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1.
Sci Rep ; 11(1): 3357, 2021 02 08.
Artículo en Inglés | MEDLINE | ID: mdl-33558597

RESUMEN

Burn injuries are most challenging to manage since it causes loss of the integrity of large portions of the skin leading to major disability or even death. Over the years, hydrogels are considered as a significant delivery system for wound treatment because of several advantages over other conventional formulations. We hypothesized that the bFGF-collagen-AgSD incorporated hydrogel formulation can accelerate the rate of burn healing in animal model and would promote fibroblast cell proliferation. Neovascularization and re-epithelialization is a hall mark of burn wound healing. In the present study, histopathological investigation and scanning electron microscopy of skin tissue of Wistar rats showed almost complete epithelialisation after 16 days in the treatment group. The developed hydrogel showed significantly accelerated wound closure compared with a standard and control group. The faster wound closure resulted from increased re-epithelialization and granulation tissue formation because of the presence of collagen and growth factor. Expressions of proteins such as TrkA, p- TrkA, ERK1/2, p-ERK1/2, NF-kß, and p-NF-kß involved in nerve growth factor (NGF) signalling pathway were analysed by western blot. All the findings obtained from this study indicated that the hydrogel can be considered as a promising delivery system against second degree burn by faster healing.


Asunto(s)
Quemaduras , Colágeno/farmacología , Factor 2 de Crecimiento de Fibroblastos/farmacología , Hidrogeles/farmacología , Sistema de Señalización de MAP Quinasas/efectos de los fármacos , Animales , Quemaduras/tratamiento farmacológico , Quemaduras/metabolismo , Quemaduras/patología , Colágeno/química , Factor 2 de Crecimiento de Fibroblastos/química , Hidrogeles/química , Inflamación/tratamiento farmacológico , Inflamación/metabolismo , Inflamación/patología , Proteína Quinasa 1 Activada por Mitógenos/metabolismo , Proteína Quinasa 3 Activada por Mitógenos/metabolismo , Ratas , Ratas Wistar , Receptor trkA/metabolismo
2.
Mater Sci Eng C Mater Biol Appl ; 72: 415-424, 2017 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-28024604

RESUMEN

One-pot synthesis methods for development of hydrophilic imaging nanoprobes have advantages over multi-pot methods due to their simple procedures, less probability for degradation of efficiency, superior control over growth and morphology, cost effectiveness, improved scope for scale-up synthesis etc. Here, we present a novel one-pot facile synthesis of hydrophilic colloidal bimodal nanoprobe (FePt-CdS) prepared through a seed-mediated nucleation and growth technique. In this facile synthesis of complex nanostructure, glutathione (GSH) was used as the capping agent to render biocompatibility and dispersibility. The microstructure, surface, optical, magnetic, biocompatibility, relaxivity and imaging property of the developed nanoprobe have been studied. The microstructural characterizations reveal average size of the particle as ~9-11nm with bleb shaped morphology. Spectroscopic characterization depicts the development of GSH capped CdS QDs on FePt, surface functionalities and their stability. The magnetic measurements confirm the superparamagnetic property in the developed bimodal nanoprobe. In addition, the GSH capping imparts excellent biocompatibility, water dispersibility, and fluorescence property to the probe. In RAW 264.7 macrophage cells, the bimodal nanoprobes exhibit intense green and red fluorescence. The magnetic resonance imaging (MRI) and fluorescence imaging (FI) study depict high transverse relaxivity and visible range fluorescent property in the synthesized FePt-CdS nanoprobe. Hence, the developed bimodal nanoprobe can be used as a potential candidate in simultaneous FI and MR imaging.


Asunto(s)
Materiales Biocompatibles/química , Compuestos de Cadmio/química , Glutatión/química , Platino (Metal)/química , Puntos Cuánticos/química , Sulfuros/química , Animales , Materiales Biocompatibles/toxicidad , Supervivencia Celular/efectos de los fármacos , Interacciones Hidrofóbicas e Hidrofílicas , Imagen por Resonancia Magnética , Magnetismo , Ratones , Microscopía Electrónica de Transmisión , Microscopía Fluorescente , Puntos Cuánticos/toxicidad , Células RAW 264.7 , Espectrometría por Rayos X , Propiedades de Superficie , Difracción de Rayos X
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