RP-HPLC METHOD FOR DETERMINATION OF OSELTAMIVIR PHOSPHATE IN CAPSULES AND SPIKED PLASMA
ANALYTICAL LETTERS, cilt.43, sa.14, ss.2200-2209, 2010 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 43 Sayı: 14
- Basım Tarihi: 2010
- Doi Numarası: 10.1080/00032711003698721
- Dergi Adı: ANALYTICAL LETTERS
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.2200-2209
- Anahtar Kelimeler: 4-Chloro-7-nitrobenzofurazan, Drug analysis, HPLC, Oseltamivir phosphate, Plasma, INFLUENZA, NEURAMINIDASE, TAMIFLU(R), VALIDATION, CHROMATOGRAPHY, CARBOXYLATE, METABOLITE, INHIBITOR, URINE, ASSAY
- İstanbul Üniversitesi Adresli: Evet
Özet
A new, sensitive RP-HPLC method was developed for the determination of oseltamivir phosphate in capsules and plasma. The method was based on the reaction of the drug with 4-chloro-7-nitrobenzofurazan in borate buffer solution of pH 8.50. Isocratic chromatography was performed on a C(18) column with acetonitrile-10 mM nitric acid (pH 3, 60 + 40, v/v) as the mobile phase with fluorescence detection (lambda ex: 470 nm, lambda em: 541 nm). Mexiletine hydrochloride was used as an internal standard. Analytical parameters were evaluated. The calibration range was linear from 50.0-750.0 ng/ml. The mean percentage recovery in capsules and plasma were 99.95% and 95.42%, respectively.
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| Times Cited: 3 (from Web of Science) |
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Cited References: 18 [ view related records ] |
| Abstract: A new, sensitive RP-HPLC method was developed for the determination of oseltamivir phosphate in capsules and plasma. The method was based on the reaction of the drug with 4-chloro-7-nitrobenzofurazan in borate buffer solution of pH 8.50. Isocratic chromatography was performed on a C(18) column with acetonitrile-10 mM nitric acid (pH 3, 60 + 40, v/v) as the mobile phase with fluorescence detection (lambda ex: 470 nm, lambda em: 541 nm). Mexiletine hydrochloride was used as an internal standard. Analytical parameters were evaluated. The calibration range was linear from 50.0-750.0 ng/ml. The mean percentage recovery in capsules and plasma were 99.95% and 95.42%, respectively. |
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