Recent developments in 99Tcm-labelled peptide-based radiopharmaceuticals:: An overview

被引:82
作者
Okarvi, SM [1 ]
机构
[1] Univ Alberta, Fac Pharm & Pharmaceut Sci, Edmonton, AB T6G 2N8, Canada
关键词
D O I
10.1097/00006231-199912000-00002
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
Nature has designed peptides to stimulate, inhibit or regulate many body functions, The development of radiolabelled peptide-based radiopharmaceuticals for imaging a variety of tumours, infection/inflammation and thrombus has seen a new era in nuclear medicine. Recently, a number of Tc-99(m)-labelled bioactive peptides have proven to be useful diagnostic imaging agents. Due to their small size, peptide molecules exhibit favourable pharmacokinetic characteristics, such as rapid uptake by target tissue and rapid blood clearance, which potentially allows images to be acquired earlier following the administration of a Tc-99(m)-labelled peptide radiopharmaceutical. The challenge is to label bioactive peptides with Tc-99(m) with high specific activity without impairing the biological properties of the peptides. Molecular engineering techniques now permit synthesis of a wide range of biologically active peptides that carry chelating groups in their structure without affecting their receptor binding properties, thus permitting a high specific activity product. This review presents recent developments in Tc-99(m)-labelled small peptides and their potential applications in the imaging of various types of diseases. In addition, the different techniques for radiolabelling small bioactive peptides, the pharmacokinetic properties of peptides, and their potential as diagnostic imaging agents are also addressed. (C) 1999 Lippincott Willlams & Wilkins).
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页码:1093 / 1112
页数:20
相关论文
共 113 条
[1]  
ALLEMANNTANNAHI.L, 1998, EUR J NUCL MED, V25, P958
[2]   COMPARISON OF THE INFECTION IMAGING PROPERTIES OF A TC-99M LABELED CHEMOTACTIC PEPTIDE WITH IN-111 IGG [J].
BABICH, JW ;
GRAHAM, W ;
BARROW, SA ;
FISCHMAN, AJ .
NUCLEAR MEDICINE AND BIOLOGY, 1995, 22 (05) :643-648
[3]  
BABICH JW, 1993, J NUCL MED, V34, P1964
[4]   Design, synthesis, and initial evaluation of high-affinity technetium bombesin analogues [J].
Baidoo, KE ;
Lin, KS ;
Zhan, YG ;
Finley, P ;
Scheffel, U ;
Wagner, HN .
BIOCONJUGATE CHEMISTRY, 1998, 9 (02) :218-225
[5]   High-affinity no-carrier-added 99mTc-labeled chemotactic peptides for studies of inflammation in vivo [J].
Baidoo, KE ;
Scheffel, U ;
Stathis, M ;
Finley, P ;
Lever, SZ ;
Zhan, YG ;
Wagner, HN .
BIOCONJUGATE CHEMISTRY, 1998, 9 (02) :208-217
[6]  
BANGARD M, 1998, EUR J NUCL MED, V25, P837
[7]  
Barrett JA, 1997, J NUCL MED, V38, P59
[8]   SYNTHESIS AND PHARMACOLOGICAL PROPERTIES OF N-TERMINAL DECAPEPTIDE OF VASOACTIVE INTESTINAL PEPTIDE (VIP) [J].
BODANSZKY, M ;
HENES, JB ;
YIOTAKIS, AE ;
SAID, SI .
JOURNAL OF MEDICINAL CHEMISTRY, 1977, 20 (11) :1461-1464
[9]  
Bodanszky M., 1984, PRACTICE PEPTIDE SYN
[10]  
Breeman W A, 1996, Q J Nucl Med, V40, P209