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通过高效液相色谱法直接测定药物和血清中的四种氟喹诺酮类药物,即依诺沙星、诺氟沙星、氧氟沙星和环丙沙星。

Direct determination of four fluoroquinolones, enoxacin, norfloxacin, ofloxacin, and ciprofloxacin, in pharmaceuticals and blood serum by HPLC.

作者信息

Samanidou V F, Demetriou C E, Papadoyannis I N

机构信息

Laboratory of Analytical Chemistry, Department of Chemistry, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.

出版信息

Anal Bioanal Chem. 2003 Mar;375(5):623-9. doi: 10.1007/s00216-003-1749-9. Epub 2003 Feb 13.

Abstract

A rapid, accurate and sensitive method has been developed for the quantitative determination of four fluoroquinolone antimicrobial agents, enoxacin, norfloxacin, ofloxacin and ciprofloxacin, with high in-vitro activity against a wide range of Gram-negative and Gram-positive organisms.A Kromasil 100 C(8) 250 mm x 4 mm, 5 microm analytical column was used with an eluting system consisting of a mixture of CH(3)CN-CH(3)OH-citric acid 0.4 mol L(-1) (7:15:78 %, v/v). Detection was performed with a variable wavelength UV-visible detector at 275 nm resulting in limits of detection: 0.02 ng per 20 microL injection for enoxacin and 0.01 ng for ofloxacin, norfloxacin and ciprofloxacin. Hydrochlorothiazide (HCT) was used as internal standard at a concentration of 2 ng microL(-1). A rectilinear relationship was observed up to 2 ng microL(-1) for enoxacin, 12 ng microL(-1) for ofloxacin, 3 ng microL(-1) for norfloxacin, and 5 ng microL(-1) for ciprofloxacin. Separation was achieved within 10 min. The statistical evaluation of the method was examined by performing intra-day (n=8) and inter-day precision assays (n=8) and was found to be satisfactory with high accuracy and precision. The method was applied to the direct determination of the four fluoroquinolones in human blood serum. Sample pretreatment involved only protein precipitation with acetonitrile. Recovery of analytes in spiked samples was 97+/-6% over the range 0.1-0.5 ng microL(-1).

摘要

已开发出一种快速、准确且灵敏的方法,用于定量测定四种氟喹诺酮类抗菌剂,即依诺沙星、诺氟沙星、氧氟沙星和环丙沙星,它们对多种革兰氏阴性菌和革兰氏阳性菌具有高体外活性。使用一根Kromasil 100 C(8) 250 mm×4 mm、5微米的分析柱,洗脱系统由CH(3)CN-CH(3)OH-0.4 mol L(-1)柠檬酸(7:15:78%,v/v)的混合物组成。采用可变波长紫外可见检测器在275 nm处进行检测,检测限为:依诺沙星每20微升进样0.02纳克,氧氟沙星、诺氟沙星和环丙沙星为0.01纳克。氢氯噻嗪(HCT)用作内标,浓度为2纳克/微升。依诺沙星在高达2纳克/微升、氧氟沙星在12纳克/微升、诺氟沙星在3纳克/微升、环丙沙星在5纳克/微升范围内观察到线性关系。10分钟内实现分离。通过进行日内(n = 8)和日间精密度测定(n = 8)对该方法进行统计评估,发现其具有高准确性和精密度,令人满意。该方法应用于直接测定人血清中的四种氟喹诺酮类药物。样品预处理仅涉及用乙腈进行蛋白质沉淀。加标样品中分析物的回收率在0.1 - 0.5纳克/微升范围内为97±6%。

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