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1.
International Journal of Biomedical Engineering ; (6): 245-250, 2023.
Article in Chinese | WPRIM | ID: wpr-989346

ABSTRACT

Black phosphorus, as a novel two-dimensional nanomaterial, has received a lot of attention from researchers for its unique structure and properties. In recent years, with the increasing cross-sectional research related to black phosphorus 2D nanomaterials in various fields such as materials science, physics, chemistry, biology, and medicine, it has shown great potential for development and application in biomedicine. The excellent photoacoustic properties and good biocompatibility of black phosphorus 2D nanomaterials make them outstanding in tumor diagnosis and treatment. In this paper, the structure and properties, preparation, and functional modification of black phosphorus two-dimensional nanomaterials and their potential applications in the bio-detection and treatment of tumors, as well as the application progress of antibacterial were reviewed.

2.
Chinese Pharmacological Bulletin ; (12): 1535-1538, 2014.
Article in Chinese | WPRIM | ID: wpr-460029

ABSTRACT

Aim To construct eukaryotic expressing plasmid of hi FGF2 ( high molecular weight isoform fi-broblast growth factor-2,hi FGF2) gene and to investi-gate its effect on apoptosis after its overexpression in HEK293 cells. Methods The DNA template primer was designed and synthesized. The pDsRed1-N1 plas-mids were digested by the restriction enzymes of Nhel and Hind III. The hi FGF2 was ligated with linearized pDsRed1-N1 by T4 DNA Ligase. The recombinant plasmid was identified by endonuclease digestion and sequenced. The recombinant hi FGF2 plasmid was transient transfected into HEK293 cells by Lipofectami-neTM 2000 Reagent. The transfection efficiency was de-tected by fluorescence inversion microscope. The cell apoptosis was detected by Annexin V-FITC/PI apopto-sis detection kit with flow cytometry analysis. Results The pDsRed1-N1 eukaryotic expression vector was consistent with the design. The recombinant hi FGF2 plasmid was transfected in HEK293 cells. The trans-fection rate was more than 70%. The FITC/PI dyeing rate in hi-FGF2 over-expression HEK297 cells was a-bout ( 29. 12 ± 2. 81 )%. Conclusions pDsRed1-N1 eukaryotic expression vector is successfully constructed and transfected into HEK293 cells. Over-expression of hi FGF2 induces cell apoptosis.

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