Patchen L C, Mount D L, Schwartz I K, Churchill F C
J Chromatogr. 1983 Nov 11;278(1):81-9. doi: 10.1016/s0378-4347(00)84758-1.
Methodology has been developed to facilitate the collection, transport, and analysis of blood samples in studies of chloroquine absorption and metabolism. The method utilizes high-performance liquid chromatography (HPLC) with fluorescence detection to quantify chloroquine and its major metabolite, desethylchloroquine, in 100-microliters quantities of blood collected on filter paper. Detection limits are 5 ng/ml for both analytes. No loss of either analyte occurred from filter-paper-collected blood spots stored over a twelve-weeks' period at room temperature. Filter-paper-collected, finger-stick blood spots give values for each analyte comparable to corresponding determinations on venous, whole-blood samples. The HPLC mobile phase selected has general applicability to the separation of antimalarial drugs. The methodology permits effective assessment of chloroquine prophylaxis compliance and parasite drug resistance in remote, malaria-endemic regions.
已开发出一种方法,以方便在氯喹吸收和代谢研究中对血样进行采集、运输和分析。该方法利用带荧光检测的高效液相色谱法(HPLC),对收集在滤纸上的100微升血量中的氯喹及其主要代谢物去乙基氯喹进行定量。两种分析物的检测限均为5纳克/毫升。在室温下储存12周的滤纸采集血斑中,两种分析物均未出现损失。滤纸采集的手指刺血斑中每种分析物的值与静脉全血样本的相应测定值相当。所选择的HPLC流动相对抗疟药物的分离具有普遍适用性。该方法可有效评估偏远疟疾流行地区氯喹预防的依从性和寄生虫耐药性。