Biomaterials for the treatment of myocardial infarction

被引:308
作者
Christman, Karen L.
Lee, Randall J.
机构
[1] Univ Calif Berkeley, Berkeley, CA 94720 USA
[2] San Francisco Joint Bioengn Grad Grp, San Francisco, CA USA
[3] Univ Calif San Francisco, Inst Cardiovasc Res, San Francisco, CA 94143 USA
关键词
D O I
10.1016/j.jacc.2006.06.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
For nearly a decade, researchers have investigated the possibility of cell transplantation for cardiac repair. More recently, the emerging fields of tissue engineering and biomaterials have begun to provide potential treatments. Tissue engineering approaches are designed to repair lost or damaged tissue through the use of growth factors, cellular transplantation, and biomaterial scaffolds. There are currently 3 biomaterial approaches for the treatment of myocardial infarction (MI). The first involves polymeric left ventricular restraints in the prevention of heart failure. The second utilizes in vitro engineered cardiac tissue, which is subsequently implanted in vivo. The final approach entails injecting cells and/or a scaffold into the myocardium to create in situ engineered cardiac tissue. This review gives an overview of the current progress in the growing field of biomaterials for the treatment of MI.
引用
收藏
页码:907 / 913
页数:7
相关论文
共 64 条
[1]   Mechanical stretch regimen enhances the formation of bioengineered autologous cardiac muscle grafts [J].
Akhyari, P ;
Fedak, PWM ;
Weisel, RD ;
Lee, TYJ ;
Verma, S ;
Mickle, DAG ;
Li, RK .
CIRCULATION, 2002, 106 (13) :I137-I142
[2]  
Anderson JM, 1996, ADVANCED BIOMATERIALS IN BIOMEDICAL ENGINEERING AND DRUG DELIVERY SYSTEMS, P163
[3]   Cardiac support device modifies left ventricular geometry and myocardial structure after myocardial infarction [J].
Blom, AS ;
Mukherjee, R ;
Pilla, JJ ;
Lowry, AS ;
Yarbrough, WM ;
Mingoia, JT ;
Hendrick, JW ;
Stroud, RE ;
McLean, JE ;
Affuso, J ;
Gorman, RC ;
Gorman, JH ;
Acker, MA ;
Spinale, FG .
CIRCULATION, 2005, 112 (09) :1274-1283
[4]   Tissue engineering via local gene delivery [J].
Bonadio, J .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2000, 78 (06) :303-311
[5]   Restraining acute infarct expansion decreases collagenase activity in borderzone myocardium [J].
Bowen, FW ;
Jones, SC ;
Narula, N ;
Sutton, MGSJ ;
Plappert, T ;
Edmunds, LH ;
Dixon, IMC .
ANNALS OF THORACIC SURGERY, 2001, 72 (06) :1950-1956
[6]   Cardiac muscle tissue engineering: toward an in vitro model for electrophysiological studies [J].
Bursac, N ;
Papadaki, M ;
Cohen, RJ ;
Schoen, FJ ;
Eisenberg, SR ;
Carrier, R ;
Vunjak-Novakovic, G ;
Freed, LE .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1999, 277 (02) :H433-H444
[7]  
Carrier RL, 1999, BIOTECHNOL BIOENG, V64, P580, DOI 10.1002/(SICI)1097-0290(19990905)64:5<580::AID-BIT8>3.0.CO
[8]  
2-X
[9]   Perfusion improves tissue architecture of engineered cardiac muscle [J].
Carrier, RL ;
Rupnick, M ;
Langer, R ;
Schoen, FJ ;
Freed, LE ;
Vunjak-Novakovic, G .
TISSUE ENGINEERING, 2002, 8 (02) :175-188
[10]   Passive epicardial containment prevents ventricular remodeling in heart failure [J].
Chaudhry, PA ;
Mishima, T ;
Sharov, VG ;
Hawkins, J ;
Alferness, C ;
Paone, G ;
Sabbah, HN .
ANNALS OF THORACIC SURGERY, 2000, 70 (04) :1275-1280