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采用反相高效液相色谱法(RP-HPLC)和薄层色谱-光密度法同时定量测定止咳糖浆中氯苯那敏、去氧肾上腺素、愈创甘油醚的含量,并检测其中的防腐剂及相关物质愈创木酚。

Simultaneous Quantification of Chlorpheniramine, Phenylephrine, Guaifenesin in Presence of Preservatives with Detection of Related Substance Guaiacol in their Cough Syrup by RP-HPLC and TLC-Densitometric Methods.

作者信息

Boltia Shereen A, Soudi Aya T, Elzanfaly Eman S, Zaazaa Hala E

机构信息

Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr El-Aini Street, Cairo, Egypt.

出版信息

J Chromatogr Sci. 2019 Jul 1;57(6):552-559. doi: 10.1093/chromsci/bmz027.

Abstract

Two sensitive chromatographic methods have been developed, and validated for chlorpheniramine maleate (CM), phenylephrine (PE) and guaifenesin (GF) determination in their mixture and in presence of GF related substance guaiacol (GL) and preservative namely; sodium benzoate (NaB). The first method was based on thin layer chromatographic separation (TLC) followed by densitometric determination of the separated spots. The separation was achieved using silica gel 60 F254 TLC plates and ethyl acetate: methanol: toluene: ammonia (7:1.5:1:0.5, by volume) as a developing system. Densitometric quantification of the three drugs was carried by the reflectance mode at 270 nm. The second method was based on the use of high-performance liquid chromatography with diode array detection, by which the proposed components were separated on a reversed phase C18 analytical column using phosphate buffer pH 2.9 (containing 0.1 g Heptane-1-sulphonic acid sodium salt) and acetonitrile (85:15, v/v) at 0.8 mL/min for 4 minutes then 1 mL/min till end of the run using flow rate online switching technique. Both methods were validated according to the ICH guidelines and successfully applied for the determination of CM, PE, and GF in pure powder and in combined cough syrup without interference from the excipients.

摘要

已开发出两种灵敏的色谱方法,并对其进行了验证,用于测定马来酸氯苯那敏(CM)、去氧肾上腺素(PE)和愈创甘油醚(GF)混合物中的含量,以及在存在GF相关物质愈创木酚(GL)和防腐剂苯甲酸钠(NaB)的情况下的含量。第一种方法基于薄层色谱分离(TLC),然后对分离出的斑点进行光密度测定。使用硅胶60 F254 TLC板和乙酸乙酯:甲醇:甲苯:氨水(体积比为7:1.5:1:0.5)作为展开系统进行分离。三种药物的光密度定量通过在270 nm处的反射模式进行。第二种方法基于使用配备二极管阵列检测的高效液相色谱法,通过该方法,在反相C18分析柱上,使用pH 2.9的磷酸盐缓冲液(含有0.1 g庚烷-1-磺酸钠盐)和乙腈(85:15,v/v),以0.8 mL/min的流速分离4分钟,然后使用流速在线切换技术以1 mL/min的流速直至运行结束,分离出所提议的成分。两种方法均根据ICH指南进行了验证,并成功应用于纯粉末和复方止咳糖浆中CM、PE和GF的测定,不受辅料的干扰。

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