Size exclusion chromatography as green support for forced degradation study of adalimumab.

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY Acta Pharmaceutica Pub Date : 2023-12-26 Print Date: 2023-12-01 DOI:10.2478/acph-2023-0044
Jelena Kovačić, Daniela Amidžić Klarić, Nikša Turk, Ana Mornar
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Abstract

Size exclusion chromatography (SEC) has become a powerful tool for analysing size variants of biologic drugs in their native form. Modern SEC can be defined by the use of chromatographic columns packed with sub-3 µm particles, allowing an increase in method throughput compared to that of conventional SEC. We performed the forced degradation study of adalimumab, the first genetically engineered fully humanised immunoglobulin G1 monoclonal antibody, and evaluated tha possibilities of an advanced SEC column packed with sub-3 µm particles for elucidation of the degradation pathway. Our results revealed the main adalimumab degradation products to be antibody fragments. Acidic and basic conditions had the most intensive effect on the degradation of the adalimumab while the drug exhibits relative stability under thermal and photolytic stress conditions. The AGREE and AGREEprep calculators were used for the evaluation of the environmental performance of the forced degradation procedure. The results of the green score evaluation are presented as round pictograms with a circle in the centre that shows the overall score of 0.81 and 0.61, respectively. Both pictograms are highlighted in green, indicating the eco-friendly conditions.

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尺寸排阻色谱法作为阿达木单抗强制降解研究的绿色支持。
尺寸排阻色谱 (SEC) 已成为分析原生生物药物尺寸变体的强大工具。现代 SEC 可以通过使用填有 3 微米以下颗粒的色谱柱来定义,与传统 SEC 相比,它可以提高方法的通量。我们对阿达木单抗(首个基因工程全人源化免疫球蛋白 G1 单克隆抗体)进行了强制降解研究,并评估了采用 3 微米以下颗粒填料的先进 SEC 色谱柱阐明降解途径的可能性。我们的研究结果表明,阿达木单抗的主要降解产物是抗体片段。酸性和碱性条件对阿达木单抗的降解影响最大,而该药物在热和光解压力条件下表现出相对的稳定性。AGREE 和 AGREEprep 计算器用于评估强制降解程序的环境性能。绿色得分的评估结果以圆形象形图的形式显示,中间的圆圈分别表示总得分 0.81 和 0.61。两个象形图均以绿色突出显示,表明生态友好的条件。
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来源期刊
Acta Pharmaceutica
Acta Pharmaceutica PHARMACOLOGY & PHARMACY-
CiteScore
5.20
自引率
3.60%
发文量
20
审稿时长
>12 weeks
期刊介绍: AP is an international, multidisciplinary journal devoted to pharmaceutical and allied sciences and contains articles predominantly on core biomedical and health subjects. The aim of AP is to increase the impact of pharmaceutical research in academia, industry and laboratories. With strong emphasis on quality and originality, AP publishes reports from the discovery of a drug up to clinical practice. Topics covered are: analytics, biochemistry, biopharmaceutics, biotechnology, cell biology, cell cultures, clinical pharmacy, drug design, drug delivery, drug disposition, drug stability, gene technology, medicine (including diagnostics and therapy), medicinal chemistry, metabolism, molecular modeling, pharmacology (clinical and animal), peptide and protein chemistry, pharmacognosy, pharmacoepidemiology, pharmacoeconomics, pharmacodynamics and pharmacokinetics, protein design, radiopharmaceuticals, and toxicology.
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