2020
DOI: 10.1016/j.jconrel.2020.05.027
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One-year chronic toxicity evaluation of single dose intravenously administered silica nanoparticles in mice and their Ex vivo human hemocompatibility

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Cited by 71 publications
(38 citation statements)
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“…Additionally, long-term toxicity studies about the chronic administration of MSN are needed. Recently, Mohammadpour et al have evaluated the effect of the intravenous administration of silica nanoparticles with different sizes and porosities for one year in animal models showing scarce toxicity [ 85 ]. The development of industrial synthetic routes which yield large amounts of high quality MSN with reproducibility between batches is also a challenge.…”
Section: Discussionmentioning
confidence: 99%
“…Additionally, long-term toxicity studies about the chronic administration of MSN are needed. Recently, Mohammadpour et al have evaluated the effect of the intravenous administration of silica nanoparticles with different sizes and porosities for one year in animal models showing scarce toxicity [ 85 ]. The development of industrial synthetic routes which yield large amounts of high quality MSN with reproducibility between batches is also a challenge.…”
Section: Discussionmentioning
confidence: 99%
“…The major toxicity pathway associated with silica is due to its surface chemistry (silanol groups) which can interact with the membrane components leading to the cells lysis and cellular components leaking (91,92). Mesoporous silica exhibited lower hemolytic effect compared to non-porous silica (25). This could be attributed to the lower density of silanol groups on the surface of mesoporous structures (93).…”
Section: Biocompatibility and Biodistributionmentioning
confidence: 99%
“…Specifically, inorganic platforms as mesoporous silica nanoparticles (MSNs) comprise a potential nanosystem for healthcare applications due to interesting characteristics such as easy functionalization, large surface area, high chemical and physical stabilities and hydroxyl groups available in their surface/ pores. In addition, MSNs tunable morphology, size, surface charges and pores make them carriers with good biocompatibility and biodegradability, low toxicity, good biodistribution and elimination (12,(21)(22)(23)(24)(25)(26)(27). Drugs loaded into MSNs pores leading to pharmacological properties maintenance besides protection against degradation and immediate drug release (23,24,28,29).…”
Section: Introductionmentioning
confidence: 99%
“…As long as the silica doses are not too large, this would prevent chronic accumulation in the organism. A recent study that evaluated the one-year toxicological behavior of intravenously-injected single-dose silica nanoparticles in mice has shown that, while large (500 nm) non-porous silica particles produced some lung, heart and kidney damage attributed to resolved thrombosis, no significant toxicity was produced by MSNs and smaller non-porous silica particles [ 35 ].…”
Section: Mesoporous Silica Nanoparticles For Drug Deliverymentioning
confidence: 99%