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局部皮肤制剂中甘氨酸和苏氨酸的测定。

Determination of glycine and threonine in topical dermatological preparations.

作者信息

Marrubini G, Caccialanza G, Massolini G

机构信息

Department of Pharmaceutical Chemistry, University of Pavia, Via Taramelli 12, 27100 Pavia, Italy.

出版信息

J Pharm Biomed Anal. 2008 Aug 5;47(4-5):716-22. doi: 10.1016/j.jpba.2008.02.024. Epub 2008 Feb 29.

Abstract

In the present study, a single HPLC method was developed for the determination of glycine and threonine in cicatrizants. Two different preparations of a cream and an ointment, and the corresponding bandages, onto which the formulations were applied, were studied. The method involved matrix solubilisation with dichloromethane, liquid-liquid isolation of gly and thr with aqueous 1N NaOH, and derivatization with phenylisothiocyanate. Reversed-phase HPLC separation was carried out by gradient elution with 20mM aqueous NaClO4 and acetonitrile (from 90% to 30% aqueous NaClO4 in 10 min) on a LiChrospher 100 RP-18 cartridge (125 mm x 4.6 mm). Analytes were determined with a UV detector set at 245 nm. Quantitation was accomplished by internal standardization with methionine. Linearity was studied in the range 60-120% of the concentrations expected for gly and thr (viz. for gly from 200 to 400 microgml(-1), and for thr from 100 to 200 microgml(-1)). In reference aqueous samples, linear correlation (r) was better than 0.99 for gly and thr, while in spiked matrix samples r ranged from 0.97 to 0.98. Recoveries were in the 95-105% interval, and precision (CV%, N=6) was better than 5% for both analytes either in cream, ointment or bandages. The method was successfully used for the quality control of topical dermatological preparations.

摘要

在本研究中,开发了一种单一的高效液相色谱法用于测定瘢痕形成剂中的甘氨酸和苏氨酸。研究了两种不同制剂(一种乳膏和一种软膏)以及涂抹有这些制剂的相应绷带。该方法包括用二氯甲烷溶解基质,用1N氢氧化钠水溶液进行甘氨酸和苏氨酸的液 - 液分离,以及用异硫氰酸苯酯进行衍生化。反相高效液相色谱分离在LiChrospher 100 RP - 18柱(125 mm×4.6 mm)上进行,采用20mM高氯酸钠水溶液和乙腈梯度洗脱(10分钟内从90%的高氯酸钠水溶液到30%)。用设置在245nm的紫外检测器测定分析物。通过用蛋氨酸进行内标法定量。在甘氨酸和苏氨酸预期浓度的60 - 120%范围内研究线性(即甘氨酸为200至400μgml⁻¹,苏氨酸为100至200μgml⁻¹)。在参考水性样品中,甘氨酸和苏氨酸的线性相关系数(r)优于0.99,而在加标基质样品中,r范围为0.97至0.98。回收率在95 - 105%之间,乳膏、软膏或绷带中两种分析物的精密度(变异系数%,N = 6)均优于5%。该方法成功用于局部皮肤科制剂的质量控制。

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