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用于迷迭香酸眼部给药的壳聚糖基纳米颗粒——体外试验

Chitosan-based nanoparticles for rosmarinic acid ocular delivery--In vitro tests.

作者信息

da Silva Sara Baptista, Ferreira Domingos, Pintado Manuela, Sarmento Bruno

机构信息

Laboratory of Pharmaceutical Technology, Department of Drug Sciences, Faculty of Pharmacy, University of Porto, Rua Jorge Viterbo Ferreira 228, 4050-313 Porto, Portugal; CBQF-Centro de Biotecnologia e Química Fina, Laboratório Associado, Escola Superior de Biotecnologia, Universidade Católica Portuguesa/Porto, Rua Arquiteto Lobão Vital, Apartado 2511, 4202-401 Porto, Portugal.

Laboratory of Pharmaceutical Technology, Department of Drug Sciences, Faculty of Pharmacy, University of Porto, Rua Jorge Viterbo Ferreira 228, 4050-313 Porto, Portugal.

出版信息

Int J Biol Macromol. 2016 Mar;84:112-20. doi: 10.1016/j.ijbiomac.2015.11.070. Epub 2015 Nov 29.

Abstract

In this study, chitosan nanoparticles were used to encapsulate antioxidant rosmarinic acid, Salvia officinalis (sage) and Satureja montana (savory) extracts as rosmarinic acid natural vehicles. The nanoparticles were prepared by ionic gelation using chitosan and sodium tripolyphosphate (TPP) in a mass ratio of 7:1, at pH 5.8. Particle size distribution analysis and transmission electron microscopy (TEM) confirmed the size ranging from 200 to 300 nm, while surface charge of nanoparticles ranged from 20 to 30 mV. Nanoparticles demonstrate to be safe without relevant cytotoxicity against retina pigment epithelium (ARPE-19) and human cornea cell line (HCE-T). The permeability study in HCE monolayer cell line showed an apparent permeability coefficient Papp of 3.41±0.99×10(-5) and 3.24±0.79×10(-5) cm/s for rosmarinic acid loaded chitosan nanoparticles and free in solution, respectively. In ARPE-19 monolayer cell line the Papp was 3.39±0.18×10(-5) and 3.60±0.05×10(-5) cm/s for rosmarinic acid loaded chitosan nanoparticles and free in solution, respectively. Considering the mucin interaction method, nanoparticles indicate mucoadhesive proprieties suggesting an increased retention time over the ocular mucosa after instillation. These nanoparticles may be promising drug delivery systems for ocular application in oxidative eye conditions.

摘要

在本研究中,壳聚糖纳米颗粒被用作抗氧化剂迷迭香酸、鼠尾草提取物和山地鼠尾草提取物的载体,作为迷迭香酸的天然运载工具。纳米颗粒通过离子凝胶法制备,使用壳聚糖和三聚磷酸钠(TPP),质量比为7:1,pH值为5.8。粒度分布分析和透射电子显微镜(TEM)证实颗粒大小在200至300纳米之间,而纳米颗粒的表面电荷在20至30毫伏之间。纳米颗粒被证明是安全的,对视网膜色素上皮细胞(ARPE - 19)和人角膜细胞系(HCE - T)没有明显的细胞毒性。在HCE单层细胞系中的渗透性研究表明,负载迷迭香酸的壳聚糖纳米颗粒和溶液中游离的迷迭香酸的表观渗透系数Papp分别为3.41±0.99×10(-5)和3.24±0.79×10(-5)厘米/秒。在ARPE - 19单层细胞系中,负载迷迭香酸的壳聚糖纳米颗粒和溶液中游离的迷迭香酸的Papp分别为3.39±0.18×10(-5)和3.60±0.05×10(-5)厘米/秒。考虑到粘蛋白相互作用方法,纳米颗粒显示出粘膜粘附特性,表明滴注后在眼粘膜上的保留时间增加。这些纳米颗粒可能是用于眼部氧化疾病应用的有前途的药物递送系统。

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