GC-MS Analysis Research Articles

Chemical Composition, Antifungal, Antibacterial, Antioxidant, Antiviral and Cytotoxic Activities of Ruta chalepensis L. Fixed Oil from Saudi Arabia

An aromatic plant is called Ruta chalepensis L. known locally as “Fidjel,” grows in rocky, arid places. Its pharmacological activities are pleiotropic. The goal of the present investigation was to use GCMS and HPLC analysis to identify the chemical constituents of oil extracted from Ruta chalepensis L. and assess its antibacterial, antifungal, antioxidant, antiviral, and anticancer properties. Linoleic acid was the most predominant acid found in Ruta chalepensis L. oil, then oleic acid, palmitic acid, and linolenic acid. 13.64 μg/mL of tocopherol (α-, β-, and γ-tocopherol) was identified. The primary phytosterols are β-sitosterol and campesterol. At 200 μL/mL of Ruta chalepensis L. oil, phenolic components rated 84.4 GAE/mL and had 94.0% antioxidant activity. Zone inhibition efficacy of Ruta chalepensis L. oil against microbial strains, particularly E. coli with a diameter of 42.3 mm, was demonstrated. MBC (30 μL/mL and 40 μL/mL) are the bactericidal action against E. coli and S. aureus, while MIC bacteriostatic (30 μL/mL) was also demonstrated. However, Ruta chalepensis L. oil was ineffective against Saccharomyces cervisia and fungal strains. Weak inhibitory impact of Ruta chalepensis L. oil was observed against the PC-3 (prostate cancer) cell line. Nonetheless, it had a significant inhibitory impact on the A2780 (ovarian cancer) cell line. At 100 μg/mL of oil, Ruta chalepensis L. oil showed a low antiviral impact (7.93±2.03%) against the herpes simplex virus type 2 (HSV-2). Oil from Ruta chalepensis L. is a promising option for the medical management of non- transmissible illnesses, since it is wealthy in antioxidants and bioactive substances.

Unusual Photochemistry in Aromatic Dithioimides: Quantitative Thione Reduction Promoted by Ether Solvents.

We report a mechanistic investigation of an aromatic dithioimide (2SS) displaying puzzling yet efficient photochemistry in ether solvents. Perplexingly, 2SS dissolved in ether solvents in a sealed and degassed vial was photochemically converted to the corresponding diimide (2OO), as determined by 1H NMR following product extraction. With no external sources of oxygen in the sample, could the oxygen in 2OO be from the ether itself? To study this unprecedented proposition, we attempt to uncover the ether's involvement in this reaction. As seen by laser-flash photolysis, 2SS appears to first react with the solvent from its singlet excited state. Following the reaction by NMR under rigorously oxygen- and water-free conditions led to the identification of a photoreductive pathway that quantitatively transformed one thione into a methylene to yield 2SH2. Subsequent oxidation of 2SH2 or irradiation of 2SS under air proved that molecular oxygen was indeed necessary to observe an oxidative pathway leading to 2OO, ruling out the initially proposed involvement of an ether oxygen. An explanation of 2SS desulfurization was further revealed through the study of solvent by-products by GC-MS analysis. Supported by DFT calculations, a mechanism is proposed to involve a chain reaction initiated by photochemically generated ether radical.

Irciniaplysins A-D: New Psammaplysin Derivatives from Philippine Marine Sponge Ircinia sp.

Four new psammaplysin derivatives (1-4) with fatty acyl substituents, designated irciniaplysins A-D, and three known psammaplysins (5-7) were isolated from a marine sponge Ircinia sp. Their structures were elucidated using extensive spectroscopic analyses. The positions of the double bonds and the branch points of the fatty acyl side chains were determined by GC-MS analysis of their fatty acid methyl ester (FAME) derivatives. Irciniaplysins A (1) and B (2) contained an unusual long-chain fatty acyl substituent with a 5,9-diene unit. The isolated compounds were evaluated for their cytotoxic activity against the human colorectal carcinoma (HCT 116) cells, however, none of these compounds showed significant activity.

Combining the pharmaceutical and toxicological properties of select essential oils with their chemical components by GC-MS analysis.

In the current investigation, a comprehensive analysis was carried out on essential oils (Eos) extracted from six aromatic plant species, namely Rosmarinus officinalis, Pelargonium graveolens, Thymus vulgaris, Origanum vulgare, Laurus nobilis, and Aloysia citrodora. An exploration was conducted into the chemical composition using Gas Chromatography-Mass Spectrometry (GC/MS), antioxidant properties assessed through DPPH, ABTS, CUPRAC, FRAP, MCA, and PBD assays, ecotoxicological impacts evaluated via allelopathy and the Daphnia magna heartbeat test, as well as bio-pharmacological effects including anticancer activity and gene expression analysis. Results revealed strong antioxidant activity in all essential oils, with T. vulgaris EO (2748.00 mg TE/g) and O. vulgare EO (2609.29 mg TE/g) leading in CUPRAC assay. R. officinalis EO showed the highest α-amylase inhibition at 1.58 mmol ACAE/g, while O. vulgare EO excelled in α-glucosidase inhibition at 1.57 mmol ACAE/g. Additionally, cytotoxic effects were evaluated on human colorectal cancer (HCT116) cells. A. citrodora, O. vulgare, and R. officinalis EOs were found the most potent anticancer, as also witnessed by their higher modulatory effects on the gene expression of BAX and Bcl-2. Collectively, the present data highlight the importance to implement the knowledge and to valorise the chain of aromatic plants.

Transcriptome analysis of Acinetobacter calcoaceticus HX09 strain with outstanding crude-oil-degrading ability.

Microbial remediation plays a pivotal role in the elimination of petroleum pollutants, making it imperative to investigate the capabilities of microorganisms in degrading petroleum. The present study describes the isolation of a promising strain, Acinetobacter sp. HX09, from petroleum-contaminated water. GC-MS analysis revealed a remarkable removal efficiency for short and medium-chain alkanes, with a rate of approximately 64% after a 7-days incubation at 30 °C. Transcriptome analysis of HX09 exhibited a predominant upregulation in gene expression levels by the induce of crude oil. Notably, genes such as alkane 1-monooxygenase, dehydrogenases and fatty acid metabolic enzymes exhibited fold changes range from 3.16 to 1.3. Based on the alkB gene sequences in HX09, the Phyre2 algorithm generated a three-dimensional structure that exhibited similarity to segments of acyl coenzyme desaturases and acyl lipid desaturases. Furthermore, three biodegradation-related gene clusters were predicted in HX09 based on the reference genome sequence. These findings contribute to our understanding of the hydrocarbon-degrading mechanisms employed by Acinetobacter species and facilitate the development of effective remediation strategies for crude oil- polluted environments.

Investigation of value-added compounds derived from oak wood using hydrothermal processing techniques and comprehensive analytical approaches (HPLC, GC-MS, FT-IR, and NMR)

In this study, slow pyrolysis of oak woods was carried out in a fixed bed tube reactor at four different temperatures ranging from 100 °C to 400 °C and at 5 °C/min speed time intervals. The compositions of the produced bio-tar and bio-oils were determined in detail using FT-IR, GC-MS, HPLC, and NMR devices. Several pyrolysis parameters were carried out to reveal the distribution of pyrolytic products under different pyrolysis temperatures (100–400 °C) and times (1–4 h). During the slow pyrolysis process, oak wood started to decompose to form organic volatile products at a set temperature of 100 °C and reached a maximum yield of volatile products at around 400 °C. GC-MS analyses revealed that different valuable components such as furans, phenolic compounds, carbonyls, linear, aromatic compounds, acids, and hydrocarbons have been formed. Based on the experimental results of the pyrolysis, it has been detected that the temperature and time interval are very effective parameters in the conversion of oak wood to the amount of liquid product.

Antibacterial Activitiy of Triterpeniod Compounds

The goal of the study was to ascertain whether particular pathogenic bacteria could be inhibited by triterpeniod substances obtained from Rosmarinus officinalis (rosemary) extracts. The time frame for completing this construction was July 2023–April 2024. At the beginning, 100 specimens were taken from patients who were undergoing treatment at the Burn Cure Center in Nineveh Governorate, Iraq Routine biochemical testing were used to determine burn infections caused by bacteria, and the Vitek2 compact system was used to confirm the diagnosis. Acinetobacter baumani and Pseudomonas auroginosa were the most common isolates. In order to extract the substance, rosemary (R. officinalis) leaves were air-dried in the shade and then processed into a fine powder using a grinding machine. A soxhlet device was used to extract 50 g of powdered leaves for six hours at 40–60 °C using 250 ml of 75% petroleum ether. Afterwards, the mixture was dried out at 40°C in a rotating evaporator. After being weighed, the extract residue was stored until needed. Using gas chromatography/mass spectrometry (GC/MS), the crude extract was examined. Ursolic acid (1.38), oleanolic acid (3.27), and other triterpeniod substances with varying ratios were identified by GC-MS analysis. The antibacterial activity of triterpeniod compounds was assessed at concentrations of 12.5%, 25%, 50%, and 100% using the well-diffusion Kirby-Bauer method. The test was evaluated in comparison to six bacterial strains. The results indicated that staphylococcus aureus (50%:22mm – 100%: 26mm), staphylococcus haemolyticus (100%: 17mm), and Acinetobacter baumani (50%:18mm – 100%: 22mm) had the highest inhibitory.

What Phenomena Happen During Pyrolysis of Plastic? FTIR AND GC-MS Analysis of Pyrolyzed Low Linear Density Polyethylene (LLDPE) Polymer Particles Completed with Bibliometric Research Trend and Pyrolysis Chemical Reaction Mechanism

This research aims to determine the compounds produced from the pyrolyzed Low Linear Density Polyethylene (LLDPE) using Fourier Transform Infrared (FTIR) and Gas Chromatography-Mass Spectroscopy (GC MS). We used pyrolysis of 985 g of 2-mm diameter LLDPE plastic ore at a temperature between 192-194°C for 135 min using a batch reactor (length x width x height = 35 cm x 24 cm x 44 cm) equipped with an outlet connected to two condensers (24°C). To ensure the chemical results, the reactor was connected in series to condensers 1 and 2. The results obtained in condenser 1 were 3 mL of 2-phase liquid with a strong odor. The upper fluid is yellow, and the lower fluid is brown. In condenser 2 (connected directly to condenser 1), 4 mL of yellow single-phase liquid was produced with a strong odor. The liquid obtained from the pyrolysis process was then analyzed by FTIR and GC-MS. FTIR results on both samples showed that the samples contained the functional groups O-H, CH₂, and C=O. The GC-MS results on condenser sample 2 showed that the pyrolysis product contained acetone compounds. This confirmed that pyrolysis caused chemical structural changes in LLDPE due to LLDPE chain bond-breaking reactions, producing many smaller chemical compounds. Additionally, some oxidation happens, which is due to the oxygen content in the reactor. This study provides new insights into the LLDPE pyrolysis mechanism and the physical and chemical properties of the liquid resulting from the pyrolysis process.

Chemical Evaluations of Boiled Hemidactylus frenatus and Scolopendridae cataracta Solutions and their Histopathological Effects on Livers and Kidneys of Rats

This study evaluated the chemical profiles of boiled Hemidacylus frenatus (wall gecko, WG) and Scolopendridae cataracta (centipede) solutions and their effects on the liver and kidneys of albino rats. The GC-MS analyses of the solutions revealed that notable among the compounds present in boiled whole wall gecko solution (BWWGS) were hexadecanoic acid, 11-octadecanoic acid and methyl stearate. Hexadecanoic acid, 9,10-epoxy-18-(trimethylsiloxy)-, methyl stearate, 6-Octadecenoic acid and n-hexadecanoic were relatively present at high levels in boiled degutted wall gecko solution (BDWGS) while 9-octadecanoic acid, hexadecanoic acid and methyl stearate were also present in boiled centipede solution (BCS). Histological examinations of the kidneys and liver showed that the most notable effects of these solutions after 28-day exposure of the rats were haemorrhage in both organs, vacuolar degeneration in the kidneys and degeneration of the hepatocytes; in dose-dependent manners. The BWWGS and BCS induced hepatic and renal morphological changes in organs of the rats that were treated with them; indicating that the solutions contained toxic substances. The toxic effect was more pronounced with BWWGS relative to BDWGS; suggesting that the gut of WG might have contained agents responsible for the higher toxicity of its boiled solution. In conclusion, the boiled wall gecko and centipede solutions were toxic to the organs of the rats because of the toxic substances detected in them.

Upgrading/Deacidification of Bio-Oils by Liquid–Liquid Extraction Using Aqueous Methanol as a Solvent

Oxygenated compounds such as acids in bio-oils (BO) have been related to the corrosion of metals and their storage instability when applied as fuels. Therefore, upgrading BO by removing acids (deacidification) can be a valuable technique to reduce corrosivity using specific separation processes. Therefore, the objective of this paper was to evaluate the effect of the water content in the solvent (aqueous methanol), the carboxylic acid content in the BO and extraction temperature on the deacidification process by liquid–liquid extraction (LLE), as well as the effect of the same parameters on the quality of the deacidified BO through physical–chemical and GC-MS analyses. The results show that an increase in the water content (5 to 25%) in the solvent and an increase in the carboxylic acids content (24.38 to 51.56 mg KOH/g) in the BO reduce the solvent’s capacity to extract carboxylic acids while increasing the temperature (25 to 35 °C) of the deacidification process promoted an increase in its capacity to remove them. Consequently, the highest deacidification efficiency (72.65%) is achieved with 5% water in methanol at 25 °C for BO1 (TAN = 24.38 mg KOH/g). Therefore, the deacidification process through LLE using aqueous methanol contributed significantly to BO upgrading.

Development of Phytoconstituents from Spathodea campanulata Flowers as Potential Antimalarial Agents

Background: Considering the majority of pharmaceutical firms focus on using herbal remedies as an alternative source of essential components, herbal remedies are extremely significant to pharmacological researchers. Spathodea campanulata is one of the members of the Bignoniaceae family. It is popular for its curative properties Aim: This research aimed to assess the possibility of bioactive elements and antioxidant impacts of the methanol fraction of Spathodea campanulata flowers. Objectives: The objective of this research was to assess the achievable bioactive elements and antioxidant impacts of the methanol fraction of Spathodea campanulata flowers. Methods: GC-MS was adopted to identify the phytoconstituents present in the extract. In the present study, we utilized computational modelling with the Schrödinger Maestro 11.2 edition to make benefit of interactions among 42 bio-active components and anti-malarial targets (1LDG and 2ANL). Results: In the methanol extract of the Spathodea campanulata flowers, phytochemical research revealed the presence of terpenoids, glycosides, carbohydrates, steroids, and flavonoids. Forty-two phytoconstituents, notably methyl-beta-d-galactopyranoside, 4-hydroxybenzoic acid, and 1,2- ethanediol monobenzoate, were determined through GC-MS analysis. Docking analysis of 42 bioactive compounds demonstrated that 1,2-ethanediol mono benzoate, 4-hydroxy benzoic acid, and methyl.beta.-d-galactopyranoside had higher G-Scores with 1LDG and 2ANL. Conclusion: In this work, multiple phytoconstituents discovered in a methanol extract of the S. campanulata flower were determined. As a result of this research, four phytoconstituents from the flower extracts may be created as an exciting new therapy for malaria.

Revealing the microbial diversity and volatile flavor formation in finger citron kombucha by metagenomic and GC-MS analysis

Kombucha is a kind of health drink formed by the metabolism of Symbiotic Culture of Bacteria and Yeast (SCOBY) composed of yeast, acetic acid bacteria and lactic acid bacteria, which is popular among researchers and fond of consumers because of its antioxidant and hypoglycemic effects. In this study, the finger citron kombucha with different fermentation time (2, 4, 6, 8 day) were analyzed by headspace solid phase micro-extraction gas chromatography-mass spectrometry (HS-SPME-GC-MS) and metagenomic sequencing. The results showed that a total of 76 volatiles were identified, including 15 key volatiles, such as linalool, geraniol, α-terpinene, and limonene, which had a great influence on the flavor of kombucha. Metagenomic analysis showed that unclassified-g-Gluconobacter, Komagataeibacter saccharivorans, Gluconobacter-sp.-R71656 and other microorganisms were the dominant species in finger citron kombucha. Through the correlation heat map analysis of volatiles and microbial composition, it was found that Gluconobacter had a positive effect on the formation of most volatiles of kombucha. In addition, Novacetimonas hansenii, Brettanomyces bruxellensis and Wickerhamiella sorbophila were also closely related to the flavor formation of kombucha. This study provided a theoretical basis for finding the key aroma-producing microorganisms in the fermentation process of finger citron kombucha and the subsequent construction of SCOBY.

Gas Chromatography-Mass Spectrometry (GC-MS) Analysis of Scaphium Affine Seed Extract and Assessment of its Anti-Hemorrhoidal Efficacy.

Seeds of plant Scaphium Affine are traditionally used by the healers of "India" for the treatment of piles. The primary objective of the study was to assess the anti-hemorrhoidal potential of the ethanolic seed extract of Scaphium affine. After the soxhlet extraction method, the seed extract from Scaphium affine was first submitted to phytochemical standardization and then GC-MS analysis. Rats were given Croton oil and Jatropha oil to develop hemorrhoids, and Scaphium affine seed extract (ESA) was administered orally for 5 days and 3 days, respectively, at doses of 1000 and 500 mg/kg. The Rectoanal coefficient (RAC) was calculated as an inflammatory marker. The hemorrhoidal tissues were also subjected to cytokine profiling, biochemical estimation and histopathology. ESA demonstrated the presence of flavonoids, saponins, phytosterols, phenols, and tannins. GCMS analysis elucidated the presence of hexadecanoic acid 2 hydroxy -1,3 propane diyl ester,9 Octadecanoic acid ethyl ester, Cyclohexane 1,4 di methyl cis, Farnesol isomer,1, E-11, Z-13 octa decatriene, Stigmasterol, N-(5 ethyl -1,3,4-thiadiazol-yl) benzamide, N, N Dinitro 1,3,5,7 tetraza bicyclo 93,3,1) as major phytoconstituents. The results depicted more potent anti-hemorrhoidal activity of ESA at 1000 mg/kg, p.o., which was evident through a decrease in RAC. A significant decline in the levels of IL-1β, IL-6, and TNF-α expression was observed, along with the restoration of altered antioxidants and enzymes. Histopathological analysis confirmed the tissue recovery as it revealed minimal inflammation and decreased dilated blood vessels in treated animals. Based on the results it can be concluded that seeds of Scaphium affine showed significant anti-hemorrhoid agents which may be attributed to their anti-inflammatory and anti-oxidant potential due to the presence of certain phytoconstituents in it. The study also supports the traditional use of seeds of Scaphium affine for the first time in the treatment of hemorrhoids.

The Utilisation of Mushroom Leftovers, Oats, and Lactose-Free Milk Powder for the Development of Geriatric Formulation.

This study aims to focus on developing a food supplement for the geriatric population using disposal mushrooms, oats, and lactose-free milk powder. Lactose intolerance is most common in older adults, raising the demand for lactose-free foods. One of the major global challenges currently faced by humankind is food waste (FW). Most of the food that is produced for human consumption has not been utilized completely (1/3rd-1/2 unutilized), resulting in agricultural food waste. Mushrooms are highly valuable in terms of their nutritional value and medicinal properties; however, a significant percentage of mushroom leftovers are produced during mushroom production that do not meet retailers' standards (deformation of caps/stalks) and are left unattended. Oats are rich in dietary fibre beta-glucan (55% water soluble; 45% water insoluble). Lactose-free milk powder, oats, and dried mushroom leftover powder were blended in different ratios. It was observed that increasing the amount of mushroom leftover powder increases the protein content while diluting calories. The product with 15% mushroom powder and 30% oat powder showed the highest sensory scores and the lowest microbial count. The GCMS and FTIR analyses confirmed the presence of ergosterol and other functional groups. The results of the XRD analysis showed that the product with 15% mushroom powder and 30% oat powder had a less crystalline structure than the product with 5% mushroom powder and 40% oat powder and the product with 10% mushroom powder and 35% oat powder, resulting in more solubility. The ICP-OES analysis showed significant concentrations of calcium, potassium, magnesium, sodium, and zinc. The coliform count was nil for the products, and the bacterial count was below the limited range (3 × 102 cfu/g). The product with 15% mushroom powder and 30% oat powder showed the best results, so this developed product is recommended for older adults.

The control effect and mechanism of antioxidants on the flavor deterioration of Sichuan pepper essential oil during thermal processing

The impacts of varying heating temperature on the flavor of Sichuan pepper essential oil (SPEO) have been studied. The high temperature heating was found to accelerate the oxidation of SPEO and caused the deterioration of its flavor (odor and pungency taste). With the intervention of antioxidants including RE, AP, and TPP, both thermal oxidation stability and flavor stability of SPEO were enhanced. Addition of 1.5% TPP had the best control effect, which significantly improved the overall flavor of heated SPEO and made the overall flavor of SPEO heated at 100°C highly similar to that of original SPEO. According to the results of GC-MS and OAV analyses, the control effect of antioxidants on odor deterioration of SPEO was mainly through significantly inhibiting the decrease in content and OAV of both linalool and terpenes, and restricting the formation of some oxygenated compounds such as aldehydes. The results of HPLC analysis showed that the control effect of antioxidants on the thermal taste stability of SPEO was mainly dependent on blocking the chemical reactions of sanshools, especially hydroxy-α-sanshool.

Unlocking nature’s potential: anticancer potential of Helichrysum sanguineum (L.) Kostel on breast cancer cells and its chemical composition

ABSTRACT Helichrysum sanguineum (L.) Kostel (H. sanguineum), a member of the Asteraceae family, has been traditionally employed for various medicinal purposes owing to its rich phytochemical composition. This study investigates the anticancer properties of various extracts of H. sanguineum (ethanol, acetonitrile, hexane, and chloroform) against breast cancer cells, shedding light on its chemical constituents and their potential therapeutic effects. In vitro assays demonstrate the profound inhibitory effects of H. sanguineum extract on human fibroblast and breast cancer cells. Furthermore, we elucidate the underlying mechanisms of action, revealing its ability to induce apoptosis and cell cycle arrest in breast cancer cells. The cytotoxicity and apoptosis outcomes in breast cancer cells varied across different extracts, yet no adverse effects were observed on healthy cells at equivalent concentrations. Furthermore, all extracts initially promoted breast cancer cell proliferation, with the chloroform extract notably reducing cancer cell proliferation even at low concentrations. GC-MS analysis identifies the major chemical constituents of the extract, including flavonoids, terpenoids, and phenolic compounds, which likely contribute to its anticancer activity. Our findings highlight the potential of H. sanguineum extract as a natural agent for breast cancer treatment and the need for further exploration of its mechanisms and clinical applications.

Anthracene detoxification by Laccases from indigenous fungal strains Trichoderma lixii FLU1 and Talaromyces pinophilus FLU12.

The persistence and ubiquity of polycyclic aromatic hydrocarbons (PAHs) in the environment necessitate effective remediation strategies. Hence, this study investigated the potential of purified Laccases, TlFLU1L and TpFLU12L, from two indigenous fungi Trichoderma lixii FLU1 (TlFLU1) and Talaromyces pinophilus FLU12 (TpFLU12), respectively for the oxidation and detoxification of anthracene. Anthracene was degraded with vmax values of 3.51 ± 0.06mg/L/h and 3.44 ± 0.06mg/L/h, and Km values of 173.2 ± 0.06mg/L and 73.3 ± 0.07mg/L by TlFLU1L and TpFLU12L, respectively. The addition of a mediator compound 2,2-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) to the reaction system significantly increased the degradation of anthracene, with up to a 2.9-fold increase in vmax value and up to threefold decrease in Km values of TlFLU1L and TpFLU12L. The GC-MS analysis of the metabolites suggests that anthracene degradation follows one new pathway unique to the ABTS system-hydroxylation and carboxylation of C-1 and C-2 position of anthracene to form 3-hydroxy-2-naphthoic acid, before undergoing dioxygenation and side chain removal to form chromone which was later converted into benzoic acid and CO2. This pathway contrasts with the common dioxygenation route observed in the free Laccase system, which is observed in the second degradation pathways. Furthermore, toxicity tests using V. parahaemolyticus and HT-22 cells, respectively, demonstrated the non-toxic nature of Laccase-ABTS-mediated metabolites. Intriguingly, analysis of the expression level of Alzheimer's related genes in HT-22 cells exposed to degradation products revealed no induction of neurotoxicity unlike untreated cells. These findings propose a paradigm shift for bioremediation by highlighting the Laccase-ABTS system as a promising green technology due to its efficiency with the discovery of a potentially less harmful degradation pathway, and the production of non-toxic metabolites.

Green Synthesis of Silver Nanoparticles using Coriandrum sativum and Murraya koenigii Leaf Extract and its Thrombolytic Activity

Background: Plants have been used for ages in traditional medicine, and it is exciting to perceive how recent research has recognized the bioactive compounds liable for their beneficial effects. Green synthesis of metal nanoparticles is a hastily emergent research area in nanotechnology. This study describes the synthesis of silver nanoparticles (AgNPs) using Coriandrum sativum and Murraya koenigii leaf extract and its thrombolytic activity. Objective: The aim of the study was to determine the clot lysis activity of Coriandrum sativum and Murraya koenigii synthesized silver nanoparticles. Methods: Leaves of Coriandrum sativum and Murraya koenigii were collected. Methanolic extraction of the plant sample was done through a Soxhlet extractor. The methanolic extract obtained from both the leaves was subjected to GC-MS analysis. The synthesized NPs from leaf extracts were monitored for analysis, where the typical X-ray diffraction pattern and its diffraction peaks were identified. 3D image of the NPs was analysed by Atomic Force Microscopy. The surface charge of nanoparticles was identified by Zeta potential. The Clot lysis activity of Coriandrum sativum and Murraya koenigii synthesized silver nanoparticles were analysed by the modified Holmstorm method. Results: The thrombolytic property of the methanolic extract of plants Coriandrum sativum showed clot lysis activity at 2.5 mg/mL with 45.99% activity, and Murraya koenigii extract with 66.56% activity. The nanoparticles (Nps) from Coriandrum sativum showed clot lysis activity at 2.5 mg/mL with 58.29% activity, and NPs from Murraya koenigii with 54.04% activity. Coriandrum sativum in GC-MS exhibited 3 peaks, whereas Murraya koenigii extract showed five peaks with notable bioactive compounds. Conclusion: These NPs were further used for biomedical applications after being fixed by an organic encapsulation agent. The present research reveals the usefulness of Coriandrum sativum and Murraya koenigii for the environmentally friendly manufacture of silver nanoparticles.

Direct evidence of gas flushing oil in deep reservoirs: Insight from integrated fluid inclusion analyses

Gas flushing of oil has been proposed as an essential process for forming some condensate gas reservoirs based on laboratory experiments and modeling but such a process has rarely been documented in subsurface reservoirs. Here, we report a unique type of yellow-ringed oil inclusions (YROIs) discovered from a deep reservoir in the Kuqa Foreland Basin, Western China that recorded the gas flushing of oil process in the subsurface. The occurrence, composition, phase state and PVT conditions of YROIs during trapping were investigated using a suite of fluid inclusion analytical methods including fluid inclusion petrography, microthermometry, fluorescence spectroscopy, PVT modeling and molecular composition analysis.YROIs found in the reservoir are three-phase (solid–liquid-vapor) fluid inclusions at room temperature with solid rings of 2–3 μm thickness and estimated volume percentages varying between 5 % and 15 %. When heated the solid ring starts to melt at around 46 °C and homogenized with the liquid phase at or above their corresponding homogenization temperatures of coeval aqueous inclusions. YROIs have fluorescence spectral peaks between 530 nm and 550 nm and an elevated spectral shoulder around 650 nm when measured at room temperature; but most spectra show a distinct “blue shift” and an absence of the 650 nm shoulder when measured at their homogenization temperatures. Some YROIs with thick yellow rings show dual spectral peaks at 570 nm and 630 nm at room temperature and their spectral peaks do not change when remeasured at their homogenization temperatures. Molecular compositions derived from synchronous fluorescence spectra and GC-MS analysis suggest that the compositions of YROIs are rich in polyaromatic compounds. PVT modeling indicates that YROIs were trapped under high pressure conditions with a pressure exceeding 50 % of the corresponding hydrostatic pressure.YROIs are interpreted to have been trapped under an elevated temperature and overpressure condition (around 110 °C and 60 MPa) relating to an intensive (wet) gas flushing of an early-charged wax-rich oil. When light hydrocarbon components in the reservoir oil were partially removed by gas, the wax/resin components rich in polyaromatic hydrocarbon compounds may precipitate due to physio-chemical fractionation. YROIs were entrapped in subsurface from a heterogeneous hydrocarbon fluid containing variable amounts of wax/resin colloids, which subsequently coalesce to form solid rings adhering to the inner wall of oil inclusions at room temperature. The presence of yellow-ringed oil inclusions in a reservoir may be indicative of a rapid gas flushing of waxy oil under high pressure, and their minimum homogenization temperature may approximate their trapping temperature.

Molecular Docking and ADMET Profiling of Pimenta Dioica Bioactives: Targeting Carboxylesterase 1

ABSTRACT The study explored the chemical composition, antioxidant activity, and potential antihyperlipidemic effects of Allspice (Pimenta dioica) leaf essential oil. The oil yield from hydro-distillation was 1.61 ± 0.35% (v/w), with major compounds identified by GC-MS analysis as eugenol (72.06 ± 3.93%), β-pinene (9.29 ± 3.33%), chavicol (6.95 ± 0.6%), limonene (3.05 ± 0.71%), and 3-octenol (1.55 ± 1.07%). The oil’s antioxidant activity (426 ± 3.5 mg TE g−1) was attributed to polyphenols. It also reduced porcine pancreatic lipase activity, suggesting potential in managing dietary lipids. Molecular docking showed strong binding to CES1, with eugenol, limonene, β-pinene, and octenol outperforming the control (probucol). ADME-Tox predictions indicated favorable pharmacological profiles with controlled lipophilicity and toxicity.