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Dual-modal imaging and excellent anticancer efficiency of cisplatin and doxorubicin loaded NaGdF(4):Yb(3+)/Er(3+) nanoparticles

NaGdF(4):Yb(3+)/Er(3+) nanoparticles were synthesized via a modified hydrothermal route. The dependence of structure and morphology on the dosage of sodium polyacrylate was studied by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The as-prepared nanoparticles could be used for...

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Detalles Bibliográficos
Autores principales: Zhang, Zhiyang, Sheng, Jiayi, Zhang, Miaomiao, Ma, Xiaoyan, Geng, Zhirong, Wang, Zhilin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081283/
https://www.ncbi.nlm.nih.gov/pubmed/35541744
http://dx.doi.org/10.1039/c8ra03898h
Descripción
Sumario:NaGdF(4):Yb(3+)/Er(3+) nanoparticles were synthesized via a modified hydrothermal route. The dependence of structure and morphology on the dosage of sodium polyacrylate was studied by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The as-prepared nanoparticles could be used for T(2) weighted magnetic resonance imaging due to the paramagnetism of Gd(3+). cis-dichlorodiamineplatinum (CDDP) could be loaded onto NaGdF(4):Yb(3+)/Er(3+) nanoparticles through binding carboxyl in the form of Pt–O bonds, and doxorubicin (DOX) could be loaded via hydrogen bonding. DOX could also be loaded onto the NaGdF(4)–CDDP composite in the same manner, and the loading efficiency of both drugs remained unchanged. Three as-prepared drug delivery systems were used for tumor inhibition both in vitro and in vivo, and the results indicated that NaGdF(4)–CDDP–DOX displayed the greatest inhibitory capacity.