首页> 外文期刊>Journal of Analytical Methods in Chemistry >Further Validation of a Rapid Screening Semiquantitative Thin-Layer Chromatographic Method for Marketed Antimalarial Medicines for Adoption in Malawi
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Further Validation of a Rapid Screening Semiquantitative Thin-Layer Chromatographic Method for Marketed Antimalarial Medicines for Adoption in Malawi

机译:快速筛选半定量薄层色谱方法用于马拉维市售抗疟药物的进一步验证

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A recently developed semiquantitative thin-layer chromatographic (SQ-TLC) assay has been employed in postmarketing surveillance of antimalarial medicines used in Malawi prior to HPLC assay. Both methods gave analogous results in a significant majority of the samples, with a good correlation (r = 0.9012) for the active pharmaceutical ingredients of the dosage forms assayed. Artemether-containing medicines had the highest percentage (92.67%) of samples with comparable results for both assays. The lowest percentage (66.67%) was observed in artesunate-containing medicines. The SQ-TLC method was validated for specificity, accuracy, precision, linearity, and stability according to the International Conference on Harmonisation guidelines, with the results falling within acceptable limits. For specificity, retention factor values of the test samples and reference standards were comparable, while accuracy and precision of 91.1 ± 5.7% were obtained for all samples. The method was linear in the range 1.0–2.0 µg/spot with a correlation coefficient of r = 0.9783. Stability tests also fell within acceptable limits. In this study, we present the validation of the SQ-TLC method and propose its adoption as a rapid screening tool for field estimation of the quality of antimalarial and other essential medicines in Malawi and other parts of the developing world prior to a more accurate HPLC assay.
机译:最近开发的半定量薄层色谱(SQ-TLC)测定法已用于在进行HPLC测定法之前对马拉维使用的抗疟药进行售后监测。两种方法在绝大部分样品中均得出相似的结果,与所测定剂型中的活性药物成分具有良好的相关性(r = 0.9012)。含有蒿甲醚的药物在样品中所占的比例最高(92.67%),两种测定的结果相近。在含青蒿琥酯的药物中观察到最低百分比(66.67%)。根据国际协调会议指南,对SQ-TLC方法的特异性,准确性,精密度,线性和稳定性进行了验证,结果在可接受的范围内。就特异性而言,测试样品和参比标准品的保留因子值相当,而所有样品的准确度和精密度均达到91.1±5.7%。该方法在1.0-2.0μg/ s范围内呈线性,相关系数为r = 0.9783。稳定性测试也落在可接受的范围内。在这项研究中,我们提出了SQ-TLC方法的验证,并提出了将其作为一种快速筛选工具,以便在更准确的HPLC之前对马拉维和其他发展中国家的抗疟药和其他基本药物的质量进行现场评估。分析。

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