Jančar, Boštjan

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Authority KeyName Variants
orcid::0000-0002-7491-859X
  • Jančar, Boštjan (5)
Projects

Author's Bibliography

Poly(D,L-lactide-co-glycolide)/hydroxyapatite core-shell nanospheres. Part 1: A multifunctional system for controlled drug delivery

Vukomanović, Marija; Škapin, Srečo Davor; Jančar, Boštjan; Maksin, Tatjana; Ignjatović, Nenad; Uskoković, Vuk; Uskoković, Dragan

(2011)

TY  - JOUR
AU  - Vukomanović, Marija
AU  - Škapin, Srečo Davor
AU  - Jančar, Boštjan
AU  - Maksin, Tatjana
AU  - Ignjatović, Nenad
AU  - Uskoković, Vuk
AU  - Uskoković, Dragan
PY  - 2011
UR  - https://dais.sanu.ac.rs/123456789/2749
AB  - Biodegradable poly(D,L-lactide-co-glycolide) (PLGA) and bioactive hydroxyapatite (HAP) are selected for the formation of a multifunctional system with the specific core-shell structure to be applied as a carrier of a drug. As a result, both components of PLGA/HAp core-shells are able to capture one part of the drug. Polymeric shells consisting of small nanospheres up to 20 nm in size act as a matrix in which one part of the drug is dispersed. In the same time, ceramic cores are formed of rod-like hydroxyapatite particles at the surface of which another part of the drug is adsorbed onto the interface between the polymer and the ceramics. The content of the loaded drug, as well as the selected solvent/non-solvent system, have a crucial influence on the resulting PLGA/HAp morphology and, finally, unimodal distribution of core-shells is obtained. The redistribution of the drug between the organic and inorganic parts of the material is expected to provide an interesting contribution to the kinetics of the drug release resulting in non-typical two-step drug release. (C) 2010 Elsevier B.V. All rights reserved.
T2  - Colloids and Surfaces B: Biointerfaces
T1  - Poly(D,L-lactide-co-glycolide)/hydroxyapatite core-shell nanospheres. Part 1: A multifunctional system for controlled drug delivery
SP  - 404
EP  - 413
VL  - 82
IS  - 2
DO  - 10.1016/j.colsurfb.2010.09.011
UR  - https://hdl.handle.net/21.15107/rcub_dais_2749
ER  - 
@article{
author = "Vukomanović, Marija and Škapin, Srečo Davor and Jančar, Boštjan and Maksin, Tatjana and Ignjatović, Nenad and Uskoković, Vuk and Uskoković, Dragan",
year = "2011",
abstract = "Biodegradable poly(D,L-lactide-co-glycolide) (PLGA) and bioactive hydroxyapatite (HAP) are selected for the formation of a multifunctional system with the specific core-shell structure to be applied as a carrier of a drug. As a result, both components of PLGA/HAp core-shells are able to capture one part of the drug. Polymeric shells consisting of small nanospheres up to 20 nm in size act as a matrix in which one part of the drug is dispersed. In the same time, ceramic cores are formed of rod-like hydroxyapatite particles at the surface of which another part of the drug is adsorbed onto the interface between the polymer and the ceramics. The content of the loaded drug, as well as the selected solvent/non-solvent system, have a crucial influence on the resulting PLGA/HAp morphology and, finally, unimodal distribution of core-shells is obtained. The redistribution of the drug between the organic and inorganic parts of the material is expected to provide an interesting contribution to the kinetics of the drug release resulting in non-typical two-step drug release. (C) 2010 Elsevier B.V. All rights reserved.",
journal = "Colloids and Surfaces B: Biointerfaces",
title = "Poly(D,L-lactide-co-glycolide)/hydroxyapatite core-shell nanospheres. Part 1: A multifunctional system for controlled drug delivery",
pages = "404-413",
volume = "82",
number = "2",
doi = "10.1016/j.colsurfb.2010.09.011",
url = "https://hdl.handle.net/21.15107/rcub_dais_2749"
}
Vukomanović, M., Škapin, S. D., Jančar, B., Maksin, T., Ignjatović, N., Uskoković, V.,& Uskoković, D.. (2011). Poly(D,L-lactide-co-glycolide)/hydroxyapatite core-shell nanospheres. Part 1: A multifunctional system for controlled drug delivery. in Colloids and Surfaces B: Biointerfaces, 82(2), 404-413.
https://doi.org/10.1016/j.colsurfb.2010.09.011
https://hdl.handle.net/21.15107/rcub_dais_2749
Vukomanović M, Škapin SD, Jančar B, Maksin T, Ignjatović N, Uskoković V, Uskoković D. Poly(D,L-lactide-co-glycolide)/hydroxyapatite core-shell nanospheres. Part 1: A multifunctional system for controlled drug delivery. in Colloids and Surfaces B: Biointerfaces. 2011;82(2):404-413.
doi:10.1016/j.colsurfb.2010.09.011
https://hdl.handle.net/21.15107/rcub_dais_2749 .
Vukomanović, Marija, Škapin, Srečo Davor, Jančar, Boštjan, Maksin, Tatjana, Ignjatović, Nenad, Uskoković, Vuk, Uskoković, Dragan, "Poly(D,L-lactide-co-glycolide)/hydroxyapatite core-shell nanospheres. Part 1: A multifunctional system for controlled drug delivery" in Colloids and Surfaces B: Biointerfaces, 82, no. 2 (2011):404-413,
https://doi.org/10.1016/j.colsurfb.2010.09.011 .,
https://hdl.handle.net/21.15107/rcub_dais_2749 .
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Ultrasound-assisted synthesis of nanostructured LiFePO4/C composite

Jugović, Dragana; Mitrić, Miodrag; Cvjetićanin, Nikola; Jančar, Boštjan; Mentus, Slavko; Uskoković, Dragan

(2008)

TY  - CONF
AU  - Jugović, Dragana
AU  - Mitrić, Miodrag
AU  - Cvjetićanin, Nikola
AU  - Jančar, Boštjan
AU  - Mentus, Slavko
AU  - Uskoković, Dragan
PY  - 2008
UR  - https://dais.sanu.ac.rs/123456789/295
AB  - Poster presented at the Women in Nano Winter School, Kranjska Gora, Slovenia, February 7-9, 2008
T1  - Ultrasound-assisted synthesis of nanostructured LiFePO4/C composite
UR  - https://hdl.handle.net/21.15107/rcub_dais_295
ER  - 
@conference{
author = "Jugović, Dragana and Mitrić, Miodrag and Cvjetićanin, Nikola and Jančar, Boštjan and Mentus, Slavko and Uskoković, Dragan",
year = "2008",
abstract = "Poster presented at the Women in Nano Winter School, Kranjska Gora, Slovenia, February 7-9, 2008",
title = "Ultrasound-assisted synthesis of nanostructured LiFePO4/C composite",
url = "https://hdl.handle.net/21.15107/rcub_dais_295"
}
Jugović, D., Mitrić, M., Cvjetićanin, N., Jančar, B., Mentus, S.,& Uskoković, D.. (2008). Ultrasound-assisted synthesis of nanostructured LiFePO4/C composite. .
https://hdl.handle.net/21.15107/rcub_dais_295
Jugović D, Mitrić M, Cvjetićanin N, Jančar B, Mentus S, Uskoković D. Ultrasound-assisted synthesis of nanostructured LiFePO4/C composite. 2008;.
https://hdl.handle.net/21.15107/rcub_dais_295 .
Jugović, Dragana, Mitrić, Miodrag, Cvjetićanin, Nikola, Jančar, Boštjan, Mentus, Slavko, Uskoković, Dragan, "Ultrasound-assisted synthesis of nanostructured LiFePO4/C composite" (2008),
https://hdl.handle.net/21.15107/rcub_dais_295 .

Synthesis and characterization of LiFePO(4)/C composite obtained by sonochemical method

Jugović, Dragana; Mitrić, Miodrag; Cvjetićanin, Nikola; Jančar, Boštjan; Mentus, Slavko; Uskoković, Dragan

(2008)

TY  - JOUR
AU  - Jugović, Dragana
AU  - Mitrić, Miodrag
AU  - Cvjetićanin, Nikola
AU  - Jančar, Boštjan
AU  - Mentus, Slavko
AU  - Uskoković, Dragan
PY  - 2008
UR  - https://dais.sanu.ac.rs/123456789/2739
AB  - Lithium iron phosphate has become of great interest as storage cathode for the next generation of rechargeable lithium batteries. Olivine structure LiFePO(4)/C composite powder was prepared by ultrasound assisted synthesis. A polyvinyl alcohol solution was used as the source of an in situ formed carbon. X-ray powder diffraction confirmed the phase purity. X-ray powder diffraction data were used for the crystal structure refinement, based on Rietveld full profile method. All relevant structural and microstructural crystal parameters that could be significant for electrochemical intercalation/deintercalation processes were determined. The Rietveld refinement also showed additional electron density on the lithium sites, indicating 3 at.% iron on the lithium site. Electrochemical characteristic of the composite was evaluated by using galvanostatic charge/discharge tests. While cycling at C/3 (C/10) rate the discharge capacity increases, starting from the value of 94.1 (116.0) mAh/g and reaching 99.5 (124.0) mAh/g at the end of the cycling. Particle morphology was revealed by both scanning and transmission electron microscopies. On the thin particle edges carbon film with a typical thickness of several nanometers can be observed, as well as small carbon agglomerates (typical size LT 6 nm) at certain spots on the substrate surface. (c) 2008 Elsevier B.V. All rights reserved.
T2  - Solid State Ionics
T1  - Synthesis and characterization of LiFePO(4)/C composite obtained by sonochemical method
SP  - 415
EP  - 419
VL  - 179
IS  - 11-12
DO  - 10.1016/j.ssi.2008.03.014
UR  - https://hdl.handle.net/21.15107/rcub_dais_2739
ER  - 
@article{
author = "Jugović, Dragana and Mitrić, Miodrag and Cvjetićanin, Nikola and Jančar, Boštjan and Mentus, Slavko and Uskoković, Dragan",
year = "2008",
abstract = "Lithium iron phosphate has become of great interest as storage cathode for the next generation of rechargeable lithium batteries. Olivine structure LiFePO(4)/C composite powder was prepared by ultrasound assisted synthesis. A polyvinyl alcohol solution was used as the source of an in situ formed carbon. X-ray powder diffraction confirmed the phase purity. X-ray powder diffraction data were used for the crystal structure refinement, based on Rietveld full profile method. All relevant structural and microstructural crystal parameters that could be significant for electrochemical intercalation/deintercalation processes were determined. The Rietveld refinement also showed additional electron density on the lithium sites, indicating 3 at.% iron on the lithium site. Electrochemical characteristic of the composite was evaluated by using galvanostatic charge/discharge tests. While cycling at C/3 (C/10) rate the discharge capacity increases, starting from the value of 94.1 (116.0) mAh/g and reaching 99.5 (124.0) mAh/g at the end of the cycling. Particle morphology was revealed by both scanning and transmission electron microscopies. On the thin particle edges carbon film with a typical thickness of several nanometers can be observed, as well as small carbon agglomerates (typical size LT 6 nm) at certain spots on the substrate surface. (c) 2008 Elsevier B.V. All rights reserved.",
journal = "Solid State Ionics",
title = "Synthesis and characterization of LiFePO(4)/C composite obtained by sonochemical method",
pages = "415-419",
volume = "179",
number = "11-12",
doi = "10.1016/j.ssi.2008.03.014",
url = "https://hdl.handle.net/21.15107/rcub_dais_2739"
}
Jugović, D., Mitrić, M., Cvjetićanin, N., Jančar, B., Mentus, S.,& Uskoković, D.. (2008). Synthesis and characterization of LiFePO(4)/C composite obtained by sonochemical method. in Solid State Ionics, 179(11-12), 415-419.
https://doi.org/10.1016/j.ssi.2008.03.014
https://hdl.handle.net/21.15107/rcub_dais_2739
Jugović D, Mitrić M, Cvjetićanin N, Jančar B, Mentus S, Uskoković D. Synthesis and characterization of LiFePO(4)/C composite obtained by sonochemical method. in Solid State Ionics. 2008;179(11-12):415-419.
doi:10.1016/j.ssi.2008.03.014
https://hdl.handle.net/21.15107/rcub_dais_2739 .
Jugović, Dragana, Mitrić, Miodrag, Cvjetićanin, Nikola, Jančar, Boštjan, Mentus, Slavko, Uskoković, Dragan, "Synthesis and characterization of LiFePO(4)/C composite obtained by sonochemical method" in Solid State Ionics, 179, no. 11-12 (2008):415-419,
https://doi.org/10.1016/j.ssi.2008.03.014 .,
https://hdl.handle.net/21.15107/rcub_dais_2739 .
38
37
47

Synthesis and characterization of LiFePO4/C composite obtained by sonochemical method

Jugović, Dragana; Mitrić, Miodrag; Cvjetićanin, Nikola; Jančar, Boštjan; Mentus, Slavko; Uskoković, Dragan

(2008)

TY  - JOUR
AU  - Jugović, Dragana
AU  - Mitrić, Miodrag
AU  - Cvjetićanin, Nikola
AU  - Jančar, Boštjan
AU  - Mentus, Slavko
AU  - Uskoković, Dragan
PY  - 2008
UR  - https://dais.sanu.ac.rs/123456789/754
AB  - Lithium iron phosphate has become of great interest as storage cathode for the next generation of rechargeable lithium batteries. Olivine structure LiFePO4/C composite powder was prepared by ultrasound assisted synthesis. A polyvinyl alcohol solution was used as the source of an in situ formed carbon. X-ray powder diffraction confirmed the phase purity. X-ray powder diffraction data were used for the crystal structure refinement, based on Rietveld full profile method. All relevant structural and microstructural crystal parameters that could be significant for electrochemical intercalation/deintercalation processes were determined. The Rietveld refinement also showed additional electron density on the lithium sites, indicating 3 at.% iron on the lithium site. Electrochemical characteristic of the composite was evaluated by using galvanostatic charge/discharge tests. While cycling at C/3 (C/10) rate the discharge capacity increases, starting from the value of 94.1 (116.0) mAh/g and reaching 99.5 (124.0) mAh/g at the end of the cycling. Particle morphology was revealed by both scanning and transmission electron microscopies. On the thin particle edges carbon film with a typical thickness of several nanometers can be observed, as well as small carbon agglomerates (typical size < 6 nm) at certain spots on the substrate surface.
T2  - Solid State Ionics
T1  - Synthesis and characterization of LiFePO4/C composite obtained by sonochemical method
SP  - 415
EP  - 419
IS  - 11-12
DO  - 10.1016/j.ssi.2008.03.014
UR  - https://hdl.handle.net/21.15107/rcub_dais_754
ER  - 
@article{
author = "Jugović, Dragana and Mitrić, Miodrag and Cvjetićanin, Nikola and Jančar, Boštjan and Mentus, Slavko and Uskoković, Dragan",
year = "2008",
abstract = "Lithium iron phosphate has become of great interest as storage cathode for the next generation of rechargeable lithium batteries. Olivine structure LiFePO4/C composite powder was prepared by ultrasound assisted synthesis. A polyvinyl alcohol solution was used as the source of an in situ formed carbon. X-ray powder diffraction confirmed the phase purity. X-ray powder diffraction data were used for the crystal structure refinement, based on Rietveld full profile method. All relevant structural and microstructural crystal parameters that could be significant for electrochemical intercalation/deintercalation processes were determined. The Rietveld refinement also showed additional electron density on the lithium sites, indicating 3 at.% iron on the lithium site. Electrochemical characteristic of the composite was evaluated by using galvanostatic charge/discharge tests. While cycling at C/3 (C/10) rate the discharge capacity increases, starting from the value of 94.1 (116.0) mAh/g and reaching 99.5 (124.0) mAh/g at the end of the cycling. Particle morphology was revealed by both scanning and transmission electron microscopies. On the thin particle edges carbon film with a typical thickness of several nanometers can be observed, as well as small carbon agglomerates (typical size < 6 nm) at certain spots on the substrate surface.",
journal = "Solid State Ionics",
title = "Synthesis and characterization of LiFePO4/C composite obtained by sonochemical method",
pages = "415-419",
number = "11-12",
doi = "10.1016/j.ssi.2008.03.014",
url = "https://hdl.handle.net/21.15107/rcub_dais_754"
}
Jugović, D., Mitrić, M., Cvjetićanin, N., Jančar, B., Mentus, S.,& Uskoković, D.. (2008). Synthesis and characterization of LiFePO4/C composite obtained by sonochemical method. in Solid State Ionics(11-12), 415-419.
https://doi.org/10.1016/j.ssi.2008.03.014
https://hdl.handle.net/21.15107/rcub_dais_754
Jugović D, Mitrić M, Cvjetićanin N, Jančar B, Mentus S, Uskoković D. Synthesis and characterization of LiFePO4/C composite obtained by sonochemical method. in Solid State Ionics. 2008;(11-12):415-419.
doi:10.1016/j.ssi.2008.03.014
https://hdl.handle.net/21.15107/rcub_dais_754 .
Jugović, Dragana, Mitrić, Miodrag, Cvjetićanin, Nikola, Jančar, Boštjan, Mentus, Slavko, Uskoković, Dragan, "Synthesis and characterization of LiFePO4/C composite obtained by sonochemical method" in Solid State Ionics, no. 11-12 (2008):415-419,
https://doi.org/10.1016/j.ssi.2008.03.014 .,
https://hdl.handle.net/21.15107/rcub_dais_754 .
38
37
47

Crystal structure of hydroxyapatite nanorods synthesized by sonochemical homogeneous precipitation

Jevtić, Marija; Mitrić, Miodrag; Škapin, Srečo Davor; Jančar, Boštjan; Ignjatović, Nenad; Uskoković, Dragan

(2008)

TY  - JOUR
AU  - Jevtić, Marija
AU  - Mitrić, Miodrag
AU  - Škapin, Srečo Davor
AU  - Jančar, Boštjan
AU  - Ignjatović, Nenad
AU  - Uskoković, Dragan
PY  - 2008
UR  - https://dais.sanu.ac.rs/123456789/2743
AB  - Using a homogeneous precipitation method in an ultrasound field, we synthesized nanosized, platelike hydroxyapatite (HAp). The internal structure of these platelike formations consists of specifically oriented and laterally connected nanorods. The synthesized HAp nanorods have a length of about 500 nm and a diameter of about 100 nm. A, closer inspection of the microstructure of a single nanorod revealed a highly regular and defect-free lattice with unique crystallographic plane orientations. The obtained structure was related to the influence of the ultrasound on the growth mechanism. The samples were characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and transmission, electron microscopy (TEM).
T2  - Crystal Growth and Design
T1  - Crystal structure of hydroxyapatite nanorods synthesized by sonochemical homogeneous precipitation
SP  - 2217
EP  - 2222
VL  - 8
IS  - 7
DO  - 10.1021/cg7007304
UR  - https://hdl.handle.net/21.15107/rcub_dais_2743
ER  - 
@article{
author = "Jevtić, Marija and Mitrić, Miodrag and Škapin, Srečo Davor and Jančar, Boštjan and Ignjatović, Nenad and Uskoković, Dragan",
year = "2008",
abstract = "Using a homogeneous precipitation method in an ultrasound field, we synthesized nanosized, platelike hydroxyapatite (HAp). The internal structure of these platelike formations consists of specifically oriented and laterally connected nanorods. The synthesized HAp nanorods have a length of about 500 nm and a diameter of about 100 nm. A, closer inspection of the microstructure of a single nanorod revealed a highly regular and defect-free lattice with unique crystallographic plane orientations. The obtained structure was related to the influence of the ultrasound on the growth mechanism. The samples were characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and transmission, electron microscopy (TEM).",
journal = "Crystal Growth and Design",
title = "Crystal structure of hydroxyapatite nanorods synthesized by sonochemical homogeneous precipitation",
pages = "2217-2222",
volume = "8",
number = "7",
doi = "10.1021/cg7007304",
url = "https://hdl.handle.net/21.15107/rcub_dais_2743"
}
Jevtić, M., Mitrić, M., Škapin, S. D., Jančar, B., Ignjatović, N.,& Uskoković, D.. (2008). Crystal structure of hydroxyapatite nanorods synthesized by sonochemical homogeneous precipitation. in Crystal Growth and Design, 8(7), 2217-2222.
https://doi.org/10.1021/cg7007304
https://hdl.handle.net/21.15107/rcub_dais_2743
Jevtić M, Mitrić M, Škapin SD, Jančar B, Ignjatović N, Uskoković D. Crystal structure of hydroxyapatite nanorods synthesized by sonochemical homogeneous precipitation. in Crystal Growth and Design. 2008;8(7):2217-2222.
doi:10.1021/cg7007304
https://hdl.handle.net/21.15107/rcub_dais_2743 .
Jevtić, Marija, Mitrić, Miodrag, Škapin, Srečo Davor, Jančar, Boštjan, Ignjatović, Nenad, Uskoković, Dragan, "Crystal structure of hydroxyapatite nanorods synthesized by sonochemical homogeneous precipitation" in Crystal Growth and Design, 8, no. 7 (2008):2217-2222,
https://doi.org/10.1021/cg7007304 .,
https://hdl.handle.net/21.15107/rcub_dais_2743 .
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209
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