Polymers as drugs

被引:35
作者
Dhal, PK [1 ]
Holmes-Farley, SR [1 ]
Huval, CC [1 ]
Jozefiak, TH [1 ]
机构
[1] Genzyme Corp, Drug Discovery & Dev, Waltham, MA 02451 USA
来源
POLYMER THERAPEUTICS I: POLYMERS AS DRUGS, CONJUGATES AND GENE DELIVERY SYSTEMS | 2006年 / 192卷
关键词
bioactive polymers; drugs; non-absorbed; polyvalent; sequestrants;
D O I
10.1007/12_020
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polymeric drugs are defined as polymers that are active pharmaceutical ingredients, i.e., they are neither drug carriers nor prodrugs. In general, the underlying concept behind these therapeutic agents is the utilization of high molecular weight and functional characteristics of polymers to selectively recognize, sequester, and remove low molecular weight and macromolecular disease causing species in the intestinal fluid. The high molecular weight nature of these therapeutically relevant polymers makes them systemically non-absorbed, thus providing a number of advantages including long-term safety profiles over traditional small molecule drug products. Furthermore, multiple functional groups in the polymers incorporate polyvalent binding interactions that can result in pharmaceutical properties not found in small molecule drugs. This article summarizes some of the most recent efforts for the discovery and development of polymeric drugs that have proceeded from discovery phase to market place. Examples include sequestration of low molecular weight species such as bile acids, phosphate, and iron ions as well as polyvalent interactions to bind toxins, viruses, and bacteria as well as polymeric enzyme inhibitors and fat binders as anti-obesity agents. Furthermore, use of functional polymers to treat autoimmune disease and sickle cell anemia has been reviewed.
引用
收藏
页码:9 / 58
页数:50
相关论文
共 174 条
[91]   Rhabdomyolysis associated with hydroxymethylglutaryl-coenzyme A reductase inhibitors [J].
Jamal, SM ;
Eisenberg, MJ ;
Christopoulos, S .
AMERICAN HEART JOURNAL, 2004, 147 (06) :956-965
[92]   Sustained clinical benefits of glatiramer acetate in relapsing multiple sclerosis patients observed for 6 years [J].
Johnson, KP ;
Brooks, BR ;
Ford, CC ;
Goodman, A ;
Guarnaccia, J ;
Lisak, RP ;
Myers, LW ;
Panitch, HS ;
Pruitt, A ;
Rose, JW ;
Kachuck, N ;
Wolinsky, JS .
MULTIPLE SCLEROSIS JOURNAL, 2000, 6 (04) :255-266
[93]  
Johnson LR, 1994, PHYSL GASTROINTESTIN
[94]  
JOZEFIAK T, 2001, Patent No. 6299868
[95]  
JOZEFIAK TH, 2001, POLYM PREPR, V42, P98
[96]   Pluronic® block copolymers as novel polymer therapeutics for drug and gene delivery [J].
Kabanov, AV ;
Batrakova, EV ;
Alakhov, VY .
JOURNAL OF CONTROLLED RELEASE, 2002, 82 (2-3) :189-212
[97]  
Kelly CP, 1998, ANNU REV MED, V49, P375
[98]   Synthetic multivalent ligands in the exploration of cell-surface interactions [J].
Kiessling, LL ;
Gestwicki, JE ;
Strong, LE .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2000, 4 (06) :696-703
[99]   Shaping of the autoreactive T-cell repertoire by a splice variant of self protein expressed in thymic epithelial cells [J].
Klein, L ;
Klugmann, M ;
Nave, KA ;
Tuohy, VK ;
Kyewski, B .
NATURE MEDICINE, 2000, 6 (01) :56-61