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Determination of pyridoxal isonicotinoyl hydrazone, cefoperozone, and ampicillin in biological fluids by high-performance liquid chromatography.

机译:高效液相色谱法测定生物体液中的吡ido醛异烟酰yl,头孢哌酮和氨苄青霉素。

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摘要

Analytical methods for the quantitation measurement of the concentrations of pyridoxal isonicotinoyl hydrazone (PIH), cefoperazone (CPZ), and ampicillin (AMP) were developed with the goal of implementation in pharmacokinetic studies. The assays were accomplished by reversed phase high performance liquid chromatography (HPLC), after suitable sample preparation. All the methods achieved separation using isocratic conditions, with absorbance detection as the means of quantitation. The quality of the chromatography was monitored through the determination of chromatographic figures of merit.;The antibiotic assays, AMP and CPZ, included matched internal standards to simplify sample preparation and quantitation. The recovery of drugs and internal standards from serum, and linearity of the methods were determined. The chromatographic retentions of other antibiotics were ascertained, and did not coelute with either analyte or internal standard.;PIH is an orphan drug proposed for the chelation treatment of iron overload conditions arising from transfusion therapy for an underlying anemia. Chromatography of standard solutions of PIH required an end-capped reversed phase column and eluent modifiers to produce well resolved peaks with precision. Recovery studies from biological fluids indicated alternative modes of drug disposition from those usually associated with drug metabolism. Evidence was obtained that indicated reaction of PIH with protein and non-protein fractions of serum. It was felt that a suitable internal standard could not be established at this time, quantitation was achieved through comparison to an external standard.;PIH was demonstrated to be present in the urine of subjects taking PIH orally, a pathway for elimination that was previously undescribed.
机译:为了实现在药代动力学研究中的目标,开发了定量测定吡ido醛异烟酰yl(PIH),头孢哌酮(CPZ)和氨苄青霉素(AMP)浓度的分析方法。在合适的样品制备后,通过反相高效液相色谱法(HPLC)完成测定。所有方法都使用等度条件实现了分离,并以吸光度检测作为定量手段。色谱质量通过测定色谱图的品质指数进行监控。抗生素测定AMP和CPZ包括匹配的内标,以简化样品制备和定量。确定了从血清中回收药物和内标物的方法的线性。确定了其他抗生素的色谱保留,并且没有与分析物或内标共洗脱。PIH是一种孤儿药物,建议用于螯合治疗因潜在贫血的输血疗法引起的铁超负荷情况。 PIH标准溶液的色谱分析需要使用封端的反相色谱柱和洗脱液改性剂,以产生精确分离的峰。从生物体液中回收的研究表明,与通常与药物代谢有关的药物处置方式不同。获得的证据表明PIH与血清蛋白和非蛋白部分反应。认为此时无法建立合适的内标,通过与外标的比较实现了定量。口服PIH的受试者尿液中存在PIH,这是以前未曾描述的消除途径。

著录项

  • 作者

    Glass, Leon Robert.;

  • 作者单位

    Cleveland State University.;

  • 授予单位 Cleveland State University.;
  • 学科 Health Sciences Pharmacology.
  • 学位 Ph.D.
  • 年度 1990
  • 页码 254 p.
  • 总页数 254
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:50:28

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