期刊
PHARMAZIE
卷 74, 期 11, 页码 658-660出版社
GOVI-VERLAG PHARMAZEUTISCHER VERLAG GMBH
DOI: 10.1691/ph.2019.8192
关键词
-
资金
- South African National Research Foundation (NRF) [105913]
- Centre of Excellence for Pharmaceutical Sciences (Pharmacen(TM)) of the North-West University, Potchefst-room Campus, South Africa
A novel HPLC method with UV detection was developed and validated in skin penetration (in vitro) studies to identify and quantify lovastatin, mevastatin, rosuvastatin and simvastatin. A Venusil XBP C-18 (2), 150 x 4.6 mm, 5 mu m column (Agela Technologies, Newark, DE) was used with gradient elution (start at 45 % acetonitrile and increase linearly to 90 % after 1 min; hold at 90 % until 6 min and then re-equilibrate at start conditions) and the mobile phase consisted of (A) Milli-Q (R) water and 0.1% orthophosphoric acid, and (B) HPLC grade acetonitrile. The flow rate was set at 1 ml/min, 240 nm UV detection and an injection volume of 10 mu l. Linearity was obtained over a range of 0.50-200.00 mu g/ml and correlation coefficients ranging from 0.998-1.000 were obtained. Average recovery ranged from 95.9-100.6 %. The LOD and LOQ values obtained from the slope of a calibration curve and the standard deviation of the response ranged from 0.0138-0.0860 mu g/ml and 0.0419-0.2615 mu g/ml, respectively, where lovastatin and simvastatin could be detected at a concentration similar to the other statins, but could only be quantified at a higher concentration than the remaining statins. The specificity of the method was proved as accurate and quantification of statins was found, even within the incorporation of other compounds.
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