» Articles » PMID: 38264689

Engineered Nanodrug Targeting Oxidative Stress for Treatment of Acute Kidney Injury

Overview
Date 2024 Jan 24
PMID 38264689
Authors
Affiliations
Soon will be listed here.
Abstract

Acute kidney injury (AKI) is a clinical syndrome characterized by a rapid decline in renal function, and is associated with a high risk of death. Many pathological changes happen in the process of AKI, including crucial alterations to oxidative stress levels. Numerous efforts have thus been made to develop effective medicines to scavenge excess reactive oxygen species (ROS). However, researchers have encountered several significant challenges, including unspecific biodistribution, high biotoxicity, and in vivo instability. To address these problems, engineered nanoparticles have been developed to target oxidative stress and treat AKI. This review thoroughly discusses the methods that empower nanodrugs to specifically target the glomerular filtration barrier and presents the latest achievements in engineering novel ROS-scavenging nanodrugs in clustered sections. The analysis of each study's breakthroughs and imperfections visualizes the progress made in developing effective nanodrugs with specific biodistribution and oxidative stress-targeting capabilities. This review fills the blank of a comprehensive outline over current progress in applying nanotechnology to treat AKI, providing potential insights for further research.

Citing Articles

Hierarchical Targeting Nanodrug with Holistic DNA Protection for Effective Treatment of Acute Kidney Injury.

Chen Q, Yang Y, Ying X, Huang C, Chen J, Wang J Adv Sci (Weinh). 2024; 12(6):e2411254.

PMID: 39703158 PMC: 11809360. DOI: 10.1002/advs.202411254.


An enzyme-mimicking reactive oxygen species scavenger targeting oxidative stress-inflammation cycle ameliorates IR-AKI by inhibiting pyruvate dehydrogenase kinase 4.

He W, Ding C, Lin T, Wang B, Wang W, Deng Z Theranostics. 2024; 14(19):7534-7553.

PMID: 39659578 PMC: 11626943. DOI: 10.7150/thno.101229.


Toxic Effects of Synthesized Bismuth Oxide/Reduced Graphene Oxide (BiO/RGO) Nanocomposites in Two Distinct Mammalian Cell Lines: Role Oxidative Stress and Apoptosis.

Lateef R, Ahmad I, Mahdi A, Lohia N, Alhadlaq H, Akhtar M Int J Nanomedicine. 2024; 19:12655-12674.

PMID: 39619053 PMC: 11608047. DOI: 10.2147/IJN.S489874.


Implantation of biomimetic polydopamine nanocomposite scaffold promotes optic nerve regeneration through modulating inhibitory microenvironment.

Pan T, Huang Y, Wei J, Lai C, Chen Y, Nan K J Nanobiotechnology. 2024; 22(1):683.

PMID: 39506841 PMC: 11542345. DOI: 10.1186/s12951-024-02962-y.


Innovative hydrogel-based therapies for ischemia-reperfusion injury: bridging the gap between pathophysiology and treatment.

Wang W, Tai S, Tao J, Yang L, Cheng X, Zhou J Mater Today Bio. 2024; 29:101295.

PMID: 39493810 PMC: 11528235. DOI: 10.1016/j.mtbio.2024.101295.


References
1.
Ziyadeh F . Mediators of diabetic renal disease: the case for tgf-Beta as the major mediator. J Am Soc Nephrol. 2003; 15 Suppl 1:S55-7. DOI: 10.1097/01.asn.0000093460.24823.5b. View

2.
Jiang D, Ge Z, Im H, England C, Ni D, Hou J . DNA origami nanostructures can exhibit preferential renal uptake and alleviate acute kidney injury. Nat Biomed Eng. 2018; 2(11):865-877. PMC: 6258029. DOI: 10.1038/s41551-018-0317-8. View

3.
Jones S, Hancock J, Jones O, Neubauer A, Topley N . The expression of NADPH oxidase components in human glomerular mesangial cells: detection of protein and mRNA for p47phox, p67phox, and p22phox. J Am Soc Nephrol. 1995; 5(7):1483-91. DOI: 10.1681/ASN.V571483. View

4.
Fan Q, Cheng K, Hu X, Ma X, Zhang R, Yang M . Transferring biomarker into molecular probe: melanin nanoparticle as a naturally active platform for multimodality imaging. J Am Chem Soc. 2014; 136(43):15185-94. PMC: 4227813. DOI: 10.1021/ja505412p. View

5.
Min Y, Caster J, Eblan M, Wang A . Clinical Translation of Nanomedicine. Chem Rev. 2015; 115(19):11147-90. PMC: 4607605. DOI: 10.1021/acs.chemrev.5b00116. View