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柠檬酸盐对α-1-蛋白酶抑制剂的稳定作用。

Stabilization of alpha-1-proteinase inhibitor by citrate.

作者信息

Coan M H, Mitra G

出版信息

Vox Sang. 1984;46(3):142-8. doi: 10.1111/j.1423-0410.1984.tb00066.x.

Abstract

alpha 1-Proteinase inhibitor has potential therapeutic value in patients with chronic deficiency (which can lead to emphysema) and in acute adult respiratory distress syndrome. Pasteurization (10 h, 60 degrees C) can reduce the risk of hepatitis B; and addition of stabilizers to the inhibitor helps prevent the loss of biological activity which occurs during pasteurization. Denaturation during heating at several temperatures was studied, using high pressure liquid chromatography, differential scanning calorimetry, and elastase inhibitory capacity to measure the extent of denaturation. The presence of 0.5 M citrate increases the Arrhenius-type activation energy 3-fold, and the enthalpy of denaturation is increased by 3.5 kJ/mol (15 kcal/mol). The onset temperature of the endotherm is increased by more than 10 degrees C. The inhibitor is further stabilized by sucrose (O.5 g/ml). In the presence of both citrate and sucrose, samples of alpha 1-proteinase inhibitor retained almost full biological activity following pasteurization for 10 h at 60 degrees C; the heating conditions used to destroy hepatitis B infectivity of other plasma derivatives.

摘要

α1-蛋白酶抑制剂对慢性缺乏症(可导致肺气肿)患者及急性成人呼吸窘迫综合征患者具有潜在治疗价值。巴氏消毒法(10小时,60摄氏度)可降低感染乙肝的风险;向抑制剂中添加稳定剂有助于防止在巴氏消毒过程中发生的生物活性丧失。利用高压液相色谱法、差示扫描量热法以及弹性蛋白酶抑制能力来测定变性程度,研究了在几个温度下加热时的变性情况。0.5M柠檬酸盐的存在使阿累尼乌斯型活化能增加了3倍,变性焓增加了3.5kJ/mol(15kcal/mol)。吸热峰的起始温度升高了10摄氏度以上。蔗糖(0.5g/ml)可进一步稳定该抑制剂。在同时存在柠檬酸盐和蔗糖的情况下,α1-蛋白酶抑制剂样品在60摄氏度下经过10小时巴氏消毒后仍保留几乎全部的生物活性;该加热条件用于破坏其他血浆衍生物的乙肝传染性。

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