High performance liquid chromatographic determination of etofibrate and its hydrolysis products.
Publikation: Beiträge in Zeitschriften › Zeitschriftenaufsätze › Forschung › begutachtet
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in: Journal of Pharmaceutical and Biomedical Analysis, Jahrgang 43, Nr. 1, 04.01.2007, S. 196–203.
Publikation: Beiträge in Zeitschriften › Zeitschriftenaufsätze › Forschung › begutachtet
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TY - JOUR
T1 - High performance liquid chromatographic determination of etofibrate and its hydrolysis products.
AU - El-Gindy, A.
AU - Hadad, Ghada M.
AU - Mahmoud, Waleed M. M.
PY - 2007/1/4
Y1 - 2007/1/4
N2 - High performance liquid chromatographic (HPLC) method is presented for the determination of etofibrate (EF) and its hydrolysis products. The method was based on HPLC separation of EF from its hydrolysis products using cyanopropyl column at ambient temperature with mobile phase consisting of acetonitrile–10 mM potassium dihydrogen phosphate, pH was adjusted to 4.1 using phosphoric acid (50:50, v/v). Quantitation was achieved with UV detection at 221 nm based on peak area. The flow rate was 1.5 ml min−1. The proposed method was used to investigate the kinetics of acidic hydrolysis process of EF at different temperatures and the apparent pseudo first-order rate constant, half-life and activation energy were calculated. The kinetics of alkaline hydrolysis process of EF using 0.01 M sodium hydroxide at different temperatures cannot be studied as the drug is rapidly hydrolyzed in alkaline medium. The pH-rate profile of hydrolysis of EF in Britton–Robinson buffer solutions within the pH range 2–10 were studied.
AB - High performance liquid chromatographic (HPLC) method is presented for the determination of etofibrate (EF) and its hydrolysis products. The method was based on HPLC separation of EF from its hydrolysis products using cyanopropyl column at ambient temperature with mobile phase consisting of acetonitrile–10 mM potassium dihydrogen phosphate, pH was adjusted to 4.1 using phosphoric acid (50:50, v/v). Quantitation was achieved with UV detection at 221 nm based on peak area. The flow rate was 1.5 ml min−1. The proposed method was used to investigate the kinetics of acidic hydrolysis process of EF at different temperatures and the apparent pseudo first-order rate constant, half-life and activation energy were calculated. The kinetics of alkaline hydrolysis process of EF using 0.01 M sodium hydroxide at different temperatures cannot be studied as the drug is rapidly hydrolyzed in alkaline medium. The pH-rate profile of hydrolysis of EF in Britton–Robinson buffer solutions within the pH range 2–10 were studied.
KW - Chemistry
KW - Etofibrate
KW - HPLC
KW - Kinetics of hydrolysis
KW - pH-rate profile
UR - http://www.scopus.com/inward/record.url?scp=33845216929&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/7afe123b-142c-389e-b85c-71ce377fafd1/
U2 - 10.1016/j.jpba.2006.07.001
DO - 10.1016/j.jpba.2006.07.001
M3 - Journal articles
VL - 43
SP - 196
EP - 203
JO - Journal of Pharmaceutical and Biomedical Analysis
JF - Journal of Pharmaceutical and Biomedical Analysis
SN - 0731-7085
IS - 1
ER -