Mechanism of tumor-targeted delivery of macromolecular drugs, including the EPR effect in solid tumor and clinical overview of the prototype polymeric drug SMANCS

被引:756
作者
Maeda, H [1 ]
Sawa, T
Konno, T
机构
[1] Kumamoto Univ, Sch Med, Dept Microbiol, Kumamoto 8600811, Japan
[2] Kumamoto Univ, Sch Med, Dept Surg, Kumamoto 8600811, Japan
关键词
SMANCS; EPR effects; clinical overview;
D O I
10.1016/S0168-3659(01)00309-1
中图分类号
O6 [化学];
学科分类号
0703 [化学];
摘要
This review article describes three aspects of polymeric drugs. The general mechanism of the EPR (enhanced permeability and retention) effect and factors involved in the effect are discussed, in view of the advantages of macromolecular therapeutics for cancer treatment, which are based on the highly selective EPR-related delivery of drug to tumor. Also described are advantages of more general water-soluble polymeric drugs as primary anticancer agents, using SMANCS as an example. Last, SMANCS/Lipiodol is discussed with reference to the type of formulation for arterial injection with most pronounced tumor selective delivery. as well as its advantages, precautions, and side effects from the clinical standpoint. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:47 / 61
页数:15
相关论文
共 52 条
[1]
AKAIKE T, 1997, NEOCARZINOSTATIN PAS, P155
[2]
[Anonymous], 1986, Protein Tailoring for Food and Medical Uses
[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]
POLYMER CONJUGATES - PHARMACOKINETIC CONSIDERATIONS FOR DESIGN AND DEVELOPMENT [J].
DUNCAN, R ;
SPREAFICO, F .
CLINICAL PHARMACOKINETICS, 1994, 27 (04) :290-306
[6]
PRECLINICAL EVALUATION OF POLYMER-BOUND DOXORUBICIN [J].
DUNCAN, R ;
SEYMOUR, LW ;
OHARE, KB ;
FLANAGAN, PA ;
WEDGE, S ;
HUME, IC ;
ULBRICH, K ;
STROHALM, J ;
SUBR, V ;
SPREAFICO, F ;
GRANDI, M ;
RIPAMONTI, M ;
FARAO, M ;
SUARATO, A .
JOURNAL OF CONTROLLED RELEASE, 1992, 19 (1-3) :331-346
[7]
IWAI K, 1984, CANCER RES, V44, P2115
[8]
Polymer conjugation to Cu,Zn-SOD and suppression of hydroxyl radical generation on exposure to H2O2: Improved stability of SOD in vitro and in vivo [J].
Kojima, Y ;
Akaike, T ;
Sato, K ;
Maeda, H ;
Hirano, T .
JOURNAL OF BIOACTIVE AND COMPATIBLE POLYMERS, 1996, 11 (03) :169-190
[9]
TARGETED CHEMOTHERAPY FOR UNRESECTABLE PRIMARY AND METASTATIC LIVER-CANCER [J].
KONNO, T ;
KAI, Y ;
YAMASHITA, R ;
NAGAMITSU, A ;
KIMURA, M .
ACTA ONCOLOGICA, 1994, 33 (02) :133-137
[10]
EFFECT OF ARTERIAL ADMINISTRATION OF HIGH-MOLECULAR-WEIGHT ANTI-CANCER AGENT SMANCS WITH LIPID LYMPHOGRAPHIC AGENT ON HEPATOMA - A PRELIMINARY-REPORT [J].
KONNO, T ;
MAEDA, H ;
IWAI, K ;
TASHIRO, S ;
MAKI, S ;
MORINAGA, T ;
MOCHINAGA, M ;
HIRAOKA, T ;
YOKOYAMA, I .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1983, 19 (08) :1053-&