9 research outputs found
Carboxymethyl guar gum nanoparticles for drug delivery applications:preparation and preliminary in-vitro investigations
Carboxymethyl guar gum nanoparticles for drug delivery applications: preparation and preliminary in-vitro investigations
Abstract Carboxymethyl guar gum (CMGG) synthesised from commercially available polysaccharide was formulated into nanoparticles via ionic gelation using trisodium trimetaphosphate (STMP) as cross-linking agent. Characterisation using a range of analytical techniques (FTIR, NMR, GPC, TGA and DLS) confirmed the CMGG structure and revealed the effect of the CMGG and STMP concentration on the main characteristics of the obtained nanoformulations. The average nanoparticle diameter was found to be around 208 nm, as determined by dynamic light scattering (DLS) and confirmed by scanning electron microscopy (SEM) and nanoparticle tracking analysis (NTA). Experiments using simulated gastric and intestinal fluids evidenced significant pH-dependent drug release behaviour of the nanoformulations loaded with Rhodamine B (RhB) as a model drug (loading capacity in excess of 83%), as monitored by UV-Vis. While dose-dependent cytotoxicity was observed, the nanoformulations appeared completely non-toxic at concentrations below 0.3 mg/mL. Results obtained so far suggest that carboxymethylated guar gum nanoparticles formulated with STMP warrant further investigations as polysaccharide based biocompatible drug nanocarriers
Des nanoparticules à base de fullerènes C60 fonctionnalisées par polyethylenimine et PEG pour delivrance d’ADN
International audienc
Des nanoparticules à base de fullerènes C60 fonctionnalisées par polyethylenimine et PEG pour delivrance d’ADN
International audienc
Transfection-capable polycationic nanovectors which include PEGylated-cyclodextrin structural units: a new synthesis pathway
Polycationic nanoentities with low variability are able to act as cooperating carriers for dsDNA complexation and transport.</p
Inclusion complexes of propiconazole nitrate with substituted β-cyclodextrins: the synthesis and in silico and in vitro assessment of their antifungal properties
Inclusion complexes with sulfobutylether-β-cyclodextrin, β-cyclodextrin sulphated sodium salt and monochlorotriazinyl-β-cyclodextrin were characterized and assessed for antifungal activity and cytotoxicity.</p
Hybrid fullerene conjugates as vectors for DNA cell-delivery
C60-PEI and C60-PEG-PEI as efficient binders of dsDNA, with good transfection up to 25%, high cytocompatibility and cell proliferation up to 200%.</p
