Multifunctional Nanotheranostics for Dual-Modal Imaging-Guided Precision Therapy of Nasopharyngeal Carcinoma

被引:3
作者
Yang, Qianyu [1 ]
Guo, Yingkun [2 ]
Zhou, Yang [3 ]
Song, Jiali [1 ]
Song, Yujun [3 ]
Li, Hanmei [4 ]
Gao, Huile [3 ]
Huang, Weiyuan [1 ]
机构
[1] Hainan Med Univ, Hainan Gen Hosp, Dept Radiol, Hainan Affiliated Hosp, Haikou 570311, Hainan, Peoples R China
[2] Sichuan Univ, West China Univ Hosp 2, Key Lab Birth Defects & Related Dis Women & Childr, Dept Radiol,Minist Educ, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Univ, West China Sch Pharm, Key Lab Drug Targeting & Drug Delivery Syst, Chengdu 610064, Sichuan, Peoples R China
[4] Chengdu Univ, Sch Food & Biol Engn, Chengdu 610106, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
nanotheranostic; magnetic resonance imaging; photodynamic therapy; imaging-guided therapy; nasopharyngealcarcinoma; PHOTODYNAMIC THERAPY; NANOPARTICLES; RADIOTHERAPY;
D O I
10.1021/acs.molpharmaceut.3c00491
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Currently, the low survival rate and poor prognosis ofpatientswith nasopharyngeal carcinoma are ascribed to the lack of early andaccurate diagnosis and resistance to radiotherapy. In parallel, theintegration of imaging-guided diagnosis and precise treatment hasgained much attention in the field of theranostic nanotechnology.However, constructing dual-modal imaging-guided nanotheranostics withdesired imaging performance as well as great biocompatibility remainschallenging. Therefore, we developed a simple but multifunctionalnanotheranostic GdCPP for the early and accurate diagnosis and efficienttreatment of nasopharyngeal carcinoma (NPC), which combined fluorescenceimaging and magnetic resonance imaging (MRI) onto a single nanoplatformfor imaging-guided subsequent photodynamic therapy (PDT). GdCPP hadan appropriate particle size (81.93 & PLUSMN; 0.69 nm) and was highlystable, resulting in sufficient tumor accumulation, which along withmassive reactive oxygen species (ROS) generation upon irradiationfurther significantly killed tumor cells. Moreover, GdCPP owned muchstronger r (1) relaxivity (9.396 mM(-1) s(-1)) compared to clinically used Gd-DTPA (5.034mM(-1) s(-1)) and exhibited better T 1WI MRI performance. Under dual-modal imaging-guidedPDT, GdCPP achieved efficient therapeutic outcomes without causingany noticeable tissue damage. The results of in vitro and in vivo studies indicated that GdCPP may bea suitable candidate for dual-modal imaging-guided precision tumortherapy.
引用
收藏
页码:4743 / 4757
页数:15
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