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Validated stability-indicating derivative and derivative ratio methods for the determination of some drugs used to alleviate respiratory tract disorders and their degradation products.验证了用于测定用于缓解呼吸道疾病的一些药物及其降解产物的衍生化和衍生比方法的稳定性。
Drug Test Anal. 2011 May;3(5):306-18. doi: 10.1002/dta.258. Epub 2011 Mar 16.
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Method development and validation of montelukast in human plasma by HPLC coupled with ESI-MS/MS: application to a bioequivalence study.采用高效液相色谱-电喷雾串联质谱法(HPLC-ESI-MS/MS)测定人血浆中孟鲁司特的方法开发与验证:在生物等效性研究中的应用
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Simultaneous estimation of Montelukast sodium and Bambuterol hydrochloride in tablets by spectrophotometry.分光光度法同时测定片剂中孟鲁司特钠和盐酸班布特罗的含量
Hindustan Antibiot Bull. 2007;49-50(1-4):29-33.
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A new spectrophotometric method for quantitative multicomponent analysis resolution of mixtures of salicylic and salicyluric acids.一种用于水杨酸和水杨尿酸混合物定量多组分分析分辨率的新分光光度法。
Talanta. 1990 Mar;37(3):347-51. doi: 10.1016/0039-9140(90)80065-n.
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Smart stability-indicating spectrophotometric methods for determination of binary mixtures without prior separation.无需预先分离即可测定二元混合物的智能稳定性指示分光光度法。
J AOAC Int. 2008 Mar-Apr;91(2):299-310.
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Analysis of glimepiride by using derivative UV spectrophotometric method.采用导数紫外分光光度法分析格列美脲。
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Analysis of ACE inhibitors in pharmaceutical dosage forms by derivative UV spectroscopy and liquid chromatography (HPLC).采用导数紫外光谱法和液相色谱法(HPLC)对药物剂型中的血管紧张素转换酶(ACE)抑制剂进行分析。
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采用分光光度技术(比值差法)同时测定皮肤软膏中的视黄酸和氢醌。

Simultaneous determination of retinoic acid and hydroquinone in skin ointment using spectrophotometric technique (ratio difference method).

机构信息

Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Kasr-El Aini Street, 11562 Cairo, Egypt.

出版信息

Saudi Pharm J. 2012 Jul;20(3):249-53. doi: 10.1016/j.jsps.2012.03.004. Epub 2012 Mar 31.

DOI:10.1016/j.jsps.2012.03.004
PMID:23960798
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3744983/
Abstract

An innovative spectrophotometric method was developed for simultaneous determination of compounds with interfering spectra in binary mixtures without previous separation, showing significant advantages over the conventional methods regarding minimal data manipulation and applicability. The proposed method was applied for the determination of retinoic acid and hydroquinone in laboratory-prepared mixtures with mean percentage recoveries 100.13 ± 0.31 and 99.99 ± 0.04, respectively, and in their pharmaceutical formulation with mean percentage recoveries 100.13 ± 0.86 and 100.07 ± 0.58, respectively. The method was validated according to USP guidelines and can be applied for routine quality control testing.

摘要

建立了一种无需预先分离即可同时测定二元混合物中具有光谱干扰化合物的分光光度新方法,与常规方法相比,该方法在数据处理和适用性方面具有显著优势。该方法用于测定实验室制备的混合物中的视黄酸和对苯二酚,平均回收率分别为 100.13 ± 0.31%和 99.99 ± 0.04%,在其药物制剂中的平均回收率分别为 100.13 ± 0.86%和 100.07 ± 0.58%。该方法符合 USP 指南,可以用于常规质量控制检测。