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固态下蛋白质的化学降解,重点是光化学反应。

Chemical degradation of proteins in the solid state with a focus on photochemical reactions.

机构信息

Department of Pharmaceutical Chemistry, 2095 Constant Avenue, University of Kansas, Lawrence, KS 66047, USA.

Department of Pharmaceutical Chemistry, 2095 Constant Avenue, University of Kansas, Lawrence, KS 66047, USA.

出版信息

Adv Drug Deliv Rev. 2015 Oct 1;93:2-13. doi: 10.1016/j.addr.2014.11.016. Epub 2014 Dec 4.

Abstract

Protein pharmaceuticals comprise an increasing fraction of marketed products but the limited solution stability of proteins requires considerable research effort to prepare stable formulations. An alternative is solid formulation, as proteins in the solid state are thermodynamically less susceptible to degradation. Nevertheless, within the time of storage a large panel of kinetically controlled degradation reactions can occur such as, e.g., hydrolysis reactions, the formation of diketopiperazine, condensation and aggregation reactions. These mechanisms of degradation in protein solids are relatively well covered by the literature. Considerably less is known about oxidative and photochemical reactions of solid proteins. This review will provide an overview over photolytic and non-photolytic degradation reactions, and specially emphasize mechanistic details on how solid structure may affect the interaction of protein solids with light.

摘要

蛋白质类药物在已上市产品中所占的比例越来越大,但蛋白质的有限溶液稳定性需要大量的研究工作来制备稳定的制剂。另一种选择是固体制剂,因为固体状态下的蛋白质在热力学上不易降解。然而,在储存期间,会发生大量动力学控制的降解反应,例如水解反应、二酮哌嗪的形成、缩合和聚集反应。这些蛋白质固体的降解机制在文献中有相对详细的描述。关于固体蛋白质的氧化和光化学反应,人们知之甚少。本文综述了光解和非光解降解反应,并特别强调了固体结构如何影响蛋白质固体与光相互作用的机制细节。

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