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作 者:李金恒[1] 刘存刚[1] 姚旋[1] 曹晓梅[1] 倪立[1] 马晶晶[1] 贺阳红[2]
机构地区:[1]南京军区南京总医院药理科,江苏南京210002 [2]南京医科大学康达学院,江苏南京210012
出 处:《医学研究生学报》2008年第7期682-684,共3页Journal of Medical Postgraduates
基 金:国家自然科学基金资助项目(批准号:30472055)
摘 要:目的:建立人血浆中柳氮磺吡啶(SASP)及其代谢物磺胺吡啶(SP)、乙酰磺胺吡啶(AcSP)浓度的高效液相色谱(HPLC)测定方法。方法:液相分离采用Hedera ODS-2分析柱,柱温:30℃,以甲醇0.05 mol/L乙酸铵溶液(含0.1%三乙胺)溶剂系统梯度洗脱,流速为1.0 ml/min,进样量20μl;检测波长243 nm。以苯巴比妥(PB)为内标,血浆样品用甲醇沉淀蛋白质后取上清液进样分析。结果:血浆中其他组分均不干扰样品的测定;在0.5-100mg/L范围内SP、AcSP和SASP均呈良好的线性关系,相关系数r均〉0.999 2;提取回收率(n=5)分别为97.1%-101.3%、97.7%-103.3%、94.9%-102.3%;日内相对标准偏差(RSD)分别为1.44%-3.04%、1.76%-3.85%、2.12%-3.22%,日间RSD分别为2.01%-3.69%、2.11%-3.99%、2.56%-3.56%。结论:本方法操作简便、选择性好、准确、灵敏,可用于柳氮磺吡啶的药代动力学研究。Objective: To develop a validated, highly sensitive and selective high performance liquid chromatographic (HPLC) method for the quantitative determination of sulfasalazine (SASP) and its metabolites sulfapyridine (SP) and N-acetylsulfapyridine (AcSP) in human plasma. Methods: After protein precipitation with methanol, 20 ul of supernatant was injected onto a Hedera ODS-2 column and the effluent measured for UV absorption at 243 nm. 0.05 mol/L ammonium acetate ( containing 0. 1% triethylamine) was used as mobile phase A and methanol as mobile phase B with the flow rate of 1.0 ml/min. A gradient elution program was applied, and phenobarbital used as the internal standard. Results: The linear concentrations of SP, AcSP and SASP ranged from 0.5 to 100 mg/L ( r 〉 0.999 2) ; the rates of extraction recovery were 97.1% - 101.3% for SP, 97.7% - 103.3% for AcSP and 94.9% - 102.3% for SASP; the intra- and inter-day RSDs were 〈 4.0%. Conclusion: The HPLC method, with its high sensitivity, accuracy and repeatability, can be used in the pharmacokinetic and bioavailability studies of SASP.
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