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POLYETHYLENE-GLYCOL MODIFICATION OF THE MONOCLONAL-ANTIBODY A7 ENHANCES ITS TUMOR-LOCALIZATION
被引:35
|
作者
:
KITAMURA, K
论文数:
0
引用数:
0
h-index:
0
机构:
BIOMEMBRANE INST,SEATTLE,WA 98104
BIOMEMBRANE INST,SEATTLE,WA 98104
KITAMURA, K
[
1
]
TAKAHASHI, T
论文数:
0
引用数:
0
h-index:
0
机构:
BIOMEMBRANE INST,SEATTLE,WA 98104
BIOMEMBRANE INST,SEATTLE,WA 98104
TAKAHASHI, T
[
1
]
TAKASHINA, K
论文数:
0
引用数:
0
h-index:
0
机构:
BIOMEMBRANE INST,SEATTLE,WA 98104
BIOMEMBRANE INST,SEATTLE,WA 98104
TAKASHINA, K
[
1
]
YAMAGUCHI, T
论文数:
0
引用数:
0
h-index:
0
机构:
BIOMEMBRANE INST,SEATTLE,WA 98104
BIOMEMBRANE INST,SEATTLE,WA 98104
YAMAGUCHI, T
[
1
]
NOGUCHI, A
论文数:
0
引用数:
0
h-index:
0
机构:
BIOMEMBRANE INST,SEATTLE,WA 98104
BIOMEMBRANE INST,SEATTLE,WA 98104
NOGUCHI, A
[
1
]
TSURUMI, H
论文数:
0
引用数:
0
h-index:
0
机构:
BIOMEMBRANE INST,SEATTLE,WA 98104
BIOMEMBRANE INST,SEATTLE,WA 98104
TSURUMI, H
[
1
]
TOYOKUNI, T
论文数:
0
引用数:
0
h-index:
0
机构:
BIOMEMBRANE INST,SEATTLE,WA 98104
BIOMEMBRANE INST,SEATTLE,WA 98104
TOYOKUNI, T
[
1
]
HAKOMORI, S
论文数:
0
引用数:
0
h-index:
0
机构:
BIOMEMBRANE INST,SEATTLE,WA 98104
BIOMEMBRANE INST,SEATTLE,WA 98104
HAKOMORI, S
[
1
]
机构
:
[1]
BIOMEMBRANE INST,SEATTLE,WA 98104
来源
:
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
|
1990年
/ 171卷
/ 03期
关键词
:
D O I
:
10.1016/0006-291X(90)90839-F
中图分类号
:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号
:
071010 ;
081704 ;
摘要
:
The F(ab')2 fragment of murine monoclonal antibody A7 was covalently bonded to polyethylene glycol (PEG, molecular weight: 5000) and the conjugate was compared to the parent F(ab')2 fragment by in vitro and in vivo studies. PEG-conjugated antibody fragment retained its antigen-binding activity in a competitive radioimmunoassay. The conjugate had a longer half-life and showed increased accumulation in tumors. Although the tumor:blood ratio for parent F(ab')2 fragment was higher than that for the conjugate, it showed higher value than whole MAb A7. The tissue:blood ratios were kept low with the conjugate, indicating that the conjugate was uptaken to normal organ with lesser extent, as compared with parent F(ab')2 fragment. Our findings indicate that this PEG-conjugated F(ab')2 fragment could be a promising carrier for use in targeting cancer chemotherapy. © 1990.
引用
收藏
页码:1387 / 1394
页数:8
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