Poly(ethylene glycol) conjugated drugs and prodrugs: A comprehensive review

被引:115
作者
Greenwald, RB [1 ]
Conover, CD [1 ]
Choe, YH [1 ]
机构
[1] Enzon Inc, Piscataway, NJ 08854 USA
来源
CRITICAL REVIEWS IN THERAPEUTIC DRUG CARRIER SYSTEMS | 2000年 / 17卷 / 02期
关键词
poly(ethylene glycol); anticancer drug conjugates; prodrugs; camptothecin; paclitaxel; EPR effect;
D O I
10.1615/critrevtherdrugcarriersyst.v17.i2.20
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Low molecular weight Poly(ethylene glycol) (PEG) (< 20,000)-drug conjugates, prepared over a 20-year period, have been scrutinized and their properties and efficacy reviewed. No commercial products have thus far been reported for these types of compounds. However, during the past 5 years a renaissance in the field of PEG-(anticancer) drug conjugates has taken place, initiated by the use of higher molecular weight PEGs (> 20,000), especially 40,000, which is estimated to have a plasma circulating half-life of approximately 8-9 h. This recent resuscitation of small organic molecule delivery by high molecular weight PEG conjugates was founded on meaningful in vivo testing using established tumor models and has led to a clinical candidate. Recent applications of high molecular weight PEG prodrug strategies to amino-containing drugs are also detailed.
引用
收藏
页码:101 / 161
页数:61
相关论文
共 144 条
[1]   INTRAMOLECULAR CATALYSIS OF AMIDE HYDROLYSIS BY CARBOXY-GROUP - RATE DETERMINING PROTON-TRANSFER FROM EXTERNAL GENERAL ACIDS IN HYDROLYSIS OF SUBSTITUTED MALEAMIC ACIDS [J].
ALDERSLE.MF ;
KIRBY, AJ ;
LANCASTE.PW ;
MCDONALD, RS ;
SMITH, CR .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1974, (12) :1487-1495
[2]  
ASHTON P, 1997, Patent No. 5681964
[3]  
BAILON P, 1997, Patent No. 0809996
[4]   Direct evidence for peptide transporter (PepT1)-mediated uptake of a nonpeptide prodrug, valacyclovir [J].
Balimane, PV ;
Tamai, I ;
Guo, AL ;
Nakanishi, T ;
Kitada, H ;
Leibach, FH ;
Tsuji, A ;
Sinko, PJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 250 (02) :246-251
[5]   AMINO-ACID AND DIPEPTIDE DERIVATIVES OF DAUNORUBICIN .2. CELLULAR PHARMACOLOGY AND ANTI-TUMOR ACTIVITY ON L1210 LEUKEMIC-CELLS INVITRO AND INVIVO [J].
BAURAIN, R ;
MASQUELIER, M ;
DEPREZDECAMPENEERE, D ;
TROUET, A .
JOURNAL OF MEDICINAL CHEMISTRY, 1980, 23 (11) :1171-1174
[6]  
Bedeschi Angelo, 1997, Drugs of the Future, V22, P1259
[7]   MECHANISM OF ALKALINE HYDROLYSIS OF P-NITROPHENYL N-METHYLCARBAMATE [J].
BENDER, ML ;
HOMER, RB .
JOURNAL OF ORGANIC CHEMISTRY, 1965, 30 (11) :3975-&
[8]  
BENTLEY MD, 1997, POLYM PREPR, V38, P584
[9]   CO-OPERATIVE EFFECTS OF FUNCTIONAL GROUPS IN PEPTIDES .1. ASPARTYL-SERINE DERIVATIVES [J].
BERNHARD, SA ;
CARTER, JH ;
KATCHALSKI, E ;
SELA, M ;
SHALITIN, Y ;
BERGER, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1962, 84 (12) :2421-&
[10]   IN-VITRO AND IN-VIVO EVALUATION OF POLYOXYETHYLENE INDOMETHACIN ESTERS AS DERMAL PRODRUGS [J].
BONINA, FP ;
MONTENEGRO, L ;
DECAPRARIIS, P ;
PALAGIANO, F ;
TRAPANI, G ;
LISO, G .
JOURNAL OF CONTROLLED RELEASE, 1995, 34 (03) :223-232