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Enantiomeric Resolution and Determination of Clenbuterol by Hplc Technique in Plasma and Pharmaceutical Formulations Using Polysaccharide Chiral Stationary Phase and Uv Detection
| Content Provider | Semantic Scholar |
|---|---|
| Author | Hefnawy, Mohamed M. Alshehri, Mona M. Sultan, Maha Taher Mostafa, Gamal A. E. |
| Copyright Year | 2013 |
| Abstract | Clenbuterol enantiomers were directly separated and determined in plasma and pharmaceutical formulation by a selective HPLC method using cellulose-based polysaccharide chiral stationary phase (CSP) known as OJ-RH. Enantiomeric resolution was achieved with a mobile phase consists of acetonitrile: 0.3M sodium perchlorate (16 %: 84 %), (v/v), a flow rate of 0.9 ml/min and a UV detection set at 247 nm. The method validated for its linearity, accuracy, and precision and robustness. The standard calibration curves were linear over the range of 0.5-50 μg/ml for each enantiomer with detection limit of 0.1 μg/ml. There was no significant difference between interand intra-day studies for each enantiomer which confirmed the reproducibility of the assay method. The method is highly specific where the co-formulated compounds did not interfere. The stability of clenbuterol enantiomers under high temperature was studied. The results showed that the drug is stable for at least 7 days at 80C. The mean extraction efficiency for R-(-)and S(+)clenbuterol from plasma was in the ranges 93-102 % at 7.5 40 μg/ml level for each enantiomers. The overall recoveries of clenbuterol enantiomers from pharmaceutical formulations were in the ranges 97 103 % with %RSD ranged from 1.81-2.35 %. The assay method proved to be chiral quality control for clenbuterol formulations by HPLC and to therapeutic drug monitoring. |
| File Format | PDF HTM / HTML |
| Alternate Webpage(s) | http://www.chalcogen.ro/1781_Hevnawy.pdf |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |