• DocumentCode
    636124
  • Title

    Development and characterization of chitosan-pluronic nanoparticles for tamoxifen delivery and cytotoxicity to MCF-7 cells

  • Author

    Othayoth, Rajath ; Karthik, V. ; Kumar, K. Sathish

  • Author_Institution
    Dept. of Biomed. Eng., SRM Univ., Chennai, India
  • fYear
    2013
  • fDate
    24-26 July 2013
  • Firstpage
    394
  • Lastpage
    401
  • Abstract
    In this study, tamoxifen-loaded chitosan-pluronic nanoparticles have been prepared by an ionic gelation (IG) method. Particle size analysis, Scanning electron microscopy (SEM), Zeta potential measurements, Fourier transform infrared spectroscopy (FT-IR) and differential scanning calorimetry (DSC) were used for nanoparticle characterization. The cytotoxicity of the nanoparticles was assayed in the MCF-7 cell line. The optimized tamoxifen loaded nanoparticles had a spherical shape with positive charge and mean diameter 150 to 300 nm. The FT-IR and DSC studies found that the drug was dispersed in amorphous form due to its potent interaction with nanoparticles matrix. The maximum encapsulation efficiency was obtained at 8mg/ml tamoxifen. The tamoxifen loaded chitosan-pluronic nanoparticles had good blood compatibility and the particles were nontoxic to the MCF-7 cell line. All study results suggest that the nanoparticles could be used as an effective drug delivery carrier for the breast cancer treatment.
  • Keywords
    Fourier transform spectra; biomedical materials; cancer; cellular transport; differential scanning calorimetry; drug delivery systems; drugs; electrokinetic effects; encapsulation; infrared spectra; materials preparation; nanofabrication; nanomedicine; nanoparticles; particle size; polymers; scanning electron microscopy; spectrochemical analysis; toxicology; DSC; FT-IR; Fourier transform infrared spectroscopy; MCF-7 cell line; amorphous form; blood compatibility; breast cancer treatment; chitosan-pluronic nanoparticle characterization; chitosan-pluronic nanoparticle development; differential scanning calorimetry; drug delivery carrier; ionic gelation method; materials preparation; maximum encapsulation efficiency; nanoparticle cytotoxicity; nanoparticle matrix; particle size analysis; positive charge; scanning electron microscopy; size 150 nm to 300 nm; tamoxifen delivery; tamoxifen-loaded chitosan-pluronic nanoparticle; zeta potential measurements; Nanoparticles; Chitosan; MCF-7 cells; ionic gelation; nanoparticles; tamoxifen;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Advanced Nanomaterials and Emerging Engineering Technologies (ICANMEET), 2013 International Conference on
  • Conference_Location
    Chennai
  • Print_ISBN
    978-1-4799-1377-0
  • Type

    conf

  • DOI
    10.1109/ICANMEET.2013.6609328
  • Filename
    6609328