Development and validation of spectrofluorimetric method for determination of haloperidol in pharmaceutical dosage forms

被引:7
作者
Rahman, Nafisur [1 ]
Siddiqui, Sana [1 ]
机构
[1] Aligarh Muslim Univ, Dept Chem, Aligarh 202002, Uttar Pradesh, India
关键词
pharmaceuticals; haloperidol; alizarin red S; spectrofluorimetry; validation; HUMAN PLASMA; METABOLITES; ASSAY;
D O I
10.1002/dta.126
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple, sensitive, and accurate spectrofluorimetric method has been developed for the determination of haloperidol in pharmaceutical preparations. The present method is based on the formation of an ion-pair complex between haloperidol and alizarin red S at pH 3.4 which is extractable with chloroform. The ion-pair complex exhibits maximum fluorescence intensity at 564 nm with excitation at 466 nm. The reaction conditions were optimized to obtain maximum fluorescence intensity. The relation between the fluorescence intensity and concentration was found to be linear over the range 0.8-20 mu g/mL with detection limit of 0.08 mu g/mL. The method was successfully employed for quantitation of the active ingredient haloperidol in pharmaceutical preparations. Statistical comparison of the results with the reference method shows excellent agreement and indicates no significant difference between the methods compared in terms of accuracy and precision. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:252 / 258
页数:7
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