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Tailored Doxorubicin-Hyaluronan Conjugate as a Potent Anticancer Glyco-Drug : An Alternative to Prodrug Approach

Podiyan, Oommen (author)
Uppsala universitet,Polymerkemi
Garousi, Javad (author)
Uppsala universitet,Polymerkemi
Sloff, Marije (author)
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Varghese, Oommen (author)
Uppsala universitet,Polymerkemi
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 (creator_code:org_t)
2013-10-15
2014
English.
In: Macromolecular Bioscience. - : Wiley. - 1616-5187 .- 1616-5195. ; 14:3, s. 327-333
  • Journal article (peer-reviewed)
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  • Releasibility of doxorubicin from drug-conjugates is believed to be a prerequisite for its anti- cancer activity. Here, a new glyco-drug approach that circumvents the releasibility restriction is reported, opening a new possibility to design efficient, target specific drug delivery system. It is discovered that stable amide coupling of doxorubicin (DOX) tohyaluronan (HA) shows dose dependent cytotoxicity to CD44 positive human coloncancer cells (HCT116) as compared to human breast cancer cells(MCF-7) and mouse fibroblast cells (NIH-3T3), which express less CD44 receptor. This direct conjugation approach is an easy scalable strategy that could be adopted to design innocuous anti-tumor nanoparticle formulations.

Subject headings

NATURVETENSKAP  -- Kemi -- Polymerkemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Polymer Chemistry (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

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