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作 者:杨惠锑 费艳秋[1] 王平全[1] 袁静[1] 施安国[1]
机构地区:[1]上海第二医科大学附属仁济医院临床药学研究室,上海市200001
出 处:《中国药房》2001年第9期542-543,共2页China Pharmacy
摘 要:目的:建立左旋多巴血药浓度的测定方法并对左旋多巴控释片进行人体药代动力学研究。方法:高效液相色谱法,色谱柱:Lichrospher 100C18柱(5um,250mm×4mm);流动相:水(含EDTA0.08mmol/L,KH2PO470mm70mmol/L,庚烷磺酸钠2.08mmol/L):甲醇(90:10);流速:1.0ml/min;荧光检测:激发波长为278nm,发射波长为325nm;血浆样品用高氯酸沉淀蛋白后直接进样。结果:方法回收率为95.50%~102.55%,最低检测限为0.25ng,日内RSD<4.29%(n=4),日间RSD<6.73%(n=4),线性范围为0.125~4.0ug/ml。8名健康受试者单次口服左旋多巴控释片250mg后,药-时曲线符合二室模型,AUC为(297.36±52.18)ug/(ml·min),Cmax为(1.04±0.42)ug/ml,Tmax为(152.65±46.71)min,T1/2a为(124.76±43.87)min,T1/2β为(157.83±30.82)min.与左旋多巴相比,Tmax和T1/2a具有显著性差异,相对生物利用度为(70.17±7.41)%。OBJECTIVE: To develop a method for the determination of levodopa in human plasma and study aarodopa's pharmacokinetics. METHODS: Experiments were performed on Waters 2010 HIPLC system with a 474 fluorecence detector (λEX = 278nm, λEm = 325nm) and a Lichrospher 100 C18 column. The mobile phase(pH3. 7) was 90% water containing 0.08 mmol/L EDTA, 70mmol/L KH2PO4, 2. 08mmol/L sodium heptanesulfonate and 10% methanal. The flow rate was 1. 0ml/min. The plasma sample was directly injected for determination after being deproteinized with perchloric acid. RESULTS: The linear range was 0. 125-4.0ug/ml,the limitation of detection was 0. 25ug/ml,within- day RSD<4.29%(n=4),between-day RSD< 6.73% (n = 4), the recoveries of levodopa were 95.50% -102.55%. After oral administration of 250mg aarodopa tablet, the re sults showed that the disposition of aarodopa was conformed to a two-compartment model with T1/2a = (124.76 ± 43.87) min, T1/2β= (157. 83±30. 82)min,Tmax =(152.65±46.71)min,Cmax (1.04±0.42)ug/ml and AUC= (297. 36±52. 18) ug/(ml min) . In comparison with levodopa tablet, Tmax and T1/ 2a were significantly different, the relative biovailability was (70. 1± 7.41) % . CONCLUSION: This method is rapid, accurate and sensitive, it is very suitable for the investigation of clinical phar- macokinetics of levodopa.
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