TARGETING OF MACROMOLECULAR CARRIERS AND LIPOSOMES BY ANTIBODIES TO MYOSIN HEAVY-CHAIN

被引:0
|
作者
KLIBANOV, AL
KHAW, BA
NOSSIFF, N
ODONNELL, SM
HUANG, L
SLINKIN, MA
TORCHILIN, VP
机构
[1] UNIV TENNESSEE, DEPT BIOCHEM, KNOXVILLE, TN 37996 USA
[2] MASSACHUSETTS GEN HOSP, DIV NUCL MED, BOSTON, MA 02114 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1991年 / 261卷 / 04期
关键词
ANTIMYOSIN; CHELATING POLYMER; LIPOSOME; MONOCLONAL ANTIBODY; MYOCARDIAL INFARCTION; RADIOIMMUNOIMAGING;
D O I
暂无
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Macromolecular carriers and liposomes were covalently coupled to monoclonal antibodies against cardiac myosin heavy chain. Deferoxamine-modified polymers bound tightly with Ga-67 and Ga-68 radioisotopes. Ternary deferoxamine-polylysine antibody conjugates specifically targeted the radioisotopes to a myosin-coated microplate. Scatchard analysis revealed a high affinity of the conjugate for the target with a K(as) of approximately 10(8) M-1. Liposomes that contained immobilized antimyosin antibodies were targeted specifically to the myosin-coated plate. Additional coating of these liposomes with polyethylene glycol reduced specific binding to the target in vitro. However, because of the presence of polyethylene glycol on the surface of liposomes, these liposomes had a long half-life and slowly cleared from the blood-stream after intravenous injection. These immunoliposomes showed up to 16- to 18-fold specific localization to the necrotic areas of the myocardium in rabbits with experimental infarction.
引用
收藏
页码:60 / 65
页数:6
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