Ion-exchange Chromatography Research Articles

Comparative studies on composition of feed additives for juvenile fish produced with bioconversion of fish raw materials

Technology of feed additive for fry feeding in fish farms is developed to provide both important nutrients (proteins, lipids, etc.) and optimal peptide composition of protein that is achieved using proteolysis of raw materials under certain conditions. For this purpose, enzymatic hydrolysis of substandard small-sized frozen pollock was used. The rational duration of the hydrolysis process was 60 min. that provided the degree of protein hydrolysis of 26–28 %. The experimental fermentolysate was concentrated to a water content of 3–4 % and presented as a feed additive TINRO-60. This product is compared with other feed additives (dried fermentolysates) produced in Russia from fish raw materials using bioconversion, such as Biomarin, Bioprom and Vakhob. General chemical composition of tested products was determined by standard methods of analytical chemistry; composition and content of fatty acids — by gas-liquid chromatography; microand macroelements, as well as toxic metals — by atomic absorption spectrophotometry; fractional composition of proteins and peptides — by high pressure gel permeation chromatography; amino acid composition — by ion exchange chromatography on a high-speed analyzer. All tested samples contain similar amount of the main feed component — protein substances. The quantitative ratio of peptide fractions is also comparable, the sum of the most active fractions (MW 0.1−10.0 kDa) in TINRO-60 and Biomarin is close to their level in tissues of Artemia, natural food for fish fry. The content of essential amino acids, EPA and DHA is significant in Biomarin, TINRO-60 and Bioprom, but almost twice lower in Vakhob. Analysis of mineral composition showed that bioconversion into dry fermentolysates does not cause concentration of toxic elements. High quality of the protein feed additive TINRO-60 produced by bioconversion of nonstandard fish raw materials under certain conditions is proved.

Detection, Optimization, Characterization, and Cytotoxic Effect of Vaginolysin Extracted from Gardnerella Vaginalis Isolated from Iraqi Women Who Had Abortions

Objective: The goal of this study is the detection of the gen that responsible for production the vaginolysin toxin, discovered the optimal condition for produce vaginolysin, purification and characterization of the toxin and show the cytotoxic effect of vaginolysin on VK2cell and HeLa cell. Methods: Among 592 specimens isolated from pregnant women suffering from vaginal inflammation and threatened with abortion(these women is suffering from strong pain in the cervical region), only 62 of isolates identified as G vaginalis. From Baghdad teaching hospital. detection of the gen that responsible for production the vaginolysin toxin. study of the optimal condition to produce vaginolysin. the purification of the toxin by using ammonium sulfate, ion exchange chromatography and gel filtration, toxin characterization of pH and temperature activity and stability, the study of cytotoxic effect of vaginolysin on VK2 and HeLa cells. Result: The optimal condition to produce the toxin is pH level in 4, best temperature is 37 0C, the best media is TSB broth , and the best hours is 24hr. . The best range for precipitation saturation ratio 50%. ion exchanges have specific activity 4 mg. gel filtrations show an increase in the specific activity of purified toxin (10U/mg). the characterization done by pH and temperature,Vaginolysin was active in 0.5 U/ mL at pH 7, and stable in pH 7 activity, the best temperature for vaginolysin activity is 0.5 U/mL at 37°C and maximum stability was recorded at 37°C . the cytotoxic effect of the toxin on VK2 cell observed the viability ratio 69.98%, at higher toxin concentration, while the result for HeLa cell viability ratio 38.77%, at higher toxin concentration. Conclusion: vaginolysin cause lysis of vaginal cell and cervical cell may lead to abortion, the killing ratio increase by increasing the concentration of the toxin and the effect of the toxin on HeLa cell is more than on VK2 cell.

Pretreatment and saccharification of corn cobs using partially purified fungal ligninozymes

AbstractCorn cobs consist primarily of a lignocellulosic material comprising hemicellulose, cellulose, and lignin in a crystalline state, which is resistant to microbial saccharification. Bioethanol production from corn cobs has rarely been attempted, especially using chemical pretreatment methods.The present study deals with the production and purification of fungal (Phanerochaete chrysosporium MTCC 787 and Pleurotus florida PAU 22‐01) extracellular ligninolytic enzymes – lignin peroxidase (LiP), manganese peroxidase (MnP), and laccase (Lac) – followed by their utilization for the biological pretreatment of corn cobs along with saccharification using commercial cellulase. Crude LiP, MnP, and Lac demonstrated specific activity of 2.23, 2.1, and 2.63 U/mg, respectively.The one‐step purification of crude enzyme using diethyl amino ethyl (DEAE) cellulose ion exchange chromatography resulted in 11.3, 10.1 and 8.62‐fold purification of LiP, MnP and Lac activity, respectively, with corresponding specific activity of 25.1 U/mg (LiP), 21.2 U/mg (MnP) and 22.7 U/mg (Lac) in the partially purified ligninozymes. Using the latter, biological pretreatment of 2.5 g corn cobs in a reaction volume of 30 mL containing approximately 200 units of Lac, Lip and MnP enzymes (in phosphate buffer, pH 6) resulted in a maximum of 78.4% delignification with a saccharification efficiency of 97.1% using commercial cellulases.

Applications of high performance liquid chromatography-mass spectrometry in proteomics

Proteomics profiling plays an important role in biomedical studies. Proteomics studies are much more complicated than genome research, mainly because of the complexity and diversity of proteomic samples. High performance liquid chromatography-mass spectrometry (HPLC-MS) is a fundamental tool in proteomics research owing to its high speed, resolution, and sensitivity. Proteomics research targets from the peptides and individual proteins to larger protein complexes, the molecular weight of which gradually increases, leading to sustained increases in structural and compositional complexity and alterations in molecular properties. Therefore, the selection of various separation strategies and stationary-phase parameters is crucial when dealing with the different targets in proteomics research for in-depth proteomics analysis. This article provides an overview of commonly used chromatographic-separation strategies in the laboratory, including reversed-phase liquid chromatography (RPLC), hydrophilic interaction liquid chromatography (HILIC), hydrophobic interaction chromatography (HIC), ion-exchange chromatography (IEC), and size-exclusion chromatography (SEC), as well as their applications and selectivity in the context of various biomacromolecules. At present, no single chromatographic or electrophoretic technology features the peak capacity required to resolve such complex mixtures into individual components. Multidimensional liquid chromatography (MDLC), which combines different orthogonal separation modes with MS, plays an important role in proteomics research. In the MDLC strategy, IEC, together with RPLC, remains the most widely used separation mode in proteomics analysis; other chromatographic methods are also frequently used for peptide/protein fractionation. MDLC technologies and their applications in a variety of proteomics analyses have undergone great development. Two strategies in MDLC separation systems are mainly used in proteomics profiling: the "bottom-up" approach and the "top-down" approach. The "shotgun" method is a typical "bottom-up" strategy that is based on the RPLC or MDLC separation of whole-protein-sample digests coupled with MS; it is an excellent technique for identifying a large number of proteins. "Top-down" analysis is based on the separation of intact proteins and provides their detailed molecular information; thus, this technique may be advantageous for analyzing the post-translational modifications (PTMs) of proteins. In this paper, the "bottom-up" "top-down" and protein-protein interaction (PPI) analyses of proteome samples are briefly reviewed. The diverse combinations of different chromatographic modes used to set up MDLC systems are described, and compatibility issues between mobile phases and analytes, between mobile phases and MS, and between mobile phases in different separation modes in multidimensional chromatography are analyzed. Novel developments in MDLC techniques, such as high-abundance protein depletion and chromatography arrays, are further discussed. In this review, the solutions proposed by researchers when encountering compatibility issues are emphasized. Moreover, the applications of HPLC-MS combined with various sample pretreatment methods in the study of exosomal and single-cell proteomics are examined. During exosome isolation, the combined use of ultracentrifugation and SEC can yield exosomes of higher purity. The use of SEC with ultra-large-pore-size packing materials (200 nm) enables the isolation of exosomal subgroups, and proteomics studies have revealed significant differences in protein composition and function between these subgroups. In the field of single-cell proteomics, researchers have addressed challenges related to reducing sample processing volumes, preventing sample loss, and avoiding contamination during sample preparation. Innovative methods and improvements, such as the utilization of capillaries for sample processing and microchips as platforms to minimize the contact area of the droplets, have been proposed. The integration of these techniques with HPLC-MS shows some progress. In summary, this article focuses on the recent advances in HPLC-MS technology for proteomics analysis and provides a comprehensive reference for future research in the field of proteomics.

Comparing the Two Methods of Ion Chromatography and Titration in Evaluating the Concentration of Sulfuric Acid Mist and Vapor in the General Air of the Electrolysis Unit of the Copper Production Industry

Comparing the Two Methods of Ion Chromatography and Titration in Evaluating the Concentration of Sulfuric Acid Mist and Vapor in the General Air of the Electrolysis Unit of the Copper Production Industry

A study on an analytical method for volatile fatty acids (VFAs) in the atmosphere by using ion chromatography and ultrapure water

A study on an analytical method for volatile fatty acids (VFAs) in the atmosphere by using ion chromatography and ultrapure water

Simultaneous determination of several forms of phosphate in food by ion exchange chromatography

The phosphate group is a group of food additives commonly used for moisturizing, improving the structure, and retaining the color and flavor of products prepared from meat, fish, milk, baked goods, and beverages. A reliable and fast ion exchange chromatography method developed for the simultaneous determination of several forms of phosphate (orthophosphoric acid; pyrophosphate, triphosphate, and hexametaphosphate) in food. Samples were extracted with deionized water at a temperature of 25 ± 5oC for 30 minutes. The extracts were determined by ion exchange chromatography under the conditions: Dionex IonPacTM AS11 column (4 x 250 mm, 9 µm) and Dionex IonPaxTM AG11 column (4 x 50 mm, 9 µm) with the gradient program of KOH concentration from 20 mM to 80 mM. The flow rate is 1 mL/min. The method has good specificity, the calibration curves of the four substances have correlation coefficient values R2 > 0.9999, repeatability and recovery meet the requirements of AOAC. The detection limits (LOD) and quantification limit (LOQ) of each substance in the phosphate group are 12 mg/kg and 40 mg/kg, respectively. The method was applied to simultaneously determine several forms of phosphate in 50 food samples: 15/50 samples detected pyrophosphate, 2/50 samples detected triphosphate, 18/50 samples detected hexametaphosphate and 44/50 samples detected ortho-phosphoric acid, 6/50 samples not detected any form of phosphate. The concentration of phosphate group in detected samples varied from 67.9 mg/kg to 2499 mg/kg.

Highly sensitive two-dimensional ion chromatography mass spectrometry method for nitrite determination in hydroxypropyl methylcellulose

Due to their potential adverse health effects, some N-nitrosamines in drug products are strictly regulated with very low maximum daily intake limits. Nitrosamines can be formed from the reaction of nitrite and secondary or tertiary amines when both species co-exist in the drug synthesis or formulation process. One key strategy to mitigate nitrosamine risk in drugs is to select low-nitrite containing pharma excipients for formulation. It is necessary to develop a sensitive method for trace nitrite determination in pharma excipients as it enables drug producers to study nitrosamine formation kinetics and select excipient suppliers. This study details the development and validation of a two-dimensional ion chromatography mass spectrometry (2D-IC/MS) method for trace nitrite determination in hydroxypropyl methylcellulose (HPMC), one of the most important pharmaceutical excipients used in many drug formulations. The 2D-IC system was operated in heart-cutting mode with a concentrator column coupling the two dimensions. A standard bore anion-exchange column was used in the first dimension (1D) to enable a large volume injection for increased sensitivity and provide improved resolution between nitrite and the interfering chloride peak. A high efficiency microbore anion-exchange column with different selectivity was used in the second dimension (2D) to resolve nitrite from other interfering species. The use of 2D-IC resulted in significantly improved resolution, solving the sensitivity loss issue due to ion suppression from an otherwise 1D separation. MS detection with selective ion monitoring and isotope labeled nitrite internal standard further improve the method specificity, accuracy, and ruggedness, as compared with conductivity detection. For trace determination, it is also extremely important to have a clean blank. For this purpose, a novel cleaning procedure using a strong anion wash was developed to remove nitrite contamination from labware. The optimized method was validated with linearity of nitrite in the concentration range of 18.5–5005.8 ng/g having a regression coefficient of >0.9999, precision with RSD at 3.5–10.1 % and recovery of 90.5–102.4 %. The limit of detection and limit of quantitation were 8.9 and 29.6 ng/g relative to the HPMC sample, or equivalent to 89 and 296 pg/g in the sample solution, respectively.

Grape Pomace Polyphenols Reduce Acute Inflammatory Response Induced by Carrageenan in a Murine Model.

Grape pomace (GP), a by-product of wine production, contains bioactive polyphenols with potential health benefits. This study investigates the anti-inflammatory properties of a polyphenolic fraction derived from GP, obtained by ultrasound-microwave hybrid extraction and purified using ion-exchange chromatography. In the inflammation model, mice were divided into six groups: intact, carrageenan, indomethacin, and three GP polyphenols treatment groups. Paw edema was induced by subplantar injection of carrageenan, and the GP polyphenols were administered intraperitoneally at doses of 10, 20, and 40 mg/kg. The anti-inflammatory effect was evaluated by measuring paw volume, and expression of inflammatory markers: cyclooxygenase-2 (COX-2), myeloperoxidase (MPO), and cytokines (IL-1β and IL-6), along with lipid peroxidation levels. The GP polyphenols significantly reduced paw edema and expression levels of COX-2, MPO, and cytokines in a dose-dependent manner effect, with the highest dose showing the greatest reduction. Additionally, lipid peroxidation levels were also decreased by GP polyphenols treatment at doses of 10 and 20 mg/kg. These findings suggest that ultrasound-microwave extraction combined with amberlite purification proved to be effective in obtaining a polyphenolic-rich fraction from GP. Thus, GP polyphenols may serve as a natural anti-inflammatory and antioxidant agent for treating inflammation and oxidative stress-related diseases.

Chemical composition of wild and domestic animals’ organism in areas of geophagy distribution in Altai Republic

Relevance. The need to study the elemental composition of the organism of wild and domestic animals in natural environments with different levels of chemical elements. Aim. To reveal features of the elemental composition of the organism of the Altai red deer (Cervus elaphus sibiricus Severtzov, 1873), wild boar (Sus scrofa scrofa Linnaeus, 1758) and domestic pigs (Sus scrofa domesticus Erxleben, 1777) in Ongudai district, Altai Republic, including the area with signs of active geophagy. Objects. Organs and tissues of wild and domestic animals. Methods. Mass spectrometry with inductively coupled plasma; atomic-emission spectrometry; ion chromatography, analytical electron microscope with energy dispersion spectrometer. Results. The median values of chemical elements concentrations in the organisms of the Altai red deer, the wild boar and the domestic pig have been determined. S, Cl and K showed the highest values in the composition of macroelements and La, Ce, Nd and Th among rare-earth and radioactive elements. Among the elemental composition features of the studied animals, an increased accumulation of Hg and Pb in the Altai red deer; metals of the Fe-group, W, as well as rare-earth and radioactive elements – in the boar; platinoids – in the domestic pig. In comparison with the results of previous studies, increased concentrations of Hg in red deer kidneys, W in boar bronchi and Pb in the brain of domestic pigs were recorded. Assumptions were made about the factors influencing the formation of the elemental composition of the body of animals. For red deer and wild boar these are the factors of nutrition (including geophagy) and features of accumulation of elements in bone tissue; for domestic pigs – features of forage and local metallogeny, including composition of natural waters.

Impact of breast cancer neoadjuvant chemotherapy on plasma and urine amino acid profile, plasma proteins and nitrogen metabolism

Neoadjuvant chemotherapy (NAC) is the preferred treatment option in locally advanced breast cancer (BC). The administration of NAC is associated with a wide range of adverse effects. This pilot observational prospective study examined the effect of NAC using anthracycline + cyclophosphamide (AC) followed by paclitaxel (PTx) on a portfolio of 22 plasma and urinary amino acids, plasma proteins (albumin, prealbumin, transferrin), and products of nitrogen metabolism (urea, creatinine, uric acid) in plasma and urine. Plasma and 24-h urine samples were obtained from ten patients with early breast cancer (N1-3 N0-2 M0), at the following time points: before the start of NAC and during the AC/PTx treatment period (a total of 8 measurements at three-weekly intervals). Amino acids were analyzed using ion exchange chromatography. There were no significant differences in the measured parameters in plasma and urine between pre-NAC and during AC- and PTx-treatment. No trend was detected. A significant difference in the portfolio of plasma and urinary amino acids was found only in the pre-treatment period compared to the control group. Levels of eight plasma amino acids (8/22) were significantly reduced and those of nine urine amino acids were increased (9/22). Nitrogenous catabolites in plasma and urine were not indicative of increased protein catabolism during the anthracycline and taxane treatment periods. A slightly positive nitrogen balance was accompanied by an average weight gain of 3.3 kg (range 0–6 kg). The AC/PTx treatment regimen did not cause significant changes in the monitored laboratory parameters.

Assessment of hydrochemical characteristics, health risks and quality of groundwater for drinking and irrigation purposes in a mountainous region of Pakistan

Renowned for its agriculture, livestock, and mining, Zhob district, Pakistan, faces the urgent problem of declining groundwater quality due to natural and human-induced factors. This deterioration poses significant challenges for residents who rely on groundwater for drinking, domestic, and irrigation purposes. Therefore, this novel study aimed to carry out a comprehensive assessment of groundwater quality in Zhob district, considering various aspects such as hydrochemical characteristics, human health risks, and suitability for drinking and irrigation purposes. While previous studies may have focused on one or a few of these aspects, this study integrates multiple analyses to provide a holistic understanding of the groundwater quality situation in the region. Additionally, the study applies a range of common hydrochemical analysis methods (acid–base titration, flame atomic absorption spectrometry, and ion chromatography), drinking water quality index (WQI), irrigation indices, and health risk assessment models, using 19 water quality parameters. This multi-method approach enhances the robustness and accuracy of the assessment, providing valuable insights for decision-makers and stakeholders. The results revealed that means of the majority of water quality parameters, such as pH (7.64), electrical conductivity (830.13 μScm–1), total dissolved solids (562.83 mgL–1), as well as various anions, and cations, were in line with drinking water norms. However, the water quality index (WQI) predominantly indicated poor drinking water quality (range = 51–75) at 50% sites, followed by good quality (range = 26–50) at 37% of the sites, with 10% of the sites exhibiting very poor quality (range = 76–100). For irrigation purposes, indices such as sodium percent (mean = 31.37%), sodium adsorption ratio (mean = 0.98 meqL–1), residual sodium carbonate (– 3.15 meqL–1), Kelley’s index (mean = 0.49), and permeability (mean = 49.11%) indicated suitability without immediate treatment. However, the magnesium hazard (mean = 46.11%) and potential salinity (mean = 3.93) demonstrated that prolonged application of groundwater for irrigation needs soil management to avoid soil compaction and salinity. Water samples exhibit characteristics of medium salinity and low alkalinity (C2S1) as well as high salinity and low alkalinity (C3S1) categories. The Gibbs diagram results revealed that rock weathering, including silicate weathering and cation exchange, is the primary factor governing the hydrochemistry of groundwater. The hydrochemical composition is dominated by mixed Ca–Mg–Cl, followed by Na–Cl and Mg–Cl types. Furthermore, the human health risk assessment highlighted that fluoride (F–) posed a higher risk compared with nitrate (NO3–). Additionally, ingestion was found to pose a higher risk to health compared to dermal contact, with children being particularly vulnerable. The average hazard index (HI) for children was 1.24, surpassing the allowable limit of 1, indicating detrimental health effects on this subpopulation. Conversely, average HI values for adult females (0.59) and adult males (0.44) were within safe levels, suggesting minimal concerns for these demographic groups. Overall, the study’s interdisciplinary approach and depth of analysis make a significant contribution to understanding groundwater quality dynamics and associated risks in Zhob district, potentially informing future management and mitigation strategies.

Doping control analysis of myo-inositol trispyrophosphate and 10 bisphosphonates in equine plasma by ion chromatography-mass spectrometry and its application to clodronic acid horse administration.

Bisphosphonates and myo-inositol trispyrophosphate (ITPP) are two classes of difficult-to-detect polar drugs that are prohibited under the rules of racing. ITPP is a drug capable of increasing the amount of oxygen in hypoxic tissues, and studies have shown that administration of ITPP increases the maximal exercise capacity in mice. The properties of ITPP make it an ideal candidate as a doping agent to enhance performance in racehorses. In recent years, ITPP had indeed been detected in racehorses and confiscated items. As for bisphosphonates, it is especially critical to control their use as since February 2019, the International Agreement on Breeding, Racing and Wagering (IABRW) by the International Federation of Horseracing Authorities (IFHA) had identified specific conditions on which bisphosphonates should not be administered to a racehorse. A recent review of literature shows that there is yet a simultaneous screening method for detecting ITPP and bisphosphonates in equine samples. This paper describes an efficient ion chromatography high-resolution mass spectrometry (IC-HRMS) method for the simultaneous detection of ITPP and 10 bisphosphonates at sub-parts-per-billion (ppb) to low-ppb levels in equine plasma after solid-phase extraction (SPE) and its application to an administration study of clodronic acid in horses.

Online Mixed-Bed Ion Exchange Chromatography for Native Top-Down Proteomics of Complex Mixtures.

Native top-down mass spectrometry (nTDMS) allows characterization of protein structure and noncovalent interactions with simultaneous sequence mapping and proteoform characterization. The majority of nTDMS studies utilize purified recombinant proteins, with significant challenges hindering application to endogenous systems. To perform native top-down proteomics (nTDP), where endogenous proteins from complex biological systems are analyzed by nTDMS, it is essential to separate proteins under nondenaturing conditions. However, it remains difficult to achieve high resolution with MS-compatible online chromatography while preserving protein tertiary structure and noncovalent interactions. Herein, we report the use of online mixed-bed ion exchange chromatography (IEC) to enable separation of endogenous proteins from complex mixtures under nondenaturing conditions, preserving noncovalent interactions for nTDP analysis. We have successfully detected large proteins (>146 kDa) and identified endogenous metal-binding and oligomeric protein complexes in human heart tissue lysate. The use of a mixed-bed stationary phase allowed retention and elution of proteins over a wide range of isoelectric points without altering the sample or mobile phase pH. Overall, our method provides a simple online IEC-MS platform that can effectively separate proteins from complex mixtures under nondenaturing conditions and preserve higher-order structure for nTDP applications.

Enzyme and Microwave Coassisted Extraction, Physicochemical Properties, and Antioxidant Activity of Polysaccharides from Baijiu Distillers' Grains

AbstractBaijiu distillers' grain is a solid waste after the fermentation of grains, and their high added value and deep processing and utilization require further study. This study uses the enzyme and microwave coassisted method to extract Baijiu distillers' grain polysaccharides (DGPs). Through optimization of the single‐factor test and response surface methodology (RSM), the optimal conditions are solid–liquid ratio 1:30, enzyme time 50 min, enzyme temperature 50 °C, enzyme pH 5.0, microwave time 6 min, and microwave power 480 W, with a maximum DGP yield of 3.98% ± 0.03. DGP is purified by DEAE‐Sepharose cellulose ion exchange chromatography to obtain four fractions, namely DGP‐1, DGP‐2, DGP‐3, and DGP‐4; the molecular weights are 2224.05, 90.99, 1478.16, and 346.19 kDa, respectively, and the main monosaccharide components are Man and Glc. The antioxidant assay shows that the four kinds of DGPs have different free radical scavenging capacities, among which DGP‐2, DGP‐3, and DGP‐4 have good antioxidant activities. Therefore, DGP can be used as a potential natural antioxidant.

Evaluation of antibiofilm activity for siderophore produced from rhizospheric Acinetobacter baumannii against of some respiratory tracts bacteria

Siderophore was extracted from Acinetobacter baumannii isolated from rhizosphere reigion in Baghdad City . The results appeared the ability of isolate (Acinetobacter baumannii 5) to produce Siderophore with diameter of (15) mm and the condition for production was temperature reached 30 degrees, and the optimum pH was 7 . Purification of siderophore through : Ion exchange chromatography for purify more stable form as ferric-siderophore complex and final step through gel filtration. The activity of purified siderophore as antibacterial agent was tested against 13 different local clinical bacterial as follows (Klebsiella pneumoniae ,Pseudomonas aeruginosa ,Acinetobacter baumannii , Escherichia.coli ,Streptococcus pyogenes ,Staph. aureus ,Enterobacter cloacea, Enterobacter aerogenes ,Enterococcus faecalis ,Burkholderia cepacian ,Serratia fiaria ,S. marcescens ,Klebsiella oxytoca ) isolates at concentration 20 mg/ml of free iron siderophore and the results showed that highest activity of siderophore was reported on Streptococcus.pyogenes with inhibition zone (26)mm, and on Acinetobacter baumannii, Serratia.marcescens and Escherichia.coli the inhibition zone was (20)mm while the lowest effects were on Serratia. fiaria and Klebsiella .oxytoca with inhibition zone (16mm). As well as, the purified siderophore showed good activity as antibiofilm of pathogenic bacteria. The highest antiadhesive percentage was observed for Escherichia.coli by percentage 64.4%.

Structural characterization and anti-ageing activity of polysaccharide from Exocarpium Citrulli

In this investigation, we have effectively extracted and characterized a new Exocarpium Citrulli polysaccharide (ECP-2) with a molecular weight of 1.67 × 106 Da using hot water extraction and ethanol precipitation techniques. Analysis was performed using high performance gel permeation chromatography, ion chromatography, Fourier transform infrared spectroscopy, nuclear magnetic resonance, and scanning electron microscopy. ECP-2 is primarily composed of galactose (32.32 %), arabinose (25.42 %), and mannose (19.75 %). Fuc, Rha, Ara, Gal, Glc, Man, and GalA molar ratios in ECP-2 is 4.65:1.50:25.42:32.32:5.78:19.75:10.57. Based on structural studies, the primary sugar residues of ECP-2 are T-α-L-Araf-(1→, →5)-α-L-Araf-(1→, T-α-D-Manp-(1→ and →3,6)-β-D-Galp-(1→. Furthermore, the anti-aging effect of ECP-2 in D-galactose model mice, while the results indicate that ECP-2 significantly enhances the activities of superoxide dismutase, glutathione peroxidase, and catalase in D-galactose model control mice. Additionally, ECP-2 effectively eliminated the lipid peroxidation product malondialdehyde, thereby restoring normal growth of the mice by regulating their defense mechanism. In conclusion, the polysaccharides of Exocarpium Citrulli, particularly ECP-2, may be appropriate for use in natural medicines and functional foods to halt or slow the aging process.

A study into the natural occurrence of inorganic ions relevant to forensic explosives investigations on human hands

The natural occurrence of 16 inorganic ions relevant to forensic explosives investigations on human hands was studied to support the evaluation of activity-level propositions when such traces are found on the hands or in the fingerprints of a suspect. A total of 594 hand swab extracts from 297 participants throughout Europe and the United States of America were analyzed using Ion Chromatography – Mass Spectrometry. The data provides a reference framework for future covert investigations and forensic casework. The results indicate that thiocyanate, chlorate, nitrite, lithium, strontium, and barium are rarely detected on the hands of individuals who have had no direct contact with explosives (P<0.03) and in quantities below 6 µg. Perchlorate contamination sporadically occurs without deliberately handling perchlorates (P=0.03), albeit at low levels (<12 µg). It also seems that the presence of perchlorate on hands is generally related to professions that involve explosives. Detecting substantial amounts of any of these rare ions on a suspect’s hands would require a specific explanation. Because legitimate activities exist that can also result in elevated levels of ions of interest on hands, the context surrounding their presence has to be carefully assessed for each individual case.

Furcellaran: Impact of Concentration, Rheological Properties, and Structure on Ice Recrystallization Inhibition Activity.

Recrystallization is considered the main damaging mechanism during the frozen storage of biologic materials. In this study, furcellaran, a polysaccharide related to κ-carrageenan, was studied for its concentration-dependent effect on ice crystal growth and recrystallization. The structure and sulfate content of the utilized furcellaran was analyzed by 1H nuclear magnetic resonance spectroscopy, ion chromatography, and high-performance size-exclusion chromatography. Additionally, the rheological properties of furcellaran solutions were investigated. Our findings demonstrate that furcellaran inhibits ice growth as effectively as κ-carrageenan. Furthermore, the rheological properties change with increasing furcellaran concentration, resulting in a gel-like consistency at 5 g/L, which coincides with decreased recrystallization inhibition activity and larger crystals. This suggests that gel formation or a gel-like consistency has to be avoided for optimal recrystallization inhibition activity.

Analysis of highly polar anionic pesticides in food of plant and animal origin by ion chromatography and tandem mass spectrometry with emphasis on addressing adverse effects caused by matrix co-extractives

Residues of various highly polar pesticides and their metabolites are commonly found in numerous food products. Some of these compounds, such as glyphosate, are not only used in large amounts in agriculture, but are also controversially discussed in public. Here, we present a method, employing ion chromatography (IC) coupled to tandem mass spectrometry (IC-MS/MS), for the analyses of glyphosate, aminomethyl phosphonic acid (AMPA), N-acetyl-glyphosate (NAGly), fosetyl, and 10 further highly polar pesticides and metabolites in various plant and animal matrices following a minimal sample preparation by means of the QuPPe method. Thorough investigations showed that an AS19 column enabled the analysis of all 14 compounds within 30 min. The best sensitivity could be obtained with the make-up solvent acetonitrile being admixed to the mobile phase at a 1:2 flow rate ratio. Matrix effects were thoroughly studied in terms of ion suppression and retention time shifts. Conductivity detection was used to monitor elution profiles of matrix co-extractives in comparison with matrix effect profiles obtained by continuous post-column infusion of a mix with 13 highly polar pesticides and metabolites. These tests indicated that a fivefold dilution of QuPPe extracts was suitable for the routine analysis of samples for MRL-conformity, as it considerably reduced matrix effects maintaining sufficient sensitivity and high recovery rates in eight different commodities. The suitability of the final method for its application in routine analysis was verified by the analysis of >130 samples containing incurred residues where the results were compared with two existing LC-MS/MS methods.Graphical