Abstract

Silver nanoparticle (Ag-NP) is well known for its high antibacterial efficacy. However, its toxicity toward mammalian cells is still a concern in clinical applications. The aim of our study was to evaluate the composition effects of Ag-NP supported by silicate nanoplatelet (NSP) with respect to the cytotoxicity and genotoxicity, and was in reference to the poly (styrene-co-maleic anhydride)-supported Ag-NP (Ag-NP/SMA). The NSP at the geometric dimension of averaged 80 x 80 x 1 nm3 was prepared from the exfoliation of natural clays and used to support different weight ratio of Ag-NP. The supporting limitation of NSP on Ag-NP was below the weight ratio of 15/85 (Ag-NP to NSP), and the detached Ag-NP from the Ag-NP/NSP (30/70) and Ag-NP/SMA hybrids were observed by TEM. Ames test was performed to assess the mutagenic potential of different compositions of Ag-NP/NSP, only Ag-NP/NSP (30/70) and Ag-NP/SMA hybrids exhibited mutagenicity when the concentration was 1.09 ppm or higher. In viewing of cytotoxicity using MTT tests toward HaCaT cells, the IC30 of Ag-NP/NSP (1/99, 7/93 and 15/85) were 1416.7, 243.6, and 148.9 ppm respectively, while Ag-NP/SMA was 64.8 ppm. The IC30 of Ag-NP/NSP (1/99, 7/93 and 15/85) were at least 833, 78 and 7 folds higher than their corresponding minimum inhibitory concentrations (MIC) respectively, and whereas Ag-NP/SMA was 6.4 folds. The Ag-NP/NSP and Ag-NP/SMA hybrids had been further investigated for genotoxicity by chromosomal aberrations and in vivo micronucleus assay within the concentration at IC10 and IC30, only Ag-NP/SMA showed a higher frequency of chromosomal aberrations. Our findings indicated that the viability of utilizing the NSP to maintain Ag-NP for antimicrobial activity, and the high-surface area of NSP served as an excellent support for associating Ag-NP and consequently rendering the mitigation of the inherent toxicity of Ag-NP in clinical uses.

Highlights

  • Nanomaterials with different physical properties and compositions [1,2,3] may give rise to new applications in biomedicines [4], drug-delivery agents [5, 6], or biosensors [7,8,9]

  • A similar trend was found while Ag-NP/nanoscale silicate platelets (NSP) of 30/70 and Ag-NP/styrene maleic anhydride polymer (SMA) significantly increased in revertant colonies at the dose over 1.09 or 2.19 ppm/plate, whereas Ag-NP/NSP of 1/99, 7/93 and 15/85 showed no mutagenic responses either with or without S9

  • Ames test provides the initial screening on the selecting non-mutagenic compositions of Ag-NP/NSP at 1/99, 7/93 and 15/ 85 for further genotoxicity tests in eukaryotic systems

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Summary

Introduction

Nanomaterials with different physical properties and compositions [1,2,3] may give rise to new applications in biomedicines [4], drug-delivery agents [5, 6], or biosensors [7,8,9]. Silver nanoparticles (Ag-NP) have been identified as effective antimicrobial agents and have been widely utilized as bactericides [10, 11] in many medical fields such as wound dressings, catheters, implants coating, and bone cements [12,13,14]. Ag-NP are less reactive than silver ions for clinical and therapeutic applications [21], there is still a serious concern on the toxicity toward mammalian cells and the environment [22,23,24,25,26]. Toxic effects to the human body are caused by absorption through skin, lung, or digestive systems [23, 24, 27], and in vitro studies have indicated that Ag-NP might enter mammalian cells and elicit cytotoxicity and genotoxicity [28, 29]. For clinical applications of Ag-NP, an important issue is to determine the balance between bactericidal efficacy and minimum harm to mammalian cells

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