Osei-Safo Dorcas, Chikowe Ibrahim, Harrison Jerry Joe Ebow Kingsley, Yeboah Daniel Konadu, Addae-Mensah Ivan
Chemistry Department, School of Mathematical and Physical Sciences, College of Basic and Applied Sciences, University of Ghana, Accra, Ghana.
Biomedical Sciences and Health Professions, College of Medicine, University of Malawi, Blantyre, Malawi.
J Anal Methods Chem. 2018 May 2;2018:2130390. doi: 10.1155/2018/2130390. eCollection 2018.
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 ( = 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 g/spot with a correlation coefficient of = 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.
在采用高效液相色谱法(HPLC)分析之前,一种最近开发的半定量薄层色谱法(SQ-TLC)已用于马拉维使用的抗疟药物的上市后监测。在绝大多数样品中,两种方法得出的结果相似,对于所分析剂型的活性药物成分具有良好的相关性(r = 0.9012)。含蒿甲醚的药物在两种分析中结果可比的样品百分比最高(92.67%)。含青蒿琥酯的药物中观察到的百分比最低(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,结果均在可接受范围内。对于特异性,测试样品和参考标准品的保留因子值具有可比性,而所有样品的准确度和精密度为91.1±5.7%。该方法在1.0-2.0 g/点范围内呈线性,相关系数r = 0.9783。稳定性测试结果也在可接受范围内。在本研究中,我们展示了SQ-TLC方法的验证,并建议将其用作一种快速筛查工具,以便在进行更准确的HPLC分析之前,对马拉维和发展中世界其他地区的抗疟药物及其他基本药物的质量进行现场评估。