Costa Mirsiane Pascoal, Abdu João Octavio Carneiro, de Moura Maria Fernanda Cobucci Soares, Silva Allana Carvalho, Zacaron Thiago Medeiros, de Paiva Mayara Rodrigues Brandão, Fabri Rodrigo Luiz, Pittella Frederico, Perrone Ítalo Tuler, Tavares Guilherme Diniz
Postgraduate Program in Pharmaceutical Science, Federal University of Juiz de Fora, Juiz de Fora 36036-900, Minas Gerais, Brazil.
Faculty of Pharmacy, Federal University of Juiz de Fora, Juiz de Fora 36036-900, Minas Gerais, Brazil.
Mol Pharm. 2025 Jul 7;22(7):3542-3562. doi: 10.1021/acs.molpharmaceut.5c00118. Epub 2025 Jun 6.
Lung diseases remain a leading cause of mortality globally, posing a substantial challenge to public health. Conditions such as asthma, tuberculosis, cystic fibrosis, pneumonia, chronic obstructive pulmonary disease (COPD), and lung cancer are highly prevalent and of increasing concern due to their rising incidence in recent years. The recent global outbreak of coronavirus disease 2019 (COVID-19) has further highlighted the urgent need for more effective therapeutic approaches to combat pulmonary diseases. In this context, growing interest in nanotechnology for pulmonary drug delivery has emerged, driven by its potential to enable localized treatment, reduce dosages, provide controlled release, enhance drug solubility, and improve bioavailability. Among the various nanomaterials explored, poly(lactic--glycolic acid) (PLGA)─a copolymer of lactic and glycolic acids─has gained regulatory approval as a safe, biodegradable, and biocompatible carrier, with an extended-release profile, making it an ideal candidate for the development of nanostructured drug delivery systems. Multiple methodologies are available for synthesizing PLGA nanoparticles tailored to pulmonary administration, supported by a wide array of devices designed to cater to individual patient needs. This review seeks to evaluate the advantages of PLGA-based nanoparticles for pulmonary drug delivery, with a focus on their potential to enhance inhalation therapy formulations.
肺部疾病仍然是全球主要的死亡原因,对公共卫生构成重大挑战。哮喘、肺结核、囊性纤维化、肺炎、慢性阻塞性肺疾病(COPD)和肺癌等病症非常普遍,且由于近年来发病率不断上升而日益受到关注。2019年冠状病毒病(COVID-19)近期在全球爆发,进一步凸显了对抗肺部疾病更有效治疗方法的迫切需求。在此背景下,受纳米技术在实现局部治疗、减少剂量、提供控释、提高药物溶解度和改善生物利用度方面的潜力驱动,人们对用于肺部给药的纳米技术的兴趣日益浓厚。在探索的各种纳米材料中,聚乳酸-乙醇酸共聚物(PLGA)——乳酸和乙醇酸的共聚物——已获得监管批准,作为一种安全、可生物降解且生物相容的载体,具有缓释特性,使其成为开发纳米结构药物递送系统的理想候选材料。有多种方法可用于合成适合肺部给药的PLGA纳米颗粒,并有一系列旨在满足个体患者需求的设备作为支撑。本综述旨在评估基于PLGA的纳米颗粒在肺部给药方面的优势,重点关注其增强吸入治疗制剂的潜力。