4.8 Review

Nanodrugs alleviate acute kidney injury: Manipulate RONS at kidney

Journal

BIOACTIVE MATERIALS
Volume 22, Issue -, Pages 141-167

Publisher

KEAI PUBLISHING LTD
DOI: 10.1016/j.bioactmat.2022.09.021

Keywords

Reactive oxygen and nitrogen species; Acute kidney injury; Nanomaterials; Antioxidant therapy; Renal physiology

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This review article introduces the potential and advantages of nanodrugs in treating acute kidney injury (AKI). Traditional small molecule drugs have limitations in AKI treatment, while nanodrugs with kidney targeting ability can overcome these limitations and achieve significant therapeutic effects.
Currently, there are no clinical drugs available to treat acute kidney injury (AKI). Given the high prevalence and high mortality rate of AKI, the development of drugs to effectively treat AKI is a huge unmet medical need and a research hotspot. Although existing evidence fully demonstrates that reactive oxygen and nitrogen species (RONS) burst at the AKI site is a major contributor to AKI progression, the heterogeneity, complexity, and unique physiological structure of the kidney make most antioxidant and anti-inflammatory small molecule drugs inef-fective because of the lack of kidney targeting and side effects. Recently, nanodrugs with intrinsic kidney tar-geting through the control of size, shape, and surface properties have opened exciting prospects for the treatment of AKI. Many antioxidant nanodrugs have emerged to address the limitations of current AKI treatments. In this review, we systematically summarized for the first time about the emerging nanodrugs that exploit the patho-logical and physiological features of the kidney to overcome the limitations of traditional small-molecule drugs to achieve high AKI efficacy. First, we analyzed the pathological structural characteristics of AKI and the main pathological mechanism of AKI: hypoxia, harmful substance accumulation-induced RONS burst at the renal site despite the multifactorial initiation and heterogeneity of AKI. Subsequently, we introduced the strategies used to improve renal targeting and reviewed advances of nanodrugs for AKI: nano-RONS-sacrificial agents, antioxidant nanozymes, and nanocarriers for antioxidants and anti-inflammatory drugs. These nanodrugs have demonstrated excellent therapeutic effects, such as greatly reducing oxidative stress damage, restoring renal function, and low side effects. Finally, we discussed the challenges and future directions for translating nanodrugs into clinical AKI treatment.

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