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三种无需分离药物辅料即可同时测定片剂中阿司匹林和水杨酸的新分光光度法的比较。

Comparison of three new spectrophotometric methods for simultaneous determination of aspirin and salicylic acid in tablets without separation of pharmaceutical excipients.

作者信息

Glombitza B W, Schmidt P C

机构信息

Department of Pharmaceutical Technology, Eberhard-Karls-University Tübingen, Germany.

出版信息

J Pharm Sci. 1994 May;83(5):751-7. doi: 10.1002/jps.2600830532.

Abstract

Simultaneous analysis of aspirin (ASA) and salicylic acid (SA) in pharmaceutical tablet preparations was performed by two multicomponent UV-spectrophotometric methods utilizing principal component regression and classical least square algorithm. Additionally, an assay procedure based on second-derivative spectroscopy was developed. The analysis was performed in turbid solutions without separation of interfering excipients. The range, as determined by the second-derivative methods, was 0.2 to 103.2 micrograms/mL for ASA and 0.07 to 44.5 micrograms/mL for SA. Sensitivity for determination of SA was 0.004% of ASA content for the second-derivative method and 0.2% of ASA content for both multicomponent methods. The methods were applied to laboratory mixtures and commercial tablet formulations containing ASA and SA. The advantage of the second-derivative method in determining small amounts of SA in commercial tablet preparations is shown in comparison with a conventional HPLC method. All UV-spectrophotometric methods are rapid, accurate, and reproducible.

摘要

采用主成分回归和经典最小二乘法两种多组分紫外分光光度法对药物片剂制剂中的阿司匹林(ASA)和水杨酸(SA)进行了同时分析。此外,还开发了一种基于二阶导数光谱的测定方法。分析在混浊溶液中进行,无需分离干扰辅料。通过二阶导数法测定,ASA的范围为0.2至103.2微克/毫升,SA的范围为0.07至44.5微克/毫升。二阶导数法测定SA的灵敏度为ASA含量的0.004%,两种多组分方法测定SA的灵敏度为ASA含量的0.2%。这些方法应用于含有ASA和SA的实验室混合物和商业片剂制剂。与传统的高效液相色谱法相比,二阶导数法在测定商业片剂制剂中少量SA方面的优势得以体现。所有紫外分光光度法均快速、准确且可重复。

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