Protamine-based nanoparticles as new antigen delivery systems

被引:27
|
作者
Vicente Gonzalez-Aramundiz, Jose [1 ,4 ]
Peleteiro Olmedo, Mercedes [2 ,3 ]
Gonzalez-Fernandez, Africa [2 ,3 ]
Alonso Fernandez, Maria Jose [1 ]
Stefania Csaba, Noemi [1 ]
机构
[1] Univ Santiago de Compostela, Sch Pharm, Dept Pharm & Pharmaceut Technol, Ctr Res Mol Med & Chron Dis CIMUS,Hlth Res Inst S, Santiago De Compostela, Spain
[2] Univ Vigo, Biomed Res Ctr CINBIO, Immunol, Vigo 36310, Pontevedra, Spain
[3] Univ Vigo, Inst Biomed Res Vigo IBIV, Vigo 36310, Pontevedra, Spain
[4] Pontificia Univ Catolica Chile, Fac Quim, Dept Farm, Santiago, Chile
关键词
Nanoparticles; Antigen delivery; Protamine; Vaccine; Hyaluronic acid; Hepatitis B; VACCINE ADJUVANTS; CHITOSAN; HYALURONAN; NANOCARRIERS; PROTEINS; OLIGOSACCHARIDES; MICROPARTICLES; BIOMATERIALS; CARRIERS; ALLERGY;
D O I
10.1016/j.ejpb.2015.09.019
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The use of biodegradable nanoparticles as antigen delivery vehicles is an attractive approach to overcome the problems associated with the use of Alum-based classical adjuvants. Herein we report, the design and development of protamine-based nanoparticles as novel antigen delivery systems, using recombinant hepatitis B surface antigen as a model viral antigen. The nanoparticles, composed of protamine and a polysaccharide (hyaluronic acid or alginate), were obtained using a mild ionic cross-linking technique. The size and surface charge of the nanoparticles could be modulated by adjusting the ratio of the components. Prototypes with optimal physicochemical characteristics and satisfactory colloidal stability were selected for the assessment of their antigen loading capacity, antigen stability during storage and in vitro and in vivo proof-of-concept studies. In vitro studies showed that antigen-loaded nanoparticles induced the secretion of cytokines by macrophages more efficiently than the antigen in solution, thus indicating a potential adjuvant effect of the nanoparticles. Finally, in vivo studies showed the capacity of these systems to trigger efficient immune responses against the hepatitis B antigen following intramuscular administration, suggesting the potential interest of protamine-polysaccharide nanoparticles as antigen delivery systems. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:51 / 59
页数:9
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