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降粘大体积盐辅料可防止蛋白质溶液凝胶化,但不能防止碳水化合物溶液凝胶化。

Viscosity-Reducing Bulky-Salt Excipients Prevent Gelation of Protein, but Not Carbohydrate, Solutions.

作者信息

Kumar Awanish, Klibanov Alexander M

机构信息

Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.

出版信息

Appl Biochem Biotechnol. 2017 Aug;182(4):1491-1496. doi: 10.1007/s12010-017-2413-8. Epub 2017 Jan 23.

DOI:10.1007/s12010-017-2413-8
PMID:28116573
Abstract

The problem of gelation of concentrated protein solutions, which poses challenges for both downstream protein processing and liquid formulations of pharmaceutical proteins, is addressed herein by employing previously discovered viscosity-lowering bulky salts. Procainamide-HCl and the salt of camphor-10-sulfonic acid with L-arginine (CSA-Arg) greatly retard gelation upon heating and subsequent cooling of the model proteins gelatin and casein in water: Whereas in the absence of additives the proteins form aqueous gels within several hours at room temperature, procainamide-HCl for both proteins and also CSA-Arg for casein prevent gel formation for months under the same conditions. The inhibition of gelation by CSA-Arg stems exclusively from the CSA moiety: CSA-Na was as effective as CSA-Arg, while Arg-HCl was marginally or not effective. The tested bulky salts did not inhibit (and indeed accelerated) temperature-induced gel formation in aqueous solutions of all examined carbohydrates-starch, agarose, alginate, gellan gum, and carrageenan.

摘要

浓缩蛋白质溶液的凝胶化问题,这对蛋白质下游加工和药用蛋白质的液体制剂均构成挑战,本文通过使用先前发现的降低粘度的大体积盐来解决。盐酸普鲁卡因酰胺以及樟脑 -10-磺酸与L-精氨酸的盐(CSA-Arg)在加热并随后冷却模型蛋白明胶和酪蛋白的水溶液时,能极大地延缓凝胶化:在没有添加剂的情况下,蛋白质在室温下几小时内就会形成水凝胶,而盐酸普鲁卡因酰胺对两种蛋白质以及CSA-Arg对酪蛋白在相同条件下可防止凝胶形成数月。CSA-Arg对凝胶化的抑制完全源于CSA部分:CSA-Na与CSA-Arg效果相同,而盐酸精氨酸则效果甚微或无效。所测试的大体积盐在所有检测的碳水化合物(淀粉、琼脂糖、藻酸盐、结冷胶和卡拉胶)的水溶液中均不抑制(实际上还加速)温度诱导的凝胶形成。

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