Daunorubicin and gambogic acid co-loaded cysteamine-CdTe quantum dots minimizing the multidrug resistance of lymphoma in vitro and in vivo


Autoria(s): Zhou, Yi; Wang, Ruju; Chen, Bing; Sun, Dan; Hu, Yong; Xu, Peipei
Data(s)

18/10/2016

Resumo

To minimize the side effects and the multidrug resistance (MDR) arising from daunorubicin (DNR) treatment of malignant lymphoma, a chemotherapy formulation of cysteamine-modified cadmium tellurium (Cys-CdTe) quantum dots coloaded with DNR and gambogic acid (GA) nanoparticles (DNR-GA-Cys-CdTe NPs) was developed. The physical property, drug-loading efficiency and drug release behavior of these DNR-GA-Cys-CdTe NPs were evaluated, and their cytotoxicity was explored by 3-[4,5-dimethylthiazol-2-y1]-2,5-diphenyltetrazolium bromide assay. These DNR-GA-Cys-CdTe NPs possessed a pH-responsive behavior, and displayed a dose-dependent antiproliferative activity on multidrug-resistant lymphoma Raji/DNR cells. The accumulation of DNR inside the cells, revealed by flow cytometry assay, and the down-regulated expression of P-glycoprotein inside the Raji/DNR cells measured by Western blotting assay indicated that these DNR-GA-Cys-CdTe NPs could minimize the MDR of Raji/DNR cells. This multidrug delivery system would be a promising strategy for minimizing MDR against the lymphoma.

Formato

application/pdf

Identificador

http://pure.qub.ac.uk/portal/en/publications/daunorubicin-and-gambogic-acid-coloaded-cysteaminecdte-quantum-dots-minimizing-the-multidrug-resistance-of-lymphoma-in-vitro-and-in-vivo(5df2015a-9319-4c48-ae71-1e9a74383ac1).html

http://dx.doi.org/0.2147/IJN.S115037

http://pure.qub.ac.uk/ws/files/114951749/Daunorubicin_and_gambogic_ac.pdf

Idioma(s)

eng

Direitos

info:eu-repo/semantics/openAccess

Fonte

Zhou , Y , Wang , R , Chen , B , Sun , D , Hu , Y & Xu , P 2016 , ' Daunorubicin and gambogic acid co-loaded cysteamine-CdTe quantum dots minimizing the multidrug resistance of lymphoma in vitro and in vivo ' International Journal of Nanomedicine , vol 2016 , no. 11 , pp. 5429-5442 . DOI: 0.2147/IJN.S115037

Tipo

article