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1.
J Nanosci Nanotechnol ; 20(12): 7398-7405, 2020 12 01.
Artigo em Inglês | MEDLINE | ID: mdl-32711606

RESUMO

Enzyme immobilization has demonstrated effective means for extending protein stability and shelf life. However, current methods negatively affect the enzyme activity, particularly for application purposes. Herein, the amino functionalized graphene oxide (GO-NH2) was synthesized and used to covalently immobilize lactase. FT-IR, UV-Vis, SEM, TEM and XPS were employed to confirm and characterize the immobilized lactase. At the resulting optimal temperature, the immobilization rate achieved 61% and the immobilized lactase maintained approximately 95% of catalyst activity. Compared with the free lactase, used as a control, the immobilized lactase was significantly more stable within acidic or basic environments, higher temperature conditions and had multiple recycle use characteristics. Furthermore, the immobilized lactase had a preserved 87% activity after storage at 4 °C for 30 days, while the free lactase was almost deactivated after 20 days under the same storage conditions. This work conforms that the amino-functionalized graphene oxide is a potential support material for lactase immobilization and can be extended to use with a variety of enzymes for a number of applications.


Assuntos
Enzimas Imobilizadas , Grafite , Estabilidade Enzimática , Enzimas Imobilizadas/metabolismo , Concentração de Íons de Hidrogênio , Espectroscopia de Infravermelho com Transformada de Fourier , Temperatura
2.
J Nanosci Nanotechnol ; 10(12): 8562-74, 2010 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-21121367

RESUMO

The expanded application of carbon nanotubes and increased annual production has recently sparked public interest concerning associated and potentially adverse exposure effects. As very little is known with regard to the toxicology and underlying mechanism of the phenomena termed "single-walled carbon nanotube (SWCNT) exposure", we conducted an in depth investigation of potential SWCNT effects on cell adhesion molecule gene expression within rat aortic endothelial cells (RAECs). RAEC exposure to SWCNT induced neutrophil adhesion to the endothelial monolayer via increased ICAM-1 and VCAM-1 expression. Due to NF-kappaB's fundamental involvement in the transcriptional regulation of cell adhesion molecules, we studied NF-kappaB/P65 activation in SWCNT treated RAECs, as well as GSH and LDH as determinants of oxidative stress, a condition that influences NF-kappaB activation. Resultant data indicates SWCNT exposure induces oxidative stress, thereby altering ICAM-1 and VCAM-1 expression. SWCNT induced nuclear NF-kB/P65 translocation can be inhibited by N-acetylcysteine, indicating elevated ICAM-1 and VCAM-1 expression is mediated by oxidative stress in RAECs, and may play important inflammatory roles in SWCNT-induced vascular endothelium damage.


Assuntos
Células Endoteliais/efeitos dos fármacos , Molécula 1 de Adesão Intercelular/biossíntese , Nanotubos de Carbono/toxicidade , Molécula 1 de Adesão de Célula Vascular/biossíntese , Acetilcisteína/farmacologia , Análise de Variância , Animais , Aorta/citologia , Aorta/efeitos dos fármacos , Aorta/metabolismo , Adesão Celular/efeitos dos fármacos , Sobrevivência Celular/efeitos dos fármacos , Células Cultivadas , Citocinas/metabolismo , Relação Dose-Resposta a Droga , Células Endoteliais/metabolismo , Expressão Gênica/efeitos dos fármacos , Glutationa/metabolismo , Histocitoquímica , Molécula 1 de Adesão Intercelular/genética , L-Lactato Desidrogenase/metabolismo , Mitocôndrias/química , Mitocôndrias/efeitos dos fármacos , Mitocôndrias/metabolismo , Nanotubos de Carbono/química , Ratos , Espécies Reativas de Oxigênio/metabolismo , Transdução de Sinais/efeitos dos fármacos , Molécula 1 de Adesão de Célula Vascular/genética
3.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-545353

RESUMO

Objective To study the oxidative damage on testis of male rats induced by micro-nano-scale SiO2. Methods Male Wistar rats were exposed to nanometer SiO2(20-40 nm) and micro-meter SiO2(1-10 ?m)by intratracheal injection once two days. The rats were killed after 5 weeks of exposure. Some indicators related to the oxidative damage in the serum and the testis were determined. Results The activity of GSH-Px and SOD in the high dose groups decreased significantly and the MDA levels increased compared to the control group;The MDA levels of nano-silicon dioxide high dose group increased in the serum. Conclusion Nano-silicon dioxide may cause lipid peroxidation in the testis with a tendency of higher toxicity than that of micro-SiO2 at the same exposed level,the detail mechanism needs further discussion.

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