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1.
J Colloid Interface Sci ; 620: 419-430, 2022 Aug 15.
Artículo en Inglés | MEDLINE | ID: mdl-35439693

RESUMEN

Cervical cancer is one of the most common cancers affecting women worldwide. There are an estimated 570.000 new cases of cervical cancer each year and conventional treatments can cause severe side effects. In this work, we developed a platform for vaginal administration of lipophilic drugs for cervical cancer treatment. We formulated mucoadhesive cubosomes for the delivery of curcumin, a lipophilic drug for cervical cancer treatment, to increase its bioavailability and local absorption. This study tests the use of cubosomes for vaginal drug administration and assesses their potential efficiency using the CAM (chick embryo chorioallantoic membrane) model. SAXS (small-angle X-ray scattering), cryo-TEM (cryo-transmission electron microscopy), and dynamic light scattering (DLS) were employed to characterise the system. With ex vivo permeation and retention studies, we find that the curcumin released from our system is retained in the vaginal mucosa. In vitro cytotoxicity assay and cellular uptake showed an increased cytotoxic effect of curcumin against HeLa cell line when incorporated into the cubosomes. The curcumin-loaded cubosomes also demonstrated an antiangiogenic effect evaluated in vivo by the CAM model.


Asunto(s)
Curcumina , Neoplasias del Cuello Uterino , Animales , Embrión de Pollo , Curcumina/farmacología , Femenino , Células HeLa , Humanos , Dispersión del Ángulo Pequeño , Neoplasias del Cuello Uterino/tratamiento farmacológico , Difracción de Rayos X
2.
Int J Nanomedicine ; 11: 4865-4874, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27703352

RESUMEN

PURPOSE: The aim of the present study was to develop nanoprobes with theranostic features, including - at the same time - photoacoustic, near-infrared (NIR) optical imaging, and photothermal properties, in a versatile and stable core-shell silica-polyethylene glycol (PEG) nanoparticle architecture. MATERIALS AND METHODS: We synthesized core-shell silica-PEG nanoparticles by a one-pot direct micelles approach. Fluorescence emission and photoacoustic and photothermal properties were obtained at the same time by appropriate doping with triethoxysilane-derivatized cyanine 5.5 (Cy5.5) and cyanine 7 (Cy7) dyes. The performances of these nanoprobes were measured in vitro, using nanoparticle suspensions in phosphate-buffered saline and blood, dedicated phantoms, and after incubation with MDA-MB-231 cells. RESULTS: We obtained core-shell silica-PEG nanoparticles endowed with very high colloidal stability in water and in biological environment, with absorption and fluorescence emission in the NIR field. The presence of Cy5.5 and Cy7 dyes made it possible to reach a more reproducible and higher doping regime, producing fluorescence emission at a single excitation wavelength in two different channels, owing to the energy transfer processes within the nanoparticle. The nanoarchitecture and the presence of both Cy5.5 and Cy7 dyes provided a favorable agreement between fluorescence emission and quenching, to achieve optical imaging and photoacoustic and photothermal properties. CONCLUSION: We obtained rationally designed nanoparticles with outstanding stability in biological environment. At appropriate doping regimes, the presence of Cy5.5 and Cy7 dyes allowed us to tune fluorescence emission in the NIR for optical imaging and to exploit quenching processes for photoacoustic and photothermal capabilities. These nanostructures are promising in vivo theranostic tools for the near future.


Asunto(s)
Neoplasias de la Mama/patología , Colorantes Fluorescentes/química , Imagen Multimodal/métodos , Nanopartículas/química , Técnicas Fotoacústicas/métodos , Polietilenglicoles/química , Dióxido de Silicio/química , Benzotiazoles/metabolismo , Neoplasias de la Mama/diagnóstico por imagen , Carbocianinas/metabolismo , Colorantes/metabolismo , Femenino , Fluorescencia , Humanos , Hipertermia Inducida/métodos , Micelas , Nanoestructuras/química , Imagen Óptica/métodos , Fototerapia , Células Tumorales Cultivadas
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