Fabrication of PLGA scaffolds using soft lithography and microsyringe deposition

被引:271
作者
Vozzi, G
Flaim, C
Ahluwalia, A
Bhatia, S
机构
[1] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92096 USA
[2] Univ Calif San Diego, Dept Med, La Jolla, CA 92096 USA
[3] Univ Pisa, Ctr Interdipartimentale Ric E Piaggio, Fac Engn, I-56100 Pisa, Italy
基金
美国国家航空航天局;
关键词
microfabrication; PLGA; microsyringe; soft lithography;
D O I
10.1016/S0142-9612(03)00052-8
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Construction of biodegradable, three-dimensional scaffolds for tissue engineering has been previously described using a variety of molding and rapid prototyping techniques. In this study, we report and compare two methods for fabricating poly(DL-lactide-co-glycolide) (PLGA) scaffolds with feature sizes of approximately 10-30 mum. The first technique, the pressure assisted microsyringe, is based on the use of a microsyringe that utilizes a computer-controlled, three-axis micropositioner, which allows the control of motor speeds and position. A PLGA solution is deposited from the needle of a syringe by the application of a constant pressure of 20-300 mm Hg, resulting in a controlled polymer deposition. The second technique is based on 'soft lithographic' approaches that utilize a poly(dimethylsiloxane) mold. Three variations of the second technique are presented: polymer casting, microfluidic perfusion, and spin coating. Polymer concentration, solvent composition, and mold dimensions influenced the resulting scaffolds as evaluated by light and electron microscopy. As a proof-of-concept for scaffold utility in tissue engineering applications, multilayer structures were formed by thermal lamination, and scaffolds were rendered porous by particulate leaching. These simple methods for forming PLGA scaffolds with microscale features may serve as useful tools to explore structure/function relationships in tissue engineering. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2533 / 2540
页数:8
相关论文
共 41 条
[1]   Biodegradation and biocompatibility of PLA and PLGA microspheres [J].
Anderson, JM ;
Shive, MS .
ADVANCED DRUG DELIVERY REVIEWS, 1997, 28 (01) :5-24
[2]   Microfluidic tectonics: A comprehensive construction platform for microfluidic systems [J].
Beebe, DJ ;
Moore, JS ;
Yu, Q ;
Liu, RH ;
Kraft, ML ;
Jo, BH ;
Devadoss, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (25) :13488-13493
[3]   Tissue Engineering at the Micro-Scale [J].
Bhatia, Sangeeta N. ;
Chen, Christopher S. .
BIOMEDICAL MICRODEVICES, 1999, 2 (02) :131-144
[4]  
Bhatia SN, 1997, J BIOMED MATER RES, V34, P189, DOI 10.1002/(SICI)1097-4636(199702)34:2<189::AID-JBM8>3.0.CO
[5]  
2-M
[6]   Microfabrication technology for vascularized tissue engineering [J].
Borenstein, JT ;
Terai, H ;
King, KR ;
Weinberg, EJ ;
Kaazempur-Mofrad, MR ;
Vacanti, JP .
BIOMEDICAL MICRODEVICES, 2002, 4 (03) :167-175
[7]   Geometric control of cell life and death [J].
Chen, CS ;
Mrksich, M ;
Huang, S ;
Whitesides, GM ;
Ingber, DE .
SCIENCE, 1997, 276 (5317) :1425-1428
[8]   Patterned deposition of cells and proteins onto surfaces by using three-dimensional microfluidic systems [J].
Chiu, DT ;
Jeon, NL ;
Huang, S ;
Kane, RS ;
Wargo, CJ ;
Choi, IS ;
Ingber, DE ;
Whitesides, GM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (06) :2408-2413
[9]   Mechanical and in vivo performance of hydroxyapatite implants with controlled architectures [J].
Chu, TMG ;
Orton, DG ;
Hollister, SJ ;
Feinberg, SE ;
Halloran, JW .
BIOMATERIALS, 2002, 23 (05) :1283-1293
[10]   Patterned delivery of immunoglobulins to surfaces using microfluidic networks [J].
Delamarche, E ;
Bernard, A ;
Schmid, H ;
Michel, B ;
Biebuyck, H .
SCIENCE, 1997, 276 (5313) :779-781