TY  - JOUR
AU  - Jauković, Valentina
AU  - Krajišnik, Danina
AU  - Daković, Aleksandra
AU  - Damjanović, Ana
AU  - Krstić, Jugoslav
AU  - Stojanović, Jovica
AU  - Čalija, Bojan
PY  - 2021
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3796
AB  - The functionality of halloysite (Hal) nanotubes as drug carriers can be improved by lumen enlargement and polymer modification. This study investigates the influence of selective acid etching on Hal functionalization with cationic biopolymer chitosan. Hal was subjected to lumen etching under mild conditions, loaded under vacuum with nonsteroidal antiinflammatory drug aceclofenac, and incubated in an acidic solution of chitosan. The functionality of pristine and etched Hal before and upon polymer functionalization was assessed by ζ-potential measurements, structural characterization (FT-IR, DSC and XRPD analysis), cell viability assay, drug loading and drug release studies. Acid etching increased specific surface area, pore volume and pore size of Hal, decreased ζ-potential and facilitated binding of the cationic polymer. XRPD and DSC analysis revealed crystalline structure of etched Hal. Successful chitosan binding and drug entrapment were further confirmed by FT-IR and DSC studies. XRPD showed surface polymer binding. DSC and FT-IR analyses confirmed the presence of the entrapped drug in its crystalline form. Drug loading was increased for ≈81% by selective lumen etching. Slight decrease of drug content occurred during chitosan functionalization due to aceclofenac diffusion in the polymer solution. The drug release was more sustained from etched Hal nanocomposites (up to ≈87% for 12 h) than from pristine Hal (up to ≈97% for 12 h) due to more intensive chitosan binding. High human fibroblast survival rates upon exposure to pristine and etched Hal before and after chitosan functionalization (>90% in the concentration of 1000 μg/mL) confirmed that both lumen etching under mild conditions and polymer functionalization had no significant effect on cytocompatibility. Based on these findings, selective lumen etching in combination with polycation modification appears to be a promising approach for improvement of Hal nanotubes functionality by increasing payload, polymer binding capacity, and sustained release properties with no significant effect on their cytocompatibility.
PB  - Elsevier Ltd
T2  - Materials Science and Engineering C
T1  - Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release
VL  - 123
DO  - 10.1016/j.msec.2021.112029
ER  - 

@article{
author = "Jauković, Valentina and Krajišnik, Danina and Daković, Aleksandra and Damjanović, Ana and Krstić, Jugoslav and Stojanović, Jovica and Čalija, Bojan",
year = "2021",
abstract = "The functionality of halloysite (Hal) nanotubes as drug carriers can be improved by lumen enlargement and polymer modification. This study investigates the influence of selective acid etching on Hal functionalization with cationic biopolymer chitosan. Hal was subjected to lumen etching under mild conditions, loaded under vacuum with nonsteroidal antiinflammatory drug aceclofenac, and incubated in an acidic solution of chitosan. The functionality of pristine and etched Hal before and upon polymer functionalization was assessed by ζ-potential measurements, structural characterization (FT-IR, DSC and XRPD analysis), cell viability assay, drug loading and drug release studies. Acid etching increased specific surface area, pore volume and pore size of Hal, decreased ζ-potential and facilitated binding of the cationic polymer. XRPD and DSC analysis revealed crystalline structure of etched Hal. Successful chitosan binding and drug entrapment were further confirmed by FT-IR and DSC studies. XRPD showed surface polymer binding. DSC and FT-IR analyses confirmed the presence of the entrapped drug in its crystalline form. Drug loading was increased for ≈81% by selective lumen etching. Slight decrease of drug content occurred during chitosan functionalization due to aceclofenac diffusion in the polymer solution. The drug release was more sustained from etched Hal nanocomposites (up to ≈87% for 12 h) than from pristine Hal (up to ≈97% for 12 h) due to more intensive chitosan binding. High human fibroblast survival rates upon exposure to pristine and etched Hal before and after chitosan functionalization (>90% in the concentration of 1000 μg/mL) confirmed that both lumen etching under mild conditions and polymer functionalization had no significant effect on cytocompatibility. Based on these findings, selective lumen etching in combination with polycation modification appears to be a promising approach for improvement of Hal nanotubes functionality by increasing payload, polymer binding capacity, and sustained release properties with no significant effect on their cytocompatibility.",
publisher = "Elsevier Ltd",
journal = "Materials Science and Engineering C",
title = "Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release",
volume = "123",
doi = "10.1016/j.msec.2021.112029"
}

Jauković, V., Krajišnik, D., Daković, A., Damjanović, A., Krstić, J., Stojanović, J.,& Čalija, B.. (2021). Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release. in Materials Science and Engineering C
Elsevier Ltd., 123.
https://doi.org/10.1016/j.msec.2021.112029

Jauković V, Krajišnik D, Daković A, Damjanović A, Krstić J, Stojanović J, Čalija B. Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release. in Materials Science and Engineering C. 2021;123.
doi:10.1016/j.msec.2021.112029 .

Jauković, Valentina, Krajišnik, Danina, Daković, Aleksandra, Damjanović, Ana, Krstić, Jugoslav, Stojanović, Jovica, Čalija, Bojan, "Influence of selective acid-etching on functionality of halloysite-chitosan nanocontainers for sustained drug release" in Materials Science and Engineering C, 123 (2021),
https://doi.org/10.1016/j.msec.2021.112029 . .

TY  - JOUR
AU  - Spasojević, Milica
AU  - Daković, Aleksandra
AU  - Rottinghaus, George E.
AU  - Obradović, Milena
AU  - Krajišnik, Danina
AU  - Marković, Marija
AU  - Krstić, Jugoslav
PY  - 2021
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3795
AB  - A natural kaolin from Serbia was modified with different amounts of octadecyldimethylbenzyl ammonium (ODMBA) - (25, 50 and 90% of kaolin cation exchange capacity). Samples were denoted as OKR-25, OKR-50 and OKR-90. Several methods (FTIR spectroscopy, thermal analysis, zeta potential measurements, and N2 physisorption) were used for characterization of the organokaolinites. Adsorption of the common mycotoxins - ochratoxin A (OCHRA) and zearalenone (ZEN) by the organokaolinites was investigated at different levels of solid phase in suspension, different initial mycotoxin concentrations and different pH values. The natural kaolin was not effective in binding OCHRA or ZEN. Adsorption of both mycotoxins by organokaolinites increased with increasing amounts of solid phase as well as with increasing levels of surfactant on the kaolin surface. OCHRA and ZEN adsorption by all organokaolinites followed non-linear adsorption isotherms, at pH 3, 7 and 9. The maximum adsorption capacity for OCHRA adsorption was at pH 3 (4.8 mg/g for OKR-25, 26.7 mg/g for OKR-50 and 39.2 mg/g for OKR-90) that was calculated from the Langmuir model. Much lower OCHRA adsorption capacities were found at pH 7 and 9 (from 0.8 mg/g to 6.9 mg/g at pH 7 and from 1.1 mg/g to 4.6 mg/g at pH 9). The following adsorption capacities for ZEN were obtained from the Langmuir isotherms, at pH 3: 4.5 mg/g for OKR-25, 12.0 mg/g for OKR-50 and 13.5 mg/g for OKR-90. At pH 7, adsorption of ZEN was 5.7 mg/g for OKR-25, 15.3 mg/g for OKR-90 and 14. 4 mg/g for OKR-90. At pH 9, ZEN adsorption capacities were 2.4, 14.1 and 8.1 mg/g for OKR-25, OKR-50 and OKR-90, respectively. Thus, at the lowest amount of ODMBA at the kaolin surface, adsorption of ZEN was similar at pH 3 and 7, while a slightly lower value was obtained for its adsorption at pH 9. With increasing amounts of organic phase at the kaolin surface, the adsorption of ZEN was practically independent of pH. Adsorption of both mycotoxins was dependent on the amount of ODMBA ions at the kaolin surface as well as on their forms in solution.
PB  - Elsevier Ltd
T2  - Applied Clay Science
T1  - Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone
VL  - 205
DO  - 10.1016/j.clay.2021.106040
ER  - 

@article{
author = "Spasojević, Milica and Daković, Aleksandra and Rottinghaus, George E. and Obradović, Milena and Krajišnik, Danina and Marković, Marija and Krstić, Jugoslav",
year = "2021",
abstract = "A natural kaolin from Serbia was modified with different amounts of octadecyldimethylbenzyl ammonium (ODMBA) - (25, 50 and 90% of kaolin cation exchange capacity). Samples were denoted as OKR-25, OKR-50 and OKR-90. Several methods (FTIR spectroscopy, thermal analysis, zeta potential measurements, and N2 physisorption) were used for characterization of the organokaolinites. Adsorption of the common mycotoxins - ochratoxin A (OCHRA) and zearalenone (ZEN) by the organokaolinites was investigated at different levels of solid phase in suspension, different initial mycotoxin concentrations and different pH values. The natural kaolin was not effective in binding OCHRA or ZEN. Adsorption of both mycotoxins by organokaolinites increased with increasing amounts of solid phase as well as with increasing levels of surfactant on the kaolin surface. OCHRA and ZEN adsorption by all organokaolinites followed non-linear adsorption isotherms, at pH 3, 7 and 9. The maximum adsorption capacity for OCHRA adsorption was at pH 3 (4.8 mg/g for OKR-25, 26.7 mg/g for OKR-50 and 39.2 mg/g for OKR-90) that was calculated from the Langmuir model. Much lower OCHRA adsorption capacities were found at pH 7 and 9 (from 0.8 mg/g to 6.9 mg/g at pH 7 and from 1.1 mg/g to 4.6 mg/g at pH 9). The following adsorption capacities for ZEN were obtained from the Langmuir isotherms, at pH 3: 4.5 mg/g for OKR-25, 12.0 mg/g for OKR-50 and 13.5 mg/g for OKR-90. At pH 7, adsorption of ZEN was 5.7 mg/g for OKR-25, 15.3 mg/g for OKR-90 and 14. 4 mg/g for OKR-90. At pH 9, ZEN adsorption capacities were 2.4, 14.1 and 8.1 mg/g for OKR-25, OKR-50 and OKR-90, respectively. Thus, at the lowest amount of ODMBA at the kaolin surface, adsorption of ZEN was similar at pH 3 and 7, while a slightly lower value was obtained for its adsorption at pH 9. With increasing amounts of organic phase at the kaolin surface, the adsorption of ZEN was practically independent of pH. Adsorption of both mycotoxins was dependent on the amount of ODMBA ions at the kaolin surface as well as on their forms in solution.",
publisher = "Elsevier Ltd",
journal = "Applied Clay Science",
title = "Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone",
volume = "205",
doi = "10.1016/j.clay.2021.106040"
}

Spasojević, M., Daković, A., Rottinghaus, G. E., Obradović, M., Krajišnik, D., Marković, M.,& Krstić, J.. (2021). Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone. in Applied Clay Science
Elsevier Ltd., 205.
https://doi.org/10.1016/j.clay.2021.106040

Spasojević M, Daković A, Rottinghaus GE, Obradović M, Krajišnik D, Marković M, Krstić J. Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone. in Applied Clay Science. 2021;205.
doi:10.1016/j.clay.2021.106040 .

Spasojević, Milica, Daković, Aleksandra, Rottinghaus, George E., Obradović, Milena, Krajišnik, Danina, Marković, Marija, Krstić, Jugoslav, "Influence of surface coverage of kaolin with surfactant ions on adsorption of ochratoxin A and zearalenone" in Applied Clay Science, 205 (2021),
https://doi.org/10.1016/j.clay.2021.106040 . .

TY  - JOUR
AU  - Čalija, Bojan
AU  - Milić, Jela
AU  - Milašinović, Nikola
AU  - Daković, Aleksandra
AU  - Trifković, Kata
AU  - Stojanović, Jovica
PY  - 2020
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3478
AB  - This study was designed to investigate functionality of tetracycline‐loaded chitosan‐halloysite nanocomposite films, with focus on evaluating the influence of chitosan molar mass on films applicability for sustained local antibiotic delivery. The films were prepared by casting and solvent evaporation using low, medium, and high molar mass chitosan. SEM analysis revealed compact, nonporous and rough surface of the nanocomposite films due to the presence of halloysite agglomerates and tetracycline crystals. Increasing chitosan molar mass led to higher values of elongation at break (from 21.65 ± 2.65 to 34.48 ± 2.34%), tensile strength (from 134.8 ± 13.21 to 246.36 ± 14.69 MPa), and elastic modulus (from 633.79 ± 128.37 to 716.55 ± 60.76 MPa) of the nanocomposite films. FT‐IR, XRPD, and thermal analyses confirmed molar mass dependent chitosan‐halloysite interactions and improved thermal stability of the nanocomposite films in comparison with chitosan films. The nanocomposite films released tetracycline in a sustained manner, with the slowest release achieved from the films consisting of low molar mass chitosan. Chitosan molar mass was confirmed to be a functionality‐related characteristic of chitosan‐halloysite nanocomposite films as potential sustained‐release carriers for topical delivery of antibiotics
PB  - Wiley Periodicals, Inc.
T2  - Journal of Applied Polymer Science
T1  - Functionality of chitosan‐halloysite nanocomposite films for sustained delivery of antibiotics: The effect of chitosan molar mass
VL  - 137
IS  - 8
DO  - 10.1002/app.48406
ER  - 

@article{
author = "Čalija, Bojan and Milić, Jela and Milašinović, Nikola and Daković, Aleksandra and Trifković, Kata and Stojanović, Jovica",
year = "2020",
abstract = "This study was designed to investigate functionality of tetracycline‐loaded chitosan‐halloysite nanocomposite films, with focus on evaluating the influence of chitosan molar mass on films applicability for sustained local antibiotic delivery. The films were prepared by casting and solvent evaporation using low, medium, and high molar mass chitosan. SEM analysis revealed compact, nonporous and rough surface of the nanocomposite films due to the presence of halloysite agglomerates and tetracycline crystals. Increasing chitosan molar mass led to higher values of elongation at break (from 21.65 ± 2.65 to 34.48 ± 2.34%), tensile strength (from 134.8 ± 13.21 to 246.36 ± 14.69 MPa), and elastic modulus (from 633.79 ± 128.37 to 716.55 ± 60.76 MPa) of the nanocomposite films. FT‐IR, XRPD, and thermal analyses confirmed molar mass dependent chitosan‐halloysite interactions and improved thermal stability of the nanocomposite films in comparison with chitosan films. The nanocomposite films released tetracycline in a sustained manner, with the slowest release achieved from the films consisting of low molar mass chitosan. Chitosan molar mass was confirmed to be a functionality‐related characteristic of chitosan‐halloysite nanocomposite films as potential sustained‐release carriers for topical delivery of antibiotics",
publisher = "Wiley Periodicals, Inc.",
journal = "Journal of Applied Polymer Science",
title = "Functionality of chitosan‐halloysite nanocomposite films for sustained delivery of antibiotics: The effect of chitosan molar mass",
volume = "137",
number = "8",
doi = "10.1002/app.48406"
}

Čalija, B., Milić, J., Milašinović, N., Daković, A., Trifković, K.,& Stojanović, J.. (2020). Functionality of chitosan‐halloysite nanocomposite films for sustained delivery of antibiotics: The effect of chitosan molar mass. in Journal of Applied Polymer Science
Wiley Periodicals, Inc.., 137(8).
https://doi.org/10.1002/app.48406

Čalija B, Milić J, Milašinović N, Daković A, Trifković K, Stojanović J. Functionality of chitosan‐halloysite nanocomposite films for sustained delivery of antibiotics: The effect of chitosan molar mass. in Journal of Applied Polymer Science. 2020;137(8).
doi:10.1002/app.48406 .

Čalija, Bojan, Milić, Jela, Milašinović, Nikola, Daković, Aleksandra, Trifković, Kata, Stojanović, Jovica, "Functionality of chitosan‐halloysite nanocomposite films for sustained delivery of antibiotics: The effect of chitosan molar mass" in Journal of Applied Polymer Science, 137, no. 8 (2020),
https://doi.org/10.1002/app.48406 . .

TY  - JOUR
AU  - Čalija, Bojan
AU  - Milić, Jela
AU  - Milašinović, Nikola
AU  - Daković, Aleksandra
AU  - Trifković, Kata
AU  - Stojanović, Jovica
AU  - Krajišnik, Danina
PY  - 2020
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3476
AB  - This study was designed to investigate functionality of tetracycline‐loaded chitosan‐halloysite nanocomposite films, with focus on evaluating the influence of chitosan molar mass on films applicability for sustained local antibiotic delivery. The films were prepared by casting and solvent evaporation using low, medium, and high molar mass chitosan. SEM analysis revealed compact, nonporous and rough surface of the nanocomposite films due to the presence of halloysite agglomerates and tetracycline crystals. Increasing chitosan molar mass led to higher values of elongation at break (from 21.65 ± 2.65 to 34.48 ± 2.34%), tensile strength (from 134.8 ± 13.21 to 246.36 ± 14.69 MPa), and elastic modulus (from 633.79 ± 128.37 to 716.55 ± 60.76 MPa) of the nanocomposite films. FT‐IR, XRPD, and thermal analyses confirmed molar mass dependent chitosan‐halloysite interactions and improved thermal stability of the nanocomposite films in comparison with chitosan films. The nanocomposite films released tetracycline in a sustained manner, with the slowest release achieved from the films consisting of low molar mass chitosan. Chitosan molar mass was confirmed to be a functionality‐related characteristic of chitosan‐halloysite nanocomposite films as potential sustained‐release carriers for topical delivery of antibiotics.
PB  - Wiley Periodicals, Inc.
T2  - Journal of Applied Polymer Science
T1  - Functionality of chitosan‐halloysite nanocomposite films for sustained delivery of antibiotics: The effect of chitosan molar mass
VL  - 137
IS  - 8
DO  - 10.1002/app.48406
ER  - 

@article{
author = "Čalija, Bojan and Milić, Jela and Milašinović, Nikola and Daković, Aleksandra and Trifković, Kata and Stojanović, Jovica and Krajišnik, Danina",
year = "2020",
abstract = "This study was designed to investigate functionality of tetracycline‐loaded chitosan‐halloysite nanocomposite films, with focus on evaluating the influence of chitosan molar mass on films applicability for sustained local antibiotic delivery. The films were prepared by casting and solvent evaporation using low, medium, and high molar mass chitosan. SEM analysis revealed compact, nonporous and rough surface of the nanocomposite films due to the presence of halloysite agglomerates and tetracycline crystals. Increasing chitosan molar mass led to higher values of elongation at break (from 21.65 ± 2.65 to 34.48 ± 2.34%), tensile strength (from 134.8 ± 13.21 to 246.36 ± 14.69 MPa), and elastic modulus (from 633.79 ± 128.37 to 716.55 ± 60.76 MPa) of the nanocomposite films. FT‐IR, XRPD, and thermal analyses confirmed molar mass dependent chitosan‐halloysite interactions and improved thermal stability of the nanocomposite films in comparison with chitosan films. The nanocomposite films released tetracycline in a sustained manner, with the slowest release achieved from the films consisting of low molar mass chitosan. Chitosan molar mass was confirmed to be a functionality‐related characteristic of chitosan‐halloysite nanocomposite films as potential sustained‐release carriers for topical delivery of antibiotics.",
publisher = "Wiley Periodicals, Inc.",
journal = "Journal of Applied Polymer Science",
title = "Functionality of chitosan‐halloysite nanocomposite films for sustained delivery of antibiotics: The effect of chitosan molar mass",
volume = "137",
number = "8",
doi = "10.1002/app.48406"
}

Čalija, B., Milić, J., Milašinović, N., Daković, A., Trifković, K., Stojanović, J.,& Krajišnik, D.. (2020). Functionality of chitosan‐halloysite nanocomposite films for sustained delivery of antibiotics: The effect of chitosan molar mass. in Journal of Applied Polymer Science
Wiley Periodicals, Inc.., 137(8).
https://doi.org/10.1002/app.48406

Čalija B, Milić J, Milašinović N, Daković A, Trifković K, Stojanović J, Krajišnik D. Functionality of chitosan‐halloysite nanocomposite films for sustained delivery of antibiotics: The effect of chitosan molar mass. in Journal of Applied Polymer Science. 2020;137(8).
doi:10.1002/app.48406 .

Čalija, Bojan, Milić, Jela, Milašinović, Nikola, Daković, Aleksandra, Trifković, Kata, Stojanović, Jovica, Krajišnik, Danina, "Functionality of chitosan‐halloysite nanocomposite films for sustained delivery of antibiotics: The effect of chitosan molar mass" in Journal of Applied Polymer Science, 137, no. 8 (2020),
https://doi.org/10.1002/app.48406 . .

TY  - JOUR
AU  - Janićijević, Jelena
AU  - Milić, Jela
AU  - Čalija, Bojan
AU  - Micov, Ana
AU  - Stepanović-Petrović, Radica
AU  - Tomić, Maja
AU  - Daković, Aleksandra
AU  - Dobričić, Vladimir
AU  - Nedić-Vasiljević, Bojana
AU  - Krajišnik, Danina
PY  - 2018
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3050
AB  - Refined diatomite from the Kolubara coal basin (Serbia) was inorganically functionalized through a simple, one-pot, non-time-consuming procedure. Model drug ibuprofen was adsorbed on the functionalized diatomite under optimized conditions providing high drug Loading (similar to 201 mg g(-1)). Physicochemical characterization was performed on the starting and modified diatomite before and after ibuprofen adsorption. Dissolution testing was conducted on comprimates containing the drug adsorbed on the modified diatomite (composite) and those containing a physical mixture of the drug with the modified diatomite. The antihyperalgesic and the antiedematous activity of ibuprofen from both composites and physical mixtures were evaluated in vivo employing an inflammatory pain model in rats. Functionalization and subsequent drug adsorption had no significant effect on the diatomite ordered porous structure. Two forms of ibuprofen most likely coexisted in the adsorbed state - the acidic form and a salt/complex with aluminium. Both comprimate types showed extended ibuprofen release in vitro, but no significant influence on the duration of the ibuprofen effect was observed upon in vivo application of the composite or physical mixture. However, both the composite and the physical mixture were more effective than equivalent doses of ibuprofen in pain suppression in rats. This potentiation of the ibuprofen antihyperalgesic effect may result from the formation of the drug complex with the carrier and can be of clinical relevance.
PB  - Royal Soc Chemistry, Cambridge
T2  - Journal of Materials Chemistry B
T1  - Potentiation of the ibuprofen antihyperalgesic effect using inorganically functionalized diatomite
VL  - 6
IS  - 36
SP  - 5812
EP  - 5822
DO  - 10.1039/c8tb01376d
ER  - 

@article{
author = "Janićijević, Jelena and Milić, Jela and Čalija, Bojan and Micov, Ana and Stepanović-Petrović, Radica and Tomić, Maja and Daković, Aleksandra and Dobričić, Vladimir and Nedić-Vasiljević, Bojana and Krajišnik, Danina",
year = "2018",
abstract = "Refined diatomite from the Kolubara coal basin (Serbia) was inorganically functionalized through a simple, one-pot, non-time-consuming procedure. Model drug ibuprofen was adsorbed on the functionalized diatomite under optimized conditions providing high drug Loading (similar to 201 mg g(-1)). Physicochemical characterization was performed on the starting and modified diatomite before and after ibuprofen adsorption. Dissolution testing was conducted on comprimates containing the drug adsorbed on the modified diatomite (composite) and those containing a physical mixture of the drug with the modified diatomite. The antihyperalgesic and the antiedematous activity of ibuprofen from both composites and physical mixtures were evaluated in vivo employing an inflammatory pain model in rats. Functionalization and subsequent drug adsorption had no significant effect on the diatomite ordered porous structure. Two forms of ibuprofen most likely coexisted in the adsorbed state - the acidic form and a salt/complex with aluminium. Both comprimate types showed extended ibuprofen release in vitro, but no significant influence on the duration of the ibuprofen effect was observed upon in vivo application of the composite or physical mixture. However, both the composite and the physical mixture were more effective than equivalent doses of ibuprofen in pain suppression in rats. This potentiation of the ibuprofen antihyperalgesic effect may result from the formation of the drug complex with the carrier and can be of clinical relevance.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Journal of Materials Chemistry B",
title = "Potentiation of the ibuprofen antihyperalgesic effect using inorganically functionalized diatomite",
volume = "6",
number = "36",
pages = "5812-5822",
doi = "10.1039/c8tb01376d"
}

Janićijević, J., Milić, J., Čalija, B., Micov, A., Stepanović-Petrović, R., Tomić, M., Daković, A., Dobričić, V., Nedić-Vasiljević, B.,& Krajišnik, D.. (2018). Potentiation of the ibuprofen antihyperalgesic effect using inorganically functionalized diatomite. in Journal of Materials Chemistry B
Royal Soc Chemistry, Cambridge., 6(36), 5812-5822.
https://doi.org/10.1039/c8tb01376d

Janićijević J, Milić J, Čalija B, Micov A, Stepanović-Petrović R, Tomić M, Daković A, Dobričić V, Nedić-Vasiljević B, Krajišnik D. Potentiation of the ibuprofen antihyperalgesic effect using inorganically functionalized diatomite. in Journal of Materials Chemistry B. 2018;6(36):5812-5822.
doi:10.1039/c8tb01376d .

Janićijević, Jelena, Milić, Jela, Čalija, Bojan, Micov, Ana, Stepanović-Petrović, Radica, Tomić, Maja, Daković, Aleksandra, Dobričić, Vladimir, Nedić-Vasiljević, Bojana, Krajišnik, Danina, "Potentiation of the ibuprofen antihyperalgesic effect using inorganically functionalized diatomite" in Journal of Materials Chemistry B, 6, no. 36 (2018):5812-5822,
https://doi.org/10.1039/c8tb01376d . .

TY  - JOUR
AU  - Marković, Marija
AU  - Daković, Aleksandra
AU  - Rottinghaus, George E.
AU  - Kragović, Milan
AU  - Petković, Andela
AU  - Krajišnik, Danina
AU  - Milić, Jela
AU  - Mercurio, Mariano
AU  - de Gennaro, Bruno
PY  - 2017
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2929
AB  - In this study, organozeolites were prepared by treatment of the natural zeolites (clinoptilolite and phillipsite) with cetylpyridinium chloride (CP) equivalent to 50 and 100% of their external cation exchange capacities (ECEC). Organoclinoptilolites (ZCPs) and organophillipsites (PCPs) were characterized by FTIR spectroscopy, thermal analysis, determination of the point of zero charge and zeta potential. Adsorption of zearalenone (ZEN) by ZCPs and PCPs at pH 3 and 7 was investigated. Results showed that adsorption of ZEN increases with increasing amounts of CP at the zeolitic surfaces for both ZCPs and PCPs but the adsorption mechanism was different. Adsorption of ZEN by ZCPs followed a linear type of isotherm at pH 3 and 7 while ZEN adsorption by PCPs showed non linear (Langmuir and Freundlich) type of isotherm at both pH values. Different interactions between the ZEN molecule (or ion) and ZCPs and PCPs occurred: partition (linear isotherms) and adsorption in addition to partition (non linear isotherms), respectively. For the highest level of organic phase at the zeolitic surfaces, the maximum adsorbed amount of ZEN was 5.73 mg/g for organoclinoptilolite and 6.86 mg/g for organophillipsite at pH 3. Slightly higher adsorption: 6.98 mg/g for organoclinoptilolite and 7.54 mg/g for organophillipsite was achieved at pH 7. The results confirmed that CP ions at both zeolitic surfaces are responsible for ZEN adsorption and that organophillipsites are as effective in ZEN adsorption as organoclinoptilolites.
PB  - Elsevier Science BV, Amsterdam
T2  - Colloids and Surfaces B: Biointerfaces
T1  - Adsorption of the mycotoxin zearalenone by clinoptilolite and phillipsite zeolites treated with cetylpyridinium surfactant
VL  - 151
SP  - 324
EP  - 332
DO  - 10.1016/j.colsurfb.2016.12.033
ER  - 

@article{
author = "Marković, Marija and Daković, Aleksandra and Rottinghaus, George E. and Kragović, Milan and Petković, Andela and Krajišnik, Danina and Milić, Jela and Mercurio, Mariano and de Gennaro, Bruno",
year = "2017",
abstract = "In this study, organozeolites were prepared by treatment of the natural zeolites (clinoptilolite and phillipsite) with cetylpyridinium chloride (CP) equivalent to 50 and 100% of their external cation exchange capacities (ECEC). Organoclinoptilolites (ZCPs) and organophillipsites (PCPs) were characterized by FTIR spectroscopy, thermal analysis, determination of the point of zero charge and zeta potential. Adsorption of zearalenone (ZEN) by ZCPs and PCPs at pH 3 and 7 was investigated. Results showed that adsorption of ZEN increases with increasing amounts of CP at the zeolitic surfaces for both ZCPs and PCPs but the adsorption mechanism was different. Adsorption of ZEN by ZCPs followed a linear type of isotherm at pH 3 and 7 while ZEN adsorption by PCPs showed non linear (Langmuir and Freundlich) type of isotherm at both pH values. Different interactions between the ZEN molecule (or ion) and ZCPs and PCPs occurred: partition (linear isotherms) and adsorption in addition to partition (non linear isotherms), respectively. For the highest level of organic phase at the zeolitic surfaces, the maximum adsorbed amount of ZEN was 5.73 mg/g for organoclinoptilolite and 6.86 mg/g for organophillipsite at pH 3. Slightly higher adsorption: 6.98 mg/g for organoclinoptilolite and 7.54 mg/g for organophillipsite was achieved at pH 7. The results confirmed that CP ions at both zeolitic surfaces are responsible for ZEN adsorption and that organophillipsites are as effective in ZEN adsorption as organoclinoptilolites.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Colloids and Surfaces B: Biointerfaces",
title = "Adsorption of the mycotoxin zearalenone by clinoptilolite and phillipsite zeolites treated with cetylpyridinium surfactant",
volume = "151",
pages = "324-332",
doi = "10.1016/j.colsurfb.2016.12.033"
}

Marković, M., Daković, A., Rottinghaus, G. E., Kragović, M., Petković, A., Krajišnik, D., Milić, J., Mercurio, M.,& de Gennaro, B.. (2017). Adsorption of the mycotoxin zearalenone by clinoptilolite and phillipsite zeolites treated with cetylpyridinium surfactant. in Colloids and Surfaces B: Biointerfaces
Elsevier Science BV, Amsterdam., 151, 324-332.
https://doi.org/10.1016/j.colsurfb.2016.12.033

Marković M, Daković A, Rottinghaus GE, Kragović M, Petković A, Krajišnik D, Milić J, Mercurio M, de Gennaro B. Adsorption of the mycotoxin zearalenone by clinoptilolite and phillipsite zeolites treated with cetylpyridinium surfactant. in Colloids and Surfaces B: Biointerfaces. 2017;151:324-332.
doi:10.1016/j.colsurfb.2016.12.033 .

Marković, Marija, Daković, Aleksandra, Rottinghaus, George E., Kragović, Milan, Petković, Andela, Krajišnik, Danina, Milić, Jela, Mercurio, Mariano, de Gennaro, Bruno, "Adsorption of the mycotoxin zearalenone by clinoptilolite and phillipsite zeolites treated with cetylpyridinium surfactant" in Colloids and Surfaces B: Biointerfaces, 151 (2017):324-332,
https://doi.org/10.1016/j.colsurfb.2016.12.033 . .

TY  - JOUR
AU  - Marković, Marija
AU  - Daković, Aleksandra
AU  - Rottinghaus, George E.
AU  - Petković, Andela
AU  - Kragović, Milan
AU  - Krajišnik, Danina
AU  - Milić, Jela
PY  - 2017
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2827
AB  - Benzalkonium chloride - BC (the mixture of alkylbenzyldimethylammonium chlorides containing the alkyl groups having chain lengths of C8 to C18 and benzyl functional group) was used as a surfactant for production of organozeolites (BZs). The natural zeolite - clinoptilolite was modified with three different levels (2, 5 and 10 mmol/100 g) of BC. FTIR spectroscopy, thermal analysis, zeta potential measurements, determination of the point of zero charge and BET were used to determine the quantity of the surfactant at the zeolitic surface. The main aim was to investigate adsorption properties of BZs towards ochratoxin A (OCHRA) and zearalenone (ZEN) under in vitro conditions. Results showed that adsorption of OCHRA and ZEN by BZs increased with increasing amounts of BC at the zeolitic surface but the adsorption mechanism was different. Adsorption of OCHRA by BZs followed nonlinear isotherms at pH 3 and 7, and higher adsorption capacity was observed at pH 3. This indicates that adsorption was dependent on the form of OCHRA in solution and that the sites at the uncovered zeolitic surface together with the surfactants contributed to OCHRA adsorption. Adsorption of ZEN by BZs showed linear isotherms at pH 3 and 7 and similar amounts were adsorbed at both pH values. This suggests that adsorption is practically independent of the form of ZEN in solution and that organic cations at the zeolitic surface are the active sites relevant for ZEN adsorption.
PB  - Elsevier Science BV, Amsterdam
T2  - Colloids and Surfaces A: Physicochemical and Engineering Aspects
T1  - Ochratoxin A and zearalenone adsorption by the natural zeolite treated with benzalkonium chloride
VL  - 529
SP  - 7
EP  - 17
DO  - 10.1016/j.colsurfa.2017.05.054
ER  - 

@article{
author = "Marković, Marija and Daković, Aleksandra and Rottinghaus, George E. and Petković, Andela and Kragović, Milan and Krajišnik, Danina and Milić, Jela",
year = "2017",
abstract = "Benzalkonium chloride - BC (the mixture of alkylbenzyldimethylammonium chlorides containing the alkyl groups having chain lengths of C8 to C18 and benzyl functional group) was used as a surfactant for production of organozeolites (BZs). The natural zeolite - clinoptilolite was modified with three different levels (2, 5 and 10 mmol/100 g) of BC. FTIR spectroscopy, thermal analysis, zeta potential measurements, determination of the point of zero charge and BET were used to determine the quantity of the surfactant at the zeolitic surface. The main aim was to investigate adsorption properties of BZs towards ochratoxin A (OCHRA) and zearalenone (ZEN) under in vitro conditions. Results showed that adsorption of OCHRA and ZEN by BZs increased with increasing amounts of BC at the zeolitic surface but the adsorption mechanism was different. Adsorption of OCHRA by BZs followed nonlinear isotherms at pH 3 and 7, and higher adsorption capacity was observed at pH 3. This indicates that adsorption was dependent on the form of OCHRA in solution and that the sites at the uncovered zeolitic surface together with the surfactants contributed to OCHRA adsorption. Adsorption of ZEN by BZs showed linear isotherms at pH 3 and 7 and similar amounts were adsorbed at both pH values. This suggests that adsorption is practically independent of the form of ZEN in solution and that organic cations at the zeolitic surface are the active sites relevant for ZEN adsorption.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Colloids and Surfaces A: Physicochemical and Engineering Aspects",
title = "Ochratoxin A and zearalenone adsorption by the natural zeolite treated with benzalkonium chloride",
volume = "529",
pages = "7-17",
doi = "10.1016/j.colsurfa.2017.05.054"
}

Marković, M., Daković, A., Rottinghaus, G. E., Petković, A., Kragović, M., Krajišnik, D.,& Milić, J.. (2017). Ochratoxin A and zearalenone adsorption by the natural zeolite treated with benzalkonium chloride. in Colloids and Surfaces A: Physicochemical and Engineering Aspects
Elsevier Science BV, Amsterdam., 529, 7-17.
https://doi.org/10.1016/j.colsurfa.2017.05.054

Marković M, Daković A, Rottinghaus GE, Petković A, Kragović M, Krajišnik D, Milić J. Ochratoxin A and zearalenone adsorption by the natural zeolite treated with benzalkonium chloride. in Colloids and Surfaces A: Physicochemical and Engineering Aspects. 2017;529:7-17.
doi:10.1016/j.colsurfa.2017.05.054 .

Marković, Marija, Daković, Aleksandra, Rottinghaus, George E., Petković, Andela, Kragović, Milan, Krajišnik, Danina, Milić, Jela, "Ochratoxin A and zearalenone adsorption by the natural zeolite treated with benzalkonium chloride" in Colloids and Surfaces A: Physicochemical and Engineering Aspects, 529 (2017):7-17,
https://doi.org/10.1016/j.colsurfa.2017.05.054 . .

TY  - CHAP
AU  - Krajišnik, Danina
AU  - Daković, Aleksandra
AU  - Janićijević, Jelena
AU  - Milić, Jela
PY  - 2017
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2819
AB  - In the last two decades several representatives of natural silica-based materials (clays, zeolites, and diatomites) have emerged in biomedical applications due to their favorable physicochemical and functionality-related characteristics along with good biocompatibility. The possibility of their use in drug delivery as carriers for NSAIDs, as one of the most widely prescribed drugs, is particularly interesting since it would overcome some of the therapy-related side effects and improve patience compliance.This chapter gives an overview of natural silica-based materials' characteristics relevant for their pharmaceutical use, along with various examples of their structure modification in order to obtain materials with improved functional properties as potential drug carriers. A review on application of these materials in drug delivery of NSAIDs is presented including evaluation of techniques used for drug silica based carrier characterization in addition to investigation of their biopharmaceutical performances.
PB  - Elsevier Inc.
T2  - Microsized and Nanosized Carriers for Nonsteroidal Anti-Inflammatory Drugs: Formulation Challenges a
T1  - Natural and Modified Silica-Based Materials as Carriers for NSAIDs
SP  - 219
EP  - 258
DO  - 10.1016/B978-0-12-804017-1.00008-X
ER  - 

@inbook{
author = "Krajišnik, Danina and Daković, Aleksandra and Janićijević, Jelena and Milić, Jela",
year = "2017",
abstract = "In the last two decades several representatives of natural silica-based materials (clays, zeolites, and diatomites) have emerged in biomedical applications due to their favorable physicochemical and functionality-related characteristics along with good biocompatibility. The possibility of their use in drug delivery as carriers for NSAIDs, as one of the most widely prescribed drugs, is particularly interesting since it would overcome some of the therapy-related side effects and improve patience compliance.This chapter gives an overview of natural silica-based materials' characteristics relevant for their pharmaceutical use, along with various examples of their structure modification in order to obtain materials with improved functional properties as potential drug carriers. A review on application of these materials in drug delivery of NSAIDs is presented including evaluation of techniques used for drug silica based carrier characterization in addition to investigation of their biopharmaceutical performances.",
publisher = "Elsevier Inc.",
journal = "Microsized and Nanosized Carriers for Nonsteroidal Anti-Inflammatory Drugs: Formulation Challenges a",
booktitle = "Natural and Modified Silica-Based Materials as Carriers for NSAIDs",
pages = "219-258",
doi = "10.1016/B978-0-12-804017-1.00008-X"
}

Krajišnik, D., Daković, A., Janićijević, J.,& Milić, J.. (2017). Natural and Modified Silica-Based Materials as Carriers for NSAIDs. in Microsized and Nanosized Carriers for Nonsteroidal Anti-Inflammatory Drugs: Formulation Challenges a
Elsevier Inc.., 219-258.
https://doi.org/10.1016/B978-0-12-804017-1.00008-X

Krajišnik D, Daković A, Janićijević J, Milić J. Natural and Modified Silica-Based Materials as Carriers for NSAIDs. in Microsized and Nanosized Carriers for Nonsteroidal Anti-Inflammatory Drugs: Formulation Challenges a. 2017;:219-258.
doi:10.1016/B978-0-12-804017-1.00008-X .

Krajišnik, Danina, Daković, Aleksandra, Janićijević, Jelena, Milić, Jela, "Natural and Modified Silica-Based Materials as Carriers for NSAIDs" in Microsized and Nanosized Carriers for Nonsteroidal Anti-Inflammatory Drugs: Formulation Challenges a (2017):219-258,
https://doi.org/10.1016/B978-0-12-804017-1.00008-X . .

TY  - JOUR
AU  - Čalija, Bojan
AU  - Milić, Jela
AU  - Janićijević, Jelena
AU  - Daković, Aleksandra
AU  - Krajišnik, Danina
PY  - 2017
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2784
AB  - This study investigated the potential of halloysite nanotubes (HNTs) to improve the sustained release properties of chitosan (CS) microparticles cross-linked ionically with tripolyphosphate (TPP). Composite CS-HNTs microparticles were obtained by a simple and eco-friendly procedure based on a coaxial extrusion technique. Prior to encapsulation, a water-soluble model drug, verapamil hydrochloride (VH), was adsorbed successfully on HNTs. The microparticles were characterized by optical microscopy, Fourier transform infrared (FTIR) spectroscopy, differential thermal analysis/thermogravimetric analysis (DTA/TG) and evaluated for encapsulation efficiency and drug-release properties. The composite particles had a slightly deformed spherical shape and micrometric size with average perimeters ranging from 485.4 +/- 13.3 to 492.4 +/- 11.9 mu m. The results of FTIR spectroscopy confirmed non-covalent interactions between CS and HNTs within composite particle structures. The DTA and TG studies revealed increased thermal stability of the composite particles in comparison to the CS-TPP particles. Drug adsorption on HNTs prior to encapsulation led to an increase in encapsulation efficiency from 19.6 +/- 2.9 to 84.3 +/- 1.9%. In contrast to the rapid release of encapsulated model drug from CS-TPP microparticles, the composite CS-HNTs microparticles released drug in a sustained manner, showing the best fit to the Bhaskar model. The results presented here imply that HNTs could be used to improve morphology, encapsulation efficiency and sustained drug-release properties of CS microparticles cross-linked ionically with TPP.
PB  - Mineralogical Soc, Twickenham
T2  - Clay Minerals
T1  - Ionically cross-linked chitosan-halloysite composite microparticles for sustained drug release
VL  - 52
IS  - 4
SP  - 413
EP  - 426
DO  - 10.1180/claymin.2017.052.04.01
ER  - 

@article{
author = "Čalija, Bojan and Milić, Jela and Janićijević, Jelena and Daković, Aleksandra and Krajišnik, Danina",
year = "2017",
abstract = "This study investigated the potential of halloysite nanotubes (HNTs) to improve the sustained release properties of chitosan (CS) microparticles cross-linked ionically with tripolyphosphate (TPP). Composite CS-HNTs microparticles were obtained by a simple and eco-friendly procedure based on a coaxial extrusion technique. Prior to encapsulation, a water-soluble model drug, verapamil hydrochloride (VH), was adsorbed successfully on HNTs. The microparticles were characterized by optical microscopy, Fourier transform infrared (FTIR) spectroscopy, differential thermal analysis/thermogravimetric analysis (DTA/TG) and evaluated for encapsulation efficiency and drug-release properties. The composite particles had a slightly deformed spherical shape and micrometric size with average perimeters ranging from 485.4 +/- 13.3 to 492.4 +/- 11.9 mu m. The results of FTIR spectroscopy confirmed non-covalent interactions between CS and HNTs within composite particle structures. The DTA and TG studies revealed increased thermal stability of the composite particles in comparison to the CS-TPP particles. Drug adsorption on HNTs prior to encapsulation led to an increase in encapsulation efficiency from 19.6 +/- 2.9 to 84.3 +/- 1.9%. In contrast to the rapid release of encapsulated model drug from CS-TPP microparticles, the composite CS-HNTs microparticles released drug in a sustained manner, showing the best fit to the Bhaskar model. The results presented here imply that HNTs could be used to improve morphology, encapsulation efficiency and sustained drug-release properties of CS microparticles cross-linked ionically with TPP.",
publisher = "Mineralogical Soc, Twickenham",
journal = "Clay Minerals",
title = "Ionically cross-linked chitosan-halloysite composite microparticles for sustained drug release",
volume = "52",
number = "4",
pages = "413-426",
doi = "10.1180/claymin.2017.052.04.01"
}

Čalija, B., Milić, J., Janićijević, J., Daković, A.,& Krajišnik, D.. (2017). Ionically cross-linked chitosan-halloysite composite microparticles for sustained drug release. in Clay Minerals
Mineralogical Soc, Twickenham., 52(4), 413-426.
https://doi.org/10.1180/claymin.2017.052.04.01

Čalija B, Milić J, Janićijević J, Daković A, Krajišnik D. Ionically cross-linked chitosan-halloysite composite microparticles for sustained drug release. in Clay Minerals. 2017;52(4):413-426.
doi:10.1180/claymin.2017.052.04.01 .

Čalija, Bojan, Milić, Jela, Janićijević, Jelena, Daković, Aleksandra, Krajišnik, Danina, "Ionically cross-linked chitosan-halloysite composite microparticles for sustained drug release" in Clay Minerals, 52, no. 4 (2017):413-426,
https://doi.org/10.1180/claymin.2017.052.04.01 . .

TY  - JOUR
AU  - Marković, Marija
AU  - Daković, Aleksandra
AU  - Krajišnik, Danina
AU  - Kragović, Milan
AU  - Milić, Jela
AU  - Langella, Alessio
AU  - de Gennaro, Bruno
AU  - Cappelletti, Piergiulio
AU  - Mercurio, Mariano
PY  - 2016
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2696
AB  - Incorporation of diclofenac sodium into phillipsite modified with cetylpyridinium chloride (CP-Cl) or hexadecyltrimethyl ammonium bromide (HDTMA-Br) was followed by batch equilibrium adsorption studies in buffer solution at pH = 7.4. Characteristics of the drug/surfactant/zeolite complexes were investigated by UV/VIS, FTIR spectroscopy, thermal (DTA/TG) analysis and-potential measurements. The obtained data confirmed that organic cations at phillipsite surface were responsible for incorporation of diclofenac sodium. Diclofenac sodium incorporated amounts increased with increasing the amount of each surfactant as well as with increasing the initial drug concentration. Langmuir model was the best model for fitting the experimental data of diclofenac adsorption on surfactant/phillipsite composites, suggesting complex adsorption mechanism. The physico-chemical properties of surfactant/phillipsite composites and enhanced incorporation of diclofenac sodium suggests that it might be possible to use these materials as drug carriers.
PB  - Elsevier Science BV, Amsterdam
T2  - Journal of Molecular Liquids
T1  - Evaluation of the surfactant/phillipsite composites as carriers for diclofenac sodium
VL  - 222
SP  - 711
EP  - 716
DO  - 10.1016/j.molliq.2016.07.127
ER  - 

@article{
author = "Marković, Marija and Daković, Aleksandra and Krajišnik, Danina and Kragović, Milan and Milić, Jela and Langella, Alessio and de Gennaro, Bruno and Cappelletti, Piergiulio and Mercurio, Mariano",
year = "2016",
abstract = "Incorporation of diclofenac sodium into phillipsite modified with cetylpyridinium chloride (CP-Cl) or hexadecyltrimethyl ammonium bromide (HDTMA-Br) was followed by batch equilibrium adsorption studies in buffer solution at pH = 7.4. Characteristics of the drug/surfactant/zeolite complexes were investigated by UV/VIS, FTIR spectroscopy, thermal (DTA/TG) analysis and-potential measurements. The obtained data confirmed that organic cations at phillipsite surface were responsible for incorporation of diclofenac sodium. Diclofenac sodium incorporated amounts increased with increasing the amount of each surfactant as well as with increasing the initial drug concentration. Langmuir model was the best model for fitting the experimental data of diclofenac adsorption on surfactant/phillipsite composites, suggesting complex adsorption mechanism. The physico-chemical properties of surfactant/phillipsite composites and enhanced incorporation of diclofenac sodium suggests that it might be possible to use these materials as drug carriers.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Journal of Molecular Liquids",
title = "Evaluation of the surfactant/phillipsite composites as carriers for diclofenac sodium",
volume = "222",
pages = "711-716",
doi = "10.1016/j.molliq.2016.07.127"
}

Marković, M., Daković, A., Krajišnik, D., Kragović, M., Milić, J., Langella, A., de Gennaro, B., Cappelletti, P.,& Mercurio, M.. (2016). Evaluation of the surfactant/phillipsite composites as carriers for diclofenac sodium. in Journal of Molecular Liquids
Elsevier Science BV, Amsterdam., 222, 711-716.
https://doi.org/10.1016/j.molliq.2016.07.127

Marković M, Daković A, Krajišnik D, Kragović M, Milić J, Langella A, de Gennaro B, Cappelletti P, Mercurio M. Evaluation of the surfactant/phillipsite composites as carriers for diclofenac sodium. in Journal of Molecular Liquids. 2016;222:711-716.
doi:10.1016/j.molliq.2016.07.127 .

Marković, Marija, Daković, Aleksandra, Krajišnik, Danina, Kragović, Milan, Milić, Jela, Langella, Alessio, de Gennaro, Bruno, Cappelletti, Piergiulio, Mercurio, Mariano, "Evaluation of the surfactant/phillipsite composites as carriers for diclofenac sodium" in Journal of Molecular Liquids, 222 (2016):711-716,
https://doi.org/10.1016/j.molliq.2016.07.127 . .

TY  - JOUR
AU  - Krajišnik, Danina
AU  - Daković, Aleksandra
AU  - Malenović, Anđelija
AU  - Kragović, Milan
AU  - Milić, Jela
PY  - 2015
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2327
AB  - The sorption of ibuprofen by modified natural zeolite composites at three concentration levels (10, 20 and 30 mmol/100 g) of cationic surfactants - benzalkonium chloride and cetylpyridinium chloride, in a buffer solution (pH 7.4), was studied. Characterization of the composites before and after ibuprofen sorption was performed by drug sorption and isotherm studies, zeta potential and Fourier Transform infrared spectroscopic analysis. The biopharmaceutical performance of cationic surfactant-modified zeolites as drug formulation excipients was evaluated by in vitro dissolution experiments from the composites with medium surfactant contents. The drug sorption was influenced by the surfactant type and amount used for the zeolite modification. Prolonged drug release over a period of 8 h (up to similar to 40%) was achieved with both groups of samples. The kinetic analysis showed that the drug release profiles were best fitted with the Higuchi and the Bhaskar models, indicating a combination of drug diffusion and ion exchange as the predominant release mechanisms.
PB  - Mineralogical Soc, Twickenham
T2  - Clay Minerals
T1  - Ibuprofen sorption and release by modified natural zeolites as prospective drug carriers
VL  - 50
IS  - 1
SP  - 11
EP  - 22
DO  - 10.1180/claymin.2015.050.1.02
ER  - 

@article{
author = "Krajišnik, Danina and Daković, Aleksandra and Malenović, Anđelija and Kragović, Milan and Milić, Jela",
year = "2015",
abstract = "The sorption of ibuprofen by modified natural zeolite composites at three concentration levels (10, 20 and 30 mmol/100 g) of cationic surfactants - benzalkonium chloride and cetylpyridinium chloride, in a buffer solution (pH 7.4), was studied. Characterization of the composites before and after ibuprofen sorption was performed by drug sorption and isotherm studies, zeta potential and Fourier Transform infrared spectroscopic analysis. The biopharmaceutical performance of cationic surfactant-modified zeolites as drug formulation excipients was evaluated by in vitro dissolution experiments from the composites with medium surfactant contents. The drug sorption was influenced by the surfactant type and amount used for the zeolite modification. Prolonged drug release over a period of 8 h (up to similar to 40%) was achieved with both groups of samples. The kinetic analysis showed that the drug release profiles were best fitted with the Higuchi and the Bhaskar models, indicating a combination of drug diffusion and ion exchange as the predominant release mechanisms.",
publisher = "Mineralogical Soc, Twickenham",
journal = "Clay Minerals",
title = "Ibuprofen sorption and release by modified natural zeolites as prospective drug carriers",
volume = "50",
number = "1",
pages = "11-22",
doi = "10.1180/claymin.2015.050.1.02"
}

Krajišnik, D., Daković, A., Malenović, A., Kragović, M.,& Milić, J.. (2015). Ibuprofen sorption and release by modified natural zeolites as prospective drug carriers. in Clay Minerals
Mineralogical Soc, Twickenham., 50(1), 11-22.
https://doi.org/10.1180/claymin.2015.050.1.02

Krajišnik D, Daković A, Malenović A, Kragović M, Milić J. Ibuprofen sorption and release by modified natural zeolites as prospective drug carriers. in Clay Minerals. 2015;50(1):11-22.
doi:10.1180/claymin.2015.050.1.02 .

Krajišnik, Danina, Daković, Aleksandra, Malenović, Anđelija, Kragović, Milan, Milić, Jela, "Ibuprofen sorption and release by modified natural zeolites as prospective drug carriers" in Clay Minerals, 50, no. 1 (2015):11-22,
https://doi.org/10.1180/claymin.2015.050.1.02 . .

TY  - JOUR
AU  - Janićijević, Jelena
AU  - Krajišnik, Danina
AU  - Čalija, Bojan
AU  - Nedić-Vasiljević, Bojana
AU  - Dobričić, Vladimir
AU  - Daković, Aleksandra
AU  - Antonijević, Milan D.
AU  - Milić, Jela
PY  - 2015
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2360
AB  - Diatomite makes a promising candidate for a drug carrier because of its high porosity, large surface area, modifiable surface chemistry and biocompatibility. Herein, refined diatomite from Kolubara coal basin, which complied with the pharmacopoeial requirements for heavy metals content and microbiological quality, was used as a starting material. Inorganic modification of the starting material was performed through a simple, one-step procedure. Significant increase in adsorbent loading with diclofenac sodium (DS) was achieved after the modification process (similar to 373 mg/g) which enabled the preparation of comprimates containing therapeutic dose of the adsorbed drug. Adsorption of DS onto modified diatomite resulted in the alteration of the drug's XRD pattern and FTIR spectrum. In vitro drug release studies in phosphate buffer pH 7.5 demonstrated prolonged DS release over 8 h from comprimates containing DS adsorbed on modified diatomite (up to 37% after 8 h) and those containing physical mixture of the same composition (up to 45% after 8 h). The results of in vivo toxicity testing on mice pointed on potential safety of both unmodified (starting) and modified diatomite. All these findings favor the application of diatomite as a potential functional drug carrier.
PB  - Elsevier Science BV, Amsterdam
T2  - International Journal of Pharmaceutics
T1  - Modified local diatomite as potential functional drug carrier-A model study for diclofenac sodium
VL  - 496
IS  - 2
SP  - 466
EP  - 474
DO  - 10.1016/j.ijpharm.2015.10.047
ER  - 

@article{
author = "Janićijević, Jelena and Krajišnik, Danina and Čalija, Bojan and Nedić-Vasiljević, Bojana and Dobričić, Vladimir and Daković, Aleksandra and Antonijević, Milan D. and Milić, Jela",
year = "2015",
abstract = "Diatomite makes a promising candidate for a drug carrier because of its high porosity, large surface area, modifiable surface chemistry and biocompatibility. Herein, refined diatomite from Kolubara coal basin, which complied with the pharmacopoeial requirements for heavy metals content and microbiological quality, was used as a starting material. Inorganic modification of the starting material was performed through a simple, one-step procedure. Significant increase in adsorbent loading with diclofenac sodium (DS) was achieved after the modification process (similar to 373 mg/g) which enabled the preparation of comprimates containing therapeutic dose of the adsorbed drug. Adsorption of DS onto modified diatomite resulted in the alteration of the drug's XRD pattern and FTIR spectrum. In vitro drug release studies in phosphate buffer pH 7.5 demonstrated prolonged DS release over 8 h from comprimates containing DS adsorbed on modified diatomite (up to 37% after 8 h) and those containing physical mixture of the same composition (up to 45% after 8 h). The results of in vivo toxicity testing on mice pointed on potential safety of both unmodified (starting) and modified diatomite. All these findings favor the application of diatomite as a potential functional drug carrier.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "International Journal of Pharmaceutics",
title = "Modified local diatomite as potential functional drug carrier-A model study for diclofenac sodium",
volume = "496",
number = "2",
pages = "466-474",
doi = "10.1016/j.ijpharm.2015.10.047"
}

Janićijević, J., Krajišnik, D., Čalija, B., Nedić-Vasiljević, B., Dobričić, V., Daković, A., Antonijević, M. D.,& Milić, J.. (2015). Modified local diatomite as potential functional drug carrier-A model study for diclofenac sodium. in International Journal of Pharmaceutics
Elsevier Science BV, Amsterdam., 496(2), 466-474.
https://doi.org/10.1016/j.ijpharm.2015.10.047

Janićijević J, Krajišnik D, Čalija B, Nedić-Vasiljević B, Dobričić V, Daković A, Antonijević MD, Milić J. Modified local diatomite as potential functional drug carrier-A model study for diclofenac sodium. in International Journal of Pharmaceutics. 2015;496(2):466-474.
doi:10.1016/j.ijpharm.2015.10.047 .

Janićijević, Jelena, Krajišnik, Danina, Čalija, Bojan, Nedić-Vasiljević, Bojana, Dobričić, Vladimir, Daković, Aleksandra, Antonijević, Milan D., Milić, Jela, "Modified local diatomite as potential functional drug carrier-A model study for diclofenac sodium" in International Journal of Pharmaceutics, 496, no. 2 (2015):466-474,
https://doi.org/10.1016/j.ijpharm.2015.10.047 . .

TY  - CHAP
AU  - Milić, Jela
AU  - Daković, Aleksandra
AU  - Krajišnik, Danina
AU  - Rottinghaus, George E.
PY  - 2014
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2259
AB  - Natural and synthetic zeolites have emerged as potential materials for biomedical application in recent years. Zeolites are hydrated microporous tektoaluminosilicates consisting of three-dimensional frameworks of SiO4 and AlO4 tetrahedra linked through shared oxygen atoms. Clinoptilolite, a mineral from the heulandite group of zeolites, ((Na,K)6(Al6Si3O)O72·nH2O), is the most abundant sedimentary zeolite in nature. In this chapter an overview of surface modifi cation of clinoptilolite by interaction with cationic surfactants is given alongside with the methods used for characterization of the surfactant modifi ed zeolites (organozeolites/composites). Diff erent organozeolites were tested under conditions for adsorption of several mycotoxins commonly found in animal feed. Study of in vitro surfactant desorption in vitro followed by in vivo acute toxicity testing was used to demonstrate the nontoxic nature of these improved mineral materials. Functionality related characteristics of modifi ed natural zeolites were analyzed for investigation of their potential use as pharmaceutical excipients for modifi ed release of active pharmaceutical ingredients.
PB  - Wiley Blackwell
T2  - Advanced Healthcare Materials
T1  - Modified Natural Zeolites-Functional Characterization and Biomedical Application
SP  - 359
EP  - 403
DO  - 10.1002/9781118774205.ch10
ER  - 

@inbook{
author = "Milić, Jela and Daković, Aleksandra and Krajišnik, Danina and Rottinghaus, George E.",
year = "2014",
abstract = "Natural and synthetic zeolites have emerged as potential materials for biomedical application in recent years. Zeolites are hydrated microporous tektoaluminosilicates consisting of three-dimensional frameworks of SiO4 and AlO4 tetrahedra linked through shared oxygen atoms. Clinoptilolite, a mineral from the heulandite group of zeolites, ((Na,K)6(Al6Si3O)O72·nH2O), is the most abundant sedimentary zeolite in nature. In this chapter an overview of surface modifi cation of clinoptilolite by interaction with cationic surfactants is given alongside with the methods used for characterization of the surfactant modifi ed zeolites (organozeolites/composites). Diff erent organozeolites were tested under conditions for adsorption of several mycotoxins commonly found in animal feed. Study of in vitro surfactant desorption in vitro followed by in vivo acute toxicity testing was used to demonstrate the nontoxic nature of these improved mineral materials. Functionality related characteristics of modifi ed natural zeolites were analyzed for investigation of their potential use as pharmaceutical excipients for modifi ed release of active pharmaceutical ingredients.",
publisher = "Wiley Blackwell",
journal = "Advanced Healthcare Materials",
booktitle = "Modified Natural Zeolites-Functional Characterization and Biomedical Application",
pages = "359-403",
doi = "10.1002/9781118774205.ch10"
}

Milić, J., Daković, A., Krajišnik, D.,& Rottinghaus, G. E.. (2014). Modified Natural Zeolites-Functional Characterization and Biomedical Application. in Advanced Healthcare Materials
Wiley Blackwell., 359-403.
https://doi.org/10.1002/9781118774205.ch10

Milić J, Daković A, Krajišnik D, Rottinghaus GE. Modified Natural Zeolites-Functional Characterization and Biomedical Application. in Advanced Healthcare Materials. 2014;:359-403.
doi:10.1002/9781118774205.ch10 .

Milić, Jela, Daković, Aleksandra, Krajišnik, Danina, Rottinghaus, George E., "Modified Natural Zeolites-Functional Characterization and Biomedical Application" in Advanced Healthcare Materials (2014):359-403,
https://doi.org/10.1002/9781118774205.ch10 . .

TY  - JOUR
AU  - Janićijević, Jelena
AU  - Krajišnik, Danina
AU  - Čalija, Bojan
AU  - Dobričić, Vladimir
AU  - Daković, Aleksandra
AU  - Krstić, Jugoslav
AU  - Marković, Marija
AU  - Milić, Jela
PY  - 2014
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2101
AB  - Inorganic modification of diatomite was performed with the precipitation product of partially neutralized aluminum sulfate solution at three different mass ratios. The starting and the modified diatomites were characterized by SEM-EDS, FTIR, thermal analysis and zeta potential measurements and evaluated for drug loading capacity in adsorption batch experiments using diclofenac sodium (DS) as a model drug. In vitro drug release studies were performed in phosphate buffer pH 6.8 from comprimates containing: the drug adsorbed onto the selected modified diatomite sample (DAMD), physical mixture of the drug with the selected modified diatomite sample (PMDMD) and physical mixture of the drug with the starting diatomite (PMDD). In vivo acute toxicity testing of the modified diatomite samples was performed on mice. High adsorbent loading of the selected modified diatomite sample (similar to 250 mg/g in 2 h) enabled the preparation of comprimates containing adsorbed DS in the amount near to its therapeutic dose. Drug release studies demonstrated prolonged release of DS over a period of 8 h from both DAMD comprimates (18% after 8 h) and PMDMD comprimates (45% after 8 h). The release kinetics for DAMD and PMDMD comprimates fitted well with Korsmeyer-Peppas and Bhaskar models, indicating that the release mechanism was a combination of non-Fickian diffusion and ion exchange process.
PB  - Elsevier Science BV, Amsterdam
T2  - Materials Science & Engineering C: Materials for Biological Applications
T1  - Inorganically modified diatomite as a potential prolonged-release drug carrier
VL  - 42
SP  - 412
EP  - 420
DO  - 10.1016/j.msec.2014.05.052
ER  - 

@article{
author = "Janićijević, Jelena and Krajišnik, Danina and Čalija, Bojan and Dobričić, Vladimir and Daković, Aleksandra and Krstić, Jugoslav and Marković, Marija and Milić, Jela",
year = "2014",
abstract = "Inorganic modification of diatomite was performed with the precipitation product of partially neutralized aluminum sulfate solution at three different mass ratios. The starting and the modified diatomites were characterized by SEM-EDS, FTIR, thermal analysis and zeta potential measurements and evaluated for drug loading capacity in adsorption batch experiments using diclofenac sodium (DS) as a model drug. In vitro drug release studies were performed in phosphate buffer pH 6.8 from comprimates containing: the drug adsorbed onto the selected modified diatomite sample (DAMD), physical mixture of the drug with the selected modified diatomite sample (PMDMD) and physical mixture of the drug with the starting diatomite (PMDD). In vivo acute toxicity testing of the modified diatomite samples was performed on mice. High adsorbent loading of the selected modified diatomite sample (similar to 250 mg/g in 2 h) enabled the preparation of comprimates containing adsorbed DS in the amount near to its therapeutic dose. Drug release studies demonstrated prolonged release of DS over a period of 8 h from both DAMD comprimates (18% after 8 h) and PMDMD comprimates (45% after 8 h). The release kinetics for DAMD and PMDMD comprimates fitted well with Korsmeyer-Peppas and Bhaskar models, indicating that the release mechanism was a combination of non-Fickian diffusion and ion exchange process.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Materials Science & Engineering C: Materials for Biological Applications",
title = "Inorganically modified diatomite as a potential prolonged-release drug carrier",
volume = "42",
pages = "412-420",
doi = "10.1016/j.msec.2014.05.052"
}

Janićijević, J., Krajišnik, D., Čalija, B., Dobričić, V., Daković, A., Krstić, J., Marković, M.,& Milić, J.. (2014). Inorganically modified diatomite as a potential prolonged-release drug carrier. in Materials Science & Engineering C: Materials for Biological Applications
Elsevier Science BV, Amsterdam., 42, 412-420.
https://doi.org/10.1016/j.msec.2014.05.052

Janićijević J, Krajišnik D, Čalija B, Dobričić V, Daković A, Krstić J, Marković M, Milić J. Inorganically modified diatomite as a potential prolonged-release drug carrier. in Materials Science & Engineering C: Materials for Biological Applications. 2014;42:412-420.
doi:10.1016/j.msec.2014.05.052 .

Janićijević, Jelena, Krajišnik, Danina, Čalija, Bojan, Dobričić, Vladimir, Daković, Aleksandra, Krstić, Jugoslav, Marković, Marija, Milić, Jela, "Inorganically modified diatomite as a potential prolonged-release drug carrier" in Materials Science & Engineering C: Materials for Biological Applications, 42 (2014):412-420,
https://doi.org/10.1016/j.msec.2014.05.052 . .

TY  - JOUR
AU  - Krajišnik, Danina
AU  - Daković, Aleksandra
AU  - Malenović, Anđelija
AU  - Đekić, Ljiljana
AU  - Kragović, Milan
AU  - Dobričić, Vladimir
AU  - Milić, Jela
PY  - 2013
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1959
AB  - In this paper, investigations of zeolite - cationic surfactant - drug composites as drug carriers were performed. For that purpose, after adsorption of the model drug - diclofenac sodium (DS) onto composites obtained by the modification of natural zeolite (NZ) with cetylpyridinium chloride (CPC) at the three different levels, i.e., 10, 20 and 30 mmol/100 g (ZCPC-10, ZCPC-20 and ZCPC-30, respectively), the release of the drug, at pH 6.8, was studied. The results of DS release from ZCPC-10 composite (DS/ZCPC-10) were compared with the DS release from corresponding physical mixture, as well as from physical mixture of NZ and DS. Characterization of the composites after adsorption of DS and the physical mixtures was realized by zeta potential measurements and by thermal analysis. Results showed that the prolonged release of DS from all the three composites, as well as from physical mixture containing ZCPC-10 and DS was achieved over a period of 8 h. The drug release from both DS/ZCPC-10 (max 55%) and corresponding physical mixture (max 38%) was remarkably lower than that from the physical mixture of NZ and DS (max 85%). The kinetic analysis for all the three composites, as well as for the physical mixture of ZCPC-10 and DS, showed that drug release profiles were best fitted with the Korsmeyer-Peppas and Bhaskar release models, indicating a combination of drug diffusion and ion exchange as the predominant release mechanisms in the dissolution medium.
PB  - Elsevier Science BV, Amsterdam
T2  - Microporous and Mesoporous Materials
T1  - An investigation of diclofenac sodium release from cetylpyridinium chloride-modified natural zeolite as a pharmaceutical excipient
VL  - 167
SP  - 94
EP  - 101
DO  - 10.1016/j.micromeso.2012.03.033
ER  - 

@article{
author = "Krajišnik, Danina and Daković, Aleksandra and Malenović, Anđelija and Đekić, Ljiljana and Kragović, Milan and Dobričić, Vladimir and Milić, Jela",
year = "2013",
abstract = "In this paper, investigations of zeolite - cationic surfactant - drug composites as drug carriers were performed. For that purpose, after adsorption of the model drug - diclofenac sodium (DS) onto composites obtained by the modification of natural zeolite (NZ) with cetylpyridinium chloride (CPC) at the three different levels, i.e., 10, 20 and 30 mmol/100 g (ZCPC-10, ZCPC-20 and ZCPC-30, respectively), the release of the drug, at pH 6.8, was studied. The results of DS release from ZCPC-10 composite (DS/ZCPC-10) were compared with the DS release from corresponding physical mixture, as well as from physical mixture of NZ and DS. Characterization of the composites after adsorption of DS and the physical mixtures was realized by zeta potential measurements and by thermal analysis. Results showed that the prolonged release of DS from all the three composites, as well as from physical mixture containing ZCPC-10 and DS was achieved over a period of 8 h. The drug release from both DS/ZCPC-10 (max 55%) and corresponding physical mixture (max 38%) was remarkably lower than that from the physical mixture of NZ and DS (max 85%). The kinetic analysis for all the three composites, as well as for the physical mixture of ZCPC-10 and DS, showed that drug release profiles were best fitted with the Korsmeyer-Peppas and Bhaskar release models, indicating a combination of drug diffusion and ion exchange as the predominant release mechanisms in the dissolution medium.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Microporous and Mesoporous Materials",
title = "An investigation of diclofenac sodium release from cetylpyridinium chloride-modified natural zeolite as a pharmaceutical excipient",
volume = "167",
pages = "94-101",
doi = "10.1016/j.micromeso.2012.03.033"
}

Krajišnik, D., Daković, A., Malenović, A., Đekić, L., Kragović, M., Dobričić, V.,& Milić, J.. (2013). An investigation of diclofenac sodium release from cetylpyridinium chloride-modified natural zeolite as a pharmaceutical excipient. in Microporous and Mesoporous Materials
Elsevier Science BV, Amsterdam., 167, 94-101.
https://doi.org/10.1016/j.micromeso.2012.03.033

Krajišnik D, Daković A, Malenović A, Đekić L, Kragović M, Dobričić V, Milić J. An investigation of diclofenac sodium release from cetylpyridinium chloride-modified natural zeolite as a pharmaceutical excipient. in Microporous and Mesoporous Materials. 2013;167:94-101.
doi:10.1016/j.micromeso.2012.03.033 .

Krajišnik, Danina, Daković, Aleksandra, Malenović, Anđelija, Đekić, Ljiljana, Kragović, Milan, Dobričić, Vladimir, Milić, Jela, "An investigation of diclofenac sodium release from cetylpyridinium chloride-modified natural zeolite as a pharmaceutical excipient" in Microporous and Mesoporous Materials, 167 (2013):94-101,
https://doi.org/10.1016/j.micromeso.2012.03.033 . .

TY  - JOUR
AU  - Krajišnik, Danina
AU  - Daković, Aleksandra
AU  - Malenović, Anđelija
AU  - Milojević-Rakić, Maja
AU  - Dondur, Vera
AU  - Radulović, Željka
AU  - Milić, Jela
PY  - 2013
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1905
AB  - Results on adsorption of diclofenac sodium (DS) by modified natural zeolite composites at three levels (10,20 and 30 mmol/100 g) of cationic surfactant-hexadecyltrimethylammonium bromide (HB), in a buffer solution, were compared. Characterization of composites before and after drug adsorption was performed by determination of electrokinetic mobility, FTIR and thermal analysis. The results indicated interactions between drug and carriers. The pharmaceutical performance of cationic surfactant-modified zeolites as drug formulation excipients was evaluated by in vitro dissolution experiments. The results were compared with the drug release from corresponding physical mixtures. Prolonged drug release over a period of 8 h (up to 30%) was achieved with both groups of samples. Furthermore, DS release reached up to 85% from physical mixtures containing drug amount closer to a therapeutic dose.
PB  - Elsevier Science BV, Amsterdam
T2  - Applied Clay Science
T1  - Investigation of adsorption and release of diclofenac sodium by modified zeolites composites
SP  - 322
EP  - 326
DO  - 10.1016/j.clay.2013.08.011
ER  - 

@article{
author = "Krajišnik, Danina and Daković, Aleksandra and Malenović, Anđelija and Milojević-Rakić, Maja and Dondur, Vera and Radulović, Željka and Milić, Jela",
year = "2013",
abstract = "Results on adsorption of diclofenac sodium (DS) by modified natural zeolite composites at three levels (10,20 and 30 mmol/100 g) of cationic surfactant-hexadecyltrimethylammonium bromide (HB), in a buffer solution, were compared. Characterization of composites before and after drug adsorption was performed by determination of electrokinetic mobility, FTIR and thermal analysis. The results indicated interactions between drug and carriers. The pharmaceutical performance of cationic surfactant-modified zeolites as drug formulation excipients was evaluated by in vitro dissolution experiments. The results were compared with the drug release from corresponding physical mixtures. Prolonged drug release over a period of 8 h (up to 30%) was achieved with both groups of samples. Furthermore, DS release reached up to 85% from physical mixtures containing drug amount closer to a therapeutic dose.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Applied Clay Science",
title = "Investigation of adsorption and release of diclofenac sodium by modified zeolites composites",
pages = "322-326",
doi = "10.1016/j.clay.2013.08.011"
}

Krajišnik, D., Daković, A., Malenović, A., Milojević-Rakić, M., Dondur, V., Radulović, Ž.,& Milić, J.. (2013). Investigation of adsorption and release of diclofenac sodium by modified zeolites composites. in Applied Clay Science
Elsevier Science BV, Amsterdam., 322-326.
https://doi.org/10.1016/j.clay.2013.08.011

Krajišnik D, Daković A, Malenović A, Milojević-Rakić M, Dondur V, Radulović Ž, Milić J. Investigation of adsorption and release of diclofenac sodium by modified zeolites composites. in Applied Clay Science. 2013;:322-326.
doi:10.1016/j.clay.2013.08.011 .

Krajišnik, Danina, Daković, Aleksandra, Malenović, Anđelija, Milojević-Rakić, Maja, Dondur, Vera, Radulović, Željka, Milić, Jela, "Investigation of adsorption and release of diclofenac sodium by modified zeolites composites" in Applied Clay Science (2013):322-326,
https://doi.org/10.1016/j.clay.2013.08.011 . .

TY  - JOUR
AU  - Krajišnik, Danina
AU  - Daković, Aleksandra
AU  - Milojević, Maja
AU  - Malenović, Anđelija
AU  - Kragović, Milan
AU  - Bajuk-Bogdanović, Danica
AU  - Dondur, Vera
AU  - Milić, Jela
PY  - 2011
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1541
AB  - In this study an investigation of a model drug sorption onto cationic surfactant-modified natural zeolites as a drug formulation excipient was performed. Natural zeolite was modified with cetylpyridinium chloride in amounts equivalent to 100, 200 and 300% of its external cation-exchange capacity. The starting material and obtained organozeolites were characterized by Fourier transform infrared spectroscopy, zeta potential measurements and thermal analysis. In vitro sorption of diclofenac sodium as a model drug was studied for all surfactant/zeolite composites by means of sorption isotherm measurements in aqueous solutions (pH 7.4). The modified zeolites with three levels of surfactant coverage within the short activation time were prepared. Zeta potential measurements and thermal analysis showed that when the surfactant loading level was equal to external cation-exchange value, almost monolayer of organic phase were present at the zeolitic surface while higher amounts of surfactant produced less extended bilayers, ordered bilayers or admicelles at the zeolitic surface. Modified zeolites, obtained in this manner, were effective in diclofenac sodium sorption and the organic phase derived from adsorbed cetylpyridinium chloride was the primary sorption phase for the model drug. The Langmuir isotherm was found to describe the equilibrium sorption data well over the entire concentration range. The separate contributions of the adsorption and partition to the total sorption of DS were analyzed mathematically. Results revealed that that adsorption and partitioning of the model drug take place simultaneously.
PB  - Elsevier Science BV, Amsterdam
T2  - Colloids and Surfaces B: Biointerfaces
T1  - Properties of diclofenac sodium sorption onto natural zeolite modified with cetylpyridinium chloride
VL  - 83
IS  - 1
SP  - 165
EP  - 172
DO  - 10.1016/j.colsurfb.2010.11.024
ER  - 

@article{
author = "Krajišnik, Danina and Daković, Aleksandra and Milojević, Maja and Malenović, Anđelija and Kragović, Milan and Bajuk-Bogdanović, Danica and Dondur, Vera and Milić, Jela",
year = "2011",
abstract = "In this study an investigation of a model drug sorption onto cationic surfactant-modified natural zeolites as a drug formulation excipient was performed. Natural zeolite was modified with cetylpyridinium chloride in amounts equivalent to 100, 200 and 300% of its external cation-exchange capacity. The starting material and obtained organozeolites were characterized by Fourier transform infrared spectroscopy, zeta potential measurements and thermal analysis. In vitro sorption of diclofenac sodium as a model drug was studied for all surfactant/zeolite composites by means of sorption isotherm measurements in aqueous solutions (pH 7.4). The modified zeolites with three levels of surfactant coverage within the short activation time were prepared. Zeta potential measurements and thermal analysis showed that when the surfactant loading level was equal to external cation-exchange value, almost monolayer of organic phase were present at the zeolitic surface while higher amounts of surfactant produced less extended bilayers, ordered bilayers or admicelles at the zeolitic surface. Modified zeolites, obtained in this manner, were effective in diclofenac sodium sorption and the organic phase derived from adsorbed cetylpyridinium chloride was the primary sorption phase for the model drug. The Langmuir isotherm was found to describe the equilibrium sorption data well over the entire concentration range. The separate contributions of the adsorption and partition to the total sorption of DS were analyzed mathematically. Results revealed that that adsorption and partitioning of the model drug take place simultaneously.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Colloids and Surfaces B: Biointerfaces",
title = "Properties of diclofenac sodium sorption onto natural zeolite modified with cetylpyridinium chloride",
volume = "83",
number = "1",
pages = "165-172",
doi = "10.1016/j.colsurfb.2010.11.024"
}

Krajišnik, D., Daković, A., Milojević, M., Malenović, A., Kragović, M., Bajuk-Bogdanović, D., Dondur, V.,& Milić, J.. (2011). Properties of diclofenac sodium sorption onto natural zeolite modified with cetylpyridinium chloride. in Colloids and Surfaces B: Biointerfaces
Elsevier Science BV, Amsterdam., 83(1), 165-172.
https://doi.org/10.1016/j.colsurfb.2010.11.024

Krajišnik D, Daković A, Milojević M, Malenović A, Kragović M, Bajuk-Bogdanović D, Dondur V, Milić J. Properties of diclofenac sodium sorption onto natural zeolite modified with cetylpyridinium chloride. in Colloids and Surfaces B: Biointerfaces. 2011;83(1):165-172.
doi:10.1016/j.colsurfb.2010.11.024 .

Krajišnik, Danina, Daković, Aleksandra, Milojević, Maja, Malenović, Anđelija, Kragović, Milan, Bajuk-Bogdanović, Danica, Dondur, Vera, Milić, Jela, "Properties of diclofenac sodium sorption onto natural zeolite modified with cetylpyridinium chloride" in Colloids and Surfaces B: Biointerfaces, 83, no. 1 (2011):165-172,
https://doi.org/10.1016/j.colsurfb.2010.11.024 . .

TY  - JOUR
AU  - Krajišnik, Danina
AU  - Milojević, Maja
AU  - Malenović, Anđelija
AU  - Daković, Aleksandra
AU  - Ibrić, Svetlana
AU  - Savić, Snežana
AU  - Dondur, Vera
AU  - Matijasević, Srdan
AU  - Radulović, Aleksandra
AU  - Daniels, Rolf
AU  - Milić, Jela
PY  - 2010
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1364
AB  - Context: In this study an investigation of cationic surfactants-modified natural zeolites as drug formulation excipient was performed. Objective: The aim of this work was to carry out a study of the purified natural zeolitic tuff with high amount of clinoptilolite as a potential carrier for molecules of pharmaceutical interest. Materials and methods: Two cationic surfactants (benzalkonium chloride and hexadecyltrimethylammonium bromide) were used for modification of the zeolitic surface in two levels (equal to and twice as external cation-exchange capacity of the zeolitic tuff). Prepared samples were characterized by Fourier transform infrared spectroscopy, thermogravimetric, high-performance liquid chromatography analysis, and powder flow determination. Different surfactant/zeolite composites were used for additional investigation of three model drugs: diclofenac diethylamine, diclofenac sodium, and ibuprofen by means of adsorption isotherm measurements in aqueous solutions. Results: The modified zeolites with two levels of surfactant coverage within the short activation time were prepared. Determination of flow properties showed that modification of zeolitic surface reflected on powder flow characteristics. Investigation of the model drugs adsorption on the obtained composites revealed that a variation between adsorption levels was influenced by the surfactant type and the amount present at the surface of the composites. Discussion and conclusion: In vitro release profiles of the drugs from the zeolite-surfactant-drug composites revealed that sustained drug release could be attained over a period of 8 hours. The presented results for drug uptake by surfactant-zeolite composites and the afterward drug release demonstrated the potential use of investigated modified natural zeolite as excipients for advanced excipients in drug formulations.
PB  - Informa Healthcare, London
T2  - Drug Development and Industrial Pharmacy
T1  - Cationic surfactants-modified natural zeolites: improvement of the excipients functionality
VL  - 36
IS  - 10
SP  - 1215
EP  - 1224
DO  - 10.3109/03639041003695121
ER  - 

@article{
author = "Krajišnik, Danina and Milojević, Maja and Malenović, Anđelija and Daković, Aleksandra and Ibrić, Svetlana and Savić, Snežana and Dondur, Vera and Matijasević, Srdan and Radulović, Aleksandra and Daniels, Rolf and Milić, Jela",
year = "2010",
abstract = "Context: In this study an investigation of cationic surfactants-modified natural zeolites as drug formulation excipient was performed. Objective: The aim of this work was to carry out a study of the purified natural zeolitic tuff with high amount of clinoptilolite as a potential carrier for molecules of pharmaceutical interest. Materials and methods: Two cationic surfactants (benzalkonium chloride and hexadecyltrimethylammonium bromide) were used for modification of the zeolitic surface in two levels (equal to and twice as external cation-exchange capacity of the zeolitic tuff). Prepared samples were characterized by Fourier transform infrared spectroscopy, thermogravimetric, high-performance liquid chromatography analysis, and powder flow determination. Different surfactant/zeolite composites were used for additional investigation of three model drugs: diclofenac diethylamine, diclofenac sodium, and ibuprofen by means of adsorption isotherm measurements in aqueous solutions. Results: The modified zeolites with two levels of surfactant coverage within the short activation time were prepared. Determination of flow properties showed that modification of zeolitic surface reflected on powder flow characteristics. Investigation of the model drugs adsorption on the obtained composites revealed that a variation between adsorption levels was influenced by the surfactant type and the amount present at the surface of the composites. Discussion and conclusion: In vitro release profiles of the drugs from the zeolite-surfactant-drug composites revealed that sustained drug release could be attained over a period of 8 hours. The presented results for drug uptake by surfactant-zeolite composites and the afterward drug release demonstrated the potential use of investigated modified natural zeolite as excipients for advanced excipients in drug formulations.",
publisher = "Informa Healthcare, London",
journal = "Drug Development and Industrial Pharmacy",
title = "Cationic surfactants-modified natural zeolites: improvement of the excipients functionality",
volume = "36",
number = "10",
pages = "1215-1224",
doi = "10.3109/03639041003695121"
}

Krajišnik, D., Milojević, M., Malenović, A., Daković, A., Ibrić, S., Savić, S., Dondur, V., Matijasević, S., Radulović, A., Daniels, R.,& Milić, J.. (2010). Cationic surfactants-modified natural zeolites: improvement of the excipients functionality. in Drug Development and Industrial Pharmacy
Informa Healthcare, London., 36(10), 1215-1224.
https://doi.org/10.3109/03639041003695121

Krajišnik D, Milojević M, Malenović A, Daković A, Ibrić S, Savić S, Dondur V, Matijasević S, Radulović A, Daniels R, Milić J. Cationic surfactants-modified natural zeolites: improvement of the excipients functionality. in Drug Development and Industrial Pharmacy. 2010;36(10):1215-1224.
doi:10.3109/03639041003695121 .

Krajišnik, Danina, Milojević, Maja, Malenović, Anđelija, Daković, Aleksandra, Ibrić, Svetlana, Savić, Snežana, Dondur, Vera, Matijasević, Srdan, Radulović, Aleksandra, Daniels, Rolf, Milić, Jela, "Cationic surfactants-modified natural zeolites: improvement of the excipients functionality" in Drug Development and Industrial Pharmacy, 36, no. 10 (2010):1215-1224,
https://doi.org/10.3109/03639041003695121 . .