Development of new chitosan/carrageenan nanoparticles for drug delivery applications

被引:213
作者
Grenha, Ana [1 ]
Gomes, Manuela E. [1 ]
Rodrigues, Marcia [1 ]
Santo, Vitor E. [1 ]
Mano, Joao F. [1 ]
Neves, Nuno M. [1 ]
Reis, Rui L. [1 ]
机构
[1] Univ Minho, Dept Polymer Engn,PT Govt Associated Lab, Res Grp 3Bs,IBB Inst Biotechnol & Bioengn, Headquarters European Inst Excellence Tissue Engn, P-4719 Braga, Portugal
关键词
carrageenan; chitosan; controlled release; ionic interaction; nanoparticles; CHITOSAN; CARRAGEENAN; BIOPOLYMERS; ALGINATE; INSULIN;
D O I
10.1002/jbm.a.32466
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
The use of polymeric nanoparticles, especially those composed of natural polymers, has become a very interesting approach in drug delivery., mainly because of the advantages offered by their small dimensions. The aim of this work was to develop a novel formulation of nanoparticles comprised of two natural marine-derived polymers, namely chitosan and carrageenan, and to evaluate their potential for the association and controlled release of macromolecules. Nanoparticles were obtained in a hydrophilic environment, under very mild conditions, avoiding the use of organic solvents or other aggressive technologies for their preparation. The developed nanocarriers presented sizes within 350-650 run and positive zeta potentials of 50-60 mV. Polymeric interactions between nanoparticles' components were evaluated by Fourier transform infrared spectroscopy. Using ovalbumin as model protein, nanoparticles evidenced loading capacity varying from 4% to 17%, and demonstrated excellent capacity to provide a controlled release for up to 3 weeks. Furthermore, nanoparticles have demonstrated to exhibit a noncytotoxic behavior in biological in vitro tests performed using L929 fibroblasts, which is critical regarding the biocompatibility of those carriers. In summary, the developed chitosan-carrageenan nanoparticles have shown promising properties to be used as carriers of therapeutic macromolecules, with potential application not only strictly in drug delivery, but also in broader areas, such as tissue engineering and regenerative medicine. (C) 2009 Wiley Periodicals, Inc. J Biomed Mater Res 92A: 1265-1272, 2010
引用
收藏
页码:1265 / 1272
页数:8
相关论文
共 24 条
[1]
Properties of radiation synthesized PVP-kappa carrageenan hydrogel blends [J].
Abad, LV ;
Relleve, LS ;
Aranilla, CT ;
Dela Rosa, AM .
RADIATION PHYSICS AND CHEMISTRY, 2003, 68 (05) :901-908
[2]
Bixler H. J., 1994, British Food Journal, V96, P12, DOI 10.1108/00070709410060763
[3]
Calvo P, 1997, J APPL POLYM SCI, V63, P125, DOI 10.1002/(SICI)1097-4628(19970103)63:1<125::AID-APP13>3.0.CO
[4]
2-4
[5]
Domish M., 1997, ADV CHITIN SCI, P664
[6]
Enhancement of nasal absorption of insulin using chitosan nanoparticles [J].
Fernández-Urrusuno, R ;
Calvo, P ;
Remuñán-López, C ;
Vila-Jato, JL ;
Alonso, MJ .
PHARMACEUTICAL RESEARCH, 1999, 16 (10) :1576-1581
[7]
Microencapsulated chitosan nanoparticles for lung protein delivery [J].
Grenha, A ;
Seijo, B ;
Remuñán-López, C .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2005, 25 (4-5) :427-437
[8]
Hirano S., 1989, POLYM ENG SCI, V59, P897
[9]
Nanoparticle technology in bone tissue engineering [J].
Kim, Kyobum ;
Fisher, John P. .
JOURNAL OF DRUG TARGETING, 2007, 15 (04) :241-252
[10]
Chitin and chitosan: Functional biopolymers from marine crustaceans [J].
Kurita, Keisuke .
MARINE BIOTECHNOLOGY, 2006, 8 (03) :203-226