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1.
Chemistry ; 18(11): 3305-15, 2012 Mar 12.
Artigo em Inglês | MEDLINE | ID: mdl-22311805

RESUMO

The use of dendritic structures for the grafting of core-shell γ-Fe(2)O(3)/polymer 300 nm superparamagnetic nanoparticles (MNPs) has been performed with four metallodendrons that were functionalized with diphosphinopalladium complexes. The catalytic performance of these nanocatalysts was optimized for the Suzuki C-C cross-coupling reaction. These results demonstrated the importance of optimizing the catalytic efficiency of grafted MNPs by optimizing the dendritic structures and the nature of the peripheral phosphine ligands. All of these nanocatalysts showed remarkable reactivity towards bromoarenes and they were recovered and efficiently reused by magnetic separation with almost no loss of reactivity, even after 25 cycles.

2.
Colloids Surf B Biointerfaces ; 181: 1019-1025, 2019 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-31382329

RESUMO

Nanoparticles, such as TiO2 particles, have a great potential for biomedical applications due to their ultra-small size and large specific surface area. However, their detection within cells is to date more than challenging. Thus, implementing fluorescence properties to nanoparticles via their controlled functionalisation with an organic chromophore is an original and efficient strategy to enable their visualization. In this work, a silylated coupling agent bearing a luminescent rhodamine B group was synthesised and grafted on the surface of anatase nanoparticles. The successful functionalisation was demonstrated via zeta potential, dynamic light scattering and diffuse reflectance infrared Fourier transform analyses. Remarkably, the obtained luminescent TiO2 particles showed an improved photocatalytic activity compared to the pristine nanoparticles. Both, as-synthesised and functionalised TiO2 nanoparticles samples appear to be non-toxic towards malignant and non-malignant cells. Moreover, the detection of the functionalised particles within cultured cells was proven to be easy and efficient via confocal fluorescence microscopy.


Assuntos
Fluorescência , Nanopartículas/química , Compostos de Organossilício/química , Processos Fotoquímicos , Titânio/química , Pesquisa Biomédica , Catálise , Microscopia Confocal , Microscopia de Fluorescência , Compostos de Organossilício/síntese química , Tamanho da Partícula , Rodaminas/química , Propriedades de Superfície
3.
Colloids Surf B Biointerfaces ; 143: 7-14, 2016 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-26998862

RESUMO

Stable, non-agglomerated TiO2 nanoparticle (NP) dispersions are a crucial requirement for an accurate NP dosing in in vitro and in vivo experiments. In this study self-synthesised TiO2 NPs were stabilised in three different cell culture media (DMEM, RPMI, BEGM) with the help of stabilising agents. Cell culture tested stabilisers (bovine serum albumin, fetal bovine serum) were compared to non-tested commercial products which are commonly utilized in the cement industry (Melflux(®) 4930 F, Melpers(®) 4343, Sika(®) ViscoCrete(®)-10110178). For a quantitative evaluation and comparison of the degree of stabilisation, a sedimentation study using UV absorbance spectroscopy was carried out and the agglomerate size was measured via dynamic light scattering. The cytotoxicity of the novel surfactants and stabilised NPs was examined in a head and neck squamous cell carcinoma-derived FaDu cell line and in human mesenchymal stem cells. We successfully stabilised TiO2 NPs with Melflux(®) 4930 F in each cell culture medium, achieving perfect stability over at least one day and agglomerate sizes of less than 100nm, while the cytotoxicity of the NPs was not affected.


Assuntos
Ácidos Carboxílicos/química , Éteres/química , Nanopartículas Metálicas/química , Titânio/química , Animais , Ácidos Carboxílicos/farmacologia , Bovinos , Linhagem Celular Tumoral , Sobrevivência Celular/efeitos dos fármacos , Meios de Cultura/química , Éteres/farmacologia , Floculação/efeitos dos fármacos , Humanos , Células-Tronco Mesenquimais/citologia , Células-Tronco Mesenquimais/efeitos dos fármacos , Células-Tronco Mesenquimais/fisiologia , Polimerização , Cultura Primária de Células , Soroalbumina Bovina/química , Soluções , Tensoativos/química , Titânio/farmacologia
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