Milinković Budinčić, Jelena

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orcid::0000-0002-1113-4456
  • Milinković Budinčić, Jelena (7)
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Author's Bibliography

Characterization of escin-loaded chitosan/xanthan-based polyelectrolyte complexes for pH-driven oral drug delivery

Ćirić, Ana; Milinković Budinčić, Jelena; Petrović, Lidija; Đekić, Ljiljana

(University of Novi Sad, Faculty of Technology Novi Sad, 2022)

TY  - CONF
AU  - Ćirić, Ana
AU  - Milinković Budinčić, Jelena
AU  - Petrović, Lidija
AU  - Đekić, Ljiljana
PY  - 2022
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/5364
AB  - Escin is a vasoprotective drug with pH-dependent aqueous solubility, used in the form of gastro-resistant tablets due to its ability to irritate the gastric mucosa. ...
PB  - University of Novi Sad, Faculty of Technology Novi Sad
C3  - 2nd International Conference on Advanced Production and Processing 20th-22nd October 2022 Novi Sad, Serbia (Book of Abstracts)
T1  - Characterization of escin-loaded chitosan/xanthan-based polyelectrolyte complexes for pH-driven oral drug delivery
SP  - 148
EP  - 148
UR  - https://hdl.handle.net/21.15107/rcub_farfar_5364
ER  - 
@conference{
author = "Ćirić, Ana and Milinković Budinčić, Jelena and Petrović, Lidija and Đekić, Ljiljana",
year = "2022",
abstract = "Escin is a vasoprotective drug with pH-dependent aqueous solubility, used in the form of gastro-resistant tablets due to its ability to irritate the gastric mucosa. ...",
publisher = "University of Novi Sad, Faculty of Technology Novi Sad",
journal = "2nd International Conference on Advanced Production and Processing 20th-22nd October 2022 Novi Sad, Serbia (Book of Abstracts)",
title = "Characterization of escin-loaded chitosan/xanthan-based polyelectrolyte complexes for pH-driven oral drug delivery",
pages = "148-148",
url = "https://hdl.handle.net/21.15107/rcub_farfar_5364"
}
Ćirić, A., Milinković Budinčić, J., Petrović, L.,& Đekić, L.. (2022). Characterization of escin-loaded chitosan/xanthan-based polyelectrolyte complexes for pH-driven oral drug delivery. in 2nd International Conference on Advanced Production and Processing 20th-22nd October 2022 Novi Sad, Serbia (Book of Abstracts)
University of Novi Sad, Faculty of Technology Novi Sad., 148-148.
https://hdl.handle.net/21.15107/rcub_farfar_5364
Ćirić A, Milinković Budinčić J, Petrović L, Đekić L. Characterization of escin-loaded chitosan/xanthan-based polyelectrolyte complexes for pH-driven oral drug delivery. in 2nd International Conference on Advanced Production and Processing 20th-22nd October 2022 Novi Sad, Serbia (Book of Abstracts). 2022;:148-148.
https://hdl.handle.net/21.15107/rcub_farfar_5364 .
Ćirić, Ana, Milinković Budinčić, Jelena, Petrović, Lidija, Đekić, Ljiljana, "Characterization of escin-loaded chitosan/xanthan-based polyelectrolyte complexes for pH-driven oral drug delivery" in 2nd International Conference on Advanced Production and Processing 20th-22nd October 2022 Novi Sad, Serbia (Book of Abstracts) (2022):148-148,
https://hdl.handle.net/21.15107/rcub_farfar_5364 .

Interactions in escin-loaded chitosan/xanthan-based polyelectrolyte complexes: evaluation of drug content and drying method impact

Ćirić, Ana; Milinković Budinčić, Jelena; Petrović, Lidija; Đekić, Ljiljana

(University of Novi Sad, Faculty of Technology Novi Sad, 2022)

TY  - CONF
AU  - Ćirić, Ana
AU  - Milinković Budinčić, Jelena
AU  - Petrović, Lidija
AU  - Đekić, Ljiljana
PY  - 2022
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/5365
AB  - Escin is an amphiphilic drug with weakly acidic properties, a saponoside with aglycone and glycone parts in the structure. It has high and pH-dependent solubility in water. ...
PB  - University of Novi Sad, Faculty of Technology Novi Sad
C3  - 2nd International Conference on Advanced Production and Processing 20th-22nd October 2022 Novi Sad, Serbia (Book of Abstracts)
T1  - Interactions in escin-loaded chitosan/xanthan-based polyelectrolyte complexes: evaluation of drug content and drying method impact
SP  - 167
EP  - 167
UR  - https://hdl.handle.net/21.15107/rcub_farfar_5365
ER  - 
@conference{
author = "Ćirić, Ana and Milinković Budinčić, Jelena and Petrović, Lidija and Đekić, Ljiljana",
year = "2022",
abstract = "Escin is an amphiphilic drug with weakly acidic properties, a saponoside with aglycone and glycone parts in the structure. It has high and pH-dependent solubility in water. ...",
publisher = "University of Novi Sad, Faculty of Technology Novi Sad",
journal = "2nd International Conference on Advanced Production and Processing 20th-22nd October 2022 Novi Sad, Serbia (Book of Abstracts)",
title = "Interactions in escin-loaded chitosan/xanthan-based polyelectrolyte complexes: evaluation of drug content and drying method impact",
pages = "167-167",
url = "https://hdl.handle.net/21.15107/rcub_farfar_5365"
}
Ćirić, A., Milinković Budinčić, J., Petrović, L.,& Đekić, L.. (2022). Interactions in escin-loaded chitosan/xanthan-based polyelectrolyte complexes: evaluation of drug content and drying method impact. in 2nd International Conference on Advanced Production and Processing 20th-22nd October 2022 Novi Sad, Serbia (Book of Abstracts)
University of Novi Sad, Faculty of Technology Novi Sad., 167-167.
https://hdl.handle.net/21.15107/rcub_farfar_5365
Ćirić A, Milinković Budinčić J, Petrović L, Đekić L. Interactions in escin-loaded chitosan/xanthan-based polyelectrolyte complexes: evaluation of drug content and drying method impact. in 2nd International Conference on Advanced Production and Processing 20th-22nd October 2022 Novi Sad, Serbia (Book of Abstracts). 2022;:167-167.
https://hdl.handle.net/21.15107/rcub_farfar_5365 .
Ćirić, Ana, Milinković Budinčić, Jelena, Petrović, Lidija, Đekić, Ljiljana, "Interactions in escin-loaded chitosan/xanthan-based polyelectrolyte complexes: evaluation of drug content and drying method impact" in 2nd International Conference on Advanced Production and Processing 20th-22nd October 2022 Novi Sad, Serbia (Book of Abstracts) (2022):167-167,
https://hdl.handle.net/21.15107/rcub_farfar_5365 .

Evaluation of chitosan/xanthan gum polyelectrolyte complexes potential for pH-dependent oral delivery of escin

Ćirić, Ana; Milinković Budinčić, Jelena; Dobričić, Vladimir; Rmandić, Milena; Barudžija, Tanja; Malenović, Anđelija; Petrović, Lidija; Đekić, Ljiljana

(Elsevier B.V., 2022)

TY  - JOUR
AU  - Ćirić, Ana
AU  - Milinković Budinčić, Jelena
AU  - Dobričić, Vladimir
AU  - Rmandić, Milena
AU  - Barudžija, Tanja
AU  - Malenović, Anđelija
AU  - Petrović, Lidija
AU  - Đekić, Ljiljana
PY  - 2022
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4272
AB  - Escin is an amphiphilic and weakly acidic drug that oral administration may lead to the irritation of gastric mucosa. The entrapment of escin into chitosan (CH)/xanthan gum (XG)-based polyelectrolyte complexes (PECs) can facilitate controlled drug release which may be beneficial for the reduction of its side effects. This study aimed to investigate the influence of escin content and drying method on the formation, physicochemical, and controlled, pH-dependent drug release properties of CH/XG-based PECs. Measurements of transmittance, con- ductivity, and rheological characterization confirmed the formation of CH/XG-based PECs with escin entrapped at escin-to-polymers mass ratios 1:1, 1:2, and 1:4. Ambient-dried PECs had higher yield, entrapment efficiency, and escin content in comparison with spray-dried ones. FT-IR spectra confirmed the interactions between CH, XG, and escin, which were stronger in ambient-dried PECs. PXRD and DSC analyses showed the amorphous escin character in all dry PECs, regardless of the drying method. The most promising controlled and pH-dependent in vitro escin release was from the ambient-dried PEC at the escin-to-polymers mass ratio of 1:1. For that reason and due to the highest yield and entrapment efficiency, this carrier has the potential to prevent the irritation of gastric mucosa after oral administration of escin.
PB  - Elsevier B.V.
T2  - International Journal of Biological Macromolecules
T1  - Evaluation of chitosan/xanthan gum polyelectrolyte complexes potential for pH-dependent oral delivery of escin
VL  - 221
SP  - 48
EP  - 60
DO  - 10.1016/j.ijbiomac.2022.08.190
ER  - 
@article{
author = "Ćirić, Ana and Milinković Budinčić, Jelena and Dobričić, Vladimir and Rmandić, Milena and Barudžija, Tanja and Malenović, Anđelija and Petrović, Lidija and Đekić, Ljiljana",
year = "2022",
abstract = "Escin is an amphiphilic and weakly acidic drug that oral administration may lead to the irritation of gastric mucosa. The entrapment of escin into chitosan (CH)/xanthan gum (XG)-based polyelectrolyte complexes (PECs) can facilitate controlled drug release which may be beneficial for the reduction of its side effects. This study aimed to investigate the influence of escin content and drying method on the formation, physicochemical, and controlled, pH-dependent drug release properties of CH/XG-based PECs. Measurements of transmittance, con- ductivity, and rheological characterization confirmed the formation of CH/XG-based PECs with escin entrapped at escin-to-polymers mass ratios 1:1, 1:2, and 1:4. Ambient-dried PECs had higher yield, entrapment efficiency, and escin content in comparison with spray-dried ones. FT-IR spectra confirmed the interactions between CH, XG, and escin, which were stronger in ambient-dried PECs. PXRD and DSC analyses showed the amorphous escin character in all dry PECs, regardless of the drying method. The most promising controlled and pH-dependent in vitro escin release was from the ambient-dried PEC at the escin-to-polymers mass ratio of 1:1. For that reason and due to the highest yield and entrapment efficiency, this carrier has the potential to prevent the irritation of gastric mucosa after oral administration of escin.",
publisher = "Elsevier B.V.",
journal = "International Journal of Biological Macromolecules",
title = "Evaluation of chitosan/xanthan gum polyelectrolyte complexes potential for pH-dependent oral delivery of escin",
volume = "221",
pages = "48-60",
doi = "10.1016/j.ijbiomac.2022.08.190"
}
Ćirić, A., Milinković Budinčić, J., Dobričić, V., Rmandić, M., Barudžija, T., Malenović, A., Petrović, L.,& Đekić, L.. (2022). Evaluation of chitosan/xanthan gum polyelectrolyte complexes potential for pH-dependent oral delivery of escin. in International Journal of Biological Macromolecules
Elsevier B.V.., 221, 48-60.
https://doi.org/10.1016/j.ijbiomac.2022.08.190
Ćirić A, Milinković Budinčić J, Dobričić V, Rmandić M, Barudžija T, Malenović A, Petrović L, Đekić L. Evaluation of chitosan/xanthan gum polyelectrolyte complexes potential for pH-dependent oral delivery of escin. in International Journal of Biological Macromolecules. 2022;221:48-60.
doi:10.1016/j.ijbiomac.2022.08.190 .
Ćirić, Ana, Milinković Budinčić, Jelena, Dobričić, Vladimir, Rmandić, Milena, Barudžija, Tanja, Malenović, Anđelija, Petrović, Lidija, Đekić, Ljiljana, "Evaluation of chitosan/xanthan gum polyelectrolyte complexes potential for pH-dependent oral delivery of escin" in International Journal of Biological Macromolecules, 221 (2022):48-60,
https://doi.org/10.1016/j.ijbiomac.2022.08.190 . .
5
4

Influence of spray-drying process on properties of chitosan/xanthan gum polyelectrolyte complexes as carriers for oral delivery of ibuprofen

Ćirić, Ana; Milinković Budinčić, Jelena; Medarević, Đorđe; Dobričić, Vladimir; Rmandić, Milena; Barudžija, Tanja; Malenović, Anđelija; Petrović, Lidija; Đekić, Ljiljana

(Savez farmaceutskih udruženja Srbije, 2022)

TY  - JOUR
AU  - Ćirić, Ana
AU  - Milinković Budinčić, Jelena
AU  - Medarević, Đorđe
AU  - Dobričić, Vladimir
AU  - Rmandić, Milena
AU  - Barudžija, Tanja
AU  - Malenović, Anđelija
AU  - Petrović, Lidija
AU  - Đekić, Ljiljana
PY  - 2022
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4179
AB  - Polyelectrolyte complexes (PECs) are attractive carriers with recognized potential to
enhance oral delivery of poorly soluble high-dosed low-molecular-weight drugs. The formulation
of solid oral dosage forms requires the drying of PECs, which may affect their physicochemical
and biopharmaceutical properties. The aim of this study was to investigate the effect of spray-
drying on the properties of ibuprofen-loaded chitosan/xanthan gum PECs and to assess the drug
release kinetics from such PECs filled into hard capsules in comparison with corresponding PECs
which are dried under ambient conditions. The yield, ibuprofen content, entrapment efficiency,
and residual moisture content of spray-dried PECs were lower than those of ambient-dried PECs.
Better flowability of spray-dried PECs was attributed to the almost spherical particle shape,
shown by scanning electron microscopy. DSC and PXRD analysis confirmed the amorphization
of ibuprofen during spray-drying. All the investigated PECs, obtained by drying under ambient
conditions as well as by spray-drying, had high rehydration capacity both in 0.1 M hydrochloric
acid (pH 1.2) and phosphate buffer pH 7.4. In vitro ibuprofen release from dried PECs was
controlled during 12 h with the release of approximately 30% of entrapped ibuprofen. Spray-dried
PECs provided better control of ibuprofen diffusion from the carrier compared to the ambient-
dried ones.
AB  - Polielektrolitni kompleksi (PEK) su atraktivni nosači sa potencijalom poboljšanja peroralne isporuke slabo rastvorljivih visokodoziranih lekovitih supstanci niske molekulske mase. Formulisanje čvrstih oralnih farmaceutskih oblika na bazi PEK zahteva njihovo sušenje, što može uticati na fizičko-hemijska i biofarmaceutska svojstva kompleksa. Cilj ove studije bio je da se ispita efekat sušenja raspršivanjem na svojstva PEK hitozana i ksantan gume u koje je inkorporiran ibuprofen i da se proceni kinetika oslobađanja lekovite supstance iz takvih PEK napunjenih u tvrde kapsule u poređenju sa odgovarajućim PEK koji su sušeni pod ambijentalnim uslovima. Prinos, sadržaj ibuprofena, efikasnost inkorporiranja i sadržaj vlage PEK sušenih raspršivanjem bili su niži nego kod PEK sušenih pod ambijentalnim uslovima. Bolja protočnost PEK osušenih raspršivanjem je posledica skoro sfernog oblika čestica, što je pokazano skenirajućom elektronskom mikroskopijom. Rezultati DSC i PXRD analiza su potvrdili amorfizaciju ibuprofena tokom sušenja raspršivanjem. Ispitivani PEK osušeni pod različitim uslovima imali su visoku sposobnost rehidratacije u 0,1 M hlorovodoničnoj kiselini (pH 1,2) i fosfatnom puferu pH 7,4. In vitro oslobađanje ibuprofena iz osušenih PEK bilo je kontrolisano tokom 12 h uz oslobađanje približno 30% inkorporiranog ibuprofena. PEK sušeni raspršivanjem obezbedili su bolju kontrolu difuzije ibuprofena iz nosača u poređenju sa onima sušenim pod ambijentalnim uslovima.
PB  - Savez farmaceutskih udruženja Srbije
T2  - Arhiv za farmaciju
T1  - Influence of spray-drying process on properties of chitosan/xanthan gum polyelectrolyte complexes as carriers for oral delivery of ibuprofen
T1  - Uticaj postupka sušenja raspršivanjem na svojstva polielektrolitnih kompleksa hitozana i ksantan gume kao nosača za peroralnu isporuku ibuprofena
VL  - 72
IS  - 1
SP  - 36
EP  - 60
DO  - 10.5937/arhfarm72-35133
ER  - 
@article{
author = "Ćirić, Ana and Milinković Budinčić, Jelena and Medarević, Đorđe and Dobričić, Vladimir and Rmandić, Milena and Barudžija, Tanja and Malenović, Anđelija and Petrović, Lidija and Đekić, Ljiljana",
year = "2022",
abstract = "Polyelectrolyte complexes (PECs) are attractive carriers with recognized potential to
enhance oral delivery of poorly soluble high-dosed low-molecular-weight drugs. The formulation
of solid oral dosage forms requires the drying of PECs, which may affect their physicochemical
and biopharmaceutical properties. The aim of this study was to investigate the effect of spray-
drying on the properties of ibuprofen-loaded chitosan/xanthan gum PECs and to assess the drug
release kinetics from such PECs filled into hard capsules in comparison with corresponding PECs
which are dried under ambient conditions. The yield, ibuprofen content, entrapment efficiency,
and residual moisture content of spray-dried PECs were lower than those of ambient-dried PECs.
Better flowability of spray-dried PECs was attributed to the almost spherical particle shape,
shown by scanning electron microscopy. DSC and PXRD analysis confirmed the amorphization
of ibuprofen during spray-drying. All the investigated PECs, obtained by drying under ambient
conditions as well as by spray-drying, had high rehydration capacity both in 0.1 M hydrochloric
acid (pH 1.2) and phosphate buffer pH 7.4. In vitro ibuprofen release from dried PECs was
controlled during 12 h with the release of approximately 30% of entrapped ibuprofen. Spray-dried
PECs provided better control of ibuprofen diffusion from the carrier compared to the ambient-
dried ones., Polielektrolitni kompleksi (PEK) su atraktivni nosači sa potencijalom poboljšanja peroralne isporuke slabo rastvorljivih visokodoziranih lekovitih supstanci niske molekulske mase. Formulisanje čvrstih oralnih farmaceutskih oblika na bazi PEK zahteva njihovo sušenje, što može uticati na fizičko-hemijska i biofarmaceutska svojstva kompleksa. Cilj ove studije bio je da se ispita efekat sušenja raspršivanjem na svojstva PEK hitozana i ksantan gume u koje je inkorporiran ibuprofen i da se proceni kinetika oslobađanja lekovite supstance iz takvih PEK napunjenih u tvrde kapsule u poređenju sa odgovarajućim PEK koji su sušeni pod ambijentalnim uslovima. Prinos, sadržaj ibuprofena, efikasnost inkorporiranja i sadržaj vlage PEK sušenih raspršivanjem bili su niži nego kod PEK sušenih pod ambijentalnim uslovima. Bolja protočnost PEK osušenih raspršivanjem je posledica skoro sfernog oblika čestica, što je pokazano skenirajućom elektronskom mikroskopijom. Rezultati DSC i PXRD analiza su potvrdili amorfizaciju ibuprofena tokom sušenja raspršivanjem. Ispitivani PEK osušeni pod različitim uslovima imali su visoku sposobnost rehidratacije u 0,1 M hlorovodoničnoj kiselini (pH 1,2) i fosfatnom puferu pH 7,4. In vitro oslobađanje ibuprofena iz osušenih PEK bilo je kontrolisano tokom 12 h uz oslobađanje približno 30% inkorporiranog ibuprofena. PEK sušeni raspršivanjem obezbedili su bolju kontrolu difuzije ibuprofena iz nosača u poređenju sa onima sušenim pod ambijentalnim uslovima.",
publisher = "Savez farmaceutskih udruženja Srbije",
journal = "Arhiv za farmaciju",
title = "Influence of spray-drying process on properties of chitosan/xanthan gum polyelectrolyte complexes as carriers for oral delivery of ibuprofen, Uticaj postupka sušenja raspršivanjem na svojstva polielektrolitnih kompleksa hitozana i ksantan gume kao nosača za peroralnu isporuku ibuprofena",
volume = "72",
number = "1",
pages = "36-60",
doi = "10.5937/arhfarm72-35133"
}
Ćirić, A., Milinković Budinčić, J., Medarević, Đ., Dobričić, V., Rmandić, M., Barudžija, T., Malenović, A., Petrović, L.,& Đekić, L.. (2022). Influence of spray-drying process on properties of chitosan/xanthan gum polyelectrolyte complexes as carriers for oral delivery of ibuprofen. in Arhiv za farmaciju
Savez farmaceutskih udruženja Srbije., 72(1), 36-60.
https://doi.org/10.5937/arhfarm72-35133
Ćirić A, Milinković Budinčić J, Medarević Đ, Dobričić V, Rmandić M, Barudžija T, Malenović A, Petrović L, Đekić L. Influence of spray-drying process on properties of chitosan/xanthan gum polyelectrolyte complexes as carriers for oral delivery of ibuprofen. in Arhiv za farmaciju. 2022;72(1):36-60.
doi:10.5937/arhfarm72-35133 .
Ćirić, Ana, Milinković Budinčić, Jelena, Medarević, Đorđe, Dobričić, Vladimir, Rmandić, Milena, Barudžija, Tanja, Malenović, Anđelija, Petrović, Lidija, Đekić, Ljiljana, "Influence of spray-drying process on properties of chitosan/xanthan gum polyelectrolyte complexes as carriers for oral delivery of ibuprofen" in Arhiv za farmaciju, 72, no. 1 (2022):36-60,
https://doi.org/10.5937/arhfarm72-35133 . .
3
3

Chitosan/Sodium Dodecyl Sulfate Complexes for Microencapsulation of Vitamin E and Its Release Profile— Understanding the Effect of Anionic Surfactant

Milinković Budinčić, Jelena; Petrović, Lidija; Đekić, Ljiljana; Aleksić, Milijana; Fraj, Jadranka; Popović, Senka; Bučko, Sandra; Katona, Jaroslav; Spasojević, Ljiljana; Škrbić, Jelena; Malenović, Anđelija

(MDPI, 2021)

TY  - JOUR
AU  - Milinković Budinčić, Jelena
AU  - Petrović, Lidija
AU  - Đekić, Ljiljana
AU  - Aleksić, Milijana
AU  - Fraj, Jadranka
AU  - Popović, Senka
AU  - Bučko, Sandra
AU  - Katona, Jaroslav
AU  - Spasojević, Ljiljana
AU  - Škrbić, Jelena
AU  - Malenović, Anđelija
PY  - 2021
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/4021
AB  - Microencapsulation of bioactive substances is a common strategy for their protection and release rate control. The use of chitosan (Ch) is particularly promising due to its abundance, biocompatibility, and interaction with anionic surfactants to form complexes of different characteristics with relevance for use in microcapsule wall design. In this study, Ch/sodium dodecyl sulfate (SDS) microcapsules, without and with cross-linking agent (formaldehyde (FA) or glutaraldehyde (GA)), were obtained by the spray drying of vitamin E loaded oil-in-water emulsion. All of the microcapsules had good stability during the drying process. Depending on the composition, their product yield, moisture content, and encapsulation efficiency varied between 11–34%, 1.14–1.62%, and 94–126%, respectively. SEM and FTIR analysis results indicate that SDS as well as cross-linkers significantly affected the microcapsule wall properties. The profiles of in vitro vitamin E release from the investigated microcapsules fit with the Korsmeyer-Peppas model (r2 > 0.9). The chemical structure of the anionic surfactant was found to have a significant effect on the vitamin E release mechanism. Ch/SDS coacervates may build a microcapsule wall without toxic crosslinkers. This enabled the combined diffusion/swelling based release mechanism of the encapsulated lipophilic substance, which can be considered favorable for utilization in food and pharmaceutical products.
PB  - MDPI
T2  - Pharmaceuticals
T1  - Chitosan/Sodium Dodecyl Sulfate Complexes for Microencapsulation of Vitamin E and Its Release Profile— Understanding the Effect of Anionic Surfactant
VL  - 15
IS  - 1
DO  - 10.3390/ph15010054
ER  - 
@article{
author = "Milinković Budinčić, Jelena and Petrović, Lidija and Đekić, Ljiljana and Aleksić, Milijana and Fraj, Jadranka and Popović, Senka and Bučko, Sandra and Katona, Jaroslav and Spasojević, Ljiljana and Škrbić, Jelena and Malenović, Anđelija",
year = "2021",
abstract = "Microencapsulation of bioactive substances is a common strategy for their protection and release rate control. The use of chitosan (Ch) is particularly promising due to its abundance, biocompatibility, and interaction with anionic surfactants to form complexes of different characteristics with relevance for use in microcapsule wall design. In this study, Ch/sodium dodecyl sulfate (SDS) microcapsules, without and with cross-linking agent (formaldehyde (FA) or glutaraldehyde (GA)), were obtained by the spray drying of vitamin E loaded oil-in-water emulsion. All of the microcapsules had good stability during the drying process. Depending on the composition, their product yield, moisture content, and encapsulation efficiency varied between 11–34%, 1.14–1.62%, and 94–126%, respectively. SEM and FTIR analysis results indicate that SDS as well as cross-linkers significantly affected the microcapsule wall properties. The profiles of in vitro vitamin E release from the investigated microcapsules fit with the Korsmeyer-Peppas model (r2 > 0.9). The chemical structure of the anionic surfactant was found to have a significant effect on the vitamin E release mechanism. Ch/SDS coacervates may build a microcapsule wall without toxic crosslinkers. This enabled the combined diffusion/swelling based release mechanism of the encapsulated lipophilic substance, which can be considered favorable for utilization in food and pharmaceutical products.",
publisher = "MDPI",
journal = "Pharmaceuticals",
title = "Chitosan/Sodium Dodecyl Sulfate Complexes for Microencapsulation of Vitamin E and Its Release Profile— Understanding the Effect of Anionic Surfactant",
volume = "15",
number = "1",
doi = "10.3390/ph15010054"
}
Milinković Budinčić, J., Petrović, L., Đekić, L., Aleksić, M., Fraj, J., Popović, S., Bučko, S., Katona, J., Spasojević, L., Škrbić, J.,& Malenović, A.. (2021). Chitosan/Sodium Dodecyl Sulfate Complexes for Microencapsulation of Vitamin E and Its Release Profile— Understanding the Effect of Anionic Surfactant. in Pharmaceuticals
MDPI., 15(1).
https://doi.org/10.3390/ph15010054
Milinković Budinčić J, Petrović L, Đekić L, Aleksić M, Fraj J, Popović S, Bučko S, Katona J, Spasojević L, Škrbić J, Malenović A. Chitosan/Sodium Dodecyl Sulfate Complexes for Microencapsulation of Vitamin E and Its Release Profile— Understanding the Effect of Anionic Surfactant. in Pharmaceuticals. 2021;15(1).
doi:10.3390/ph15010054 .
Milinković Budinčić, Jelena, Petrović, Lidija, Đekić, Ljiljana, Aleksić, Milijana, Fraj, Jadranka, Popović, Senka, Bučko, Sandra, Katona, Jaroslav, Spasojević, Ljiljana, Škrbić, Jelena, Malenović, Anđelija, "Chitosan/Sodium Dodecyl Sulfate Complexes for Microencapsulation of Vitamin E and Its Release Profile— Understanding the Effect of Anionic Surfactant" in Pharmaceuticals, 15, no. 1 (2021),
https://doi.org/10.3390/ph15010054 . .
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Study of vitamin E microencapsulation and controlled release from chitosan/sodium lauryl ether sulfate microcapsules

Milinković Budinčić, Jelena; Petrović, Lidija; Đekić, Ljiljana; Fraj, Jadranka; Bučko, Sandra; Katona, Jaroslav; Spasojević, Ljiljana

(Elsevier Ltd, 2021)

TY  - JOUR
AU  - Milinković Budinčić, Jelena
AU  - Petrović, Lidija
AU  - Đekić, Ljiljana
AU  - Fraj, Jadranka
AU  - Bučko, Sandra
AU  - Katona, Jaroslav
AU  - Spasojević, Ljiljana
PY  - 2021
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3774
AB  - Potential benefit of microencapsulation is its ability to deliver and protect incorporated ingredients such as vitamin E. Microcapsule wall properties can be changed by adding of coss-linking agents that are usually considered toxic for application. The microcapsules were prepared by a spray-drying technique using coacervation method, by depositing the coacervate formed in the mixture of chitosan and sodium lauryl ether sulfate to the oil/water interface. All obtained microcapsules suspensions had slightly lower mean diameter compared to the starting emulsion (6.85 ± 0.213 μm), which shows their good stability during the drying process. The choice and absence of cross-linking agents had influence on kinetics of vitamin E release. Encapsulation efficiency of microcapsules without cross-linking agent was 73.17 ± 0.64 %. This study avoided the use of aldehydes as cross-linking agents and found that chitosan/SLES complex can be used as wall material for the microencapsulation of hydrophobic active molecules in cosmetic industry.
PB  - Elsevier Ltd
T2  - Carbohydrate Polymers
T1  - Study of vitamin E microencapsulation and controlled release from chitosan/sodium lauryl ether sulfate microcapsules
VL  - 251
DO  - 10.1016/j.carbpol.2020.116988
ER  - 
@article{
author = "Milinković Budinčić, Jelena and Petrović, Lidija and Đekić, Ljiljana and Fraj, Jadranka and Bučko, Sandra and Katona, Jaroslav and Spasojević, Ljiljana",
year = "2021",
abstract = "Potential benefit of microencapsulation is its ability to deliver and protect incorporated ingredients such as vitamin E. Microcapsule wall properties can be changed by adding of coss-linking agents that are usually considered toxic for application. The microcapsules were prepared by a spray-drying technique using coacervation method, by depositing the coacervate formed in the mixture of chitosan and sodium lauryl ether sulfate to the oil/water interface. All obtained microcapsules suspensions had slightly lower mean diameter compared to the starting emulsion (6.85 ± 0.213 μm), which shows their good stability during the drying process. The choice and absence of cross-linking agents had influence on kinetics of vitamin E release. Encapsulation efficiency of microcapsules without cross-linking agent was 73.17 ± 0.64 %. This study avoided the use of aldehydes as cross-linking agents and found that chitosan/SLES complex can be used as wall material for the microencapsulation of hydrophobic active molecules in cosmetic industry.",
publisher = "Elsevier Ltd",
journal = "Carbohydrate Polymers",
title = "Study of vitamin E microencapsulation and controlled release from chitosan/sodium lauryl ether sulfate microcapsules",
volume = "251",
doi = "10.1016/j.carbpol.2020.116988"
}
Milinković Budinčić, J., Petrović, L., Đekić, L., Fraj, J., Bučko, S., Katona, J.,& Spasojević, L.. (2021). Study of vitamin E microencapsulation and controlled release from chitosan/sodium lauryl ether sulfate microcapsules. in Carbohydrate Polymers
Elsevier Ltd., 251.
https://doi.org/10.1016/j.carbpol.2020.116988
Milinković Budinčić J, Petrović L, Đekić L, Fraj J, Bučko S, Katona J, Spasojević L. Study of vitamin E microencapsulation and controlled release from chitosan/sodium lauryl ether sulfate microcapsules. in Carbohydrate Polymers. 2021;251.
doi:10.1016/j.carbpol.2020.116988 .
Milinković Budinčić, Jelena, Petrović, Lidija, Đekić, Ljiljana, Fraj, Jadranka, Bučko, Sandra, Katona, Jaroslav, Spasojević, Ljiljana, "Study of vitamin E microencapsulation and controlled release from chitosan/sodium lauryl ether sulfate microcapsules" in Carbohydrate Polymers, 251 (2021),
https://doi.org/10.1016/j.carbpol.2020.116988 . .
55
20
49

Encapsulation and release of vitamin C in double W/O/W emulsions followed by complex coacervation in gelatin-sodium caseinate system

Fraj, Jadranka; Petrović, Lidija; Đekić, Ljiljana; Milinković Budinčić, Jelena; Bučko, Sandra; Katona, Jaroslav

(Elsevier Ltd, 2021)

TY  - JOUR
AU  - Fraj, Jadranka
AU  - Petrović, Lidija
AU  - Đekić, Ljiljana
AU  - Milinković Budinčić, Jelena
AU  - Bučko, Sandra
AU  - Katona, Jaroslav
PY  - 2021
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3695
AB  - The objective of this study was to produce and characterize microcapsules for simultaneous encapsulation hydrophilic and lipophilic active substances. For this purpose, double emulsification process was employed, followed by complex coacervation in the system of two oppositely charged biopolymers, gelatin and sodium caseinate (NaCAS). Properties of the microcapsules wall have been regulated by cross-linking of the gelatin/NaCAS complex at the interface with genipin. Vitamins C and E were selected as model hydrophilic and lipophilic bioactive compounds for this study. Investigations of surface morphology, encapsulation efficiency (EE) and kinetic of vitamin C release have shown that genipin concentration as well as interaction in gelatin/NaCAS system make an influence on microcapsules properties. Genipin concentration of 2 mmol/g, was chosen as the optimal and the highest EE of the vitamins were obtained at proteins mass ratio of 2:1. The results of release kinetic determination of the vitamins showed that release mechanism is simple diffusion.
PB  - Elsevier Ltd
T2  - Journal of Food Engineering
T1  - Encapsulation and release of vitamin C in double W/O/W emulsions followed by complex coacervation in gelatin-sodium caseinate system
VL  - 292
DO  - 10.1016/j.jfoodeng.2020.110353
ER  - 
@article{
author = "Fraj, Jadranka and Petrović, Lidija and Đekić, Ljiljana and Milinković Budinčić, Jelena and Bučko, Sandra and Katona, Jaroslav",
year = "2021",
abstract = "The objective of this study was to produce and characterize microcapsules for simultaneous encapsulation hydrophilic and lipophilic active substances. For this purpose, double emulsification process was employed, followed by complex coacervation in the system of two oppositely charged biopolymers, gelatin and sodium caseinate (NaCAS). Properties of the microcapsules wall have been regulated by cross-linking of the gelatin/NaCAS complex at the interface with genipin. Vitamins C and E were selected as model hydrophilic and lipophilic bioactive compounds for this study. Investigations of surface morphology, encapsulation efficiency (EE) and kinetic of vitamin C release have shown that genipin concentration as well as interaction in gelatin/NaCAS system make an influence on microcapsules properties. Genipin concentration of 2 mmol/g, was chosen as the optimal and the highest EE of the vitamins were obtained at proteins mass ratio of 2:1. The results of release kinetic determination of the vitamins showed that release mechanism is simple diffusion.",
publisher = "Elsevier Ltd",
journal = "Journal of Food Engineering",
title = "Encapsulation and release of vitamin C in double W/O/W emulsions followed by complex coacervation in gelatin-sodium caseinate system",
volume = "292",
doi = "10.1016/j.jfoodeng.2020.110353"
}
Fraj, J., Petrović, L., Đekić, L., Milinković Budinčić, J., Bučko, S.,& Katona, J.. (2021). Encapsulation and release of vitamin C in double W/O/W emulsions followed by complex coacervation in gelatin-sodium caseinate system. in Journal of Food Engineering
Elsevier Ltd., 292.
https://doi.org/10.1016/j.jfoodeng.2020.110353
Fraj J, Petrović L, Đekić L, Milinković Budinčić J, Bučko S, Katona J. Encapsulation and release of vitamin C in double W/O/W emulsions followed by complex coacervation in gelatin-sodium caseinate system. in Journal of Food Engineering. 2021;292.
doi:10.1016/j.jfoodeng.2020.110353 .
Fraj, Jadranka, Petrović, Lidija, Đekić, Ljiljana, Milinković Budinčić, Jelena, Bučko, Sandra, Katona, Jaroslav, "Encapsulation and release of vitamin C in double W/O/W emulsions followed by complex coacervation in gelatin-sodium caseinate system" in Journal of Food Engineering, 292 (2021),
https://doi.org/10.1016/j.jfoodeng.2020.110353 . .
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