Faculty of Pharmacy, Osaka Medical and Pharmaceutical University, Takatsuki, Osaka, Japan.
School of Pharmaceutical Sciences, Wakayama Medical University, Wakayama, Japan.
Expert Opin Drug Deliv. 2024 Jun;21(6):945-963. doi: 10.1080/17425247.2024.2376702. Epub 2024 Jul 8.
INTRODUCTION: Dry powder inhaler (DPI) formulations are gaining attention as universal formulations with applications in a diverse range of drug formulations. The practical application of DPIs to pulmonary drugs requires enhancing their delivery efficiency to the target sites for various treatment modalities. Previous reviews have not explored the relation between particle morphology and delivery to different pulmonary regions. This review introduces new approaches to improve targeted DPI delivery using novel particle design such as supraparticles and metal-organic frameworks based on cyclodextrin. AREAS COVERED: This review focuses on the design of DPI formulations using polysaccharides, promising excipients not yet approved by regulatory agencies. These excipients can be used to design various particle morphologies by controlling their physicochemical properties and manufacturing methods. EXPERT OPINION: Challenges associated with DPI formulations include poor access to the lungs and low delivery efficiency to target sites in the lung. The restricted applicability of typical excipients contributes to their limited use. However, new formulations based on polysaccharides are expected to establish a technological foundation for the development of DPIs capable of delivering modalities specific to different lung target sites, thereby enhancing drug delivery.
简介:干粉吸入器(DPI)制剂作为通用制剂越来越受到关注,可应用于多种药物制剂。将 DPIs 实际应用于肺部药物需要提高其向各种治疗方式的目标部位的输送效率。以前的综述没有探讨颗粒形态与向不同肺部区域输送之间的关系。本综述介绍了使用基于环糊精的超粒子和金属有机框架等新型粒子设计来改善靶向 DPI 输送的新方法。 涵盖领域:本综述重点介绍了使用多糖设计 DPI 制剂的方法,多糖是一种有前途的赋形剂,但尚未获得监管机构的批准。通过控制这些赋形剂的物理化学性质和制造方法,可以设计出各种颗粒形态。 专家意见:DPI 制剂面临的挑战包括肺部难以进入和向肺部目标部位输送效率低。典型赋形剂的应用受限导致其使用受限。然而,基于多糖的新配方有望为开发能够针对不同肺部目标部位输送特定模式的 DPIs 奠定技术基础,从而增强药物输送。
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