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Development and Evaluation of Stimuli-Responsive Chimeric Nanostructures

  1. Author:
    Naziris, Nikolaos
    Pippa, Natassa
    Stellas, Dimitrios
    Chrysostomou, Varvara
    Pispas, Stergios
    Demetzos, Costas
    Libera, Marcin
    Trzebicka, Barbara
  2. Author Address

    Section of Pharmaceutical Technology, Department of Pharmacy, School of Health Sciences, National and Kapodistrian University of Athens, Athens, Greece., Theoretical and Physical Chemistry Institute, National Hellenic Research Foundation, Athens, Greece., Biomedical Research Foundation, Academy of Athens, Athens, Greece., Vaccine Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, Maryland, USA., Section of Pharmaceutical Technology, Department of Pharmacy, School of Health Sciences, National and Kapodistrian University of Athens, Athens, Greece. demetzos@pharm.uoa.gr., Centre of Polymer and Carbon Materials, Polish Academy of Sciences, Zabrze, Poland.,
    1. Year: 2018
    2. Date: Oct
    3. Epub Date: 2018 07 20
  1. Journal: AAPS PharmSciTech
    1. 19
    2. 7
    3. Pages: 2971-2989
  2. Type of Article: Article
  3. ISSN: 1530-9932
  1. Abstract:

    Chimeric/mixed stimuli-responsive nanocarriers are promising agents for therapeutic and diagnostic applications, as well as in the combinatorial field of theranostics. Herein, we designed chimeric nanosystems, composed of natural phospholipid and pH-sensitive amphiphilic diblock copolymer, in different molar ratios and assessed the polymer lyotropic effect on their properties. Initially, polymer-grafted bilayers were evaluated for their thermotropic behavior by thermal analysis. Chimeric liposomes were prepared through thin-film hydration and the obtained vesicles were studied by light scattering techniques, to measure their physicochemical characteristics and colloidal stability, as well as by imaging techniques, to elucidate their global and membrane morphology. Finally, in vitro screening of the systems 39; toxicity was held. The copolymer effect on the membrane phase transition strongly depended on the pH of the surrounding environment. Chimeric nanoparticles were around and above 100 160;nm, while electron microscopy revealed occasional morphology diversity, probably affecting the toxicity of the systems. The latter was assessed to be tolerable, while dependent on the nanosystems 39; material concentration, polymer concentration, and polymer composition. All experiments suggested that the thermodynamic and biophysical properties of the nanosystems are copolymer-composition- and concentration-dependent, since different amounts of incorporated polymer would produce divergent effects on the lyotropic liquid crystal membrane. Certain chimeric systems can be exploited as advanced drug delivery nanosystems, based on their overall promising profiles.

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External Sources

  1. DOI: 10.1208/s12249-018-1112-2
  2. PMID: 30030723
  3. WOS: 000452587900023
  4. PII : 10.1208/s12249-018-1112-2

Library Notes

  1. Fiscal Year: FY2017-2018
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