Poly(L-histidine)-chitosan/alginate complex microcapsule as a novel drug delivery agent

被引:21
作者
Chen, Ai-Zheng [1 ,2 ]
Chen, Mei-Ying [1 ]
Wang, Shi-Bin [1 ,2 ]
Huang, Xiao-Nan [1 ]
Liu, Yuan-Gang [1 ,2 ]
Chen, Zong-Xiang [1 ]
机构
[1] Huaqiao Univ, Coll Chem Engn, Xiamen 361021, Peoples R China
[2] Huaqiao Univ, Inst Biomat & Tissue Engn, Xiamen 361021, Peoples R China
基金
中国国家自然科学基金;
关键词
poly(amino acid); controlled release; microcapsules; chitosan; alginate; RELEASE; MICROSPHERES; ACID; HYDROGELS;
D O I
10.1002/app.35371
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Novel poly(L-histidine)-chitosan/alginate complex microcapsules were prepared from biodegradable polymers poly(L-histidine) (PLHis) in the presence of chitosan at acetate buffer solution pH 4.6. Microcapsules obtained are spherical and well-dispersed with a smooth surface and a narrow size distribution. The microcapsules can encapsulate the protein model drug hemoglobin (Hb) efficiently. The results show that the complex microcapsules with low, medium, or high molecular weight of chitosan (0.05%, w/v), the highest encapsulation efficiencies obtained are 91.3%, 85.9%, and 94.2% with loading efficiencies of 47.8%, 44.3%, and 39.7%, respectively. The release profiles indicate that Hb-loaded microcapsules conform to first-order release kinetic in whole procedure, and 84.8%, 71.4%, and 87.3% of Hb were released during 72-h incubation in PBS pH6.8 for microcapsules with low, medium, and high molecular weight chitosan (0.05%, w/v), respectively. The results also indicate that particle size and drug loading efficiency have a significant influence on the release profile and encapsulation efficiency. Our results reveal that the PLHis-chitosan/alginate complex microcapsules are able to encapsulate and release Hb and are potential carriers for protein drugs. (C) 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012
引用
收藏
页码:3728 / 3736
页数:9
相关论文
共 26 条
[1]   Protein direct delivery to dendritic cells using nanoparticles based on amphiphilic poly(amino acid) derivatives [J].
Akagi, Takami ;
Wang, Xin ;
Uto, Tomofumi ;
Baba, Masanori ;
Akashi, Mitsuru .
BIOMATERIALS, 2007, 28 (23) :3427-3436
[2]   Poly(L-histidine) with several aminoethyl groups for a new pH-sensitive DNA carrier [J].
Asayama, S ;
Sekine, T ;
Hamaya, A ;
Kawakami, H ;
Nagaoka, S .
POLYMERS FOR ADVANCED TECHNOLOGIES, 2005, 16 (07) :567-570
[3]   Design of a poly(L-histidine)-carbohydrate conjugate for a new pH-sensitive drug carrier [J].
Asayama, S ;
Kawakami, H ;
Nagaoka, S .
POLYMERS FOR ADVANCED TECHNOLOGIES, 2004, 15 (08) :439-444
[4]   Structure and interactions in covalently and ionically crosslinked chitosan hydrogels for biomedical applications [J].
Berger, J ;
Reist, M ;
Mayer, JM ;
Felt, O ;
Peppas, NA ;
Gurny, R .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2004, 57 (01) :19-34
[5]   Poly(D,L-lactic acid) surfaces modified by silk fibroin: effects on the culture of osteoblast in vitro [J].
Cai, KY ;
Yao, KD ;
Lin, SB ;
Yang, ZM ;
Li, XQ ;
Xie, HQ ;
Qing, TW ;
Gao, LB .
BIOMATERIALS, 2002, 23 (04) :1153-1160
[6]   Effects of aldehydes and methods of cross-linking on properties of calcium alginate microspheres prepared by emulsification [J].
Chan, LW ;
Heng, PWS .
BIOMATERIALS, 2002, 23 (05) :1319-1326
[7]  
Chen A. Z., 2009, Journal of Biomimetrics, Biomaterials, and Tissue Engineering, V3, P25, DOI 10.4028/www.scientific.net/JBBTE.3.25
[8]   Characteristics of poly-L-ornithine-coated alginate microcapsules [J].
Darrabie, MD ;
Kendall, WF ;
Opara, EC .
BIOMATERIALS, 2005, 26 (34) :6846-6852
[9]   New derivatives of polyglutamic acid as drug carrier systems [J].
Hoste, K ;
Schacht, E ;
Seymour, L .
JOURNAL OF CONTROLLED RELEASE, 2000, 64 (1-3) :53-61
[10]   On the importance and mechanisms of burst release in matrix-controlled drug delivery systems [J].
Huang, X ;
Brazel, CS .
JOURNAL OF CONTROLLED RELEASE, 2001, 73 (2-3) :121-136