Particulate atomisation design methods for the development and engineering of advanced drug delivery systems: A review

IF 5.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY International Journal of Pharmaceutics Pub Date : 2024-09-27 DOI:10.1016/j.ijpharm.2024.124771
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Abstract

The role and opportunities presented by particulate technologies (due to novel processing methods and advanced materials) have multiplied over the last few decades, leading to promising and ideal properties for drug delivery. For example, the dissolution and bioavailability of poorly soluble drug substances and achieving site- specific drug delivery with a desired release profile are crucial aspects of forming (to some extent) state-of-the-art platforms. Atomisation techniques are intended to achieve efficient control over particle size, improved processing time, improved drug loading efficiency, and the opportunity to encapsulate a broad range of viable yet sensitive therapeutic moieties. Particulate engineering through atomization is accomplished by employing various mechanisms such as air, no air, centrifugal, electrohydrodynamic, acoustic, and supercritical fluid driven processes. These driving forces overcome capillary stresses (e.g., liquid viscosity, surface tension) and transform formulation media (liquid) into fine droplets. More frequently, solvent removal, multiple methods are included to reduce the final size distribution. Nevertheless, a thorough understanding of fluid mechanics, thermodynamics, heat, and mass transfer is imperative to appreciate and predict outputs in real time. More so, in recent years, several advancements have been introduced to improve such processes through complex particle design coupled with quality by-design (QbD) yielding optimal particulate geometry in a predictable manner. Despite these valuable and numerous advancements, atomisation techniques face difficulty scaling up from laboratory scales to manufacturing industry scales. This review details the various atomisation techniques (from design to mechanism) along with examples of drug delivery systems developed. In addition, future perspectives and bottlenecks are provided while highlighting current and selected seminal developments in the field.

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用于开发和设计先进给药系统的微粒雾化设计方法:综述。
过去几十年来,微粒技术(由于新型加工方法和先进材料)所发挥的作用和带来的机遇成倍增加,为给药带来了前景广阔的理想特性。例如,溶解性差的药物物质的溶解性和生物利用度,以及实现特定部位给药和理想的释放曲线,都是形成(在一定程度上)最先进平台的关键方面。雾化技术旨在实现对粒度的有效控制,缩短加工时间,提高药物负载效率,并有机会封装各种可行但敏感的治疗分子。雾化微粒工程是通过采用各种机制(如空气、无空气、离心、电流体动力、声波和超临界流体驱动过程)来实现的。这些驱动力可克服毛细管应力(如液体粘度、表面张力),将配方介质(液体)转化为细小液滴。更常见的方法是去除溶剂,采用多种方法来减少最终的粒度分布。然而,要了解并实时预测输出结果,就必须对流体力学、热力学、传热和传质有透彻的了解。此外,近年来,通过复杂的颗粒设计和质量设计(QbD),以可预测的方式获得最佳颗粒几何形状,从而改进了此类工艺。尽管取得了这些宝贵的进步,但雾化技术仍难以从实验室规模扩展到制造业规模。本综述详细介绍了各种雾化技术(从设计到机制)以及所开发的给药系统实例。此外,还提供了未来展望和瓶颈问题,同时重点介绍了该领域当前和选定的开创性发展。
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来源期刊
CiteScore
10.70
自引率
8.60%
发文量
951
审稿时长
72 days
期刊介绍: The International Journal of Pharmaceutics is the third most cited journal in the "Pharmacy & Pharmacology" category out of 366 journals, being the true home for pharmaceutical scientists concerned with the physical, chemical and biological properties of devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture and evaluation. This includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials. The journal has special sections on pharmaceutical nanotechnology and personalized medicines, and publishes research papers, reviews, commentaries and letters to the editor as well as special issues.
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