Epidermal growth factor radiopharmaceuticals:: 111In chelation, conjugation to a blood-brain barrier delivery vector via a biotin-polyethylene linker, pharacokinetics, and in vivo imaging of experimental brain tumors

被引:63
作者
Kurihara, A [1 ]
Deguchi, Y [1 ]
Pardridge, WM [1 ]
机构
[1] Univ Calif Los Angeles, Sch Med, Dept Med, Los Angeles, CA 90095 USA
关键词
D O I
10.1021/bc980123x
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Epidermal growth factor (EGF) is a potential peptide radiopharmaceutical for detection of brain tumors, because many human gliomas overexpress the EGF receptor (EGFR). The transport of EGF to the brain, however, is restricted by the blood-brain barrier (BBB). The purpose of the present study was to develop a vector-mediated brain delivery system for radiolabeled EGF. Human EGF was monobiotinylated with NHS-PEG(3400)-biotin, where NHS is N-hydroxysuccinimide and PEG(3400) is poly(ethylene glycol) of 3400 Da molecular mass. EGF-PEG(3400)-biotin was radiolabeled with either I-125 or In-111 through the metal chelator, diethylenetriaminepentaacetic acid (DTPA). The radiolabeled EGF was then conjugated to a BBB delivery vector comprised of a complex of the OX26 monoclonal antibody (MAb) to the rat transferrin receptor, which was coupled to streptavidin (SA). Following intravenous injection in rats, the I-125 conjugate was rapidly degraded in vivo, while the In-111 conjugate was metabolically stable. The brain delivery of [In-111]DTPA-EGF-PEG(3400)-biotin was enabled by conjugation with OX26/SA and was optimized by co-injection of unlabeled EGF to saturate EGF receptors in the liver. The specific binding of the [In-111]DTPA-EGF-PEG(3400)-biotin conjugated to OX26/SA to the EGF receptor was confirmed in C6 rat glioma cells, which had been transfected with a gene encoding for the human EGF receptor under the regulation of a dexamethasone-inducible promoter. In vivo studies of CG-EGFR experimental tumors in Fischer 344 rats demonstrated successful brain imaging only when the peptide radiopharmaceutical was conjugated to the BBB delivery system, although the C6-EGFR tumors did not express EGFR in vivo. In conclusion, these studies describe the molecular formulation of a peptide radiopharmaceutical that can be used for imaging brain tumors behind the BBB.
引用
收藏
页码:502 / 511
页数:10
相关论文
共 23 条
[11]   LOCALIZATION OF BINDING-SITES FOR EPIDERMAL GROWTH-FACTOR (EGF) IN RAT-KIDNEY - EVIDENCE FOR THE EXISTENCE OF LOW AFFINITY EGF BINDING-SITES ON THE BRUSH-BORDER MEMBRANE [J].
KIM, DC ;
HANANO, M ;
KANAI, Y ;
OHNUMA, N ;
SUGIYAMA, Y .
PHARMACEUTICAL RESEARCH, 1992, 9 (11) :1394-1401
[12]   AMPLIFICATION, ENHANCED EXPRESSION AND POSSIBLE REARRANGEMENT OF EGF RECEPTOR GENE IN PRIMARY HUMAN-BRAIN TUMORS OF GLIAL ORIGIN [J].
LIBERMANN, TA ;
NUSBAUM, HR ;
RAZON, N ;
KRIS, R ;
LAX, I ;
SOREQ, H ;
WHITTLE, N ;
WATERFIELD, MD ;
ULLRICH, A ;
SCHLESSINGER, J .
NATURE, 1985, 313 (5998) :144-147
[13]   EPIDERMAL GROWTH-FACTOR DOES NOT CROSS THE BLOOD-BRAIN-BARRIER [J].
NAVE, KA ;
PROBSTMEIER, R ;
SCHACHNER, M .
CELL AND TISSUE RESEARCH, 1985, 241 (02) :453-457
[14]   ENKEPHALIN AND BLOOD-BRAIN-BARRIER - STUDIES OF BINDING AND DEGRADATION IN ISOLATED BRAIN MICRO-VESSELS [J].
PARDRIDGE, WM ;
MIETUS, LJ .
ENDOCRINOLOGY, 1981, 109 (04) :1138-1143
[15]   Drug delivery to the brain [J].
Pardridge, WM .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1997, 17 (07) :713-731
[16]   Combined use of carboxyl-directed protein pegylation and vector-mediated blood-brain barrier drug delivery system optimizes brain uptake of brain-derived neurotrophic factor following intravenous administration [J].
Pardridge, WM ;
Wu, DF ;
Sakane, T .
PHARMACEUTICAL RESEARCH, 1998, 15 (04) :576-582
[17]  
Sagita M, 1998, CANCER RES, V58, P914
[18]   Carboxyl-directed pegylation of brain-derived neurotrophic factor markedly reduces systemic clearance with minimal loss of biologic activity [J].
Sakane, T ;
Pardridge, WM .
PHARMACEUTICAL RESEARCH, 1997, 14 (08) :1085-1091
[19]   TRANSPORT OF [I-125] TRANSFERRIN THROUGH THE RAT BLOOD-BRAIN-BARRIER [J].
SKARLATOS, S ;
YOSHIKAWA, T ;
PARDRIDGE, WM .
BRAIN RESEARCH, 1995, 683 (02) :164-171
[20]   EPIDERMAL GROWTH-FACTOR RECEPTOR EXPRESSION IN HUMAN GLIOMAS [J].
TORP, SH ;
HELSETH, E ;
DALEN, A ;
UNSGAARD, G .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 1991, 33 (01) :61-64