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荧光光谱法测定家兔中丹参素血浓度及其药物动力学参数

SPECTROFLUOROMETRIC DETERMINATION OF RABBITPLASMA LEVEL AND PHARMACOKINETICPARAMETERS OF "DAN-SHEN-SU

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【作者】 何怀冰; 王蓓; 陈沄; 秦芝玲; 张德成; 金吉琴; 李端; 戎大梅;

【Author】 HE HUAIBING, WANG BEI, OHEN YUN, QIN ZHILING (T. L. CHING)(Department of Analytical Chemistry, Faculty of Pharmacy, Shanghai First Medical College, Shanghai)ZHANG DECHENG, JIN JIQIN, LI DUAN, BONG DAMEI(Department of Chemistry of Natural Products, "Pharmacology and Biochemistry,Facuty of Pharmacy, and Central Laboratory of Instrumental Analysis, ShanghaiFirst Medical College, Shanghai)

【机构】 上海第一医学院药学系分析化学教研室,上海第一医学院药学系分析化学教研室,上海第一医学院药学系分析化学教研室,上海第一医学院药学系分析化学教研室,上海第一医学院药学系天然药物化学,上海第一医学院附属红旗药厂,上海第一医学院药学系药理生物化学教研室,上海第一医学药学系院仪器分析中心实验室 1981届药学系毕业生; ,1981届药学系毕业生;

【摘要】 本文报道血样经醋酸乙脂提取、分离丹参素后,用荧光光谱法加以测定。丹参素醋酸乙脂液激发光谱与荧光发射光谱峰的波长各为λΕχ285nm,λΕχ314nm;浓度在1.0~9.0×10-6g/ml,范围与荧光强度呈线性关系;溶液的荧光强度稳定。由本法测得血浆中的丹参素回收率平均为76.47士2.427%(CV=3.174%,n=20);血药浓度-时间(1gc-t)曲线表明,丹参素的药物动力学为单室模型,其消除速率常数和生物半衰期为:Kel=0.04561士0.0141(min-1);t(1/2)=16.58士5.768(min)。

【Abstract】 A spectrofluorometric procedure for the determination of rabbit plasma level of "DAN-SHEN-SU" [D( + )×-3, 4-dihydroxyphenyl lactic acid] was proposed, and ita phamacokinetic parameters were obtained from the corresponding plasma level-time curve measured.In ethyl acetate medium, "DAN-SHEN-SU" showed an emission maximum at 314 nm (the excitation maximum was at 285 nm) and its concentration ranging form 1.0 to 9.0 × 10-6g/ml presented a linear relation with the fluorescent intensity which remained stable for three hours, correlation coefficient, x=0.9996; regression line, 0= 1.0168 ±10-7F-1. 815 ±10-7.The data of fluorescent intensity of"DAN-SHEN-SU"extracted with ethyl acetate from rabbit plasma within the above concentration range were also quite satisfactory, r=0.9997; C = 1.497±10-7F-1.470±10-7.The average recovery of "DAN-SHEN-SU" from plasma was 76.47 ±2.427%, coefficient of variation, 0. V. = 3.147% (n = 20).According to the existing experimental conditions, the rabbit plasma levels of "DAN-SHEN-SU" administered intravenously were measured. The resultant graph of log plasma concentration-time plotted was a straight line, suggesting that the pharmacokinetics of "DAN-SHEN-SU" was a one-compartment open body model with the following parameters: elimination rate constant, Kel = 0.04561 ±0.0141 (min-1); biological half life time t1±2 = 16.58±5.768(min).

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