Biodegradable poly(L-lactide-r-trimethene carbonate) copolymers (P(LLA-co-TMC)) with different compositions were synthesized. The degradation of the copolymers was carried out in phosphate buffer saline solutions (pH = 7.4) at 37 °C. The compositions, structure and properties of the copolymers in degradation were characterized with 1H-NMR, DSC, XRD, GPC, and SEM. The weight loss of the P(LLA-co-TMC) 50/50 was much faster than that of P(LLA-co-TMC) 85/15 and PLLA homopolymer. Interestingly, though the molecular weight of the compolymers decreased greatly during degradation, the compositions were rarely varied. After long time degradation, the PLLA segments were induced to crystallize in the P(LLA-co-TMC) 85/15 copolymer. The SEM observation of the surface and cross-section of P(LLA-co-TMC) 85/15 copolymer films found it was similar to the bulk degradation of PLLA homopolymer.
Inorganic polyhedral oligomeric silsesquioxane(POSS) was used as the core for the synthesis of poly(Llysine) peptide dendrimer via copper-catalyzed azide–alkyne click chemistry. The inorganic/organic composite dendrimer was characterized by MS,1H NMR, FTIR, GPC and DLS.
α-Cyclodextrin/poly(ethylene glycol)(α-CD/PEG) polyrotaxane nanoparticles were prepared via a self-assembly method. Anticancer drug methotrexate(MTX) was loaded in the nanoparticles. The interaction between MTX and polyrotaxane was investigated. The formation, morphology, drug release and in vitro anticancer activity of the MTX loaded polyrotaxane nanoparticles were studied. The results show that the MTX could be efficiently absorbed on the nanoparticles, and hydrogen bonds were formed between MTX andα-CDs. The typical channel-type stacking assembly style of polyrotaxane nanoparticles was changed after MTX was loaded. The mean diameter of drug loaded polyrotaxane nanoparticles were around 200 nm and the drug loading content was as high as about 20%. Drug release profiles show that most of the loaded MTX was released within 8 hours and the cumulated release rate was as high as 98%. The blank polyrotaxane nanoparticles were nontoxicity to cells. The in vitro anticancer activity of the MTX loaded polyrotaxane nanoparticles was higher than that of free MTX.
A novel method to prepare crosslinked polyethyleneimine(CPEI)hollow nanospheres was reported.Uniform silica nanospheres were used as templates,3-aminopropyl trimethoxysilane(APS)was immobilized on the surface of silica nanospheres as couple agent.Aziridine was initiated ring-opening polymerization with the amino groups in APS to form polyethyleneimine(PEI)shell layer.1,4-Butanediol diacrylate was utilized to crosslink PEI polymeric shell.The silica nanospheres in core were etched by hydrofluoric acid to obtain hollow CPEI nanospheres.The hollow nanospheres were characterized by X-ray photoelectron spectroscopy(XPS),transmission electron microscopy(TEM),and thermogravimetric analysis(TGA).
Inclusion complexes(ICs) composed ofα-cyclodextrins(α-CD) and biodegradable comblike copolymers with poly(α,β-malic acid)(PMA) backbones and methylated poly(ethylene glycol)(mPEG) side chains were prepared by the host-guest reaction.Two series of ICs with mPEG750 and mPEG2000 were prepared.The stoichiometry(EG/CD) of all the ICs in mPEG2000 series was 3.1,no matter what the graft degree was.While in mPEG750 series,the stoichiometry(EG/CD) was very different:it increased with the amount of mPEG decreasing...
