Abstract
HPMA copolymer-RGDfK (HPMA-RGDfK) conjugates bearing either aminohexylgeldanamycin (AHGDM) or docetaxel (DOC) were synthesized and characterized. In vitro stability and binding were evaluated. Cytotoxicity toward ovarian cancer cells was evaluated and the ability of the conjugates to induce cell death was assessed by combination index analysis. Conjugates bearing AHGDM were more stable and exhibited slower drug release than those bearing DOC. Both conjugates demonstrated the ability to bind to avb3 integrins. In combination, HPMA-RGDfK conjugates demonstrated marked synergism as compared to their non-targeted counterparts and free drug controls. HPMA-RGDfK conjugates bearing AHGDM and DOC induce synergistic cytotoxicity in vitro, suggesting their potential as a promising combination therapy.
Keywords:
docetaxel; geldanamycin; ovarian cancer; targeted drug delivery.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Antibiotics, Antineoplastic* / chemistry
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Antibiotics, Antineoplastic* / pharmacokinetics
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Antibiotics, Antineoplastic* / pharmacology
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Benzoquinones* / chemistry
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Benzoquinones* / pharmacokinetics
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Benzoquinones* / pharmacology
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Cell Death / drug effects
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Cell Line, Tumor
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Docetaxel
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Drug Screening Assays, Antitumor
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Female
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Humans
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Integrin alphaVbeta3 / antagonists & inhibitors
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Lactams, Macrocyclic* / chemistry
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Lactams, Macrocyclic* / pharmacokinetics
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Lactams, Macrocyclic* / pharmacology
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Methacrylates* / chemistry
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Methacrylates* / pharmacokinetics
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Methacrylates* / pharmacology
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Oligopeptides* / chemistry
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Oligopeptides* / pharmacokinetics
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Oligopeptides* / pharmacology
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Ovarian Neoplasms / drug therapy*
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Ovarian Neoplasms / metabolism
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Ovarian Neoplasms / pathology
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Taxoids* / chemistry
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Taxoids* / pharmacokinetics
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Taxoids* / pharmacology
Substances
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Antibiotics, Antineoplastic
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Benzoquinones
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Integrin alphaVbeta3
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Lactams, Macrocyclic
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Methacrylates
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Oligopeptides
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Taxoids
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Docetaxel
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arginyl-glycyl-aspartic acid
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hydroxypropyl methacrylate
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geldanamycin