金属和氧化物纳米颗粒对细菌毒性的研究进展

阐述了纳米颗粒的组分、尺寸、形状和表面电荷等性质与毒性的关系,介绍了纳米颗粒对革兰氏阴性菌和革兰氏阳性菌的毒性差异,指出了分散介质、暴露方式等毒性试验条件对纳米颗粒细菌毒性的影响,讨论了纳米颗粒对细菌毒性的可能机制,如氧化损伤、破坏细胞壁、作用于蛋白和核酸以及释放出金属离子等。针对目前纳米毒性研究尚处于起步阶段的现状,提出了建立纳米材料的毒性评价方法,加强从分子生物学水平开展对毒性机制的研究等建议。     

纳米银的生物分布及其影响因素研究进展

纳米银(AgNPs)以其独特的抗菌性能在生物医药和消费品中得到大量应用。然而,随着人类接触AgNPs的机会增多,AgNPs暴露的潜在危害也不容忽视。体内研究表明,AgNPs可以通过经口、呼吸、腹腔、静脉等途径进入机体,进而通过血液或淋巴液的流动分散到全身不同组织器官。而不同的暴露方式、暴露剂量、AgNPs粒径、表面包被和电荷以及暴露器官本身的特点可能对AgNPs在体内的分布与蓄积产生影响。因此,本文系统地总结了AgNPs进入生物体的途径及其在生物体内的组织分布,讨论了影响AgNPs体内生物分布和蓄积的因素。     

磺胺与金属氧化物纳米颗粒对发光菌的急性联合毒性及其机制初探

磺胺与金属氧化物纳米颗粒同作为抗菌剂对环境与人体健康皆有危害。为探究其对细菌的毒性作用,测定了4种磺胺,包括磺胺氯哒嗪(SCP)、磺胺吡啶(SPY)、磺胺甲基异恶唑(SMZ)、磺胺嘧啶(SD),与3种金属氧化物纳米颗粒,纳米ZnO(n-ZnO)、纳米CuO(n-CuO)、纳米Cr_2O_3(n-Cr_2O_3)对发光菌(Vibriofischeri)的单一毒性及二元急性联合毒性。结果表明,SCP对V.fischeri的单一毒性明显大于其他3种磺胺;n-ZnO的单一毒性远大于n-CuO和n-Cr_2O_3;磺胺与金属氧化物纳米颗粒的二元急性联合毒性效应表现为拮抗、相加和协同,协同居多,说明金属氧化物纳米颗粒增加了磺胺的生物毒性,两者在环境中的共存带来了更大的环境生态风险。     

Size and shape effects of MnFe2O4 nanoparticles as catalysts for reductive degradation of dye pollutants

• Size and shape-dependent MnFe₂O₄ NPs were prepared via a facile method. • Ligand-exchange chemistry was used to prepare the hydrophilic MnFe₂O₄ NPs. • The catalytic properties of MnFe₂O₄ NPs toward dye degradation were fully studied. • The catalytic activities of MnFe₂O₄ NPs followed Michaelis–Menten behavior. • All the MnFe₂O₄ NPs exhibit selective degradation to different dyes. The magnetic nanoparticles that are easy to recycle have tremendous potential as a suitable catalyst for environmental toxic dye pollutant degradation. Rationally engineering shapes and tailoring the size of nanocatalysts are regarded as an effective manner for enhancing performances. Herein, we successfully synthesized three kinds of MnFe₂O₄ NPs with distinctive sizes and shapes as catalysts for reductive degradation of methylene blue, rhodamine 6G, rhodamine B, and methylene orange. It was found that the catalytic activities were dependent on the size and shape of the MnFe₂O₄ NPs and highly related to the surface-to-volume ratio and atom arrangements. Besides, all these nanocatalysts exhibit selectivity to different organic dyes, which is beneficial for their practical application in dye pollutant treatment. Furthermore, the MnFe₂O₄ NPs could be readily recovered by a magnet and reused more than ten times without appreciable loss of activity. The size and shape effects of MnFe₂O₄ nanoparticles demonstrated in this work not only accelerate further understanding the nature of nanocatalysts but also contribute to the precise design of nanoparticles catalyst for pollutant degradation.     

Influence of phosphate on deposition and detachment of TiO2 nanoparticles in soil

We examined influence of phosphate on transport of TiO₂ NPs in soil. Deposition was reduced at higher pH and by adsorption of phosphate in soil. Release was more for NPs initially deposited at higher pH. Release was more for NPs initially deposited in the presence of phosphate. Surface roughness and charge heterogeneity play a role in the deposition/ release. The widespread use of TiO₂ nanoparticles (NPs) makes inevitable their release into the soil. Phosphate is also widespread within soil, and is likely copresent with TiO₂ NPs. However, the influence of phosphate on deposition/release— and thereby on transport— of TiO₂ NPs in soil is yet to be elucidated. In this study we conducted saturated column experiments to systematically examine the transport of TiO₂ NPs in soil amended with phosphate at different ionic strengths (ISs) (1, 10, 100 mmol/L NaCl) and pHs (4 and 9). Results show that the deposition of TiO₂ NPs decreased with decreasing IS, increasing pH, and when soil absorbed phosphate. These observations are qualitatively in agreement with Derjaguin-Landau-Verwey-Overbeek (DLVO) interaction energy calculations, because the repulsive energy barrier is larger and secondary minimum depth is smaller at a lower IS, higher pH, and in the presence of phosphate. Accordingly, both primary- and secondary-minimum deposition were inhibited. Interestingly, although the deposition was less at higher pH and in the presence of phosphate, the subsequent spontaneous detachment and detachment by reduction of solution IS in these cases were greater. In addition, the presence of phosphate in the solution can cause a small quantity of attached TiO₂ NPs to detach, even without perturbations of physical and chemical conditions. Our study was the first to investigate the influence of phosphate on detachment of TiO₂ NPs and the results have important implication for accurate prediction of fate and transport of TiO₂ NPs in subsurface environments.     

Size-dependent in vitro cytotoxicity assay of gold nanoparticles

Gold nanoparticles (AuNps) may serve as a promising model to address the size-dependent biological response of cell lines. Their size can be controlled with great precision during chemical synthesis. AuNps have potential applications in drug delivery, cancer diagnosis, and therapy, in the food industry, and for environmental remediation. However, some of the recent literature contains conflicting data regarding the cytotoxicity of gold nanoparticles. Against this background, a systematic study of water soluble gold nanoparticles stabilized by citrate ranging in size from 3?nm to 45?nm were synthesized. The cytotoxicity of these particles were tested by employing the (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide reduction assay), the neutral red cellular uptake assay, and lactate dehydrogenase release assay. Noticeable differences in the cytotoxic effects depending on the assay, and the nanoparticle size have been found. Citrate stabilized gold nanoparticles with sizes of 3?nm, 8?nm, and 30?nm were more sensitive to the cell lines and caused gradual cell death within 24?h at higher concentrations. This results in IC50 values ranging from 57 to 78?μgmL^?1 depending on the particle size, and cell line combinations. In contrast, AuNps with diameters of 5?nm, 6?nm, 10?nm, 17?nm, and 45?nm were nontoxic up to three to four fold higher concentrations, and at long-term exposure.     

Toxicity of cadmium nanoparticles to Bacillus subtilis

The study deals with the toxicological impact of cadmium nanoparticles (Cd NPs) on Bacillus subtilis as a model Gram-positive bacterium. Cadmium oxide (CdO) NPs (～22 nm) and cadmium sulfide (CdS) NPs (～3 nm) were used in this study. Both the NPs were found to inhibit the cell viability of B. subtilis when added to the culture at mid-log phase, the viable cell number declined with increasing concentration of Cd NPs. At mid-log phase, 15 mg L^?1 CdO NPs inhibited growth by ～50%, whereas at 30 mg L^?1 growth completely ceased. Under the same conditions, CdS NPs inhibited growth by ～50% at a concentration of 8 mg L^?1, and at 20 mg L^?1 growth was completely retarded. The cells changed their morphological features to a filamentous form with increasing Cd NPs exposure time, leading to associated with clumping. NPs treated cells when stained with 4′, 6-diamino-2-phenylindole, showed filamentous multinucleated bead structure, suggesting irregularities in cell division. Increasing intracellular oxidative stress due to Cd NPs exposure might be one of the reasons for the cell morphological changes and toxicity in B. subtilis.     

The Toxicology of Silica Nanoparticles: A Review

Silica nanoparticles are increasingly used in industrial, cosmetics, and medical applications. Workers in nanosilica production industries, laboratory personnel in drug production industries, patients taking drugs with nanosilica in its formulations, and everyone in society who uses cosmetics are potentially at risk to health effects induced by silica nanoparticles. Like other nanomaterials, nanosilica has unique physical and chemical properties that modify its toxic effects compared to bulk silica or microparticles of silica. Nanosilica toxicology has been studied by various in vitro and in vivo protocols and on humans, studies which are collected and summarized in the present publication. The toxic effects are outlined based on the type of body compartment, viz. cardiovascular, dermal, respiratory, neural, hepatic, genetic, immune, reproductive, and renal system. Further information, especially the experimental protocols and toxicological endpoints, are summarized in tables.     

Effects of three different nanoparticles on bioaccumulation,oxidative stress,osmoregulatory, and immune responses of Carcinus aestuarii

Abstract

In this study, the toxicity of CuO (40?nm), α-Al₂O₃ (40?nm), and α-Fe₂O₃ (20–40?nm) nanoparticles was comparatively investigated on Carcinus aestuarii. Crabs were semi-statically exposed to 1?mg/L of each for 14?days and their accumulation and distribution in tissue and hemolymph, potential oxidative stress mechanism, total hemocyte counts and types, and the osmoregulatory and ionoregulatory responses were determined. The tissue distribution of CuO nanoparticles was hepatopancreas?>?hemolymph?≥?gill?> muscle, for α-Fe₂O₃ gill?>?hepatopancreas?>?muscle?> hemolymph, and for α-Al₂O₃ gill?>?muscle?≥?hemolymph?> hepatopancreas. While α-Al₂O₃ and α-Fe₂O₃ NPs, induced lipid peroxidation and changes in antioxidant enzyme activity in the hepatopancreas tissue, the oxidative damage caused by the CuO nanoparticles was minimal. All three nanoparticles, copper in particular, elicit osmoregulatory and ionoregulatory toxicity at this concentration, due to the inhibition of Na⁺, K⁺-ATPase activity in the gill and depletion of hemolymph and carcass ion concentrations.     

纳米氧化镍对3种绿藻的毒性效应

通过配制不同浓度(0,60,120,180,240,300mg/L)纳米氧化镍(nNiO)悬浊液,对四尾栅藻(Scenedesmus quadricauda)、普通小球藻(Chlorella vulgaris)和羊角月牙藻(Selenastrum capricornutum)进行连续胁迫10d的毒性试验,测定nNiO对3种绿藻生长状况、叶绿素a、蛋白质、脂质过氧化物丙二醛(MDA)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)的影响.结果表明,nNiO胁迫对四尾栅藻、普通小球藻和羊角月牙藻的生长均有一定抑制作用,在同一时间段内,总体呈明显剂量效应;nNiO低浓度(60~120mg/L)胁迫对供试藻的影响表现为“抑制—促进—抑制”,在一定时间内对供试藻有促进生长的作用;nNiO胁迫对四尾栅藻、普通小球藻和羊角月牙藻的毒性效应表现为叶绿素a和蛋白质含量减少,MDA含量升高,抗氧化活性降低;羊角月牙藻对nNiO的耐受性较强,四尾栅藻和普通小球藻较敏感.