2021
DOI: 10.23937/2572-4061.1510036
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Recent Advances on Renal Toxicity of Engineered Nanoparticles-A Review

Abstract: Kidney is considered as the secondary target organ of nanoparticle (NP) toxicity. Since it is the primary organ of excretion, NPs are expected to adversely affect the renal system. Therefore, a comprehensive review of recent knowledge on renal toxicity of engineered nanoparticles (ENPs) was made. Mechanistic paradigms of their toxicity have also been discussed.

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Cited by 8 publications
(4 citation statements)
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“…It is worth noting that NPs can reach various organs, including the kidney, liver, and spleen, through the circulatory system, irrespective of the route of exposure ( 36 ). The kidney, being the primary site for excretion, is particularly susceptible to the adverse effects of NP toxicity, which can impact renal function ( 37 ).…”
Section: Discussionmentioning
confidence: 99%
“…It is worth noting that NPs can reach various organs, including the kidney, liver, and spleen, through the circulatory system, irrespective of the route of exposure ( 36 ). The kidney, being the primary site for excretion, is particularly susceptible to the adverse effects of NP toxicity, which can impact renal function ( 37 ).…”
Section: Discussionmentioning
confidence: 99%
“…In the next decade, most materials will be in the nanoscale forms of existing goods such as titanium dioxide, silica, clays, polymers, metal powders, and chemicals. There has been a limited amount of research on the toxicity of CNTs and fullerenes [79][80][81]. To the best of our knowledge, there has been no methodical study of the hydrolytic, oxidative, photochemical, and biological stability of nanomaterials in natural and engineered environmental systems that have been published in peerreviewed literature.…”
Section: Nanomaterials and Water Purification Challengesmentioning
confidence: 99%
“…Similar to every drug, nanoparticles are, to a certain level, toxic [94]. For example, NPs, can translocate across biological barriers and affect secondary target organs [95], they can have adverse effects on certain cancer cells (e.g., activate cancer cells instead of damaging them) [96], agglomerate on the surface of other cells, such as endothelial cells [97] and platelets [98], or form cluster with a large HD [97], influencing their renal excretion resulting in an increased lifetime in the body. Therefore, efforts have to be dedicated to designing NPs to reduce their toxicity.…”
Section: Future and Perspectivesmentioning
confidence: 99%