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加工和制剂因素对片剂中 Catalase 活性的影响。

Effect of processing and formulation factors on Catalase activity in tablets.

机构信息

Research Center Pharmaceutical Engineering GmbH, Inffeldgasse 13, 8010 Graz, Austria.

iMed.UL - Faculdade de Farmácia da Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003 Lisboa, Portugal.

出版信息

Int J Pharm. 2024 Oct 25;664:124626. doi: 10.1016/j.ijpharm.2024.124626. Epub 2024 Aug 28.

Abstract

The manufacturing of tablets containing biologics exposes the biologics to thermal and shear stresses, which are likely to induce structural changes (e.g., aggregation and denaturation), leading to the loss of their activity. Saccharides often act as stabilizers of proteins in formulations, yet their stabilizing ability throughout solid oral dosage processing, such as tableting, has been barely studied. This work aimed to investigate the effects of formulation and process (tableting and spray-drying) variables on catalase tablets containing dextran, mannitol, and trehalose as potential stabilizers. Non-spray-dried and spray-dried formulations were prepared and tableted (100, 200, and 400 MPa). The enzymatic activity, number of aggregates, reflecting protein aggregation and structure modifications were studied. A principal component analysis was performed to reveal underlying correlations. It was found that tableting and spray-drying had a notable negative effect on the activity and number of aggregates formed in catalase formulations. Overall, dextran and mannitol failed to preserve the catalase activity in any unit operation studied. On the other hand, trehalose was found to preserve the activity during spray-drying but not necessarily during tableting. The study demonstrated that formulation and process variables must be considered and optimized together to preserve the characteristics of catalase throughout processing.

摘要

片剂的制造过程会使生物制剂暴露在热和剪切应力下,这可能会导致其结构发生变化(例如聚集和变性),从而导致其活性丧失。糖通常在制剂中作为蛋白质的稳定剂,但它们在片剂等固体制剂加工过程中的稳定能力几乎没有得到研究。本工作旨在研究制剂和工艺(压片和喷雾干燥)变量对含有右旋糖酐、甘露醇和海藻糖作为潜在稳定剂的过氧化氢酶片剂的影响。制备了非喷雾干燥和喷雾干燥的制剂并进行压片(100、200 和 400 MPa)。研究了酶活性、聚集体数量,以反映蛋白质聚集和结构修饰。进行了主成分分析以揭示潜在的相关性。结果发现,压片和喷雾干燥对过氧化氢酶制剂中形成的酶活性和聚集体数量有显著的负面影响。总体而言,右旋糖酐和甘露醇在研究的任何单元操作中都未能保持过氧化氢酶的活性。另一方面,海藻糖在喷雾干燥过程中被发现可以保持活性,但在压片过程中不一定。该研究表明,必须综合考虑和优化制剂和工艺变量,以在整个加工过程中保持过氧化氢酶的特性。

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