Alginate-chitosan coated layered double hydroxide nanocomposites for enhanced oral vaccine delivery

被引:86
作者
Yu, Xinying [1 ]
Wen, Tinggang [1 ]
Cao, Pei [1 ]
Shan, Liang [1 ]
Li, Li [1 ]
机构
[1] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Brisbane, Qld 4072, Australia
关键词
Polymer coating; Layered double hydroxide nanoparticle; Oral delivery; Alginate; Chitosan; DRUG-DELIVERY; NANOPARTICLES; EFFICIENT; NANOMATERIALS; PERMEATION; OVERCOME; REMOVAL; PROTEIN; MUCUS; PB2+;
D O I
10.1016/j.jcis.2019.08.027
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Layered double hydroxide nanoparticles (LDHs) have shown the excellent capability and good adjuvant function as a nanocarrier for protein antigen delivery to enhance the immune response. Furthermore, LDHs have good biocompatibility and low cytotoxicity. However, their oral vaccine delivery efficiency is limited due to acidic/enzyme degradation in the stomach and low bioavailability in the small intestine. To overcome these challenges, alginate-chitosan coated LDHs nanocomposites (ALG-CHT-LDH) have been developed and used as a carrier for oral protein vaccine delivery. The physicochemical properties of ALG-CHT-LDH have been determined by dynamic light scattering (DLS), transmission electron microscopy (TEM), and ultraviolet visible (UV-Vis) spectroscopy. Protein release properties of LDHs with/without polymer coating have been investigated at various pHs. The protein release profile of ALG-CHT-LDH nanocomposites indicated that ALG-CHT coating could partially protect protein release at the acidic condition (pH 1.2). The cellular uptake efficiency of protein delivered by ALG-CHT-LDH for the intestine cells and macrophages were studied. After alginate layer falls from ALG-CHT-LDH nanocomposite, flow cytometry analysis (FACS) data suggest that chitosan-coated LDHs significantly enhance the internalization of proteins at the Caco2 and macrophage cells. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:258 / 265
页数:8
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