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使用高效液相色谱法(HPLC)对生物素酶缺乏症患者尿液中的生物胞素进行定量测定。

Quantitative determination of biocytin in urine of patients with biotinidase deficiency using high-performance liquid chromatography (HPLC).

作者信息

Suormala T M, Baumgartner E R, Bausch J, Holick W, Wick H

机构信息

University Children's Hospital, Basel, Switzerland.

出版信息

Clin Chim Acta. 1988 Oct 31;177(3):253-69. doi: 10.1016/0009-8981(88)90070-8.

Abstract

A specific method for the quantitative determination of biocytin from urine of biotinidase deficient patients is described using HPLC-separation and quantitative determination by an avidin binding method. Partial purification of biocytin from urine was achieved with an anion exchange resin and concentration of the eluate by lyophilization. The recovery of biocytin from urines was 95.3 +/- 5.9 (mean +/- SD). The precision of biocytin estimation in patients urines including the HPLC-sample preparation procedure varied between 5.9% and 10.5% (CV). Biocytin concentrations were measured in urine samples of 5 patients obtained during and/or before biotin therapy. Before treatment biocytin excretion ranged from 6.2-28.8 nmol/mmol creatinine. During therapy biocytin excretion increased to the 1.3 to 4-fold level in 3 out of 4 patients. However, there was no dose-related increase of biocytin excretion when pharmacological doses were administered. Apart from biocytin and biotin, patients excrete additional biotin derivatives. Some of these have been preliminary identified as bisnorbiotin and oxidation products of bisnorbiotin, biocytin and biotin.

摘要

描述了一种使用高效液相色谱分离和抗生物素蛋白结合法定量测定生物素酶缺乏患者尿液中生物胞素的具体方法。通过阴离子交换树脂对尿液中的生物胞素进行部分纯化,并通过冻干浓缩洗脱液。生物胞素从尿液中的回收率为95.3±5.9(平均值±标准差)。包括高效液相色谱样品制备程序在内的患者尿液中生物胞素估计的精密度在5.9%至10.5%(变异系数)之间。在生物素治疗期间和/或之前,对5名患者的尿液样本进行了生物胞素浓度测量。治疗前,生物胞素排泄量为6.2 - 28.8 nmol/mmol肌酐。治疗期间,4名患者中有3名患者的生物胞素排泄量增加到1.3至4倍水平。然而,给予药理剂量时,生物胞素排泄量没有剂量相关的增加。除了生物胞素和生物素外,患者还排泄其他生物素衍生物。其中一些已初步鉴定为双降生物素以及双降生物素、生物胞素和生物素的氧化产物。

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