Washing Steps Research Articles

Ionic Liquids as Potential Cleaning and Restoration Agents for Cellulosic Artefacts

This study explores the efficacy of 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide and 1-hexyl-3-methylimidazolium chloride as cleaning agents for aged cellulosic artifacts. A 10% v/v acetone solution of these ionic liquids (ILs) effectively removes the brownish-yellow color of aged paper in a 10 min immersion treatment. Colorimetric analysis shows a remarkable increase in lightness (L*) by up to 40% and a decrease in red/brownish tones (b*) after IL treatment. The cleaning process also deacidifies the paper, shifting the pH to neutral-slightly basic levels and enhancing its long-term stability. Optimal pH outcomes are achieved, with ionic liquid consumption values of 0.4–0.6 g/g of paper. The FTIR analysis revealed structural changes in cellulose induced by the washing step, which is mainly due to the reorganization effect imparted by the ionic liquids. Furthermore, ILs mobilized degraded compounds and acidic species, aiding in their extraction during the restoration process. Mechanical testing indicated an enhancement in the overall tensile strength and strain at break values for IL-treated papers by up to 33%. This study demonstrates the multiple benefits of alkylimidazolium ionic liquids for preserving and restoring cultural heritage artifacts made of cellulosic materials.

Sustainable Tailoring of Lignin Nanoparticles Assisted by Green Solvents

AbstractThis work aimed at studying the self‐assembly of lignin macromolecules towards lignin nanoparticles (LNPs) with green solvents and shedding light on a tailor‐made production of LNPs through a meticulous study of different variables. The methodology (antisolvent to lignin solution – method A; or lignin solution to antisolvent – method B), the lignin solvent, the flow rate of solvent/antisolvent addition, the lignin solution loading and the washing step (centrifugation vs dialysis) were examined. Remarkably, method B enabled achieving desired LNPs (127.4–264.9 nm), while method A induced the formation of lignin microparticles (582.8–7820 nm). Among lignin solvents, ethanol allowed the preparation of LNPs with the lowest hydrodynamic diameter (method B=127.4 nm), while the largest particles (method A=7820 nm) were obtained with ethylene glycol. These latest particles were characterized as heterogeneous, irregular, and highly aggregated when compared for instance with γ‐valerolactone counterparts, which showed the most homogeneous (PDI=0.057–0.077) and spherical particles. Moreover, decreasing lignin solution loading enabled the reduction on LNP size and Zeta potential. Dialysed samples allowed the formation of LNPs with lower hydrodynamic size, reduced aggregation, and higher homogeneity. Furthermore, dialysis provided high stability to LNPs, avoiding particle coalescent phenomenon.

Tetrazine‐Isonitrile Bioorthogonal Fluorogenic Reactions Enable Multiplex Labeling and Wash‐Free Bioimaging of Live Cells

AbstractDeveloping fluorogenic probes for simultaneous live cell labeling of multiple targets is crucial for understanding complex cellular events. The emerging [4+1] cycloaddition between tetrazine and isonitriles holds promise as a bioorthogonal tool, yet existing tetrazine probes lack reactivity and fluorogenicity. Here, we present the development of a series of tetrazine‐functionalized bioorthogonal probes. By incorporating pyrazole adducts into the fluorophore scaffolds, the post‐reacted probes displayed remarkable fluorescence turn‐on ratios, up to 3184‐fold. Moreover, these modifications are generalizable to various fluorophores, enabling a broad emission range from 473 to 659 nm. Quantum chemical calculations further elucidate the turn‐on mechanisms. These probes enable the simultaneous labeling of multiple targets in live cells, without the need for a washing step. Consequently, our findings pave the way for advanced multiplex imaging and detection techniques for cellular studies.

Tetrazine-Isonitrile Bioorthogonal Fluorogenic Reactions Enable Multiplex Labeling and Wash-Free Bioimaging of Live Cells.

Developing fluorogenic probes for simultaneous live cell labeling of multiple targets is crucial for understanding complex cellular events. The emerging [4+1] cycloaddition between tetrazine and isonitriles holds promise as a bioorthogonal tool, yet existing tetrazine probes lack reactivity and fluorogenicity. Here, we present the development of a series of tetrazine-functionalized bioorthogonal probes. By incorporating pyrazole adducts into the fluorophore scaffolds, the post-reacted probes displayed remarkable fluorescence turn-on ratios, up to 3184-fold. Moreover, these modifications are generalizable to various fluorophores, enabling a broad emission range from 473 to 659 nm. Quantum chemical calculations further elucidate the turn-on mechanisms. These probes enable the simultaneous labeling of multiple targets in live cells, without the need for a washing step. Consequently, our findings pave the way for advanced multiplex imaging and detection techniques for cellular studies.

Pemberdayaan Masyarakat Kampung Pelangi Melalui Pelatihan Langkah Cuci Tangan Pakai Sabun pada Ibu Rumah Tangga Di Kelurahan Guntung Paikat Kota Banjarbaru

Banjarbaru City is the second city with the highest number of cases after Banjarmasin with 4,411 cases and 123 deaths in 2021. Several health behaviors that can reduce the possibility of being infected with the COVID-19 virus are implementing Clean and Healthy Living Behavior, one of which is by implementing the behavior of washing hands with soap. Therefore, training activities aim to increase the knowledge and behavior of housewives regarding PHBS, especially the practice of washing hands with soap in the household setting. The training method used uses an active participatory method so that participants are free to express opinions and ask questions and practice hand washing steps directly. The target of this activity is 30 housewives in Kampung Pelangi, Guntung Paikat Village, Banjarbaru City. This activity is divided into three stages, namely preparation, implementation and evaluation. The evaluation results showed that there was an increase in the knowledge of the training participants before and after the training. It is hoped that future activities can involve other groups in the household, such as involving the head of the house

Improved sensitivity and automation of amulti-step upconversion lateral flow immunoassay using a3D-printed actuation mechanism.

The development of sensitive point-of-care (POC) assay platforms is of interest for reducing the cost and time of diagnostics. Lateral flow assays (LFAs) are the gold standard for POC systems, but their sensitivity as such is inadequate, for example, in the case of cardiac diagnostics. The performance can be improved by incorporating different steps, such as pre-incubation to prolong the interaction time between sample and reporter for immunocomplex formation, and washing steps for background reduction. However, for POC assays, manual steps by the assay conductor are not desired. In this research, upconverting nanoparticles (UCNPs) were coated with poly(acrylic acid) (PAA) and conjugated to anti-cTnI antibodies, yielding non-clustering particles with low non-specific binding. The performance of cTnI-LFA in the PAA-anti-cTnI-UCNPs was compared to thesame UCNPs with a commercial carboxyl surface. A kitchen-timer mechanism was embedded in a 3D-printed housing to produce a low-cost actuator facilitating a timed pre-incubation step for reporter and sample, and a washing step, to enable a multi-step cTnI-LFA with minimized manual labour. PAA-UCNPs showed improved mobility on nitrocellulose compared to those with a commercial surface. The mechanical actuator system was shown to improve sensitivity compared to a labour-intensive multi-step dipstick method, despite pre-incubation occurring during shaking and heating in the dipstick method. The limit of detection decreased from 7.6 to 1.5ng/L cTnI in human plasma. The presented actuator can be easily modified for sensitivity improvement in the LFA for different analytes via pre-incubation and washing steps.

A, The IMPLEMENTATION OF CLEAN AND HEALTHY LIVING BEHAVIOR THROUGH HAND HYGIENE WITH 6 STEPS OF HAND WASHING AS PREVENTION OF DISEASE TRANSMISSION

School as an institution that has an organization that has a curriculum as a form of activity that is neatly planned and arranged (Nurochim, 2019). Health Education (PENKES) is given to children with the aim of improving healthy living habits so that they can be responsible for themselves and their environment as well as participating in health-related activities (Mardhianti, 2013), (Rindafit, 2015). Hands are a part of the body that comes into direct contact with dirt, the habit of children who do not wash their hands after contact with dirty objects causes the entry of bacteria into the body, the result is that diseases will be lodged in the child's body such as worms, diarrhea, cough, and other infectious diseases. Health education about hand washing is important to be given to children to foster clean and healthy living behavior. Hand washing with soap is one of the actions of clean and healthy living behavior (PHBS) which aims to break the chain of disease spread through direct or indirect contact so as to prevent disease transmission. The purpose of this activity is expected to increase understanding and awareness in children to wash their hands based on hand washing steps to improve health status and prevent infectious diseases.

Evaluation of the impact of olive milling on the mineral oil contamination of extra‐virgin olive oils

AbstractMineral oil saturated (MOSH) and aromatic hydrocarbons (MOAH) are environmental and processing contaminants also found in extra‐virgin olive oil. Knowledge on contamination sources can help minimize them. The main objective of this work was to investigate the impact of milling operations. To this purpose, samples from 25 processing lines (at 5 different processing stages) were analyzed by online high‐performance liquid chromatography—gas chromatography—flame ionization detection. A protocol for eliminating endogenous n‐alkanes was tested and applied when necessary. Generally, transport to the mill had a negligible impact. The washing step had a mitigation impact, more evident on samples with higher contamination. On average, total MOSH decreased of 2.1 mg kg–1. Despite the reduction determined by washing, the entire milling process resulted in an increase in contamination (> 30%) for 20% of the processing lines. Total average MOSH and MOAH contamination increased by 2.3 and 0.6 mg kg–1, respectively.Practical Applications: This work aims to improve the knowledge on the presence and sources of mineral oil hydrocarbons (MOH), contaminants of petrogenic origin, in extra‐virgin olive oil. In particular, this work investigates the impact of processing at the mill, including the transport stage, as well as the potential of the washing step in reducing the contamination. For the first time, a systematic study on this topic has been carried out. The knowledge of the contribution of individual steps in the production process to final product contamination is of paramount importance in identifying critical points on which to take action to mitigate contamination, and this is of great interest for all operators of the sector and for protecting consumer health, especially when considering possible presence of MOAH, which may include genotoxic and carcinogenic compounds.

Copper Nanosheet-Based Wash-Free Fluorescence Imaging of Cancer Cells.

Near-infrared fluorescence (NIRF) probes greatly facilitate in vivo imaging of various biologically important species. However, there are several significant limitations such as consuming washing steps, photobleaching, and low signal intensity. Herein, we synthesized fluorescent copper nanosheets templated with DNA scaffolds (DNS/CuNSs). We employ them and Cy5.5 of the fluorescence resonance energy transfer (FRET) system, which have a larger Stokes shift (∼12-fold) than the traditional NIRF dye Cy5.5. Based on their excellent fluorescence properties, we employ DNS/CuNSs-Cy5.5 for fluorescence probes in cancer cell imaging. Compared with the free Cy5.5 fluorescence probe, the novel fluorescence imaging probe implements wash-free imaging and exhibits enhanced anti-photobleaching ability (∼5.5-fold). Moreover, the FRET system constructed by DNS/CuNSs has a higher signal amplification ability (∼4.17-fold), which is more similar to that of Cu nanoclusters prepared with DNA nanomonomers as a template. This work provides a new idea for cancer cell MCF-7 imaging and is expected to promote the development of cancer cell fluorescence imaging.

Red-emissive carbon quantum dots minimize phototoxicity for rapid and long-term lipid droplet monitoring

Long-term fluorescence monitoring of subcellular organelles is crucial for cellular physiology and pathology studies. Lipid droplets (LDs) are increasingly recognized for their involvement in various biological processes, to influence disease development through diverse behaviors However, existing LD probes face challenges in achieving high targeting and long-term monitoring due to poor photostability and long-term phototoxicity. Carbon quantum dots (CQDs) have gained prominence due to their exceptional fluorescence properties, but their prevalent blue excitation wavelength presents difficulties for long-term imaging. Herein, we synthesized red-emissive carbon quantum dot (R-CQDs) with superior photobleaching resistance and red-emission, thus enabling harmlessly fluorescence monitoring of cells longer than 3 h. In addition, R-CQD exhibits suitable amphiphilicity and remarkable solvatochromic effect, allowing rapid targeting to LDs for immediate imaging without cumbersome washing steps. Hence, R-CQD shows high performance for extended observation of dynamic LD behavior in various biological processes, which is confirmed by documenting the course of LDs during starvation as well as lipotoxicity. Compared to commercial probes, R-CQD extends live cell imaging time by at least 9-fold, facilitating the study of LD behavioral characteristics under diverse physiological or pathological conditions. This work provides a reliable fluorescence tool for tracking intercellular microenvironment dynamically thus to understand the divers biological or disease mechanism.

Dry and Hydrothermal Co-Carbonization of Mixed Refuse-Derived Fuel (RDF) for Solid Fuel Production

The present study aims to test several conditions of the thermochemical pretreatment of torrefaction and carbonization to improve the physical and combustible properties of the Portuguese RDF. Therefore, two different types of RDF were submitted alone or mixed in 25%, 50%, and 75% proportions to dry carbonization processes in a range of temperatures between 250 to 350 °C and residence time between 15 and 60 min. Hydrothermal carbonization was also carried out with RDF samples and their 50% mixture at temperatures of 250 and 300 °C for 30 min. The properties of the 51 chars and hydrochars produced were analyzed. Mass yield, apparent density, proximate and elemental analysis, ash mineral composition, and higher heating value (HHV), among others, were determined to evaluate the combustion behavior improvement of the chars. The results show that after carbonization, the homogeneity and apparent density of the chars were increased compared to the raw RDF wastes. The chars and hydrochars produced present higher HHV and lower moisture and chlorine content. In the case of chars, a washing step seems to be essential to reduce the chlorine content to allow them to be used as an alternative fuel. In conclusion, both dry and wet carbonization demonstrated to be important pretreatments of the RDF to produce chars with improved physical and combustion properties.

Exploiting mechanochemical activation and molten-salt-assisted reduction-diffusion approach in bottom-up synthesis of Sm2Fe17N3

Sm2Fe17N3 powders were prepared by a novel molten-salt mechanochemically assisted reduction-diffusion (RD) approach. CaCl2, plays a critical role during mechanochemical processing as a dispersant, facilitating the RD process by dissolving the precursors in a molten flux and further assisting during the washing step by efficient removal of by-products thus minimizing the surface oxidation of Sm2Fe17N3 powder particles. Various milling times and RD temperatures were examined, and synthesis conditions were optimized to achieve pure-phase Sm2Fe17N3 powders with low aggregation of magnetic particles. Powders synthesized at 950 °C RD exhibited the highest hard-magnetic properties: coercivity Hc of 13.5 kOe, and maximum energy product (BH)max of 19.4 MGOe. This was attributed to the formation of fine single-phase Sm2Fe17N3 particles as well as minimal oxidation of particle surface. Furthermore, by densifying the Sm2Fe17N3 powders with high-pressure spark plasma sintering, a bulk magnet with (BH)max of 16.5 MGOe and a relative density of 86 % was produced indicating that the obtained Sm2Fe17N3 powders had low oxygen content.

A novel biosensor based on antibody-controlled strand displacement amplification (SDA) and hybridization chain reaction (HCR) for tetracycline detection

The specificity of antibodies and efficient amplification of nucleic acid molecules play an important role in developing biosensors for monitoring human and environmental health. Herein, integrating their capabilities by site-selective modification of small molecules on DNA, a biosensor based on antibody-controlled strand displacement amplification (SDA) and hybridization chain reaction (HCR) was developed. The SDA–HCR reaction was activated by the competitive binding of antibodies to free small molecules and small molecule-conjugated DNA. As a proof-to-concept, we developed a biosensor capable of detecting tetracycline (TC) with high sensitivity and specificity. First, TC was labeled with azide group through chemical modification, and TC–DNA was prepared by copper-free click chemistry. Further, the antibody-controlled SDA–HCR reaction was developed through serial optimization. By this method, TC could be detected in a linear range of 0.01–100 µM with a detection limit of 0.006 µM, and the recovery of actual samples was 96.62–100.31 % with 1.70–4.00 % RSD, suggesting satisfactory performance by the biosensor. Using this method, TC or any other small molecules can be detected without washing, immobilization, and multiple additional steps, which would simplify detection to a great degree. Consequently, the distinctive strategy proposed in this work may find more applications in the detection of other small molecules.

Extraction of proteinaceous components and biominerals from cold water fish fileting side streams: a review

Fileting is a popular form of processing methods and in addition to being sold fresh or frozen, filets are used for preparation products battered and breaded filets. This generates considerable amount of side streams like skin, frames, and cut-offs which forms around 30–70% of the total body weight. The European Waste Framework Directive 2008 and recent amendments [EU WFD (2018/851)] stipulates comprehensive regulations which the manufacturers must follow while handling the side streams generated during the processing. This demands a detailed compilation of information regarding the yield, classification and valorization potential of side streams associated with the fileting operations of the cold-water finfishes. The side streams are a rich source of proteins including structural proteins like collagen and biominerals such as hydroxyapatite which find multiple application in food and pharmaceutical industry. Previously, the recovery of these components was performed by extensive chemical treatment with acids or bases, including subsequent washing steps. Nowadays, green extraction methods, defined as technologies with reduced energy and chemical consumption, should be considered to achieve a green shift in the food industry. Nevertheless, industrial upscaling of green extraction methods and subsequent refinement of the isolated compounds must be further evaluated and improved in order to achieve a green shift in food industry by using side-stream derived compounds as ingredients. Moreover, legislations as well as national and international regulations must be considered and evaluated. Even though a number of articles are recently available regarding seafood side stream valorization, this review focus on side streams generated predominantly from cold water fish species and also discusses sustainable green technologies to be included during the recovery process.

Polycarbonate ethanolysis with imidazolium-based ionic liquids: Recovery of high-purity BPA and value-added by-product

Depolymerization using ionic liquids (ILs) is an efficient and eco-friendly method for recycling waste poly(bisphenol A carbonate) (PC). To use IL for PC ethanolysis, the effect of IL structure on PC depolymerization should be investigated. In this study, we investigated PC ethanolysis using imidazolium-based ILs with different alkyl chain lengths (ethyl, butyl, and hexyl groups) as both the catalyst and solvent to afford the monomer bisphenol-A and a value-added byproduct, diethyl carbonate. 1-Ethyl-3-methyl imidazolium acetate ([EMIM][Ac]) exhibited the highest depolymerization efficiency, and an additional wash step increased the purity of the recovered BPA. A 100 % PC conversion rate, 90.9 % BPA yield, 99.9 % BPA purity, and 99 % [EMIM][Ac] reusability over five depolymerization cycles were observed in the PC ethanolysis using [EMIM][Ac]. In addition, recovered BPA behaved identically to commercially available BPA in the polymerization of PC. This strategy could help reduce the worldwide production of new BPA for PC synthesis.

A one-step immunoassay based on switching peptides for diagnosis of porcine epidemic diarrhea virus (PEDV) using screened Fv-antibodies.

In this study, a one-step immunoassay for porcine epidemic diarrhea virus (PEDV) based on Fv-antibodies and switching peptides was developed, and the assay results of PEDV were obtained by just mixing samples without any further reaction or washing steps. The Fv-antibodies with binding affinity to the spike protein of PEDV were screened from the Fv-antibody library using the receptor-binding domain (RBD) of the spike protein as a screening probe. Screened Fv-antibodies with binding affinities to the RBD antigen were expressed, and the binding constants (KD) were calculated to be 83-142 nM. The one-step immunoassay for the detection of PEDV was configured as a displacement immunoassay using a fluorescence-labeled switching peptide. The one-step immunoassay based on switching peptides was performed using PEDV, and the limit of detection (LOD) values for PEDV detection were estimated to be Ct = 39.7-36.4. Compared with the LOD value for a conventional lateral flow immunoassay (Ct = 33.0), the one-step immunoassay showed a remarkably improved LOD for the detection of PEDV. Finally, the interaction between the screened Fv-antibodies and the PEDV RBD was investigated using docking simulations and compared with the amino acid sequences of the receptors on host cells, such as aminopeptidase N (APN) and angiotensin-converting enzyme-2 (ACE-2).

A local hydroxyl group-modified copper site directs the oxidation of carbon monoxide.

A washing step is employed to adjust the residual surface hydroxyl groups on the Cu-TiO2 catalysts, which in turn influences the local environment of copper species. Hydroxyl groups control both copper dispersion and the Cu+/Cu2+ ratio. Notably, a higher [Cu+]/[OH-] ratio is associated with an enhanced reaction rate in CO conversion.

A pilot study for decellularizing human and porcine cornea for future use in corneal regeneration

Purpose: To effectively decellularize human and porcine corneas for future use in corneal regeneration by using an already established decellularization technique being efficient in decellularizing blood vessels.Methods: One human and 4 porcine corneas were decellularized by using various washing steps with 3‐[(3‐cholamidopropyl) dimethylammonio]‐1‐propanesulfonate (CHAPS) detergent, Benzonase, Ethylenediaminetetraacetic acid (EDTA), 5% Dextran or 5% D‐Mannitol. The quality of the decellularization process was assessed by quantitative and qualitative measurement of DNA content, glycosaminoglycans (GAGs), immunofluorescent staining for Collagen I, V and keratocan, and Transmission Electron Microscopy (TEM) to observe the structure of the collagen fibrils was used.Results: The decellularization process showed 99,94% and 99,52% DNA content reduction in the human and porcine corneas when using Dextran, respectively, while more DNA remained in the porcine corneas when D‐Mannitol was used. Similar pattern was observed in the preservation of GAGs, with the highest amount being found in the human cornea, and less in the porcine corneas. H&E and Immunofluorescent staining showed no presence of cell nuclei when compared to the control native corneas, while Alcian blue staining qualitatively confirmed the presence of GAGs. Collagen I, V and keratocan were still present in the decellularized corneas when compared to the native ones, while TEM microscopy further confirmed the similar patterns of the collagen fibrils in the decellularized‐, compared to the native‐ corneas.Conclusions: This pilot study showed that our decellularization method is effective in decellularizing human and porcine corneas, with very high amount of DNA being removed from the corneas, while the GAGs were preserved to an acceptable extent, and the structure and pattern of the collagen fibrils maintained.

Engineering strong man-made cellulosic fibers: a review of the wet spinning process based on cellulose nanofibrils.

With the goal of sustainable development, manufacturing continuous high-performance fibers based on sustainable resources is an emerging research direction. However, compared to traditional synthetic fibers, plant fibers have limited length/diameter and uncontrollable natural defects, while regenerated cellulose fibers such as viscose and Lyocell suffer from inferior mechanical properties. Wet-spun fibers based on nanocelluloses especially cellulose nanofibrils (CNFs) offer superior mechanical performance since CNFs are the fundamental high-performance building blocks of plant cell walls. This review aims to summarize the progress of making CNF wet-spun fibers, emphasizing on the whole wet spinning process including spinning suspension preparation, spinning, coagulation, washing, drying and post-stretching steps. By establishing the relationships between the nano-scale assembling structure and the macroscopic changes in the CNF dope from gels to dried fibers, effective methods and strategies to improve the mechanical properties of the final fibers are analyzed and proposed. Based on this, the opportunities and challenges for potential industrial-scale production are discussed.

Safety evaluation of the food enzyme phosphoinositide phospholipase C from the genetically modified Pseudomonas fluorescens strain PIC.

The food enzyme phosphoinositide phospholipase C (1-phosphatidyl-1D-myo-inositol-4,5-bisphosphate inositoltrisphosphohydrolase EC 3.1.4.11.) is produced with the genetically modified Pseudomonas fluorescens strain PIC by DSM Food specialties B.V. The genetic modifications do not give rise to safety concerns. The food enzyme is free from viable cells of the production organism and its DNA. It is intended to be used in the processing of fats and oils for the production of refined edible fats and oils by degumming. Since residual amounts of the total organic solids are removed by the washing and purification steps applied during degumming, dietary exposure estimation and toxicity testing were considered unnecessary. A search for the similarity of the amino acid sequence of the food enzyme to known allergens was made and no matches were found. The Panel considered that the risk of allergic reactions by dietary exposure cannot be excluded, but the likelihood for this to occur is low. Based on the data provided, the Panel concluded that this food enzyme does not give rise to safety concerns under the intended conditions of use.