A Dilemma in the Glycosaminoglycan-Based Therapy: Synthetic or Naturally Unique Molecules?

被引:35
作者
Pomin, Vitor H. [1 ]
机构
[1] Univ Fed Rio de Janeiro, Univ Hosp Clementino Fraga Filho, Inst Med Biochem Leopoldo de Meis, Program Glycobiol, BR-21941913 Rio De Janeiro, RJ, Brazil
关键词
carbohydrate-based drugs; chemical synthesis; drug development; glycosaminoglycans; enzymatic synthesis; oligosaccharide synthesis; FUCOSYLATED CHONDROITIN SULFATE; DEPOLYMERIZED HOLOTHURIAN GLYCOSAMINOGLYCAN; HEPARIN-INDUCED THROMBOCYTOPENIA; SOLID-PHASE SYNTHESIS; ACID BUILDING-BLOCKS; GIANT AFRICAN SNAIL; ACHARAN SULFATE; CHEMOENZYMATIC SYNTHESIS; ANTICOAGULANT ACTIVITY; KERATAN SULFATE;
D O I
10.1002/med.21356
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Glycosaminoglycans (GAGs) are widely explored in the biomedical market as functional ingredients in pharmaceutical or nutraceutical preparations. This extensive application of GAGs is justified by their multiple activities across several systems including, but not limited to, coagulation, thrombosis, inflammation, cancer, angiogenesis, cell differentiation, tissue repair, and microbial infections. Therapeutic GAGs are commonly extracted from mammalian tissues. Although functional in diverse systems, mammalian GAGs present serious downsides in therapy such as contamination risk from the mammalian tissues. In order to overcome some of the downsides, two new GAG sources have been appearing as alternatives to the mammalian-derived molecules. They are the synthetic GAGs and those extracted from nonmammalian origins such as invertebrate animals. This report overviews the general aspects of each GAG alternative and compares critically their pros and cons attributes in light of the prospects for the future of GAG-based therapy. (C) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:1195 / 1219
页数:25
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