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    Supramolecular Copolymer

    Micelles Based on the

    Complementary Multiple Hydrogen

    Bonds of Nucleobases for Drug

    Delievery

    Wang D. et al

    Presented bySunita Sharma

    1/30/2012

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    Background

    Main Cancer Treatments

    SurgeryInvasive and onlyeffective in stage I and IIcancer treatment.

    Radiation therapyCan possibly damagenormal tissue and organsnear the tumor

    ChemotherapyDrugs only present in thebody for a limited timeperiod

    Block Copolymer Micelles

    Improve solubility andbioavailability of hydrophobicdrugs in water.

    Size allows prolong drugcirculation time afteradministration

    Programmable delivery systemwhich the release of drugs can becontrolled via pH of environment.

    Main paper objective based uponthe finding that rapid drug releasewill reduce drug resistance incells.

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    Supramolecular Polymers

    Supramolecular polymer is a polymer whose monomerrepeat units are held together by non-covalent bonds,like co-ordination, pi-pi interaction and hydrogenbonding.

    In this article, two polymers have been used toassemble is supramolecular polymer PCL-A andPEG-U

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    Purpose and method

    Synthesis of PCL-A and U-PEG

    Synthesis of PCL-A:U-PEG micelles

    Insure pH-Triggered DOX Release

    Cell Internalization and DOX Release

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    Synthesis and

    Characterization of PCL-A

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    Synthesis and

    Characterization of U-PEG

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    Synthesis of PCL-A:U-PEG

    micellesTable 2. Properti es of the PCL-A:U-PEG Micelles

    sample CMCa(mg/ mL) diameterb ( nm) PDIb

    PCL25-A:U-PEG114 6.5 102 142 0.097

    PCL40-A:U-PEG114 3.9 102 156 0.093

    PCL49-A:U-PEG114 1.8 102 172 0.139

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    Insure pH-Triggered DOX

    Release

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    Cell Internalization and

    DOX Release

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    Conclusion

    Successful development of stimuli responsivemicelles, self assembled from PCL-A:U-PEG

    These micelles strongly respond to mild acidic

    pH and release the drug inside the shell, leadingto increased drug efficacy

    Stimuli responsive micelles are promising

    candidates for improvements in drug deliverysystems.

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    Questions?

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    Supplemental Info

    ! "#"

    Akali Catalyst

    !

    ! ! ! !

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    ReferenceWang, D.; Su, Y.; Jin, C.; Zhu, B.; Pang, Y.; Zhu, P.; Liu, J.; Tu, C.;

    Yan, D.; Zhu, X. Biomacromolecules2011

    , 12, 1370-1379.

    Toncheva, V.; Schacht, E.; Ng, S. y.; Barr, J.; Heller, J. J. DrugTargeting2003, 11, 345-353.