Yu Tao, Wang Ying-Ying, Yang Ming, Schneider Craig, Zhong Weixi, Pulicare Sarah, Choi Woo-Jin, Mert Olcay, Fu Jie, Lai Samuel K, Hanes Justin
Center for Nanomedicine, Johns Hopkins University School of Medicine, 400 N. Broadway, Baltimore, MD 21231, USA.
Drug Deliv Transl Res. 2012 Apr;2(2). doi: 10.1007/s13346-011-0048-9.
Mucus secretions coating entry points to the human body that are not covered by skin efficiently trap and clear conventional drug carriers, limiting controlled drug delivery at mucosal surfaces. To overcome this challenge, we recently engineered nanoparticles that readily penetrate a variety of human mucus secretions, which we termed mucus-penetrating particles (MPP). Here, we report a new biodegradable MPP formulation based on diblock copolymers of poly(lactic-glycolic acid) and poly(ethylene glycol) (PLGA-PEG). PLGA-PEG nanoparticles prepared by a solvent diffusion method rapidly diffused through fresh, undiluted human cervicovaginal mucus (CVM) with an average speed only eightfold lower than their theoretical speed in water. In contrast, PLGA nanoparticles were slowed more than 12,000-fold in the same CVM secretions. Based on the measured diffusivities, as much as 75% of the PLGA-PEG nanoparticles are expected to penetrate a 10-μm-thick mucus layer within 30 min, whereas virtually no PLGA nanoparticles are expected to do so over the same duration. These results encourage further development of PLGA-PEG nanoparticles as mucus-penetrating drug carriers for improved drug and gene delivery to mucosal surfaces.
覆盖人体未被皮肤覆盖的入口点的黏液分泌物能够有效地捕获并清除传统药物载体,从而限制了黏膜表面的可控药物递送。为了克服这一挑战,我们最近设计了一种能够轻易穿透多种人体黏液分泌物的纳米颗粒,我们将其称为黏液穿透颗粒(MPP)。在此,我们报告一种基于聚乳酸-乙醇酸共聚物和聚乙二醇(PLGA-PEG)的二嵌段共聚物的新型可生物降解MPP制剂。通过溶剂扩散法制备的PLGA-PEG纳米颗粒能够快速扩散穿过新鲜、未稀释的人宫颈阴道黏液(CVM),其平均速度仅比其在水中的理论速度低八倍。相比之下,PLGA纳米颗粒在相同的CVM分泌物中的速度减慢了超过12000倍。根据测得的扩散系数,预计高达75%的PLGA-PEG纳米颗粒能够在30分钟内穿透10μm厚的黏液层,而在相同时间段内几乎没有PLGA纳米颗粒能够做到这一点。这些结果鼓励进一步开发PLGA-PEG纳米颗粒作为黏液穿透药物载体,以改善药物和基因向黏膜表面的递送。