Bukara, Katarina

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  • Bukara, Katarina (8)

Author's Bibliography

Mapping of hemoglobin in erythrocytes and erythrocyte ghosts using two photon excitation fluorescence microscopy

Bukara, Katarina; Jovanić, Svetlana; Drvenica, Ivana; Stančić, Ana; Ilić, Vesna Lj.; Rabasović, Mihailo D.; Pantelić, Dejan; Jelenković, Branislav; Bugarski, Branko; Krmpot, Aleksandar

(Spie-Soc Photo-Optical Instrumentation Engineers, Bellingham, 2017)

TY  - JOUR
AU  - Bukara, Katarina
AU  - Jovanić, Svetlana
AU  - Drvenica, Ivana
AU  - Stančić, Ana
AU  - Ilić, Vesna Lj.
AU  - Rabasović, Mihailo D.
AU  - Pantelić, Dejan
AU  - Jelenković, Branislav
AU  - Bugarski, Branko
AU  - Krmpot, Aleksandar
PY  - 2017
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3747
AB  - The present study describes utilization of two photon excitation fluorescence (2PE) microscopy for visualization of the hemoglobin in human and porcine erythrocytes and their empty membranes (i.e., ghosts). High-quality, label-and fixation-free visualization of hemoglobin was achieved at excitation wavelength 730 nm by detecting visible autofluorescence. Localization in the suspension and spatial distribution (i.e., mapping) of residual hemoglobin in erythrocyte ghosts has been resolved by 2PE. Prior to the 2PE mapping, the presence of residual hemoglobin in the bulk suspension of erythrocyte ghosts was confirmed by cyanmethemoglobin assay. 2PE analysis revealed that the distribution of hemoglobin in intact erythrocytes follows the cells' shape. Two types of erythrocytes, human and porcine, characterized with discocyte and echinocyte morphology, respectively, showed significant differences in hemoglobin distribution. The 2PE images have revealed that despite an extensive washing out procedure after gradual hypotonic hemolysis, a certain amount of hemoglobin localized on the intracellular side always remains bound to the membrane and cannot be eliminated. The obtained results open the possibility to use 2PE microscopy to examine hemoglobin distribution in erythrocytes and estimate the purity level of erythrocyte ghosts in biotechnological processes.
PB  - Spie-Soc Photo-Optical Instrumentation Engineers, Bellingham
T2  - Journal of Biomedical Optics
T1  - Mapping of hemoglobin in erythrocytes and erythrocyte ghosts using two photon excitation fluorescence microscopy
IS  - 2
VL  - 22
DO  - 10.1117/1.JBO.22.2.026003
ER  - 
@article{
author = "Bukara, Katarina and Jovanić, Svetlana and Drvenica, Ivana and Stančić, Ana and Ilić, Vesna Lj. and Rabasović, Mihailo D. and Pantelić, Dejan and Jelenković, Branislav and Bugarski, Branko and Krmpot, Aleksandar",
year = "2017",
abstract = "The present study describes utilization of two photon excitation fluorescence (2PE) microscopy for visualization of the hemoglobin in human and porcine erythrocytes and their empty membranes (i.e., ghosts). High-quality, label-and fixation-free visualization of hemoglobin was achieved at excitation wavelength 730 nm by detecting visible autofluorescence. Localization in the suspension and spatial distribution (i.e., mapping) of residual hemoglobin in erythrocyte ghosts has been resolved by 2PE. Prior to the 2PE mapping, the presence of residual hemoglobin in the bulk suspension of erythrocyte ghosts was confirmed by cyanmethemoglobin assay. 2PE analysis revealed that the distribution of hemoglobin in intact erythrocytes follows the cells' shape. Two types of erythrocytes, human and porcine, characterized with discocyte and echinocyte morphology, respectively, showed significant differences in hemoglobin distribution. The 2PE images have revealed that despite an extensive washing out procedure after gradual hypotonic hemolysis, a certain amount of hemoglobin localized on the intracellular side always remains bound to the membrane and cannot be eliminated. The obtained results open the possibility to use 2PE microscopy to examine hemoglobin distribution in erythrocytes and estimate the purity level of erythrocyte ghosts in biotechnological processes.",
publisher = "Spie-Soc Photo-Optical Instrumentation Engineers, Bellingham",
journal = "Journal of Biomedical Optics",
title = "Mapping of hemoglobin in erythrocytes and erythrocyte ghosts using two photon excitation fluorescence microscopy",
number = "2",
volume = "22",
doi = "10.1117/1.JBO.22.2.026003"
}
Bukara, K., Jovanić, S., Drvenica, I., Stančić, A., Ilić, V. Lj., Rabasović, M. D., Pantelić, D., Jelenković, B., Bugarski, B.,& Krmpot, A.. (2017). Mapping of hemoglobin in erythrocytes and erythrocyte ghosts using two photon excitation fluorescence microscopy. in Journal of Biomedical Optics
Spie-Soc Photo-Optical Instrumentation Engineers, Bellingham., 22(2).
https://doi.org/10.1117/1.JBO.22.2.026003
Bukara K, Jovanić S, Drvenica I, Stančić A, Ilić VL, Rabasović MD, Pantelić D, Jelenković B, Bugarski B, Krmpot A. Mapping of hemoglobin in erythrocytes and erythrocyte ghosts using two photon excitation fluorescence microscopy. in Journal of Biomedical Optics. 2017;22(2).
doi:10.1117/1.JBO.22.2.026003 .
Bukara, Katarina, Jovanić, Svetlana, Drvenica, Ivana, Stančić, Ana, Ilić, Vesna Lj., Rabasović, Mihailo D., Pantelić, Dejan, Jelenković, Branislav, Bugarski, Branko, Krmpot, Aleksandar, "Mapping of hemoglobin in erythrocytes and erythrocyte ghosts using two photon excitation fluorescence microscopy" in Journal of Biomedical Optics, 22, no. 2 (2017),
https://doi.org/10.1117/1.JBO.22.2.026003 . .
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Biomembranes from slaughterhouse blood erythrocytes as prolonged release systems for dexamethasone sodium phosphate

Drvenica, Ivana; Bukara, Katarina; Ilić, Vesna Lj.; Mišić, Danijela; Vasić, Borislav; Gajić, Radoš B.; Đorđević, Verica; Veljović, Đorđe; Belić, Aleksandar; Bugarski, Branko

(Wiley, Hoboken, 2016)

TY  - JOUR
AU  - Drvenica, Ivana
AU  - Bukara, Katarina
AU  - Ilić, Vesna Lj.
AU  - Mišić, Danijela
AU  - Vasić, Borislav
AU  - Gajić, Radoš B.
AU  - Đorđević, Verica
AU  - Veljović, Đorđe
AU  - Belić, Aleksandar
AU  - Bugarski, Branko
PY  - 2016
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3329
AB  - The present study investigated preparation of bovine and porcine erythrocyte membranes from slaughterhouse blood as bio-derived materials for delivery of dexamethasone-sodium phosphate (DexP). The obtained biomembranes, i.e., ghosts were characterized in vitro in terms of morphological properties, loading parameters, and release behavior. For the last two, an UHPLC/-HESI-MS/MS based analytical procedure for absolute drug identification and quantification was developed. The results revealed that loading of DexP into both type of ghosts was directly proportional to the increase of drug concentration in the incubation medium, while incubation at 37 degrees C had statistically significant effect on loaded amount of DexP (P lt 0.05). The encapsulation efficiency was about fivefold higher in porcine compared to bovine ghosts. Insight into ghosts' surface morphology by field emission-scanning electron microscopy and atomic force microscopy confirmed that besides inevitable effects of osmosis, DexP inclusion itself had no observable additional effect on the morphology of the ghosts carriers. DexP release profiles were dependent on erythrocyte ghost type and amount of residual hemoglobin. However, sustained DexP release was achieved and shown over 3 days from porcine ghosts and 5 days from bovine erythrocyte ghosts.
PB  - Wiley, Hoboken
T2  - Biotechnology Progress
T1  - Biomembranes from slaughterhouse blood erythrocytes as prolonged release systems for dexamethasone sodium phosphate
EP  - 1055
IS  - 4
SP  - 1046
VL  - 32
DO  - 10.1002/btpr.2304
ER  - 
@article{
author = "Drvenica, Ivana and Bukara, Katarina and Ilić, Vesna Lj. and Mišić, Danijela and Vasić, Borislav and Gajić, Radoš B. and Đorđević, Verica and Veljović, Đorđe and Belić, Aleksandar and Bugarski, Branko",
year = "2016",
abstract = "The present study investigated preparation of bovine and porcine erythrocyte membranes from slaughterhouse blood as bio-derived materials for delivery of dexamethasone-sodium phosphate (DexP). The obtained biomembranes, i.e., ghosts were characterized in vitro in terms of morphological properties, loading parameters, and release behavior. For the last two, an UHPLC/-HESI-MS/MS based analytical procedure for absolute drug identification and quantification was developed. The results revealed that loading of DexP into both type of ghosts was directly proportional to the increase of drug concentration in the incubation medium, while incubation at 37 degrees C had statistically significant effect on loaded amount of DexP (P lt 0.05). The encapsulation efficiency was about fivefold higher in porcine compared to bovine ghosts. Insight into ghosts' surface morphology by field emission-scanning electron microscopy and atomic force microscopy confirmed that besides inevitable effects of osmosis, DexP inclusion itself had no observable additional effect on the morphology of the ghosts carriers. DexP release profiles were dependent on erythrocyte ghost type and amount of residual hemoglobin. However, sustained DexP release was achieved and shown over 3 days from porcine ghosts and 5 days from bovine erythrocyte ghosts.",
publisher = "Wiley, Hoboken",
journal = "Biotechnology Progress",
title = "Biomembranes from slaughterhouse blood erythrocytes as prolonged release systems for dexamethasone sodium phosphate",
pages = "1055-1046",
number = "4",
volume = "32",
doi = "10.1002/btpr.2304"
}
Drvenica, I., Bukara, K., Ilić, V. Lj., Mišić, D., Vasić, B., Gajić, R. B., Đorđević, V., Veljović, Đ., Belić, A.,& Bugarski, B.. (2016). Biomembranes from slaughterhouse blood erythrocytes as prolonged release systems for dexamethasone sodium phosphate. in Biotechnology Progress
Wiley, Hoboken., 32(4), 1046-1055.
https://doi.org/10.1002/btpr.2304
Drvenica I, Bukara K, Ilić VL, Mišić D, Vasić B, Gajić RB, Đorđević V, Veljović Đ, Belić A, Bugarski B. Biomembranes from slaughterhouse blood erythrocytes as prolonged release systems for dexamethasone sodium phosphate. in Biotechnology Progress. 2016;32(4):1046-1055.
doi:10.1002/btpr.2304 .
Drvenica, Ivana, Bukara, Katarina, Ilić, Vesna Lj., Mišić, Danijela, Vasić, Borislav, Gajić, Radoš B., Đorđević, Verica, Veljović, Đorđe, Belić, Aleksandar, Bugarski, Branko, "Biomembranes from slaughterhouse blood erythrocytes as prolonged release systems for dexamethasone sodium phosphate" in Biotechnology Progress, 32, no. 4 (2016):1046-1055,
https://doi.org/10.1002/btpr.2304 . .
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Comparative studies on osmosis based encapsulation of sodium diclofenac in porcine and outdated human erythrocyte ghosts

Bukara, Katarina; Drvenica, Ivana; Ilić, Vesna Lj.; Stančić, Ana; Mišić, Danijela; Vasić, Borislav; Gajić, Radoš; Vučetić, Dušan; Kiekens, Filip; Bugarski, Branko

(Elsevier Science Bv, Amsterdam, 2016)

TY  - JOUR
AU  - Bukara, Katarina
AU  - Drvenica, Ivana
AU  - Ilić, Vesna Lj.
AU  - Stančić, Ana
AU  - Mišić, Danijela
AU  - Vasić, Borislav
AU  - Gajić, Radoš
AU  - Vučetić, Dušan
AU  - Kiekens, Filip
AU  - Bugarski, Branko
PY  - 2016
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3318
AB  - The objective of our study was to develop controlled drug delivery system based on erythrocyte ghosts for amphiphilic compound sodium diclofenac considering the differences between erythrocytes derived from two readily available materials - porcine slaughterhouse and outdated transfusion human blood. Starting erythrocytes, empty erythrocyte ghosts and diclofenac loaded ghosts were compared in terms of the encapsulation efficiency, drug releasing profiles, size distribution, surface charge, conductivity, surface roughness and morphology. The encapsulation of sodium diclofenac was performed by an osmosis based process - gradual hemolysis. During this process sodium diclofenac exerted mild and delayed antihemolytic effect and increased potassium efflux in porcine but not in outdated human erythrocytes. FTIR spectra revealed lack of any membrane lipid disorder and chemical reaction with sodium diclofenac in encapsulated ghosts. Outdated human erythrocyte ghosts with detected nanoscale damages and reduced ability to shrink had encapsulation efficiency of only 8%. On the other hand, porcine erythrocyte ghosts had encapsulation efficiency of 37% and relatively slow drug release rate. More preserved structure and functional properties of porcine erythrocytes related to their superior encapsulation and release performances, define them as more appropriate for the usage in sodium diclofenac encapsulation process.
PB  - Elsevier Science Bv, Amsterdam
T2  - Journal of Biotechnology
T1  - Comparative studies on osmosis based encapsulation of sodium diclofenac in porcine and outdated human erythrocyte ghosts
EP  - 22
SP  - 14
VL  - 240
DO  - 10.1016/j.jbiotec.2016.10.017
ER  - 
@article{
author = "Bukara, Katarina and Drvenica, Ivana and Ilić, Vesna Lj. and Stančić, Ana and Mišić, Danijela and Vasić, Borislav and Gajić, Radoš and Vučetić, Dušan and Kiekens, Filip and Bugarski, Branko",
year = "2016",
abstract = "The objective of our study was to develop controlled drug delivery system based on erythrocyte ghosts for amphiphilic compound sodium diclofenac considering the differences between erythrocytes derived from two readily available materials - porcine slaughterhouse and outdated transfusion human blood. Starting erythrocytes, empty erythrocyte ghosts and diclofenac loaded ghosts were compared in terms of the encapsulation efficiency, drug releasing profiles, size distribution, surface charge, conductivity, surface roughness and morphology. The encapsulation of sodium diclofenac was performed by an osmosis based process - gradual hemolysis. During this process sodium diclofenac exerted mild and delayed antihemolytic effect and increased potassium efflux in porcine but not in outdated human erythrocytes. FTIR spectra revealed lack of any membrane lipid disorder and chemical reaction with sodium diclofenac in encapsulated ghosts. Outdated human erythrocyte ghosts with detected nanoscale damages and reduced ability to shrink had encapsulation efficiency of only 8%. On the other hand, porcine erythrocyte ghosts had encapsulation efficiency of 37% and relatively slow drug release rate. More preserved structure and functional properties of porcine erythrocytes related to their superior encapsulation and release performances, define them as more appropriate for the usage in sodium diclofenac encapsulation process.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Journal of Biotechnology",
title = "Comparative studies on osmosis based encapsulation of sodium diclofenac in porcine and outdated human erythrocyte ghosts",
pages = "22-14",
volume = "240",
doi = "10.1016/j.jbiotec.2016.10.017"
}
Bukara, K., Drvenica, I., Ilić, V. Lj., Stančić, A., Mišić, D., Vasić, B., Gajić, R., Vučetić, D., Kiekens, F.,& Bugarski, B.. (2016). Comparative studies on osmosis based encapsulation of sodium diclofenac in porcine and outdated human erythrocyte ghosts. in Journal of Biotechnology
Elsevier Science Bv, Amsterdam., 240, 14-22.
https://doi.org/10.1016/j.jbiotec.2016.10.017
Bukara K, Drvenica I, Ilić VL, Stančić A, Mišić D, Vasić B, Gajić R, Vučetić D, Kiekens F, Bugarski B. Comparative studies on osmosis based encapsulation of sodium diclofenac in porcine and outdated human erythrocyte ghosts. in Journal of Biotechnology. 2016;240:14-22.
doi:10.1016/j.jbiotec.2016.10.017 .
Bukara, Katarina, Drvenica, Ivana, Ilić, Vesna Lj., Stančić, Ana, Mišić, Danijela, Vasić, Borislav, Gajić, Radoš, Vučetić, Dušan, Kiekens, Filip, Bugarski, Branko, "Comparative studies on osmosis based encapsulation of sodium diclofenac in porcine and outdated human erythrocyte ghosts" in Journal of Biotechnology, 240 (2016):14-22,
https://doi.org/10.1016/j.jbiotec.2016.10.017 . .
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Ordered mesoporous silica to enhance the bioavailability of poorly water-soluble drugs: Proof of concept in man

Bukara, Katarina; Schueller, Laurent; Rosier, Jan; Martens, Mark A.; Daems, Tinne; Verheyden, Loes; Eelen, Siemon; Van Speybroeck, Michiel; Libanati, Cristian; Martens, Johan A.; Van Den Mooter, Guy; Frerart, Francoise; Jolling, Koen; De Gieter, Marjan; Bugarski, Branko; Kiekens, Filip

(Elsevier Science Bv, Amsterdam, 2016)

TY  - JOUR
AU  - Bukara, Katarina
AU  - Schueller, Laurent
AU  - Rosier, Jan
AU  - Martens, Mark A.
AU  - Daems, Tinne
AU  - Verheyden, Loes
AU  - Eelen, Siemon
AU  - Van Speybroeck, Michiel
AU  - Libanati, Cristian
AU  - Martens, Johan A.
AU  - Van Den Mooter, Guy
AU  - Frerart, Francoise
AU  - Jolling, Koen
AU  - De Gieter, Marjan
AU  - Bugarski, Branko
AU  - Kiekens, Filip
PY  - 2016
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3326
AB  - Formulating poorly water soluble drugs using ordered mesoporous silica materials is an emerging approach to tackle solubility-related bioavailability problems. The current study was conducted to assess the bioavailability-enhancing potential of ordered mesoporous silica in man. In this open-label, randomized, two-way cross-over study, 12 overnight fasted healthy volunteers received a single dose of fenofibrate formulated with ordered mesoporous silica-or a marketed product based on micronized fenofibrate. Plasma concentrations of fenofibric acid, the pharmacologically active metabolite of fenofibrate, were monitored up to 96 h post-dose. The rate (C-max/dose increased by 77%; t(max) reduced by 0.75 h) and extent of absorption (AUC(0-24h)/dose increased by 54%) of fenofibrate were significantly enhanced following administration of the ordered mesoporous silica based formulation. The results of this study serve as a proof of concept in man for this novel formulation approach.
PB  - Elsevier Science Bv, Amsterdam
T2  - European Journal of Pharmaceutics and Biopharmaceutics
T1  - Ordered mesoporous silica to enhance the bioavailability of poorly water-soluble drugs: Proof of concept in man
EP  - 225
SP  - 220
VL  - 108
DO  - 10.1016/j.ejpb.2016.08.020
ER  - 
@article{
author = "Bukara, Katarina and Schueller, Laurent and Rosier, Jan and Martens, Mark A. and Daems, Tinne and Verheyden, Loes and Eelen, Siemon and Van Speybroeck, Michiel and Libanati, Cristian and Martens, Johan A. and Van Den Mooter, Guy and Frerart, Francoise and Jolling, Koen and De Gieter, Marjan and Bugarski, Branko and Kiekens, Filip",
year = "2016",
abstract = "Formulating poorly water soluble drugs using ordered mesoporous silica materials is an emerging approach to tackle solubility-related bioavailability problems. The current study was conducted to assess the bioavailability-enhancing potential of ordered mesoporous silica in man. In this open-label, randomized, two-way cross-over study, 12 overnight fasted healthy volunteers received a single dose of fenofibrate formulated with ordered mesoporous silica-or a marketed product based on micronized fenofibrate. Plasma concentrations of fenofibric acid, the pharmacologically active metabolite of fenofibrate, were monitored up to 96 h post-dose. The rate (C-max/dose increased by 77%; t(max) reduced by 0.75 h) and extent of absorption (AUC(0-24h)/dose increased by 54%) of fenofibrate were significantly enhanced following administration of the ordered mesoporous silica based formulation. The results of this study serve as a proof of concept in man for this novel formulation approach.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "European Journal of Pharmaceutics and Biopharmaceutics",
title = "Ordered mesoporous silica to enhance the bioavailability of poorly water-soluble drugs: Proof of concept in man",
pages = "225-220",
volume = "108",
doi = "10.1016/j.ejpb.2016.08.020"
}
Bukara, K., Schueller, L., Rosier, J., Martens, M. A., Daems, T., Verheyden, L., Eelen, S., Van Speybroeck, M., Libanati, C., Martens, J. A., Van Den Mooter, G., Frerart, F., Jolling, K., De Gieter, M., Bugarski, B.,& Kiekens, F.. (2016). Ordered mesoporous silica to enhance the bioavailability of poorly water-soluble drugs: Proof of concept in man. in European Journal of Pharmaceutics and Biopharmaceutics
Elsevier Science Bv, Amsterdam., 108, 220-225.
https://doi.org/10.1016/j.ejpb.2016.08.020
Bukara K, Schueller L, Rosier J, Martens MA, Daems T, Verheyden L, Eelen S, Van Speybroeck M, Libanati C, Martens JA, Van Den Mooter G, Frerart F, Jolling K, De Gieter M, Bugarski B, Kiekens F. Ordered mesoporous silica to enhance the bioavailability of poorly water-soluble drugs: Proof of concept in man. in European Journal of Pharmaceutics and Biopharmaceutics. 2016;108:220-225.
doi:10.1016/j.ejpb.2016.08.020 .
Bukara, Katarina, Schueller, Laurent, Rosier, Jan, Martens, Mark A., Daems, Tinne, Verheyden, Loes, Eelen, Siemon, Van Speybroeck, Michiel, Libanati, Cristian, Martens, Johan A., Van Den Mooter, Guy, Frerart, Francoise, Jolling, Koen, De Gieter, Marjan, Bugarski, Branko, Kiekens, Filip, "Ordered mesoporous silica to enhance the bioavailability of poorly water-soluble drugs: Proof of concept in man" in European Journal of Pharmaceutics and Biopharmaceutics, 108 (2016):220-225,
https://doi.org/10.1016/j.ejpb.2016.08.020 . .
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In Vivo Performance of Fenofibrate Formulated With Ordered Mesoporous Silica Versus 2-Marketed Formulations: A Comparative Bioavailability Study in Beagle Dogs

Bukara, Katarina; Schueller, Laurent; Rosier, Jan; Daems, Tinne; Verheyden, Loes; Eelen, Siemon; Martens, Johan A.; Van den Mooter, Guy; Bugarski, Branko; Kiekens, Filip

(Wiley-Blackwell, Hoboken, 2016)

TY  - JOUR
AU  - Bukara, Katarina
AU  - Schueller, Laurent
AU  - Rosier, Jan
AU  - Daems, Tinne
AU  - Verheyden, Loes
AU  - Eelen, Siemon
AU  - Martens, Johan A.
AU  - Van den Mooter, Guy
AU  - Bugarski, Branko
AU  - Kiekens, Filip
PY  - 2016
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/3240
AB  - The present study aims to evaluate the in vitro and in vivo performance of ordered mesoporous silica (OMS) as a carrier for the poorly water-soluble compound fenofibrate. Fenofibrate was loaded into OMS via incipient wetness impregnation to obtain a 29% drug load and formulated into capsules. Two capsule dosage forms (containing 33.5 and 16.75 mg fenofibrate, respectively) were compared with the commercially available forms-Lipanthyl (R) (fenofibrate microcrystals) and Tricor (R) (fenofibrate nanocrystals). In vitro dissolution tests showed that the amount of fenofibrate released from Lipanthyl (R) and Tricor (R) was approximately 30%, whereas approximately 66% and 60% of the drug was released from OMS capsules containing 33.5 and 16.75 mg of fenofibrate, respectively. Storage of OMS capsules loaded with 33.5 mg of fenofibrate at 25 degrees C/60% relative humidity (RH) or 40 degrees C/75% RH did not alter the release kinetics, nor the physical state of the compound, pointing the stability of the present formulation. The in vivo study in dogs confirmed satisfying level of safety and tolerability of fenofibrate-OMS formulation (eq. 33.5 mg) with the potential to improve the absorption of fenofibrate. Though some variability in the data, this formulation is promising to be further investigated in a clinical trial setting.
PB  - Wiley-Blackwell, Hoboken
T2  - Journal of Pharmaceutical Sciences
T1  - In Vivo Performance of Fenofibrate Formulated With Ordered Mesoporous Silica Versus 2-Marketed Formulations: A Comparative Bioavailability Study in Beagle Dogs
EP  - 2385
IS  - 8
SP  - 2381
VL  - 105
DO  - 10.1016/j.xphs.2016.05.019
ER  - 
@article{
author = "Bukara, Katarina and Schueller, Laurent and Rosier, Jan and Daems, Tinne and Verheyden, Loes and Eelen, Siemon and Martens, Johan A. and Van den Mooter, Guy and Bugarski, Branko and Kiekens, Filip",
year = "2016",
abstract = "The present study aims to evaluate the in vitro and in vivo performance of ordered mesoporous silica (OMS) as a carrier for the poorly water-soluble compound fenofibrate. Fenofibrate was loaded into OMS via incipient wetness impregnation to obtain a 29% drug load and formulated into capsules. Two capsule dosage forms (containing 33.5 and 16.75 mg fenofibrate, respectively) were compared with the commercially available forms-Lipanthyl (R) (fenofibrate microcrystals) and Tricor (R) (fenofibrate nanocrystals). In vitro dissolution tests showed that the amount of fenofibrate released from Lipanthyl (R) and Tricor (R) was approximately 30%, whereas approximately 66% and 60% of the drug was released from OMS capsules containing 33.5 and 16.75 mg of fenofibrate, respectively. Storage of OMS capsules loaded with 33.5 mg of fenofibrate at 25 degrees C/60% relative humidity (RH) or 40 degrees C/75% RH did not alter the release kinetics, nor the physical state of the compound, pointing the stability of the present formulation. The in vivo study in dogs confirmed satisfying level of safety and tolerability of fenofibrate-OMS formulation (eq. 33.5 mg) with the potential to improve the absorption of fenofibrate. Though some variability in the data, this formulation is promising to be further investigated in a clinical trial setting.",
publisher = "Wiley-Blackwell, Hoboken",
journal = "Journal of Pharmaceutical Sciences",
title = "In Vivo Performance of Fenofibrate Formulated With Ordered Mesoporous Silica Versus 2-Marketed Formulations: A Comparative Bioavailability Study in Beagle Dogs",
pages = "2385-2381",
number = "8",
volume = "105",
doi = "10.1016/j.xphs.2016.05.019"
}
Bukara, K., Schueller, L., Rosier, J., Daems, T., Verheyden, L., Eelen, S., Martens, J. A., Van den Mooter, G., Bugarski, B.,& Kiekens, F.. (2016). In Vivo Performance of Fenofibrate Formulated With Ordered Mesoporous Silica Versus 2-Marketed Formulations: A Comparative Bioavailability Study in Beagle Dogs. in Journal of Pharmaceutical Sciences
Wiley-Blackwell, Hoboken., 105(8), 2381-2385.
https://doi.org/10.1016/j.xphs.2016.05.019
Bukara K, Schueller L, Rosier J, Daems T, Verheyden L, Eelen S, Martens JA, Van den Mooter G, Bugarski B, Kiekens F. In Vivo Performance of Fenofibrate Formulated With Ordered Mesoporous Silica Versus 2-Marketed Formulations: A Comparative Bioavailability Study in Beagle Dogs. in Journal of Pharmaceutical Sciences. 2016;105(8):2381-2385.
doi:10.1016/j.xphs.2016.05.019 .
Bukara, Katarina, Schueller, Laurent, Rosier, Jan, Daems, Tinne, Verheyden, Loes, Eelen, Siemon, Martens, Johan A., Van den Mooter, Guy, Bugarski, Branko, Kiekens, Filip, "In Vivo Performance of Fenofibrate Formulated With Ordered Mesoporous Silica Versus 2-Marketed Formulations: A Comparative Bioavailability Study in Beagle Dogs" in Journal of Pharmaceutical Sciences, 105, no. 8 (2016):2381-2385,
https://doi.org/10.1016/j.xphs.2016.05.019 . .
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Antioksidativna aktivnost etanolnih ekstrakata Thymus serpyllum

Jovanović, Aleksandra A.; Zdunić, Gordana; Ćujić, Nada; Šavikin, Katarina; Bukara, Katarina; Lević, Steva; Bugarski, Branko

(Faculty of Technology, Zvornik, 2015)

TY  - CONF
AU  - Jovanović, Aleksandra A.
AU  - Zdunić, Gordana
AU  - Ćujić, Nada
AU  - Šavikin, Katarina
AU  - Bukara, Katarina
AU  - Lević, Steva
AU  - Bugarski, Branko
PY  - 2015
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/6449
AB  - Wild Thyme (Thymus serpyllum, Lamiaceae) is a subshrub from the Lamiaceae family, with
plants that are rich in essential oils and antioxidative polyphenolic substances. Reducing
potential of phenolic compounds gives them a special role in the adsorption and neutralization
of free radicals. In the present study, we used a method of maceration, lasting 15, 30, 60 and 90
minutes, degree of fragmentation 0.7, two types of solvent (50% and 96% ethanol) and ratio
drugs:solvent 1:20. In Folin-Ciocalteu method, the higest total polyphenols content was obtained
in 50% ethanolic extract after 90 minutes of extraction, while the lowest total polyphenols
content was recorded in 96% ethanolic extract after 15 minutes (1173,21 mg GA/g DW and
102,56 mg GA/g DW, respectively). Ethanolic extracts were analized for antioxidant activity by
using spectrophotometric methods, DPPH method and ABTS method. There is signifficant
difference between antioxidant activity in 50% and in 96% ethanolic extracts. The worse result
was obtained with 96% ethanol as extractant after 15 minutes of maceration (IC50 31,323 mg/ml
and 0,116 mM Trolox/g DW). This study found that both total polyphenols and antioxidant
activities determined were significantly affected by the type of solvent and time of extraction.
Also, the levels of total soluble phenolic compounds were positively correlated with free radical
scavenging activities against DPPH and ABTS radicals.
AB  - Majčina dušica (Thymus serpyllum, Lamiaceae) je višegodišnji busen iz familije Lamiaceae, koju
čine biljke bogate etarskim uljima i antioksidativnim polifenolnim supstancama. Antioksidativnu
aktivnost fenolne komponente duguju svom redukujućem potencijalu, koji im daje posebnu ulogu
u adsorpciji i neutralizaciji slobodnih radikala. U ovoj studiji ekstrakti T. serpyllum su dobijeni
metodom maceracije, u trajanju od 15, 30, 60 i 90 minuta, korišćenjem droge stepena
usitnjenosti 0,7, dva rastvarača (50% i 96% etanola) i odnosa droga:rastvarač 1:20. FolinCiocalteu metodom je određen sadržaj ukupnih polifenola, gde je 50% etanolni ekstrakt, nakon
90 minuta ekstrakcije sadržao najveću količinu ukupnih polifenola, dok su najniže vrednosti
zabeležene kod 96% etanolnog ekstrakta, nakon 15 minuta (1173,21 mg GA/g suve droge,
odnosno 102,56 mg GA/g suve droge). Primenom spektrofotometrijskih metoda, DPPH metode i
ABTS metode, određena je antioksidativna aktivnost 50% i 96% etanolnih ekstrakata T.
serpyllum. Statistika je pokazala da postoji značajna razlika između antioksidativnog kapaciteta
50% i 96% etanolnih ekstrakata. Najlošiju antioksidativnu aktivnost poseduje 96% etanolni
ekstrakt, nakon 15 minuta ekstrakcije (IC50 31,323 mg/ml i 116 mM Troloxa/g suve droge).
Sadržaj ukupnih fenola i antioksidativna aktivnost ekstrakata zavise od tipa rastvarača
korišćenog za ekstrakciju i vremena ekstrakcije. Ovaj rad pokazuje da postoji pozitivna
korelacija između sadržaja ukupnih polifenola i kapaciteta neutralizacije DPPH i ABTS
radikala.
PB  - Faculty of Technology, Zvornik
C3  - IV International Congress of Engineering, Environment and Materials in Processing Industry
T1  - Antioksidativna aktivnost etanolnih ekstrakata Thymus serpyllum
EP  - 452
SP  - 444
DO  - 10.7251/EEMSR1501444J
ER  - 
@conference{
author = "Jovanović, Aleksandra A. and Zdunić, Gordana and Ćujić, Nada and Šavikin, Katarina and Bukara, Katarina and Lević, Steva and Bugarski, Branko",
year = "2015",
abstract = "Wild Thyme (Thymus serpyllum, Lamiaceae) is a subshrub from the Lamiaceae family, with
plants that are rich in essential oils and antioxidative polyphenolic substances. Reducing
potential of phenolic compounds gives them a special role in the adsorption and neutralization
of free radicals. In the present study, we used a method of maceration, lasting 15, 30, 60 and 90
minutes, degree of fragmentation 0.7, two types of solvent (50% and 96% ethanol) and ratio
drugs:solvent 1:20. In Folin-Ciocalteu method, the higest total polyphenols content was obtained
in 50% ethanolic extract after 90 minutes of extraction, while the lowest total polyphenols
content was recorded in 96% ethanolic extract after 15 minutes (1173,21 mg GA/g DW and
102,56 mg GA/g DW, respectively). Ethanolic extracts were analized for antioxidant activity by
using spectrophotometric methods, DPPH method and ABTS method. There is signifficant
difference between antioxidant activity in 50% and in 96% ethanolic extracts. The worse result
was obtained with 96% ethanol as extractant after 15 minutes of maceration (IC50 31,323 mg/ml
and 0,116 mM Trolox/g DW). This study found that both total polyphenols and antioxidant
activities determined were significantly affected by the type of solvent and time of extraction.
Also, the levels of total soluble phenolic compounds were positively correlated with free radical
scavenging activities against DPPH and ABTS radicals., Majčina dušica (Thymus serpyllum, Lamiaceae) je višegodišnji busen iz familije Lamiaceae, koju
čine biljke bogate etarskim uljima i antioksidativnim polifenolnim supstancama. Antioksidativnu
aktivnost fenolne komponente duguju svom redukujućem potencijalu, koji im daje posebnu ulogu
u adsorpciji i neutralizaciji slobodnih radikala. U ovoj studiji ekstrakti T. serpyllum su dobijeni
metodom maceracije, u trajanju od 15, 30, 60 i 90 minuta, korišćenjem droge stepena
usitnjenosti 0,7, dva rastvarača (50% i 96% etanola) i odnosa droga:rastvarač 1:20. FolinCiocalteu metodom je određen sadržaj ukupnih polifenola, gde je 50% etanolni ekstrakt, nakon
90 minuta ekstrakcije sadržao najveću količinu ukupnih polifenola, dok su najniže vrednosti
zabeležene kod 96% etanolnog ekstrakta, nakon 15 minuta (1173,21 mg GA/g suve droge,
odnosno 102,56 mg GA/g suve droge). Primenom spektrofotometrijskih metoda, DPPH metode i
ABTS metode, određena je antioksidativna aktivnost 50% i 96% etanolnih ekstrakata T.
serpyllum. Statistika je pokazala da postoji značajna razlika između antioksidativnog kapaciteta
50% i 96% etanolnih ekstrakata. Najlošiju antioksidativnu aktivnost poseduje 96% etanolni
ekstrakt, nakon 15 minuta ekstrakcije (IC50 31,323 mg/ml i 116 mM Troloxa/g suve droge).
Sadržaj ukupnih fenola i antioksidativna aktivnost ekstrakata zavise od tipa rastvarača
korišćenog za ekstrakciju i vremena ekstrakcije. Ovaj rad pokazuje da postoji pozitivna
korelacija između sadržaja ukupnih polifenola i kapaciteta neutralizacije DPPH i ABTS
radikala.",
publisher = "Faculty of Technology, Zvornik",
journal = "IV International Congress of Engineering, Environment and Materials in Processing Industry",
title = "Antioksidativna aktivnost etanolnih ekstrakata Thymus serpyllum",
pages = "452-444",
doi = "10.7251/EEMSR1501444J"
}
Jovanović, A. A., Zdunić, G., Ćujić, N., Šavikin, K., Bukara, K., Lević, S.,& Bugarski, B.. (2015). Antioksidativna aktivnost etanolnih ekstrakata Thymus serpyllum. in IV International Congress of Engineering, Environment and Materials in Processing Industry
Faculty of Technology, Zvornik., 444-452.
https://doi.org/10.7251/EEMSR1501444J
Jovanović AA, Zdunić G, Ćujić N, Šavikin K, Bukara K, Lević S, Bugarski B. Antioksidativna aktivnost etanolnih ekstrakata Thymus serpyllum. in IV International Congress of Engineering, Environment and Materials in Processing Industry. 2015;:444-452.
doi:10.7251/EEMSR1501444J .
Jovanović, Aleksandra A., Zdunić, Gordana, Ćujić, Nada, Šavikin, Katarina, Bukara, Katarina, Lević, Steva, Bugarski, Branko, "Antioksidativna aktivnost etanolnih ekstrakata Thymus serpyllum" in IV International Congress of Engineering, Environment and Materials in Processing Industry (2015):444-452,
https://doi.org/10.7251/EEMSR1501444J . .

Flow cytometric determination of osmotic behaviour of animal erythrocytes toward their engineering for drug delivery

Kostić, Ivana T.; Ilić, Vesna Lj.; Bukara, Katarina; Mojsilović, Slavko B.; Đurić, Zorka Ž.; Draškovič, Petra; Bugarski, Branko

(Association of Chemical Engineers of Serbia, 2015)

TY  - JOUR
AU  - Kostić, Ivana T.
AU  - Ilić, Vesna Lj.
AU  - Bukara, Katarina
AU  - Mojsilović, Slavko B.
AU  - Đurić, Zorka Ž.
AU  - Draškovič, Petra
AU  - Bugarski, Branko
PY  - 2015
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2900
AB  - Despite the fact that the methods based on the osmotic properties of the cells are the most widely used for loading of drugs in human and animal erythrocytes, data related to the osmotic properties of erythrocytes derived from animal blood are scarce. This work was performed with an aim to investigate the possibility of use the flow cytometry as a tool for determination the osmotic behaviour of porcine and bovine erythrocytes, and thus facilitates the engineering of erythrocytes from animal blood to be drug carriers. The method of flow cytometry successfully provided the information about bovine and porcine erythrocyte osmotic fragility, and made the initial steps in assessment of erythrocyte shape in a large number of erythrocytes. Although this method is not able to confirm the swelling of porcine erythrocytes, it indicated the differences in porcine erythrocytes that had basic hematological parameters inside and outside the reference values. In order to apply/use the porcine and bovine erythrocytes as drug carriers, the method of flow cytometry, confirming the presence of osmotically different fractions of red blood cells, indicated that various amounts of the encapsulated drug in porcine and bovine erythrocytes can be expected.
AB  - Uprkos činjenici da su metode koje se baziraju na osmotskim osobinama ćelija najčešće korišćene metode za inkapsulaciju lekova u humane i životinjske eritrocite, podaci o osmotskim osobinama eritrocita životinjskog porekla su vrlo oskudni. Cilj ovog rada bio je ispitivanje mogućnosti korišćenja metode protočne citometrije za određivanje osmotskih osobina svinjskih i goveđih eritrocita, čime bi se olakšao inženjering pomenutih životinjskih eritrocita za otpuštanje lekova. Metodom protočne citometrije uspešno su dobijene informacije o osmotskoj fragilnosti svinjskih i goveđih eritrocita i načinjeni su početni koraci u proceni oblika velikog broja eritrocita. Iako ova metoda nije uspela da potvrdi bubrenje svinjskih eritrocita, ukazala je na razliku u uzorcima svinjskih eritrocita koji su imali osnovne hematološke parametre izvan i unutar referentnih vrednosti. U cilju primene svinjskih i goveđih eritrocita kao nosača lekova, metoda protočne citometrije je, potvrdivši prisustvo osmotski različitih frakcija eritrocita, ukazala na to da se različite količine inkapsuliranog leka u pojedinačnim, kako svinjskim, tako i goveđim eritrocitima mogu očekivati.
PB  - Association of Chemical Engineers of Serbia
T2  - Hemijska industrija
T1  - Flow cytometric determination of osmotic behaviour of animal erythrocytes toward their engineering for drug delivery
T1  - Određivanje osmotskih osobina životinjskih eritrocita protočnom citometrijom u cilju njihovog inženjeringa kao nosača lekova
EP  - 76
IS  - 1
SP  - 67
VL  - 69
DO  - 10.2298/HEMIND140124021K
ER  - 
@article{
author = "Kostić, Ivana T. and Ilić, Vesna Lj. and Bukara, Katarina and Mojsilović, Slavko B. and Đurić, Zorka Ž. and Draškovič, Petra and Bugarski, Branko",
year = "2015",
abstract = "Despite the fact that the methods based on the osmotic properties of the cells are the most widely used for loading of drugs in human and animal erythrocytes, data related to the osmotic properties of erythrocytes derived from animal blood are scarce. This work was performed with an aim to investigate the possibility of use the flow cytometry as a tool for determination the osmotic behaviour of porcine and bovine erythrocytes, and thus facilitates the engineering of erythrocytes from animal blood to be drug carriers. The method of flow cytometry successfully provided the information about bovine and porcine erythrocyte osmotic fragility, and made the initial steps in assessment of erythrocyte shape in a large number of erythrocytes. Although this method is not able to confirm the swelling of porcine erythrocytes, it indicated the differences in porcine erythrocytes that had basic hematological parameters inside and outside the reference values. In order to apply/use the porcine and bovine erythrocytes as drug carriers, the method of flow cytometry, confirming the presence of osmotically different fractions of red blood cells, indicated that various amounts of the encapsulated drug in porcine and bovine erythrocytes can be expected., Uprkos činjenici da su metode koje se baziraju na osmotskim osobinama ćelija najčešće korišćene metode za inkapsulaciju lekova u humane i životinjske eritrocite, podaci o osmotskim osobinama eritrocita životinjskog porekla su vrlo oskudni. Cilj ovog rada bio je ispitivanje mogućnosti korišćenja metode protočne citometrije za određivanje osmotskih osobina svinjskih i goveđih eritrocita, čime bi se olakšao inženjering pomenutih životinjskih eritrocita za otpuštanje lekova. Metodom protočne citometrije uspešno su dobijene informacije o osmotskoj fragilnosti svinjskih i goveđih eritrocita i načinjeni su početni koraci u proceni oblika velikog broja eritrocita. Iako ova metoda nije uspela da potvrdi bubrenje svinjskih eritrocita, ukazala je na razliku u uzorcima svinjskih eritrocita koji su imali osnovne hematološke parametre izvan i unutar referentnih vrednosti. U cilju primene svinjskih i goveđih eritrocita kao nosača lekova, metoda protočne citometrije je, potvrdivši prisustvo osmotski različitih frakcija eritrocita, ukazala na to da se različite količine inkapsuliranog leka u pojedinačnim, kako svinjskim, tako i goveđim eritrocitima mogu očekivati.",
publisher = "Association of Chemical Engineers of Serbia",
journal = "Hemijska industrija",
title = "Flow cytometric determination of osmotic behaviour of animal erythrocytes toward their engineering for drug delivery, Određivanje osmotskih osobina životinjskih eritrocita protočnom citometrijom u cilju njihovog inženjeringa kao nosača lekova",
pages = "76-67",
number = "1",
volume = "69",
doi = "10.2298/HEMIND140124021K"
}
Kostić, I. T., Ilić, V. Lj., Bukara, K., Mojsilović, S. B., Đurić, Z. Ž., Draškovič, P.,& Bugarski, B.. (2015). Flow cytometric determination of osmotic behaviour of animal erythrocytes toward their engineering for drug delivery. in Hemijska industrija
Association of Chemical Engineers of Serbia., 69(1), 67-76.
https://doi.org/10.2298/HEMIND140124021K
Kostić IT, Ilić VL, Bukara K, Mojsilović SB, Đurić ZŽ, Draškovič P, Bugarski B. Flow cytometric determination of osmotic behaviour of animal erythrocytes toward their engineering for drug delivery. in Hemijska industrija. 2015;69(1):67-76.
doi:10.2298/HEMIND140124021K .
Kostić, Ivana T., Ilić, Vesna Lj., Bukara, Katarina, Mojsilović, Slavko B., Đurić, Zorka Ž., Draškovič, Petra, Bugarski, Branko, "Flow cytometric determination of osmotic behaviour of animal erythrocytes toward their engineering for drug delivery" in Hemijska industrija, 69, no. 1 (2015):67-76,
https://doi.org/10.2298/HEMIND140124021K . .
2
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Erythrocyte membranes from slaughterhouse blood as potential drug vehicles: Isolation by gradual hypotonic hemolysis and biochemical and morphological characterization

Kostić, Ivana T.; Ilić, Vesna Lj.; Đorđević, Verica; Bukara, Katarina; Mojsilović, Slavko B.; Nedović, Viktor; Bugarski, Diana; Veljović, Đorđe; Misić, Danijela M.; Bugarski, Branko

(Elsevier, Amsterdam, 2014)

TY  - JOUR
AU  - Kostić, Ivana T.
AU  - Ilić, Vesna Lj.
AU  - Đorđević, Verica
AU  - Bukara, Katarina
AU  - Mojsilović, Slavko B.
AU  - Nedović, Viktor
AU  - Bugarski, Diana
AU  - Veljović, Đorđe
AU  - Misić, Danijela M.
AU  - Bugarski, Branko
PY  - 2014
UR  - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/2738
AB  - The present study was aimed at investigating the effect of isolation process-gradual hypotonic hemolysis on chosen parameters of the erythrocyte membranes (ghosts) originating from bovine and porcine slaughterhouse blood. The estimation of the gradual hypotonic hemolysis as a drug loading procedure for the erythrocyte ghosts was performed as well. Based on the results derived from analysis of the osmotic properties of the erythrocytes, the gradual hemolysis was performed with high volume of erythrocytes and 35 mM hypotonic sodium-phosphate/NaCl, enabling  gt 90% of hemolysis for both types of erythrocytes. Detailed insight into ghosts' morphology by field emission-scanning electron microscopy revealed a distortion from erythrocyte shape and an altered surface texture with increased bilayer curvature for both samples. Compared to erythrocytes, an average diameter of ghosts from both type of erythrocytes decreased for only about 10%. The reported unidispersity of the isolated ghosts is of great importance for their potential application as vehicles of active compounds. Gradual hemolysis did not lead to substantial loss of cholesterol and membrane/cytoskeleton proteins. This result indicated the ghosts' possibility to mimic the chemical and structural anisotropic environment of in vivo cell membranes, which is of significance for drug diffusion and partition coefficients. Induced shift of phosphatidylserine to external surface of the ghosts demonstrated their potential application as vehicles for targeted drug delivery to cells of reticuloendothelial system. Ultra high-performance liquid chromatography and Fourier transform infrared spectroscopy revealed the presence of a drug model - dexamethasone-sodium phosphate, and its interaction with structural components in both types of erythrocyte ghosts.
PB  - Elsevier, Amsterdam
T2  - Colloids and Surfaces B-Biointerfaces
T1  - Erythrocyte membranes from slaughterhouse blood as potential drug vehicles: Isolation by gradual hypotonic hemolysis and biochemical and morphological characterization
EP  - 259
SP  - 250
VL  - 122
DO  - 10.1016/j.colsurfb.2014.06.043
ER  - 
@article{
author = "Kostić, Ivana T. and Ilić, Vesna Lj. and Đorđević, Verica and Bukara, Katarina and Mojsilović, Slavko B. and Nedović, Viktor and Bugarski, Diana and Veljović, Đorđe and Misić, Danijela M. and Bugarski, Branko",
year = "2014",
abstract = "The present study was aimed at investigating the effect of isolation process-gradual hypotonic hemolysis on chosen parameters of the erythrocyte membranes (ghosts) originating from bovine and porcine slaughterhouse blood. The estimation of the gradual hypotonic hemolysis as a drug loading procedure for the erythrocyte ghosts was performed as well. Based on the results derived from analysis of the osmotic properties of the erythrocytes, the gradual hemolysis was performed with high volume of erythrocytes and 35 mM hypotonic sodium-phosphate/NaCl, enabling  gt 90% of hemolysis for both types of erythrocytes. Detailed insight into ghosts' morphology by field emission-scanning electron microscopy revealed a distortion from erythrocyte shape and an altered surface texture with increased bilayer curvature for both samples. Compared to erythrocytes, an average diameter of ghosts from both type of erythrocytes decreased for only about 10%. The reported unidispersity of the isolated ghosts is of great importance for their potential application as vehicles of active compounds. Gradual hemolysis did not lead to substantial loss of cholesterol and membrane/cytoskeleton proteins. This result indicated the ghosts' possibility to mimic the chemical and structural anisotropic environment of in vivo cell membranes, which is of significance for drug diffusion and partition coefficients. Induced shift of phosphatidylserine to external surface of the ghosts demonstrated their potential application as vehicles for targeted drug delivery to cells of reticuloendothelial system. Ultra high-performance liquid chromatography and Fourier transform infrared spectroscopy revealed the presence of a drug model - dexamethasone-sodium phosphate, and its interaction with structural components in both types of erythrocyte ghosts.",
publisher = "Elsevier, Amsterdam",
journal = "Colloids and Surfaces B-Biointerfaces",
title = "Erythrocyte membranes from slaughterhouse blood as potential drug vehicles: Isolation by gradual hypotonic hemolysis and biochemical and morphological characterization",
pages = "259-250",
volume = "122",
doi = "10.1016/j.colsurfb.2014.06.043"
}
Kostić, I. T., Ilić, V. Lj., Đorđević, V., Bukara, K., Mojsilović, S. B., Nedović, V., Bugarski, D., Veljović, Đ., Misić, D. M.,& Bugarski, B.. (2014). Erythrocyte membranes from slaughterhouse blood as potential drug vehicles: Isolation by gradual hypotonic hemolysis and biochemical and morphological characterization. in Colloids and Surfaces B-Biointerfaces
Elsevier, Amsterdam., 122, 250-259.
https://doi.org/10.1016/j.colsurfb.2014.06.043
Kostić IT, Ilić VL, Đorđević V, Bukara K, Mojsilović SB, Nedović V, Bugarski D, Veljović Đ, Misić DM, Bugarski B. Erythrocyte membranes from slaughterhouse blood as potential drug vehicles: Isolation by gradual hypotonic hemolysis and biochemical and morphological characterization. in Colloids and Surfaces B-Biointerfaces. 2014;122:250-259.
doi:10.1016/j.colsurfb.2014.06.043 .
Kostić, Ivana T., Ilić, Vesna Lj., Đorđević, Verica, Bukara, Katarina, Mojsilović, Slavko B., Nedović, Viktor, Bugarski, Diana, Veljović, Đorđe, Misić, Danijela M., Bugarski, Branko, "Erythrocyte membranes from slaughterhouse blood as potential drug vehicles: Isolation by gradual hypotonic hemolysis and biochemical and morphological characterization" in Colloids and Surfaces B-Biointerfaces, 122 (2014):250-259,
https://doi.org/10.1016/j.colsurfb.2014.06.043 . .
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