AI Article Synopsis

  • Acute Kidney Injury (AKI) is linked to harmful reactive oxygen species, but current treatments are ineffective due to poor kidney targeting and side effects.
  • Researchers developed a new nanodrug using poly(ursolic acid) (PUA) as a carrier for the antioxidant resveratrol (RES), showing that it can effectively reduce oxidative stress and protect kidney cells.
  • In animal models, the PUA nanoparticles not only improved drug delivery to the kidneys but also displayed anti-inflammatory properties, suggesting they may be a strong candidate for AKI treatment.

Article Abstract

Acute kidney injury (AKI) is a common kidney disease associated with excessive reactive oxygen species (ROS). Unfortunately, due to the low kidney targeting and undesired side effects, the existing antioxidant and anti-inflammatory drugs are unavailable for AKI management in clinic. Therefore, it's essential to develop effective nanodrugs with high renal targeting and biocompatibility for AKI treatment. Herein, we reported a novel nanodrug for AKI treatment, utilizing poly(ursolic acid) (PUA) as a bioactive nanocarrier and resveratrol (RES) as a model drug. The PUA polymer was synthesized form ursolic acid with intrinsic antioxidant and anti-inflammatory activities, and successfully encapsulated RES through a nanoprecipitation method. Subsequently, we systemically investigated the therapeutic potential of RES-loaded PUA nanoparticles (PUA NPs@RES) against AKI. In vitro results demonstrated that PUA NPs@RES effectively scavenged ROS and provided substantial protection against HO-induced cellular damage. In vivo studies revealed that PUA NPs significantly improved drug accumulation in the kidneys and exhibited favorable biocompatibility. Furthermore, PUA NPs alone exhibited additional anti-inflammatory and antioxidant effect, synergistically enhancing therapeutic efficacy in AKI mouse models when combined with RES. Overall, our study successfully developed an effective nanodrug using self-therapeutic nanocarriers, presenting a promising option for the treatment of AKI.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10726514PMC
http://dx.doi.org/10.1186/s12951-023-02254-xDOI Listing

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