Fractionation Of Extract Research Articles

Dichloromethane -methanol fraction of Mahonia nepalensis containing Berberine, Jatrorrhizine, and tetrahydroberberine as corrosion inhibitor for mild steel

A potentially superior alternative source of environmentally acceptable corrosion inhibitors for metallic materials is plant extracts. This study reports on the use of compounds separated from Mahonia nepalensis (MN) bark extract as an environmentally friendly corrosion inhibitor for mild steel (MS) in 1 M H2SO4. The organic layer was separated from MN bark extracts and then Berberine, Jatrorrhizine, and Tetrahydroberberine were identified and quantified by Liquid column mass spectroscopy (LC-MS) in dichloromethane (DCM) −Methanol fraction of Mahonia nepalensis. The DCM − Methanol fraction of extract was characterized by Ultra violet − visible spectroscopy (UV–Vis) and Fourier Transform Infrared (FTIR). The DCM-Methanol fractions in 1 M H2SO4 were applied to study corrosion inhibition of MS by potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). The results showed above 91 % inhibition efficiency (IE) for DCM-Methanol fraction containing 2.12 ppm berberine, jatrorrhizine, and tetrahydroberberine at room temperature indicating that it is an effective and cheap candidate for the corrosion prevention of MS in industry. The potentiodynamic polarization demonstrated a reduction in current density without affecting the reaction mechanism but reduced the hydrogen reduction indicated by suppression in cathodic current. Based on polarization curves and open circuit potential, it exhibited mixed inhibitory behavior. Similarly, EIS analysis revealed a drop in double-layer capacitance accompanied by an increase in charge transfer resistance. EIS and a scanning electron microscope (SEM) with energy dispersive X-ray spectroscopy (EDX) ascertain the adsorption of inhibitor molecules forming a protective layer on the MS surface.

The effect of Coix lachrymal L. seed extract on the expression of inflammation and fibrogenesis genes in human retinal pigment epithelial cells.

Proliferative vitreoretinopathy (PVR) is a vision-threatening condition associated with retinal-detachment (RD), primarily caused by fibrocellular scar membrane formation. This study investigates the therapeutic potential of adlay seed extract fractions in mitigating PVR-associated pathways, focusing on oxidative stress, proliferation, inflammation, and fibrogenesis in retinal pigment epithelial (RPE) cells. Adlay seed extract fractions (methanolic: MeOH and residual: Res) were obtained through solvent extraction and characterized for carbohydrate, protein, flavonoid content, and antioxidant activity. RPE cells were cultured, and their viability in response to adlay fractions was assessed using the MTT assay. Gene expression analysis of IL-1β, IL-6, LIF, TGF-β, Snail and α-SMA genes was conducted via real-time PCR after treatment with adlay fractions. The Res fraction exhibited higher levels of protein, carbohydrate, flavonoids, and phenols compared to the MeOH fraction, along with significantly enhanced antioxidant activity. Both fractions showed inhibitory effects on RPE cell viability, with the Res fraction demonstrating a more pronounced impact. Gene expression analysis revealed a significant decrease in IL-6 and TGF-β expression with the MeOH fraction treatment, while the Res fraction led to decreased expression of IL-6, LIF, TGF-β, Snail and α-SMA, indicating a more comprehensive modulation of PVR-associated pathways. This study highlights the potential therapeutic benefits of adlay seed extract fractions in mitigating PVR-associated pathways in RPE cells. The Res fraction, particularly rich in bioactive compounds and exhibiting potent antioxidant activity, shows promise in attenuating oxidative stress, proliferation, inflammation, and fibrogenesis, critical processes in PVR development. These findings underscore the potential of adlay seed extracts as a novel therapeutic strategy for PVR warranting further investigation and clinical validation.

Evaluation of Sedative activity of Cannabis Sativa in mice

Background: Cannabis sativa Linn. (Family: Cannabaceae) is commonly cultivated in Bangladesh in moist areas such as riverbanks, lakes, canals, and roadsides. The leaves of this plant are traditionally used to treat insomnia, depression, and neurodegenerative diseases. Objective: The study's objective is to investigate the sedative effects and phytochemical composition of the Cannabis sativa species in Nigeria. Methods: The elevated plus maze was used to assess the sedative effect of various fractions of aqueous methanol extracts of Cannabis sativa at a dosage of 100 mg/kg in mice. Comparisons were made between the sedative action of the extract and diazepam, which was used as the positive control. Additionally, acute toxicity was also evaluated during the assessment. Results: During the elevated plus-maze test, various parameters such as the number of entries in open arms and the number of entries in closed arms were recorded. The administration of different fractions of aqueous methanol extracts of Cannabis sativa resulted in a significant increase (p < 0.001) in the time spent in and the number of entries into open arms compared to the control group. Conclusion: The findings suggest that various concentrations of water-methanol extracts from Cannabis sativa exhibit sedative effects that are superior to those of the control (diazepam), supporting the use of this plant in traditional medicine. Further research should be conducted to investigate the active components of Cannabis sativa and understand the mechanism of its effects before proceeding to clinical trials.

In vivo biological screening of extract and bioactive compound from Ficus benghalensis L. and their in silico molecular docking analysis.

Ficus benghalensis has been used by local health care practitioners to treat pain, inflammation, rheumatism, and other health issues. In this study, the crude extract and diverse fractions, along with the isolated compound of F. benghalensis were examined for their roles as muscle relaxants, analgesics, and sedatives. The extract and isolated compound 1 were screened for muscle-relaxant, analgesic, and sedative actions. The acetic acid-mediated writhing model was utilized for analgesic assessment, the muscle relaxant potential was quantified through traction and inclined plan tests, and the open field test was applied for sedative effects. The extract/fractions (25, 50, and 100 mg/kg) and isolated compounds (2.5, 5, 10, and 20 mg/kg) were tested at various doses. A profound (p< 0.001) reduce in the acetic acid-mediated writhing model was observed against carpachromene (64.44%), followed by ethyl acetate (60.67%) and methanol (58.42%) fractions. A marked (p< 0.001) muscle relaxant activity was noticed against the isolated compound (71.09%), followed by ethyl acetate (66.98%) and methanol (67.10%) fractions. Regarding the sedative effect, a significant action was noted against the isolated compound (71.09%), followed by ethyl acetate (66.98%) and methanol (67.10%) fractions. Furthermore, the binding modes of the isolated compounds were explored using molecular docking. The molecular docking study revealed that the isolated compound possessed good binding affinity for COX2 and GABA. Our isolated compound may possess inhibitory activity against COX2 and GABA receptors. The extract and isolated compounds of Ficus benghalensis can be used as analgesics, muscle relaxants, and sedatives. However, detailed molecular and functional analyses are essential to ascertain their function as muscle relaxants, analgesics, and sedatives.

Wound-Healing Activity of Solvent Fractions and Antiinflammatory Activity of Crude Extract and Solvent Fractions of Acokanthera schimperi Schweinf (Apocynaceae) Leaves in Mice Model

BackgroundIn Ethiopia, Acokanthera schimperi is frequently used to treat wounds and other conditions. Nothing has been published to date on the anti-inflammatory properties of A. schimperi leaves or the wound-healing effects of solvent fractions, despite a report on the crude extract's ability to heal wounds being available in the literature. PurposeTherefore, this experiment has been initiated to look into the solvent fractions' ability to heal wounds and the anti-inflammatory properties of the A. schimperi leaf 80% methanol extract and its fractions in mice. Study designThe experimental study design was conducted to evaluate wound healing and the anti-inflammatory properties of the A. schimperi leaf 80% methanol extract and its fractions in mice. MethodsThe plant's leaf crude extract was fractionated using ethyl acetate, chloroform, and distilled water. The resulting fractions were then combined with a simple ointment base to make an ointment at 5% and 10% w/w. Next, using excision and incision wound models, the ointments' ability to promote wound healing was assessed. The excision model was utilised to estimate wound contraction and epithelization time, whereas the incision model was utilised to measure tensile strength. By dissolving 1% carrageenan in 0.9% saline (w/v) and giving oral dosages of the crude extract and solvent fractions (100, 200, and 400 mg/kg), the anti-inflammatory efficacy of the leaves was assessed concurrently with a carrageenan-induced hind paw edema model. ResultsSignificant wound healing activity was seen in both models in wounds treated with 5% and 10% (w/w) solvent fraction ointment, as shown by higher tissue breaking strength (with 51.38% maximum effect by 10% (w/w) ethyl acetate fraction ointment), shorter epithelization times (within 15.92 days by ethyl acetate fraction ointment 10%), and increased wound contraction (99.40% by ethyl acetate fraction ointment 10%). The extract (hydromethanolic) and solvent fractions also showed notable dose-related decreases in inflammation. ConclusionThe study's findings supported A. schimperi's traditional use as a wound healing agent by showing that the solvent fractions of the plant's leaves promoted wound healing, at least in part, through their anti-inflammatory effect.

Anti-diabetic and anti-inflammatory activities of Marrubiin isolated from Marrubium vulgare: Indications of its interaction with PPAR γ

BackgroundThe aerial parts of Marrubium vulgare L. were used for many ailments like catarrh to diabetes in many parts of Latin America and Asia. PurposeIdentifying the active principle responsible for anti-diabetic activity of methanol extract of M. vulgare leaves and to predict the possible targets. Study designAll the activity investigations were conducted simultaneously for the extract, fraction, and isolated compounds to decipher the activity profile in comparison to each other which allowed the identification of an active principle followed by use of in silico methods to identify the possible target/s. MethodsThe aerial parts of M. vulgare were extracted using methanol. A chloroform fraction was prepared. Marrubiin and marrubinone B were isolated from this fraction. The anti-hyperglycemic, hypoglycemic, and postprandial blood glucose lowering activities were investigated using streptozotocin-induced diabetic and non-diabetic rat models. Pro-inflammatory cytokine inhibitory potential was investigated using LPS induced acute-inflammatory mouse model and RAW 264.7 cells. Further, antioxidant activity was investigated using a DPPH assay. The in silico analysis, using the Swiss-target prediction tool, was carried out to predict the probable targets of the isolated molecules. ResultsMarrubiin exhibited anti-hyperglycemic effect in diabetic rats followed by hypoglycemia, and postprandial blood glucose lowering in non-diabetic rats. Methanol extract (Mv extract) and chloroform fraction (Mv fraction) showed anti-hyperglycemic and hypoglycemic effects. Moderate inhibition of IL-1β, TNF-α, and IL-6 was observed for marrubiin, marrubinone B, Mv extract, and Mv fraction, in vitro and in vivo. Neither marrubiin nor marrubinone B could quench the DPPH free radicals while Mv extract and Mv fraction could show 80 % suppression. In silico analysis has predicted that marrubiin can interact with PPAR γ but not marrubinone B. ConclusionsMarrubiin and marrubinone B were responsible for the anti-inflammatory effect of Mv extract and Mv fraction while not contributing to the antioxidant effect. Marrubiin was found to be responsible for the anti-diabetic activity of Mv extract. The predicted interaction propensity of marrubiin with PPAR γ could explain its dual activity observed in the experimental setup.

Phytochemical Analysis, Antioxidant Activity of Wild Medicinal Plants of Himalayan Range

Plants that are indigenous to the Himalayas have been exploited for their therapeutic properties for over 6,500 years. Using their deep knowledge of the local flora and fauna, traditional healers in the region are able to treat a wide variety of maladies with herbal treatments. People who live in rural areas of the Himalayas rely on wild medicinal plants for their health, and we need to do everything in our power to ensure that these plants continue to thrive in the harsh desert climate of the Himalayas. Raw materials that are obtained from wild plants are in high demand all around the world, particularly among pharmaceutical companies, ethnomedics, and practitioners of traditional medicine as well as other medical practitioners. India has been a top exporter of raw herbal medications all over the world. This is mostly due to the number of medicinal plants that can be found in the Himalayas. The aim of this study was to determine the Phytochemical analysis and antioxidant activity of various parts of 20 selected wild medicinal plants, found in the Himalayan regions in India, China, Nepal, Bhutan and Pakistan including Swertia bimaculate, Ficus neriifolia, Rubus treutleri, Periploca calophylla, G. depressa, Buddleja napaulensis, Habenaria edgeworthii, Pyracantha crenulate, Roscoea procera, Allium rubellum, Berberis chitria, Capsella bursa-pastoris, Artemisia maritima, C. glanduliferum, C. distans, Juniperus macropoda, Origanum vulgare, Valeriana jatamansi, Polygonatum verticillatum, Meconopsis aculeate and Fragaria nubicolais. There were several different parts of the species that were examined to determine their total polyphenol, flavonoid, alkaloid, saponin, and tannin concentrations. One fraction of the plant extracts was found to contain a higher quantity of phytochemicals when compared to the other portions. Through the utilisation of the DPPH and FRAP model systems, the antioxidant capacity of a number of different components was assessed. The high-performance liquid chromatography (HPLC) technique can be combined with the DPPH and/or ABTS tests in order to rapidly screen extracts for the presence of active chemicals.

Determination of Total Flavonoid Content from Extract and Fractions of Mangrove Leaves (Rhizopora mucronata)

Indonesia is an archipelagic country with a very wide coastal area. Lombok Island has a coastal area with quite extensive mangrove forest areas. Rhizopora mucronata was the most dominant species found in the region. The Rhizopora mucronata species was a plant from the Rhizoporaceae family reported to have antibacterial, antifungal, and antioxidant activity. These biological activities were caused by the presence of secondary metabolite compounds in R. mucronata, one of which is flavonoids. Research regarding the flavonoid content of R. mucronata leaves has not been explored. Therefore, the study aimed to determine the total flavonoid content in extracts and fractions of R. mucronata leaves using the spectrophotometric UV-Vis method. R. mucronata mangrove leaves simplicia were extracted using the sonication method using 96% ethanol solvent, then fractionated using the liquid-liquid extraction method with n-hexane, ethyl acetate, and water. The percentage yield of 96% ethanol extract, water fraction, ethyl acetate fraction, and n-hexane fraction respectively were 42.33%; 43.147%; 40.49%; 9.74%; and 32.49%. The TLC test showed the presence of flavonoid compounds detected in the extract and fractions which were marked with blue spots. The total flavonoid contents in the 96% ethanol extract, water fraction, ethyl acetate fraction, and n-hexane fraction were respectively (12,980; 14,160; 23,880; and 25,350) mg Quercetin equivalent/gram sample (mg QE/ g). The total flavonoid content of the extract and fractions of R. mucronata leaves were analyzed using the One-way ANOVA test method. The total flavonoid content in the n-hexane fraction and ethyl acetate fraction was significantly higher than the 96% ethanol extract and water fraction. The total flavonoid content of R. mucronata leaves was relatively high, which contributes to several of its biological activities.

Evaluation of antimicrobial activity of plant extracts and column fractions of hexane extract against Mycobacterium kansaii

The aim of this study is to assess the antibacterial efficacy of aerial parts of the Ageratum conyzoides plant extracts and column fractions against Mycobacterium kansaii. The antimicrobial experiments were performed using five doses (0.1 µg/ml, 1 µg/ml, 10 µg/ml, 100 µg/ml, 1000 µg/ml) of plant extracts and column fractions. The results showed notable inhibitory effects on Mycobacterium kansaii. The results indicated that the extract of A. conyzoides exhibited action against all the tested bacterial isolates, with the level of activity varying depending on the concentration. The hexane extract exhibited antibacterial activity, with mean zones of inhibition measuring 97.88±9.46 and 27.1±3.33, while the ethanol extract showed a mean zone of inhibition of 100.6±3.42 and 36.77±1.74 against M.kansaii, respectively. Nevertheless, the hexane extract's three column fractions exhibited average inhibition zones of 98.60±1.0 and 23.11±4.35, 90.02±10.22 and 21.94±6.77, 99.32±3.04 and 17.23±5.26 for the third, fourth, and fifth (last sample) respectively. The findings of this study provide evidence for the conventional utilization of the Ageratum plant and emphasize the necessity for further comprehensive research to explore potential alternatives to current antibacterial medications.

Myeloprotective potential of leaves extract fractions of Cnidoscolus aconitifolius in myelo suppression

Chemotherapy has been associated with myelosuppression. Myeloprotection is the main remedy to myelosuppression. Nature has been endowed with natural molecules rich in therapeutic components and one of such nature is Cnidoscolus aconitifolius (CA) which has been reported to be rich in antioxidants. The aim of the study was to investigate myelo-protective potential of CA in myelo-suppressed animal model. Albino rats (n = 32) were divided into 8 groups of 4 rats each labelled A-H out of which 7 groups (B-H) were induced intraperitoneally for myelosuppression with cyclophosphamide (CP) and only 6 groups (C-H) were treated with CA extracts for four weeks. Group A served as normal control, groups B-H was induced for myelosuppression with cyclophosphamide. Group B served as myelo-suppressed control, groups C, D and E, received 100mg/kg body weight (bw) methanol fractions of CA while groups F, G and H received 200mg/kg body weight methanol fractions of CA. Two milliliters of blood were collected into ethylenediaminetetraacetic acid containers for total white blood cell count and absolute granulocyte count on days 3, 12 and 21 using mindray auto analyser BC-360. On day 30, bone marrow (BM) was harvested from one rat per group for BM examination and cellularity. Following administration of (CP), myelosuppression set in as observed in significant decreased (P &lt; 0.05) in total white blood cell (TWBC) count and absolute granulocyte count. Extract fractions of CA caused significant increase (P &lt; 0.05) in TWBC count and absolute granulocyte count in all the treated groups on days 12 and 21 compared with baseline. Bone marrow cellularity of all the treated groups revealed normal myeloid erythroid ratio indicating normal marrow cellularity. The findings in this study suggested myelo-protection by Cnidoscolus aconitifolius against cyclophosphamide induced myelosuppression.

In vivo evaluation of anti-diarrheal activity of hydroalcoholic extract and solvent fractions of the leaf of Leucas deflexa Hook.f (Lamiaceae) in rodents

The emergence of antibiotic-resistant bacteria has intensified the search for novel antidiarrheal drug. Plant-derived extracts offer promising alternatives due to their ability to modulate gut motility and enhance water absorption. The leaves of Leucas deflexa Hook.f., a plant native to Ethiopia, have been traditionally utilized in the treatment of diarrheal diseases. Nonetheless, its traditional application has yet to be scientifically confirmed. Hence, the aim of the present study was to evaluate antidiarrheal activity of the crude extract and fractions of the leaf of Leucas deflexa Hook.f (Lamiaceae). Healthy Swiss albino mice were randomly divided into five groups per experimental model: castor oil-induced diarrhea, gastrointestinal motility, and anti-enteropooling assays. The control group received distilled water (10ml/kg), while the positive control was treated with loperamide (3mg/kg). The remaining groups were administered various dosages (LD100, LD200, and LD400 mg/kg) of a hydroalcoholic extract or its fractions from Leucas deflexa Hook.f. The crude extract and chloroform fraction substantially (P<0.001) delayed the onset of diarrhea, reduced fecal frequency, and decreased total fecal weight at all administered doses compared to the negative control. The butanol and aqueous fractions exhibited a substantial antidiarrheal effect at doses of 200mg/kg and 400mg/kg, respectively. All treatments, including the crude extract, chloroform, butanol, and aqueous fractions, substantially (P<0.001) reduced the volume and weight of intestinal contents at various doses. Additionally, the chloroform, aqueous fraction, and crude extract at doses of 100, 200, and 400mg/kg substantially inhibited gastrointestinal motility compared to the negative control. The results of this study corroborate the traditional use of Leucas deflexa leaves in the treatment of diarrhea. These findings give a scientific justification for further exploration of the underlying mechanisms and potential therapeutic applications of this plant extract.

Phytochemical and volatile components evaluation of antimicrobial root extracts of &lt;i&gt;Dichrostachys cinerea&lt;/i&gt; (sickle bush)(&lt;i&gt;Fabaceae&lt;/i&gt;) (L) Wight &amp; Arn

The crude ethanolic extract of the root of Dichrostachys cinerea (Fabaceae) was screened for phytochemicals and antimicrobial activity against Staphylococcus aureus, Escherichia coli, Pseudomonas aureginosa, Salmonella typhi, and Candida albicans using agar-well diffusion method. The phytochemical screening of the root extract results showed the presence of alkaloids, flavonoids, essential oils, phenols, terpenes, tannins, unsaturated sterols, and saponins. However, coumarins, and anthocyanins were absent. The crude extract was subjected to column chromatographic fractionation to give nine fractions of which two, DCR1 and DCR2, were subjected to gas chromatography-mass spectrometry (GC-MS) analysis. The crude extract and column chromatographic fractions DCR1 and DCR2 gave MIC of 1 mg/mL against Staphylococcus aureus, but were not active against the other test organisms. The gas chromatography-mass spectrometry analysis of the antibacterial fractions, DCR1 and DCR2, based on standard MS library data revealed the presence of caryophellene, phthalates, a phenol and fatty acids and their ester derivatives. These phytoconstituents could account for the biological properties of the extracts of the plant. The results of this work therefore support its use in ethno-medicinal preparations, particularly against infections.

In Vitro Antibacterial Activity of Adiantum capillus Veneris Extraction with Methanol, Chloroform, and Ether Solvents against Methicillin-resistant Staphylococcus aureus.

The increasing problem of multi-drug resistant (MDR) pathogens is a worldwide concern, especially in the pharmaceutical industry. At the same time, medicinal plants have renewed interest because of their wide variety of bioactive phytochemicals, which could be used to develop new antimicrobial drugs. This renewed interest is partly due to the growing resistance to traditional drugs and their associated side effects. The objective of this study is to assess the antimicrobial properties of the total extract and various fractions of Adiantum capillus veneris against Methicillin-resistant Staphylococcus aureus (MRSA). The aerial parts of Adiantum capillus veneris were subjected to extraction using methanol, chloroform, and ether, and the resulting extracts were tested for their antimicrobial activity against MRSA. Additionally, essential oil was obtained from the aerial parts using a Clevenger apparatus and boiling water. Furthermore, Gas Chromatography-Mass Spectrometry (GC/MS) was utilized to analyze the phytochemicals isolated from the extracts of Adiantum capillus veneris. The essential oil was obtained through distillation and then analyzed using GC/MS. The antimicrobial activity was evaluated using the agar diffusion method. GC/MS analysis revealed that the composition was primarily phytol (59.9%), constituting 99.3% of phyto-constituents. However, both the total extract and the individual fractions exhibited no inhibitory effects against MRSA strains.

Brine shrimp lethality and antioxidant property of &lt;i&gt;Lagenaria breviflora&lt;/i&gt; (Benth.) Roberty fruit crude extract and fractions

Background: Oxidative injury plays a pivotal impact in the development of human diseases, and it is a major component of the pathophysiology of several inflammation-linked human medical disorders. Objective: The focus of this study was to evaluate the cytotoxicity and antioxidant potential of the fruit of Lagenaria breviflora (Benth.) Roberty (LB). Methods: The antioxidant capacity of L. breviflora's crude and solvent fractions was assessed using standard techniques by measuring the total phenolic content, total flavonoid content, and DPPH radical scavenging activity. The data we0re analyzed using One-way ANOVA, and Dunnett's Multiple Comparison was used to establish the threshold. Results: The total flavonoid contents of fruit methanol extract, LB hexane, chloroform, and ethyl acetate fractions were 32.00 ± 0.94, 224.32 ±0.05, 224.06 ±0.14, and 2615.67 ± 13.20 mg gallic acid equivalent/g of extract, respectively. In contrast, the total phenolic contents were 5218.83 ± 3.18, 2615.67 ± 13.20, and 4553.00 ± 24.27 mg gallic acid equivalent/g of extract, respectively. The crude extract of LB, hexane fraction, chloroform, and ethyl acetate fraction displayed IC50 values of 242.57 ± 8.90, 262.91 ± 6.49, 96.17 ± 2.74, and 221.45 ± 0.83 μg/mL, respectively, for their ability to scavenge DPPH radicals. Ascorbic acid and rutin had IC50 values of 2.76 ± 0.01 and 20.6 ± 9.26 μg/mL, respectively. Conclusions: Fruit from L. breviflora (LB) exhibited strong antioxidant potential, which may have resulted from the fruit's phenolic and flavonoid content. This demonstrates the reason this herb is used in traditional medicine. Keywords: Oxidative stress, brine shrimp lethality assay, total phenolic contents, total flavonoid contents, DPPH, Lagenaria breviflora fruit.

Antioxidant and Anti-Inflammatory Effects of Nettle Polyphenolic Extract: Impact on Human Colon Cells and Cytotoxicity Against Colorectal Adenocarcinoma.

Urtica dioica L. is one of the most widely utilized medicinal plants commonly applied in the form of tea, juice, and dietary supplements. This study aimed to assess the effect of the U. dioica ethanol-water extract (UdE) and polyphenolic fraction isolated from the extract (UdF) on normal human colon epithelial cells and to evaluate their protective activity against induced oxidative stress. The cytotoxic potential against human colorectal adenocarcinoma (HT29) and the anti-inflammatory effects were also investigated. UPLC-MS-DAD analysis revealed that both extracts were abundant in caffeic acid derivatives, specifically chlorogenic and caffeoylmalic acids, and therefore, they showed significant protective and ROS scavenging effects in normal human colon epithelial cells. Moreover, they had no negative impact on cell viability and morphology in normal cells and the extracts, particularly UdF, moderately suppressed adenocarcinoma cells. Furthermore, UdF significantly decreased IL-1β levels in HT29 cells. Our research indicates that U. dioica may provide significant health advantages because of its antioxidant and anti-inflammatory effects.

Exploring the anticancer potential of Lasia spinosa rhizomes: insights from molecular docking and DFT investigations on chlorogenic acid and beyond

Lasia spinosa (L.) Thwaites rhizomes (LSR), historically utilised in traditional medicine for various health sufferings, including cancer, represent an intriguing yet underexplored reservoir of bioactive constituents. Our study focused on exploring the anticancer potential of LSR and its phytoconstituents. The methanol extract of LSR exhibited significant cytotoxicity against various cancer cell lines compared to other extracts. The fractionation of methanol extract resulted in the isolation of chlorogenic acid (CA), oleanolic acid, β-amyrin, and lyonoresinol. Molecular docking analysis of these isolated compounds targeted at the active sites of CDK-2, VEGFR-2, and ToP-2A enzymes revealed the superior docking score of CA compared to the other constituents. Additionally, density functional theory studies indicated the strong electrophilic nature of CA and its potential for robust enzyme binding interactions. Subsequent MTT assays focusing on CA exhibited significant activity against all tested cell lines, with IC50 values ranging from 21.56 to 72.60 μg/ml, comparable to quercetin.

Comparative Study of the Chemical Characterisation of Bioactive Compounds in Different Fractions of Ethanol Extract of Amaranthus Spinosus Leaves

In the evolution of pharmaceutical research, and to discover novel drugs, as well as therapeutic agents the exploration of plant-derived secondary metabolites offers a promising avenue. The current investigation has identified several phytochemicals in the various fractions of the sample being studied. Comparative study on the fractions showed certain phytocompounds were soluble in the solvents of fractionation. Compounds such as n-Hexadecenoic acid, Phthalic anhydride, Dodecanoic acid had affinity for both solvents, however, in varying concentrations as they were more abundant in the n-Hexane fraction. The result of the GCMS showed the presence of 12 compounds in the n-Hexane fraction, with the most abundant being cis-Vaccenic acid (40.39 %), n-Hexadecanoic acid (13.21 %), 9,12-Octadecadienoic acid (Z, Z)- (11.52 %), Octadecanoic acid (10.33 %), and Linoelaidic acid (9.84 %), which are reported to exhibit various biological activities. The FTIR analysis of this fraction further revealed functional groups such as Alcohol, Carboxylic acid, Alkene, Alkane, Aldehyde, Carbon dioxide, Nitrile, Allene, conjugated alkene, phenol, and Alkyl &amp; Aryl Halides. GC-MS result of chloroform fraction further revealed the presence of 13 phytochemical compounds, of which the abundant phytochemical compounds are Linoelaidic acid (32.99 %), Z,Z-10,12-Hexadecadien-1-ol acetate (17.12 %), Nonanoic acid (14.81 %), and Cyclohexene, 4-pentyl-1-(4-propylcyclohexyl)- (12.08 %), while the FT-IR result showed the presence of sixteen (16) peaks, with functional groups such as Alcohols, phenols, thiol, thiocyanate, and δ-lactone. This study therefore infers that the pharmacological potential of the plant may be linked to the presence of the bioactive compounds in it as revealed by this study, however, recommended further study to identify the pharmacological activity of the other compounds with unknown activities, explore more pharmacological activities of the known compounds to solidify the claims on them further, and further carry out toxicity studies on the compounds to ascertain their safety.

Anti-Aging Activities and LC-MS Analysis of Chrysophyllum cainito Leaves Extract

Star apple (Chrysophyllum cainito L.), or Apple-nam in Thai, is a medium-sized tree in the Sapotaceae family. It is native to Middle America and distributed in Thailand and Southeast Asia. It has antioxidation, anti-inflammatory and anti-diabetic properties. The active compounds in star apples are flavonoids. This research aimed to study the biological activities and chemical constituents of crude extract and active fractions from the leaves of star apples. The leaf powder was defatted with dichloromethane and further extracted with ethanol using ultrasound-assisted extraction. The ethanol extract was separated by quick column chromatography given 7 fractions (CCE1-CCE7). The total phenolic content and antioxidant activity of the extract and chromatographic fractions were determined. The active fractions were further studied for tyrosinase inhibition, collagenase inhibition and cell proliferation properties. The result showed that the highest total phenolic content was observed in ethanol extract. The high polar fraction, CCE6, displayed the highest antioxidation activity with radical scavenging of 0.34 ± 0.01 mg AAE/mL in the DPPH assay and a FRAP value of 1.36 ± 0.01 mg AAE/mL in the FRAP assay. The CCE6 also exhibited the highest anti-tyrosinase and anti-collagenase activities with a percentage of 67.14 ± 1.34 and 70.32 ± 2.88, respectively and showed the best activity in cell proliferation with a percentage of 24.68 ± 2.94. The analysis of the components using the negative ionization LC-MS technique revealed that gallic acid and quercetin-3-galactoside are the major constituents in the ethanol extract. While the fraction CCE6 showed glucosyl (2E,6E,10x)-10,11-dihydroxy-2,6-farnesadienoate and p-mentha-1,3,5,8-tetraene as the predominant compounds. HIGHLIGHTS The ethanol extract was prepared using ultrasound-assisted extraction. The first report of tyrosinase and collagenase inhibition, as well as cell proliferation properties, of the cainito leaves extract and chromatographic fractions. The major components of the ethanol extract of cainito leaves in Thailand and its active fraction by LC-MS technique were reported for the first time. GRAPHICAL ABSTRACT

Identification of an active fraction of Kangfuxin in the treatment of periodontitis in a rat model.

Periodontitis is a serious gum infection that disrupts the soft tissue around teeth. This study aimed to identify the most effective fraction of the Chinese medicine Kangfuxin for periodontitis treatment in a rat model. Kangfuxin solution was subjected to sequential extraction using chloroform, ethyl acetate, n-butanol, and water. The extracts were evaporated, dissolved in DMSO, diluted in water, and administered to rats via gavage (0.5 mL/day) for 2 weeks. The n-butanol extract was further fractionated using macroporous resin chromatography with 10%, 30%, 50%, 70%, and 90% ethanol elution. Levels of inflammatory cytokines IL-6, IL-1β, and TNF-α in periodontitis samples were examined by ELISA. Leukocyte infiltration in the cementum was analysed by haematoxylin and eosin (H&E) staining. The n-butanol extract showed the best anti-inflammatory effect, reducing IL-6, IL-1β, and TNF-α levels in periodontitis samples and alleviating tissue damage and leukocyte infiltration in the cementum. Further fractionation revealed that the 50% ethanol fraction of the n-butanol extract had the most potent action in attenuating inflammation. This fraction suppressed the activation of the PI3K-AKT-mTOR signalling pathway in periodontitis samples. Application of a PI3K activator counteracted the anti-inflammatory effect of the 50% ethanol fraction. We identified a potent anti-inflammatory fraction (50% ethanol fraction of the n-butanol extract) of Kangfuxin for periodontitis treatment. This fraction suppressed the activity of the PI3K-AKT-mTOR signalling pathway in periodontitis samples. Further research is needed to isolate and characterise the specific bioactive compounds within this fraction.

Chemical constituents and antimicrobial activity of the aerial part of Solanum betaceum Cav. (Solanaceae)

A new saponin namely diosgeninoside (25 R-spirost-5-en-3-O-[β-D-glucopyranosyl (1→2) - β-D-glucuronic acid]) and a new fatty acid betacic acid: (Z)-8(S*),9(S*),10(R*)-trihydroxy-11-octadecenoic acid together with six known compounds: N-trans-coumaroyl tyramine, ergosta-7,22-dien-3β,5α,6β-triol, β-sitosterol, and β-sitosterol-3-O-β-D-glucopyranoside, L-threitol and soya-cerebroside I were isolated from the methanolic extract of Solanum betaceum. The structures were elucidated by interpretation of their 1D and 2D NMR spectra and spectrometric data. The methanolic extract, the EtOAc and n-BuOH fractions, and several isolated compounds were tested for antibacterial activity against four bacteria (Staphylococcus aureus; Staphylococcus epidermidis; Escherichia coli; and Pseudomonas aeruginosa). The methanolic extract and the EtOAc fraction showed moderate activity against Staphylococcus aureus and Pseudomonas aeruginosa with MIC value of 128 µg/mL. Compound 1 showed moderate activity against Staphylococcus aureus with MIC value of 64 µg/mL.