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出 处:《分析化学》1996年第10期1212-1215,共4页Chinese Journal of Analytical Chemistry
基 金:国家自然科学基金;中国科学院长春应用化学研究所电分析化学开放研究实验室基金
摘 要:对无环鸟苷和鸟嘌呤的高效毛细管电泳(HPCE)分离测定条件进行了详细研究,建立了以2-氨基-5-巯基-3,4-噻二唑为内标的快速、灵敏的HPCE定量分析方法。当无环鸟苷和鸟嘌呤的浓度分别在10~300mg/L和5~300mg/L范围时,可进行定量分析,最低检出限分别为8.52mg/L和2.80mg/L。该方法用于无环鸟苷产品的质量检测,结果准确。用于尿液中的无环鸟苷和鸟嘌呤的快速测定,相对标准偏差小于4.5%。无环鸟苷和鸟嘌呤的回收率分别优于81%和86%。In this paper, the separation and determination conditions of acyclic guanosine and guanine by high performance capillary electrophoresis have been studied systematically. A simple and reproducible HPCE method for determining acyclic guanosine and guanine in acyclic guanosine product and urine is presented. 2-amino-5-mercapto-3, 4-dithiazole was used as an internal standard. Results showed that the linear ranges of determination for acyclic guanosine and guanine are 10~300 mg/L and 5-300 mg/L, and the detection limits are 8. 52mg/L and 2. 80 mg/L (S/N= 2) respectively. The recoveries are more than 81% for acyclic guanosine and 86% for guanine in urine. RSD is less than 4. 5%.
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