Abstract:Nanotoxicology is argued and considered one of the emerging topics. In this study, polyaniline (PANI)/2-acrylamido-2-methylpropanesulfonic acid (AMPSA) capped silver nanoparticles (NPs)/graphene oxide (GO) quantum dots (QDs) nanocomposite (PANI/Ag (AMPSA)/GO QDs NC) as a nanoadsorbent has a potential for removal of toxic hexavalent chromium (Cr(VI)) ions from water. The acute toxicity of this NC was evaluated on Artemia salina and freshwater Ostracods (Cypridopsis vidua) larvae for 48 h. The measurements were … Show more
“…One of the most attractive and widely studied nanostructured materials with antimicrobial activity on its own is silver nanoparticles (Ag NPs), which also offer high chemical stability, high surface-to-volume ratio, relatively low synthesis cost, ease of preparation, and high reactivity [ 26 , 27 ]. Ag NPs’ antibacterial activity has been attributed to their attachment to bacterial membranes, inducing disruption, leakage of bacterial inner components, and even inhibition of protein synthesis [ 13 ].…”
“…One of the most attractive and widely studied nanostructured materials with antimicrobial activity on its own is silver nanoparticles (Ag NPs), which also offer high chemical stability, high surface-to-volume ratio, relatively low synthesis cost, ease of preparation, and high reactivity [ 26 , 27 ]. Ag NPs’ antibacterial activity has been attributed to their attachment to bacterial membranes, inducing disruption, leakage of bacterial inner components, and even inhibition of protein synthesis [ 13 ].…”
“…Artemia salina , a zooplanktonic crustacean, is used as a model organism for acute toxicity testing by the United States Environmental Protection Agency (US-EPA) . The assay is correlated with the toxicity data of rodents and humans and is generally used in testing acute toxicity of toxic materials, bioactive molecules, or metallodrugs …”
{[Ag8(Mef)8(μ2-S,O-DMSO)2(μ2-O-DMSO)2(O-DMSO)8]·2(H2O)} (1), [Ag(Mef)(tpP)2] (2),
[Ag(Mef)(tpAs)3] (3), and {2 [Ag(Mef)(tpSb)3] (DMSO)} (4) were obtained by the conjugation
of mefenamic acid (MefH), a nonsteroidal anti-inflammatory drug (NSAID),
with a mitochondriotropic derivative of pnictogen tpE (tp = triphenyl
group; E = P, As, and Sb) through silver(I). Their hydrophilicity
was adjusted by their dispersion into sodium lauryl sulfate (SLS),
forming SLS@1–4. 1–4 and SLS@1–4 were characterized
by their spectral data and X-ray crystallography. They inhibit the
proliferation of human breast adenocarcinoma cells MCF-7 (hormone-dependent
(HD)) and MDA-MB-231 (hormone-independent (HI)). X-ray fluorescence
reveals the Ag cellular uptake. The in vitro and in vivo nongenotoxicity was confirmed with micronucleus
(MN), Artemia salina, and Allium cepa assays. Their mechanism of action was studied by cell morphology,
DNA fragmentation, acridine orange/ethidium bromide (AO/EB) staining,
cell cycle arrest, mitochondrial membrane permeabilization tests,
DNA binding affinity, and LOX inhibitory activity and was rationalized
by regression analysis.
“…Consistent with our in vitro experiments and previous publications, GOQDs possess high biocompatibility, paving the way for potential application in PNI treatment. [ 34 ]…”
The understanding of nanomaterial biology determines material selection and scaffold fabrication in regenerative medicine. The translational application of advanced functional nanomaterials, like graphene and derivatives, requires an in‐depth investigation on the sophisticated material‐cell action network. To achieve the therapeutic convergence between biocompatibility and bioeffectiveness, herein, series of graphene derivatives are screened and the superiority of graphene oxide quantum dots (GOQDs) is confirmed. Thereby, a GOQD functionalized nerve scaffold is fabricated for peripheral nerve repair with electrospinning and freeze‐drying technology. The behavioral, electrophysiological, and pathological analysis confirms that GOQDs promote nerve structural reconstruction and attenuate denervation‐induced myopathy. Macrophages perceive the implanted materials and initiate a variety of biological processes. GOQDs activate the macrophage ERK/CERB/VEGF pathway in vitro and in vivo, thereby contributing to intraneural vascularization. In addition, an enzyme‐activated degradation route of GOQDs is explored and the implanted scaffolds trigger negligible scar formation and blood toxicity. These findings demonstrate the ability of the GOQD, a biocompatible graphene derivative, to facilitate intraneural vascularization and regeneration of injured peripheral nerves through a macrophage intracellular signaling‐mediated mechanism. This enlightens the authors to continuously explore the mechanisms behind the material nanobiology‐dependent therapeutic convergence between biocompatibility and bioeffectiveness for clinical translation.
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