A green approach to nanoplastic detection: SERS with untreated filter paper for polystyrene nanoplastics.

Plastic pollution at the nanoscale continues to pose adverse effects on environmental sustainability and human health. However, the detection of nanoplastics (NPLs) remains challenging due to limitations in methodology and instrumentation. Herein, a "green approach" for surface-enhanced Raman spectroscopy (SERS) was exploited to detect polystyrene nanospheres (PSNSs) in water, employing untreated filter paper and a simple syringe-filtration set-up. This SERS protocol not only enabled the filtration of nano-sized PSNSs, which are smaller than the pore size of the ordinary filter paper, but also offered SERS enhancement by utilizing quasi-spherical-shaped silver nanoparticles (AgNPs) as the SERS-active substrate. The filtering of NPLs was accomplished by adding an aggregating agent to the nanoparticle mixture, which caused the aggregation of NPLs and AgNPs, resulting in a larger cluster and more hot spots for SERS detection. The optimal aggregating agent and its concentration, as well as the volume ratio between the AgNPs and NPLs, were also optimized. This SERS method successfully detected and quantified PSNSs of various sizes (i.e., 100, 300, 460, 600, and 800 nm) down to a limit of detection (LOD) of about 0.31 µg mL-1. The method was also validated against the presence of several interferents (i.e., salts, sugars, amino acids, and surfactants) and was proven practical, as evidenced by the detection of 800nm PSNSs in drinking and tap water (LODs of 1.47 and 1.55 µg mL-1, respectively).

Using polyvinyl alcohol-ionic hydrogels containing a wound healing agent to manage wounds in different environments.

OBJECTIVE: To explore the effects of pH on properties of polyvinyl alcohol (PVA)-ionic hydrogels containing wound healing promoters. METHOD: PVA was combined with a natural wound healing promoter (silk sericin (SS)), and an anionic agent (eosin (ES)) or cationic agent (methylene blue (MB)), and made into hydrogels. Properties of the hydrogels and behaviour at different pHs were investigated. RESULTS: The density and gel fraction of PVA/SS-ES hydrogel and PVA/SS-MB hydrogel were considerably lower compared with hydrogel without SS. The swelling ratio and degradation of the hydrogels increased with increasing SS concentration in all pH solutions. The influence of SS in interrupting long-chain PVA molecules was confirmed based on changes in Fourier-transform infrared spectroscopy (FTIR). The SS released from the gels was found to interact with the ionic agent and influenced the release profile of the ionic agent. Surprisingly, the anionic agent in PVA/SS-ES hydrogel showed 70% release in high pH solution whereas the cationic agent in PVA/SS-MB hydrogel showed 86% release in low pH solution. Moreover, the active agent could accumulate on the skin layer and had a positive effect on a specific wound area. CONCLUSION: Based on the results obtained in this study, it is suggested to use anionic hydrogels containing wound healing promoter for wounds at high pH and cationic hydrogels containing wound healing promoter for wounds with low pH. Ability to improve wound healing using a natural healing agent combined with ionic agents and controlling the pH of hydrogels will help in developing quick and low-cost treatment for wounds.

MCR-ALS with sample insertion constraint to enhance the sensitivity of surface-enhanced Raman scattering detection.

The multivariate curve resolution-alternative least squares (MCR-ALS) algorithm was modified with sample insertion constraint to deconvolute the overlapping peaks in SERS spectra. The developed method was evaluated by the spectral data simulated using a Gaussian distribution function to generate two independent peaks corresponding to a capping agent and an analyte. The spectra were generated with different overlapping levels and various intensity ratios of the analyte to the capping agent. By using MCR-ALS with the sample insertion constraint, the peak of the capping agent was completely excluded to obtain a calibration model of the analyte with R2 > 0.95 under all conditions. Furthermore, our developed method was later applied to a real SERS measurement to quantify carbofuran (analyte) using the azo-coupling reaction with p-ATP (capping agent) on silver nanoparticles as a SERS substrate. A calibration model of derivative carbofuran phenol was generated with R2 = 0.99 and LOD = 28.19 ppm. To assess the performance of the calibration model, the model was used to estimate the concentration of carbofuran in an external validation set. It was found that the RMSE of prediction was only 2.109 with a promising R2 = 0.97.

Antibiofilm activity and cytotoxicity of silk sericin against Streptococcus mutans bacteria in biofilm: an in vitro study.

OBJECTIVE: To investigate the potential of sericin extracted by different methods to inhibit biofilm formation (prevention) and disrupt already formed biofilm (treatment). METHOD: In this in vitro study, sericin was extracted by heat, acid, alkali and urea. Streptococcus mutans bacteria were cultivated in the presence of various concentrations of sericin to evaluate antibiofilm formation using cell density assay (inhibition effect before biofilm formed). Conversely, various concentrations of sericin were added to a biofilm already formed by Streptococcus mutans bacteria, and the viability of bacteria assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay (disruption effects after biofilm formed). Structures of extracted sericin were evaluated using circular dichroism and Fourier-transform infrared spectrometer. RESULTS: The urea-extracted sericin at all concentrations (12.5mg/ml, 25mg/ml, 50mg/ml and 100mg/ml) showed the highest potential antibiofilm activity in terms of both inhibition and disruption effects, compared with sericin extracted by heat, acid or alkali. The heat-extracted and acid-extracted sericin were found to reduce the biofilm formation dose-dependently, while the alkali-extracted sericin did not show either inhibition or disruption effect on the bacterial biofilm. The urea-extracted sericin also killed the bacteria residing within the biofilm, possibly due to its modified structure which may destabilise the bacterial cell wall, leading to membrane disintegration and, finally, cell death. CONCLUSION: Our results demostrated the antibiofilm activity of sericin. This could form the basis of further research on the mechanism and application of sericin as a novel antibiofilm agent.

Distinguishing Enantiomers by Tip-Enhanced Raman Scattering: Chemically Modified Silver Tip with an Asymmetric Atomic Arrangement.

Discrimination between enantiomers is achieved by tip-enhanced Raman scattering (TERS) using a silver tip that is chemically modified by an achiral para-mercaptopyridine (pMPY) probe molecule. Differences in the relative intensities of the pMPY spectra were monitored for three pairs of enantiomers containing hydroxy (-OH) and/or amino (-NH2 ) groups. The N: or N+ -H functionality of the pMPY-modified tip participates in hydrogen-bond interactions with a particular molecular orientation of each chiral isomer. The asymmetric arrangement of silver atoms at the apex of the tip induces an asymmetric electric field, which causes the tip to become a chiral center. Differences in the charge-transfer (CT) states of the metal-achiral probe system in conjunction with the asymmetric electric field produce different enhancements in the Raman signals of the two enantiomers. The near-field effect of the asymmetric electric field, which depends on the number of analyte functional groups capable of hydrogen-bond formation, improves the degree of discrimination.

Local structural changes in graphene oxide layers induced by silver nanoparticles.

Structural changes of graphene oxide (GO) in silver/graphene oxide (AGO) nanocomposites are investigated using tip-enhanced Raman scattering (TERS). Because of markedly high spatial resolution of the TERS technique, the measurements of molecular information at specific nano-scaled positions can be achieved by constructing line-profile TERS spectra straight from the center of silver nanoparticles (AgNPs) on GO layers. The results show evidences that AgNPs cause shortening of C-C bonds beneath AgNPs, flattening of GO layers, and critical bending on GO layers. Additionally, a connection of carbon atoms via a C-C network subsequently expands structural changes with a distance of 200-250 nm from the center of AgNPs, even though this distance is larger than the size of AgNPs. The proposed model of GO structural changes unveils new understanding about changes in properties from GO to AGO nanocomposites, which will contribute to a development of advanced nanostructures/nanocomposites in the near future.

Bringing macromolecules into cells and evading endosomes by oxidized carbon nanoparticles.

A great challenge exists in finding safe, simple, and effective delivery strategies to bring matters across cell membrane. Popular methods such as viral vectors, positively charged particles and cell penetrating peptides possess some of the following drawbacks: safety issues, lysosome trapping, limited loading capacity, and toxicity, whereas electroporation produces severe damages on both cargoes and cells. Here, we show that a serendipitously discovered, relatively nontoxic, water dispersible, stable, negatively charged, oxidized carbon nanoparticle, prepared from graphite, could deliver macromolecules into cells, without getting trapped in a lysosome. The ability of the particles to induce transient pores on lipid bilayer membranes of cell-sized liposomes was demonstrated. Delivering 12-base-long pyrrolidinyl peptide nucleic acids with d-prolyl-(1S,2S)-2-aminocyclopentanecarboxylic acid backbone (acpcPNA) complementary to the antisense strand of the NF-κB binding site in the promoter region of the Il6 gene into the macrophage cell line, RAW 264.7, by our particles resulted in an obvious accumulation of the acpcPNAs in the nucleus and decreased Il6 mRNA and IL-6 protein levels upon stimulation. We anticipate this work to be a starting point in a new drug delivery strategy, which involves the nanoparticle that can induce a transient pore on the lipid bilayer membrane.

Selective colors reflection from stratified aragonite calcium carbonate plates of mollusk shells.

An interaction between the incident light and the structural architecture within the shell of Asian green mussel (Perna viridis) induces observable pearlescent colors. In this paper, we investigate the influence of the structural architecture on the expressed colors. After a removal of the organic binder, small flakes from crushed shells show vivid rainbow reflection under an optical microscope. An individual flake expresses vivid color under a bright-field illumination while become transparent under a dark-field illumination. The expressed colors of the aragonite flakes are directly associated with its structural architecture. The flakes with aragonite thickness of 256, 310, and 353 nm, respectively, appear blue, green, and red under an optical microscope. The spectral simulation corroborates the experimentally observed optical effects as the flakes with thicker aragonite layers selectively reflected color with longer wavelengths. Flakes with multiple aragonite thicknesses expressed multi-color as the upper aragonite layers allow reflected colors from the lower layers to be observed.

Chemometric analysis of spectroscopic data on shape evolution of silver nanoparticles induced by hydrogen peroxide.

The study on the shape evolution of metal nanoparticles (MNPs) is crucial to gain an understanding on controlling the shape and size of metal nanostructures. In this work, a detailed study on shape evolution of silver (Ag) nanospheres to nanoplates induced by hydrogen peroxide (H2O2) was performed. According to the growth mechanism of Ag nanoplates, the spectrophotometric method combined with chemometric analysis has potential to reveal the structural evolution process as observed by surface plasmon resonance phenomena. The extinction spectra of the evolving nanostructures were analyzed by factor analysis and error indicator functions. Five major components attributed to the different particle shapes and sizes were theoretically predicted. Furthermore, the concentration profiles and pure spectra of these components were resolved using multivariate curve resolution-alternative least squares (MCR-ALS) analysis. The evolution profiles show that the spherical Ag particles systematically evolved into plate structures of different sizes. Larger nanoplates were obtained when higher concentrations of H2O2 were employed. An evidence of nanoplate disintegration was observed when a large amount of H2O2 was employed. The predicted structural morphologies of each component given by chemometric calculation were in excellent agreement with those observed by transmission electron microscope (TEM) images.

Size-independent quantification of nanoplastics in various aqueous media using surfaced-enhanced Raman scattering.

In this work, we successfully developed an intriguing preparation strategy to reduce the size-dependent effect of nanoplastics (NPLs), which is the limitation of NPLs quantification by surface-enhanced Raman scattering (SERS). This simple and low-cost technique enabled us to quantify different sizes (i.e., 100, 300, 600, and 800 nm) of polystyrene nanospheres (PS NSs) in various aqueous media. The SERS substrate was simply prepared by sputtering gold particles to cover on a glass cover slide. By dissolving PS NSs in toluene and preconcentrating by coffee-ring effect, SERS measurement can quantify NPLs at a very low concentration with a limit of detection (LOD) of approximately 0.10-0.26 µg/mL. The experiment was also conducted in the presence of interferences, including salts, sugars, amino acids, and detergents. The method was validated for quantitative analysis using a mixture of 100-, 300-, 600-, and 800-nm PS NSs in a ratio of 1:1:1:1 in real-world media (i.e., tap water, mineral water, and river water), which successfully approaches the evaluation of PS NSs in the range of 10-40 µg/mL with an LOD of approximately 0.32-0.52 µg/mL.

Effect of Lavandula angustifolia and Cananga odorata on decrease of blood pressure in high blood pressure volunteers: A randomized controlled trial.

INTRODUCTION: Hypertension is one of the most dangerous diseases. However, medicine for hypertension may cause adverse effects. Thus, alternative treatments may be beneficial to patients. The aims of the study were to evaluate efficacy and safety of sticker pads containing lavender and ylang ylang oil (LY pads) on decrease blood pressure. MATERIALS AND METHODS: The LY pads had been developed since 2018. The safety of LY pads in healthy volunteers' study and the efficacy and safety of LY pads in high blood pressure volunteers' study were conducted at Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, Thailand in October 2020 to December 2022. In the safety of LY pads in healthy volunteers' study, the LY pad was attached to the shirts of 56 healthy volunteers for 2 h. Adverse reactions, irritation score, and quality of life were assessed. In the efficacy and safety of the LY pads in high blood pressure volunteers' study, 34 high blood pressure volunteers were randomly divided into the LY group or the placebo group. The volunteers attached the pad to their shirt for 14 days. Blood pressure, pulse rate, and adverse reactions were investigated. RESULTS: The LY pad was safe for humans. Using the LY pad for 2 h had no significant adverse reactions in healthy volunteers. Moreover, it significantly improved quality of life (p<0.05). The blood pressure of the LY pad group after at least 3 days use was significantly lower than before using the pad (p<0.05). The systolic blood pressure difference and pulse rate difference were also superior in the LY pad group compared to the placebo group (p<0.05). CONCLUSIONS: The LY pad was safe in healthy volunteers and could reduce blood pressure in high blood pressure volunteers without adverse effects. Thus, it may be a supportive or alternative treatment for hypertension.

An ionic surfactant-mediated Langmuir-Blodgett method to construct gold nanoparticle films for surface-enhanced Raman scattering.

A gold nanoparticle film for surface-enhanced Raman scattering (SERS) was successfully constructed by an ionic surfactant-mediated Langmuir-Blodgett (LB) method. The gold film was formed by adding ethanol to a gold colloid/hexane mixture in the presence of dodecyltrimethylammonium bromide (DTAB). Consequently, gold nanoparticles (AuNPs) assembled at the water/hexane interface due to the decrease in surface charge density of AuNPs. Since DTAB binds the gold surface by a coulombic force, rather than a chemical bonding, it is easily replaced by target molecules for SERS purposes. The SERS enhancement factor of the 80 nm gold nanoparticle film was approximately 1.2 × 10(6) using crystal violet (CV) as a Raman dye. The SERS signal from the proposed DTAB-mediated film was approximately 10 times higher than that from the octanethiol-modified gold film, while the reproducibility and stability of this film compared to an octanethiol-modified film were similar. This method can also be applied to other metal nanostructures to fabricate metal films for use as a sensitive SERS substrate with a higher enhancement factor.

Micrometer-sized gold nanoplates: starch-mediated photochemical reduction synthesis and possibility of application to tip-enhanced Raman scattering (TERS).

In this report, we propose a novel starch-mediated photochemical reduction method for synthesizing micrometer-sized gold nanoplates and the possibility of using them as a tip-enhanced Raman scattering (TERS) substrate. To reduce gold ions, a starch chain firstly forms a complex with AuCl(4)(-), and the gold ion is subsequently reduced by receiving an electron from a chloride ion and generating a chloride radical when the [AuCl(4)(-)-starch] complex is irradiated by sunlight. Due to the slow reaction rate and the capability of starch as a template, gold structure can thermodynamically grow along the (111) facet which is the lowest energy facet of the gold face-centered cubic (fcc) crystal. This method can provide various shapes of gold plates such as triangle, truncated triangle, hexagon, polygon, etc. The plate size can be controlled in the range from a few micrometers to more than one hundred micrometers by increasing the acidity of solution while the plate thickness is less than 100 nm. Potential application of the gold plates as TERS substrates is demonstrated by collecting Raman signals while approaching a silver-coated tungsten tip to the surface of the micrometer-sized gold nanoplate covered by crystal violet (CV) molecules. The results show that less than one hundred CV molecules can be detected in our study.

Progress of tip-enhanced Raman scattering for the last two decades and its challenges in very recent years.

Tip-enhanced Raman scattering (TERS) has recently attracted remarkable attention as a novel nano-spectroscopy technique. TERS, which provides site-specific information, can be performed on any material surface regardless of morphology. Moreover, it can be applied in various environments, such as ambient air, ultrahigh vacuum (UHV), solutions, and electrochemical environments. This review reports on one hand progress of TERS for the last two decades, and on the other hand, its challenges in very recent years. Part of the progress of TERS starts with the prehistory and history of TERS, and then, the characteristics and advantages of TERS are described. Significant emphasis is put on the development of TERS instrumentation and equipment such as ultrahigh vacuum TERS, liquid TERS, electrochemical-TERS, and tip-preparations. Applications of TERS, particularly those with nanocarbons, biological materials, and surface and interface analysis, are mentioned in some detail. In the part on challenges, we focus on the very recent advances in TERS; progress in spatial resolution to the angstrom scale is the hottest topic. Recent TERS studies performed under UHV, for example chemical imaging at the angstrom scale and Raman detection of bond breaking and making of a chemisorbed up-standing single molecules at single-bond level, are reviewed. Of course, there is no clear border between the two parts. In the last part the perspective of TERS is discussed.

Selection of cryoprotectants for freezing and freeze-drying of gold nanoparticles towards further uses in various applications.

Recently, cryopreservation of AuNPs without aggregation has been attempted to improve their long-term stability. This study investigated criteria to select cryoprotectants for AuNPs using a variety of materials, including sugar (sucrose), surfactant (Tween 20), polymers (polyvinyl alcohol (PVA) and polyvinylpyrrolidone (PVP)), and biopolymer (pectin). For cryoprotective performance, UV-vis spectroscopy reveals the potential of all cryoprotectants for preventing citrate-capped AuNPs (cit-AuNPs) from irreversible aggregation under freezing. While sucrose, PVP, and pectin were more suitable than Tween 20 and PVA as cryoprotectants for lyophilization of AuNPs with the maintained redispersability. For storage and further use, Luria-Bertani agar plate, dynamic light scattering (DLS), and transmission electron microscopy (TEM) results indicate impacts of the cryoprotectant coexisted with AuNPs after resuspension and imply that washing of the restored AuNPs is encouraged. Otherwise, running the restored AuNPs through applications, such as functionalization, protein conjugation, and surface-enhanced Raman scattering (SERS), without washing the cryoprotectant could lead to inaccurate results. This study also serves as a guideline for a comprehensive practice flow of AuNP handling, encompassing the synthesis step, cryopreservation, and use after resuspension.

Coupling reaction-based ultrasensitive detection of phenolic estrogens using surface-enhanced resonance Raman scattering.

Studies have shown that many adverse health effects are associated with human exposure to dietary or environmental estrogens. Therefore, the development of rapid and highly sensitive detection methods for estrogens is very important and necessary to maintain hormonal concentration below the safety limit. Herein, we demonstrate a simple and rapid approach to detect trace amounts of phenolic estrogen based on surface-enhanced resonance Raman scattering (SERRS). Because of a coupling reaction between diazonium ions and the phenolic estrogens, azo compounds are formed with strong SERRS activity, which allows phenolic estrogen recognition at subnanomolar levels in solution. The proposed protocol has multiplexing capability, because each SERRS fingerprint of the azo dyes specifically corresponds to the related estrogen. Moreover, it is universal and highly selective, not only for phenolic estrogens but also for other phenolic molecules, even in complex systems.

Highly sensitive and selective determination of iodide and thiocyanate concentrations using surface-enhanced Raman scattering of starch-reduced gold nanoparticles.

In this report, we propose a novel technique for the determination of the concentrations of iodide and thiocyanate by surface-enhanced Raman scattering (SERS) of starch-reduced gold nanoparticles. Starch-reduced gold nanoparticles show an intrinsic Raman peak at 2125 cm(-1) due to the -C≡C- stretching mode of a synthesized byproduct. Because of the high adsorptivity of iodide on a gold surface, the intensity of the SERS peak at 2125 cm(-1) decreases with an increase in the iodide concentration. Thiocyanate also strongly adsorbs on a gold surface, and a new peak appears at around 2100 cm(-1), attributed to the -C≡N stretching vibration in a SERS spectrum of starch-reduced gold nanoparticles. These two peaks were successfully used to determine the iodide and thiocyanate concentrations separately, even in their mixture system. The detection limit of this technique for iodide is 0.01 µM with a measurement range of 0.01-2.0 µM, while the detection limit of this technique for thiocyanate is 0.05 µM with a measurement range of 0.05-50 µM. This technique is highly selective for iodide and thiocyanate ions without interference from other coexisting anions such as other halides, carbonate, and sulfate.

Superior Technique for the Production of Agarose Dressing Containing Sericin and Its Wound Healing Property.

Finding a simple and eco-friendly production technique that matches to the natural agent and results in a truly valuable natural scaffold production is still limited amongst the intensively competitive natural scaffold development. Therefore, the purpose of this study was to develop natural scaffolds that were environmentally friendly, low cost, and easily produced, using natural agents and a physical crosslinking technique. These scaffolds were prepared from agarose and sericin using the freeze-drying method (D) or freeze-thawing together with the freeze-drying method (TD). Moreover, plasticizers were added into the scaffold to improve their properties. Their physical, mechanical, and biological properties were investigated. The results showed that scaffolds that were prepared using the TD method had stronger bonding between sericin and other compounds, leading to a low swelling ratio and low protein release of the scaffolds. This property may be applied in the development of further material as a controlled drug release scaffold. Adding plasticizers, especially glycerin, into the scaffolds significantly increased elongation properties, leading to an increase in elasticity of the scaffold. Moreover, all scaffolds could activate cell migration, which had an advantage on wound healing acceleration. Accordingly, this study was successful in developing natural scaffolds using natural agents and simple and green crosslinking methods.

Luminescent nanohybrid of ZnO quantum dot and cellulose nanocrystal as anti-counterfeiting ink.

Luminescent quantum dot (QD) ink is currently a powerful tool for generating hidden information on paper substrates. Herein, we fabricated a nanohybrid ink of bacterial cellulose nanocrystal (BCNC) and UV-responsive ZnO QD via electrostatic self-assembly for improving solvent resistance and message encryption process. Under investigations on the printed areas, the nanohybrid can slightly infiltrate into the paper fibers and form a thin layer on the top of paper substrates, conferring an enhanced print permanence against wetting conditions while maintaining the daylight unobservability and its luminescent stability. The water resistance of the proposed nanohybrid ink enables developing a higher security level that the prints can be submerged in CuCl2 aqueous solutions to quench the luminescent message. The concealed message can eventually be revealed under UV light again after submerging in EDTA solution. Our ZnO QD/BCNC nanohybrid with eco-friendly nature therefore exhibits great potential as security marking ink for counterfeit protection with sustainable uses.

Development of Eugenol-Embedded Calcium Citrate Nanoparticles as a Local Anesthetic Agent.

Eugenol is a major phenolic component derived from clove oil with potential medical applications. Of particular interest, it has been used as a therapeutic agent in topical applications because of its analgesic and local anesthetic properties. However, topical formulations of eugenol produce skin irritation, which limits its clinical applications. One promising strategy to overcome this disadvantage is by using a biocompatible material that could be an appropriate topical vehicle for eugenol. Researchers have recently focused on the development of eugenol-embedded calcium citrate nanoparticles (Eu-CaCit NPs) without adverse effects. The Eu-CaCit NPs were developed as a topical delivery system and their biocompatibility and penetration ability were evaluated. Eu-CaCit NPs at 1.2 mg/mL did not show cytotoxicity effects in human cells. Moreover, the Eu-CaCit NPs presented the ability to penetrate the dermis layer of the human intact skin following 12 h exposure. All the results concluded that Eu-CaCit NPs have shown a potential as a carrier for topical delivery of eugenol. These novel nanoparticles represent a promising alternative for topical application of local anesthetic with natural pain relievers.