Fractionation Of Leaf Extract Research Articles

Effect of Justicia insularis Leaf Extract and Fractions on Oxidative Stress Markers, Liver Function Parameters and Liver Histology of Plasmodium berghei -Infected Mice

Justicia insularis (Family-Acanthaceae) is used in Ibibio ethnomedicine to treat malaria. The leaf extract and fractions of J. insularis were investigated for antioxidative stress and hepatoprotective activities in Plasmodium berghei-infected mice. The leaf extract (100-300 mg/kg, p.o.) exerted significant (p<0.05) antimalarial activity against P. berghei infection in curative test with ethyl acetate fraction demonstrating the highest activity. The extract/fractions treatment caused significant (p<0.05) reductions in liver enzymes (ALT, AST and ALP), total and conjugated bilirubin of the treated infected mice and also decreased significantly (p<0.05) total protein and albumin levels of the treated mice relative to control. The leaf extract and fractions further improved significantly (p<0.05) the levels of oxidative stress markers enzymes and molecules (CAT, GPx, GST, SOD) of the treated infected mice with no significant (p>0.05) effect on GSH. The MDA levels in the livers of the treated infected mice were significantly (p<0.05) reduced relative to control. Histology of liver sections revealed absence or significant reductions in pathological features in infected mice treated with leaf extract (100 mg/kg), DCM and ethyl acetate fractions compared to untreated infected mice. These results suggest that the leaf extract/fractions of Justicia insularis possess antioxidative stress and hepatoprotective potentials, which is an added advantage to its antimalarial property.

Antiplasmodial activities of n-hexane and water fractions of Dennettia tripetala leaf extract in Wistar rats

Many people die from malaria, a global health crisis. Most global malaria cases and deaths occur in sub-Saharan Africa. The rising resistance of Plasmodium spp. to antimalarial medications is hindering efforts to eradicate the illness. This study tested Dennettia tripetala leaf extract, N-hexane, and water fractions for antimalarial activity in rats. We used standard methods to screen Dennettia tripetala solvent (N-hexane and water) for phytochemical components. We tested the antimalarial potential of rats using Peters' 4-day suppressive, Rane's curative, and prophylactic tests. After conducting an exhaustive investigation, it was discovered that both fractions contained varying amounts of flavonoids, alkaloids, terpenoids, and saponins. There was a significant amount of antimalarial activity demonstrated by both fractions across all test models (P<0.05). Compared to the water fraction, Dennettia tripetala's n-hexane fraction was highly chemosuppressive and curative. Dennettia tripetala n-hexane has chemoprophylactic, curative, and chemosuppressive effects. The curative effect was 62.3% to 72.4%, and the chemosuppressive effect was 51.2% to 88.5%. Chemoprophylactic activity was 32.1%–61.2%. At 250–1500 mg/kg, Combretum nigricans butanol suppressed 40.3%, 54.1%, and 69.1%, respectively. Therapeutic effects were 26.2%, 36.9%, and 34.5%, while chemoprophylaxis was 48.4%, 70.0%, and 87.4%. Both Dennettia tripetala solvent fractions have antimalarial activity, suggesting they may be effective in different malaria therapy stages.

Assessment of Piper longum L. (Piperaceae) leaves toxicity on the adults of Tribolium castaneum (Herbst, 1797) (Coleoptera: Tenebrionidae)

BackgroundNumerous insect pests attack stored grains causing both qualitative and quantitative losses. The most damaging pest that infests dry stored produce is the red flour beetle, Tribolium castaneum, a secondary pest of stored goods. This pest, especially in its adult stage, exhibits resistance to chemical insecticides, thereby rendering the traditional pesticides ineffective in controlling it. Phyto-derivatives, which are strong insecticides and also ecologically benign, have gained interest as non-chemical solutions for controlling this pest. Hence, the objective of this study was to investigate the potential of Piper longum leaf extract insecticidal action as an environmentally benign insecticide for the first time against the adults of T. castaneum. In this study, P. longum leaf ethanol extract was tested against the adults of T. castaneum by petri dish bioassay method. Ad hoc studies to verify significant mortality for the initial confirmation of adulticidal activity were conducted for 24 h at different dosages of 62.5, 125, 250, 500 and 1000 mg/L of P. longum leaf ethanol extract. Thereafter, dosages set at 10, 20, 30 and 40 mg/L for the fractions of P. longum leaf ethanol extract were conducted. Prior to this, the leaf extract of this plant was subjected to column chromatography for fractionation. The fractions tested for adulticidal activity were subjected to gas chromatography–mass spectroscopy.ResultsSignificant adulticidal action with 100% adult mortality was observed in ethanol extract of P. longum leaves. Among the fourteen fractions (F0–F13) obtained tested, only fractions, F5, F10 and F13, demonstrated adulticidal activity, and the remaining fractions displayed poor activity. One hundred per cent morality was noted in T. castaneum adults after 96 h at 40 mg/L in F5 and F10, and in F13 at 20 mg/L, and their respective LD50 values were 17.6, 26.6 and 10.0 mg/L. The fractions F5, F10 and F13 contained fatty acids, viz., hexadecanoic acid, dotriacontane and heptacosane in F5; tetradecanoic acid and nonadecanoic acid in F10; and octadecanoic acid, aspartame and tridecanoic acid in F13, revealed through gas chromatography–mass spectroscopy.ConclusionsThe results of the study showed that P. longum ethanol leaf extract revealed significant adulticidal activity and is a promising toxic agent to the adults of T. castaneum. The fatty acids in the ethanolic leaf extract fractions of P. longum could have caused toxicity to the adults of T. castaneum. According to the current literature survey, this is the first research report on the adulticidal activity of P. longum leaf extracts against the adults of T. castaneum.

Fractionated Leaf Extracts of Ocimum gratissimum Inhibit the Proliferation and Induce Apoptosis of A549 Lung Adenocarcinoma Cells.

Previous in vitro studies in our laboratory demonstrated that ethyl acetate (P2) and water- soluble (PS/PT1) fractionated leaf extracts of Ocimum gratissimum inhibit the proliferation of prostate cancer cells. It has been reported that the crude aqueous extract induces apoptosis in lung adenocarcinoma cells; however, the efficacy of the fractionated extracts against these cells remains unclear. In the present study, we hypothesized that the ability of the fractionated extracts to inhibit proliferation and induce apoptosis is associated with the activation of pro-apoptotic proteins and induction of DNA condensation in A549 cells. Ocimum gratissimum was cultivated and its leaves were harvested, extracted, and fractionated to produce fractions P2 and PS/PT1. Anti-proliferative activity was assessed by direct cell count. For morphological characterization of apoptosis, 4',6-diamidino-2-phenylindole staining was employed. Western blot analysis was performed to evaluate the apoptotic activity of the fractionated extracts. In data generated from anti-proliferation studies, P2 significantly inhibited cell proliferation in a concentration-dependent manner; PS/PT1 elicited a decrease in the viability of cells, occurring at 500 µg/mL. 4',6-diamidino-2-phenylindole staining revealed the induction of apoptosis, as evidenced by the formation of apoptotic bodies. Increased levels of pro-apoptotic proteins were observed as the concentrations of the fractionated extracts increased. These results suggest that fractionated leaf extracts of Ocimum gratissimum inhibit the proliferation and induce apoptosis of A549 cells.

Enhancing anticancer activity of Clerodendrum viscosum vent. extracts by solvent fractionation: An in vitro and in silico mechanistic study

Clerodendrum viscosum Vent. is a well-known plant in Indian and Chinese traditional medicine systems. While studies showed its crude leaf extract's cytotoxicity against HT-29 and HeLa cells, various non-bioactive compounds present in crude extracts may influence overall bioactivity. This study aimed to separate the most bioactive fractions from Clerodendrum viscosum’s crude extracts that exhibit anticancer potential against HepG2 cells. Crude extracts were fractionated using a solvent-polarity-based process and their anticancer activity was investigated through in vitro, in silico, and network pharmacology approaches. Nonpolar leaf (CVLH) and root (CVRH) fractions showed maximum cytotoxicity in HepG2 cells without affecting noncancer-origin WRL68 cells. Both extracts induced oxidative stress, DNA damage, cell cycle arrest, and apoptosis in HepG2 cells, with CVRH exhibiting a superior effect. GC-MS analysis identified various anticancer phytochemicals differentially present in CVLH and CVRH. Network pharmacology with these phytochemicals predicted Bcl-2 as the primary target, while molecular docking confirmed lupeol, stigmasterol, alpha-amyrin, cycloartenol, and calysterol being the top five phytochemicals exhibiting strong binding against Bcl-2, androgen receptor (AR), and epidermal growth factor receptor (EGFR). Western blot confirmed an elevated Bax/Bcl-2 ratio in HepG2 cells by CVLH and CVRH. In summary, the nonpolar fractions of Clerodendrum viscosum leaf and root crude extracts showed enhanced anticancer activity, suggesting their potential pharmaceutical applications.

Tinospora malabarica leaf extract fractions-derived silver nanoparticles and their spectral characterisation: evaluation of their toxicity properties against agricultural pests Spodoptera litura and Helicoverpa armigera

ABSTRACT Our study specifically delves into the synthesis of AgNPs utilizing Tinospora malabarica leaf extract fractions (Tm-LMEFs) and explore their efficacy in combating the larvae have progressed to the synthesized AgNPs (Tm-AgNPS) and the leaf methanol extract fractions (LMEFs), our investigation focused on their impact on the targeted larvae species over a 24-h exposure period. Significantly noteworthy mortality rates were observed across all Spodoptera litura and Helicoverpa armigera post-treatment, indicating pronounced efficacy. Notably, the Tm-AgNPS exhibited higher toxicity compared to the LMEFs these selected polyphagous insect pests. Quantitative analysis yielded the highest mortality (98.99%/90.44% and 55.33%/49.60%) values for the synthesized Tm-AgNPs against S. litura and H. armigera, with no observed mortality in the control group. This study marks the first instance of exploring both Tm-LMEFs, Tm-AgNPs and enzyme activity have toxicity properties against selected agriculture pests, highlighting their promising role in pest management and environmental sustainability.

Evaluation of the merit of ethanolic extract of Annona reticulata as an anti-cancer agent in human colon cancer cell lines (HCT-116)

Background Colon cancer is the third most common cancer type worldwide. Novel alternative therapeutic anti-cancer drugs against colon cancer with less toxicity are to be explored . This study was aimed to explore the anti-proliferative and anti-migratory activity of various fractions of Annona reticulata ethanolic leaf extract on human colon cancer cell lines (HCT-116) and to explore the potential molecular targets from the most potent plant extract fraction. Methods After obtaining ethical clearance from the institutional ethics committee, the extract and fractions were prepared and a preliminary analysis of the phytochemical was done qualitatively. Total phenolic and flavonoids were determined. Ethanolic leaf extract and its fractions were subjected to cytotoxicity analysis using the sulforhodamine B assay and the most promising fraction which showed the highest viability was selected to study anti-migratory activity. The anti-migratory effect was studied using a scratch wound healing assay. Gas chromatography-mass spectrometry (GC-MS) was done to identify the major phytocompounds present in the fraction. The major five phytocompounds identified from the GC-MS were subjected to bioinformatics analysis. Result Among the four fractions, the petroleum ether fraction exhibited the highest anti-proliferative activity. The migration of colon cancer cells was significantly inhibited by the extract and petroleum ether fraction. The major phytocompounds identified from GC-MS were phytol (13.03%), 2,6-bis (3,4-methylenedioxyphenyl)-3,7-dioxabicyclo (3.3.0) octane (11.95%), gamma.-sitosterol (10.45%), alpha.-tocopherol-beta.-D-mannoside (7.50%) and 3-amino-4-piperonyl-5-pyrazolone (5.84%). The bioinformatics analysis of these phytochemicals showed a high potential to affect the levels of key proteins driving colon cancer progression, inhibiting the enzymes and proteins overexpressed in cancer. Conclusion The outcome of this study endorses the potential of phytochemicals of the petroleum ether fraction of ethanolic leaf extract of Annona reticulata for the development of a new chemotherapeutic agent in the treatment of colon cancer.

Efficacy of Albizia malacophylla (A.Rich.) Walp. (Leguminosae) methanol (80%) leaf extract and solvent fractions against Plasmodium berghei-induced malaria in mice model

Ethnopharmacological relevanceNovel drugs are needed to address the issue of malarial infection resistance; natural items can be a different source of these medications. Albizia malacophylla (A. Rich.) Walp. (Leguminosae) is listed as one of the antimalarial medicinal plants in Ethiopian folk medicine. However, there are no reports regarding the biological activity or phytochemistry of the plant. Aim of the studyThus, this study aimed to evaluate the A. malacophylla crude extract and solvent fractions' in vivo antimalarial activity utilizing 4-day suppressive, preventative, and curative tests in mice infected with P. berghei. Materials and methodsThe parasite Plasmodium berghei, which causes rodent malaria, was used to infect healthy male Swiss Albino mice, weighing 23–28 g and aged 6–8 weeks. Solvent fractions such as methanol, water, and chloroform were given in addition to an 80% methanolic extract at 100, 200, and 400 mg/kg doses. A Conventional test such as parasitemia, survival time, body weight, temperature, and packed cell capacity were employed to ascertain factors such as the suppressive, curative, and preventive tests. ResultsEvery test substance dramatically reduced the number of parasites in every experiment. Crude extract (with the highest percentage suppression of 67.78%) performs better antimalarial effect than the methanol fraction, which is the most efficient solvent fraction with a percentage suppression of 55.74%. With a suppression value of 64.83% parasitemia level, the therapeutic effects of 80% methanolic crude extract were greater than its curative and preventative effects in a four-day suppressive test. The survival period (17 days) was longer with the hydroalcoholic crude extract dose of 400 mg/kg than with other doses of the materials under investigation. ConclusionsThe results of this investigation validate the antimalarial characteristics of A. malacophylla leaf extract. The crude extract prevented weight loss, a decline in temperature, and a reduction in PCV. The results demonstrate that the plant has a promising antimalarial effect against P. berghei, hence supporting the traditional use of the plant. Therefore, it could serve as a foundation for the development of new antimalarial drugs.

Therapeutic effect of the solvent fraction of hexane leaf extract of Tapinanthus bangwensis (Engl. & K. Krause) (Loranthaceae) in alloxan-induced pathology in diabetic rats

Plant-based products are gradually replacing pharmaceuticals in treating ailments, including diabetes, due to their safety, cost-effectiveness, potency, and availability. Therefore, the current study looked into the therapeutic effect of the solvent fraction of hexane leaf extract of Tapinanthus bangwensis (HEXETACF) (Loranthaceae) in alloxan-induced pathology in diabetic rats. The biochemical parameters were estimated using analytical grade kits via spectrophotometric method. The laboratory rats were distributed into group W (five rats on feed and water), group X (seven rats + 150 mg/kg alloxan solution only), group Y (seven rats + 150 mg/kg alloxan solution + 200 mg/kg BW silymarin for 21 days), and group Z (seven rats + 150 mg/kg alloxan solution + 250 mg/kg BW HEXETACF for 21 days). The results showed that HEXETACF and silymarin (SILY) reduced blood glucose concentration by 33.77% and 34.80%, respectively, after the 21st day of treatment (p < 0.05). Additionally, alkaline phosphatase (ALP) and alanine aminotransferase (ALT) activity in SILY and HEXETACF were significantly decreased compared to the diabetic group (p < 0.05), but no significant decrease in aspartate aminotransferase (AST) activity was observed between the test samples and the diabetic group. Furthermore, the test samples lowered malondialdehyde (MDA) levels, by improving glutathione, superoxide dismutase (SOD), and catalase (CAT) activity. The HEXETACF and SILY significantly decreased triglyceride levels (TG) compared to the diabetic group at p < 0.05. They also reduced low-density lipoprotein (LDL) and cholesterol levels and increased the high-density lipoprotein levels compared to the diabetic group. Additionally, no significant decrease in serum electrolytes (Na+, K+, and Cl-), urea, and creatinine (including albumin and total protein) values was observed in HEXETACF and SILY, while hematological indices increased compared to the diabetic group. Histology results revealed that the test samples had normalized glomeruli, β-islet cells, and hepatocytes. However, a trace of mild congestion was noticed in the STDG. But edemic blood congestion was observed in the diabetic group. In conclusion, the current result demonstrated that HEXETACF may be a promising antidiabetic agent that could replace mSILY.

Evaluation of phytochemical, in vitro antibacterial and rate of kill assay of <i>Terminalia avicennioides</i> leaf against some bacteria associated with diarrhoea

The study was aimed to evaluate the phytochemical constituents, in vitro antibacterial and rate of kill assay of Terminalia avicennioides leaf extract against some bacteria associated with diarrhoea. The phytochemical constituents of the ethanol of Terminalia avicennioides leaf, aqueous, n- butanol, and ethyl acetate fractions of the leaf extract were determined using standard analytical methods. The antibacterial activities of the leaf extract and extract fractions against clinical isolates of Salmonella Typhimurium and Escherichia coli isolated from diarrhoeaic patients were determined in vitro by agar diffusion, dilution and time - kill methods. The result of phytochemical screening revealed the presence of carbohydrates, cardiac glycosides, saponins, flavonoides, tannins, alkaloids, phenols and triterpenes. The crude extract and extract fractions of T. avicennioides leaf were effective against the test bacterial isolates at varied concentration of extracts but the n-butanol fraction was more effective with Minimum inhibitory and Minimum Bactericidal Concentration of 6.25 and 12.5mg/ml. The clinical isolates of E. coli and S. Typhimurium were completely killed within 180 minutes of exposure to ethanol leaf extract and extract fractions at varied MBCs of 12.5 mg/ml and 25.0 mg/ml. The clinical isolates of E. coli and S. Typhimurium were more susceptible to n-butanol fraction within 120 minutes of exposure to the extract fraction.

Cytotoxicity Test of Ethyl Acetate Fraction and Ethanol Fraction of Papaya Leaf Extract (Carica Papaya. L) Against Hep-2 Laryngeal Cancer Cells

Papaya leaves are used as medicine for fever, malaria, increased appetite, constipation, and anti-cancer. In the previous study using the Brine Shrimp Lethality Test (BSLT), an ethanol extract of papaya leaf had an LC50 value of 23.73 mg/mL. This suggests that papaya leaves are a compound, that uses a 70% ethanol extract of papaya leaves and has cytotoxic potential. Research objectives: This research aimed to determine the cytotoxic effect of the ethanol and ethyl acetate fractions of a 70 % ethanol extract of papaya leaf against Hep-2 cells. Performed in vitro by the direct calculation method (viable cell count), so its LC50 is known. The ethanol and ethyl acetate fraction of papaya leaf extract as a test solution was made in 5 concentrations, with concentrations of 20.93; 16.26; 12.64; 9.82, and 7.63 µg/ml. Result: The results obtained the LC50 ethanol fraction of 11.2616 μg/ml and the ethyl acetate fraction of LC50 12.4 of 882 μg/ml. Conclusion: Based on this, it can be concluded that the fraction of ethanol and ethyl acetate extracts of papaya (Carica papaya L.) have cytotoxic properties against Hep-2 cells in a range that goes very, very toxic, i.e., 5–50 µg/ml, and have the potential to be developed as an anticancer drug.

B-HEMATIN INHIBITION ACTIVITY OF THE METHANOL LEAF EXTRACT AND RESIDUAL AQUEOUS FRACTION OF FICUS ASPERIFOLIA

Chemotherapy is still regarded as the major intervention in fighting the malaria scourge despite the recent introduction of malaria vaccine. Screening of medicinal plants provides opportunities for the discovery of the potential drug molecules. Ficus asperifolia (Miq) family Moraceae has been traditionally employed in the treatment of many diseases including pain, fever and malaria. The aim of this study was to examine the anitmalarial activity of both the methanol leaf extract (MEFA) and residual aqueous fraction of Ficus asperifolia (RAF) through the determination of their heme polymerization inhibition ability. The powdered leaf was extracted using 70%

Competitive Adsorption of Phenolic Acids, Secoiridoids, and Flavonoids in Quercetin Molecularly Imprinted Polymers and Application for Fractionation of Olive Leaf Extracts.

The competitive adsorption of phenolic acids, secoiridoids, and flavonoids in a molecularly imprinted polymer (MIP) functionalized with 4-vinylpiridine (4VP) moieties is analyzed here considering vanillic acid, oleuropein, and quercetin as reference molecules. Measured adsorption isotherms highlight a much stronger binding capacity of the quercetin-MIP particles toward quercetin as compared with vanillic acid and oleuropein. The acquired data were used to design and scale-up sorption/desorption processes aiming at the fractionation of olive leaf extracts. We show that a simple adsorption process, avoiding many pre-preparation steps, is possible when working at a high extract concentration due to the strong binding capacity of the MIP for flavonoids, even when using aqueous mixtures with a large alcoholic content. Solvent-gradient/temperature-swing desorption led to a sequence of fractions with enrichment of non-flavonoids at low alcoholic content while glycosylated flavonoids were enriched in fractions with 40% < alcohol content < 80%. Enrichment factors of 13 and 12 were measured for luteolin-7-O-glucoside and apigenin-7-O-glucoside, respectively. Flavonoid aglycones were enriched in fractions with alcohol content >80% (enrichment factors >20 for luteolin and quercetin). The findings reported here demonstrate the usefulness of the developed materials and sorption/desorption conditions for agricultural residue valorization and circular bioeconomy.

In vitro Investigation and GC-MS Analysis of the Chemical Constituents in the Fraction of Hexane Leaf Extract of Tapinanthus bangwensis (Engl. and K. Krause) Loranthaceae

In vitro Investigation and GC-MS Analysis of the Chemical Constituents in the Fraction of Hexane Leaf Extract of Tapinanthus bangwensis (Engl. and K. Krause) Loranthaceae

Identification and Toxicity Profiling of Column Fractions of Ethanol Leaf Extract of Ziziphus mauritiana

Different plants may contain varying amounts of phytochemicals and also different degrees of toxicity. This study aimed to evaluate the phytochemicals present in the most active column fraction of ethanol leaf extract of the Ziziphus mauritiana plant and their toxic effects using brine shrimp lethality assay and animal model. Crude ethanol extract was obtained by maceration while fraction was achieved using a column chromatography experiment. Toxicity was evaluated with brine shrimp lethality assay and albino rat’s models while characterization was achieved with liquid chromatography-mass spectrophotometry. Ziziphus mauritiana leaves revealed 42 fractions pooled into seven fractions. Fraction three (3) was the most toxic with the brine shrimp lethality assay of (31.48ug/ml) and its toxicological evaluation revealed an adverse effect on the hematological parameter, biochemical indices, and histo-architecture of the liver and kidney of the experimental model studied. LCMS analysis of the most toxic fraction revealed the presence of Antirrhinoside, Lucidumol A, Apigenin 7-glucuronide-4'-(6''-malonylglucoside), Dioscoreside C, Camellioside D, and others which have been reported for various pharmacological effects including adverse effects, The mode of toxicity may be synergistic, individual, or antagonistic which may explain the moderate toxicity observed in animal model. Administration of these fractions may lead to toxicity despite their potential.

EVALUATION OF ANTIDIABETIC, ANTI-INFLAMMATORY, AND ANTIOXIDANT ACTIVITIES OF DIFFERENT FRACTIONS OF ETHANOLIC EXTRACT OF LEAVES OF Bauhinia variegata BY In vitro METHOD AND ISOLATION OF PHYTOCONSTITUENTS

Today, diabetes is a common morbidity, and the occurrence of the disease is attributed to various pathophysiological states of the human body, including inflammation and free radical oxidants. Previous types of research also reported the involvement of free radical oxidants in the development of secondary complications of diabetes. The scavenging of free radicals by antioxidants turns out to be a defense mechanism and can also alter disease states. Therefore, the study was designed to evaluate the properties of Bauhinia variegata L. leaves in controlling diabetes, inflammation, and free radicals. The ethanolic leaf extract was prepared and the extract was then fractionated with solvents, which were further used to perform pharmacological screening by in vitro methods. The IC50 values of the chloroform fraction (BVC) of leaf extract were recorded as the lowest among the test materials for all in vitro studies. The IC50 values of BVC in the study of inhibition of α-amylase and α-glucosidase enzymes were 31.08±1.53 and 25.33±1.52 g/mL, respectively. In the study of inhibition of bovine serum albumin and egg albumin denaturation, BVC showed efficacy with IC50 values of 23.75±1.35 and 28.15±1.32 g/mL, respectively. The fraction showed free radical scavenging activity in DPPH and nitric oxide assay, with IC50 values of 27.78±1.61 and 34.93±1.49 g/mL, respectively. In addition, two pure compounds, namely chrysoeriol and β-amyrin palmitate, were isolated from this bioactive fraction. Thus, the results proved all the claimed pharmacological effects of the leaves of Bauhinia variegata L. and also justified the hypothesis of the current study.

Detection of Antibacterial Fraction of Ethanol Extract of Folium Sambung Nyawa (Gynura procumbens) in Salmonella typhi

Background: Folium Sambung Nyawa, a native plant in Indonesia, is known for its abundant medicinal properties. Among its various secondary metabolites, flavonoids stand out, being polyphenolic compounds found in numerous plants and foods. Flavonoids exhibit a wide range of bioactive properties, including antibacterial, anti-inflammatory, anti-diabetic, anti-cancer, anti-ageing, and antioxidant effects. Objective: This study aimed to assess the antibacterial potential of Sambung Nyawa Leaf extract fractions against Salmonella typhi bacteria. Methods: The antibacterial activity was evaluated using the paper disc diffusion method to determine the inhibition zones. Three fractions---n-hexane, ethyl acetate, and water---were tested at concentrations of 10%, 20%, and 30% each, along with negative controls (DMSO) and positive controls (Chloramphenicol). Results: Flavonoid examination using synode reagent yielded positive results. Among the fractions tested, the 30% ethyl acetate fraction exhibited the most promising antibacterial activity, with an inhibition zone of 7.65 mm, indicating strong efficacy against Salmonella typhi bacteria. Conclusion: The findings suggest that the ethyl acetate fraction of the concentrated Sambung Nyawa leaf extract possesses potent antibacterial properties against Salmonella typhi bacteria

Optimization of serum formula active fraction of moringa leaf extract (Moringa oleifera Lambk) as antibacterial against Staphylococcus aureus

This study aims to determine the optimum formula for the serum active fraction of Moringa leaves with a combination of carbopol, NaCMC and propylene glycol as antibacterial. Material and methods the fractionation of the extract were tested on Staphylococcus aureus bacteria using the diffusion method. The ethyl acetate fraction which has antibacterial activity at a concentration of 15% was made into serum preparations with a combination of carbopol, NaCMC and propyleneglycol. Making serum formulas using the simplex lattice design method resulted in 14 serum formulas. Testing of the physical quality of the preparations carried out included organoleptic tests, homogeneity, pH, adhesion, viscosity, spreadability, and antibacterial activity. The results of the study on the ethyl acetate fraction of Moringa leaves with a concentration of 15% had antibacterial activity against S. aureus with an inhibition zone of 14.36 ± 1.1 mm. The TLC test the chemical compounds contained in the ethyl acetate fraction of Moringa leaves were flavonoids, saponins and tannins. The optimum combination proportions for serum preparations obtained variation values, namely carbopol 0.67% and NaCMC 3% and propylengliol 5.32%.

Evaluation of the merit of ethanolic extract of Annona reticulata as an anti-cancer agent in human colon cancer cell lines (HCT-116)

Background Colon cancer is the fourth most common cancer type worldwide. Novel alternative therapeutic anti-cancer drugs against colon cancer with less toxicity are to be explored . This study was aimed to explore the anti-proliferative and anti-migratory activity of various fractions of Annona reticulata ethanolic leaf extract on human colon cancer cell lines (HCT-116) and to explore the potential molecular targets from the most potent plant extract fraction. Methods After obtaining ethical clearance from the institutional ethics committee, the extract and fractions were prepared and a preliminary analysis of the phytochemical was done qualitatively. Total phenolic and flavonoids were determined. Ethanolic leaf extract and its fractions were subjected to cytotoxicity analysis using the sulforhodamine B assay and the most promising fraction which showed the highest viability was selected to study anti-migratory activity. The anti-migratory effect was studied using a scratch wound healing assay. Gas chromatography-mass spectrometry (GC-MS) was done to identify the major phytocompounds present in the fraction. The major five phytocompounds identified from the GC-MS were subjected to bioinformatics analysis. Result Among the four fractions, the petroleum ether fraction exhibited the highest anti-proliferative activity. The migration of colon cancer cells was significantly inhibited by the extract and petroleum ether fraction. The major phytocompounds identified from GC-MS were phytol (13.03%), 2,6-bis (3,4-methylenedioxyphenyl)-3,7-dioxabicyclo (3.3.0) octane (11.95%), gamma.-sitosterol (10.45%), alpha.-tocopherol-beta.-D-mannoside (7.50%) and 3-amino-4-piperonyl-5-pyrazolone (5.84%). The bioinformatics analysis of these phytochemicals showed a high potential to affect the levels of key proteins driving colon cancer progression, inhibiting the enzymes and proteins overexpressed in cancer. Conclusion The outcome of this study endorses the potential of phytochemicals of the petroleum ether fraction of ethanolic leaf extract of Annona reticulata for the development of a new chemotherapeutic agent in the treatment of colon cancer.

Chromatographic Profiles and Determination of Total Flavonoid Content of the Ethyl Acetate Fraction of Kalangkala Leaves (Litsea Angulata Blum) Using Uv-Vis Spectrophotometry

Background: Kalangkala is a fruit plant typical of Kalimantan and belongs to the species of the genus Litsea which is thought to have potential as a natural antioxidant. Empirically, some people in South Kalimantan use the kalangkala plant, especially the seeds of the fruit, to treat boils. One of the compounds that have antioxidant and antibacterial content is flavonoids.Objectives: To determine the thin layer chromatography profile of the total flavonoid compound of the ethyl acetate fraction and to calculate the total flavonoid content of the ethyl acetate fraction of the leaf extract of Kalangkala (Litsea angulata Blum).Method: Thin Layer Chromatography Profile and Determination of Total Flavonoid Content of the Ethyl Acetate Fraction of Kalangkala Leaf Extract using the UV-Vis Spectrophotometry method. The data were then analyzed qualitatively and quantitatively.Results: The chromatographic profile of the total flavonoids of the ethyl acetate fraction of Kalangkala leaf eluent that was most optimal was Ethyl acetate : n-Hexane (3:7) because it showed the most stains, namely 5 stains. And in the uv-vis spectrophotometry method, the total flavonoid content of the ethyl acetate fraction of Kalangkala leaves (Litsea angulata Blum) was 0.9 mg QE/g.Conclusion: Kalangkala leaf extract on the TLC profile using ethyl acetate : n-Hexane (3:7) showed a total of 5 stains. And the value of the total flavonoid content of the ethyl acetate fraction of kalangkala leaves was 0.9 mg QE/g.