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
相关论文
共 40 条
[1]   Preparation, characterization, and potential application of chitosan, chitosan derivatives, and chitosan metal nanoparticles in pharmaceutical drug delivery [J].
Ahmed, Tarek A. ;
Aljaeid, Bader M. .
DRUG DESIGN DEVELOPMENT AND THERAPY, 2016, 10 :483-507
[2]   Bionanocomposites based on alginate-zein/layered double hydroxide materials as drug delivery systems [J].
Alcantara, A. C. S. ;
Aranda, P. ;
Darder, M. ;
Ruiz-Hitzky, E. .
JOURNAL OF MATERIALS CHEMISTRY, 2010, 20 (42) :9495-9504
[3]   Alginate coated chitosan core shell nanoparticles for oral delivery of enoxaparin: In vitro and in vivo assessment [J].
Bagre, Archana Pataskar ;
Jain, Keerti ;
Jain, Narendra K. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2013, 456 (01) :31-40
[4]   Oral delivery of proteins by biodegradable nanoparticles [J].
Bakhru, Sasha H. ;
Furtado, Stacia ;
Morello, A. Peter ;
Mathiowitz, Edith .
ADVANCED DRUG DELIVERY REVIEWS, 2013, 65 (06) :811-821
[5]  
Dalmo R., 2016, ADJUVANTS DELIVERY M
[6]   Functional nanoparticles exploit the bile acid pathway to overcome multiple barriers of the intestinal epithelium for oral insulin delivery [J].
Fan, Weiwei ;
Xia, Dengning ;
Zhu, Quanlei ;
Li, Xiuying ;
He, Shufang ;
Zhu, Chunliu ;
Guo, Shiyan ;
Hovgaard, Lars ;
Yang, Mingshi ;
Gan, Yong .
BIOMATERIALS, 2018, 151 :13-23
[7]  
Fujita Y, 2017, MICRO NANO TECHNOL, P149
[8]   The role of mucus as an invisible cloak to transepithelial drug delivery by nanoparticles [J].
Garcia-Diaz, Maria ;
Birch, Ditlev ;
Wan, Feng ;
Nielsen, Hanne Morck .
ADVANCED DRUG DELIVERY REVIEWS, 2018, 124 :107-124
[9]   Pre-coating layered double hydroxide nanoparticles with albumin to improve colloidal stability and cellular uptake [J].
Gu, Zi ;
Zuo, Huali ;
Li, Li ;
Wu, Aihua ;
Xu, Zhi Ping .
JOURNAL OF MATERIALS CHEMISTRY B, 2015, 3 (16) :3331-3339
[10]   Scalable fabrication of size-controlled chitosan nanoparticles for oral delivery of insulin [J].
He, Zhiyu ;
Santos, Jose Luis ;
Tian, Houkuan ;
Huang, Huahua ;
Hu, Yizong ;
Liu, Lixin ;
Leong, Kam W. ;
Chen, Yongming ;
Mao, Hai-Quan .
BIOMATERIALS, 2017, 130 :28-41