Controlling interlayer diffusion to achieve sustained, multiagent delivery from layer-by-layer thin films

被引:229
作者
Wood, Kris C.
Chuang, Helen F.
Batten, Robert D.
Lynn, David M.
Hammond, Paula T.
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] Univ Wisconsin, Dept Chem & Biol Engn, Madison, WI 53706 USA
关键词
D O I
10.1073/pnas.0602884103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We present the fabrication of conformal, hydrolytically degradable thin films capable of administering sustained, multiagent release profiles. Films are constructed one molecular layer at a time by using the layer-by-layer, directed-deposition technique; the subsequent hydrolytic surface erosion of these systems results in the release of incorporated materials in a sequence that reflects their relative positions in the film. The position of each species is determined by its ability to diffuse throughout the film architecture, and, as such, the major focus of this work is to define strategies that physically block interlayer diffusion during assembly to create multicomponent, stratified films. By using a series of radiolabeled polyelectrolytes as experimental probes, we show that covalently crosslinked barriers can effectively block interlayer diffusion, leading to compartmentalized structures, although even very large numbers of ionically crosslinked (degradable or nondegradable) barrier layers cannot block interlayer diffusion. By using these principles, we designed degradable films capable of extended release as well as both parallel and serial multiagent release. The ability to fabricate multicomponent thin films with nanoscale resolution may lead to a host of new materials and applications.
引用
收藏
页码:10207 / 10212
页数:6
相关论文
共 25 条
[1]   Materials science - Smart biomaterials [J].
Anderson, DG ;
Burdick, JA ;
Langer, R .
SCIENCE, 2004, 305 (5692) :1923-1924
[2]   Semi-automated synthesis and screening of a large library of degradable cationic polymers for gene delivery [J].
Anderson, DG ;
Lynn, DM ;
Langer, R .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (27) :3153-3158
[3]   Microencapsulation of uncharged low molecular weight organic materials by polyelectrolyte multilayer self-assembly [J].
Caruso, F ;
Yang, WJ ;
Trau, D ;
Renneberg, R .
LANGMUIR, 2000, 16 (23) :8932-8936
[4]   Fuzzy nanoassemblies: Toward layered polymeric multicomposites [J].
Decher, G .
SCIENCE, 1997, 277 (5330) :1232-1237
[5]   Thin polymer layers formed by polyelectrolyte multilayer techniques on biological surfaces [J].
Elbert, DL ;
Herbert, CB ;
Hubbell, JA .
LANGMUIR, 1999, 15 (16) :5355-5362
[6]   Surface analysis of erodible multilayered polyelectrolyte films: Nanometer-scale structure and erosion profiles [J].
Fredin, NJ ;
Zhang, JT ;
Lynn, DM .
LANGMUIR, 2005, 21 (13) :5803-5811
[7]   Multicompartment films made of alternate polyelectrolyte multilayers of exponential and linear growth [J].
Garza, JM ;
Schaaf, P ;
Muller, S ;
Ball, V ;
Stoltz, JF ;
Voegel, JC ;
Lavalle, P .
LANGMUIR, 2004, 20 (17) :7298-7302
[8]   Recent explorations in electrostatic multilayer thin film assembly [J].
Hammond, PT .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 1999, 4 (06) :430-442
[9]   Form and function in multilayer assembly: New applications at the nanoscale [J].
Hammond, PT .
ADVANCED MATERIALS, 2004, 16 (15) :1271-1293
[10]   Controlling the growth regime of polyelectrolyte multilayer films:: Changing from exponential to linear growth by adjusting the composition of polyelectrolyte mixtures [J].
Hübsch, E ;
Ball, V ;
Senger, B ;
Decher, G ;
Voegel, JC ;
Schaaf, P .
LANGMUIR, 2004, 20 (05) :1980-1985