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1.
Journal of Prevention and Treatment for Stomatological Diseases ; (12): 586-590, 2019.
Artigo em Chinês | WPRIM | ID: wpr-750437

RESUMO

@#Surface modification of titanium implants is a hot topic for improving osteointegration and includes physical, chemical, bioactive and anodization methods. Among these methods, anodization methods can form TiO2 nanotube structures with a uniform and stable structure, and TiO2 nanotubes and substrates have high binding strengths and osteogenic properties and represent an excellent method for implant modification. TiO2 nanotube osteogenesis is closely related to its morphology, diameter and physicochemical characteristics. Therefore, the structure of TiO2 nanotubes with optimal osteogenic performance can be prepared by regulating these factors. At present, research on TiO2 nanotubes is mostly focused on composite treatments with TiO2 nanotubes, namely, the combination of other implant modification methods (physical method, chemical method, biological method) and TiO2 nanotubes to form a composite structure to work synergistically to treat osteogenesis. TiO2 nanotube composite treatment is a good prospective application for the further preparation of TiO2 nanotube-modified structures with strong osteogenic properties.

2.
Acta cir. bras ; 30(10): 654-659, graf
Artigo em Inglês | LILACS | ID: lil-764395

RESUMO

PURPOSE:To demonstrate the relationship between of sphingosine-1-phosphate (S1P) expression and subarachnoid hemorrhage (SAH).METHODS:The basilar arteries from a "double-hemorrhage" rabbit model of SAH were used to investigate the relation between S1P expression and SAH. Various symptoms, including blood clots, basilar artery cross-sectional area, and S1P phosphatase expression were measured at day 3, 5, 7, 9.RESULTS: The expression of S1P was enhanced in the cerebral vasospasm after subarachnoid hemorrhage in the rabbits. And S1P expression was consistent with the basilar artery cross-sectional area changes at day 3, 5, 7, 9.CONCLUSION: Sphingosine-1-phosphate expression in the cerebral arterial may be a new indicator in the development of cerebral vasospasm after subarachnoid hemorrhage and provide a new therapeutic method for SAH.


Assuntos
Animais , Coelhos , Lisofosfolipídeos/análise , Esfingosina/análogos & derivados , Hemorragia Subaracnóidea/patologia , Vasoespasmo Intracraniano/patologia , Artéria Basilar/patologia , Modelos Animais de Doenças , Citometria de Fluxo , Distribuição Aleatória , Esfingosina/análise , Hemorragia Subaracnóidea/complicações , Hemorragia Subaracnóidea/metabolismo , Fatores de Tempo , Vasoespasmo Intracraniano/etiologia , Vasoespasmo Intracraniano/metabolismo
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