首页> 外文期刊>Bulletin of Faculty of Pharmacy, Cairo University >Spectrophotometric, chemometric and chromatographic determination of naphazoline hydrochloride and chlorpheniramine maleate in the presence of naphazoline hydrochloride alkaline degradation product
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Spectrophotometric, chemometric and chromatographic determination of naphazoline hydrochloride and chlorpheniramine maleate in the presence of naphazoline hydrochloride alkaline degradation product

机译:盐酸萘甲唑啉碱降解产物存在下的分光光度法,化学计量法和色谱法测定盐酸萘甲唑啉和马来酸氯苯那敏

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Four accurate and sensitive methods were developed and validated for determination of naphazoline hydrochloride (NAP) and chlorpheniramine maleate (CLO) in the presence of naphazoline hydrochloride alkaline degradation product (NAP Deg). The first method is a spectrophotometric one , where NAP was determined by the fourth derivative (D 4 ) spectrophotometric method by measuring the peak amplitude at 302nm, while CLO was determined by the second derivative of the ratio spectra (DD 2 ) spectrophotometric method at 276.4nm. The second method is a chemometric-assisted spectrophotometric method in which partial least squares (PLS-1) and partial component regression (PCR) were used for the determination of NAP, CLO and NAP Deg using the information contained in their absorption spectra of ternary mixture. The third method is a TLC-densitometric one where NAP, CLO and NAP Deg were separated using HPTLC silica gel F254 plates using ethyl acetate:methanol:ammonia: (8:2:0.5, by volume) as the developing system followed by densitometric measurement at 245nm. The fourth method is HPLC method where NAP, CLO and NAP Deg were separated using ODS C 18 column and a mobile phase consisting of 0.1M KH 2 PO 4 (pH=7):methanol (55:45 v/v) delivered at 1.5mLmin ?1 followed by UV detection at 265nm. The proposed methods have been successfully applied to the analysis of NAP and CLO in pharmaceutical formulations without interference from the dosage form additives and the results were statistically compared with a reported method.
机译:开发了四种准确而灵敏的方法,并在存在萘甲唑啉盐酸盐碱性降解产物(NAP Deg)的情况下,对测定萘甲唑啉盐酸盐(NAP)和马来酸氯苯那敏(CLO)的方法进行了验证。第一种方法是分光光度法,其中NAP是通过四阶导数(D 4)分光光度法通过测量302nm处的峰振幅来确定的,而CLO是通过比率光谱(DD 2)分光光度法在276.4处的二阶导数确定的纳米第二种方法是化学辅助分光光度法,其中使用偏最小二乘(PLS-1)和偏分成分回归(PCR)来利用三元混合物吸收光谱中包含的信息来确定NAP,CLO和NAP Deg。 。第三种方法是TLC密度法,其中使用HPTLC硅胶F254板,以乙酸乙酯:甲醇:氨:(体积比为8:2:0.5)作为显影系统,分离NAP,CLO和NAP Deg,然后进行光密度测量在245nm。第四种方法是HPLC方法,其中使用ODS C 18色谱柱分离NAP,CLO和NAP Deg,并以1.5的流速输送由0.1M KH 2 PO 4(pH = 7):甲醇(55:45 v / v)组成的流动相mLmin≥1,然后在265nm处进行UV检测。所提出的方法已成功地应用于药物制剂中NAP和CLO的分析,而不受剂型添加剂的干扰,并将结果与​​报道的方法进行了统计比较。

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