Gas Chromatography-mass Spectrometry Research Articles

Preliminary phase results of GC-MS analysis and cytotoxic activity of Argemone mexicana leaves methanol extract against MCF-7 cell lines

Argemone mexicana leaves (AML) contain a variety of bioactive components such as fatty acids, amino acids, phenolics and alkaloids, including Berberine, Isoquinoline, Scoulerine, Stylopine, Thalifone, Benzylisoquinolines, Protopine, and Tetrahydroberberine. This study aimed to examine the gas chromatography and mass spectrometry (GC-MS) analysis of AML extract and its cytotoxic activity on MCF-7 cell lines to identify an alternative source for anticancer treatment. The 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay was utilized to assess the viability of AML extract-treated cells, while the apoptotic assay involved Acridine orange staining to determine the mode of cell death based on morphological and nuclear fragmentation. The GC-MS analysis was used to identify the biologically active compounds. The results showed that the percentage of cell viability after AML extract treatment ranged from 28.50% to 64.28% for concentrations of 1000 to 125 μg/ml (IC50 = 258.87 μg/ml). Statistical analysis revealed a significant difference in cell viability (p < 0.05). Exposure of cells to AML extract stimulated apoptosis through membrane blebbing, cell shrinkage, cytoplasm condensation, and nuclear fragmentation. Forty-one compounds were identified by GC-MS in the AML extract. Based on the peak area, some major compounds included n-Hexadecanoic acid (palmitic acid), 9,12-Octadecadienoic acid (Z, Z)-, Phytol, 9,12,15-Octadecatrienoic acid (Z, Z, Z)-, and 1-methyl piperidine. In conclusion, the bioactive compounds are apparently responsible for the cytotoxic effects of the AML extract, and the in-vitro results highlight the extract’s potential as a source of natural anticancer drugs. However, further investigation is necessary to confirm this.

Cleistopholis patens root bark extract exerts cardioprotective effect against doxorubicin-induced myocardial toxicity in rats

Abstract Background Myocardial Infarction still persists as the most prevalent cardiovascular disease and is a top cause of morbidity and mortality in doxorubicin treated cancer patients. This study evaluated the prophylactic effect of the ethanol root bark extract of Cleistopholis patens (ERBECP) against doxorubicin-induced myocardial infarction in wistar rats. Extraction, preliminary phytochemical analysis, acute toxicity study and body weight (b.w.) of ERBECP were achieved using standard methods. Phyto-constituents in ERBECP were indentified using Gas Chromatography-Mass Spectrometry (GC–MS) technique. Thirty (30) male albino Wistar rats of average b.w. ranging between 100 and 130 g were divided into six groups of five rats each. Groups I, II and III served as normal, doxorubicin (DOX) and standard (Vasoprin 150 mg/kg b.w) controls respectively, while groups IV, V and VI were orally pre-treated with the extract (200, 400 and 600 mg/kgb.w) for two weeks prior to intraperitoneal induction of cardiotoxicity with DOX (20 mg/kg bw) on day 14. Results Disturbances in serum cardiac function bio-markers such as; Cardiac Troponin-I (CTnI), Creatine Kinase (CK), Lactate Dehydrogenase (LDH), Aspartate aminotransferase (AST), Alanine aminotransferase (ALT). Lipid profile markers such as; Total cholesterol (TC), Triacylglycerol (TAG), Low Density Lipoprotein (LDL), High Density Lipoprotein (HDL). Oxidative stress markers such as; Malondialdehyde (MDA), Superoxide Dismutase (SOD), Catalase (CAT), Glutathione (GSH) confirmed the induction of myocardial infarction. Histological assessment of heart tissues was performed to validate biochemical results. The GC–MS analysis of ERBECP identified a total of 69 compounds. Safety profile of the aqueous extract was safe for the animals up to the highest dose of 5000 mg/kg b.w. Pre-treatment of DOX group with ERBECP could significantly increase the b.w. compared to the DOX-treated group during the experimental period of 2 weeks. There were significant (p < 0.05) alterations in the levels of CTnI, CK, LDH, AST, ALT and lipid profile indices in the DOX control rats. Also, significant (p < 0.05) increase was observed in MDA and decrease in SOD, CAT and GSH in the DOX control rats. However, administration of the extract significantly (p < 0.05) normalized these alterations and reversed the architectural changes in the heart. The 69 compounds were screened against the target protein (CBR1); we identified seven hits based on the docking score and interactions with the active site residues. All the C. patens constituents had MW (g/mol) less than 500, HBA < 10 and HBD not more than 5. Apart, 9-Octadecenoic acid (Z)-, 2,3-dihydroxy propyl ester and Estra-1,3,5(10)-trien-17. beta. -ol, all the constituents had LD50 lower than 2000 mg/kg. Conclusions The findings reveals ERBECP demonstrated promising potential and can be exploited in the development novel cardiac therapeutic agents.

IDENTIFICATION OF SECONDARY METABOLITES BY GAS CHROMATOGRAPHY WITH MASS SPECTROSCOPY IN CALLUS TISSUES OF CISTANCHE DESERTICOLA Y.C. MA

The aim of this study is to analyze the types of secondary metabolite compounds found in cistanche (Cistanche deserticola) plants. Methanolic extracts of callus tissues and shoots (stolon) of cistanche were obtained by lyophilic drying and grinding to powdered state using 80% methanol. Secondary metabolites within cystanche callus were first identified by GC-MS (gas chromatography-mass spectroscopy). The identification results of the methanolic extracts revealed various types of compounds including fatty acids (hexadecanoic acid, methyl ester); phenolic compounds and their derivatives (phenol, 2,4-bis(1,1-dimethylethyl)-, 2-methoxy-4-vinylphenol, homovanillyl alcohol, phenol, 2,6-dimethoxy;) sterols (γ-sitosterol); sugars, glycosides and other carbohydrates (ethyl α-D-glucopyranoside, sucrose), glycols and their derivatives (tetraethylene glycol, diethylene glycol monodododecyl ether), etc. Some of the detected compounds may be precursors or by-products of phenylethanoid glycosides biosynthesis. We also found a correlation between callus color and its chemical composition of secondary metabolites. The data can be used for further optimization of C. deserticola cultivation methods to increase the content of target secondary metabolites.

Immunization of male BALB/c and C57BL/6 mice similar modulates chemical signals detected in both chromatographic and behavioral tests

The odor plays a key role in communication between animals and the choice of a mate. The odor of urine of males becomes less attractive to mature females after infection or activation of the immune system. The development of the immune response in the early stages is related with the production of both pro-inflammatory and anti-inflammatory cytokines. To investigate the chemical basis of the observed differences and examine the influence of female interactions with the odor of antigen-treated males, we immunized males of inbred BALB/c (Th1) and C57BL/6 (Th2) mice with hemocyanin (KLH). For females of both tested strains, the attraction of the odor of male urine collected 3 days after immunization was lower compared with the odor of control males. Herewith, BALB/c females sniffed the urine of immunized males less frequently, and C57BL/6 females demonstrated a shorter duration of grooming in olfactory tests with urine of immunized males. The altered response of females to the odor of male urine collected on day 3 after KLH injection matched with antigen-induced modulation of relative levels of volatile organic compounds (VOCs) detected in urine samples by gas chromatography and mass spectroscopy (GC-MS). In males of both strains, after KLH injection, an increase in the content of nonanal, benzothiazole, as well as 2-sec-butyl-4,5-dihydrothiazole, and [1,4,5]-oxadithiepane was shown. At the same time, no compounds were found, the content of which changes in different directions in the urine of males after immunization, depending on the strain of the animal.

Antibacterial, Antioxidant and Cytotoxicity Assessment of Crassocephalum crepidioides Leaf Extract

The goal of the present investigation was to demonstrate the antibacterial activity of different solvent extracts (methanol, ethanol, cold aqueous and hot aqueous) of Crassocephalum crepidioides against ATCC bacterial cultures of Staphylococcus aureus, Escherichia coli, Methicillin resistant Staphylococcus aureus, Pseudomonas aeruginosa and its antioxidant potential. Furthermore, the chemical constituents present in the extract was perused by Gas chromatography-mass spectroscopy (GC-MS), along with in vitro cytotoxicity assessment. All the extracts were shown to be sensitive against S. aureus, MRSA and P. aeruginosa except for the ethanolic extract which was resistant to P. aeruginosa. Of all the extracts, hot aqueous extract found to be the most effective. It was found that Minimum inhibitory concentration (MIC) value of hot aqueous extract against S. aureus, MRSA and P. aeruginosa were 5 mg/mL, 5 mg/mL and 40 mg/mL, respectively. DPPH results showed that C. crepidioides leaf extract has potent antioxidant activity with IC50 value of 57.9 µg/mL. 22 compounds were detected in hot aqueous extract through Gas chromatography-mass spectroscopy. The results of the cytotoxicity evaluation displayed that the IC50 value of the hot aqueous extract of C. crepidioides on Vero cell lines was 292 µg/mL. This study concludes that C. crepidioides leaf extract is non-toxic, has various bioactive components and strong antibacterial and antioxidant activities, thus making it a promising therapeutic agent for various biomedical applications.

Mycosynthesis of silver nanoparticles from endophytic Aspergillus parasiticus and their antibacterial activity against methicillin-resistant Staphylococcus aureus in vitro and in vivo

BackgroundMethicillin-resistant Staphylococcus aureus (MRSA) is a drug-resistant and biofilm-forming pathogenic bacteria with severe morbidity and mortality. MRSA showed resistance against currently available antibiotics. Thus, there is an urgent need to develop novel effective treatments with minimal side effects to eliminate MRSA.AimIn this study, we aimed to mycosynthesize silver nanoparticles (AgNPs) using the endophytic fungus Aspergillus parasiticus isolated from leaves of Reseda Arabica and to examine their antibacterial activity against MRSA.ResultsScreening of fungal secondary metabolites using gas chromatography–mass spectroscopy (GC–MS) analysis revealed the presence of high content of bioactive compounds with antibacterial activities. AP-AgNPs were mycosynthesized for the first time using ethyl acetate extract of A. parasiticus and characterized by imaging (transmission electron microscopy (TEM), UV–Vis spectroscopy, zeta potential, X-ray diffraction (XRD), energy-dispersive X-ray analysis (EDX), and Fourier transform infrared spectroscopy (FTIR)). The agar well diffusion method revealed the antibacterial activity of AP-AgNPs against MRSA with 25 μg/mL of minimum inhibitory concentration (MIC). AP-AgNPs were shown to exert antibacterial action via a bactericidal mechanism based on flow cytometry, scanning electron microscopy, and transmission electron microscopy assessment. Our data demonstrated the effective interaction of AP-AgNPs with the bacterial cell membrane, which resulted in cell membrane damage and disruption of cell surface structure. Furthermore, AP-AgNPs successfully prevented the development of MRSA biofilms by disturbing cell adhesion and destructing mature biofilm reaching over 80% clearance rate. Interestingly, topical application of AP-AgNPs to superficial skin infection induced by MRSA in mice effectively promoted wound healing and suppressed bacterial burden.ConclusionOur results provide a novel green nanoparticle drug design with effective therapeutic potential against MRSA-induced skin infection.

Elucidating the augmented resistance profile of Scedosporium/Lomentospora species to azoles in a cystic fibrosis mimic environment.

Scedosporium/Lomentospora species are ranked as the second most frequently isolated filamentous fungi from cystic fibrosis (CF) patients. Previously, we demonstrated that the minimum inhibitory concentration (MIC) for voriconazole and posaconazole increased when performed on a mucin-containing synthetic CF sputum medium (SCFM) compared to the standard medium, RPMI-1640. In this study, we have expanded the MIC comparison to four additional azoles and investigated characteristics linked to azole resistance in Scedosporium apiospermum, Scedosporium minutisporum, Scedosporium aurantiacum and Lomentospora prolificans. MIC was assayed by CLSI protocol, efflux pump activity was assessed by rhodamine 6G and sterols were analysed by gas chromatography-mass spectrometry (GC-MS). Overall, MICs for fluconazole, itraconazole, voriconazole, posaconazole, miconazole and ketoconazole increased by least 2-fold when susceptibility tests were performed using SCFM compared to RPMI. The activity of efflux pumps was similar in both media; however, in RPMI, but not in SCFM, the activity was induced by voriconazole and fluconazole. Additionally, MICs for those antifungals decreased more noticeably in SCFM than in RPMI in the presence of the efflux pump inhibitor PaβN. The SCFM-grown cells presented fewer sterols in their composition, and consequently higher membrane fluidity, than RPMI-grown cells. GC-MS analysis demonstrated a remodulation in the sterol profile in SCFM- compared to RPMI-grown cells. Accordingly, when the MIC assay was performed in the presence of the membrane stressor NaCl (3%), the susceptibility to voriconazole and fluconazole increased more in SCFM- than RPMI-grown cells. Scedosporium/Lomentospora species undergo cellular adaptations in SCFM that favours their growth in face of the challenges imposed by azole antifungals.

Association between serum unsaturated fatty acids levels and infertility among American women from the National Health and Nutrition Examination Survey 2013-2014.

Some research indicates that unsaturated fatty acids (UFAs) in the diet could enhance reproductive outcomes in infertile women. However, other research holds different views, possibly due to differences in the conversion rates of UFAs from various foods and bioavailability in the body. Therefore, this research examined the link between serum UFAs and infertility issues. This research included reproductive-age women participating in the 2013-2014 American National Health and Nutrition Examination Survey (NHANES). Serum levels of four UFAs, including palmitoleic acid (16:1n-7), vaccenic acid (18:1n-7), oleic acid (18:1n-9), and linoleic acid (18:2n-6) were measured through gas chromatography-mass spectrometry. Infertility data was collected by affirmative responses to targeted questionnaire items. Associations between serum UFA levels and infertility were evaluated utilizing Poisson regression models and smooth curve fitting methods. Sensitivity analysis was also conducted. This study included 535 women, aged between 18 and 45. Poisson regression analysis, both adjusted and unadjusted for confounders, revealed no associations between palmitoleic acid, vaccenic acid, oleic acid, or linoleic acid and female infertility (all P > 0.05). However, four UFAs all showed non-linear relationships with infertility in smooth curve fitting analysis. Sensitivity analysis confirmed the stability of the findings. This research established non-linear associations between serum UFAs and infertility in American women. Specifically, maintaining appropriate serum levels of these UFAs may lower infertility risk. These findings offer new insights and practical dietary recommendations for improving female fertility.

Phytochemical screening, nutritional, antinutritional, antioxidant, GCMS and mineral analysis of Zanthoxylum rhetsa (Roxb.) DC: Insights from tribal consumption in Mizoram, Northeast India

The plant Zanthoxylum rhetsa Roxb, a member of the Rutaceae family, holds dual significance in certain communities, particularly in Mizoram, Northeast India, where it is valued for its medicinal properties and consumed as a vegetable. This study comprehensively analyzes the phytochemical, nutritional, antinutritional, and antioxidant properties and the mineral content of Z. rhetsa, a plant traditionally consumed by tribal communities in this region. Minerals such as aluminum, copper, iron, manganese, nickel, and zinc were measured using Atomic Absorption Spectroscopy (AAS). Gas Chromatography-Mass Spectrometry (GC-MS) analysis was conducted to determine the chemical composition of the samples. Phytochemical screening revealed the existence of several bioactive components, such as tannins and flavonoids, while nutritional studies validated the plant's abundance of key nutrients. Among the minerals, manganese was found in the highest concentration (481.356 mg/100 g of DW), while nickel was present in the lowest concentration (1.614 mg/100 g of DW). The total calorific content was ascertained to be 51.344 Kcal/100g, adequate for dietary requirements. Additionally, the total phenolic content measured was 8.28 mg/g in gallic acid equivalent, and the total flavonoid content was 43.04 mg/g in quercetin equivalents. The existence of antinutritional compounds in differing amounts necessitates meticulous evaluation, particularly with the intake of fruits that may possess elevated levels of these substances. This comprehensive assessment highlights the nutritional significance of Z. rhetsa in local diets, emphasizing its dual role as a source of beneficial nutrients and potential antinutritional factors.

Analysis and Characterization of Pericopsis mooniana Seed Oil for Potential Applications in Cosmetics and Nutritional Supplements

Pericopsis mooniana is renowned for wood applications, while its bark and leaves find uses in ayurvedic medicine. The shifting of global cosmetic and nutritional supplement industries towards plant-based oils has led to explore novel sources. No prior studies were done on P. mooniana seed oil. Therefore this study aims to characterize the seed oil of P. mooniana by determining Fatty Acids (FA) composition as their methyl esters, nonpolar constituents in unsaponifiable matter, and other physio-chemcial properties. The oil was extracted using the soxhlet extraction method. Ash and moisture contents of seeds, Acid Value (AV), Iodine Value (IV), smoke point and thermal stability of oil were also determined. Prepared fatty acid methyl esters and chemical constituents in unsaponifiable matter were identified and quantified using Gas Chromatography-Mass Spectrometry method. Results indicated a substantial oil yield of 36.71± 0.01% with moisture content of 5.60 ± 0.19%, ash content of 3.65 ± 0.38%, AV of 2.97 ± 0.40 mg KOH/g, IV of 16.02 ± 0.14 g I2/100g, smoke point of 233.6 ± 8.57°C, decomposition temperature of 409.95 ± 1.74°C and yield of unsaponifiable matter of 1.35 ± 0.01%. The dominant FAs are oleic (41.02%) and linoleic (38.12%) acids. Major unsaponifiable matter constituents are squalene (4.01 mg/g), beta.-sitosterol (2.63 mg/g), stigmasterol (1.23 mg/g), phytol (1.45 mg/g), geranylgeraniol (1.03 mg/g) and amyrin (0.95 mg/g). Based on the finding of this study, it can be concluded that P. mooniana seed oil has the potential to be utilized in both cosmetic and nutritional supplement industries.

GC-MS/HPLC Profiling and Sono-Maceration Mediated Extraction of Osbeckia Parvifolia Polyphenols: In Silico and In Vitro Analysis on Anti-Proliferative Activity in Ovarian Cancer Cell Lines.

Osbeckia parvifolia, an endemic edible plant of Western Ghats, was investigated in the present study for its polyphenolic compounds, including content, constituents, extraction through an ultrasonic-assisted maceration technique and therapeutic potential in biomedical applications. The methanolic extract (OPM) exhibited an IC50 value of 1.25 μg/mL against 2,2-Diphenyl-1-picrylhydrazyl (DPPH) radicals. Furthermore, the ethyl acetate and methanolic extracts also strongly inhibited 5-lipoxygenase, especially OPM (84.93 %), which was comparable to standard curcumin. OPM also elicited cytotoxicity in SKOV3 ovarian cancer cells (93.80 %), surpassing paclitaxel. Bio-accessibility analysis demonstrated that the release of phenolic compounds and antioxidant potential were very high (above 100 %), revealing the possibility of synergistic efficacy of polyphenolic complexes in drug development. Gas Chromatography -Mass Spectrometry (GC-MS) analysis revealed 22 bioactive polyphenolic compounds in OPM, such as epicatechin, quercetin, and psoralidin. This was confirmed by High Performance Liquid Chromatography (HPLC) and High-Pressure Thin Layer Chromatography (HPTLC) analyses, which revealed a high quantity of catechin (37.45 mg/g). Molecular docking revealed the significant binding affinity of these proteins for the ovarian oncoproteins PI3K (-8.52 kcal/mol) and Casp-8 (-8.41 kcal/mol). Adsorption, Distribution, Metabolism, Excretion and Toxicity (ADMET) profiling indicated the favorable pharmacokinetic properties of these compounds, supporting their candidacy in drug formulations against ovarian cancer.

P63 affects distinct metabolic pathways during keratinocyte senescence, evaluated by metabolomic profile and gene expression analysis.

Unraveling the molecular nature of skin aging and keratinocyte senescence represents a challenging research project in epithelial biology. In this regard, depletion of p63, a p53 family transcription factor prominently expressed in human and mouse epidermis, accelerates both aging and the onset of senescence markers in vivo animal models as well as in ex vivo keratinocytes. Nonetheless, the biochemical link between p63 action and senescence phenotype remains largely unexplored. In the present study, through ultrahigh performance liquid chromatography-tandem mass spectroscopy (UPLC-MS/MS) and gas chromatography/mass spectrometry (GC/MS) metabolomic analysis, we uncover interesting pathways linking replicative senescence to metabolic alterations during p63 silencing in human keratinocytes. Integration of our metabolomic profiling data with targeted transcriptomic investigation empowered us to demonstrate that absence of p63 and senescence share similar modulation profiles of oxidative stress markers, pentose phosphate pathway metabolites and lyso-glycerophospholipids, the latter due to enhanced phospholipases gene expression profile often under p63 direct/indirect gene control. Additional biochemical features identified in deranged keratinocytes include a relevant increase in lipids production, glucose and pyruvate levels as confirmed by upregulation of gene expression of key lipid synthesis and glycolytic enzymes, which, together with improved vitamins uptake, characterize senescence phenotype. Silencing of p63 in keratinocytes instead, translates into a blunted flux of metabolites through both glycolysis and the Krebs cycle, likely due to a p63-dependent reduction of hexokinase 2 and citrate synthase gene expression. Our findings highlight the potential role of p63 in counteracting keratinocyte senescence also through fine regulation of metabolite levels and relevant biochemical pathways. We believe that our research might contribute significantly to the discovery of new implications of p63 in keratinocyte senescence and related diseases.

Antibacterial Activity, GC MS Analysis and In Silico Validation of Bioactive Compound from Endophytic Fungus Lasiodiplodia pseudotheobromae EF-9.

Secondary metabolites synthesized by endophytic fungi have garnered significant interest for their broad applications in treating various ailments. In this study involving 20 plant samples, 11 endophytic fungi were isolated and cultured, and Lasiodiplodia pseudotheobromae EF-9, derived from Hibiscus rosa-sinensis, demonstrated greater antibacterial efficacy than the other isolated endophytes. Phylogenetic analyses using 18S rRNA gene confirmed the EF-9 identity as L. pseudotheobromae. Following mass production, the active compound was partially purified using column chromatography. The fraction collected at the 60th min exhibited good antibacterial activity against Bacillus coagulans (MTCC 6735) and Shigella flexneri (ATCC 12022), with an inhibition zone of approximately 20 mm in diameter. UV spectral studies revealed a wide absorption band at 430 nm. High Performance Liquid Chromatography (HPLC) of the active fraction showed a distinct peak with a retention time of 4.216 min at 430 nm absorbance. Gas Chromatography-Mass Spectrometry (GC-MS) identified the active compound in the L. pseudotheobromae EF-9 culture broth extract as Bis(2-ethylhexyl) phthalate, which displayed a peak at 16.856 min and covered 66.69% of the area in the spectral analysis.

Assessment of Pelargonium graveolens flower essential oil: Antimicrobial, antioxidant, enzyme inhibition and in vivo topical analgesic and anti-inflammatory efficacy as treatment for atopic dermatitis

Background Atopic dermatitis (AD) is a chronic inflammatory skin condition characterized by pruritus and skin barrier dysfunction. This study aims to evaluate the therapeutic potential of Pelargonium graveolens (Geraniaceae) in managing AD symptoms through its essential oil. Methods The chemical composition of Pelargonium graveolens flower essential oil (PFEO) was analyzed using gas chromatography-mass spectrometry (GC-MS). Its antimicrobial, antioxidant, and anti-inflammatory properties were assessed, along with the inhibitory effects of PFEO on key enzymes involved in skin repair: tyrosinase, elastase, and collagenase. An in vivo evaluation of a gel formulation containing PFEO was also conducted to assess its anti-inflammatory and analgesic efficacy. Results GC-MS analysis identified major compounds in PFEO, including Geraniol (22.83%), beta-citronellol (19.51%), naphthalenemethanol (15.36%), and Geranyl tiglate (9.38%), with minor constituents such as linalool (3.81%) and neryl formate (1.31%). PFEO exhibited bacteriostatic activity against various bacterial and fungal strains, including Pseudomonas aeruginosa, Staphylococcus aureus, Methicillin-Resistant Staphylococcus aureus (MRSA), Bacillus anthracis, Streptococcus pyogenes, Staphylococcus epidermidis, Candida albicans, and Malassezia spp. The essential oil also demonstrated significant antioxidant properties and inhibited key enzymes linked to skin alterations in AD. Conclusions PFEO shows promising therapeutic potential for managing symptoms of atopic dermatitis due to its antimicrobial, antioxidant, and anti-inflammatory properties, as well as its analgesic effects. The findings support further exploration of PFEO as a natural alternative in the treatment of AD.

Study protocol: the ‘Endoscope CRC’ cohort, a prospective biobank study on the development and evaluation of diagnostic and prognostic biomarker profiles for colorectal cancer and premalignant lesions

IntroductionEarly detection of colorectal cancer (CRC) and clinically relevant (advanced) adenomas leads to a significant reduction of CRC-related mortality and morbidity. However, the faecal immunochemical test (FIT) suffers from a...

Comparative volatiles profiling of two marjoram products via GC-MS analysis in relation to the antioxidant and antibacterial effects.

Marjoram (Origanum majorana L.), also known as "sweet marjoram" or "sweet oregano" is a Mediterranean herbaceous perennial herb cultivated in Egypt and widely consumed as an herbal supplement for treatment of several ailments. The main goal of this study was to assess volatiles' variation in marjoram samples collected from two different widely consumed commercial products using two different extraction techniques viz. head space solid phase microextraction (HS-SPME) and petroleum ether using gas chromatography mass spectrometry (GC-MS) analysis and multivariate data analysis. A total of 20 major aroma compounds were identified in samples extracted with HS-SPME found enriched in monoterpene hydrocarbons and oxygenated compounds. The major volatiles included β-phellandrene (20.1 and 14.2%), γ-terpinene (13.4 and 11.7%), 2-bornene (12.3 and 11.5%), p-cymene (9.8 and 4.6%) terpenen-4-ol (16.4 and 7.5%), sabinene hydrate (16.02 and 8.8%) and terpineol (4.2 and 3.2%) in MR and MI, respectively. Compared with HS-SPME, 51 aroma compounds were identified in marjoram samples extracted with petroleum ether, found more enriched in aliphatic hydrocarbons (42.8 and 73.8%) in MR and MI, respectively. While a higher identification score was observed in the case of solvent extraction, SPME appeared to be more selective in the recovery of oxygenated terpenes to account more for marjoram aroma. Multivariate data analysis using principal component analysis (PCA) revealed distinct discrimination between volatile composition of both marjoram samples. The total phenolic and flavonoid contents in marjoram samples were at (111.9, 109.1µg GA/mg) and (18.3, 19.5µg rutin eq/mg) in MR and MI, respectively. Stronger antioxidant effects were observed in MR and MI samples with IC50 at 45.5 and 56.8µg/mL respectively compared to IC50 6.57µg/mL for Trolox as assayed using DPPH assay. Moderate anti-bacterial effect was observed in MR and MI samples and expressed as a zone of inhibition mostly against Bacillus subtilis (16.03 and 15.9mm), B. cereus (12.9 and 13.7mm), Enterococcus faecalis (14.03 and 13.97mm), and Enterobacter cloacae (11.6 and 11.6mm) respectively.

Forensic Comparison of Amphetamine Chemical Profiles by Bayesian Predictive Modelling

ABSTRACTForensic chemists frequently employ statistical profiling approaches to assess the degree of similarity between samples of illicit drugs. Such profiling information can help reveal connections between nodes in distribution networks and manufacturing laboratories. For amphetamine, the routine method of comparing a pair of samples includes the use of a dissimilarity measure based on the Pearson correlation coefficient calculated between their chemical profiles obtained through gas chromatography–mass spectrometry. This simple measure of (dis)similarity has been shown distinguish pairs sharing a common origin (e.g., same production batch) to a reasonable level of accuracy. However, Pearson correlation fails to capture all the relevant notions of similarity between chemical profiles of amphetamine. We present a new statistical method for forensic drug comparison that uses a more sophisticated statistical modelling approach to determine similarity between samples. We show that this leads to improved performance over the correlation‐based approach. The proposed method is easily extendable and has an intuitive interpretation both from chemistry and forensic perspectives, which supports wide applicability to illicit drug profiling in practice.

Lingguizhugan decoction alleviates obesity in rats on a high-fat diet through the regulation of lipid metabolism and intestinal microbiota

BackgroundIndividuals with obesity often experience elevated blood lipid levels, leading to a chronic low-grade inflammatory state, exacerbating liver oxidative stress, and increasing the risk of various metabolic diseases. Recent evidence suggests that intestinal microbiota and short-chain fatty acids (SCFAs) play crucial roles in the development and progression of obesity. While the mechanisms by which Lingguizhugan decoction (LGZGD) intervenes in obesity by improving lipid metabolism, enhancing insulin sensitivity, and reducing inflammatory responses are well-documented, its potential in intestinal microbiota and SCFAs remains unclear. This study aims to explore the impact of LGZGD on high-fat diet (HFD) induced obesity in rats and its regulatory effects on intestinal microbiota and SCFAs, providing new insights for obesity prevention and treatment.MethodsFifty-one male SD rats were randomly divided into groups, with six in the normal control group (NC) receiving a ddH2O treatment and a standard diet. The remaining 45 rats were fed a high-fat diet (HFD) using D12451 feed. After 10 weeks, the rats on the HFD gained 20% more weight than the NC group, confirming the successful modeling of obesity. These rats were then randomly divided into the following groups: ddH2O high-fat diet model group (MC), 20 mg/kg/day Orlistat positive control group (Orlistat), 1.62 g/kg/day low-dose LGZGD group (LGZGL), and 3.24 g/kg/day high-dose LGZGD group (LGZGH) for 8 weeks. We evaluated changes in body weight, serum total cholesterol (TC), total triacylglycerol (TG), low-density lipoprotein cholesterol (LDL), and high-density lipoprotein cholesterol (HDL) levels. Fat and liver tissues were collected for pathological analysis. Intestinal contents were aseptically collected for 16S rRNA gene sequencing and gas chromatography–mass spectrometry (GC–MS) to assess gut microbiota and SCFA levels.ResultsLGZGD reduces body weight, TC, TG, LDL, and HDL levels, significantly reducing hepatic steatosis. Besides, it restored the richness and diversity of gut microbiota, which was reduced by HFD, altering the overall structure. Specifically, LGZGD significantly promoted the growth of Muribaculaceae and Dubosiella while inhibiting the growth of Christensenellaceae_R_7_group and UCG_005. It also restricts the production of caproic acid. Correlation analysis indicated positive correlations: Muribaculaceae with Butyric acid and Isovaleric acid; UCG_005 with TC, LDL, and HDL; and Christensenellaceae_R_7_group with TC and LDL.ConclusionLGZGD increased the abundance of beneficial gut microbiota in HFD-induced obese rats, improved gut microbiota dysbiosis, and inhibited the increase in caproic acid content. These results suggest that LGZGD can mitigate HFD-induced obesity, and its active components warrant further investigation.

Environmental Detoxification of Benzimidazole Fungicide Fuberidazole via Microbial Action in Liquid Cultures

Mitigation of the environment from hazardous pesticides is clamant for all living things. The behavior of the fungicide Fuberidazole was investigated toward biodegradation. Biotransformation experiments were conducted by bacterial strains isolated from soils including, Xanthomonas citri (XC), and Pseudomonas syringae (PS), and fungal strains including, Aspergillus flavus (AF), Aspergillus niger (AN) and Penicillium chrysogenum (PC). Analysis and quantification of Fuberidazole degradation and its metabolites were performed by gas chromatography mass spectrometry and UV-visible spectrophotometry. Pseudomonas syringae and Penicillium chrysogenum displayed great bioremedial potential and degraded 91 and 86% of Fuberidazole after 35 days. Significant metabolites such as Benzimidazole 2-carboxylic acid, Benzimidazole, and 1-(1H-benzimidazole-2-yl)ethanone were produced in the current experiment. The increasing order of half-life for all strains was obtained as, PS (10.3) < PC (10.6) < AN (11) < AF (11.9) = XC (11.9) days. Experimental results demonstrated the capability of bacterial cells to efficiently utilize Fuberidazole as a nutrition source and the significance of favorable environmental conditions for its dissipation.

Advanced sensing and analytical techniques for quality control of tobacco flavoring

Abstract Assuring stability and uniformity in tobacco cut filler flavoring is crucial for cigarette product quality. This review focuses on advanced sensing and analytical techniques like gas chromatography-mass spectrometry and electronic nose technology. These methods analyze the chemical composition of flavoring liquids and detect volatile components in tobacco cut filler samples, thereby evaluating flavoring stability and uniformity. The review also acknowledges additional technologies like near-infrared spectroscopy and continuous flow analysis. Strengths and weaknesses of these detection techniques are discussed, providing insights into quality control of tobacco cut filler flavoring.&amp;#xD;