Biodegradable polymer nanoparticles that rapidly penetrate the human mucus barrier

被引:337
作者
Tang, Benjamin C. [1 ]
Dawson, Michelle [1 ]
Lai, Samuel K. [1 ,2 ]
Wang, Ying-Ying [3 ]
Suk, Jung Soo [3 ]
Yang, Ming [3 ]
Zeitlin, Pamela [2 ,4 ]
Boyle, Michael P. [5 ]
Fu, Jie [1 ,2 ]
Hanes, Justin [1 ,2 ,3 ,6 ,7 ]
机构
[1] Johns Hopkins Univ, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Inst NanoBioTechnol, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Div Pediat Resp Sci, Baltimore, MD 21287 USA
[5] Johns Hopkins Univ, Sch Med, Div Pulm & Crit Care Med, Johns Hopkins Adult Cyst Fibrosis Program, Baltimore, MD 21205 USA
[6] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21287 USA
[7] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21287 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
cystic fibrosis; drug delivery; gene therapy; mucosa; mucus-penetrating particle; PEGYLATED POLY(ANHYDRIDE) NANOPARTICLES; CONTROLLED DRUG-DELIVERY; PARTICLE TRACKING; CERVICAL-MUCUS; IN-VIVO; TRANSPORT; BIOADHESIVE; DEPOSITION; CLEARANCE; RETENTION;
D O I
10.1073/pnas.0905998106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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(lacticco-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.
引用
收藏
页码:19268 / 19273
页数:6
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