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摘 要:本文提出了采用内标法,将HPLC用于吡罗昔康凝胶有效成分测定的新方法。讨论了流动相及内标的选择,进样量和空白基质的影响等。在优化的实验条件下,吡罗昔康浓度在0.02~0.2mg/mL范围内,其浓度与吡罗昔康和内标的峰面积之比呈线性关系。应用于实际样品分析,其结果与紫外分光光度法一致,平均回收率为99.6%,相对标准偏差为1.0%。方法简单,准确度高,专属性强,可用于吡罗昔康凝胶样品的稳定性考察和质量控制。
A Study on the HPLC Method for the Determination of Piroxicam Gel CHEN Hao(Huazhong Agricultural
University, Wuhan, 430070) Abstract:In this paper, a new method for the determination of Piroxicam gel by the
use of HPLC was reported. The main factors, including the selection of mobile
phase and internal reference materials and effects of inject ion volume and
matrix were investigated. Under optimum chromatographic condition s, the
calibration graph was linear in the range of 0.02-0.2 mg/mL, the average
recovery was 99.6% with a relative standard deviation of 1.0%. The method has be
en applied to the determination of Piroxicam gel, and their results were in good
agreement with those obtained by UV method. The proposed method was simple, acc
urate, specific and applicable to the analysis of Piroxicam gel and quality cont
rol. |
作者单位:陈浩(华中农业大学理学系,武汉,430070) 糜志远(湖北工学院生物工程系,武汉,430068) 刘万忠(湖北省药品检验所,武汉,430064) 参考文献: [1]Brogden R N, Heel R C, Speight T M,
Averg G S. Drugs[J], 1984, 28: 292. 收稿日期:2000年7月11日 出版日期:2000年12月20日 |
原载于《分析科学学报》2000 Vol.16 No.6 P.470-471
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