Anti-CD24 Nano-targeted Delivery of Docetaxel for the Treatment of Prostate Cancer

Abstract Nanoparticle (NP)-mediated, noninvasively targeted and image-guided therapies have potential to improve efficacy and safety of cancer therapeutics. We report synthesis and use of poly(lactide-co-glycolide)-polyethylene glycol (PLGA-PEG) NPs for targeted delivery of docetaxel. We synthesized...

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Published inNanomedicine Vol. 13; no. 1; pp. 263 - 273
Main Authors Bharali, Dhruba J., PhD, Sudha, Thangirala, PhD, Cui, Huadong, PhD, MD, Mian, Badar M., MD, Mousa, Shaker A., PhD
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.01.2017
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Summary:Abstract Nanoparticle (NP)-mediated, noninvasively targeted and image-guided therapies have potential to improve efficacy and safety of cancer therapeutics. We report synthesis and use of poly(lactide-co-glycolide)-polyethylene glycol (PLGA-PEG) NPs for targeted delivery of docetaxel. We synthesized docetaxel encapsulated NPs conjugated to anti-CD24 (for targeting) and/or an optical probe (for tracking) and evaluated efficacy in a prostate cancer mouse model. We observed preferential accumulation of anti-CD24 conjugated NPs (encapsulating docetaxel) compared to the non-conjugated NPs 24 hours after a single injection into luciferase-expressing PC3M prostate cancer tumor. In the same mouse model, we found significant ( P < 0.01) accumulation of docetaxel (~10-fold higher) in tumor after treatment with PLGA-PEG NPs encapsulating docetaxel and conjugated to anti-CD24 compared to non-conjugated NPs. Enhanced accumulation was associated with reduced tumor mass and tumor viability. These data support the potential impact of nano-targeted delivery of chemotherapy in enhancing the differential tumor delivery and anticancer efficacy in prostate cancer.
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ISSN:1549-9634
1549-9642
DOI:10.1016/j.nano.2016.08.017