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A review of polysaccharide cytotoxic drug conjugates for cancer therapy
► Biocompatibility, molecular weight and type of linkers are the core factors in rational drug-conjugate design. ► Conjugates generally show lower in vitro cytotoxicity in comparison with free drug. ► Superiority of the conjugates is the performance in vivo where distribution determines efficacy and...
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Published in: | Carbohydrate polymers 2013-02, Vol.92 (2), p.1280-1293 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | ► Biocompatibility, molecular weight and type of linkers are the core factors in rational drug-conjugate design. ► Conjugates generally show lower in vitro cytotoxicity in comparison with free drug. ► Superiority of the conjugates is the performance in vivo where distribution determines efficacy and safety. ► Better simulation and using more reliable in vitro cell culture models accelerate finding the best in vivo candidates.
The most considerable challenges facing effective cancer therapy are systemic toxicity of cytotoxic drugs, their lack of tumor localizing and an even distribution throughout the whole body. Besides, short half-lives and undesirable pharmacokinetics are among the other drawbacks that inhibit effective cancer chemotherapy. Conjugation of low molecular weight drugs to polysaccharides has been used as a way to address these problems. This review will focus on polysaccharide drug conjugates and will provide an overview on various conjugation studies which have been accomplished for these carriers with cytotoxic drugs. Although a wide variety of anticancer agents including some toxins have been the subject of conjugation techniques, in this review, low molecular weight cytotoxic drugs conjugated covalently to the carriers are considered. |
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ISSN: | 0144-8617 1879-1344 |
DOI: | 10.1016/j.carbpol.2012.10.036 |