Mechanisms of Controlled Release from Silk Fibroin Films

被引:72
作者
Hines, Daniel J.
Kaplan, David L. [1 ]
机构
[1] Tufts Univ, Dept Chem & Biol Engn, Medford, MA 02155 USA
关键词
DRUG-RELEASE; IN-VITRO; BIOMATERIAL COATINGS; SOLUTE RELEASE; DELIVERY; MICROSPHERES; DEGRADATION; SCAFFOLDS; MATRICES;
D O I
10.1021/bm101421r
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The controlled release of fluorescein-iso-thio-cyanate (FITC)-labeled dextrans from methanol-treated and untreated silk fibroin films was modeled to characterize the release kinetics and mechanisms. Silk films were prepared with FITC-dextrans of various molecular weights (4, 10, 20, 40 kDa). Methanol treatment was used to promote crystallinity. The release data were assessed with two different models, an empirical exponential equation commonly fit to release data and a mechanism-based semiempirical model derived from Fickian diffusion through a porous film. The FITC-dextran release kinetics were evaluated as a function of molecular weight and compared between the untreated- and methanol-treated films. For the empirical model, the estimated values of the model parameters decreased with the molecular weight of the analyte and showed no significant difference between untreated- and methanol-treated films. For the diffusion-based model, the estimated diffusion coefficient was smaller for the methanol-treated films than for the untreated films. Also, the diffusion coefficient was observed to decrease linearly with increasing molecular weight of the analyte. The percent of FITC-dextran loading entrapped and not released was less for the methanol-treated films than for untreated films and linearly increased with molecular weight. A linear regression was fit to the relationship between molecular weight and the percent of entrapped FITC-dextran particles. Using these defined linear relationships, we present an updated version of the diffusion model for simulating release of FITC-dextran of varied molecular weights from methanol-treated and untreated silk films.
引用
收藏
页码:804 / 812
页数:9
相关论文
共 34 条
[1]   Silk-based biomaterials [J].
Altman, GH ;
Diaz, F ;
Jakuba, C ;
Calabro, T ;
Horan, RL ;
Chen, JS ;
Lu, H ;
Richmond, J ;
Kaplan, DL .
BIOMATERIALS, 2003, 24 (03) :401-416
[2]   Mathematical modeling and simulation of drug release from microspheres: Implications to drug delivery systems [J].
Arifin, Davis Yohanes ;
Lee, Lai Yeng ;
Wang, Chi-Hwa .
ADVANCED DRUG DELIVERY REVIEWS, 2006, 58 (12-13) :1274-1325
[3]   Silk fibroin as a novel coating material for controlled release of theophylline [J].
Bayraktar, O ;
Malay, Ö ;
Özgarip, Y ;
Batigün, A .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2005, 60 (03) :373-381
[4]  
CUSSLER E, 2003, DIFFUDION MASS TRANS, P15611
[5]   PLGA-based microparticles: elucidation of mechanisms and a new, simple mathematical model quantifying drug release [J].
Faisant, N ;
Siepmann, J ;
Benoit, JP .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2002, 15 (04) :355-366
[6]  
Grathwohl P., 1998, Diffusion in Natural Porous Media: Contaminant Transport, Sorption/Desorption and Dissolution Kinetics, P43
[7]   Silk fibroin as an organic polymer for controlled drug delivery [J].
Hofmann, S ;
Foo, CTWP ;
Rossetti, F ;
Textor, M ;
Vunjak-Novakovic, G ;
Kaplan, DL ;
Merkle, HP ;
Meinel, L .
JOURNAL OF CONTROLLED RELEASE, 2006, 111 (1-2) :219-227
[8]   In vitro degradation of silk fibroin [J].
Horan, RL ;
Antle, K ;
Collette, AL ;
Huang, YZ ;
Huang, J ;
Moreau, JE ;
Volloch, V ;
Kaplan, DL ;
Altman, GH .
BIOMATERIALS, 2005, 26 (17) :3385-3393
[9]   Determining beta-sheet crystallinity in fibrous proteins by thermal analysis and infrared spectroscopy [J].
Hu, Xiao ;
Kaplan, David ;
Cebe, Peggy .
MACROMOLECULES, 2006, 39 (18) :6161-6170
[10]   Drug release from biodegradable injectable thermosensitive hydrogel of PEG-PLGA-PEG triblock copolymers [J].
Jeong, B ;
Bae, YH ;
Kim, SW .
JOURNAL OF CONTROLLED RELEASE, 2000, 63 (1-2) :155-163