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两种使用氯胺-T估算阿苯达唑及其剂型的简单方法。

Two simple methods for the estimation of albendazole and its dosage forms using chloramine-T.

作者信息

Basavaiah K, Prameela H C

机构信息

Department of Chemistry, University of Mysore, Manasagangotri, Mysore 570 006, India.

出版信息

Farmaco. 2003 Jul;58(7):527-34. doi: 10.1016/S0014-827X(03)00067-3.

Abstract

Two simple, rapid and reliable methods for the determination of albendazole are described. Both methods involve the use of chloramine-T as the oxidimetric reagent. In the titrimetric method, a known excess of chloramine-T is added to an acidified solution of sample, and after a specified time, the residual oxidant is determined iodometrically. Spectrophotometric procedure also involves the addition of a measured excess of chloramine-T in buffer medium of pH 2.70+/-0.1 and after the reaction is ensured to be complete, the surplus oxidant is determined by a well established colour reaction involving metol and primary arylamine that results in charge-transfer complex measurable at 520 nm. In both methods, the amount of chloramine-T corresponds to the drug content. Reaction conditions were examined and optimised. Titrimetry is based on a 1:3 stoichiometric reaction between albendazole and chloramine-T and is applicable in the range of 1-15 mg. In spectrophotometry, the absorbance was found to decrease linearly with increasing concentration of albendazole, which is corroborated by the calculated correlation coefficient value of -0.9998. The system obeys Beer's law for 2.5-25 microg x ml(-1) of albendazole. The molar absorptivity and Sandell sensitivity were calculated to be 6.24 x 10(3) l mol(-1) cm(-1) and 42.54 ng cm(-2), respectively. The limits of detection and quantification were calculated to be 1.15 and 3.83 microg x ml(-1), respectively. The proposed methods were successfully applied to the determination of albendazole in commercially available dosage forms. The reliability of the assays was established by parallel determination by the official method and recovery studies.

摘要

本文描述了两种简单、快速且可靠的阿苯达唑测定方法。两种方法均使用氯胺 -T作为氧化还原试剂。在滴定法中,向酸化的样品溶液中加入已知过量的氯胺 -T,在规定时间后,用碘量法测定剩余的氧化剂。分光光度法同样是在pH 2.70±0.1的缓冲介质中加入测量过量的氯胺 -T,确保反应完全后,通过一种成熟的涉及米吐尔和伯芳胺的显色反应来测定过量的氧化剂,该反应会产生在520 nm处可测量的电荷转移络合物。在两种方法中,氯胺 -T的用量都与药物含量相对应。对反应条件进行了考察和优化。滴定法基于阿苯达唑与氯胺 -T之间1:3的化学计量反应,适用于1 - 15 mg的范围。在分光光度法中,发现吸光度随阿苯达唑浓度的增加呈线性下降,计算得到的相关系数值为 -0.9998,证实了这一点。该体系在2.5 - 25 μg·ml⁻¹的阿苯达唑浓度范围内符合比尔定律。计算得到的摩尔吸光系数和桑德尔灵敏度分别为6.24×10³ l·mol⁻¹·cm⁻¹和42.54 ng·cm⁻²。检测限和定量限分别计算为1.15和3.83 μg·ml⁻¹。所提出的方法成功应用于市售剂型中阿苯达唑的测定。通过与官方方法平行测定和回收率研究确定了该分析方法的可靠性。

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