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HPTLC determination of ceftriaxone, cefixime and cefotaxime in dosage forms

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Authors
Agbaba, Danica
Erić-Jovanović, S
Živanov-Stakić, Dobrila
Vladimirov, S
Article (Published version)
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Abstract
The objective of this investigation was to develop an HPTLC method for the determination of ceftriaxone, cefixime and cefotaxime, cephalosporins widely used in clinical practice. High performance thin-layer chromatography of cephalosporins was performed on pre-coated silica gel HPTLC plates with concentration zones (2.5×10cm), development with mobile phase ethylacetate-acetone-methanol-water (5:2.5:2.5:1.5 v/v). A TLC scanner (Camag, Muttenz, Switzerland) set at 270 nm was used for direct evaluation of the chromatograms in reflectance/absorbance mode. The calibration curves were established dependant of peak height (linear and polinomial regression) and peak area (polinomial regression) vs ng level (125-500 ng for all cephalosporins investigated). Coefficients of variation obtained from calibration curves were compared. Precision (c.v.: 1.12-2.91% (peak height vs ng) and c.v.: 1.05-2.75% (peak area vs ng)), and detection limits (ng level) were found to be satisfactory. The method is re...producible and convenient for quantitative analysis of ceftriaxone, cefixime and cefotaxime raw materials and their different dosage forms.

Source:
Journal de Pharmacie de Belgique, 1998, 53, 3, 150-
Publisher:
  • APB Algemene Pharmaceutische Bond

ISSN: 0047-2166

Scopus: 2-s2.0-33750157551
[ Google Scholar ]
2
Handle
https://hdl.handle.net/21.15107/rcub_farfar_202
URI
https://farfar.pharmacy.bg.ac.rs/handle/123456789/202
Collections
  • Radovi istraživača / Researchers’ publications
Institution/Community
Pharmacy
TY  - JOUR
AU  - Agbaba, Danica
AU  - Erić-Jovanović, S
AU  - Živanov-Stakić, Dobrila
AU  - Vladimirov, S
PY  - 1998
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/202
AB  - The objective of this investigation was to develop an HPTLC method for the determination of ceftriaxone, cefixime and cefotaxime, cephalosporins widely used in clinical practice. High performance thin-layer chromatography of cephalosporins was performed on pre-coated silica gel HPTLC plates with concentration zones (2.5×10cm), development with mobile phase ethylacetate-acetone-methanol-water (5:2.5:2.5:1.5 v/v). A TLC scanner (Camag, Muttenz, Switzerland) set at 270 nm was used for direct evaluation of the chromatograms in reflectance/absorbance mode. The calibration curves were established dependant of peak height (linear and polinomial regression) and peak area (polinomial regression) vs ng level (125-500 ng for all cephalosporins investigated). Coefficients of variation obtained from calibration curves were compared. Precision (c.v.: 1.12-2.91% (peak height vs ng) and c.v.: 1.05-2.75% (peak area vs ng)), and detection limits (ng level) were found to be satisfactory. The method is reproducible and convenient for quantitative analysis of ceftriaxone, cefixime and cefotaxime raw materials and their different dosage forms.
PB  - APB Algemene Pharmaceutische Bond
T2  - Journal de Pharmacie de Belgique
T1  - HPTLC determination of ceftriaxone, cefixime and cefotaxime in dosage forms
VL  - 53
IS  - 3
SP  - 150
UR  - https://hdl.handle.net/21.15107/rcub_farfar_202
ER  - 
@article{
author = "Agbaba, Danica and Erić-Jovanović, S and Živanov-Stakić, Dobrila and Vladimirov, S",
year = "1998",
abstract = "The objective of this investigation was to develop an HPTLC method for the determination of ceftriaxone, cefixime and cefotaxime, cephalosporins widely used in clinical practice. High performance thin-layer chromatography of cephalosporins was performed on pre-coated silica gel HPTLC plates with concentration zones (2.5×10cm), development with mobile phase ethylacetate-acetone-methanol-water (5:2.5:2.5:1.5 v/v). A TLC scanner (Camag, Muttenz, Switzerland) set at 270 nm was used for direct evaluation of the chromatograms in reflectance/absorbance mode. The calibration curves were established dependant of peak height (linear and polinomial regression) and peak area (polinomial regression) vs ng level (125-500 ng for all cephalosporins investigated). Coefficients of variation obtained from calibration curves were compared. Precision (c.v.: 1.12-2.91% (peak height vs ng) and c.v.: 1.05-2.75% (peak area vs ng)), and detection limits (ng level) were found to be satisfactory. The method is reproducible and convenient for quantitative analysis of ceftriaxone, cefixime and cefotaxime raw materials and their different dosage forms.",
publisher = "APB Algemene Pharmaceutische Bond",
journal = "Journal de Pharmacie de Belgique",
title = "HPTLC determination of ceftriaxone, cefixime and cefotaxime in dosage forms",
volume = "53",
number = "3",
pages = "150",
url = "https://hdl.handle.net/21.15107/rcub_farfar_202"
}
Agbaba, D., Erić-Jovanović, S., Živanov-Stakić, D.,& Vladimirov, S.. (1998). HPTLC determination of ceftriaxone, cefixime and cefotaxime in dosage forms. in Journal de Pharmacie de Belgique
APB Algemene Pharmaceutische Bond., 53(3), 150.
https://hdl.handle.net/21.15107/rcub_farfar_202
Agbaba D, Erić-Jovanović S, Živanov-Stakić D, Vladimirov S. HPTLC determination of ceftriaxone, cefixime and cefotaxime in dosage forms. in Journal de Pharmacie de Belgique. 1998;53(3):150.
https://hdl.handle.net/21.15107/rcub_farfar_202 .
Agbaba, Danica, Erić-Jovanović, S, Živanov-Stakić, Dobrila, Vladimirov, S, "HPTLC determination of ceftriaxone, cefixime and cefotaxime in dosage forms" in Journal de Pharmacie de Belgique, 53, no. 3 (1998):150,
https://hdl.handle.net/21.15107/rcub_farfar_202 .

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