High-performance Liquid Research Articles

Is vitamin D deficiency a more frequent finding in hirsutism or not?

Evidence shows that vitamin D (Vit D) insufficiency is associated with some hormonal disorders. Hirsutism is a prevalent hormonal condition, which is usually associated with excess of androgenic hormones. Disturbance of Vit D level affects the regulation of these hormones and may be associated with hirsutism. This study compared the Vit D levels of women with and without hirsutism. The study aimed to answer the question "Do women with hirsutism more commonly have lower levels of vitamin D compared to women without hirsutism". In this cross-sectional study, 202 women were included (101 with hirsutism and 101 without hirsutism). 25-hydroxy Vit D level was assessed using high-performance liquid chromatography (HPLC). All data was analyzed based on a significance level < 0.05. The age distribution was similar in both groups (P > 0.05). The mean level of Vit D had no statistically significant differences between the hirsutism group (21.40 ng/ml) and non-hirsutism group (21.20 ng/ml) (P > 0.05). Also, no significant correlations between menstrual patterns, body mass index and presence of polycystic ovaries, with different levels of Vit D were observed in hirsute women (P > 0.05). The study found no significant difference in Vit D levels between individuals with and without hirsutism. About half of the individuals in both groups had Vit D deficiency. But these findings do not rule out the possible role of vitamin D deficiency in the development of hirsutism.

Screening and diversity analysis of Dibutyl phthalate degrading bacteria in agricultural soil in Chengdu, China.

Dibutyl phthalate (DBP) with teratogenicity, carcinogenesis, and mutagenesis, is a ubiquitous endocrine disruptor in the environment. The widespread usage of plastic mulch has resulted in a severe DBP pollution problem in agricultural soil. One of the most vital ways to mitigate the DBP pollution problem is to use DBP degrading bacteria to reduce the concentration of DBP in agricultural soil. DBP degrading bacteria studied in previous studies mainly come from sewage treatment plants, rivers, landfills, bioreactors, and other environmental media. At the same time, there was relatively little research on DBP degrading bacteria in agricultural soil. Therefore, using the pure culture approach, the candidate DBP degrading strains were isolated and screened from vegetable plots contaminated with plastic mulch in Dayi County, Chengdu City, Sichuan Province, China. The taxonomy of the strains was determined using the 16 sedimentation ribosomal deoxyribonucleic acid (16S rDNA) molecular technique. Furthermore, ultraviolet and visible spectrophotometry and high performance liquid chromatography (HPLC) were used to assess the degrading capability of strains. The findings showed that a total of twenty-six DBP degrading strains were screened from vegetable plots contaminated with plastic mulch in Dayi County, Chengdu City, Sichuan Province, China, and these strains belonged to two phyla: Proteobacteria and Bacillota, eight families, including Pseudomonas, Enterobacteriaceae, and Bacillaceae, as well as ten genera, such as Enterobacter, Pseudomonas, and Bacillus. One of them, the strain SWDB-7 was a potentially new species in the Enterobacter genus. The most prominent genus of the isolated strains was Enterobacter. There were significant variations in the degradation capability of different obtained DBP degrading strains. and their degradation efficiency was 14.12%-91.86%. With a total DBP removal rate of 91.86%, strain SWDB-15 had the most effective degrading capability among them. To sum up, the DBP degrading strains in vegetable plots contaminated with plastic mulch in Dayi County, Chengdu City, Sichuan Province, China are rich in diversity and capable of breaking down DBP.

Integrating Biological Early Warning Systems with High-Resolution Online Chemical Monitoring in Wastewater Treatment Plants.

Detection of micropollutants (MPs) in wastewater effluents using traditional toxicity tests or chemical analysis with discrete samples is challenging due to concentration dynamics. This study evaluates a continuous monitoring approach for detecting MPs in wastewater effluents using a combination of biological early warning systems (BEWS). Three BEWS with Chlorella vulgaris, Daphnia magna, and Gammarus pulex were operated in parallel in a full-scale municipal wastewater treatment plant. Concentrations of MPs were monitored by simultaneous online chemical analysis using high performance liquid chromatography-high resolution mass spectrometry (MS2Field). Over 5 weeks, behavioral changes observed in the BEWS occasionally exceeded acute toxicity thresholds, triggering alarms. These changes were related to MPs identified by the MS2Field, to abiotic factors, or to operational parameters of the BEWS. For one toxic event, behavioral responses were linked to a pesticide, not authorized in Switzerland, at concentrations close to literature EC50 values. Verification tests confirmed that the pesticide in the effluent was the most likely cause for the organism response. The study demonstrates the potential of BEWS as a stand-alone technique for detecting contamination peaks in wastewater, and identifies key limitations and critical factors that need to be addressed to optimize the use of BEWS in wastewater monitoring.

Whole genome analysis, detoxification of ochratoxin a and physiological characterization of a novel Bacillus velezensis MM35 isolated from soil

Ochratoxin A (OTA) is a significant global contaminant that poses severe challenges to food safety and public health. This study aims to isolate the OTA-degrated probiotics and evaluate genetic and biological characteristic. Here, The degradation rate of a new strain named Bacillus velezensis MM35 isolated from soil was the highest (87.10% within 48 h), and its culture supernatant was the main component of OTA degradation (63.95%) by high performance liquid chromatography. Further investigation revealed that the extracellular enzyme that degrades OTA in the culture supernatant of MM35 may be a small molecule enzyme with certain heat resistance. Genome-wide analysis showed that MM35 contains a cluster of carboxypeptidases encoding OTA-degrading potential, and had good metabolic and catalytic synthesis ability, and strong application potential in the synthesis and degradation of carbohydrates and proteins. A variety of secondary metabolites with antibacterial properties, such as non-ribosomal peptide synthetase and terpenoids, were identified in its metabolites. Consistent with the predicted results, MM35 showed various enzyme production characteristics such as cellulase and xylanase. Furthermore, MM35 could inhibit the growth of a variety of pathogenic bacteria, and showed high co-aggregation ability to Escherichia coli and Salmonella typhimurium. In addition, MM35 has certain tolerance to harsh environments such as strong acid, bile salt, and high temperature. Additionally, the adhesion rate of MM35 was 5.4%, and the invasion rate was 2.1% in IPEC-J2 cells. In summary, the data suggest MM35 isolated strain has high OTA degradation efficiency, antibacterial activity and intestinal colonization, which provided a new way for the treatment of OTA contamination in food and feed industries.

Profiling of agronomic traits and folic acid in five dessert bananas (Musa spp.)

Many varieties of Musa spp. have been used as edible fruits around the world. Bananas belong to the genus Musa, whose fruits contain high calories and nutritional values. There is little data on agronomic traits and folic acid (FA) concentrations of different types of dessert bananas in Vietnam. This study aimed to determine such information in the fruits of five banana varieties, including Cau, Xiem, Gia Huong, Com, and Dole. Agronomic characteristics were considered, including fruit size and weight, peel colour and pulp firmness, while FA concentrations were quantified by high-performance liquid chromatography. The results showed significant differences among agronomic values and FA contents. Dole had the heaviest weight (175.48 g), followed by Xiem (123.71 g), Gia Huong (121.77 g), Com (103.12 g) and Cau (52.07 g). The size (length × width) of 5 cultivars has significant differences, including Dole (16.22 × 4.17 cm), Xiem (11.78 × 4.44 cm), Gia Huong (15.44 × 4.22 cm), Com (11.59 × 3.88 cm) and Cau (9.00 × 3.79 cm). For the colour results, most banana cultivars had yellow peels, except Gia Huong which remained green colour at ripening stages (b/a&lt;0). The pulp firmness is expressed with the hardest value from Xiem (0.59 N), then Dole (0.36 N), Com (0.32 N), Cau and Gia Huong (0.29 N). The FA concentrations ranged 3-12 μg /100 g fresh weight. The cultivar Cau had the highest level of FA per 100 g fresh weight (12.04 μg), followed by Gia Huong (8.76 μg), Dole (6.00 μg), Xiem (4.62 μg), and Com (3.14 μg). The FA contents were positively correlated with the colour brightness L, performed by Pearson value, with r = 0.755 (p&lt;0.001). On the other hand, an inverse correlation was found between FA concentration and the fruit weight (r = -0.542, p&lt;0.001) and the pulp firmness (r = -0.337, p&lt;0.05). In conclusion on 5 varieties of dessert bananas, measured values of agronomic traits and FA have been recorded, and Pearson analysis shows a positive relation between FA and colour brightness and a negative one between FA and fruit weight/firmness.

Transcending Resolution Limits in HPLC and Diffusion NMR.

Mixture analysis is crucial in many areas of chemistry, and a wide variety of separation methods are in use. A common method for physical separation is high-performance liquid chromatography (HPLC), but resolution is a problem: chemically similar species coelute. An alternative approach is diffusion-ordered NMR spectroscopy (DOSY), in which the signals of mixture components are separated according to the diffusion coefficient. Again, separation is limited if species diffuse similarly or have overlap in their NMR spectra. Using the two techniques in combination can resolve both NMR spectra and the elution profiles of individual components, even where both techniques fail when used in isolation. Recording diffusion NMR data as a function of HPLC retention time gives a three-dimensional (3D) data set that can be analyzed using multiway statistical methods. PARAFAC analysis of diffusion NMR data measured from HPLC eluate for commercial "monoacetin" (a mixture of glycerol and its mono-, di-, and triacetates) yielded fully resolved and quantitative NMR spectra and elution profiles for all four components, whereas neither HPLC nor diffusion NMR applied independently was able to resolve the components.

Anti-leishmanial activity of Hypericum Scabrum extract against Leishmania major

Leishmaniasis is a vector-borne disease and one of the most significant neglected tropical diseases. Current anti-leishmanial treatments are often ineffective over extended periods and are associated with toxic side effects, highlighting the urgent need for new, effective, and safe alternative treatments for this infectious disease. The objective of this study was to evaluate the anti-leishmanial effects of a hydroalcoholic extract of Hypericum scabrum (H. scabrum), comparing its efficacy to that of the control drug glucantime against the standard strain of Leishmania major. The H. scabrum plants were collected from the western regions of Iran. A hydroalcoholic extract was prepared from the flower and stem of the plant using a maceration method. High-performance liquid chromatography analysis was conducted to identify the chemical compounds present in the extract. Promastigotes of L. major were cultured, and the anti-leishmanial activity of the extracts was assessed at concentrations ranging from 12.5 to 800 µg/ml using the MTT [3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide] assay. The half-maximal inhibitory concentration (IC50) values for the H. scabrum plant extract at 24, 48, and 72 h were 245.47, 141.25 and 85.11 μg/ml, respectively. The IC50 values for glucantime (the control drug) at 24 h, 48 h, and 72 h were 30.19, 21.37, and 12.58 μg/ml, respectively. While the H. scabrum extract exhibited a lower effect compared to the control drug, it still demonstrated a significant inhibitory effect on the promastigote form of L. major. Given that the plant extract of H. scabrum has demonstrated promising anti-leishmanial effects against L. major promastigotes, further studies are warranted to evaluate the efficacy of these extracts in animal models of leishmaniasis.

Effect of the Type of Herbal Preparations (Powdered Plant Material vs. Dry Ethanolic Extracts) on the Bioaccessibility of Bearberry (Arctostaphylos uva-ursi (L.) Spreng.) Phytochemicals in Simulated Digestion Conditions

The main aim of this study was to determine the potential bioaccessibility of bearberry phytochemicals influenced by the type of herbal preparations. Herbal preparations–powdered plant materials and dry extracts obtained using various ethanol concentrations (0%, 20%, 40%, 60%, 80%, and 100%) were subjected to simulated gastric or gastrointestinal digestion for the evaluation of the bioaccessibility of the phytochemicals. The phytochemical characterization of the plant material, dry extracts, and potentially bioaccessible fractions was performed using high-performance liquid chromatography (HPLC) and spectrophotometric assays. The content of the main compounds, i.e., arbutin, hydroquinone, hyperoside, pentagalloylglucose, and picein, as well as the total phenolic content and in vitro antioxidant activity through the ABTS•+-scavenging activity and Fe3+-reducing power were determined. The bioaccessibility of arbutin, i.e., the main compound in bearberry, was high, in most cases exceeding 95%, and was generally unaffected by the experimental factors; however, the changes in the content of the other compounds, the total phenolic content, and the antioxidant activity were more prominent and influenced by the type of the herbal preparation and the stage of digestion. Given the compromise between the abundance of the bearberry phytochemicals, the antioxidant activity, and the resulting potential bioaccessibility of these phytochemicals, the dry extracts prepared with 40% ethanol seem to be the most promising for phytopharmaceutical purposes and functional food applications.

Albumin nanoparticles-mediated doxorubicin delivery enhances the anti-tumor efficiency in ovarian cancer cells through controlled release.

Doxorubicin (DOX) is an anthracycline commonly used as a first-line treatment option for various malignancies, either as a stand-alone treatment or in combination with other chemotherapeutic agents. However, its efficacy in advanced cancer stages requires high doses, resulting in significant cytotoxicity to normal cells and severe side effects. Nanotechnology offers a promising strategy to mitigate these drawbacks through controlled drug release. In this study, bovine serum albumin nanoparticles (BSA-NPs) were synthesized via the desolvation method and successfully loaded with DOX (DOX-BSA-NPs). Characterization using dynamic light scattering, scanning electron microscopy, Fourier-transform infrared spectroscopy, UV-visible spectroscopy, and high-performance liquid chromatography confirmed efficient drug loading. In vitro studies demonstrated that DOX-BSA-NPs enabled sustained drug release and enhanced intracellular delivery. After treatment with DOX-BSA-NPs, ovarian cancer cells showed a twofold increase in cytotoxicity compared to free DOX. Scratch assays further revealed a significant reduction in cancer cell migration and invasion. Additionally, LDH assays and Annexin V-FITC flow cytometry indicated a shift toward apoptosis over necrosis, enhancing the anti-tumor efficacy of DOX. This was supported by increased reactive oxygen species production, upregulation of pro-apoptotic genes, downregulation of anti-apoptotic genes, and elevated caspase 3 and 7 activity, collectively promoting apoptosis. These findings underscore the potential of DOX-BSA-NPs as a superior alternative for targeted and controlled drug delivery, offering enhanced therapeutic efficacy and reduced side effects in ovarian cancer treatment.

Quality Markers of Fufang Shenqi Oral Liquid Based on Integrated Fingerprint Analysis, Chemical Pattern Recognition, and Quantification.

Fufang Shenqi Oral Liquid (FFSQOL) is an important Chinese medicine compound preparation with a wide range of clinical applications, which is mainly used to regulate immune function, improve cardiovascular function, and have anti-inflammatory and antibacterial effects. At present, it is of great importance to establish the quality evaluation method of FFSQOL and to investigate its quality markers (Q-markers). The aim of this study is to establish a quality evaluation method for FFSQOL and screen its Q-markers to provide a scientific basis for its quality control. Fourteen batches of FFSQOL were subjected to high-performance liquid chromatography (HPLC) fingerprint and similarity analysis. The components of FFSQOL were identified, and their content was determined. This was combined with cluster analysis (CA) and principal component analysis (PCA) to determine the Q-markers of FFSQOL. In this study, an HPLC fingerprint was established for 14 batches of FFSQOL, identifying 12 common peaks and six major components. Four components were identified as stable and reproducible: gallic acid (504.94 ~ 1219.04 μg/mL), caffeic acid (452.15 ~ 783.01 μg/mL), 7-O-glucoside (1097.72 ~ 2440.41 μg/mL), and formononetin (176.2 ~ 177.51 μg/mL). Quality evaluation of the 14 batches was conducted using chemical pattern recognition analysis. CA results indicated two distinct groups, and PCA revealed that principal components 1 and 2 were the main factors influencing batch differences. A combination of HPLC fingerprint, content determination results, and chemical pattern recognition analysis was employed to identify Q-markers for FFSQOL. The markers identified were gallic acid, caffeic acid, calycosin 7-O-glucoside, and formononetin. In this study, a quality evaluation method for FFSQOL was established through the implementation of fingerprint, content determination, and chemical pattern recognition analysis, resulting in the identification of four Q-Markers of FFSQOL, which laid the foundation for the formulation of FFSQOL quality standards.

Investigation of the anti-Huanglongbing effects using antimicrobial lipopeptide and phytohormone complex powder prepared from Bacillus amyloliquefaciens MG-2 fermentation

Global citrus production has been severely affected by citrus Huanglongbing (HLB) disease, caused by Candidatus Liberibacter asiaticus (Clas), and the development of effective control methods are crucial. This study employed antimicrobial lipopeptide and phytohormone complex powder (L1) prepared from the fermentation broth of the endophytic plant growth promoting bacterium (PGPB) of Bacillus amyloliquefaciens strain MG-2 to treat Candidatus Liberibacter asiaticus (CLas)-infected ‘Citrus reticulata ‘Chun Jian’ plants. Real-time fluorescence quantitative polymerase chain reaction (qPCR) and PCR were employed for disease detection. The results revealed that after 15 spray-drench treatments with L1 solution, the HLB infection rate decreased from 100 to 50%, the bacterial titer decreased by 51.9% compared with a 27.9% decrease in the control group. L1 treatment triggered the production of reactive oxygen species, increased lignin content, and increased defense enzyme activities (p &amp;lt; 0.05). Defense-related gene expression significantly increased within 12 h of treatment. In addition, L1 application also promoted plant growth, as evidenced by higher transpiration rates and net photosynthetic rates as well as increased leave or root density. Root flora analysis revealed that the abundances of Burkholderia_thailandensis, unclassified_g_Burkholderia-Caballeronia-Paraburkholderia, unclassified_g__Allorhizobium-Neorhizobium-Pararhizobium-Rhizobium, and Pseudomonas_mosselii were 1.64, 1.46, 5.84, and 6.93 times greater, respectively, than those in the control group. The levels of phenylpropanoids, polyketides, lipids, lipid-like molecules, organic acids, and derivatives, significantly increased following L1 treatment (FC &amp;gt; 2, p &amp;lt; 0.05). Additionally, salicylic acid, dihydrojasmonic acid, and isopentenyl adenosine levels in leaves markedly increased. High-performance liquid chromatography (HPLC) confirmed that L1 contained surfactin, iturin and fengycin cyclic-lipopeptides (CLPs) as well as indole-3-acetic acid (IAA), 3-indolebutyric acid (IBA), indole-3-carboxylic acid and indole-3-carboxaldehyde auxins, N6-entopentenyladenine and t-zeatin-riboside cytokinins, abscisic acid, 1-aminocyclicpanecarboxylic acid, salicylic acid, and gibberellin A1, A3 and A4 phytohormones. These findings provide insight into multiple mechanisms by which endophytic Bacillus PGPB L1 is able to combat HLB disease, to promote citrus plant growth, and to optimize the root flora for soil health which offering an innovative strategy for sustainable management of this severe disease and improving citrus plant growth and productivity

Non-affinity platform for processing knob-into-hole bispecific antibody

Bispecific antibodies hold significant potential as next-generation biotherapeutics owing to their ability to simultaneously bind to two targets. However, the development of bispecific antibodies as biotherapeutics has been hindered by the high levels of byproducts produced, including both high molecular weight and low molecular weight variants. In addition, the inevitable expression of homodimers in host cells presents further obstacles to the commercial development of bispecific antibodies as therapeutics. These byproducts, which share similar physicochemical properties with the target, pose several challenges for downstream purification processes. In this study, we present a non-protein A purification platform that employ a one-step polishing chromatography to purify bispecific antibodies. Mixed-mode Capto adhere resin was used to capture the target protein at pH 7.90 ± 0.10, followed by anion exchange chromatography as a polishing step. Overall, the results of this two-step chromatography purification method demonstrated at final product purity of 98% as assessed by size-exclusion high-performance liquid chromatography (SEC-HPLC) and 98% by reversed-phase-high-performance liquid chromatography (RP-HPLC), with residual host cell proteins controlled at 10 ppm and an excellent recovery rate of approximately 60%. This study presents a non-protein A capture platform, offering a simplified, streamlined, and competitive alternative to conventional affinity chromatography.Graphical

Exopolygalacturonase Production from the Novel Strain Lichtheimia sp. UV-16 and Enzyme Hydrolysis Properties.

A pectinase-producing strain, Lichtheimia sp. X-8, was isolated from the soil for the first time. Subsequently, Lichtheimia sp. UV-16, with a 1.23-fold increase in pectinase activity, was obtained via UV mutagenesis, and optimization of its liquid fermentation process boosted pectinase activity from 455.6 ± 12.7 to 3202.0 ± 82.1 U/mL. The crude enzyme was purified by salting out and anion exchange resin, with a purification ratio of 2.28-fold and a yield of 36.5%. The optimal reaction temperature for the pure enzyme was 60 °C with an optimal pH of 5.5. Thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC) confirmed that the enzyme was an exopolygalacturonase, achieving over 99% efficiency in pectin hydrolysis. Furthermore, incorporating pure enzymes into juice pulps can substantially enhance the juice yield, which makes this polygalacturonase a promising application in the beverage industry.

Phytochemical characterization and anti-arthritic potential of green-synthesized CuO nanoparticles derived from the Bistorta amplexicaulis root extract

IntroductionRheumatoid arthritis is an autoimmune disease that mainly causes joint damage. The patient experiences loss of appetite, pain, fever, and fatigue. The present study was designed to phytochemically characterize and evaluate the anti-arthritic activity of green-synthesized copper oxide (CuO) nanoparticles (NPs) using the hydroalcoholic extract of Bistorta amplexicaulis roots in an adjuvant-induced arthritic rat model.Material and MethodsFor this purpose, crude powdered plant material was used for proximate analysis, and the plant extract was assessed for qualitative phytochemical analysis, mineral contents, and flavonoid and phenolic contents, as well as quantitative phytochemical analysis through reversed-phase high-performance liquid chromatography (RP-HPLC) and Fourier-transform infrared (FTIR) spectroscopy. The in vitro antioxidant activity of both extracts was determined by the 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay. The biosynthesized CuO NPs from the Bistorta amplexicaulis extract showed anti-arthritic activity due to the presence of flavonoids and phenols, which showed a pain reliever effect by blocking the cyclo-oxygenase enzyme and has immune suppressant activity, thus securing the joint from destruction. The nanoparticles were characterized by zeta size, zeta potential, scanning electron microscopy (SEM), and FTIR spectroscopy. Forty-eight albino rats were divided randomly into six treatment groups.Results and DisscussionThe zeta size and zeta potential of the nanoparticles were 186.8 nm and −9.23 mV, respectively. Joint stiffness, spleen weight, thymus weight, and paw thickness showed a significant decrease after treatment with NPs. The hematological parameters such as red blood cells (RBCs) and hemoglobin showed a significant increase, while platelets and white blood cells (WBCs) showed a significant decrease in NP-treated groups. C-reactive protein (CRP), rheumatoid factor (RF), liver and kidney function biomarkers, tumor necrosis factor-α (TNF-α), and interleukin-6 (IL-6) levels showed a significant decrease at both low and high doses of green-synthesized CuO nanoparticles from the Bistorta amplexicaulis root extract. The final data were analyzed by one way and two-way analysis of variance (ANOVA) and Tukey’s multi-comparison test.ConclusionSo, from this study, it was concluded that both the plant root extract and green-synthesized CuO nanoparticles have anti-arthritic potential, but CuO NPs showed remarkable results.

Different Correlation Patterns Between Circulating Amino Acids and Body Temperature in Fibromyalgia Syndrome: A Cross-Sectional Study

The aim of this study was to analyze the association between circulating amino acids and central and peripheral body temperature in subjects with and without fibromyalgia syndrome (FMS). A total of 47 patients with FMS and 59 healthy subjects were included in the study. The concentration of amino acids was determined in serum samples using a fluorimeter coupled with a high-performance liquid chromatography system. An infrared thermography camera was used to estimate peripheral hand temperatures. The core temperature of the body was estimated using an infrared thermometer, which was applied to the axillary and tympanic areas. Correlations between several thermographic variables of the hands and tryptophan, methionine, 3-methylhistidine, histidine, glutamic acid, and tyrosine were identified exclusively within the FMS group. In contrast, correlations between aminoadipic acid and serine and thermographic variables were observed only in the healthy control group. The concentrations of asparagine and lysine correlated with thermographic variables in both groups. The essential amino acid leucine was found to correlate with axillary temperature in FMS patients. However, it should be noted that the observed associations between aminoadipic acid and tryptophan blood concentrations and axillary temperature were limited to the control group. Several correlations were identified between circulating amino acids and different body temperatures in both healthy controls and patients with FMS. However, the correlation pattern differs significantly between FMS patients and healthy controls. These findings suggest the possibility of a change in the function of several amino acids in the thermoregulatory process in patients with FMS.

Using phenolic compounds from the Mediterranean Sea west of Egypt to categorize the sediment quality

Background and aimDespite having a low population, Egypt’s west coast is heavily industrialized resulting in large amounts of industrial wastewater that are dumped directly into the sea, severely polluting the area with various toxins. Numerous human activities release phenolic chemicals into the environment, which can be found in water and sediment. These materials are used to make compounds such as dyes, pesticides, explosives, and pharmaceuticals in a variety of industrial processes. Insufficient research has been done on the infiltration of phenolic compounds, which are organic serious pollutants, into the aquatic environment along the Mediterranean coast of Egypt, particularly the western shore. The research investigates the ecological dangers and concentration of eleven phenolic compounds found in bottom sediments on Egypt’s coastal area west of Alexandria.MethodsBefore analysis, stainless steel sieves were used in a mechanical sieving system to homogenize and size-fractionate samples of superficial sediment that were gathered from each of the 15 measurement locations along Egypt’s west coast. Total nitrogen and total organic carbon were also determined. Samples of dried bottom sediment were extracted with a solution of NaOH and methanol in order to determine the phenolic compounds, the final concentrated extract volume of each sample was reduced to 1.0 ml under a mild stream of purified nitrogen gas. A high performance liquid chromatograph (HPLC) (Series 1100, Agilent Technology Inc., Santa Clara, CA, USA) fitted with an autosampler, vacuum degasser, quaternary pump, and diode array detector was used to analyze eleven phenolic compounds.ResultsThe mean concentration of total eleven phenolic ranged between 1.02–5.62 µg g−1 with the mean value of 3.17 µg g−1 (SD, ±1.68), respectively. It was discovered that the concentration of additional phenolic compounds was not uniform, with their share of less than 10% in the total phenolic compounds.ConclusionPhenol was the most prevalent compound, with pentachlorophenol (PCP) coming in second with a normal centralization of 18.454 and 10.785 µg g−1, respectively. It was found that the remaining phenolic compounds had heterogeneous convergences, with less than 10% of them contributing to the total amount of phenolic compounds. Due to several activities, including force stations that utilize tar instead of gas, the oil pipe organization, and several tourist towns, the SidiKirir and Dabaa zones had the highest quantities of phenol and pentachlorophenol.

Antibacterial, antioxidant, cytotoxicity, and phytochemical screening of Moringa oleifera leaves

Bacterial resistance to antibiotics remains a significant clinical challenge, contributing to persistently high rates of morbidity and mortality. Achieving treatment success is increasingly difficult, necessitating the evaluation of new antibiotics and complementary approaches, including source control and alternative therapies. This study aimed to investigate the antibacterial, antioxidant, cytotoxic, and phytochemical properties of Moringa oleifera leaf extract using high-performance liquid chromatography (HPLC), and to evaluate the pharmacokinetic properties of its major compound. The extract demonstrated strong antibacterial activity against standard strains and foodborne bacterial species. It also showed significant antioxidant potential, supported by the presence of high concentrations of phenolic and flavonoid compounds. HPLC analysis identified multiple bioactive compounds, with quercetin as the predominant component. The cytotoxicity study confirmed the safety of the extract at low and moderate concentrations, and ADMET analysis indicated favorable pharmacokinetic characteristics of quercetin. In conclusion, Moringa oleifera exhibits promising potential for medical and food industry applications due to its significant antibacterial and antioxidant activities, combined with a strong safety profile and rich phytochemical content.

Method validation and antioxidant activities of Hyperacanthus amoenus and Carissa bispinosa.

Plant foliages used as feed additives pose a health risk due to high oxidant concentrations. Oxidants cause oxidative stress and high rate of morbidities and mortalities. Hence, the aim of the study was to validate the methods to quantify gallic acid (GA) and quercetin (Q) as putative antioxidants, and to evaluate antioxidant activities in feed (F),Hyperacanthus amoenus(HA) andCarissa bispinosa(CB) extracts. Extraction was carried out with 62.5% methanol. Method validations for linearity, accuracy and precision were performed on high performance liquid chromatography. Quantitative analysis of GA and Q and testing of 2,2-diphenyl-2-picrylhydrazyl (DPPH) scavenging activities in the extracts were performed. The lowest limit of detection (LOD) and limit of quantitation (LOQ) of 0.011 µg/mL and 0.032 µg/mL were determined in HA, respectively. The methods were accurate and precise as the relative standard deviations (%RSD) were less than 15%. The GA concentrations in CB and HA extracts were statistically significant (p 0.05) and their values were 0.65 ± 0.03 x 106µg/kg dry weight (DW) (0.13%) and 0.28 ± 0.06 x 106µg/kg DW (0.002%), respectively. All extracts showed very strong radical scavenging activities with their IC50values ranging between 5.87 µg/mL and 6.86 µg/mL.Contribution:These accurate, repeatable, precise and reliable methods can be used to provide a valuable basis for GA and Q analysis in various shrub foliages. Though high GA concentrations have potential to act as antioxidants, they may have adverse health and growth performance effects when used as feed additives, while lower Q concentrations may have no effects on livestock.

In vitro simulated digestion and Caco-2 cell absorption to explore potential of soy protein isolates as whey protein substitutes in canine and feline food.

Digestive properties and bioavailability of soy protein isolate and whey protein in canine and feline were evaluated using in vitro simulated digestion and cell absorption experiments. The amino acids and peptides in soybean protein isolate and whey protein after digestion were detected by high-performance liquid chromatography and liquid mass spectrometry. Gastrointestinal digestion rates of soy protein isolate and whey protein were analyzed by fitting digestive kinetics curves. The degree of absorption and utilization of amino acids and peptides from the digestive products was evaluated by establishing a Caco-2 cell model. The results demonstrated that soy protein isolate, like whey protein, could produce large amounts of free amino acids and peptides distributed 100-1500 Da. The gastrointestinal digestion speed of soy protein isolate was similar with whey protein. It is worth noting from the intestinal absorption of Caco-2 cell that more than 15 amino acids produced by soy protein isolate and whey protein could be absorbed, and a large number of peptides were also utilized by Caco-2 cell. The bioavailability of soy protein isolates and whey protein for dogs respectively reached 6.30% and 9.00%, and it reached 7.40% and 16.40% in cats, respectively. Soy isolate proteins can be digested and absorbed by pets like whey proteins. These findings may provide significant strategies and support for the application of plant-based proteins in pet foods.

Screening Study on Serine Protease Inhibitory Activity of 10 Plant Species.

In this research, in vitro serine protease inhibitory activity of 10 plant species was evaluated, and extracts that showed strong activity were analyzed through high-performance liquid chromatography (HPLC). Rhododendron caucasicum Pall. (leaf) and Potentilla reptans L. were found to have the highest chymotrypsin inhibitory activities (83.77% and 82.01% inhibition). The highest trypsin inhibitory activity was observed in R. caucasicum (flower) (82.86% inhibition), followed by Cruciata laevipes Opiz (82.22% inhibition). Extracts showing potent enzyme inhibition were fractioned and subjected to activity tests. The highest chymotrypsin inhibitory activity was observed in the n-hexane fraction of P. reptans (92.90% inhibition). In comparison, the highest trypsin inhibitory activity was found in the ethyl acetate fraction of Lythrum salicaria L. (89.81% inhibition). HPLC studies determined that the 80% ethanol extract of P. reptans contained chlorogenic acid. The screened plants were generally rich in phenol and flavonoid content and showed strong antioxidant activity.