Biodegradable micelles from a hyaluronan-poly(ε-caprolactone) graft copolymer as nanocarriers for fibroblast growth factor 1

被引:11
作者
Lin, Ta-Chiang [1 ,2 ]
Chen, Jui-Hsiang [3 ]
Chen, Yu-Hua [3 ]
Teng, Tse-min [3 ]
Su, Chiu-Hun [3 ]
Hsu, Shan-hui [2 ,4 ]
机构
[1] Natl Taiwan Univ, NTU ITRI Nano Ctr, Taipei 10617, Taiwan
[2] Natl Taiwan Univ, Inst Polymer Sci & Engn, Taipei 10617, Taiwan
[3] Ind Technol Res Inst, Mat & Chem Res Labs, Hsinchu, Taiwan
[4] Natl Taiwan Univ, Res Ctr Dev Biol & Regenerat Med, Taipei 10617, Taiwan
关键词
FIBROBLAST-GROWTH-FACTOR; ATOMIC-FORCE MICROSCOPY; CONTROLLED-RELEASE; HYALURONIC-ACID; TRIBLOCK COPOLYMERS; PEPTIDE AMPHIPHILE; IN-VITRO; DELIVERY; ANGIOGENESIS; DEGRADATION;
D O I
10.1039/c3tb21134g
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
A novel copolymer (HA-g-PCL) was prepared by grafting hydrophobic poly(epsilon-caprolactone) (PCL) chains onto the backbone of hydrophilic hyaluronic acid (HA) with a grafting ratio of similar to 7%. The copolymer formed micelles with a size of similar to 60 nm in aqueous solution over a critical concentration of similar to 4 mu g mL(-1). Each micelle consisted of about four copolymer chains. Fibroblast growth factor 1 (FGF1) may be encapsulated in micelles by various methods. In particular, FGF1 loaded to micelles through 1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide hydrochloride (EDC) conjugation provided efficient (similar to 87%) and large amount (up to similar to 175 mu g FGF1 per mg HA-g-PCL, or on average one FGF1 molecule per micelle) of loading as well as reduced burst release of FGF1. FGF1-loaded micelles remained functional after 21 days. Experimental rats receiving FGF1-loaded micelles showed better wound contraction and faster sebaceous gland formation than those receiving free FGF1 or empty micelles. We conclude that novel HA-g-PCL micelles are good nanocarriers for the controlled release of FGF1 and may be applied to encapsulate other bioactive molecules for therapeutic purposes.
引用
收藏
页码:5977 / 5987
页数:11
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