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Fluorescent-Tagged Biodegradable Polycaprolactone Block Copolymer FRET Probe for Intracellular Bioimaging in Cancer Cells

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dc.contributor.author Kulkarni, Bhagyashree en_US
dc.contributor.author JAYAKANNAN, MANICKAM en_US
dc.date.accessioned 2019-07-01T05:34:35Z
dc.date.available 2019-07-01T05:34:35Z
dc.date.issued 2017-09 en_US
dc.identifier.citation ACS Biomaterials Science and Engineering, 3 (9), 2185-2197. en_US
dc.identifier.issn 2373-9878 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3250
dc.identifier.uri https://doi.org/10.1021/acsbiomaterials.7b00426 en_US
dc.description.abstract The present investigation reports a new fluorophore-tagged biodegradable polycaprolactone (PCL) block copolymer FRET-probe for intracellular imaging in cancer therapy. A hydroxyl functionalized π-conjugated oligo-phenylenevinylene (OPV) chromophore was tailor-made, and it was incorporated in a t-butyl ester substituted polycaprolactone block copolymer via ring opening polymerization. This blue-luminescent OPV-PCL triblock self-assembled as <200 nm spherical nanoparticles (FRET donor), and it encapsulated water insoluble Nile red (NR, FRET acceptor) to yield an OPV-NR FRET probe. Selective photo excitation of the OPV chromophore in block nanoassemblies enabled the excitation energy transfer from the OPV to NR and facilitated the efficient FRET process in aqueous medium. Time-correlated fluorescent decay dynamics and detailed photophysical studies were carried out to estimate the Förster distance, donor–acceptor distance, and the excitation energy transfer efficiency. These parameters confirmed the occurrence of the FRET process within the confined nanoparticle environment. The PCL chains in the FRET probe were susceptible to enzymatic biodegradation in intracellular environments, and the degradation process controlled the FRET on/off mechanism. Cytotoxicity studies revealed that the FRET probe was biocompatible and nontoxic to cells, and the FRET-probe was found to be readily taken up by the cancer cells, and it was internalized in the cytoplasm and peri-nuclear environment. Selective photoexcitation of the OPV chromophore in a confocal microscope exhibited dual emission from the FRET probe. The cancer cells exhibited blue luminescence (self-emission) with respect to the OPV chromophore (in the blue channel) and bright red-luminescence from the NR dye followed by the FRET process at the cellular level (in the red channel). The dual luminescence characteristics, biodegradation and biocompatibility, make the newly designed PCL-OPV-NR FRET probe an excellent biomedical nanodevice for bioimaging applications, and the proof-of-concept was established in cervical (HeLa) and breast cancer (MCF 7) cell lines. en_US
dc.language.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject Fluorescent-Tagged Biodegradable en_US
dc.subject Polycaprolactone en_US
dc.subject Intracellular Bioimaging in Cancer Cells en_US
dc.subject Bioimaging en_US
dc.subject Block copolymers en_US
dc.subject Enzyme-responsive en_US
dc.subject FRET en_US
dc.subject Polycaprolactone en_US
dc.subject 2017 en_US
dc.title Fluorescent-Tagged Biodegradable Polycaprolactone Block Copolymer FRET Probe for Intracellular Bioimaging in Cancer Cells en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle ACS Biomaterials Science and Engineering en_US
dc.publication.originofpublisher Foreign en_US


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