Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/620
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dc.contributor.authorBhaskar, Sangeeta-
dc.date.accessioned2015-07-02T08:23:35Z-
dc.date.available2015-07-02T08:23:35Z-
dc.date.issued2012-08-
dc.identifier.urihttp://hdl.handle.net/123456789/620-
dc.description.abstractPURPOSE: Cancer is a multifactorial syndrome; hence, multidimensional therapy with a chemo-immunotherapeutic conjugate could be more effective in curing the disease. METHODS: We used SP-LPS, a bio-polymer having potent immunostimulatory activity, for conjugation with paclitaxel to make a chemo-immunotherapeutic conjugate. Its physicochemical characterization was done by HPLC, NMR and IR spectra. Stability was measured at different pH, temperature and in tissue homogenates. Chemotherapeutic and immunostimulatory activity was evaluated in vitro and also in tumor microenvironment. RESULTS: The conjugate self assembled into nanoparticulate structure, probably due to micelle formation. Stability was pH and temperature dependent. The conjugate exhibited chemotherapeutic and immunotherapeutic activity in vitro. In vivo antitumor activity was significantly higher and a higher percentage of activated immune cells were found in the tumor microenvironment of the conjugate-treated mice as compared to Taxol®-treated group. CONCLUSIONS: This conjugate is a potential chemo-immunotherapeutic compound for the treatment of cancer with advantages over present day chemotherapy with Taxol in terms of higher anticancer activity, less toxicity and ease of delivery.en_US
dc.publisherSpringeren_US
dc.titleAnticancer and immunostimulatory activity by conjugate of paclitaxel and non-toxic derivative of LPS for combined chemo-immunotherapy.en_US
dc.contributor.coauthorRoy, Aniruddha-
dc.contributor.coauthorChandra, Sourav-
dc.contributor.coauthorMamilapally, Swapna-
dc.keywordChemo-immunotherapy . Immunostimulation . Paclitaxel . Polymer-Dug conjugate . SP-LPSen_US
dc.journalPharm Resen_US
dc.volumeno29en_US
dc.issueno8en_US
dc.pages2294-2309en_US
Appears in Collections:Product Development Cell Unit I, Publications

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