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采用胶束液相色谱法测定止咳感冒药中的活性成分。

Determination of active ingredients in cough-cold preparations by micellar liquid chromatography.

作者信息

Gil-Agustí M, Monferrer-Pons L, García-Alvarez-Coque M C, Esteve-Romero J

机构信息

Dpto de Ciencias Experimentales, Area de Quimica Analitica, Universitat Jaume I, Campus Riu Sec, 12080, Castelló, Spain.

出版信息

Talanta. 2001 May 30;54(4):621-30. doi: 10.1016/s0039-9140(01)00315-0.

Abstract

The chromatographic behaviour of some active ingredients in cough-cold pharmaceutical preparations, the antihistamine chlorpheniramine (or the dextro enantiomer dexchlorpheniramine), and the phenethylamines phenylephrine, phenylpropanolamine and pseudoephedrine, has been studied using a C(18) column, micellar mobile phases of sodium dodecyl sulphate (SDS) and pentanol, and with UV detection. All possible combinations of chlorpheniramine/phenethylamine were resolved and determined using a mobile phase of 0.15 M SDS-6% (v/v) pentanol at pH 7, with analysis time below 7 min. Repeatabilities and within laboratory precisions were evaluated at four different drug concentrations in the range 0.5-25 mug ml(-1) (n=5), resulting RSDs below 1.6%. The drug amounts found in the analysis of 14 commercialised preparations agreed with those declared by the manufacturers within the tolerance limits, and with those obtained using an aqueous 60% (v/v) methanol reference mobile phase. No interference was observed from other accompanying drugs such as acetylsalicylic acid, ascorbic acid, betamethasone, caffeine, codeine phosphate, diphenhydramine, lactose, paracetamol, and prednisolone. The studied combinations required a rather high amount of methanol in conventional RPLC to be eluted from the column. In contrast, the proposed procedure used a much lower amount of organic solvent (pentanol), which is highly retained in the SDS solution, being also less toxic than methanol.

摘要

使用C(18)柱、十二烷基硫酸钠(SDS)和戊醇的胶束流动相,并通过紫外检测,研究了止咳感冒药制剂中某些活性成分、抗组胺药氯苯那敏(或右旋对映体右氯苯那敏)以及苯乙胺类药物去氧肾上腺素、苯丙醇胺和伪麻黄碱的色谱行为。使用pH值为7的0.15 M SDS - 6%(v/v)戊醇流动相,可分离并测定氯苯那敏/苯乙胺的所有可能组合,分析时间在7分钟以下。在0.5 - 25 μg ml(-1)范围内的四种不同药物浓度下(n = 5)评估了重复性和实验室内精密度,相对标准偏差(RSD)低于1.6%。对14种商业化制剂分析中发现的药物含量在制造商声明的公差范围内,并且与使用60%(v/v)甲醇水参考流动相获得的结果一致。未观察到其他伴随药物如乙酰水杨酸、抗坏血酸、倍他米松、咖啡因、磷酸可待因、苯海拉明、乳糖、对乙酰氨基酚和泼尼松龙的干扰。在传统反相液相色谱法中,所研究的组合从柱上洗脱需要相当大量的甲醇。相比之下,所提出的方法使用的有机溶剂(戊醇)量要少得多,戊醇在SDS溶液中保留性很强,且毒性也比甲醇小。

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