synergistic action

协同作用
  • 文章类型: Journal Article
    可生物降解的聚合物微球在骨组织工程中作为其在不规则损伤骨修复中的非侵入性优势而变得吸引人。然而,目前用于BTE的微球仍然缺乏足够的成骨能力来诱导有效的骨再生。在这项研究中,我们开发了同时负载氧化镁(MgO)和氧化锌(ZnO)的成骨复合微球,两者都是成骨活性物质,使用一种容易和可扩展的乳化方法。成骨复合微球表现出连续但互补的释放曲线,其特征是在生理环境中迅速释放Mg2和逐渐释放Zn2。从而将生物活性离子的浓度保持在持续的高水平。因此,复合微球中Mg2和Zn2的结合导致仿生矿化的协同增强以及成骨相关基因和蛋白质在细胞水平上的表达上调。通过临界大小的颅骨率缺陷模型,超声成像显示成骨复合微球具有较强的成骨能力,可促进新骨形成,组织学和免疫组织化学评估。总之,这些成骨复合微球作为Mg2+和Zn2+的微载体,在递送治疗性离子治疗骨缺损方面具有巨大的潜力。
    Biodegradable polymer microspheres in bone tissue engineering have become appealing as their non-invasive advantages in irregular damage bone repair. However, current microspheres used in BTE still lack sufficient osteogenic capacity to induce effective bone regeneration. In this study, we developed osteogenic composite microspheres concurrently loaded with magnesium oxide (MgO) and zinc oxide (ZnO), both of which are osteogenic active substances, using a facile and scalable emulsification method. The osteogenic composite microspheres exhibited a sequential yet complementary release profile characterized by a rapid release of Mg2+ and a gradual release of Zn2+ in a physiological environment, thereby maintaining the concentration of bioactive ions at a sustained high level. As a result, the combination of Mg2+ and Zn2+ in the composite microspheres led to a synergistic enhancement in biomimetic mineralization and the upregulation in the expression of osteogenic-related genes and proteins at the cellular level. Through a critical-sized calvarial rate defect model, the osteogenic composite microspheres were demonstrated to have strong osteogenic ability to promote new bone formation via ultrasonic imaging, histological and immunohistochemical evaluations. In sum, these osteogenic composite microspheres as microcarriers of Mg2+ and Zn2+ have great potential in the delivery of therapeutic ions for treating bone defects.
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  • 文章类型: Journal Article
    设计和建造用于整体水分解和尿素电解的高效电催化剂对于促进能量转化和实现绿色制氢具有重要意义。在这项工作中,我们通过简单的水热和磷化过程构建了多相异质结。掺杂P的NiFe2O4(P-NiFe2O4)纳米颗粒均匀地锚定在通过NiFe合金自催化生长的竹状N掺杂碳纳米管(NCNT)上。通过P掺杂的协同作用,优化了活性物种的电子结构和配位环境,分散良好的超细NiFe2O4和具有良好导电性的NCNTs基体,提高其电催化的数量和活性。因此,P-NiFe2O4/NCNTs/NiFe表现出优异的HER和OER活性,在1MKOH中10mAcm-2时的过电位为111和266mV,分别。使用P-NiFe2O4/NCNT/NiFe作为阳极和阴极的对称整体水分解电池在1MKOH中的1.604V电压下可提供10mAcm-2。值得注意的是,双电极电池需要1.467V的低电压才能在1MKOH溶液和0.6M尿素中实现10mAcm-2的电流密度。这种设计的催化剂表现出优异的反应动力学和催化稳定性。这项工作为过渡金属基催化剂用于制氢提供了有用的指导。
    The design and construction of highly efficient electrocatalysts for overall water splitting and urea electrolysis are significantly important for promoting energy conversion and realizing green hydrogen production. In this work, we constructed a multi-phase heterojunction through a simple hydrothermal and phosphorization process. The P-doped NiFe2O4 (P-NiFe2O4) nanoparticles were uniformly anchored on the bamboo-like N-doped carbon nanotubes (NCNTs) grown via a NiFe-alloy autocatalysis. The electronic structure and coordination environment of active species were optimized by the synergistic action of P doping, well-dispersed ultrafine NiFe2O4, and NCNTs matrix with good conductivity, enhancing their quantity and activity for electrocatalysis. Consequently, the P-NiFe2O4/NCNTs/NiFe exhibits excellent HER and OER activities with an overpotential of 111 and 266 mV at 10 mA cm-2 in 1 M KOH, respectively. The symmetrical overall water-splitting cell using P-NiFe2O4/NCNTs/NiFe as both anode and cathode delivers 10 mA cm-2 at a voltage of 1.604 V in 1 M KOH. Notably, the two-electrode cell requires a low voltage of 1.467 V to achieve a current density of 10 mA cm-2 in 1 M KOH solution with 0.6 M urea. This designed catalysts display outstanding reaction kinetics and catalytic stability. This work provides useful guidance for applying transition metal-based catalysts for hydrogen production.
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  • 文章类型: Journal Article
    为了拓宽南瓜多糖(WESP/SWESP)和咖啡酸(CAA)的应用范围,提高马铃薯淀粉(PS)产品的品质,WESP/SWESP和CAA对糊化的影响,流变学,热力学,研究了PS的微观结构和体外消化。同时,进一步分析了WESP/SWESP和CAA对PS的协同作用。不同的是,由于WESP和SWESP具有不同的单糖组成和结构,他们对系统有不同的影响。糊化性能结果表明,WESP/SWESP和CAA的存在显著降低了峰值粘度,槽粘度,PS的分解粘度和最终粘度,特别是在联合作用下。在流变试验中,所有样品凝胶均属于假塑性流体和弱凝胶体系(tanδ<1)。此外,热力学性质显示,WESP/SWESP与CAA的协同作用具有较好的回生延迟效应。在三元体系中,WESP/SWESP,CAA和PS可以构成新的网络结构,进步凝胶体系的稳固性。此外,红外光谱的结果,拉曼光谱,X射线衍射和扫描电子显微镜显示,三元体系可以促进PS链螺旋结构的积累和缠绕,并使PS凝胶网络结构更加有序和稳定。此外,与PS凝胶相比,三元体系RDS较低,SDS和RS含量较高,提示同时加入WESP/SWESP和CAA更有利于降低PS的水解速率。这项工作揭示了WESP/SWESP之间的相互作用,CAA和PS,改善了PS的理化和消化特性。为提高马铃薯淀粉相关产品质量和开发功能性食品提供理论依据。
    In order to broaden the application range of squash polysaccharide (WESP/SWESP) and caffeic acid (CAA) and improve the quality of potato starch (PS) products, the effects of WESP/SWESP and CAA on the gelatinization, rheology, thermodynamics, microstructure and in vitro digestion of PS were investigated. Meanwhile, the synergistic effect of WESP/SWESP and CAA on PS was further analyzed. Differently, due to WESP and SWESP had different monosaccharide composition and structure, they had different effects on the system. Pasting properties results showed that the presence of WESP/SWESP and CAA significantly reduced the peak viscosity, trough viscosity, breakdown viscosity and final viscosity of PS, especially under the combined action. In rheological tests, all sample gels belonged to the pseudoplastic fluids and weak gel system (tan δ < 1). Besides, thermodynamic properties revealed that WESP/SWESP and CAA synergistic effect had better retrogradation delay effect. In the ternary system, WESP/SWESP, CAA and PS can form a new network structure and improve the stability of the gel system. In addition, the results of infrared spectroscopy, Raman spectroscopy, x-ray diffraction and scanning electron microscopy exhibited that the ternary system can promote the accumulation and winding of the spiral structure of PS chain, and make the structure of PS gel network more orderly and stable. Furthermore, compared with PS gel, the ternary system had lower RDS and higher SDS and RS content, suggesting that the addition of WESP/SWESP and CAA at the same time was more conducive to reducing the hydrolysis rate of PS. This work revealed the interaction between WESP/SWESP, CAA and PS, which improved the physicochemical and digestive properties of PS. It will provide a theoretical basis for improving the quality of potato starch-related products and developing functional foods.
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  • 文章类型: Journal Article
    多粘菌素是抵抗多药耐药(MDR)革兰氏阴性细菌感染的最后一道防线。然而,携带移动粘菌素抗性基因-1(mcr-1)的超级细菌的出现威胁到了最后的手段。考虑到细菌性肺炎中基质金属蛋白酶3(MMP-3)的高浓度,粘菌素(CST)在肺中的血浆积累有限,和离子银(Ag+)的潜在毒性,我们设计了一个可行的临床转化平台,MMP-3高性能肺靶向生物响应递送系统,我们命名为“CST&Ag@CNMS”。该系统表现出优异的肺靶向能力(>80%的肺部),MMP-3生物响应性释放特性(按需释放95%),和体外协同杀菌活性(最小抑制浓度降低2-4倍)。在mcr-1+CST耐药鼠肺炎模型中,CST&Ag@CNMS治疗提高了生存率(70%vs.20%),减少细菌负担(2-3对数菌落形成单位[CFU]/g组织),并显著减轻炎症反应。在这项研究中,CST和Ag@CNMS的表现优于游离CST和AgNO3的组合。我们还证明了CST&Ag@CNMS在体外和体内的优异生物安全性和生物降解性。这些发现表明CST和Ag@CNMS用于治疗由携带mcr-1的CST抗性细菌引起的肺部感染的临床转化潜力。
    Polymyxins are the last line of defense against multidrug-resistant (MDR) Gram-negative bacterial infections. However, this last resort has been threatened by the emergence of superbugs carrying the mobile colistin resistance gene-1 (mcr-1). Given the high concentration of matrix metalloproteinase 3 (MMP-3) in bacterial pneumonia, limited plasma accumulation of colistin (CST) in the lung, and potential toxicity of ionic silver (Ag+), we designed a feasible clinical transformation platform, an MMP-3 high-performance lung-targeted bio-responsive delivery system, which we named \"CST&Ag@CNMS\". This system exhibited excellent lung-targeting ability (>80% in lungs), MMP-3 bio-responsive release property (95% release on demand), and synergistic bactericidal activity in vitro (2-4-fold minimum inhibitory concentration reduction). In the mcr-1+ CST-resistant murine pneumonia model, treatment with CST&Ag@CNMS improved survival rates (70% vs. 20%), reduced bacteria burden (2-3 log colony-forming unit [CFU]/g tissue), and considerably mitigated inflammatory response. In this study, CST&Ag@CNMS performed better than the combination of free CST and AgNO3. We also demonstrated the superior biosafety and biodegradability of CST&Ag@CNMS both in vitro and in vivo. These findings indicate the clinical translational potential of CST&Ag@CNMS for the treatment of lung infections caused by CST-resistant bacteria carrying mcr-1.
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  • 文章类型: Journal Article
    工业含铊(Tl)废水的处理对于减轻与这种有毒金属相关的环境风险和健康威胁至关重要。将Mn氧化物(MnOx)掺入过滤系统是有效去除Tl(I)的有希望的解决方案。然而,需要进一步的研究来阐明MnOx增强过滤背后的潜在机制及其稳定运行的规则。在这项研究中,石灰石,一种具有成本效益的材料,被选为过滤介质。含Mn(II)的原水,Tl(I),和其他污染物是在对实际工业废水状况进行彻底调查后制备的。添加KMnO4以诱导石灰石表面上MnO2的形成,而长期运行导致锰氧化微生物(MnOM)的富集。结果揭示了双重机制。首先,大多数Mn(II)被KMnO4氧化形成MnO2附着在石灰石砂上,Tl(I)和残余Mn(II)都吸附在新形成的MnO2上。随后,MnOM分泌的酶促进了剩余Mn(II)的氧化,导致在长期操作期间产生具有许多空位的生物锰氧化物(BioMnOx)。生成的BioMnOx不仅吸附了Mn(II)和Tl(I),而且促进了它们的氧化过程。这种方法提供了一种有效且可持续的方法,用于从工业废水中去除Mn(II)和Tl(I)。从而解决铊污染废水带来的挑战。
    Treatment of industrial thallium(Tl)-containing wastewater is crucial for mitigating environmental risks and health threats associated with this toxic metal. The incorporation of Mn oxides (MnOx) into the filtration system is a promising solution for efficient Tl(I) removal. However, further research is needed to elucidate the underlying mechanism behind MnOx-enhanced filtration and the rules of its stable operation. In this study, limestone, a cost-effective material, was selected as the filter media. Raw water with Mn(II), Tl(I), and other pollutants was prepared after a thorough investigation of actual industrial wastewater conditions. KMnO4 was added to induce the formation of MnO2 on limestone surfaces, while long-term operation led to enrichment of manganese oxidizing microorganisms (MnOM). Results revealed a dual mechanism. Firstly, most Mn(II) were oxidized by KMnO4 to form MnO2 attaching to limestone sands, and both Tl(I) and residual Mn(II) were adsorbed onto the newly formed MnO2. Subsequently, enzymes secreted by MnOM facilitated oxidation of remaining Mn(II), resulting in the generation of biogenic manganese oxides (BioMnOx) with numerous vacancies during long-term operation. The generated BioMnOx not only adsorbed Mn(II) and Tl(I) but also promoted their oxidation process. This approach offers an effective and sustainable method for removing both Mn(II) and Tl(I) from industrial wastewater, thereby addressing the challenges posed by thallium-contaminated effluents.
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  • 文章类型: Journal Article
    这项研究评估了从中国西部传统乳制品中分离出的75株乳酸菌(LAB)的益生菌特性。其中,发酵LimosilactobacillusfermentumWXZ2-1,植物乳杆菌TXZ2-35,CrystorumCompanilactobacillusQHS9和CrystorumCompanilactobillusQHS10表现出潜在的益生菌特征。对这4个菌株的抗氧化能力进行了评估,表明发酵乳杆菌WXZ2-1表现出最高的抗氧化能力。此外,与唾液链球菌共培养时。嗜热菌和德氏乳杆菌。保加利亚,发酵乳杆菌WXZ2-1在生长培养基和羊奶中表现出协同作用。探讨其对羊奶发酵的影响,将不同量的发酵乳杆菌WXZ2-1添加到羊奶中,和它的物理化学性质,抗氧化活性,风味物质,和代谢组学进行了分析。研究发现,在羊乳发酵中掺入发酵乳杆菌WXZ2-1显著改善了羊乳的质构特性,抗氧化能力,和发酵羊奶的味道。这些发现强调了发酵乳杆菌WXZ2-1作为一种有价值的益生菌菌株的潜力,用于增强发酵羊奶的功能和可取性,有助于开发具有改善健康益处和增强质量属性的新型功能食品。
    This study evaluated 75 strains of lactic acid bacteria (LAB) isolated from traditional dairy products in western China for their probiotic properties. Among them, Limosilactobacillus fermentum WXZ 2-1, Lactiplantibacillus plantarum TXZ 2-35, Companilactobacillus crustorum QHS 9, and Companilactobacillus crustorum QHS 10 demonstrated potential probiotic characteristics. The antioxidant capacity of these 4 strains was assessed, revealing that L. fermentum WXZ 2-1 exhibited the highest antioxidant capacity. Furthermore, when cocultured with Streptococcus salivarius ssp. thermophilus and Lactobacillus delbrueckii ssp. bulgaricus, L. fermentum WXZ 2-1 demonstrated a synergistic effect in growth medium and goat milk. To explore its effect on goat milk fermentation, different amounts of L. fermentum WXZ 2-1 were added to goat milk, and its physicochemical properties, antioxidant activity, flavor substances, and metabolomics were analyzed. The study found that the incorporation of L. fermentum WXZ 2-1 in goat milk fermentation significantly improved the texture characteristics, antioxidant capacity, and flavor of fermented goat milk. These findings highlight the potential of L. fermentum WXZ 2-1 as a valuable probiotic strain for enhancing the functionality and desirability of fermented goat milk, contributing to the development of novel functional foods with improved health benefits and enhanced quality attributes.
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  • 文章类型: Journal Article
    从采矿和冶炼操作产生的工业废水中长期稳定地去除铊(Tl)仍然具有挑战性。虽然砂滤器通常用于同时去除Mn(II)和其他重金属,它们在处理Tl污染的废水方面具有有限的功效。为了解决这个差距,我们在没有添加微生物的情况下操作了实验室规模的Mn砂过滤器(MF),以研究Mn(II)和Tl(I)去除的效率和机理。流出物Mn(II)和Tl(I)浓度的趋势表明三个操作阶段:启动,发育和成熟。随着时间的推移,Tl(I)的去除效率逐渐提高,最终达到约80%。在整个操作中,Tl(I)经由表面络合和离子交换而被螯合。此外,在操作过程中,狮身人面像和其他典型的锰氧化微生物(MnOM)的富集通过产生生物氧化锰(BioMnOx)促进了Mn(II)和Tl(I)的氧化和螯合。此外,在操作过程中准确控制水质和操作条件也可以提高去除效率。总之,Mn氧化物的物理化学作用和微生物的生化作用协同促进了Mn(II)和Tl(I)的螯合。这些发现为含th工业废水的长期稳定处理提供了一种新颖且可持续的方法。
    The long-term and stable removal of thallium (Tl) from industrial wastewater generated by mining and smelting operations remains challenging. While sand filters are commonly applied for the simultaneous removal of Mn(II) and other heavy metals, they have limited efficacy in treating Tl-contaminated wastewater. To address this gap, we operated a lab-scale Mn sand filter (MF) without added microorganisms to investigate the efficiency and mechanisms of Mn(II) and Tl(I) removal. Trends in effluent Mn(II) and Tl(I) concentrations indicated three operational stages: start-up, developing and maturation. Over time, the removal efficiency of Tl(I) gradually improved, plateauing at approximately 80 % eventually. Throughout operation, Tl(I) was sequestrated via surface complexation and ion exchange. Besides, enrichment of Sphingobium and other typical manganese oxidizing microorganisms (MnOM) during operation facilitated Mn(II) and Tl(I) oxidation and sequestration by generating biogenic manganese oxides (BioMnOx). Additionally, the accurate control of water quality and operating conditions during operation could also enhance removal efficiency. In summary, physicochemical actions of Mn oxides and biochemical actions of microorganisms synergistically contributed to the sequestration of Mn(II) and Tl(I). These findings provided a novel and sustainable method for the long-term and stable treatment of industrial wastewater containing thallium.
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  • 文章类型: Journal Article
    这项研究研究了超滤膜分离级分(>10kDa,UF-1;3-10kDa,UF-2;和<3kDa,UF-3)来自冷冻鱼糜上的鲤鱼水解产物。掺入UF-3的鱼糜凝胶表现出致密,具有均匀孔隙的连续结构,即使在经历了六个冻融(F-T)循环之后,SEM和LF-NMR分析显示,截留水的减少最少(从95.1%到91.1%),游离水的增加最少(从4.5%到6.6%)。通过分子对接分析,UF-3中的三种主要肽被鉴定为与肌球蛋白头袋形成强大的相互作用,由氢键促进,静电力,和疏水相互作用。此外,分子动力学模拟表明,这三种肽通过紧密结合碱性氨基酸(Arg,Lys)和疏水性氨基酸(Phe,Leu,Ile,Met,和Val)肌球蛋白头袋中的残留物,主要受静电能(-156.95、-321.38和-267.53千卡/摩尔,分别)和范德华能量(-395.05、-347.46和-319.16千卡/摩尔,分别)。值得注意的是,关键作用位点被确定为肌球蛋白Lys599.肽的亲水性和疏水性热点残基协同作用以稳定冷冻鱼糜中的肌球蛋白结构。
    This study investigated the cryoprotective mechanism of ultrafiltration membrane-separated fractions (>10 kDa, UF-1; 3-10 kDa, UF-2; and <3 kDa, UF-3) derived from silver carp hydrolysates on frozen surimi. The surimi gel incorporating UF-3 exhibited a compact, continuous structure with uniform pores, even after undergoing six freeze-thaw (F-T) cycle, with the minimal reduction in entrapped water (from 95.1 % to 91.1 %) and least increase in free water (from 4.5 % to 6.6 %) as revealed by SEM and LF-NMR analysis. Through molecular docking analysis, three major peptides in UF-3 were identified to form robust interactions with the myosin head pocket, facilitated by hydrogen bonds, electrostatic forces, and hydrophobic interactions. Furthermore, molecular dynamics simulations demonstrated that the three peptides effectively prevented myosin from unfolding and aggregating by tightly binding to basic amino acids (Arg, Lys) and hydrophobic amino acids (Phe, Leu, Ile, Met, and Val) residues in the myosin head pocket, primarily governed by electrostatic energies (-156.95, -321.38, and -267.53 kcal/mol, respectively) and van der Waals energies (-395.05, -347.46, and -319.16 kcal/mol, respectively). Notably, the key action site was identified as Lys599 on myosin. The hydrophilic and hydrophobic hotspot residues of the peptides worked synergistically to stabilize the myosin structure in frozen surimi.
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  • 文章类型: Journal Article
    铜和铁是工业上备受关注的基本金属元素。普鲁士蓝(PB)是一类重要的金属有机骨架(MOFs);然而,结构和性质之间缺乏这种联系,以及属性差异,限制了它们的潜在应用。在本文中,合成了掺杂和不掺杂Fe的Cu基普鲁士蓝纳米立方体。随着反应时间的增加,不掺杂Fe的铜基普鲁士蓝纳米立方体(PB:CuNCs)的形貌从长方体变为圆形,最后长回长方体.然而,具有Fe掺杂的Cu基普鲁士蓝纳米立方体(PB:CuFeNCs)直接从立方体生长并最终塌陷。纳米立方体显示出从400nm到700nm的可调谐光谱的显著红移。与PB:CuNCs相比,PB:CuFeNCs在808nm辐照下具有较高的温升和较好的光热效应。PB:CuFeNCs的催化效率随pH变化而变化,并在pH为5.5时达到其最大值1.021mM。还证实了近红外辐射等离子体光热效应增强的催化反应。这项工作强调了开发的PB:Cu和PB:CuFeNCs用于光热增强共催化纳米材料的潜力。
    Copper and iron are the basic metal elements that have attracted much attention in industry. Prussian blue (PB) is a significant class of metal-organic frameworks (MOFs); however, the lack of such linkages between the structure and properties, as well as properties differences, limits their potential applications. In this paper, the Cu-based Prussian blue nanocubes with and without Fe doping were synthesized. With the increasing reaction time, the morphology of the Cu-based Prussian blue nanocubes without Fe doping (PB:Cu NCs) changes from cuboidal to circular, and finally grows back to cuboidal. However, Cu-based Prussian blue nanocubes with Fe doping (PB: CuFe NCs) grow directly from the cube and eventually collapse. The nanocubes show a notable red shift with the tunable spectra from 400 nm to 700 nm. Compared with PB: Cu NCs, the PB: CuFe NCs have higher temperature rise under 808 nm irradiation and better photothermal efficacy. The catalytic efficiency of PB: CuFe NCs changes with the pH and reaches its maximum value of 1.021 mM with a pH of 5.5. The enhanced catalytic reaction by the near-infrared radiation plasmonic photothermal effect is also confirmed. This work highlights the potential of the developed PB: Cu and PB: CuFe NCs for photothermal-enhanced co-catalysis nanomaterials.
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  • 文章类型: Journal Article
    抗生素耐药性的流行率上升是目前一个严重的问题;因此,正在探索和开发新型抗菌药物,以解决由多种耐药病原体引起的感染。生物CuO,ZnO,和WO3纳米颗粒可以被认为是这样的试剂。大肠杆菌临床分离株,金黄色葡萄球菌,耐甲氧西林金黄色葡萄球菌(MRSA),将口腔和阴道样品中的白色念珠菌和白色念珠菌用在黑暗和光照条件下孵育的单一和组合金属纳米颗粒处理,以了解纳米颗粒的协同作用及其光催化抗菌活性。生物CuO和ZnO纳米颗粒在黑暗孵育下表现出显着的抗微生物作用,而光活化不会改变。然而,光活化的WO3纳米粒子显着减少了所有测试生物的活细胞数量的75%,因此被证明是一种有前途的抗菌剂。CuO的组合,ZnO,和WO3纳米颗粒表现出协同作用,因为与单一元素纳米颗粒的作用相比,观察到它们的抗微生物性质显著增加(>90%)。通过测量丙二醛(MDA)的产生,评估了由于ROS(活性氧)产生引起的脂质过氧化作用,金属纳米颗粒在组合和分离中的抗菌作用机理。以及使用活/死染色和使用流式细胞术和荧光显微镜定量对细胞完整性的损害。
    The rising prevalence of antibiotic-resistance is currently a grave issue; hence, novel antimicrobial agents are being explored and developed to address infections resulting from multiple drug-resistant pathogens. Biogenic CuO, ZnO, and WO3 nanoparticles can be considered as such agents. Clinical isolates of E. coli, S. aureus, methicillin-resistant S. aureus (MRSA), and Candida albicans from oral and vaginal samples were treated with single and combination metal nanoparticles incubated under dark and light conditions to understand the synergistic effect of the nanoparticles and their photocatalytic antimicrobial activity. Biogenic CuO and ZnO nanoparticles exhibited significant antimicrobial effects under dark incubation which did not alter on photoactivation. However, photoactivated WO3 nanoparticles significantly reduced the number of viable cells by 75% for all the test organisms, thus proving to be a promising antimicrobial agent. Combinations of CuO, ZnO, and WO3 nanoparticles demonstrated synergistic action as a significant increase in their antimicrobial property (>90%) was observed compared to the action of single elemental nanoparticles. The mechanism of the antimicrobial action of metal nanoparticles both in combination and in isolation was assessed with respect to lipid peroxidation due to ROS (reactive oxygen species) generation by measuring malondialdehyde (MDA) production, and the damage to cell integrity using live/dead staining and quantitating with the use of flow cytometry and fluorescence microscopy.
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