Engineering metalloporphyrin-integrated nanosystems for targeted sono-/ chemo- dynamic therapy of leptomeningeal carcinomatosis through intrathecal administration

被引:17
作者
Niu, Huicong [1 ,2 ,3 ]
Chen, Jiajie [2 ,4 ]
Jin, Jie [1 ,5 ]
Qi, Xuejiao [1 ]
Bai, Kaixuan [1 ]
Shu, Chaoqin [2 ,6 ]
Wu, Aijun [2 ,6 ]
Xiao, Yin [7 ,8 ]
Wu, Chengtie [2 ,4 ]
Bu, Hui [1 ]
Zhu, Yufang [2 ,4 ]
机构
[1] Hebei Med Univ, Hosp 2, Shijiazhuang 050000, Hebei, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 200050, Peoples R China
[3] Hebei Gen Hosp, Dept Neurol, Shijiazhuang 050000, Hebei, Peoples R China
[4] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
[5] Third Hosp Shijiazhuang, Shijiazhuang 050000, Hebei, Peoples R China
[6] Univ Shanghai Sci & Technol, Sch Mat Sci & Engn, Shanghai 200093, Peoples R China
[7] Queensland Univ Technol, Ctr Biomed Technol, Tissue Engn & Bone Res, Brisbane, Qld, Australia
[8] Australia China Ctr Tissue Engn & Regenerat Med, Brisbane, Qld, Australia
关键词
Leptomeningeal carcinomatosis; Nanomedicine; Intrathecal injection; Sonodynamic therapy; Chemodynamic therapy; METAL-ORGANIC FRAMEWORKS; BREAST-CANCER; TUMOR; NANOPARTICLES; METASTASIS; SURVIVAL; DELIVERY; RELEASE; OXYGEN;
D O I
10.1016/j.cej.2022.135373
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Leptomeningeal carcinomatosis (LMC) is a severe complication of cancers that markedly shortens survival and lowers the quality of patients' life, and it still lacks adequate therapeutic programs. Nanomedicine-mediated therapy has recently presented promising to treat malignant tumors, whereas it remains challenging to deliver nanomedicines for high-efficacy LMC treatment owing to the existence of brain-related delivery barriers. Herein, a novel and effective strategy of combined sonodynamic/chemodynamic therapy (SDT/CDT) of LMC by intrathecal injection of a tumor-targeted metalloporphyrin-integrated nanosystem (MOF@MP-RGD) is developed for the first time. Thereinto, intrathecal administration can directly transport such nanosystems into the cerebrospinal fluid (CSF) around the brain and spinal cord to overcome the brain-related barriers for improving delivery. By building of the orthotopic LMC model, the nanosystems are demonstrated to be effectively accumulated in the LMC area post intrathecal administration due to the arginine-glycine-aspartate (RGD) active targeting, and subsequently excreted out of the body by metabolism process. In vivo evaluations reveal the desirable LMC tumor inhibition and survival prolongation of the combined SDT/CDT based on such biocompatible nanosystems, that is superior to the clinically-used chemotherapeutic drug. Therefore, the combination of intrathecal delivery and nanomedicine-mediated therapy holds great potential for clinical LMC treatment.
引用
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页数:13
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