A core鈥搒
hell structured multifunctional carrier with nanocrystalline silicon (ncSi) as t
he core and a water-soluble block copolymer as t
he s
hell based on a poly(methacrylic acid) (PMAA) inner s
hell and polyethylene glycol (MPEG) outer s
hell (ncSi-MPM) was synt
hesized for drug delivery. T
he morphology, composition, and properties of t
he resulting ncSi-MPM were determined by compre
hensive multianalytical characterization, including
1H NMR spectroscopy, FTIR spectroscopy, XPS spectroscopy, TEM, DLS, and fluorescence spectroscopy analyses. T
he size of t
he resulting ncSi-MPM nanocarriers ranged from 40 to 110 nm under a simulated physiological environment. T
he loading efficiency of model drug doxorubicin (DOX) was approximately 6.1鈥?.4 wt % for ncSi-MPM and t
he drug release was pH controlled. Cytotoxicity studies demonstrated that DOX-loaded ncSi-MPM showed high anticancer activity against Hela cells. Hemolysis percentages (<2%) of ncSi-MPM were within t
he scope of safe values. Fluorescent imaging studies showed that t
he nanocarriers could be used as a tracker at t
he cellular level. Integration of t
he above functional components may result in ncSi-MPM becoming a promising multifunctional carrier for drug delivery and biomedical applications.
Keywords:
nanocrystalline silicon; cytotoxicity; controlled release; drug delivery