导数分光光度法测定人白蛋白制剂中胆红素的可能性

O. I. Lazovskaya, V. Senchuk, V. Leontiev
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引用次数: 0

摘要

在获得高结合能力的人白蛋白药物制剂用于解毒治疗时,控制胆红素残留量是一个紧迫的任务。因此,本研究的目的是研究导数分光光度法测定人白蛋白药物制剂中胆红素的可能性。通过对一阶光谱的记录,结合峰值试验,可以得到516 nm波长处吸收带最小值|dA/dλ|与添加的胆红素浓度的线性关系,并可以确定“Albupharm,输液用溶液,200mg/ml”(JV Pharmland LLC,白俄罗斯共和国)药物制剂中胆红素浓度为8.58±0.23 μM,具有统计学意义。并对从胆红素中提纯白蛋白的工艺效率进行了总结。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ABOUT POSSIBILITY OF APPLYING DERIVATIVE SPECTROPHOTOMETRY FOR BILIRUBIN ASSAY IN HUMAN ALBUMIN MEDICINAL PREPARATIONS
When obtaining human albumin medicinal preparations with a high binding capacity to be used in detoxification therapy, an urgent task is to control residual content of bilirubin. Hence the purpose of this investigation is to study the possibility of applying derivative spectrophotometry for bilirubin assay in human albumin medicinal preparations. Record of the first-order spectra in combination with the spike test made it possible to obtain a linear dependence of the value |dA/dλ| in the minimum of the absorption band at a wavelength of 516 nm from the concentration of added bilirubin and to determine statistically significant bilirubin concentration in the medicinal preparation "Albupharm, solution for infusions, 200mg/ml" (JV Pharmland LLC, Republic of Belarus), which was 8,58 ± 0,23 μM, and also to draw a conclusion about the efficiency of purification technology of albumin from bilirubin.
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