粘液
乙二醇
PLGA公司
纳米颗粒
癸二酸
可生物降解聚合物
药物输送
黏膜黏附
PEG比率
材料科学
乙醇酸
生物物理学
聚合物
化学
化学工程
纳米技术
毒品携带者
高分子化学
乳酸
有机化学
细菌
生物
生态学
遗传学
财务
工程类
经济
作者
Benjamin C. Tang,Michelle Dawson,Samuel K. Lai,Yingying Wang,Jung Soo Suk,Ming Yang,Pamela L. Zeitlin,Michael Boyle,Jie Fu,Justin Hanes
标识
DOI:10.1073/pnas.0905998106
摘要
Protective mucus coatings typically trap and rapidly remove foreign particles from the eyes, gastrointestinal tract, airways, nasopharynx, and female reproductive tract, thereby strongly limiting opportunities for controlled drug delivery at mucosal surfaces. No synthetic drug delivery system composed of biodegradable polymers has been shown to penetrate highly viscoelastic human mucus, such as non-ovulatory cervicovaginal mucus, at a significant rate. We prepared nanoparticles composed of a biodegradable diblock copolymer of poly(sebacic acid) and poly(ethylene glycol) (PSA-PEG), both of which are routinely used in humans. In fresh undiluted human cervicovaginal mucus (CVM), which has a bulk viscosity approximately 1,800-fold higher than water at low shear, PSA-PEG nanoparticles diffused at an average speed only 12-fold lower than the same particles in pure water. In contrast, similarly sized biodegradable nanoparticles composed of PSA or poly(lactic-co-glycolic acid) (PLGA) diffused at least 3,300-fold slower in CVM than in water. PSA-PEG particles also rapidly penetrated sputum expectorated from the lungs of patients with cystic fibrosis, a disease characterized by hyperviscoelastic mucus secretions. Rapid nanoparticle transport in mucus is made possible by the efficient partitioning of PEG to the particle surface during formulation. Biodegradable polymeric nanoparticles capable of overcoming human mucus barriers and providing sustained drug release open significant opportunities for improved drug and gene delivery at mucosal surfaces.
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