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1.
Artif Organs ; 40(4): 385-93, 2016 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-26526301

RESUMEN

Artificial ligaments utilized in reconstruction of anterior cruciate ligament (ACL) are usually made of polyethylene terepthalate (PET) because of its good mechanical properties in vivo. However, it was found that the deficiencies in hydrophilicity and biocompatibility of PET hindered the process of ligamentization. Therefore, surface modification of the PET is deemed as a solution in resolving such problem. Silk fibroin (SF), which is characterized by good biocompatibility and low immunogenicity in clinical applications, was utilized to prepare a coating on the PET ligament (PET+SF) in this work. At first, decrease of hydrophobicity and appearance of amino groups were found on the surface of artificial PET ligament after coating with SF. Second, mouse fibroblasts were cultured on the two different kinds of ligament in order to clarify the possible effect of SF coating. It was proved that mouse fibroblasts display better adhesion and proliferation on PET+SF than PET ligament according to the results of several technical methods including SEM observation, cell adhesive force and spread area test, and mRNA analysis. Meanwhile, methylthiazolyldiphenyl-tetrazolium bromide and DNA content tests showed that biocompatibility of PET+SF is better than PET ligament. In addition, collagen deposition tests also indicated that the quantity of collagen in PET+SF is higher than PET ligament. Based on these results, it can be concluded that SF coating is suggested to be an effective approach to modify the surface of PET ligament and enhance the "ligamentization" process in vivo accordingly.


Asunto(s)
Materiales Biocompatibles Revestidos/farmacología , Fibroblastos/citología , Fibroínas/farmacología , Ligamentos , Tereftalatos Polietilenos/farmacología , Animales , Adhesión Celular/fisiología , Proliferación Celular/fisiología , Ensayo de Materiales , Ratones
2.
Analyst ; 137(10): 2394-9, 2012 May 21.
Artículo en Inglés | MEDLINE | ID: mdl-22489283

RESUMEN

Recently, metal-selective fluorescent chemosensors have attracted intense attention for their simple and real-time tracking of metal ions in environmental samples. However, most of the existing fluorescent sensors are one-off sensors and thus suffer from large amount of reagent consumption, significant experimental cost and raising the risk of environmental pollution. In this paper, we developed a green (low reagent consumption, low-toxicity reagent use), recyclable, and visual sensor for Cu(2+) in aqueous solution by using a fluorescent gold nanoclusters membrane (FGM) as the sensing unit, basing on our findings on gold nanoclusters (Au NCs) that the bovine serum albumin (BSA)-coated Au NCs exhibit excellent membrane-forming ability under the isoelectric point of BSA, and thus enable us to obtain a new type of sensing membrane (i.e. FGM) by denaturing Au NCs; the fluorescence of FGM can be significantly quenched by Cu(2+) ion, and the quenched fluorescence can be totally recovered by histidine; the as-prepared FGM is very stable and recyclable, which makes it an ideal sensing material.


Asunto(s)
Cobre/análisis , Oro/química , Nanopartículas del Metal/química , Agua/química , Animales , Bovinos , Colorantes Fluorescentes/química , Concentración de Iones de Hidrógeno , Proteínas Inmovilizadas/química , Iones/química , Membranas Artificiales , Albúmina Sérica Bovina/química , Rayos Ultravioleta
3.
Neurosci Res ; 135: 21-31, 2018 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-29288689

RESUMEN

Extracellular/acellular matrix has been attracted much research interests for its unique biological characteristics, and ACM modified neural scaffolds shows the remarkable role of promoting peripheral nerve regeneration. In this study, skin-derived precursors pre-differentiated into Schwann cells (SKP-SCs) were used as parent cells to generate acellular(ACM) for constructing a ACM-modified neural scaffold. SKP-SCs were co-cultured with chitosan nerve guidance conduits (NGC) and silk fibroin filamentous fillers, followed by decellularization to stimulate ACM deposition. This NGC-based, SKP-SC-derived ACM-modified neural scaffold was used for bridging a 10 mm long rat sciatic nerve gap. Histological and functional evaluation after grafting demonstrated that regenerative outcomes achieved by this engineered neural scaffold were better than those achieved by a plain chitosan-silk fibroin scaffold, and suggested the benefits of SKP-SC-derived ACM for peripheral nerve repair.


Asunto(s)
Dermis Acelular , Tratamiento Basado en Trasplante de Células y Tejidos/métodos , Quitosano/química , Fibroínas/química , Traumatismos de los Nervios Periféricos/terapia , Células de Schwann/trasplante , Nervio Ciático/lesiones , Andamios del Tejido , Animales , Materiales Biocompatibles/química , Regeneración Nerviosa , Traumatismos de los Nervios Periféricos/patología , Ratas , Células de Schwann/citología , Células de Schwann/ultraestructura , Nervio Ciático/ultraestructura , Piel/citología , Ingeniería de Tejidos
4.
Sci Rep ; 8(1): 3443, 2018 02 21.
Artículo en Inglés | MEDLINE | ID: mdl-29467542

RESUMEN

The repair of peripheral nerve laceration injury to obtain optimal function recovery remains a big challenge in the clinic. Misdirection of regenerating axons to inappropriate target, as a result of forced mismatch of endoneurial sheaths in the case of end-to-end nerve anastomosis or nerve autografting, represents one major drawback that limits nerve function recovery. Here we tested whether tubulation repair of a nerve defect could be beneficial in terms of nerve regeneration accuracy and nerve function. We employed sequential retrograde neuronal tracing to assess the accuracy of motor axon regeneration into the tibial nerve after sciatic nerve laceration and entubulation in adult Sprague-Dawley rats. In a separate cohort of rats with the same sciatic nerve injury/repair protocols, we evaluated nerve function recovery behaviorally and electrophysiologically. The results showed that tubulation repair of the lacerated sciatic nerve using a 3-6-mm-long bioabsorbable guidance conduit significantly reduced the misdirection of motor axons into the tibial nerve as compared to nerve autografting. In addition, tubulation repair ameliorated chronic flexion contracture. This study suggests that tubulation repair of a nerve laceration injury by utilizing a bioresorbable nerve guidance conduit represents a potential substitute for end-to-end epineurial suturing and nerve autografting.


Asunto(s)
Regeneración Tisular Dirigida/métodos , Traumatismos de los Nervios Periféricos/terapia , Nervio Ciático/lesiones , Animales , Axones/patología , Materiales Biocompatibles/uso terapéutico , Femenino , Regeneración Nerviosa , Traumatismos de los Nervios Periféricos/fisiopatología , Ratas Sprague-Dawley , Recuperación de la Función , Nervio Ciático/fisiopatología , Andamios del Tejido
6.
Int J Nanomedicine ; 9: 4569-80, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-25302023

RESUMEN

BACKGROUND: Application of artificial ligament in anterior cruciate ligament reconstruction is one of the research focuses of sports medicine but the biological tendon-bone healing still remains a problem. The preliminary study of hydroxyapatite (HAP) coating on the polyethylene terephthalate (PET) surface could effectively induce the osteoblast differentiation, but the tendon-bone healing was still not stable. As a green synthesis process, the biomimetic mineralization can simulate the natural bone growth in vitro and in vivo. METHODS: HAP crystals were grown under the guide of silk fibroin (SF) PET surface by biomimetic route. Several techniques including scanning electron microscopy, attenuated total reflectance Fourier transform infrared spectroscopy, X-ray diffraction, and energy-dispersive X-ray spectroscopy were utilized for proving the introduction of both SF and HAP. The viability and osseointegration of bone marrow stromal cells on the surface of three kinds of ligament, including PET group (non-coating group), PET+SF group (SF-coating group), and PET+SF+HAP group (combined HAP- and SF-coating group), were analyzed by CCK-8 assays and alkaline phosphatase (ALP) detection. Seventy-two mature male New Zealand rabbits were randomly divided into three groups. Among them, 36 rabbits were sacrificed for mechanical testing, and histological examination for the others. RESULTS: The SF and SF+HAP were successfully coated on the surface of PET fiber. The CCK-8 assay showed that the cell proliferation on PET+SF+HAP group was better than the other two groups from 24 to 120 hours. After 14 days of culture, the cells in the PET+SF+HAP group delivered higher levels of ALP than the other two groups. After 3 days of culture, the expression level of integrin ß1 in the PET+SF+HAP group and PET+SF group were higher than in the PET group. The mean load to failure and the stiffness value of the PET+SF+HAP group were both higher than the other two groups. Hematoxylin and eosin staining showed that new bone tissue formation was only found in the PET+SF+HAP group 8 weeks postoperatively. Masson staining showed that in the PET+SF+HAP group 8 weeks postoperatively, the PET fibers were almost completely encircled by collagen. Histomorphometric analysis showed that the width of the graft-bone interface in the PET+SF+HAP group was narrower than that in the other two groups 4 and 8 weeks postoperatively. The mRNA level of BMP-7 in the PET+SF+HAP groups was significantly higher than those in the other two groups 4 and 8 weeks postoperatively. CONCLUSION: The study showed that the combined SF and HAP coating by biomimetic route on the surface of PET artificial ligament could induce graft osseointegration in the bone tunnel, providing theoretical and experimental foundation for manufacturing novel artificial ligaments meeting the clinical needs.


Asunto(s)
Materiales Biocompatibles Revestidos/farmacología , Durapatita/farmacología , Fibroínas/farmacología , Oseointegración/efectos de los fármacos , Tereftalatos Polietilenos/química , Prótesis e Implantes , Cicatrización de Heridas/efectos de los fármacos , Animales , Huesos/efectos de los fármacos , Huesos/lesiones , Huesos/patología , Adhesión Celular/efectos de los fármacos , Diferenciación Celular/efectos de los fármacos , Proliferación Celular/efectos de los fármacos , Materiales Biocompatibles Revestidos/química , Colágeno/metabolismo , Durapatita/química , Fibroínas/química , Ligamentos/efectos de los fármacos , Ligamentos/fisiología , Masculino , Conejos
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