Optimization and Validation of an LC Method for the Determination of Cefdinir in Dosage Form and Human Urine
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In: Chromatographia, Vol. 70, No. 11/12, 12.2009, p. 1593–1598.
Research output: Journal contributions › Journal articles › Research › peer-review
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TY - JOUR
T1 - Optimization and Validation of an LC Method for the Determination of Cefdinir in Dosage Form and Human Urine
AU - Hadad, Ghada M.
AU - Emara, Samy
AU - Mahmoud, Waleed M. M.
PY - 2009/12
Y1 - 2009/12
N2 - A simple and reliable liquid chromatographic method has been developed and validated for the determination of cefdinir in human urine and capsule samples. A chromatographic separation was achieved on a C18 column using a mobile phase consisting of potassium dihydrogen phosphate (10 mM, pH 4.5)–acetonitrile (90:10, v/v). Quantitation was achieved with UV detection at 285 nm, based on peak area with linear calibration curve at a concentration range of 0.7–39 µg mL−1. This method was successfully applied for the establishment of an urinary excretion pattern after oral dose.
AB - A simple and reliable liquid chromatographic method has been developed and validated for the determination of cefdinir in human urine and capsule samples. A chromatographic separation was achieved on a C18 column using a mobile phase consisting of potassium dihydrogen phosphate (10 mM, pH 4.5)–acetonitrile (90:10, v/v). Quantitation was achieved with UV detection at 285 nm, based on peak area with linear calibration curve at a concentration range of 0.7–39 µg mL−1. This method was successfully applied for the establishment of an urinary excretion pattern after oral dose.
KW - Chemistry
KW - Column liquid chromatography
KW - Urinary excretion pattern
KW - Cefdinir
UR - http://www.scopus.com/inward/record.url?scp=72349097752&partnerID=8YFLogxK
U2 - 10.1365/s10337-009-1365-8
DO - 10.1365/s10337-009-1365-8
M3 - Journal articles
VL - 70
SP - 1593
EP - 1598
JO - Chromatographia
JF - Chromatographia
SN - 0009-5893
IS - 11/12
ER -