水活度作为冻干制剂中抗体储存稳定性的指标。

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Maximilian Zäh, Christoph Brandenbusch, Sebastian Groël, Gerhard Winter, Gabriele Sadowski
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引用次数: 0

摘要

冻干法仍然是保存单克隆抗体等敏感生物药品的关键方法。传统上,稳定机制被解释为玻璃化,它可以最大限度地减少冻干饼中的分子迁移率,而水替代,它可以恢复被水去除破坏的分子相互作用。本研究提出了一种新的设计策略,将水活度和玻璃化转变温度作为预测冻干配方长期稳定性的主要指标。水活度计算为水活度系数和(残余)水含量的乘积,是分子相互作用和冻干物中残余水含量影响的相互指标。通过使用扰动链统计关联流体理论模型计算活度系数并使用Gordon-Taylor方程计算Tg来预测有益的赋形剂组合,该研究确定了有利的赋形剂系统,如蔗糖/异托因混合物,提供了具有广泛稳定性范围的配方窗口。该方法通过稳定性研究进行了验证,证实了在0.025-0.25水活度范围内的配方具有高(长期)稳定性。这项工作通过将水赋形剂相互作用和剩余水分含量整合到预测模型中来推进配方开发,超越了传统的经验方法,并为设计稳定的生物制药配方提供了强有力的途径。这使得在合理的赋形剂浓度和组合下,尽管残余水分较低(因此,玻璃化转变温度较高),仍能实现高/有利的水活度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Water Activity as an Indicator for Antibody Storage Stability in Lyophilized Formulations.

Lyophilization remains a key method for preserving sensitive biopharmaceuticals such as monoclonal antibodies. Traditionally, stabilization mechanisms have been explained by vitrification, which minimizes molecular mobility in the lyophilized cake, and water replacement, which restores molecular interactions disrupted by water removal. This study proposes a novel design strategy that combines water activity and glass-transition temperature as the main indicators to predict long-term stability in lyophilized formulations. The water activity, calculated as the product of water activity coefficient and (residual) water content, serves as a mutual indicator of molecular interactions and influence of residual water content in the lyophilizate. By predicting beneficial excipient combinations through activity coefficient calculations using the perturbed-chain statistical association fluid theory model and calculating Tg using the Gordon-Taylor equation, the study identifies favorable excipient systems, such as sucrose/ectoine mixtures, providing formulation windows that offer broad stability ranges. The approach was validated with stability studies, confirming that formulations within a water activity range of 0.025-0.25 exhibit high (long-term) stability. This work advances formulation development by integrating water-excipient interactions and residual moisture content into a predictive model, moving beyond traditional empirical methods and offering a robust pathway to the design of stable biopharmaceutical formulations. This makes it possible to achieve high/favorable water activities despite low residual moisture (thus, high glass-transition temperatures) with plausible excipient concentrations and combinations.

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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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