Suppr超能文献

采用分光光度技术分析Allercet感冒胶囊中的对乙酰氨基酚、伪麻黄碱和西替利嗪。

Analysis of paracetamol, pseudoephedrine and cetirizine in Allercet Cold capsules using spectrophotometric techniques.

作者信息

Youssef Souha H, Hegazy Maha Abdel-Monem, Mohamed Dalia, Badawey Amr Mohamed

机构信息

Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, October University for Modern Sciences and Arts, 6 October City, 11787, Egypt.

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

出版信息

Chem Cent J. 2018 Jun 1;12(1):67. doi: 10.1186/s13065-018-0436-z.

Abstract

Paracetamol (PAR), Pseudoephedrine hydrochloride (PSE) and cetirizine dihydrochloride (CET) is a ternary mixture that composes tablets which are popular for the relief of flu in Egypt. The spectra of the drugs were overlapped and no spectrophotometric methods were reported to resolve the mixture. This research proposes four spectrophotometric methods that are efficient and require water only as a solvent. The first method was ratio subtraction-ratio difference method (RSDM) where PAR was initially removed from the mixture by ratio subtraction and determined at 292.4 nm, then PSE and CET were quantified by subtracting the amplitudes of their ratio spectra between 257.0 and 230.0 nm for PSE and between 228.0 and 257.0 nm for CET. The second method was derivative ratio spectra-zero crossing (DRZC) which was based on determining both PSE and CET from the zero-crossing points of the first and third derivative of their ratio spectra at 252.0 and 237.0 nm, respectively while PAR was determined using its first derivative at 292.4 nm. Moreover, the ternary mixture was resolved using successive derivative ratio (SDR) method where PAR, PSE and CET were determined at 310.2, 257.0 and 242.4 nm, respectively. The fourth proposed method was pure component contribution algorithm (PCCA) which was applied to quantify the drugs at their λ. Recovery percentages for RSDM were 100.7 ± 1.890, 99.69 ± 0.8400 and 99.38 ± 1.550; DRZC were 101.8 ± 0.8600, 99.04 ± 1.200 and 98.95 ± 1.300; SDR were 101.9 ± 1.060, 99.59 ± 1.010 and 100.2 ± 0.6300; PCCA were 101.6 ± 1.240, 99.10 ± 0.5400 and 100.4 ± 1.800 for PAR, PSE and BRM; respectively. The suggested methods were effectively applied to analyze laboratory prepared mixtures and their combined dosage form.

摘要

对乙酰氨基酚(PAR)、盐酸伪麻黄碱(PSE)和盐酸西替利嗪(CET)是一种三元混合物,由片剂组成,在埃及这种片剂常用于缓解流感症状。这三种药物的光谱相互重叠,尚未有分光光度法用于解析该混合物。本研究提出了四种分光光度法,这些方法高效且仅需用水作为溶剂。第一种方法是比率减法 - 比率差值法(RSDM),即首先通过比率减法从混合物中去除PAR,并在292.4nm处测定其含量,然后通过分别减去PSE在257.0至230.0nm之间以及CET在228.0至257.0nm之间的比率光谱幅度来定量PSE和CET。第二种方法是导数比率光谱 - 零交叉法(DRZC),该方法基于分别从PSE和CET比率光谱的一阶和三阶导数的零交叉点(分别为252.0nm和237.0nm)测定PSE和CET,而PAR则通过其在292.4nm处的一阶导数进行测定。此外,使用逐次导数比率(SDR)法解析该三元混合物,其中PAR、PSE和CET分别在310.2nm、257.0nm和242.4nm处测定。提出的第四种方法是纯组分贡献算法(PCCA),用于在各药物的λ处对其进行定量。RSDM法对PAR、PSE和BRM的回收率分别为100.7±1.890、99.69±0.8400和99.38±1.550;DRZC法分别为101.8±0.8600、99.04±1.200和98.95±1.300;SDR法分别为101.9±1.060、99.59±1.010和100.2±0.6300;PCCA法分别为101.6±1.240、99.10±0.5400和100.4±1.800。所建议的方法有效地应用于分析实验室制备的混合物及其复方剂型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/202f/5984616/ec1a2f5f7f6b/13065_2018_436_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验