Khetre A B, Sinha P K, Damle Mrinalini C, Mehendre R
Department of Pharmaceutical Chemistry, AISSMS College of Pharmacy, Pune-411 001, India.
Indian J Pharm Sci. 2009 Sep;71(5):509-14. doi: 10.4103/0250-474X.58178.
This study describes the development and validation of stability indicating HPLC method for voriconazole, an antifungal drug. Voriconazole was subjected to stress degradation under different conditions recommended by International Conference on Harmonization. The sample so generated was used to develop a stability-indicating high performance liquid chromatographic method for voriconazole. The peak for voriconazole was well resolved from peaks of degradation products, using a Hypersil C18 (250x4.6 mm) column and a mobile phase comprising of acetonitrile: water (40:60, v/v), at flow rate of 1 ml/min. Detection was carried out using photodiode array detector. A linear response (r > 0.99) was observed in the range of 5-25 mug/ml. The method showed good recoveries (average 100.06%) and relative standard deviation for intra and inter-day were </= 1.5 %. The method was validated for specificity and robustness also.
本研究描述了抗真菌药物伏立康唑稳定性指示高效液相色谱法的开发与验证。伏立康唑在国际协调会议推荐的不同条件下进行了强制降解。如此产生的样品用于开发伏立康唑的稳定性指示高效液相色谱法。使用Hypersil C18(250x4.6 mm)色谱柱和由乙腈:水(40:60,v/v)组成的流动相,流速为1 ml/min,伏立康唑的峰与降解产物的峰得到了很好的分离。使用光电二极管阵列检测器进行检测。在5-25μg/ml范围内观察到线性响应(r>0.99)。该方法显示出良好的回收率(平均100.06%),日内和日间相对标准偏差均≤1.5%。该方法还针对特异性和稳健性进行了验证。