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干粉吸入器设计、配方及性能的演变

Evolution of dry powder inhaler design, formulation, and performance.

作者信息

Newman S P, Busse W W

机构信息

Pharmaceutical Profiles Limited, Ruddington, Nottingham, UK.

出版信息

Respir Med. 2002 May;96(5):293-304. doi: 10.1053/rmed.2001.1276.

Abstract

Many companies are now prioritizing the development of dry powder inhalers (DPIs) above pressurized formulations of asthma drugs. A well-designed DPI and an appropriate powder formulation can optimize the effectiveness of inhaled drug therapy. A DPI must be able to deliver medications effectively for most patients, and an ideal inhaler would provide a dose that does not vary with inspiratory flow rate. Recent regulatory guidelines, among which the U.S. FDA draft guidance is the most stringent, demand consistent dose delivery from an inhaler throughout its life and consistency of doses from one inhaler to another. However, the properties of free micronized powders often interfere with drug handling and with drug delivery reducing dose consistency. Recent advances in formulation technology can increase lung dose and reduce its variability. While a perfect DPI may never exist, both device and formulation technology are evolving to rectify perceived deficiencies in earlier systems.

摘要

如今,许多公司都将干粉吸入器(DPI)的研发置于哮喘药物的加压制剂之上。设计良好的DPI和合适的粉末制剂能够优化吸入药物治疗的效果。DPI必须能够为大多数患者有效递送药物,而理想的吸入器应提供不随吸气流量速率变化的剂量。近期的监管指南中,美国食品药品监督管理局(FDA)的草案指南最为严格,要求吸入器在其整个使用周期内都能持续一致地递送剂量,且不同吸入器之间的剂量也要保持一致。然而,游离微粉化粉末的特性常常会干扰药物处理和药物递送,降低剂量的一致性。制剂技术的最新进展能够增加肺部给药剂量并减少其变异性。虽然完美的DPI可能永远不会出现,但设备和制剂技术都在不断发展,以纠正早期系统中被认为存在的缺陷。

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