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高效液相色谱法测定人血浆中某些抗炎、弱镇痛和促尿酸排泄药物及其在药代动力学中的应用。

HPLC-determination of some antiinflammatory, weak analgesic and uricosuric drugs in human blood plasma and its application to pharmacokinetics.

作者信息

Nielsen-Kudsk F

出版信息

Acta Pharmacol Toxicol (Copenh). 1980 Oct;47(4):267-73. doi: 10.1111/j.1600-0773.1980.tb03653.x.

Abstract

HPLC-determination of naproxen, indomethacin, ketoprofen, fenoprofen ibuprofen, diclofenac sodium, tolfenamic acid, phenylbutazone, mofebutazone, salicylic acid, acetylsalicylic acid, phenacetin, paracetamol, sulfinpyrazone and probenecid by means of an adjustable, rapid accurate and specific method is described. Plasma samples of 0.2 ml were deproteinised and the drugs extracted simultaneously with pure acetonitrile. Aliquots of 25 mul of this primary extract were directly injected on the column. As elution solvent for drug screening was basically used 55% methanol in 50 mM phosphate buffer at pH 4.0. Optimal separation of some drugs or reasonable elution times for others were obtained by varying the methanol concentration of the elution solvent or possibly its pH. The method used for individual drug determinations is very applicable for therapeutic monitoring purposes as well as for use in pharmacokinetic investigations. As an example, the practical detection limit for naproxen in plasma was about 0.2 microgram ml-1. By concentrating the extract this could be lowered to about 0.04 microgram ml-1. The method was applied in a study of the pharmacokinetics of naproxen in a person, who ingested a single oral dose of 2.5 mg kg-1. Pronounced two-compartment kinetics were found. Vc was 0.038 1 kg-1, Vdss 0.138 1 kg-1, t 1/2 (beta) 21.3 hrs, t 1/2 (alpha) 0.99 hr and t 1/2 (ka) 0.67 hr.

摘要

描述了一种通过可调节、快速、准确且特异的方法,利用高效液相色谱法测定萘普生、吲哚美辛、酮洛芬、非诺洛芬、布洛芬、双氯芬酸钠、托芬那酸、保泰松、莫比布宗、水杨酸、乙酰水杨酸、非那西丁、对乙酰氨基酚、磺吡酮和丙磺舒的方法。取0.2 ml血浆样品进行脱蛋白处理,并用纯乙腈同时提取药物。取25 μl该初提取物直接进样到色谱柱上。作为药物筛选的洗脱溶剂,基本采用pH 4.0的50 mM磷酸盐缓冲液中55%的甲醇。通过改变洗脱溶剂的甲醇浓度或其pH值,可实现某些药物的最佳分离或其他药物的合理洗脱时间。用于单个药物测定的该方法非常适用于治疗监测目的以及药代动力学研究。例如,血浆中萘普生的实际检测限约为0.2 μg/ml-1。通过浓缩提取物,可将其降至约0.04 μg/ml-1。该方法应用于一项萘普生药代动力学研究,研究对象为口服单剂量2.5 mg/kg-1的个体。发现有明显的二室动力学。Vc为0.038 l/kg-1,Vdss为0.138 l/kg-1,t 1/2(β)为21.3小时,t 1/2(α)为0.99小时,t 1/2(ka)为0.67小时。

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