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一种用于定量局部用药物乳膏制剂中紫苏醇的高效液相色谱法。

An HPLC method for quantitation of perillyl alcohol in a topical pharmaceutical cream formulation.

作者信息

Gupta Abhishek, Stratton Steven P, Myrdal Paul B

机构信息

Cardinal Health, Inhalation Formulation, P.O. Box 13341, Research Triangle Park, NC 27709, USA.

出版信息

J Pharm Biomed Anal. 2005 Mar 9;37(3):447-52. doi: 10.1016/j.jpba.2004.02.039. Epub 2005 Jan 13.

Abstract

A reverse phase high performance liquid chromatographic method for quantitation of perillyl alcohol in a topical cream pharmaceutical formulation was developed. Previously reported methods for analyzing drugs in lipid formulations are relatively complex and time consuming, with extraction, purification and derivatization involved. Through a simple dilution of the cream formulation in isopropyl alcohol, the present assay method enables the direct injection of the samples, on an Alltima C18 5 mu, 150 mm x 2.1 mm, narrow bore column (Alltech Associates, Deerfield, IL). The method includes an isocratic run with acetonitrile-water (40:60, v/v) at 0.35 mL/min for 12 min, followed by a gradient wash with isopropyl alcohol for 20 min, to ensure that all formulation excipients are eluted. Ultraviolet detection was performed at 210 nm with a retention time for perillyl alcohol of 7 min. The high sensitivity assay utilizes a small (5 microL) injection volume for the accurate and precise analysis of perillyl alcohol from a complex cream formulation.

摘要

建立了一种反相高效液相色谱法,用于定量测定局部乳膏药物制剂中的紫苏醇。先前报道的分析脂质制剂中药物的方法相对复杂且耗时,涉及萃取、纯化和衍生化。通过将乳膏制剂简单稀释于异丙醇中,本测定方法可直接进样,使用Alltima C18 5μm、150mm×2.1mm窄径柱(Alltech Associates,迪尔菲尔德,伊利诺伊州)。该方法包括以0.35mL/min的流速用乙腈 - 水(40:60,v/v)等度洗脱12分钟,随后用异丙醇梯度洗脱20分钟,以确保所有制剂辅料均被洗脱。在210nm处进行紫外检测,紫苏醇的保留时间为7分钟。该高灵敏度测定法采用小进样体积(5μL),用于准确、精确地分析复杂乳膏制剂中的紫苏醇。

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