Freeze-Drying as a Tool for Preparing Porous Materials: From Proof of Concept to Recent Pharmaceutical Applications.

IF 3.4 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Kawthar K Abla, Mohammed M Mehanna
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引用次数: 0

Abstract

Freeze-drying (FD) is the most extensive drying technique in pharmaceutical and biopharmaceutical industries. It relies on three main steps: freezing, primary, and secondary drying, where the sample is frozen and then dried by ice sublimation. FD possesses several features, mainly its suitability for heat-sensitive materials and its ability to produce dry products with improved physicochemical characteristics. Although FD is a gentle drying process, it can cause numerous stresses that induce chemical and physical instabilities. Herein, the addition of suitable excipients along with optimizing the process parameters is critical in attaining lyophilizates with high-quality attributes. Besides, the freeze-drying method has been explored as a unique route to produce porous materials with different applications. This work aims to dismantle the basics of freeze-drying and its role in developing porous materials, mainly amorphous and co-amorphous solid-dispersions, orodispersible tablets and films, as well as porous dressings and 3D scaffolds for effective wound healing and tissue engineering, respectively. The challenges and limitations of lyophilization have also been addressed.

冷冻干燥作为制备多孔材料的工具:从概念证明到最近的制药应用。
冷冻干燥(FD)是制药和生物制药工业中应用最广泛的干燥技术。它依赖于三个主要步骤:冷冻,一次干燥和二次干燥,其中样品被冷冻,然后通过冰升华干燥。FD具有几个特点,主要是适合热敏性物料,能够生产物理化学特性改善的干燥产品。虽然FD是一种温和的干燥过程,但它会引起许多应力,从而导致化学和物理不稳定。在此,添加合适的赋形剂以及优化工艺参数对于获得具有高质量属性的冻干物至关重要。此外,冻干方法已被探索为一种独特的途径来生产具有不同用途的多孔材料。这项工作旨在拆除冷冻干燥的基础及其在开发多孔材料中的作用,主要是无定形和共无定形固体分散体,或分散片剂和薄膜,以及用于有效伤口愈合和组织工程的多孔敷料和3D支架。冻干的挑战和局限性也已解决。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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