Stanković, B.S

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  • Stanković, B.S (4)
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  • Stanković, B. (1)
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Author's Bibliography

Polymorphism at position-174 of the interleukin-6 gene influences outcome of etanercept therapy in rheumatoid arthritis

Arsenović-Ranin, Nevena; Jančić, Ivan; Sefik-Bukilica, Mirjana; Živojinović, S.; Damjanov, Nemanja; Spasovski, Vesna; Srzentić, Sanja; Stanković, B.; Pavlović, S.

(Wiley-Blackwell, Hoboken, 2012)

TY  - CONF
AU  - Arsenović-Ranin, Nevena
AU  - Jančić, Ivan
AU  - Sefik-Bukilica, Mirjana
AU  - Živojinović, S.
AU  - Damjanov, Nemanja
AU  - Spasovski, Vesna
AU  - Srzentić, Sanja
AU  - Stanković, B.
AU  - Pavlović, S.
PY  - 2012
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/1652
PB  - Wiley-Blackwell, Hoboken
C3  - Immunology
T1  - Polymorphism at position-174 of the interleukin-6 gene influences outcome of etanercept therapy in rheumatoid arthritis
VL  - 137
SP  - 24
EP  - 24
UR  - https://hdl.handle.net/21.15107/rcub_farfar_1652
ER  - 
@conference{
author = "Arsenović-Ranin, Nevena and Jančić, Ivan and Sefik-Bukilica, Mirjana and Živojinović, S. and Damjanov, Nemanja and Spasovski, Vesna and Srzentić, Sanja and Stanković, B. and Pavlović, S.",
year = "2012",
publisher = "Wiley-Blackwell, Hoboken",
journal = "Immunology",
title = "Polymorphism at position-174 of the interleukin-6 gene influences outcome of etanercept therapy in rheumatoid arthritis",
volume = "137",
pages = "24-24",
url = "https://hdl.handle.net/21.15107/rcub_farfar_1652"
}
Arsenović-Ranin, N., Jančić, I., Sefik-Bukilica, M., Živojinović, S., Damjanov, N., Spasovski, V., Srzentić, S., Stanković, B.,& Pavlović, S.. (2012). Polymorphism at position-174 of the interleukin-6 gene influences outcome of etanercept therapy in rheumatoid arthritis. in Immunology
Wiley-Blackwell, Hoboken., 137, 24-24.
https://hdl.handle.net/21.15107/rcub_farfar_1652
Arsenović-Ranin N, Jančić I, Sefik-Bukilica M, Živojinović S, Damjanov N, Spasovski V, Srzentić S, Stanković B, Pavlović S. Polymorphism at position-174 of the interleukin-6 gene influences outcome of etanercept therapy in rheumatoid arthritis. in Immunology. 2012;137:24-24.
https://hdl.handle.net/21.15107/rcub_farfar_1652 .
Arsenović-Ranin, Nevena, Jančić, Ivan, Sefik-Bukilica, Mirjana, Živojinović, S., Damjanov, Nemanja, Spasovski, Vesna, Srzentić, Sanja, Stanković, B., Pavlović, S., "Polymorphism at position-174 of the interleukin-6 gene influences outcome of etanercept therapy in rheumatoid arthritis" in Immunology, 137 (2012):24-24,
https://hdl.handle.net/21.15107/rcub_farfar_1652 .

Low serum alpha-1-antitrypsin specific activity in monoclonal gammopathies

Jelić-Ivanović, Zorana; Stanković, B; Topić, Aleksandra; Spasojević-Kalimanovska, Vesna; Spasić, S

(Edizioni Minerva Medica, Turin, 2000)

TY  - JOUR
AU  - Jelić-Ivanović, Zorana
AU  - Stanković, B
AU  - Topić, Aleksandra
AU  - Spasojević-Kalimanovska, Vesna
AU  - Spasić, S
PY  - 2000
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/246
AB  - Background. Serum alpha(1)-antitrypsin (alpha 1AT) antigen concentration is elevated in malignancies as the result of acute phase reaction. In the present study, we examined whether the alpha 1AT elevation in monoclonal gammopathies was accompanied by an adequate increase of its functional activity. Methods. In this case-control study, serum alpha 1AT concentration was measured in 187 ambulatory patients with monoclonal gammopathies and 320 healthy blood donors matched according to sex and age. The alpha 1AT antigen concentration was assayed by immunonephelometry, whereas its functional activity was measured as trypsin inhibitory capacity (TIC), The specific alpha 1AT inhibitory activity (SIA) was calculated, defined as the TIC/antigen concentration ratio. Results. The alpha 1AT antigen concentrations obtained in the patients' samples were very significantly higher as compared with the corresponding values in the control group (mean+/-SD =134+/-41.9% of normal, p lt 0.001). However, the TIC values were higher in the patients than in the healthy controls only by 4% (104+/-23.8%, p lt 0.05). The specific alpha 1AT activity was very significantly lower in the patients, as compared with the controls (p lt 0.001), indicating that serum alpha 1AT in monoclonal gammopathies was partially inactive. Conclusions. As poor correlation between the TIC values and the antigen concentrations was obtained in the patient group as well as the decreased specific alpha 1AT activities, the TIC values in patients with monoclonal gammopathies should be interpreted with caution.
PB  - Edizioni Minerva Medica, Turin
T2  - Panminerva Medica
T1  - Low serum alpha-1-antitrypsin specific activity in monoclonal gammopathies
VL  - 42
IS  - 1
SP  - 17
EP  - 21
UR  - https://hdl.handle.net/21.15107/rcub_farfar_246
ER  - 
@article{
author = "Jelić-Ivanović, Zorana and Stanković, B and Topić, Aleksandra and Spasojević-Kalimanovska, Vesna and Spasić, S",
year = "2000",
abstract = "Background. Serum alpha(1)-antitrypsin (alpha 1AT) antigen concentration is elevated in malignancies as the result of acute phase reaction. In the present study, we examined whether the alpha 1AT elevation in monoclonal gammopathies was accompanied by an adequate increase of its functional activity. Methods. In this case-control study, serum alpha 1AT concentration was measured in 187 ambulatory patients with monoclonal gammopathies and 320 healthy blood donors matched according to sex and age. The alpha 1AT antigen concentration was assayed by immunonephelometry, whereas its functional activity was measured as trypsin inhibitory capacity (TIC), The specific alpha 1AT inhibitory activity (SIA) was calculated, defined as the TIC/antigen concentration ratio. Results. The alpha 1AT antigen concentrations obtained in the patients' samples were very significantly higher as compared with the corresponding values in the control group (mean+/-SD =134+/-41.9% of normal, p lt 0.001). However, the TIC values were higher in the patients than in the healthy controls only by 4% (104+/-23.8%, p lt 0.05). The specific alpha 1AT activity was very significantly lower in the patients, as compared with the controls (p lt 0.001), indicating that serum alpha 1AT in monoclonal gammopathies was partially inactive. Conclusions. As poor correlation between the TIC values and the antigen concentrations was obtained in the patient group as well as the decreased specific alpha 1AT activities, the TIC values in patients with monoclonal gammopathies should be interpreted with caution.",
publisher = "Edizioni Minerva Medica, Turin",
journal = "Panminerva Medica",
title = "Low serum alpha-1-antitrypsin specific activity in monoclonal gammopathies",
volume = "42",
number = "1",
pages = "17-21",
url = "https://hdl.handle.net/21.15107/rcub_farfar_246"
}
Jelić-Ivanović, Z., Stanković, B., Topić, A., Spasojević-Kalimanovska, V.,& Spasić, S.. (2000). Low serum alpha-1-antitrypsin specific activity in monoclonal gammopathies. in Panminerva Medica
Edizioni Minerva Medica, Turin., 42(1), 17-21.
https://hdl.handle.net/21.15107/rcub_farfar_246
Jelić-Ivanović Z, Stanković B, Topić A, Spasojević-Kalimanovska V, Spasić S. Low serum alpha-1-antitrypsin specific activity in monoclonal gammopathies. in Panminerva Medica. 2000;42(1):17-21.
https://hdl.handle.net/21.15107/rcub_farfar_246 .
Jelić-Ivanović, Zorana, Stanković, B, Topić, Aleksandra, Spasojević-Kalimanovska, Vesna, Spasić, S, "Low serum alpha-1-antitrypsin specific activity in monoclonal gammopathies" in Panminerva Medica, 42, no. 1 (2000):17-21,
https://hdl.handle.net/21.15107/rcub_farfar_246 .

Use of pralidoxime-Pd(II) complex for the spectrophotometric determination of the cholinesterase reactivator (PAM-2Cl) in the urine

Karljiković-Rajić, Katarina; Stanković, B.S

(1990)

TY  - JOUR
AU  - Karljiković-Rajić, Katarina
AU  - Stanković, B.S
PY  - 1990
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/56
AB  - A simple and rapid method for the spectrophotometric determination of pralidoxime chloride in urine, based on complex formation with palladium(II) without preliminary mineralization of the sample, is described. The proposed method is shown to be reproducible and in good agreement with a reference method, which involved spectrophotometric determination of corresponding oximate ions in ammonium hydroxide solution at 336 nm. Our results indicate that the proposed method is reliable, rapid and of sufficient sensitivity for pralidoxime chloride analysis in urine.
T2  - Clinica Chimica Acta
T1  - Use of pralidoxime-Pd(II) complex for the spectrophotometric determination of the cholinesterase reactivator (PAM-2Cl) in the urine
VL  - 193
IS  - 3
SP  - 119
EP  - 124
DO  - 10.1016/0009-8981(90)90243-L
ER  - 
@article{
author = "Karljiković-Rajić, Katarina and Stanković, B.S",
year = "1990",
abstract = "A simple and rapid method for the spectrophotometric determination of pralidoxime chloride in urine, based on complex formation with palladium(II) without preliminary mineralization of the sample, is described. The proposed method is shown to be reproducible and in good agreement with a reference method, which involved spectrophotometric determination of corresponding oximate ions in ammonium hydroxide solution at 336 nm. Our results indicate that the proposed method is reliable, rapid and of sufficient sensitivity for pralidoxime chloride analysis in urine.",
journal = "Clinica Chimica Acta",
title = "Use of pralidoxime-Pd(II) complex for the spectrophotometric determination of the cholinesterase reactivator (PAM-2Cl) in the urine",
volume = "193",
number = "3",
pages = "119-124",
doi = "10.1016/0009-8981(90)90243-L"
}
Karljiković-Rajić, K.,& Stanković, B.S. (1990). Use of pralidoxime-Pd(II) complex for the spectrophotometric determination of the cholinesterase reactivator (PAM-2Cl) in the urine. in Clinica Chimica Acta, 193(3), 119-124.
https://doi.org/10.1016/0009-8981(90)90243-L
Karljiković-Rajić K, Stanković B. Use of pralidoxime-Pd(II) complex for the spectrophotometric determination of the cholinesterase reactivator (PAM-2Cl) in the urine. in Clinica Chimica Acta. 1990;193(3):119-124.
doi:10.1016/0009-8981(90)90243-L .
Karljiković-Rajić, Katarina, Stanković, B.S, "Use of pralidoxime-Pd(II) complex for the spectrophotometric determination of the cholinesterase reactivator (PAM-2Cl) in the urine" in Clinica Chimica Acta, 193, no. 3 (1990):119-124,
https://doi.org/10.1016/0009-8981(90)90243-L . .
1
3

Spectrophotometric determination of pralidoxime chloride in pharmaceutical preparations

Karljiković-Rajić, Katarina; Stanković, B.S; Granov, A

(1989)

TY  - JOUR
AU  - Karljiković-Rajić, Katarina
AU  - Stanković, B.S
AU  - Granov, A
PY  - 1989
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/46
T2  - Pharmazie
T1  - Spectrophotometric determination of pralidoxime chloride in pharmaceutical preparations
VL  - 44
IS  - 7
SP  - 497
EP  - 498
UR  - https://hdl.handle.net/21.15107/rcub_farfar_46
ER  - 
@article{
author = "Karljiković-Rajić, Katarina and Stanković, B.S and Granov, A",
year = "1989",
journal = "Pharmazie",
title = "Spectrophotometric determination of pralidoxime chloride in pharmaceutical preparations",
volume = "44",
number = "7",
pages = "497-498",
url = "https://hdl.handle.net/21.15107/rcub_farfar_46"
}
Karljiković-Rajić, K., Stanković, B.S,& Granov, A.. (1989). Spectrophotometric determination of pralidoxime chloride in pharmaceutical preparations. in Pharmazie, 44(7), 497-498.
https://hdl.handle.net/21.15107/rcub_farfar_46
Karljiković-Rajić K, Stanković B, Granov A. Spectrophotometric determination of pralidoxime chloride in pharmaceutical preparations. in Pharmazie. 1989;44(7):497-498.
https://hdl.handle.net/21.15107/rcub_farfar_46 .
Karljiković-Rajić, Katarina, Stanković, B.S, Granov, A, "Spectrophotometric determination of pralidoxime chloride in pharmaceutical preparations" in Pharmazie, 44, no. 7 (1989):497-498,
https://hdl.handle.net/21.15107/rcub_farfar_46 .
4

Spectrophotometric and potentiometric determination of acidic constants of oxo-phenyl pyridinium monoxime and dioxime

Milovanović, L.T; Karljiković-Rajić, Katarina; Stanković, B.S

(Springer-Verlag, 1988)

TY  - JOUR
AU  - Milovanović, L.T
AU  - Karljiković-Rajić, Katarina
AU  - Stanković, B.S
PY  - 1988
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/38
AB  - The UV absorption spectra of 1-(1-hydroxyimino-2-oxo-2-phenyl) pyridinium chloride (compound I) and 1-(1-hydroxyimino-2-oxo-2-phenyl)-4-hydroxyiminomethyl pyridinium chloride (compound II) in water solution at different pH values have been measured. The spectral changes, with changing pH, in aqueous solutions are attributed to the dissociation of individual functional groups of the compounds. The mixed acidic constants (pK′a) of the investigated monoxime and dioxime, have been determined spectrophotometrically in the series of Britton-Robinson's buffer solutions in the pH range 3.0-5.19 and 7.70-9.90 (t=25±0.5°C, I=0.2). The following pK′a values have been obtained for monoxime pK′a1=4.30 and for dioxime pK′a1=4.28, pK′a2=8.36. Thermodynamic acidic constants (pKa) have been determined on the basis of potentiometric titrations and they have been found to be pKa1=4.32 for compound I and pKa1=4.27, pKa2=8.51 for compound II. The values obtained by transferring pK′a into pKa are in good agreement with the values obtained potentiometrically.
PB  - Springer-Verlag
T2  - Monatshefte für Chemie Chemical Monthly
T1  - Spectrophotometric and potentiometric determination of acidic constants of oxo-phenyl pyridinium monoxime and dioxime
VL  - 119
IS  - 10
SP  - 1069
EP  - 1078
DO  - 10.1007/BF00809259
ER  - 
@article{
author = "Milovanović, L.T and Karljiković-Rajić, Katarina and Stanković, B.S",
year = "1988",
abstract = "The UV absorption spectra of 1-(1-hydroxyimino-2-oxo-2-phenyl) pyridinium chloride (compound I) and 1-(1-hydroxyimino-2-oxo-2-phenyl)-4-hydroxyiminomethyl pyridinium chloride (compound II) in water solution at different pH values have been measured. The spectral changes, with changing pH, in aqueous solutions are attributed to the dissociation of individual functional groups of the compounds. The mixed acidic constants (pK′a) of the investigated monoxime and dioxime, have been determined spectrophotometrically in the series of Britton-Robinson's buffer solutions in the pH range 3.0-5.19 and 7.70-9.90 (t=25±0.5°C, I=0.2). The following pK′a values have been obtained for monoxime pK′a1=4.30 and for dioxime pK′a1=4.28, pK′a2=8.36. Thermodynamic acidic constants (pKa) have been determined on the basis of potentiometric titrations and they have been found to be pKa1=4.32 for compound I and pKa1=4.27, pKa2=8.51 for compound II. The values obtained by transferring pK′a into pKa are in good agreement with the values obtained potentiometrically.",
publisher = "Springer-Verlag",
journal = "Monatshefte für Chemie Chemical Monthly",
title = "Spectrophotometric and potentiometric determination of acidic constants of oxo-phenyl pyridinium monoxime and dioxime",
volume = "119",
number = "10",
pages = "1069-1078",
doi = "10.1007/BF00809259"
}
Milovanović, L.T, Karljiković-Rajić, K.,& Stanković, B.S. (1988). Spectrophotometric and potentiometric determination of acidic constants of oxo-phenyl pyridinium monoxime and dioxime. in Monatshefte für Chemie Chemical Monthly
Springer-Verlag., 119(10), 1069-1078.
https://doi.org/10.1007/BF00809259
Milovanović L, Karljiković-Rajić K, Stanković B. Spectrophotometric and potentiometric determination of acidic constants of oxo-phenyl pyridinium monoxime and dioxime. in Monatshefte für Chemie Chemical Monthly. 1988;119(10):1069-1078.
doi:10.1007/BF00809259 .
Milovanović, L.T, Karljiković-Rajić, Katarina, Stanković, B.S, "Spectrophotometric and potentiometric determination of acidic constants of oxo-phenyl pyridinium monoxime and dioxime" in Monatshefte für Chemie Chemical Monthly, 119, no. 10 (1988):1069-1078,
https://doi.org/10.1007/BF00809259 . .
1

Determination of acidic constants of some phenyl-hydroxyiminoethyl quinolinium compounds

Karljiković, Katarina; Stanković, B.S; Milosavljević, E.B; Binenfeld, Z.J.

(Springer-Verlag, 1986)

TY  - JOUR
AU  - Karljiković, Katarina
AU  - Stanković, B.S
AU  - Milosavljević, E.B
AU  - Binenfeld, Z.J.
PY  - 1986
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/24
AB  - Mixed acidic constants (pK′a) of quinolinium oximes [1-(2-phenyl-2-hydroxyiminoethyl)-1-quinolinium chloride (F-1), 1-(2-phenyl-2-hydroxyiminoethyl)-1-isoquinolinium chloride (F-2), 1-(2-phenyl-2-hydroxyiminoethyl)-1-(4′-methyl)-quinolinium chloride (F-3), and 1-(2-phenyl-2-hydroxyiminoethyl)-1-(6′-methyl)-quinolinium chloride (F-4)] have been determined via their UV absorption spectra recorded in the series of Britton-Robinson's buffer solutions in the pH region 8.74-11.28 (t=25±0.5°C, μ=0.2). The obtained pK′a values are in good agreement with those achieved by applying graphical methods. The following pK′a values have been obtained: 9.93 for F-1, 9.90 for F-2, and 10.02 for F-3 and F-4. On the basis of potentiometric titrations thermodynamic acidic constants (pKa) of compounds F-1, F-2, F-3, and F-4 have been determined and they were found to be 9.82, 9.71, 9.91, and 9.86, respectively. The values obtained by transferring pKa into pK′a are in good agreement with the values obtained spectrophotometrically.
PB  - Springer-Verlag
T2  - Monatshefte für Chemie Chemical Monthly
T1  - Determination of acidic constants of some phenyl-hydroxyiminoethyl quinolinium compounds
VL  - 117
IS  - 5
SP  - 661
EP  - 670
DO  - 10.1007/BF00817903
ER  - 
@article{
author = "Karljiković, Katarina and Stanković, B.S and Milosavljević, E.B and Binenfeld, Z.J.",
year = "1986",
abstract = "Mixed acidic constants (pK′a) of quinolinium oximes [1-(2-phenyl-2-hydroxyiminoethyl)-1-quinolinium chloride (F-1), 1-(2-phenyl-2-hydroxyiminoethyl)-1-isoquinolinium chloride (F-2), 1-(2-phenyl-2-hydroxyiminoethyl)-1-(4′-methyl)-quinolinium chloride (F-3), and 1-(2-phenyl-2-hydroxyiminoethyl)-1-(6′-methyl)-quinolinium chloride (F-4)] have been determined via their UV absorption spectra recorded in the series of Britton-Robinson's buffer solutions in the pH region 8.74-11.28 (t=25±0.5°C, μ=0.2). The obtained pK′a values are in good agreement with those achieved by applying graphical methods. The following pK′a values have been obtained: 9.93 for F-1, 9.90 for F-2, and 10.02 for F-3 and F-4. On the basis of potentiometric titrations thermodynamic acidic constants (pKa) of compounds F-1, F-2, F-3, and F-4 have been determined and they were found to be 9.82, 9.71, 9.91, and 9.86, respectively. The values obtained by transferring pKa into pK′a are in good agreement with the values obtained spectrophotometrically.",
publisher = "Springer-Verlag",
journal = "Monatshefte für Chemie Chemical Monthly",
title = "Determination of acidic constants of some phenyl-hydroxyiminoethyl quinolinium compounds",
volume = "117",
number = "5",
pages = "661-670",
doi = "10.1007/BF00817903"
}
Karljiković, K., Stanković, B.S, Milosavljević, E.B,& Binenfeld, Z.J.. (1986). Determination of acidic constants of some phenyl-hydroxyiminoethyl quinolinium compounds. in Monatshefte für Chemie Chemical Monthly
Springer-Verlag., 117(5), 661-670.
https://doi.org/10.1007/BF00817903
Karljiković K, Stanković B, Milosavljević E, Binenfeld Z. Determination of acidic constants of some phenyl-hydroxyiminoethyl quinolinium compounds. in Monatshefte für Chemie Chemical Monthly. 1986;117(5):661-670.
doi:10.1007/BF00817903 .
Karljiković, Katarina, Stanković, B.S, Milosavljević, E.B, Binenfeld, Z.J., "Determination of acidic constants of some phenyl-hydroxyiminoethyl quinolinium compounds" in Monatshefte für Chemie Chemical Monthly, 117, no. 5 (1986):661-670,
https://doi.org/10.1007/BF00817903 . .
2
1