The Role of Phase Separation and Local Mobility in the Stabilization of a Lyophilized IgG2 Formulation

IF 3.4 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Ashley Lay-Fortenbery, Ryan E. Holcomb, Charles S. Henry, Mark Cornell Manning, Eric J. Munson
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Abstract

The utility of employing solid-state NMR (SSNMR) to assess parameters governing the stability of a lyophilized IgG2 protein was the focus of the present work. Specifically, the interaction between the sugar stabilizer (sucrose) and protein component was measured using SSNMR and compared to physical and chemical stability data obtained from thermally stressed samples. 1H T1 and 1H T1⍴ relaxation times were measured by SSMNR for 5 different formulation conditions, and the resultant values were used to examine local mobility and phase separation, respectively. From the SSNMR measurements, it was found local mobility decreased as the sucrose to protein weight ratio increased. The decrease in local mobility corresponded to an increase in storage stability (both chemical and physical) of the lyophilized solids up to a critical weight ratio of sucrose to protein. Additionally, 1H T1⍴ measurements obtained on formulations having higher protein to sucrose weight ratios indicated phase separation of the protein and sucrose phases was occurring, at least on a small scale. Along with an increase in local mobility, phase separation in these specific formulations is thought to have played a role in their decreased storage stability in the solid state.

Graphical Abstract

Abstract Image

相分离和局部流动性在稳定冻干 IgG2 制剂中的作用
本研究的重点是利用固态核磁共振(SSNMR)评估影响冻干 IgG2 蛋白稳定性的参数。具体来说,使用 SSNMR 测量了糖稳定剂(蔗糖)和蛋白质成分之间的相互作用,并与热应力样品获得的物理和化学稳定性数据进行了比较。通过 SSMNR 测量了 5 种不同配方条件下的 1H T1 和 1H T1⍴ 弛豫时间,所得数值分别用于检测局部流动性和相分离。SSNMNR 测量结果表明,随着蔗糖与蛋白质重量比的增加,局部流动性降低。在蔗糖与蛋白质的重量比达到临界值时,局部迁移率的降低与冻干固体储存稳定性(化学和物理)的提高相对应。此外,对蛋白质与蔗糖重量比更高的配方进行的 1H T1⍴ 测量表明,至少在小范围内,蛋白质相和蔗糖相正在发生相分离。随着局部流动性的增加,这些特定配方中的相分离被认为是导致其固态储存稳定性降低的原因之一。
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来源期刊
AAPS PharmSciTech
AAPS PharmSciTech 医学-药学
CiteScore
6.80
自引率
3.00%
发文量
264
审稿时长
2.4 months
期刊介绍: AAPS PharmSciTech is a peer-reviewed, online-only journal committed to serving those pharmaceutical scientists and engineers interested in the research, development, and evaluation of pharmaceutical dosage forms and delivery systems, including drugs derived from biotechnology and the manufacturing science pertaining to the commercialization of such dosage forms. Because of its electronic nature, AAPS PharmSciTech aspires to utilize evolving electronic technology to enable faster and diverse mechanisms of information delivery to its readership. Submission of uninvited expert reviews and research articles are welcomed.
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