Gene delivery using ultrasound contrast agents

被引:133
作者
Unger, EC [1 ]
Hersh, E [1 ]
Vannan, M [1 ]
McCreery, T [1 ]
机构
[1] Univ Arizona, Dept Radiol, Tucson, AZ 85724 USA
来源
ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES | 2001年 / 18卷 / 04期
关键词
ultrasound contrast agents; microbubbles; gene therapy;
D O I
10.1046/j.1540-8175.2001.00355.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
With the human genome product and continuing advances in molecular biology many therapeutic genes have been discovered. In the cardiovascular system, gene therapy has the potential to improve myocardial vascularization and ameliorate congestive heart failure. For successful development of clinical gene therapy, however, effective gene delivery vectors are needed. Ultrasound contrast agents can be used to develop new, more effective vectors for gene delivery. Ultrasound contrast agents lower the threshold for cavitation by ultrasound energy. Using physical properties of microbubbles and coating materials, genetic drugs have been incorporated into ultrasound contrast agents. Gene-bearing microbubbles can be injected IV and ultrasound energy applied to the target region. As the microbubbles enter the region of insonation, the microbubbles cavitate, locally releasing DNA. Cavitation also likely causes a local shockwave that improves cellular uptake of DNA. With transthoracic ultrasound using commercially available diagnostic ultrasound system and an IV injection of gene-bearing microbubbles, high levels of transgene expression are observed in the insonated region of the myocardium. This new technology using microbubbles and ultrasound for gene delivery merits further study and development.
引用
收藏
页码:355 / 361
页数:7
相关论文
共 50 条
[1]   Systemic effect of human growth hormone after intramuscular injection of a single dose of a muscle-specific gene medicine [J].
Anwer, K ;
Shi, M ;
French, MF ;
Muller, SR ;
Chen, W ;
Liu, QS ;
Proctor, BL ;
Wang, JJ ;
Mumper, RJ ;
Singhal, A ;
Rolland, AP ;
Alila, HW .
HUMAN GENE THERAPY, 1998, 9 (05) :659-670
[2]   GAUGING THE LIKELIHOOD OF CAVITATION FROM SHORT-PULSE, LOW-DUTY CYCLE DIAGNOSTIC ULTRASOUND [J].
APFEL, RE ;
HOLLAND, CK .
ULTRASOUND IN MEDICINE AND BIOLOGY, 1991, 17 (02) :179-185
[3]   Constitutive expression of phVEGF165 after intramuscular gene transfer promotes collateral vessel development in patients with critical limb ischemia [J].
Baumgartner, I ;
Pieczek, A ;
Manor, O ;
Blair, R ;
Kearney, M ;
Walsh, K ;
Isner, JM .
CIRCULATION, 1998, 97 (12) :1114-1123
[4]   Assessment of myocardial perfusion by intermittent harmonic power Doppler using SonoVue, a new ultrasound contrast agent [J].
Broillet, A ;
Puginier, J ;
Ventrone, R ;
Schneider, M .
INVESTIGATIVE RADIOLOGY, 1998, 33 (04) :209-215
[5]  
Caplice Noel M, 1999, Int J Cardiovasc Intervent, V2, P141
[6]   Immune modulation by IL-10 gene transfer via viral vector and plasmid DNA: Implication for gene therapy [J].
Chun, S ;
Daheshia, M ;
Lee, S ;
Rouse, BT .
CELLULAR IMMUNOLOGY, 1999, 194 (02) :194-204
[7]  
COSGROVE DO, 1999, TXB CONTRAST MEDIA, P451
[8]  
Ernst H, 1996, J CLIN ULTRASOUND, V24, P31, DOI 10.1002/(SICI)1097-0096(199601)24:1<31::AID-JCU5>3.0.CO
[9]  
2-M
[10]   A novel non-viral vector for DNA delivery based on low molecular weight, branched polyethylenimine:: Effect of molecular weight on transfection efficiency and cytotoxicity [J].
Fischer, D ;
Bieber, T ;
Li, YX ;
Elsässer, HP ;
Kissel, T .
PHARMACEUTICAL RESEARCH, 1999, 16 (08) :1273-1279