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Implication of Nanoparticles to Combat Chronic Liver and Kidney Diseases: Progress and Perspectives

期刊

BIOMOLECULES
卷 12, 期 10, 页码 -

出版社

MDPI
DOI: 10.3390/biom12101337

关键词

kidney; liver; toxicity; nanoparticles; anti-inflammatory; antioxidant; pro-oxidant

资金

  1. Region Centre-Val de Loire (ARD Biomedicaments)

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Liver and kidney diseases are common worldwide, and the use of nanoparticles has shown potential for safe delivery of medications with minimal side effects. Nanoparticles have anti-inflammatory and antioxidant effects, and can also induce apoptosis in malignant liver and kidney cells.
Liver and kidney diseases are the most frequently encountered problems around the globe. Damage to the liver and kidney may occur as a result of exposure to various drugs, chemicals, toxins, and pathogens, leading to severe disease conditions such as cirrhosis, fibrosis, hepatitis, acute kidney injury, and liver and renal failure. In this regard, the use of nanoparticles (NPs) such as silver nanoparticles (AgNPs), gold nanoparticles (AuNPs), and zinc oxide nanoparticles (ZnONPs) has emerged as a rapidly developing field of study in terms of safe delivery of various medications to target organs with minimal side effects. Due to their physical characteristics, NPs have inherent pharmacological effects, and an accidental buildup can have a significant impact on the structure and function of the liver and kidney. By suppressing the expression of the proinflammatory cytokines iNOS and COX-2, NPs are known to possess anti-inflammatory effects. Additionally, NPs have demonstrated their ability to operate as an antioxidant, squelching the generation of ROS caused by substances that cause oxidative stress. Finally, because of their pro-oxidant properties, they are also known to increase the level of ROS, which causes malignant liver and kidney cells to undergo apoptosis. As a result, NPs can be regarded as a double-edged sword whose inherent therapeutic benefits can be refined as we work to comprehend them in terms of their toxicity.

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