Role of polyanhydrides as localized drug carriers

被引:119
作者
Jain, JP
Modi, S
Domb, AJ
Kumar, N
机构
[1] Natl Inst Pharmaceut Educ & Res, Dept Pharmaceut, SAS Nagar 160062, Punjab, India
[2] Hebrew Univ Jerusalem, Dept Med Chem & Nat Prod, IL-91120 Jerusalem, Israel
关键词
biodegradable polymers; polyanhydrides; localized delivery; cancer; implants;
D O I
10.1016/j.jconrel.2004.12.021
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Many drugs that are administered in an unmodified form by conventional systemic routes fail to reach target organs in an effective concentration, or are not effective over a length of time due to a facile metabolism. Various types of targeting delivery systems and devices have been tried over a long period of time to overcome these problems. Targeted delivery or localized drug delivery offers an advantage of reduced body burden and systemic toxicity of the drugs, especially useful for highly toxic drugs like anticancer agents. Local drug delivery via polymer is a simple approach and hypothesized to avoid the above stated problems. Polyanhydrides are a unique class of polymer for drug delivery because some of them demonstrate a near zero order drug release and relatively rapid biodegradation in vivo. Further, the release rate of polyanhydride fabricated device can be altered over a thousand fold by simple changes in the polymer backbone. Hence, these are one of the best-suited polymers for drug delivery, with biodegradability and biocompatibility. The review focuses on the advantages of polyanhydride carriers in localized drug delivery along with their degradability behavior, toxicological profile and role in various disease conditions. (c) 2005 Elsevier B.V All rights reserved.
引用
收藏
页码:541 / 563
页数:23
相关论文
共 157 条
[1]   Transporting therapeutics across the blood-brain barrier [J].
Abbott, NJ ;
Romero, IA .
MOLECULAR MEDICINE TODAY, 1996, 2 (03) :106-113
[2]   Effect of geometry on the erosion characteristics of polyanhydride matrices [J].
Akbari, H ;
D'Emanuele, A ;
Attwood, D .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1998, 160 (01) :83-89
[3]  
ALBERTSSON AC, 1997, PURE APPL CHEM, V34, P1457
[4]   Antigenicity of recombinant proteins after regioselective immobilization onto polyanhydride-based copolymers [J].
Allard, L ;
Cheynet, V ;
Oriol, G ;
Gervasi, G ;
Imbert-Laurenceau, E ;
Mandrand, B ;
Delair, T ;
Mallet, F .
BIOCONJUGATE CHEMISTRY, 2004, 15 (03) :458-466
[5]   Aminosalicylate-based biodegradable polymers:: Syntheses and in vitro characterization of poly(anhydride-ester)s and poly(anhydride-amide) [J].
Anastasiou, TJ ;
Uhrich, KE .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2003, 41 (22) :3667-3679
[6]   Rationalizing the design of polymeric biomaterials [J].
Angelova, N ;
Hunkeler, D .
TRENDS IN BIOTECHNOLOGY, 1999, 17 (10) :409-421
[7]  
BAPAT VR, 2004, PROGR CONTROLLED NOV, P1
[8]   Survival and functional status after resection of recurrent glioblastoma multiforme [J].
Barker, FG ;
Chang, SM ;
Gutin, PH ;
Malec, MK ;
McDermott, MW ;
Prados, MD ;
Wilson, CB .
NEUROSURGERY, 1998, 42 (04) :709-720
[9]   Mechanisms of angioplasty and stent restenosis: implications for design of rational therapy [J].
Bennett, MR ;
O'Sullivan, M .
PHARMACOLOGY & THERAPEUTICS, 2001, 91 (02) :149-166
[10]   INHIBITION OF VASCULAR SMOOTH-MUSCLE CELL-PROLIFERATION IN-VITRO AND IN-VIVO BY C-MYC ANTISENSE OLIGODEOXYNUCLEOTIDES [J].
BENNETT, MR ;
ANGLIN, S ;
MCEWAN, JR ;
JAGOE, R ;
NEWBY, AC ;
EVAN, GI .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (02) :820-828