State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, China
Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen DK-2100, Denmark
Biomacromolecules. 2019 Apr 8;20(4):1789-1797. doi: 10.1021/acs.biomac.9b00175. Epub 2019 Mar 28.
The fate of intravenously injected nanoparticles (NPs) is significantly affected by nano-protein interaction and corona formation. However, such an interaction between NPs and digestive enzymes occurring in the gastrointestinal tract (GIT) and its impacts on epithelial cell uptake are little known. We synthesized the poly(3-hydroxybutyrate- co-3-hydroxyhexanoate)-based cationic NPs (CNPs) and investigated the CNP-digestive enzyme interaction and its effect on the cellular uptake. The formation of enzyme corona was confirmed by size/zeta potential analysis, morphology, sodium dodecyl sulfate polyacrylamide gel electrophoresis, and enzyme quantification. The cellular uptake of CNPs by Caco-2 cells was significantly reduced upon the formation of enzyme corona. Our findings demonstrate the digestive enzyme corona formation and its inhibited effect on the epithelial cell uptake of CNPs for the first time. Understanding the enzyme corona could offer a new insight into the fate of nanomedicines in the GIT, and this understanding would be highly beneficial for guiding future nanomedicine designs.
静脉注射纳米颗粒(NPs)的命运受到纳米蛋白相互作用和冠形成的显著影响。然而,人们对 NPs 与胃肠道(GIT)中存在的消化酶之间的这种相互作用及其对上皮细胞摄取的影响知之甚少。我们合成了基于聚(3-羟基丁酸酯-共-3-羟基己酸酯)的阳离子 NPs(CNPs),并研究了 CNPs-消化酶相互作用及其对细胞摄取的影响。通过粒径/ζ 电位分析、形态学、十二烷基硫酸钠聚丙烯酰胺凝胶电泳和酶定量证实了酶冠的形成。酶冠形成后,Caco-2 细胞对 CNPs 的摄取明显减少。我们的研究结果首次证明了消化酶冠的形成及其对 CNPs 上皮细胞摄取的抑制作用。了解酶冠可以为纳米药物在 GIT 中的命运提供新的见解,这一认识对于指导未来的纳米医学设计将非常有益。