• Title of article

    cis-Dichlorodiamminoplatinum (II) glyconanoparticles by drug-induced ionic gelation technique targeted to prostate cancer: Preparation, optimization and in vitro characterization

  • Author/Authors

    Jafari Malek، نويسنده , , Soheyl and Khoshchehreh، نويسنده , , Reyhaneh and Goodarzi، نويسنده , , Navid and Khoshayand، نويسنده , , Mohammad-Reza and Amini، نويسنده , , Mohsen and Atyabi، نويسنده , , Fatemeh and Esfandyari-manesh، نويسنده , , Mehdi and Tehrani، نويسنده , , Shirin and Mohammad Jafari، نويسنده , , Razieh and Maghazei، نويسنده , , Mohammed Shahab and Alvandifar، نويسنده , , Farhad and Ebrahimi، نويسنده , , Marzieh and Dinarvand، نويسنده , , Rassoul، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2014
  • Pages
    9
  • From page
    350
  • To page
    358
  • Abstract
    AbstractBackground stem cells (CSC) have been proposed as the reason of cancer relapse which are characterized mainly based on CD44+ phenotype with other supplementary markers. The aim of the present study is to fabricate cis-dichlorodiamminoplatinum (II) (CDDP) loaded glyconanoparticles using hyaluronic acid (HA) which is also known as the endogenous substrate for CD44 in vivo. s is purpose, a drug-induced ionic gelation technique has been used to prepare CDDP-incorporated nanoparticles. To optimize the fabrication technique, stirring rate, stirring time, and HA/CDDP ratio have been selected as the main factors from other factors and subjected to face-centered central composite design for optimization purposes. The optimized nanoparticles were further characterized using different complementary methods including FTIR, SEM, AFM and DSC. To evaluate the biological effectiveness of CDDP nanoparticles release study, MTS assay, tumor cell clonogenicity and sphere formation assay have been performed as well. s cal CDDP nanoparticles with Z-average approx. 150 nm with low PdI were prepared by adjusting the selected variables. FTIR results indicated the presence of inclusion complexes between CDDP and HA which lead to preparing nanoparticles with high entrapment efficiency and drug content of 87.4 and 43.74 percentage respectively. In vitro release study showed a sustained release of CDDP up to 4 days, and cellular studies confirmed that nanoparticles formation keeps the anticancer activity of formulated CDDP while moderate increase in cancer stem cell suppression. sion ms hyaluronic acid could be successfully exploited as carrier in cancer-targeted drug delivery with a look at targeting the CSCs.
  • Keywords
    Hyaluronic acid , polysaccharide , Cancer stem cell , prostate cancer , Nanomedicine
  • Journal title
    Colloids and Surfaces B Biointerfaces
  • Serial Year
    2014
  • Journal title
    Colloids and Surfaces B Biointerfaces
  • Record number

    1978887