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Conductometric and indirect AAS determination of antimalarials.

机译:电导和间接AAS测定抗疟药。

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摘要

Two methods are described for the determination of amodiaquine hydrochloride, chloroquine phosphate and primaquine phosphate, based on the formation of their ion-associates with [Cd(2+), Co(2+), Mn(2+) and Zn(2+)] thiocyanate, ammonium reineckate and/or sodium cobaltinitrite. The molar combining ratio reveal that (1:1) (drug:reagent) ion associates are formed for all reagents except for ammonium reineckate which form (1:2) ion associates with all studied drugs. The optimum conditions for the ion-association have been studied. Conductometric method was applied for the direct determination of the suggested drugs in bulk powders, whereas indirect atomic absorption spectrometric method, depending on the measurement of the excess metal ion present in supernatant solutions after precipitation of the ion associates is used to calculate the drug concentration. Optimum concentration ranges for the determination of aminoquinoline antimalarial drugs under consideration were 0.46-12.90 and 0.155-3.87 mg using conductometric and indirect atomic absorption spectral methods, respectively. The proposed procedures have been applied successfully to the analysis of these drugs in certain formulations and the results are favourably comparable to the official methods.
机译:描述了两种测定氨二喹盐酸盐,磷酸氯喹和磷酸伯氨喹的方法,基于它们与[Cd(2 +),Co(2 +),Mn(2+)和Zn(2+)的离子缔合的形成)]硫氰酸盐,雷内铵铵和/或钴铝酸钠矿。摩尔混合比表明,除再狭窄的铵盐铵与所有研究药物形成(1:2)离子缔合外,所有试剂均形成(1:1)(药物:试剂)离子缔合。研究了离子缔合的最佳条件。电导法用于直接测定散装粉末中建议的药物,而间接原子吸收光谱法则取决于对离子缔合剂沉淀后上清液中过量金属离子的测量,以计算药物浓度。使用电导法和间接原子吸收光谱法测定氨基喹啉抗疟药的最佳浓度范围分别为0.46-12.90和0.155-3.87 mg。拟议的程序已成功应用于某些制剂中这些药物的分析,其结果可与官方方法相媲美。

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