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基于与四氰基对苯二醌二甲烷和氯冉酸形成电荷转移络合物的选择性5-羟色胺再摄取抑制剂的分光光度分析

Spectrophotometric analysis of selective serotonin reuptake inhibitors based on formation of charge-transfer complexes with tetracyanoquinodimethane and chloranilic acid.

作者信息

Darwish Ibrahim A, Refaat Ibrahim H

机构信息

Assiut University, Faculty of Pharmacy, Department of Pharmaceutical Analytical Chemistry, Assiut 71526, Egypt.

出版信息

J AOAC Int. 2006 Mar-Apr;89(2):326-33.

Abstract

A simple, accurate, and sensitive spectrophotometric method for analysis of selective serotonin reuptake inhibitors (SSRIs) has been developed and validated. The analysis was based on the formation of colored charge-transfer complexes between the intact molecule of SSRI drug as an n-electron donor and each of tetracyanoquinodimethane (TCNQ) or p-chloranilic acid (pCA) as electron acceptors. The formed complexes were measured spectrophotometrically at 842 and 520 nm for TCNQ and pCA, respectively. Different variables and parameters affecting the reactions were studied and optimized. Under the optimum reaction conditions, linear relationships with good correlation coefficients (0.9975-0.9996) were found between the absorbances and the concentrations of the investigated drugs in the concentration ranges of 4-50 and 20-400 microg/mL with TCNQ and pCA, respectively. With all the investigated drugs, TCNQ gave more sensitive assays than pCA; the limits of assay detection were 2.5-4.8 and 20-40 microg/mL with TCNQ and pCA, respectively. The intra- and interassay precisions were satisfactory; the relative standard deviations did not exceed 2%. The proposed procedures were successfully applied to the analysis of the studied drugs in pure form and pharmaceutical formulations with good accuracy; the recovery values were 98.4-102.8 +/- 1.24-1.81%. The results obtained from the proposed method were statistically comparable with those obtained from the previously reported methods.

摘要

已开发并验证了一种用于分析选择性5-羟色胺再摄取抑制剂(SSRI)的简单、准确且灵敏的分光光度法。该分析基于作为n电子供体的SSRI药物完整分子与作为电子受体的四氰基对苯二醌二甲烷(TCNQ)或对氯苯醌(pCA)各自形成的有色电荷转移络合物。分别在842nm和520nm处用分光光度法测定形成的络合物,其中842nm用于测定与TCNQ形成的络合物,520nm用于测定与pCA形成的络合物。研究并优化了影响反应的不同变量和参数。在最佳反应条件下,分别在4 - 50μg/mL和20 - 400μg/mL的浓度范围内,发现吸光度与所研究药物浓度之间存在具有良好相关系数(0.9975 - 0.9996)的线性关系,其中TCNQ对应的浓度范围是4 - 50μg/mL,pCA对应的浓度范围是20 - 400μg/mL。对于所有研究的药物,TCNQ比pCA给出的测定更灵敏;TCNQ和pCA的测定检测限分别为2.5 - 4.8μg/mL和20 - 40μg/mL。批内和批间精密度令人满意;相对标准偏差不超过2%。所提出的方法成功应用于纯品和药物制剂中所研究药物的分析,准确度良好;回收率值为98.4 - 102.8±1.24 - 1.8 %。所提出方法得到的结果与先前报道方法得到的结果在统计学上具有可比性。

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