Tang Benjamin C, Dawson Michelle, Lai Samuel K, Wang Ying-Ying, Suk Jung Soo, Yang Ming, Zeitlin Pamela, Boyle Michael P, Fu Jie, Hanes Justin
Department of Chemical and Biomolecular Engineering, The Johns Hopkins University, Baltimore, MD 21218, USA.
Proc Natl Acad Sci U S A. 2009 Nov 17;106(46):19268-73. doi: 10.1073/pnas.0905998106. Epub 2009 Nov 9.
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.
保护性黏液涂层通常会捕获并迅速清除眼睛、胃肠道、气道、鼻咽部和女性生殖道中的外来颗粒,从而极大地限制了在黏膜表面进行可控药物递送的机会。尚未有由可生物降解聚合物组成的合成药物递送系统能够以显著速率穿透高黏弹性的人体黏液,例如非排卵期宫颈阴道黏液。我们制备了由聚(癸二酸)和聚(乙二醇)(PSA-PEG)的可生物降解二嵌段共聚物组成的纳米颗粒,这两种聚合物都常用于人体。在新鲜未稀释的人体宫颈阴道黏液(CVM)中,其在低剪切力下的本体黏度比水高约1800倍,PSA-PEG纳米颗粒的扩散平均速度仅比在纯水中的相同颗粒低12倍。相比之下,由PSA或聚(乳酸-乙醇酸共聚物)(PLGA)组成的尺寸相似的可生物降解纳米颗粒在CVM中的扩散速度比在水中至少慢3300倍。PSA-PEG颗粒还能迅速穿透囊性纤维化患者肺部咳出的痰液,囊性纤维化是一种以高黏弹性黏液分泌为特征的疾病。在制剂过程中,PEG有效地分配到颗粒表面,使得纳米颗粒能够在黏液中快速运输。能够克服人体黏液屏障并实现持续药物释放的可生物降解聚合物纳米颗粒为改善黏膜表面的药物和基因递送提供了重要机遇。