Literature DB >> 23957812

LHRH-targeted nanogels as a delivery system for cisplatin to ovarian cancer.

Natalia V Nukolova1, Hardeep S Oberoi, Yi Zhao, Vladimir P Chekhonin, Alexander V Kabanov, Tatiana K Bronich.   

Abstract

Targeted drug delivery using multifunctional polymeric nanocarriers is a modern approach for cancer therapy. Our purpose was to prepare targeted nanogels for selective delivery of chemotherapeutic agent cisplatin to luteinizing hormone-releasing hormone (LHRH) receptor overexpressing tumor in vivo. Building blocks of such delivery systems consisted of innovative soft block copolymer nanogels with ionic cores serving as a reservoir for cisplatin (loading 35%) and a synthetic analogue of LHRH conjugated to the nanogels via poly(ethylene glycol) spacer. Covalent attachment of (D-Lys6)-LHRH to nanogels was shown to be possible without loss in either the ligand binding affinity or the nanogel drug incorporation ability. LHRH-nanogel accumulation was specific to the LHRH-receptor positive A2780 ovarian cancer cells and not toward LHRH-receptor negative SKOV-3 cells. The LHRH-nanogel cisplatin formulation was more effective and less toxic than equimolar doses of free cisplatin or untargeted nanogels in the treatment of receptor-positive ovarian cancer xenografts in mice. Collectively, the study indicates that LHRH mediated nanogel-cisplatin delivery is a promising formulation strategy for therapy of tumors that express the LHRH receptor.

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Year:  2013        PMID: 23957812      PMCID: PMC3809768          DOI: 10.1021/mp4003688

Source DB:  PubMed          Journal:  Mol Pharm        ISSN: 1543-8384            Impact factor:   4.939


  32 in total

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10.  Cisplatin-loaded core cross-linked micelles: comparative pharmacokinetics, antitumor activity, and toxicity in mice.

Authors:  Hardeep S Oberoi; Natalia V Nukolova; Frederic C Laquer; Larisa Y Poluektova; Jiangeng Huang; Yazen Alnouti; Masanao Yokohira; Lora L Arnold; Alexander V Kabanov; Samuel M Cohen; Tatiana K Bronich
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Review 4.  Polymeric micelles for the delivery of poorly soluble drugs: From nanoformulation to clinical approval.

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7.  Intracellularly Swollen Polypeptide Nanogel Assists Hepatoma Chemotherapy.

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8.  Decapeptide functionalized targeted mesoporous silica nanoparticles with doxorubicin exhibit enhanced apoptotic effect in breast and prostate cancer cells.

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  9 in total

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