Wei Hao, Jiang Dawei, Yu Bo, Ni Dalong, Li Mengting, Long Yin, Ellison Paul A, Siamof Cerise M, Cheng Liang, Barnhart Todd E, Im Hyung-Jun, Yu Faquan, Lan Xiaoli, Zhu Xiaohua, He Qianjun, Cai Weibo
Department of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Departments of Radiology and Medical Physics, University of Wisconsin-Madison, Madison, WI, 53705, USA.
Bioact Mater. 2022 Apr 23;19:282-291. doi: 10.1016/j.bioactmat.2022.04.006. eCollection 2023 Jan.
Acute kidney injury (AKI) leads to unacceptably high mortality due to difficulties in timely intervention and less efficient renal delivery of therapeutic drugs. Here, a series of polyvinylpyrrolidone (PVP)-curcumin nanoparticles (PCurNP) are designed to meet the renal excretion threshold (∼45 kDa), presenting a controllable delivery nanosystem for kidney targeting. Renal accumulation of the relatively small nanoparticles, Zr-PCurNP M10 with the diameter between 5 and 8 nm, is found to be 1.7 times and 1.8 times higher than the accumulation of Zr-PCurNP M29 (20-50 nm) and M40 (20-50 nm) as revealed by PET imaging. Furthermore, serum creatinine analysis, kidney tissues histology, and tubular injury scores revealed that PCurNP M10 efficiently treated cisplatin-induced AKI. Herein, PCurNP offers a novel and simple strategy for precise PET image-guided drug delivery of renal protective materials.
急性肾损伤(AKI)由于难以及时干预且治疗药物的肾脏递送效率较低,导致死亡率高得令人难以接受。在此,设计了一系列聚乙烯吡咯烷酮(PVP)-姜黄素纳米颗粒(PCurNP)以满足肾脏排泄阈值(约45 kDa),从而呈现一种用于肾脏靶向的可控递送纳米系统。PET成像显示,直径在5至8纳米之间的相对较小的纳米颗粒Zr-PCurNP M10在肾脏中的蓄积量分别比Zr-PCurNP M29(20 - 50纳米)和M40(20 - 50纳米)高1.7倍和1.8倍。此外,血清肌酐分析、肾脏组织组织学检查和肾小管损伤评分显示,PCurNP M10能有效治疗顺铂诱导的急性肾损伤。在此,PCurNP为精确的PET图像引导下肾脏保护材料的药物递送提供了一种新颖且简单的策略。