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优化红外显微镜技术,以评估在水性制剂中单个亚可见颗粒内胰岛素分子的二级结构。

Optimization of Infrared Microscopy to Assess Secondary Structure of Insulin Molecules Within Individual Subvisible Particles in Aqueous Formulations.

机构信息

Department of Pharmacy, University of Copenhagen, Copenhagen, Denmark; Novo Nordisk A/S, Måløv, Denmark.

Novo Nordisk A/S, Måløv, Denmark.

出版信息

J Pharm Sci. 2019 Mar;108(3):1117-1129. doi: 10.1016/j.xphs.2018.10.028. Epub 2018 Oct 26.

Abstract

The analysis of subvisible particles is currently challenging but pivotal to the understanding and control of the quality of protein therapeutics. While a range of characterization methods is available for subvisible particles, information on the protein conformation in a particle-considered a possible parameter in eliciting unwanted immunogenicity of protein therapeutics-is especially challenging in the lower micrometer range using existing analytical technologies. Using 6 different protein particle populations, we show that transmission Fourier transform infrared (FTIR) microscopy can determine protein secondary structure in single particles down to 10 μm. The analytical setup presented here is able to immobilize protein particles and obtain transmission FTIR spectra on individual protein particles in their intact aqueous environment. Spectra of dried particles, on the other hand, were found to occasionally differ from spectra of particles in aqueous environment. In summary, using the analytical setup described in this study, transmission FTIR microscopy uniquely provides information on single protein particles in particle populations in their aqueous environment without interference from the background protein solution.

摘要

目前,对亚可见颗粒的分析具有一定挑战性,但对于理解和控制蛋白质治疗药物的质量至关重要。虽然有一系列用于亚可见颗粒的特征分析方法,但在使用现有分析技术的情况下,对于粒径处于较低微米范围内的颗粒中的蛋白质构象信息(被认为是引发蛋白质治疗药物产生非预期免疫原性的一个可能参数)特别具有挑战性。利用 6 种不同的蛋白质颗粒群体,我们证明了传输傅里叶变换红外(FTIR)显微镜可以确定单个颗粒中的蛋白质二级结构,粒径低至 10μm。本文介绍的分析设置能够将蛋白质颗粒固定,并在其完整的水相环境中获得单个蛋白质颗粒的传输 FTIR 光谱。另一方面,干燥颗粒的光谱偶尔会与水相环境中颗粒的光谱有所不同。总之,使用本研究中描述的分析设置,传输 FTIR 显微镜独特地提供了颗粒群体中单颗粒的信息,而不会受到背景蛋白质溶液的干扰。

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