Radiolabeled liposomes for scintigraphic imaging

被引:65
作者
Boerman, OC [1 ]
Laverman, P
Oyen, WJG
Corstens, FHM
Storm, G
机构
[1] Univ Nijmegen, Med Ctr, Dept Nucl Med, Nijmegen, Netherlands
[2] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Dept Pharmaceut, Utrecht, Netherlands
关键词
D O I
10.1016/S0163-7827(00)00013-8
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
Liposomes have been investigated extensively as carriers for drugs in attempts to achieve selective deposition and/or reduced toxicity. Liposomes radiolabeled with gamma emitters such as Ga-67, In-111 and Tc-99m, can be used for imaging purposes. Liposomes as formulated in the past, are rapidly taken up by cells of the mononuclear phagocyte system (MPS), primarily those located in liver and spleen. The recent development of long-circulating liposomes (LCLs), yielded liposomes that oppose recognition by the MPS. The development of these LCLs with enhanced circulatory half-lives has broadened the potential of liposomes to scintigraphically visualize pathologic processes in vivo. Liposomes have been proposed for tumor imaging, infection imaging and blood pool imaging. Strategies have been developed that allow rapid, easy and efficient labeling of preformed liposomes with In-111 and Tc-99m. There is now a vast body of preclinical evidence showing that LCLs can be used to image a wide variety of tumors as well as inflammatory lesions. The first studies in patients show that radiolabeled liposomes can image tumor and inflammatory lesions with good sensitivity and good specificity. Here, the present status of liposome-based radiopharmaceuticals for scintigraphic application is reviewed. (C) 2000 Published by Elsevier Science Ltd.
引用
收藏
页码:461 / 475
页数:15
相关论文
共 74 条
[1]   LIPOSOME DISPOSITION INVIVO .3. DOSE AND VESICLE-SIZE EFFECTS [J].
ABRA, RM ;
HUNT, CA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1981, 666 (03) :493-503
[2]   ATTACHMENT OF TC-99M TO LIPID VESICLES CONTAINING THE LIPOPHILIC CHELATE DIPALMITOYLPHOSPHATIDYLETHANOLAMINE DTTA [J].
AHKONG, QF ;
TILCOCK, C .
NUCLEAR MEDICINE AND BIOLOGY, 1992, 19 (08) :831-840
[3]   (99m)Technetium-stannous oxinate as marker of liposome formulations [J].
Alafandy, M ;
Goffinet, G ;
Umbrain, V ;
DHaese, J ;
Camu, F ;
Legros, FJ .
NUCLEAR MEDICINE AND BIOLOGY, 1996, 23 (07) :881-887
[4]   PHARMACOKINETICS OF STEALTH VERSUS CONVENTIONAL LIPOSOMES - EFFECT OF DOSE [J].
ALLEN, TM ;
HANSEN, C .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1068 (02) :133-141
[5]   LARGE UNILAMELLAR LIPOSOMES WITH LOW UPTAKE INTO THE RETICULOENDOTHELIAL SYSTEM [J].
ALLEN, TM ;
CHONN, A .
FEBS LETTERS, 1987, 223 (01) :42-46
[6]  
Awasthi V, 1998, J NUCL MED, V39, P1089
[7]   ENHANCED LOCALIZATION OF LIPOSOMES WITH PROLONGED BLOOD-CIRCULATION TIME IN INFECTED LUNG-TISSUE [J].
BAKKERWOUDENBERG, IAJM ;
LOKERSE, AF ;
TENKATE, MT ;
STORM, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1138 (04) :318-326
[8]   LIPOSOMES WITH PROLONGED BLOOD-CIRCULATION AND SELECTIVE LOCALIZATION IN KLEBSIELLA-PNEUMONIAE INFECTED LUNG-TISSUE [J].
BAKKERWOUDENBERG, IAJM ;
LOKERSE, AF ;
TENKATE, MT ;
MOUTON, JW ;
WOODLE, MC ;
STORM, G .
JOURNAL OF INFECTIOUS DISEASES, 1993, 168 (01) :164-171
[9]  
BEAUMIER PL, 1983, RES COMMUN CHEM PATH, V39, P277
[10]  
BOERMAN OC, 1995, J NUCL MED, V36, P1639