Early phase tumor accumulation of macromolecules: a great difference in clearance rate between tumor and normal tissues

被引:376
作者
Noguchi, Y
Wu, J
Duncan, R
Strohalm, J
Ulbrich, K
Akaike, T
Maeda, H
机构
[1] Kumamoto Univ, Sch Med, Dept Microbiol, Kumamoto 860, Japan
[2] Univ London, Sch Pharm, Ctr Polymer Therapeut, London WC1N 1AX, England
[3] Acad Sci Czech Republ, Inst Macromol Chem, CR-16206 Prague, Czech Republic
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 1998年 / 89卷 / 03期
关键词
polymer drugs; tumor targeting accumulation; EPR effect; tumor vascular permeability; tissue clearance;
D O I
10.1111/j.1349-7006.1998.tb00563.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The objective of this study was to investigate the molecular weight (MW) and time-dependence of the phenomenon termed "the enhanced permeability and retention" (EPR) effect in solid tumor, in particular to determine and define the early phase accumulation of macromolecules in tumor and normal tissues and the relationship between blood concentration and tissue clearance, As a model, radioiodinated N-(2-hydroxypropyl)methacrylamide (HPMA) copolymers of MW ranging from 4.5 K to 800 K were administered i.v. to mice bearing sarcoma 180 tumor, Within 10 min all HPMA copolymers accumulated effectively in the tumor regardless of MW (1.0-1.5% of injected dose per g of tumor), However, higher MW copolymers (>50 K) showed significantly increased tumor accumulation after 6 h, while the lower MW copolymers (<40 K) were cleared rapidly from tumor tissue due to rapid diffusion back into the bloodstream, Blood clearance was also MW-dependent; the lower MW copolymers displayed rapid clearance, with kidney radioactivity of the copolymers of MW <20 K representing 24% of injected dose per g kidney at 1 min after i.v. administration, Within 10 min these copolymers passed through the kidney and were excreted in the urine. Higher MW copolymers consistently showed kidney levels of 3-5% dose per g kidney in the early phase with no time-dependent accumulation in kidney, There was also no progressive accumulation in muscle or liver, regardless of polymer MW. These results suggest the "EPR effect" in solid tumor primarily arises from in the difference in clearance rate between the solid tumor and the normal tissues after initial penetration of the polymers into these tissues.
引用
收藏
页码:307 / 314
页数:8
相关论文
共 40 条
[1]  
CARTLIDGE S A, 1987, Journal of Controlled Release, V4, P265, DOI 10.1016/0168-3659(87)90018-6
[2]  
CASSIDY J, 1989, BIOCHEM PHARMACOL, V38, P857
[3]  
Doi K, 1996, CANCER-AM CANCER SOC, V77, P1598, DOI 10.1002/(SICI)1097-0142(19960415)77:8<1598::AID-CNCR27>3.0.CO
[4]  
2-U
[5]  
Duncan R, 1996, STP PHARMA SCI, V6, P237
[6]   PINOCYTIC UPTAKE AND INTRACELLULAR DEGRADATION OF N-(2-HYDROXYPROPYL)METHACRYLAMIDE COPOLYMERS - A POTENTIAL-DRUG DELIVERY SYSTEM [J].
DUNCAN, R ;
REJMANOVA, P ;
KOPECEK, J ;
LLOYD, JB .
BIOCHIMICA ET BIOPHYSICA ACTA, 1981, 678 (01) :143-150
[7]   TARGETING OF N-(2-HYDROXYPROPYL)METHACRYLAMIDE CO-POLYMERS TO LIVER BY INCORPORATION OF GALACTOSE RESIDUES [J].
DUNCAN, R ;
KOPECEK, J ;
REJMANOVA, P ;
LLOYD, JB .
BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 755 (03) :518-521
[8]   INCREASED VASCULAR-PERMEABILITY IN ORGANS MEDIATED BY THE SYSTEMIC ADMINISTRATION OF LYMPHOKINE-ACTIVATED KILLER CELLS AND RECOMBINANT INTERLEUKIN-2 IN MICE [J].
ETTINGHAUSEN, SE ;
PURI, RK ;
ROSENBERG, SA .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1988, 80 (03) :177-188
[9]  
IWAI K, 1987, ANTICANCER RES, V7, P321
[10]  
IWAI K, 1984, CANCER RES, V44, P2115