Delivery of drugs with ultrasound

被引:63
作者
Lindner, JR [1 ]
Kaul, S [1 ]
机构
[1] Univ Virginia, Med Ctr, Div Cardiovasc, Cardiac Imaging Ctr, Charlottesville, VA 22908 USA
来源
ECHOCARDIOGRAPHY-A JOURNAL OF CARDIOVASCULAR ULTRASOUND AND ALLIED TECHNIQUES | 2001年 / 18卷 / 04期
关键词
contrast echocardiography; contrast ultrasound; microbubbles; drug delivery;
D O I
10.1046/j.1540-8175.2001.00329.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this article we discuss the potential role of microbubbles, traditionally used as ultrasound contrast agents, for site-specific drug delivery. To reach this goal, microbubbles capable of carrying a drug payload are being developed. To ensure that these microbubbles reach sufficient local concentration at disease sites, specific targeting for diseased tissues can be accomplished using several strategies. These strategies rely on either the intrinsic properties of microbubble shells or conjugation of monoclonal antibodies or other ligands to these shells that recognize antigens expressed in regions of disease. Site-specific delivery of antiinflammatory, antineoplastic, and thrombolytic drugs with microbubbles can be further enhanced by the ability to locally destroy microbubbles within an acoustic field, thereby releasing drugs and improving drug efficacy without systemic adverse effects. In the case of thrombi, ultrasound-mediated microbubble destruction also may facilitate the process of clot Lysis. This review also will consider current limitations and technological advances required for the development of this field.
引用
收藏
页码:329 / 337
页数:9
相关论文
共 36 条
[1]  
AHMAD I, 1992, CANCER RES, V52, P4817
[2]   Optical and acoustical observations of the effects of ultrasound on contrast agents [J].
Dayton, PA ;
Morgan, KE ;
Klibanov, AL ;
Brandenburger, GH ;
Ferrara, KW .
IEEE TRANSACTIONS ON ULTRASONICS FERROELECTRICS AND FREQUENCY CONTROL, 1999, 46 (01) :220-232
[3]   In vivo targeting of acoustically reflective liposomes for intravascular and transvascular ultrasonic enhancement [J].
Demos, SM ;
Alkan-Onyuksel, H ;
Kane, BJ ;
Ramani, K ;
Nagaraj, A ;
Greene, R ;
Klegerman, M ;
McPherson, DD .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1999, 33 (03) :867-875
[4]   INDUCTION OF ANGIOGENESIS DURING THE TRANSITION FROM HYPERPLASIA TO NEOPLASIA [J].
FOLKMAN, J ;
WATSON, K ;
INGBER, D ;
HANAHAN, D .
NATURE, 1989, 339 (6219) :58-61
[5]   ENHANCEMENT OF FIBRINOLYSIS INVITRO BY ULTRASOUND [J].
FRANCIS, CW ;
ONUNDARSON, PT ;
CARSTENSEN, EL ;
BLINC, A ;
MELTZER, RS ;
SCHWARZ, K ;
MARDER, VJ .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (05) :2063-2068
[6]   Polyethylene glycol modification: Relevance of improved methodology to tumour targeting [J].
Francis, GE ;
Delgado, C ;
Fisher, D ;
Malik, F ;
Agrawal, AK .
JOURNAL OF DRUG TARGETING, 1996, 3 (05) :321-&
[7]  
Gastl G, 1997, ONCOLOGY-BASEL, V54, P177
[8]   Patterns and emerging mechanisms of the angiogenic switch during tumorigenesis [J].
Hanahan, D ;
Folkman, J .
CELL, 1996, 86 (03) :353-364
[9]   Tumor infarction in mice by antibody-directed targeting of tissue factor to tumor vasculature [J].
Huang, XM ;
Molema, G ;
King, S ;
Watkins, L ;
Edgington, TS ;
Thorpe, PE .
SCIENCE, 1997, 275 (5299) :547-550
[10]   IN-VIVO MYOCARDIAL KINETICS OF AIR-FILLED ALBUMIN MICROBUBBLES DURING MYOCARDIAL CONTRAST ECHOCARDIOGRAPHY - COMPARISON WITH RADIOLABELED RED-BLOOD-CELLS [J].
JAYAWEERA, AR ;
EDWARDS, N ;
GLASHEEN, WP ;
VILLANUEVA, FS ;
ABBOTT, RD ;
KAUL, S .
CIRCULATION RESEARCH, 1994, 74 (06) :1157-1165