Preparation and biodistribution of copper-67-labeled porphyrins and porphyrin-A6H immunoconjugates

被引:23
作者
Bhalgat, MK
Roberts, JC
MercerSmith, JA
Knotts, BD
Vessella, RL
Lavallee, DK
机构
[1] UNIV UTAH,DEPT MED CHEM,SALT LAKE CITY,UT 84112
[2] LOS ALAMOS NATL LAB,MED RADIOISOTOPES RES PROGRAM,LOS ALAMOS,NM 87545
[3] UNIV WASHINGTON,DEPT UROL,SEATTLE,WA 98195
[4] CUNY HUNTER COLL,NEW YORK,NY 10021
来源
NUCLEAR MEDICINE AND BIOLOGY | 1997年 / 24卷 / 02期
关键词
antibody delivery; renal cell carcinoma; copper-67; porphyrin chelators; targeting;
D O I
10.1016/S0969-8051(96)00215-6
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
The synthetic porphyrins, N-benzyl-5,10,15,20-tetrakis(4-carboxyphenyl)porphine (N-bzHTCPP) and N-4-nitrobenzyl-5-(4-carboxyphenyl)-10,15,20-tris(4-sulfophenyl) porphine (N-bzHCS(3)P), represent excellent radiocopper chelating agents that may find utility in antibody mediated diagnosis and/or therapy. N-bzHCS(3)P was conjugated to an anti-renal cell carcinoma (RCC) antibody, A6H, and labeled with copper 67. (CuCS3P)-Cu-67-A6H was studied for its biodistribution in human RCC xenograft bearing nude mice, along with the radiolabeled free porphyrins. The porphyrins resulted in tumor:blood ratios in the range of 3 to 4 after 48 h. The radiolabeled antibody achieved a tumor:blood ratio of over 16 after 45 h, indicating accumulation at the desired site. However, unwanted localization also occurred in the liver and spleen, which will have to be rectified before realizing the full potential of this approach. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:179 / 185
页数:7
相关论文
共 45 条