Colloidal systems for tumor targeting

被引:25
作者
Storm, G
Crommelin, DJA
机构
来源
HYBRIDOMA | 1997年 / 16卷 / 01期
关键词
D O I
10.1089/hyb.1997.16.119
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The potential and limitations of targeted delivery of anticancer agents with colloidal particulate carriers is the subject of this contribution, Because over the years liposomes have gained the most attention as carrier system in the category of colloidal carrier systems, this paper focuses on the utility of the liposomal system for tumor targeting. It is imperative that an intended therapeutic application of liposomes should be well matched with the liposome behavior in vivo. Therefore, the in vivo fate of the first-generation liposomes and the more recently developed second-generation liposomes (surface-modified liposomes such as the immunoliposomes and long-circulating liposomes) is analyzed in terms of accessibility of target sites, time-, and site-controlled drug release and potential target sites for rational targeted delivery are discussed. A few examples of areas in cancer chemotherapy, with a strong rationale for the use of liposomes, are given, It is concluded that, although several options are available on the drawing board, issues such as tumor cell heterogeneity, access to the target site, shedding of antigens, and target site-specific release of the liposome-associated drug need to be addressed early in the development process.
引用
收藏
页码:119 / 125
页数:7
相关论文
共 58 条
[1]  
Allen Theresa M., 1994, Journal of Liposome Research, V4, P1, DOI 10.3109/08982109409037027
[2]   SUBCUTANEOUS ADMINISTRATION OF LIPOSOMES - A COMPARISON WITH THE INTRAVENOUS AND INTRAPERITONEAL ROUTES OF INJECTION [J].
ALLEN, TM ;
HANSEN, CB ;
GUO, LSS .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1150 (01) :9-16
[3]   LIPOSOMES WITH PROLONGED CIRCULATION TIMES - FACTORS AFFECTING UPTAKE BY RETICULOENDOTHELIAL AND OTHER TISSUES [J].
ALLEN, TM ;
HANSEN, C ;
RUTLEDGE, J .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 981 (01) :27-35
[4]   LIPOSOMES CONTAINING SYNTHETIC LIPID DERIVATIVES OF POLY(ETHYLENE GLYCOL) SHOW PROLONGED CIRCULATION HALF-LIVES INVIVO [J].
ALLEN, TM ;
HANSEN, C ;
MARTIN, F ;
REDEMANN, C ;
YAUYOUNG, A .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1066 (01) :29-36
[5]  
ALLEN TM, 1995, STEALTH LIPOSOMES, P193
[6]  
BERGERS JJ, 1992, LIPOSOME TECHNOLOGY, V2, P141
[7]   SPECIFIC TARGETING WITH POLY(ETHYLENE GLYCOL)-MODIFIED LIPOSOMES - COUPLING OF HOMING DEVICES TO THE ENDS OF THE POLYMERIC CHAINS COMBINES EFFECTIVE TARGET BINDING WITH LONG CIRCULATION TIMES [J].
BLUME, G ;
CEVC, G ;
CROMMELIN, MDJA ;
BAKKERWOUDENBERG, IAJM ;
KLUFT, C ;
STORM, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1149 (01) :180-184
[8]   LIPOSOMES FOR THE SUSTAINED DRUG RELEASE INVIVO [J].
BLUME, G ;
CEVC, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1029 (01) :91-97
[9]  
Crommelin D. A. J., 1993, PHOSPHOLIPIDS HDB, P335
[10]   ACTIVE TARGETING WITH PARTICULATE CARRIER SYSTEMS IN THE BLOOD COMPARTMENT [J].
CROMMELIN, DJA ;
SCHERPHOF, G ;
STORM, G .
ADVANCED DRUG DELIVERY REVIEWS, 1995, 17 (01) :49-60