Preparation and characterization of gold nanoparticles prepared with aqueous extracts of Lamiaceae plants and the effect of follow-up treatment with atmospheric pressure glow microdischarge

AbstractThe unique properties of gold nanoparticles (AuNPs) make them attractive for use in a number of fields, ranging from cosmetology to medicine. If AuNPs are to be widely used in industrial and medical applications, it is necessary to develop environmentally friendly methods for their synthesis. This can be accomplished by replacing the traditional chemical compounds for the reduction of the Au(III) ions to Au0 during AuNPs synthesis with natural plant extracts or with atmospheric pressure plasmas. Here, the properties of three aqueous plant extracts (Mentha piperita, Melissa officinalis, and Salvia officinalis) in the synthesis of AuNPs were compared and optimized under standardized conditions. The effects of the type of plant extract, the reaction temperature, and the precursor concentration on the production and size of the obtained AuNPs were examined using UV–Vis absorption spectrophotometry, dynamic light scattering (DLS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). It was observed that the size of the produced AuNPs was dependent on the aqueous plant extract used, and that under the optimized conditions, the aqueous leaf extract of M. piperita resulted in the production of AuNPs with the smallest volume-weighted diameter. Additionally, the bioactive compounds present in each extract were studied. Attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) indicated that different chemical groups could be involved in the AuNPs synthesis, while a Folin–Ciocalteu (FC) assay revealed a clear role of phenolic compounds. Finally, it was shown that the treatment of the synthesized AuNPs, which were obtained after bioreduction using the plant extracts, with atmospheric pressure glow microdischarge (μAPGD) resulted in their agglomeration and enlargement

Fermented juices as reducing and capping agents for the biosynthesis of size-defined spherical gold nanoparticles

Gold nanoparticles (AuNPs) are of scientific and industrial significance; however, the traditional synthesis methods employ toxic compounds. Hence, non-toxic and environmentally friendly AuNPs synthesis methods are of special interest. Here, AuNPs were produced using four solutions of fermented grape juices. UV/Vis absorption spectrophotometry and transmission electron microscopy indicated that AuNPs synthesized with a solution based on semi-sweet red grapes were mostly spherical with narrow size distribution (average diameter of 82.1 ± 36.2 nm). AuNPs of similar spherical morphology but smaller size were obtained using a solution based on semi-dry red grapes (57.1 ± 16.4 nm). A large variety of AuNPs shapes and broader size distribution were produced when solutions based on semi-sweet or dry white grapes were applied. In this case, the average sizes of the AuNPs were 271.6 ± 130.2 nm and 76.0 ± 47.2 nm, respectively. Using energy dispersive X-ray spectroscopy, Au, C, and O were detected, confirming formation of biogenic AuNPs in all cases. Mie theory calculations for AuNPs synthesized with the aid of solutions based on red grapes suggest that their optical properties are different and best suited for distinct downstream applications. Attenuated total reflectance Fourier transform infrared spectroscopy, the Folin-Ciocalteu assay, and the Bertrand's method were used to examine bioactive compounds present in the solutions applied for synthesis. Phenolics, and to a lesser extent reducing sugars, were identified as likely playing a significant role in reduction and stabilization of the AuNPs. These results display the great potential of these solutions for green synthesis of size defined AuNPs, and illustrate that different grape varieties may be used to obtain AuNPs with unique properties. Keywords: Nanostructures, Bioreduction process, Phenolics, Reducing sugars, Mie scatterin

Application of Silver Nanostructures Synthesized by Cold Atmospheric Pressure Plasma for Inactivation of Bacterial Phytopathogens from the Genera Dickeya and Pectobacterium

Pectinolytic bacteria are responsible for significant economic losses by causing diseases on numerous plants. New methods are required to control and limit their spread. One possibility is the application of silver nanoparticles (AgNPs) that exhibit well-established antibacterial properties. Here, we synthesized AgNPs, stabilized by pectins (PEC) or sodium dodecyl sulphate (SDS), using a direct current atmospheric pressure glow discharge (dc-APGD) generated in an open-to-air and continuous-flow reaction-discharge system. Characterization of the PEC-AgNPs and SDS-AgNPs with UV/Vis absorption spectroscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, and selected area electron diffraction revealed the production of spherical, well dispersed, and face cubic centered crystalline AgNPs, with average sizes of 9.33 ± 3.37 nm and 28.3 ± 11.7 nm, respectively. Attenuated total reflection-Fourier transformation infrared spectroscopy supported the functionalization of the nanostructures by PEC and SDS. Antibacterial activity of the AgNPs was tested against Dickeya spp. and Pectobacterium spp. strains. Both PEC-AgNPs and SDS-AgNPs displayed bactericidal activity against all of the tested isolates, with minimum inhibitory concentrations of 5.5 mg∙L−1 and 0.75–3 mg∙L−1, respectively. The collected results suggest that the dc-APGD reaction-discharge system can be applied for the production of defined AgNPs with strong antibacterial properties, which may be further applied in plant disease management

Plant Extracts Activated by Cold Atmospheric Pressure Plasmas as Suitable Tools for Synthesis of Gold Nanostructures with Catalytic Uses

Because cold atmospheric pressure plasma (CAPP)-based technologies are very useful tools in nanomaterials synthesis, in this work we have connected two unique in their classes approaches—a CAPP-based protocol and a green synthesis method in order to obtain stable-in-time gold nanoparticles (AuNPs). To do so, we have used an aqueous Gingko biloba leave extract and an aqueous Panax ginseng root extract (untreated or treated by CAPP) to produce AuNPs, suitable for catalytical uses. Firstly, we have adjusted the optical properties of resulted AuNPs, applying UV/Vis absorption spectrophotometry (UV/Vis). To reveal the morphology of Au nanostructures, transmission electron microscopy (TEM) in addition to energy dispersive X-ray scattering (EDX) and selected area X-ray diffraction (SAED) was utilized. Moreover, optical emission spectrometry (OES) in addition to a colorimetric method was used to identify and determine the concentration of selected RONS occurring at the liquid-CAPP interface. Additionally, attenuated total reflectance Fourier transform-infrared spectroscopy (ATR FT-IR) was applied to reveal the active compounds, which might be responsible for the AuNPs surface functionalization and stabilization. Within the performed research it was found that the smallest in size AuNPs were synthesized using the aqueous P. ginseng root extract, which was activated by direct current atmospheric pressure glow discharge (dc-APGD), generated in contact with a flowing liquid cathode (FLC). On the contrary, taking into account the aqueous G. biloba leave extract, the smallest in size AuNPs were synthesized when the untreated by CAPP aqueous G. biloba leave extract was involved in the Au nanostructures synthesis. For catalytical studies we have chosen AuNPs produced using the aqueous P. ginseng root extract activated by FLC-dc-APGD as well as AuNPs synthesized using the aqueous G. biloba leave extract also activated by FLC-dc-APGD. Those NPs were successfully used as homogenous catalysts for the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP)

A Mini-Review on Anion Exchange and Chelating Polymers for Applications in Hydrometallurgy, Environmental Protection, and Biomedicine

The rapidly increasing demand for technologies aiming to resolve challenges of separations and environmental protection causes a sharp increase in the demand for ion exchange (IX) and chelating polymers. These unique materials can offer target-selective adsorption properties vital for the removal or recovery of harmful and precious materials, where trace concentrations thereof make other techniques insufficient. Hence, recent achievements in syntheses of IX and chelating resins designed and developed in our research group are discussed within this mini-review. The aim of the present work is to reveal that, due to the diversified and unique physiochemical characteristics of the proposed materials, they are not limited to traditional separation techniques and could be used in multifunctional areas of applications, including catalysis, heat management, and biomedicine

Rhenium Nanostructures Loaded into Amino-Functionalized Resin as a Nanocomposite Catalyst for Hydrogenation of 4-Nitrophenol and 4-Nitroaniline

The present work presents a new nanocomposite catalyst with rhenium nanostructures (ReNSs) for the catalytic hydrogenation of 4-nitrophenol and 4-nitroaniline. The catalyst, based on an anion exchange resin with functionality derived from 1,1′-carboimidazole, was obtained in the process involving anion exchange of ReO4– ions followed by their reduction with NaBH4. The amino functionality present in the resin played a primary role in the stabilization of the resultant ReNSs, consisting of ≈1% (w/w) Re in the polymer mass. The synthesized and capped ReNSs were amorphous and had the average size of 3.45 ± 1.85 nm. Then, the obtained catalyst was used in a catalytic reduction of 4-nitrophenol (4-NP) and 4-nitroaniline (4-NA). Following the pseudo-first-order kinetics, 5 mg of the catalyst led to a 90% conversion of 4-NP with the mass-normalized rate constant (km1) of 6.94 × 10−3 min−1 mg−1, while the corresponding value acquired for 4-NA was 7.2 × 10−3 min−1 mg−1, despite the trace amount of Re in the heterogenous catalyst. The obtained material was also conveniently reused

Polymerization-Driven Immobilization of dc-APGD Synthesized Gold Nanoparticles into a Quaternary Ammonium-Based Hydrogel Resulting in a Polymeric Nanocomposite with Heat-Transfer Applications

A new method for the production of nanocomposites, composed of gold nanoparticles (AuNPs) and (vinylbenzyl)trimethylammonium chloride-co-N,N-methylene bisacrylamide (VBTAC-co-MBA) hydrogel, is described. Raw-AuNPs of defined optical and granulometric properties were synthesized using direct current atmospheric pressure glow discharge (dc-APGD) generated in contact with a solution of HAuCl4. Different approaches to the polymerization-driven synthesis of Au/VBTAC-co-MBA nanocomposites were tested. It was established that homogenous dispersion of AuNPs in this new nanomaterial with was achieved in the presence of NaOH in the reaction mixture. The new nanocomposite was found to have excellent heat-transfer properties

The Influence of Cold Atmospheric Pressure Plasma-Treated Media on the Cell Viability, Motility, and Induction of Apoptosis in Human Non-Metastatic (MCF7) and Metastatic (MDA-MB-231) Breast Cancer Cell Lines

Breast cancer remains the most common type of cancer, occurring in middle-aged women, and often leads to patients’ death. In this work, we applied a cold atmospheric pressure plasma (CAPP)-based reaction-discharge system, one that is unique in its class, for the production of CAPP-activated media (DMEM and Opti-MEM); it is intended for further uses in breast cancer treatment. To reach this aim, different volumes of DMEM or Opti-MEM were treated by CAPP. Prepared media were exposed to the CAPP treatment at seven different time intervals and examined in respect of their impact on cell viability and motility, and the induction of the apoptosis in human non-metastatic (MCF7) and metastatic (MDA-MB-231) breast cancer cell lines. As a control, the influence of CAPP-activated media on the viability and motility, and the type of the cell death of the non-cancerous human normal MCF10A cell line, was estimated. Additionally, qualitative and quantitative analyses of the reactive oxygen and nitrogen species (RONS), generated during the CAPP operation in contact with analyzed media, were performed. Based on the conducted research, it was found that 180 s (media activation time by CAPP) should be considered as the minimal toxic dose, which significantly decreases the cell viability and the migration of MDA-MB-231 cells, and also disturbs life processes of MCF7 cells. Finally, CAPP-activated media led to the apoptosis of analyzed cell lines, especially of the metastatic MDA-MB-231 cell line. Therefore, the application of the CAPP system may be potentially applied as a therapeutic strategy for the management of highly metastatic human breast cancer

Atmospheric Pressure Plasma-Mediated Synthesis of Platinum Nanoparticles Stabilized by Poly(vinylpyrrolidone) with Application in Heat Management Systems for Internal Combustion Chambers

Poly(vinylpyrrolidone)-stabilized Pt nanoparticles (PVP-PtNPs) were produced in a continuous-flow reaction-discharge system by application of direct current atmospheric pressure glow discharge (dc-APGD) operated between the surface of a flowing liquid anode (FLA) and a pin-type tungsten cathode. Synthesized PVP-PtNPs exhibited absorption across the entire UV/Vis region. The morphology and elemental composition of PVP-PtNPs were determined with transmission electron microscopy (TEM) and energy dispersive X-ray scattering (EDX), respectively. As assessed by TEM, PVP-PtNPs were approximately spherical in shape, with an average size of 2.9 ± 0.6 nm. EDX proved the presence of Pt, C, and O. Dynamic light scattering (DLS) and attenuated total reflectance Fourier transform-infrared spectroscopy (ATR FT-IR) confirmed PtNPs functionalization with PVP. As determined by DLS, the average size of PtNPs stabilized by PVP was 111.4 ± 22.6 nm. A fluid containing resultant PVP-PtNPs was used as a heat conductive layer for a spiral radiator managing heat generated by a simulated internal combustion chamber. As compared to water, the use of PVP-PtNPs enhanced efficiency of the system, increasing the rate of heat transfer by 80% and 30% during heating and cooling, respectively