TY  - JOUR
AU  - Milić, J.
AU  - Ćurčić, Marijana
AU  - Brnjas, Zvonko
AU  - Carapina, H
AU  - Ranđelović, J
AU  - Krinulović, Katarina
AU  - Jovović, Aleksandar
PY  - 2019
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3254
AB  - Assessing the socio-economic impact of dangerous chemicals, including persistent organic pollutants (POPs) as a specific segment, includes analysis of their impacts on human health, on the environment and on local economic development. Abundant evidence of these effects of dangerous chemicals throughout the world is provided by published research. According to WHO, these chemicals cause around 4.9 million deaths (8.3%) and 86 million Disability-Adjusted Life Years (5.7%) globally; according to very conservative estimates, 20% of cancer deaths are the consequence of the cancerous effects of chemicals in the work place. Their impact on economic development is manifested primarily through reduced productivity of society due to health impairment of both the population and natural resources. Specific research, the results of which are presented in this article, has been focused on the impact of POPs on human health. This impact is presented in very general terms through estimation of the monetized cost effects for treating those diseases and cancers assumed to be caused by POPs in Serbia. The cost estimation based on available data amounts to approximately € 68 million for a 5-year period.
PB  - Elsevier B.V.
T2  - Scientia Horticulturae
T1  - The socio-economic impact timeline in Serbia for persistent organic pollutants (POPs)
VL  - 688
SP  - 486
EP  - 493
DO  - 10.1016/j.scitotenv.2019.06.161
ER  - 

@article{
author = "Milić, J. and Ćurčić, Marijana and Brnjas, Zvonko and Carapina, H and Ranđelović, J and Krinulović, Katarina and Jovović, Aleksandar",
year = "2019",
abstract = "Assessing the socio-economic impact of dangerous chemicals, including persistent organic pollutants (POPs) as a specific segment, includes analysis of their impacts on human health, on the environment and on local economic development. Abundant evidence of these effects of dangerous chemicals throughout the world is provided by published research. According to WHO, these chemicals cause around 4.9 million deaths (8.3%) and 86 million Disability-Adjusted Life Years (5.7%) globally; according to very conservative estimates, 20% of cancer deaths are the consequence of the cancerous effects of chemicals in the work place. Their impact on economic development is manifested primarily through reduced productivity of society due to health impairment of both the population and natural resources. Specific research, the results of which are presented in this article, has been focused on the impact of POPs on human health. This impact is presented in very general terms through estimation of the monetized cost effects for treating those diseases and cancers assumed to be caused by POPs in Serbia. The cost estimation based on available data amounts to approximately € 68 million for a 5-year period.",
publisher = "Elsevier B.V.",
journal = "Scientia Horticulturae",
title = "The socio-economic impact timeline in Serbia for persistent organic pollutants (POPs)",
volume = "688",
pages = "486-493",
doi = "10.1016/j.scitotenv.2019.06.161"
}

Milić, J., Ćurčić, M., Brnjas, Z., Carapina, H., Ranđelović, J., Krinulović, K.,& Jovović, A.. (2019). The socio-economic impact timeline in Serbia for persistent organic pollutants (POPs). in Scientia Horticulturae
Elsevier B.V.., 688, 486-493.
https://doi.org/10.1016/j.scitotenv.2019.06.161

Milić J, Ćurčić M, Brnjas Z, Carapina H, Ranđelović J, Krinulović K, Jovović A. The socio-economic impact timeline in Serbia for persistent organic pollutants (POPs). in Scientia Horticulturae. 2019;688:486-493.
doi:10.1016/j.scitotenv.2019.06.161 .

Milić, J., Ćurčić, Marijana, Brnjas, Zvonko, Carapina, H, Ranđelović, J, Krinulović, Katarina, Jovović, Aleksandar, "The socio-economic impact timeline in Serbia for persistent organic pollutants (POPs)" in Scientia Horticulturae, 688 (2019):486-493,
https://doi.org/10.1016/j.scitotenv.2019.06.161 . .

TY  - CONF
AU  - Ćurčić, Marijana
AU  - Milić, J.
AU  - Brnjas, Zvonko
AU  - Ranđelović, J.
AU  - Jovović, Aleksandar
AU  - Krinulović, Katarina
AU  - Bacanović, V.
AU  - Stevanović-Carapina, Hristina
AU  - Ćurčić, Marijana
PY  - 2015
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2344
PB  - Elsevier Ireland Ltd, Clare
C3  - Toxicology Letters
T1  - PBDEs and PFOS as new POPs chemicals in Serbian regulation - Socio economic analysis for the purpose of risk management
VL  - 238
IS  - 2, Supplement
SP  - S339
EP  - S339
DO  - 10.1016/j.toxlet.2015.08.967
ER  - 

@conference{
author = "Ćurčić, Marijana and Milić, J. and Brnjas, Zvonko and Ranđelović, J. and Jovović, Aleksandar and Krinulović, Katarina and Bacanović, V. and Stevanović-Carapina, Hristina and Ćurčić, Marijana",
year = "2015",
publisher = "Elsevier Ireland Ltd, Clare",
journal = "Toxicology Letters",
title = "PBDEs and PFOS as new POPs chemicals in Serbian regulation - Socio economic analysis for the purpose of risk management",
volume = "238",
number = "2, Supplement",
pages = "S339-S339",
doi = "10.1016/j.toxlet.2015.08.967"
}

Ćurčić, M., Milić, J., Brnjas, Z., Ranđelović, J., Jovović, A., Krinulović, K., Bacanović, V., Stevanović-Carapina, H.,& Ćurčić, M.. (2015). PBDEs and PFOS as new POPs chemicals in Serbian regulation - Socio economic analysis for the purpose of risk management. in Toxicology Letters
Elsevier Ireland Ltd, Clare., 238(2, Supplement), S339-S339.
https://doi.org/10.1016/j.toxlet.2015.08.967

Ćurčić M, Milić J, Brnjas Z, Ranđelović J, Jovović A, Krinulović K, Bacanović V, Stevanović-Carapina H, Ćurčić M. PBDEs and PFOS as new POPs chemicals in Serbian regulation - Socio economic analysis for the purpose of risk management. in Toxicology Letters. 2015;238(2, Supplement):S339-S339.
doi:10.1016/j.toxlet.2015.08.967 .

Ćurčić, Marijana, Milić, J., Brnjas, Zvonko, Ranđelović, J., Jovović, Aleksandar, Krinulović, Katarina, Bacanović, V., Stevanović-Carapina, Hristina, Ćurčić, Marijana, "PBDEs and PFOS as new POPs chemicals in Serbian regulation - Socio economic analysis for the purpose of risk management" in Toxicology Letters, 238, no. 2, Supplement (2015):S339-S339,
https://doi.org/10.1016/j.toxlet.2015.08.967 . .

TY  - JOUR
AU  - Ivanović, D.
AU  - Medenica, Mirjana
AU  - Jančić, Biljana
AU  - Knežević, N.
AU  - Malenović, Anđelija
AU  - Milić, J.
PY  - 2007
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/964
AB  - The main objective of the work discussed in this paper was evaluation of a chromatographic method for simultaneous determination of hydrochlorothiazide (HCTZ), lisinopril (L), and their impurities in pharmaceuticals. Chlorothiazide (CTZ) and disulfonamide (DSA), as potential impurities in hydrochlorothiazide, and diketopiperazine (DKP), as an impurity of lisinopril, were analyzed. The chromatographic behaviour of these substances on different columns was studied using mobile phases of different polarity. The optimum separations were achieved by gradient elution on a 4.6 mm x 20 mm, 3.5 mu m particle size, C-18 column. The mobile phase was a gradient prepared by mixing 7:93 (v/v) acetonitrile-25 mm potassium dihydrogen phosphate, pH 5, and 50:50 (v/v) acetonitrile-25 mm potassium dihydrogen phosphate pH 5 in different ratios. The flow rate was 1.0 mL min(-1). UV detection was performed at 215 nm. Methylparaben was used as internal standard. The method was validated for selectivity, linearity, precision,. and accuracy. The limits of detection, LOD, and quantification, LOQ, were determined experimentally. Because of its speed and accuracy the method can be used for quality-control analysis.
PB  - Univ Silesia, Inst Chemistry, Katowice
T2  - Acta Chromatographica
T1  - Validation of an analytical procedure for simultaneous determination of hydrochlorothiazide, lisinopril, and their impurities
VL  - 18
SP  - 143
EP  - 156
UR  - https://hdl.handle.net/21.15107/rcub_farfar_964
ER  - 

@article{
author = "Ivanović, D. and Medenica, Mirjana and Jančić, Biljana and Knežević, N. and Malenović, Anđelija and Milić, J.",
year = "2007",
abstract = "The main objective of the work discussed in this paper was evaluation of a chromatographic method for simultaneous determination of hydrochlorothiazide (HCTZ), lisinopril (L), and their impurities in pharmaceuticals. Chlorothiazide (CTZ) and disulfonamide (DSA), as potential impurities in hydrochlorothiazide, and diketopiperazine (DKP), as an impurity of lisinopril, were analyzed. The chromatographic behaviour of these substances on different columns was studied using mobile phases of different polarity. The optimum separations were achieved by gradient elution on a 4.6 mm x 20 mm, 3.5 mu m particle size, C-18 column. The mobile phase was a gradient prepared by mixing 7:93 (v/v) acetonitrile-25 mm potassium dihydrogen phosphate, pH 5, and 50:50 (v/v) acetonitrile-25 mm potassium dihydrogen phosphate pH 5 in different ratios. The flow rate was 1.0 mL min(-1). UV detection was performed at 215 nm. Methylparaben was used as internal standard. The method was validated for selectivity, linearity, precision,. and accuracy. The limits of detection, LOD, and quantification, LOQ, were determined experimentally. Because of its speed and accuracy the method can be used for quality-control analysis.",
publisher = "Univ Silesia, Inst Chemistry, Katowice",
journal = "Acta Chromatographica",
title = "Validation of an analytical procedure for simultaneous determination of hydrochlorothiazide, lisinopril, and their impurities",
volume = "18",
pages = "143-156",
url = "https://hdl.handle.net/21.15107/rcub_farfar_964"
}

Ivanović, D., Medenica, M., Jančić, B., Knežević, N., Malenović, A.,& Milić, J.. (2007). Validation of an analytical procedure for simultaneous determination of hydrochlorothiazide, lisinopril, and their impurities. in Acta Chromatographica
Univ Silesia, Inst Chemistry, Katowice., 18, 143-156.
https://hdl.handle.net/21.15107/rcub_farfar_964

Ivanović D, Medenica M, Jančić B, Knežević N, Malenović A, Milić J. Validation of an analytical procedure for simultaneous determination of hydrochlorothiazide, lisinopril, and their impurities. in Acta Chromatographica. 2007;18:143-156.
https://hdl.handle.net/21.15107/rcub_farfar_964 .

Ivanović, D., Medenica, Mirjana, Jančić, Biljana, Knežević, N., Malenović, Anđelija, Milić, J., "Validation of an analytical procedure for simultaneous determination of hydrochlorothiazide, lisinopril, and their impurities" in Acta Chromatographica, 18 (2007):143-156,
https://hdl.handle.net/21.15107/rcub_farfar_964 .

TY  - JOUR
AU  - Dragičević-Curić, Nina
AU  - Stupar, Mirjana
AU  - Milić, J.
AU  - Zorić, T
AU  - Krajišnik, Danina
AU  - Vasiljević, D
PY  - 2005
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/574
AB  - The aim of this study was to develop and characterize hydrophilic gels containing chlorophyllin(CHL)loaded liposomes as well as to evaluate their stability. Two different CHL-loaded liposome dispersions using non-hydrogenated and hydrogenated soybean lecithin were prepared, characterized for their particle size, polydispersity index and trapping efficiency and incorporated in Carbopol(R) 940 NF hydrogel. The gels obtained were analyzed for flow properties, pH values and CHL content. The control liposome-free gel was obtained by incorporating the CHL solution in the hydrogel. The stability of the gels was evaluated in terms of rheological properties, pH values and CHL content during 6 months' storage at 20 +/- 2 degrees C. Suitable gel formulations for topical use were obtained revealing shear-thinning plastic flow behaviour without significant thixotropy during the whole period of examination. High yield values of the samples during the whole period indicated a long-term stability of the gel formulations. The gel formulations expressed a mild acid value acceptable for topical preparations. After 6 months' storage the CHL content was highest in the gel containing non-hydrogenated lecithin liposomes, followed by the gel containing hydrogenated lecithin liposomes and liposome-free gel, indicating that the encapsulation of CHL in liposomes led to a greater stability of CHL.
PB  - Govi-Verlag  Pharmazeutischer Verlag Gmbh, Eschborn
T2  - Pharmazie
T1  - Hydrophilic gels containing chlorophyllin-loaded liposomes: development and stability evaluation
VL  - 60
IS  - 8
SP  - 588
EP  - 592
UR  - https://hdl.handle.net/21.15107/rcub_farfar_574
ER  - 

@article{
author = "Dragičević-Curić, Nina and Stupar, Mirjana and Milić, J. and Zorić, T and Krajišnik, Danina and Vasiljević, D",
year = "2005",
abstract = "The aim of this study was to develop and characterize hydrophilic gels containing chlorophyllin(CHL)loaded liposomes as well as to evaluate their stability. Two different CHL-loaded liposome dispersions using non-hydrogenated and hydrogenated soybean lecithin were prepared, characterized for their particle size, polydispersity index and trapping efficiency and incorporated in Carbopol(R) 940 NF hydrogel. The gels obtained were analyzed for flow properties, pH values and CHL content. The control liposome-free gel was obtained by incorporating the CHL solution in the hydrogel. The stability of the gels was evaluated in terms of rheological properties, pH values and CHL content during 6 months' storage at 20 +/- 2 degrees C. Suitable gel formulations for topical use were obtained revealing shear-thinning plastic flow behaviour without significant thixotropy during the whole period of examination. High yield values of the samples during the whole period indicated a long-term stability of the gel formulations. The gel formulations expressed a mild acid value acceptable for topical preparations. After 6 months' storage the CHL content was highest in the gel containing non-hydrogenated lecithin liposomes, followed by the gel containing hydrogenated lecithin liposomes and liposome-free gel, indicating that the encapsulation of CHL in liposomes led to a greater stability of CHL.",
publisher = "Govi-Verlag  Pharmazeutischer Verlag Gmbh, Eschborn",
journal = "Pharmazie",
title = "Hydrophilic gels containing chlorophyllin-loaded liposomes: development and stability evaluation",
volume = "60",
number = "8",
pages = "588-592",
url = "https://hdl.handle.net/21.15107/rcub_farfar_574"
}

Dragičević-Curić, N., Stupar, M., Milić, J., Zorić, T., Krajišnik, D.,& Vasiljević, D.. (2005). Hydrophilic gels containing chlorophyllin-loaded liposomes: development and stability evaluation. in Pharmazie
Govi-Verlag  Pharmazeutischer Verlag Gmbh, Eschborn., 60(8), 588-592.
https://hdl.handle.net/21.15107/rcub_farfar_574

Dragičević-Curić N, Stupar M, Milić J, Zorić T, Krajišnik D, Vasiljević D. Hydrophilic gels containing chlorophyllin-loaded liposomes: development and stability evaluation. in Pharmazie. 2005;60(8):588-592.
https://hdl.handle.net/21.15107/rcub_farfar_574 .

Dragičević-Curić, Nina, Stupar, Mirjana, Milić, J., Zorić, T, Krajišnik, Danina, Vasiljević, D, "Hydrophilic gels containing chlorophyllin-loaded liposomes: development and stability evaluation" in Pharmazie, 60, no. 8 (2005):588-592,
https://hdl.handle.net/21.15107/rcub_farfar_574 .

TY  - JOUR
AU  - Savić, Snežana
AU  - Tamburić, Slobodanka
AU  - Savić, Miroslav
AU  - Cekić, Nebojša
AU  - Milić, J.
AU  - Vuleta, G
PY  - 2004
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/528
AB  - It is known that, depending on the concentration, treatment with urea could improve skin barrier function, despite its penetration-enhancing properties. This controversial skin effect of urea has been explored systematically in this study in terms of the effect of vehicle on the performance of urea. In the first part, a series of four semi-solid emulsions with 5% (w/w) urea, varying in the type of emulsion, nature of emulsifier and polarity of oil ingredients, have been evaluated with regard to their skin hydrating and transepidermal water loss (TEWL)-modifying properties. Placebo samples were tested alongside the urea-containing ones. Two best performing moisturisers from the above were chosen for the second part of the study, in which sodium lauryl sulphate (SLS)-irritated skin was treated with both placebo and urea-containing samples. In addition to TEWL and skin hydration level, the erythema index (EI) was measured before, during and after the treatment. The results have shown that barrier-improving and hydrating abilities of urea are bi-directional and dependent on both the type of vehicle used for its delivery and the state of skin.
PB  - Elsevier Science BV, Amsterdam
T2  - International Journal of Pharmaceutics
T1  - Vehicle-controlled effect of urea on normal and SLS-irritated skin
VL  - 271
IS  - 1-2
SP  - 269
EP  - 280
DO  - 10.1016/j.ijpharm.2003.11.033
ER  - 

@article{
author = "Savić, Snežana and Tamburić, Slobodanka and Savić, Miroslav and Cekić, Nebojša and Milić, J. and Vuleta, G",
year = "2004",
abstract = "It is known that, depending on the concentration, treatment with urea could improve skin barrier function, despite its penetration-enhancing properties. This controversial skin effect of urea has been explored systematically in this study in terms of the effect of vehicle on the performance of urea. In the first part, a series of four semi-solid emulsions with 5% (w/w) urea, varying in the type of emulsion, nature of emulsifier and polarity of oil ingredients, have been evaluated with regard to their skin hydrating and transepidermal water loss (TEWL)-modifying properties. Placebo samples were tested alongside the urea-containing ones. Two best performing moisturisers from the above were chosen for the second part of the study, in which sodium lauryl sulphate (SLS)-irritated skin was treated with both placebo and urea-containing samples. In addition to TEWL and skin hydration level, the erythema index (EI) was measured before, during and after the treatment. The results have shown that barrier-improving and hydrating abilities of urea are bi-directional and dependent on both the type of vehicle used for its delivery and the state of skin.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "International Journal of Pharmaceutics",
title = "Vehicle-controlled effect of urea on normal and SLS-irritated skin",
volume = "271",
number = "1-2",
pages = "269-280",
doi = "10.1016/j.ijpharm.2003.11.033"
}

Savić, S., Tamburić, S., Savić, M., Cekić, N., Milić, J.,& Vuleta, G.. (2004). Vehicle-controlled effect of urea on normal and SLS-irritated skin. in International Journal of Pharmaceutics
Elsevier Science BV, Amsterdam., 271(1-2), 269-280.
https://doi.org/10.1016/j.ijpharm.2003.11.033

Savić S, Tamburić S, Savić M, Cekić N, Milić J, Vuleta G. Vehicle-controlled effect of urea on normal and SLS-irritated skin. in International Journal of Pharmaceutics. 2004;271(1-2):269-280.
doi:10.1016/j.ijpharm.2003.11.033 .

Savić, Snežana, Tamburić, Slobodanka, Savić, Miroslav, Cekić, Nebojša, Milić, J., Vuleta, G, "Vehicle-controlled effect of urea on normal and SLS-irritated skin" in International Journal of Pharmaceutics, 271, no. 1-2 (2004):269-280,
https://doi.org/10.1016/j.ijpharm.2003.11.033 . .

TY  - JOUR
AU  - Krajišnik, Danina
AU  - Milić, J.
PY  - 2003
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/420
AB  - In the course of investigation of the effects of polymeric emulsifier (Simulgel(R)A) on the structural characteristics and physical stability (during storage time) of semisolid o/w emulsion systems with different emulsifier concentrations, dispersed droplets of an internal oil phase (4.5-11.5 mum size) were discovered. The degree of dispersity was increased along with increasing polymeric emulsifier concentration (from 1 to 5% m/m), which was shown by microscopic analysis. Experiments were also carried out using pH, electrical conductivity, and rheological (rotational and oscillatory) measurements. Emulsion samples expressed a mild acid value acceptable for topical preparations during a 6-month period. Electrical conductivity of fresh samples ranged from 0.423 to 2.009 mS/cm and after a 6-month period this slightly increased to 0.663-2.890 mS/cm. All emulsion samples revealed plastic flow behavior in fresh state, with changes in flow pattern during storage time. Viscoelastic properties defined by the oscillatory rheometry results were in good correlation with parameters of rotational rheometry and degree of internal phase dispersity. High yield stress values (flow tests) and favorable low values of damping factor (oscillatory studies) both indicated good internal structuring and long-term stability of sample containing 3% m/m of polymeric emulsifier.
PB  - Taylor & Francis Ltd, Abingdon
T2  - Drug Development and Industrial Pharmacy
T1  - Polymer-stabilized emulsion systems: Structural characteristics and physical stability evaluation
VL  - 29
IS  - 6
SP  - 701
EP  - 711
DO  - 10.1081/DDC-120021319
ER  - 

@article{
author = "Krajišnik, Danina and Milić, J.",
year = "2003",
abstract = "In the course of investigation of the effects of polymeric emulsifier (Simulgel(R)A) on the structural characteristics and physical stability (during storage time) of semisolid o/w emulsion systems with different emulsifier concentrations, dispersed droplets of an internal oil phase (4.5-11.5 mum size) were discovered. The degree of dispersity was increased along with increasing polymeric emulsifier concentration (from 1 to 5% m/m), which was shown by microscopic analysis. Experiments were also carried out using pH, electrical conductivity, and rheological (rotational and oscillatory) measurements. Emulsion samples expressed a mild acid value acceptable for topical preparations during a 6-month period. Electrical conductivity of fresh samples ranged from 0.423 to 2.009 mS/cm and after a 6-month period this slightly increased to 0.663-2.890 mS/cm. All emulsion samples revealed plastic flow behavior in fresh state, with changes in flow pattern during storage time. Viscoelastic properties defined by the oscillatory rheometry results were in good correlation with parameters of rotational rheometry and degree of internal phase dispersity. High yield stress values (flow tests) and favorable low values of damping factor (oscillatory studies) both indicated good internal structuring and long-term stability of sample containing 3% m/m of polymeric emulsifier.",
publisher = "Taylor & Francis Ltd, Abingdon",
journal = "Drug Development and Industrial Pharmacy",
title = "Polymer-stabilized emulsion systems: Structural characteristics and physical stability evaluation",
volume = "29",
number = "6",
pages = "701-711",
doi = "10.1081/DDC-120021319"
}

Krajišnik, D.,& Milić, J.. (2003). Polymer-stabilized emulsion systems: Structural characteristics and physical stability evaluation. in Drug Development and Industrial Pharmacy
Taylor & Francis Ltd, Abingdon., 29(6), 701-711.
https://doi.org/10.1081/DDC-120021319

Krajišnik D, Milić J. Polymer-stabilized emulsion systems: Structural characteristics and physical stability evaluation. in Drug Development and Industrial Pharmacy. 2003;29(6):701-711.
doi:10.1081/DDC-120021319 .

Krajišnik, Danina, Milić, J., "Polymer-stabilized emulsion systems: Structural characteristics and physical stability evaluation" in Drug Development and Industrial Pharmacy, 29, no. 6 (2003):701-711,
https://doi.org/10.1081/DDC-120021319 . .