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高效液相色谱法研究注射液加替沙星在家兔体内的药代动力学 被引量:2

Pharmacokinetics study of Gatifloxacin injection in vivo rabbit by HPLC
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摘要 目的:建立测定家兔血清中加替沙星药物浓度的高效液相方法,进一步研究注射液加替沙星在家兔体内的药代动力学。方法:通过对健康家兔耳缘静脉注射加替沙星后,分别在1,3,5,7.5,15,30,60,120,180,240,360m in时进行血液采集,用高效液相色谱法中的定量分析。结果:加替沙星C0=39.6947,药物的分布半衰期t1/2a=0.0215,药物的消除半衰期t1/2b=1.4292,K12=23.8976,K21=6.2912,K e l=2.4807,Clb=1.2499,AUC=16.0017,Vd=2.5776,单剂量静脉注射二室模型表达式:C=32.424e(-32.1846t)+7.2707e(-0.4849t)。结论:本法快速、准确,重现性好,为该药物的临床血药浓度监测和药代动力学研究提供依据。 Objective:To establish a method used to determine medicine concentration in rabbit serum by HPI.C and further study Gatifloxacin injection pharmacokinetics in vivo rabbit. Method:After injecting Gatifloxacin to ear edge by intravenous injection,we made quantitative analysis by HPLC to collect blood at 1,3,5,7. 5,15,30,60,120,180,240 and 360 min, respectively. Results :Gatifloxacin Co = 39. 6947 ,medicine distribution half life t1/2a = 0. 0215, elimination half life t1/2b= 1. 4292,K12 = 23. 8976,K21 =6. 2912,Kel= 2. 4807 ,C1b = 1. 2499, AUC= 16. 0017 ,and Vd = 2. 5776. And two--compartment model expression of single dose intravenous injection:C=32.424e(-32.1846t)+7.2707e(-0.4849t). Conclusion. It is a rapid and accurate method with better reproducibility. Therefore, the concentration in blood and pharmacokinetics. method can offer a basis for monitoring clinic medicine concentration in blood and pharmacokinetics.
出处 《黑龙江医药科学》 2008年第3期32-34,共3页 Heilongjiang Medicine and Pharmacy
关键词 加替沙星 药代动力学 高效液相色谱法 Gatifloxacin pharmacokinetics HPLC
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