Quantitative Phytochemical Analysis Research Articles

Quantitative and qualitative phytochemical analysis of ethanol leaf extract of Pleiocarpa mutica

This research project examined Pleiocarpa mutica leaf extract, extracted from ethanol using both quantitative and qualitative phytochemical analysis. Sourced is at Ugbene-Ajima in the Uzo-Uwani Local Government Area of Enugu State, Nigeria, where fresh Pleiocarpa mutica leaves were collected. After been gathered, the newly sprouted P. mutica leaves were cleaned. We then shade-dried the leaves until they were crispy, rotating them frequently to prevent them from rotting. A mechanical grinder was utilized to reduce the dried leaves to a powdered state while a maceration flask was used to macerate 1.5 kg of the known weight of the ground leaves in 10 liters of 100% ethanol. In using a muslin cloth, the mixture was filtered into a flask with a flat bottom after being left for 72 hours with irregular stirring. Quantitative phytochemical analysis procedures identified the specific concentration of a certain chemical constituent present in a plant sample using methods such as mass spectrometry, chromatography, and spectrophotometry. This makes it possible to determine the concentration of a component in the plant material. Qualitative phytochemical analysis techniques focus on identifying the presence or absence of several chemical groups in a plant sample. Discovering the existence of substances such as alkaloids, phenols, terpenoids, and flavonoids often requires a range of chemical analyses or the use of specific reagents. Thus, the standard quantitative and qualitative phytochemical analysis technique were used to investigate the chemical composition of plants and identify bioactive compounds that may offer nutritional, medicinal, or pharmacological advantages. Hence, it has been shown that the ethanol leaves extract of P. mutica contains various concentrations of phytochemical constituents, which might be responsible for its biological activities.

Effect of flavonoid-rich fraction of Pleiocarpa mutica leaves on phospholipase A2 activity

Pleiocarpa mutica (Apocynaceae) is a pharmaceutical plant investigated to identify the usefulness and efficacy of the shrubs in the treatment of various ailments. Also, flavonoids are polypenolic compounds frequently found in nature and are divided into flavones, anthocyanidins, isoflavones, catechins, flavonols, chalcones, and flavonones based on the structure of their chemicals. Hence, fresh leaves of Pleiocarpa mutica were collected from Ugbene-Ajima, Uzo-Uwani Local Government Area, Enugu State, Nigeria. The extraction of a flavonoid-rich fraction of P. mutica leaves was conducted by dissolving a certain amount of crude extract in 20 mL of 10% H2SO4 in a tiny flask and then heating the mixture in a water bath for 30 minutes at 100 °C to initiate hydrolysis. However, quantitative phytochemical analysis of the P. mutica flavonoid-rich fraction was carried out by utilizing standard conventional protocols. Newly drawn human blood samples were centrifuged for 10 minutes at 3,000 rpm, with the supernatant (plasma) being disposed of. After being measured and reconstituted as a 40% (v/v) suspension with phosphate-buffered saline, the red blood cells were rinsed three times with an equivalent volume of normal saline. The fraction substantially (p < 0.05) reduced the activity of phospholipase A2 in a concentration-dependent approach when compared to the standard drug (prednisolone), with a range of 0.2 mL to 1.0 mL reducing the amount of the enzyme by 47.58% to 63.61%. These results showed that the flavonoid-rich fraction of Pleiocarpa mutica leaves is potent in curtailing the inflammatory response through inhibition of phospholipase A2 activity.

Evaluation of <i>in vitro</i> anti-trypanosomal activities of leaves, stem bark and root bark extracts of <i>Acacia nilotica</i> (L) Willd ex Del., <i>Guiera senegalensis</i> j. F. Gmel and <i>Ziziphus abyssinica</i> Hochst ex A. rich

Currently, the control and treatment of African trypanosomiasis are limited by the number of chemotherapeutic drugs with associated side effects. Consequently, there is an urgent need for a non-toxic herbal treatment for African trypanosomiasis. Leaf, stem, and root bark extracts of Acacia nilotica L. and Guiera senegalensis J. F. Gmel and Ziziphus abyssinica Hochst ex A. Rich were sequentially extracted using hexane, ethyl acetate, methanol and water as solvents and evaluated for in vitro anti-trypanosomal activities against Trypanosoma brucei, and phytochemical contents. Results revealed that out of the 36 extracts, Methanol leaf extracts of G. senegalensis, aqueous leaf extract of G. senegalensis, methanol leaf extract of A. nilotica and methanol leaf extract of Z. abyssinica leaf extract (MIC 3.93±2.88, 10.98±3.21, 16.91±3.21 and 18.88±3.44 μg/ml respectively), gave the best in vitro anti-trypanosomal activity against T. b. brucei compare to the control. The quantitative phytochemical analysis of the 4 most trypanocidal plant extracts revealed the presence of alkaloids, flavonoids, terpene, quinines, saponins and tannins, with alkaloids and flavonoids having the highest concentrations (4.3.13±0.05 mg/100 g and 4.5±0.02 mg/100 g respectively) in the methanol leaf extract of G. senegalensis and quinone with the lowest concentration (0.1±0.07 mg/100 g).The methanol leaf extracts of G. senegalensis were found to have the most in vitro anti-trypanosomal activities (MIC of 3.93±2.88 ug/ml), possibly due to the high content of alkaloids and flavonoids. The results of this study revealed the potential of G. senegalensis for the treatment of African trypanosomiasis. Consequently, further studies are needed with this plant to evaluate its in vivo anti-trypanosomal potential, the structures of the bioactive compounds responsible for its activity, and its other medicinal properties.

A comparative study on the synergistic activities of fractions and crude essential oil of Syzygium aromaticum

BackgroundSyzygium aromaticum has been used for over a century because it has biological qualities for several health-related problems, and the crude essential oils are known to contain several components that could be responsible for synergistic or antagonistic potentials in relation to their biological uses. The study was designed to compare the biological activities of the crude essential oil from the bud of Syzygium aromaticum and fractions obtained from column chromatography.Materials and methodsThe essential oil was extracted by hydrodistillation, and two prominent fractions, C1 and C2, were obtained from the column chromatography separation of the crude essential oil. The quantitative phytochemical analysis was done by standard methods, the antioxidant activity was determined by 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid (ABTS) scavenging assays. The antifungal activities were assessed by the agar diffusion method, while the anti-inflammatory activity was done using a lipoxygenase inhibitory assay. The major component observed in the crude and fractions was determined by gas chromatography–mass spectrometry (GC–MS) analysis.ResultsThe phytochemical analysis showed that phenolic acid, tannin, saponin, flavonoids, alkaloids, cardiac glycosides, and terpenoids were present in variable quantities in all of the fractions and crude essential oil. The half-maximal inhibitory concentration (IC50) value for DPPH scavenging activity ranged from 226.1 to 301.2 µg/mL while that of ABTS scavenging activity ranged from 211.0 to 316.0 µg/mL. The lowest value of IC50 for both DPPH and ABTS was observed in fraction C1. The crude essential oil with a minimum inhibitory concentrations (MIC) value of 8.00 mg/mL was the most efficient against Candida albicans, Aspergillus penicillum, and Aspergillus niger. The anti-inflammatory assay showed C1 to have the lowest value of IC50 for the lipoxygenase assay. The major component observed in the crude essential oil as well as fraction C1 was eugenol, while fraction C2 had β-caryophyllene as the major component.ConclusionsThe result showed that all fractions as well as the crude essential oil exhibited antioxidant, antifungal, and anti-inflammatory activities, and the crude essential oil was synergic only with respect to its antifungal activity, while fraction C1 was more efficient as an anti-inflammatory and antioxidant agent.

In vitro and in silico based assessment of biological activity of endemic Allium species: LC-MS/MS analysis of onions

In this study, the beneficial biological activity of four Allium species was examined to determine the metabolite components, antioxidant, antimicrobial, antiproliferative, wound healing, and enzyme inhibitory activities. All in vitro tests were compared to their reference compounds. The quantitative phytochemical analysis was distinctively profiled fifteen metabolites. The extract of A. eldivanense exhibited promising inhibitory effect against AChE (IC50: 0.335 ± 0.04 mg mLˉˡ), BChE (IC50: 0.375 ± 0.04 mg mLˉˡ), α-glucosidase (IC50: 0.148 ± 0.01 mg mLˉˡ), and tyrosinase (IC50: 11.87 ± 1.07 μg mLˉˡ) enzymes. The extract from A. olympicum and A. ilgazense exhibited ABTS scavenging activity closer to that of BHT among four antioxidant assays. A. eldivanense showed antibacterial ability ranging from 4 to 8 mg mLˉˡ concentrations, and the extract is promising compared to ampicillin. A. peroninianum demonstrated the highest cytotoxic effect (IC50: 84.03 μg mLˉˡ) on cervical cancer cells, and all Allium extracts applied to the HeLa cell line significantly slowed down wound closure. The molecular implementation studies predicate the in vitro enzyme inhibitory findings, and the major compounds in the onion extract have the highest affinity for the targets. The findings suggested that Allium species have potential biological activities according to the comprehensive in vitro and in silico analysis.

Antioxidant and antibacterial evaluation of leaf extracts of Prunus cerasoides Buch.-Ham. ex D.Don; An In Vitro and In Silico study

BackgroundMany infectious bacteria have changed throughout time and there are alarmingly large number of antibiotic resistant species that can withstand the inhibitory impact of these treatments., Plants are new sources of antibacterial agents hence there is a need to determine and evaluate the antioxidant activity, antibacterial properties of medicinal plants ObjectiveThe present study focuses on qualitative, quantitative phytochemical analysis, antioxidant, and antimicrobial evaluation of leaves’ extracts of Prunus cerasoides Buch. -Ham. ex D. Don. Materials and methodsThe Antioxidant activity of leaves extracts of Prunus cerasoides Buch. -Ham. ex D.Don was determined by DPPH method. Antibacterial activity was determined by serial dilution method. Further docking interactions were investigated using Maestro 12.7 (Schrodinger 2021) and ADME by using QikProp tool of Schrodingers 2021. ResultsThe leaves’ extracts of Prunus cerasoides Buch. -Ham. ex D.Don showed potent antioxidant and antibacterial activities. Methanol extract was found to be the most active against all the four strains of bacteria and showed MIC value (3.125 μg/mL) against both E. coli and S. aureus. Ethyl acetate and methanol extracts had the highest radical scavenging activity. Further molecular docking and ADME studies for phytoconstituents of Prunus cerasoides Buch. -Ham. ex D. Don. using different bacterial protein targets of reported phytoconstituents of Prunus cerasoides Buch. -Ham. ex D. Don. and found that emodin, amygdalin and aromadendrin were the phytoconstituents having good docking score and drug likeliness properties. ConclusionsThe leaves extracts of Prunus cerasoides Buch. -Ham. ex D.Don showed potent free radical scavenging property as well as antibacterial activity.

Phytochemical Analysis of Selected Medicinal Pslants from Eastern Ghats of Andhra Pradesh

The objective of the present investigation is to appraise the qualitative and quantitative phytochemical analysis, DPPH and Hydroxyl radical scavenging activity along with a total antioxidant capacity of water extract obtained from six medicinal plants, i.e., Acalypha alnifolia, Caesalpinia bonduc, Carissa spinarum, Commiphora caudata, Moringa concanensis and Terminalia tomentosa. The phytochemical analysis of the six medicinal plants water extracts revealed total phenolic content (TPC) in the range of 27.77 to 3.35 GAE mg/g dwt. The highest TPC is present in A. alnifolia and the lowest is noticed in T. tomentosa. The total flavonoid content is present in between 1.68 to 1.48 QE mg/g dry weight and a higher amount of flavonoid content was observed in A. alnifolia and lowest present in C. bonduc. Antioxidant activity results of the six medicinal plants showed that the highest total antioxidant capacity was observed in Carissa spinarum and lowest in T. tomentosa. DPPH method was used to know the antioxidant capacity of aqueous extract of the six medicinal plants. Among the tested plants A. alnifolia, Carissa spinarum and Moringa concanensis strongly reduced DPPH purple color by expressing ~80% as maximum inhibition. DPPH was strongly inhibited by T. tomentosa (IC50 value 25 μg/ml). Hydroxyl radical was strongly (~96%) inhibited by T. tomentosa and lowest IC50 value was expressed by A. alnifolia (36.4 μg/ml). The study results indicate that all six medicinal plants are rich sources of natural antioxidant components.

Quantitative Analysis of Phytochemical Compounds and Antihyperglycemic Potential of Robusta Coffee from West Lampung

West Lampung Regency in Lampung Province produces high quality robusta coffee with a distinct, strong bitter flavour. Bitter flavour indicates the amount of bioactive substances produced by plants called phytochemicals. The aim of this study is to analyse the phytochemical compounds and antihyperglycemic potential of robusta coffee beans from West Lampung, Indonesia. Quantitative phytochemical analysis was carried out using the thin layer chromatography method and spectrophotometry. Animal experimental design using robusta coffee on hyperglycemia conditions in mice which was induced by alloxan 170 mg/kgBW subcutaneously and given by 1 ml of brewed robusta coffee for 10 days. The robusta coffee from West Lampung contained total caffeine 4,014.87 µg/g, total flavonoid content (TFC) 93.6 mg quercetin equivalent per gram of sample, with total alkaloid content (TAC) 0.848 mg of quinine equivalent per gram of sample, total tannin content (TTC) 182.3 mg of tannic acid equivalent per gram of sample, and total saponin content (TSC) 24.2 mg of quillaja bark equivalent per gram of sample. The administration of 1 ml/mice/day of robusta coffee brewed for 10 days did not show a decrease in blood sugar level in hyperglycemic mice, due to the short duration of the study, so the role of coffee in decreasing hyperglycemia conditions has not been optimally observed.

Biochemical analysis of Justicia carnea leaves used as a hematinic

Justicia carnea is the largest genus of Acanthaceae and is a medicinal plant used widely in Nigeria, reported to have diverse functions, including blood-boosting potential. The phytochemicals, vitamins, minerals, amino acid and proximate compositions of the leaf extract of Justicia carnea were determined using standard methods. Results of the quantitative phytochemical analyses on the leaves of Justicia carnea recorded appreciable presence of flavonoids, alkaloids, saponins, tannins, cyanogenic glycosides, oxalate, and phytate using GC-FID. Ribalinidine with 42.08±0.03 mg/kg was the highest alkaloid, Flavan -3-ol was 21.18±0.02 mg/kg, presented the highest amount of flavonoids, and phytate with 25.69±0.07 mg/kg as the highest antinutrient. Analysis of Justicia carnea leaves recorded iron (8.61mg/kg) as the major elemental content followed by potassium (5.29±0.11mg/kg). The concentrations of vitamins in Justicia carnea leaves showed vitamin C, with the highest value of (232.32±12.26 mg/100g) followed by Vitamin A (22.16±2.12 mg/kg). The results of proximate composition on Justicia carnea leaves showed a high concentration of carbohydrate (60.35±3.05%) and appreciable amounts of ash (15.02±1.01%), fibre (9.29±0.93%), protein (8.40±0.41%), and low amount of lipid (1.50±0.09%). The amino acid results showed the presence of both essential and non-essential amino acids with their concentrations in increasing and decreasing orders. These results obtained showed that leaves of Justicia carnea may serve as rich source of natural antioxidants, this may be attributed to its rich phytochemicals, nutrients and vitamin compositions and could be recommended as a potential source of useful bioactive constituents as vegetable supplement and has no toxic effect and as an effective hematinic supplement when prepared adequately.

Phytochemical analysis and antioxidant activities ethanol extract of propolis Trigona spp. from different vegetation in Lombok, West Nusa Tenggara, Indonesia

Abstract. Tirtasari K, Suwanti LT, Mufasirin, Hastutiek P, Indasari EN, Kurnijasanti R, Plumeriastuti H, Safitri E, Hestianah EP. 2024. Phytochemical analysis and antioxidant activities ethanol extract of propolis Trigona spp. from different vegetation in Lombok, West Nusa Tenggara, Indonesia. Biodiversitas 25: 404-411. Propolis is a natural substance containing a resin that is collected by honey bees from various plants and has a significant effect on human health such as antibacterial, antifungal, anti-inflammatory, antiviral, anesthetic, antioxidant, antitumoural, antiprotozoal, anticancer, antihypertensive, anticarcinogenic, antihepatotoxic and has cytotoxic activity. Cultivation of Trigona spp. in Lombok is growing rapidly. Trigona spp. produces more propolis than honey bees of Apis spp., but bee products that are maximally utilized are only honey, and propolis has not been utilized optimally. Currently, there is no scientific validation of the phytochemical content, bioactive compounds, and biological activities of ethanol extract propolis Trigona spp. from Lombok, West Nusa Tenggara. So, this study aimed to determine the phytochemical compounds, bioactive compounds, and antioxidant activity of propolis. Gas Chromatography-Mass Spectrometry (GC-MS) analysis was performed to determine the bioactive compounds of ethanol extract propolis. DPPH (2,2-diphenyl-1-picrylhydrazyl) was used to evaluate antioxidant activity. The composition of propolis compounds is different for each propolis depending on the bee species and the vegetation source from which the resin was collected. In this research, propolis was collected from different vegetation sources (cashews, moringa, coffee, and lote trees). This study used qualitative and quantitative phytochemical analysis and the antioxidant DPPH test. Different components and percentages cause significant variations in the results obtained from phytochemical tests. The content is different in various propolis, there are saponins, flavonoids, and tannins. The highest antioxidant activity was found in propolis with moringa resin 38.4150 (very strong), followed by lote tree resin -66.0420 (strong), cashew resin 81.8140 (strong), and coffee resin 100.7465 (moderate).

Phytochemical analysis, antioxidant, antimicrobial, and toxicity studies of Schima wallichii growing in Nepal

ABSTRACT The present study focuses on qualitative and quantitative phytochemical and biological analysis in bark and leaf extracts of Schima wallichii growing in Gulmi, Nepal. TPC and TFC were measured using the Folin-Ciocalteu reagent and the aluminum chloride colorimetric method, respectively. The DPPH assay was used for antioxidant activity, and antimicrobial activity was studied with the agar-well diffusion method. The presence of polyphenols, flavonoids, quinones, coumarins, saponins, terpenoids, and tannins was detected by qualitative phytochemical analysis. Total phenolic content in an aqueous leaf extract and methanol bark extract ranged from 199 ± 5 to 219 ± 8 mg GAE/g. Similarly, the flavonoid content found between 6.0 ± 1.7 in bark to 33 ± 2 mg QE/g in leaf extract. The antioxidant activity of IC50 36 ± 3, 39 ± 1, 52 ± 3, and 73 ± 4 µg/mL for methanolic bark extract, methanolic leaf, aqueous bark, and aqueous leaf extracts, respectively. The bark methanol extract showed the most antibacterial activity with ZOI of 10.0 ± 0.3, 8.0 ± 0.3, 14 ± 0, and 11 ± 1 mm against Klebsiella pneumoniae, Staphylococcus aureus, Bacillus subtilis, and Escherichia coli, respectively. Plant extracts were found to be nontoxic to mildly toxic to the brine shrimp nauplii. The plant is found to be rich in phenolics, and flavonoids showing significant antioxidant and antibacterial activities, and is nontoxic against brine shrimp nauplii. The plant imparts a health-promoting effect that needs to be explored in pharmaceutical research.

Phytochemical profiling, antibacterial and antioxidant potential of different parts of invasive plant Sonchus wightianus DC

The aim of the present investigation was to elucidate the phytochemical characterisation, antimicrobial and antioxidant efficacies of methanol extracts of leaf, stem, and root parts of S. wightianus. The phytochemical characterisation by GC-MS analysis revealed the presence of different phytocompounds such as Lupenone (38.02% in leave extract), Leupeyl acetate (33.43% in root extract), 24- Noursa −3, 12- diene (27.16% stem extract). S. wightianus methanol extracts demonstrate IC50, 8.52 µg/ml, 7.72 µg/ml and 9.08 µg/ml using DPPH, FRAP and MCA scavenging assay, respectively. The antibacterial activity of different methanol extracts was evaluated against four microorganisms with a mean zone diameter of inhibition ranging from 13 to 19 mm. For quantitative phytochemical analysis, the highest Total Phenolic Content (TPC) and Total Flavonol Content (TFC-2) were found for steam methanol extract (321.7 mg GAE/g of dry extract, 162.4 mg QE/g of dry extract respectively).

Study of Curcuma diversity from Central Java, Indonesia for sunscreen and antioxidant activity based on quantitative phytochemical analysis

Abstract. Nurhasnawati H, Sundu R, Sukmawati A. 2023. Study of Curcuma diversity from Central Java, Indonesia for sunscreen and antioxidant activity based on quantitative phytochemical analysis. Biodiversitas 24: 6880-6887. Indonesia is home to various plants, including those of the genus Curcuma. This study aimed to determine the effect of total phenolic and flavonoid content of Curcuma on antioxidant activity and SPF values. It is known that this rhizome contains secondary metabolites such as flavonoids and phenols, which are known to have antioxidant potential and are believed to act as natural ingredients for sun protection products. The samples used in this study were rhizomes of five Curcuma species from Central Java, namely C. aeruginosa, C. longa, C. mango, C. xanthorrhiza, and C. zedoaria. Alkaloids, flavonoids and tannins are present in all samples. UV-Vis spectrophotometry was used with the following results: the flavonoid total content ranged from 0.94-243.5 mg QE/g, while the total phenolic from 11.27-109.23 mg GAE/g. The DPPH and ABTS test for antioxidant activity showed that C. longa had the highest activity with an IC50 of 78.79 and 0.4273 ppm. The highest SPF values in C. longa were 31.55-36.97 (high protection). The results of the data analysis using the Spearman correlation test revealed a significant correlation between the antioxidant activity and SPF with the flavonoid and phenolic content of the Curcuma extracts.

Phytochemical, proximate, and elemental analysis of chia seed (<i>Salvia hispanica</i> L.) from Dawanau grain market, Kano State, Nigeria

Plants have shown a lots of importance in the field of phytomedicine, phamacognosy andherbal sciences, the seed of chia seed (Salvia hispanica) was collected from local farmers atDawanau grain market Kano State with the aim of determination of phytochemicals, proximate and elemental Analysis and were identified at the herbarium of plant science department of Bayero University Kano with assertion number (BUKHAN 0539), 250g of the processed seed were macerated in 500 ml of methanol, water, ethyl acetate and hexane for 72hrs. Standard method was followed for qualitative and quantitative phytochemical analysis, proximate and elemental analysis, furthermore thin layer chromatography and Fourier transform infrared microscopic analysis was conducted. The result of the analysis shows that flavonoid and carbohydrate was present throughout the solvents used, while all the proximate and heavy metal analysis were found to be within the limit of EP/WHO 2011 and WHO 1984 with the exception of Manganese. The result of the thin layer Chromatography result has the retention factor and number of spot. The FTIR analysis of the extract reveal that the I.R spectra indicated the present of different functional group such as amine, ketones, carboxylic acid and phenol. Conclusively the plant sample has shown the present of phytochemical substances that are remarkably useful in the field of ethonomedicine.

Appraisal of phytochemical constituents, antioxidant and antibacterial activities of folkloric Pentanema confertiflorum rootbark extracts

BackgroundMedicinal plants have cultural prominence in the management of ailments worldwide. The different organs of Pentanema confertiflorum (hereafter referred as P. confertiflorum) as have been used to ameliorate different diseases in Ethiopia. Thus, this study focused on the qualitative and quantitative phytochemical analysis, antioxidant, and antibacterial screening of P. confertiflorum rootbark solvent fractions. MethodsThe rootbark of P. confertiflorum was successively soaked with petroleum ether, chloroform, and methanol. The total phenolic (TPC), flavonoid (TFC), and alkaloid contents (TAC) of the different crude extracts were determined through Folin-Ciocalteu Reagent (FCR), aluminum chloride colorimetric, and bromocresol green (BCG) assays, respectively. In addition, 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging and ferric-reducing antioxidant power (FRAP) assays were employed to determine the antioxidant activity of crude extracts. Moreover, the antimicrobial activity of the crude extracts was assessed against different bacteria strains via the disc diffusion method. ResultsThe qualitative phytochemical investigation study resonated with the abundance of several secondary metabolites, especially in the methanolic rootbark extract (MRBE). In addition, the MRBE had the highest TPC (76.7 mg GAE/g extracts), TFC (86.89 mg QE/g extracts), and TAC (80.68 mg ATE/g extracts) as compared to petroleum ether and chloroform extracts. Consistent with its TPC, TFC, and TAC, the MRBE demonstrated better antioxidant activity against DPPH radical scavenging (IC50 = 44.53 ppm) and FRAP assays (EC50 = 42.72 ppm). Moreover, all the rootbark extracts induced dose-dependent antibacterial activity against Streptococci pyogenes and Staphylococcus aureus, Klebsiella pneumoniae, and Escherichia coli. ConclusionsThe preliminary findings suggested the presence of a strong correlation between the folkloric use of P. confertiflorum and its observed antioxidant and antibacterial activity. Rigorous studies on the extracts such as the isolation and characterization of bioactive compounds, and detailed bioactivity and toxicity studies are desirable to bring about safe and effective lead compounds.

Characterization and in-vitro plant-based control of hindgut bacteria isolated from Odontotermes obesus Rambur (Termitidae) and Heterotermes indicola Wasmann (Rhinotermitidae).

Termites cause a serious menace to wooden structures all over the world. They rely mostly on entozoic fauna residing in their hindgut for the digestion of cellulosic and hemicellulosic materials. One of the ways to control termites is through their gut symbionts. The present study was designed to characterize the hindgut bacteria isolated from Odontotermes obesus and Heterotermes indicola. Furthermore, the growth inhibitory effect of eight tropical plant extracts was investigated to find out potential control agents for these bacterial isolates. The characterization of bacteria was carried out based on their morphology, Gram staining, biochemical and amplification of 16SrRNA gene. Amplified products were sequenced to confirm their relationship with bacterial isolates from termites of other regions. The growth inhibitory effect of ethanolic leaf extracts of eight plants was evaluated in an invitro agar well diffusion method. Qualitative and quantitative phytochemical analysis of the most effective plant was carried out to learn about bioactive agents. The results confirmed the presence of five bacteria from each termite species. The Bacillus cereus, Escherichia coli, and Lysinibacillus fusiformis were common to both termites whereas Lysinibacillus xylanilyticus and Lysinibacillus macrolides were found in O. obesus only and H. indicola harbor Bacillus subtilis and Shigella sonnei in addition to common three ones. Among the plant extracts of Carica papaya, Eucalyptus camaldulensis, Osmium basilicum, Grevillea robusta, Eucalyptus globulus, Pongamia pinnata, Mentha longifolia, and Melia azedarach, the G. robusta > E. camaldulensis > O. basilicum were found to have growth inhibitory effects with increasing concentrations from 100 to 2000 µg/mL. The biodiversity of the bacterial fauna is important for the biological control of termites. Leaf extracts of these medicinal plants can be used to control termite infestation in an environment-friendly manner to save huge economic loss.

Synthesis of Zinc Oxide Nanoparticles using Extract of Cynodon dactylon and Assessment of their Biological Activity against Staphylococcus aureus and Escherichia coli

Nanotechnology is a groundbreaking technology that that has been widely applied in creating materials which are useful in various fields. It's important to maintain eco-friendly approaches for synthesis of nanoparticles by diversifying the substrate sources. In this study, the researchers used aqueous extract of Cynodon dactylon to synthesize zinc oxide nanoparticles (ZnONPs). Quantitative phytochemical analysis of the extract showed high concentrations of alkaloids, flavonoids, carbohydrates, proteins, amino acids, and phenolic compounds. In contrast, moderate concentrations of tannins, oils, and fats, and low concentrations of phlorotannins, saponin, triterpenoids, and cardiac glycosides were found. Sterols, anthraquinone glycosides, gums, and mucilages were not detected in the extract. The synthesized ZnONPs showed absorbance ranging from 293 nm to 336 nm, with a peak at 307 nm. Fourier transform infrared (FTIR) spectroscopy revealed that the surface of the ZnONPs contained alcohol (intermolecular bonded), alkyne, amine salt, alkane, alkyne, aromatic compounds, conjugated alkene, amine, nitro compound, sulfonyl chloride, alkylaryl ether, and sulfoxide. Dynamic light scatering (DLS) analysis of the ZnONPs showed that its average size was 35.34±1.64 nm, and the polydispersity index was 0.6335. Spectrum of X ray diffraction indicated that peaks formed at 2θ and their corresponding orientation planes are 31.92o (100), 34.62o (002), 36.44o (101), 47.64o (102), 56.84o (110), 63.3o (200), and 68.16o (112). Transmission electron micrograph revealed the spherical shape, and nonuniform sizes of ZnONPs, which ranged from 0.52 nm to 8.32 nm. Antibacterial analysis of biosynthesized ZnONPs recorded 16±3.2 mm and 6.0±2.2 mm; 6.7±2.1 mm and 4.33±1.3 mm, 0.0±0.0 mm and 1.0±1.41 mm, against Staphylococcus aureus and Escherichia coli, at 53.3 mg/mL, 26.7 mg/mL and 13.3 mg/ml concentrations, respectively. At sub-inhibitory concentrations, biosynthesized ZnONPs demonstrated effective dose-dependent antibiofilm formation activity against E. coli and S. aureus. Consequently, extract of Cynodon dactylon is suitable for biosynthesis of ZnONPs with effective antibacterial and antibiofilm formation activities.

Quantitative and Qualitative Phytochemical Analysis of Manilkara zapota (Sapodilla) Extract and Its Antibacterial Activity on Some Gram-Positive and Gram-Negative Bacteria.

A molecule's antibacterial and antiviral action is exclusively linked to substances that selectively eradicate bacteria and viruses or inhibit their growth without significantly damaging adjacent tissues. The purpose of this research is to evaluate quantitative and qualitative phytochemical analysis and the antibacterial effects of Manilkara zapota fruit extract on some Gram-positive (Staphylococcus aureus, Enterococcus faecalis, Micrococcus luteus, Bacillus cereus, and Listeria monocytogenes) and Gram-negative (Escherichia coli, Pseudomonas aeruginosa, and Klebsiella pneumoniae) bacteria in laboratory conditions. Qualitative chemical screening was used to identify different classes of active chemical compounds, and quantitative analysis of the chemical composition of the plant was used to measure the contents of flavonoid, total phenol, anthocyanin, and antioxidant activity. Antibacterial effects of Manilkara zapota ethanol extract were determined by disk diffusion methods, minimum inhibitory concentration (MIC), and minimum bactericidal concentration (MBC). Qualitative chemical screening revealed the presence of flavonoids, tannins, quinones, terpenoids, and glycosides while the presence of saponins was not observed. The bacterial inhibition zones against Listeria monocytogenes, Enterococcus faecalis, Pseudomonas aeruginosa, Staphylococcus aureus, Micrococcus luteus, Escherichia coli, Klebsiella pneumoniae, and Bacillus cereus are 15.44 ± 0.33, 12.23 ± 0.11, 8.85 ± 0.2, 14.22 ± 0.33, 15 ± 0.44, 9.33 ± 0.13, 10.33 ± 0.36 and 14.55 ± 0.45 mm, respectively. MIC and MBC of the extract in Gram-positive bacteria were 25 and 50, and in Gram-negative bacteria were 50 and 100 mg/ml, respectively. The findings imply that Manilkara zapota extract includes a good amount of plant compounds and can be a significant source for a variety of uses, including antibacterial.

Qualitative and quantitative phytochemical analysis of brown seaweed Sargassum polycystum collected from Bangladesh with its antioxidant activity determination

Seaweeds possess considerable potential for developing and enhancing pharmaceutical drugs because of their wide variety as abundant sources of numerous bioactive secondary metabolites, making them well-suited for developing and enhancing pharmaceutical drugs. This study evaluated the antioxidant, secondary metabolites, total phenolic content, and total flavonoid content of various crude extracts (methanol, ethanol) and their fractions (50 % and 70 %) of Sargassum polycystum. Fourier transform infrared (FT‐IR) analysis was also performed to identify the active chemical composition of the crude extracts. The results showed that various extracts contained varying concentrations of terpenoid, saponin, phlobatannin, cardiac glycosides, phenolic, and flavonoid. FT-IR analysis confirmed the presence of phenols, carboxylic acid, ketones, ethers, aromatics, amides, and sulfonates. 100 % methanolic extract contained the maximum concentrations of total phenols (80.13 mg of GAE/g) and total flavonoids (38.33 mg of quercetin/g). 100 % methanol extracts exhibited higher antioxidant activity in the DPPH assay (78.32 %, IC50 = 1.59 mg/ml) and ABTS assay (69.82 %, IC50 = 2.39 mg/ml). The bio-functional activity of crude extracts depended on their extract and concentration. The present study demonstrates that the macroalgae S. polycystum contains noteworthy secondary metabolites and natural antioxidants, indicating their potential utilization in various pharmacological and functional food applications.

Quantitative Screening of Phytochemicals of five Red Seaweeds from the Northern Kerala Coast, India

The Quantitative analysis of 5 phytochemical parameters: Tannins, Flavonoids, Phenols, Steroids, and Terpenoids has been done for 5 Red seaweeds belonging to the family –Rhodophyceae i.e. Gracilaria corticata, Grateloupia lithophila, Gelidium micropterum, Chondracanthus acicularis, and Centroceras clavulatum, from the Northern Kerala coast: Thikkodi, Elathur, Kappad and Beypore, located in the Kozhikode district. Methanolic extracts of the seaweeds were used for the Phytochemical component screening. The study found that Flavonoid content was the lowest among other parameters ranging from 2.61±0.04 mg QE/g dw to 5.57±0.23 QE/g dw. The steroid was found to be higher in the case of C. acicularis (61.32±0.04 mg BSE/g dw) and C. clavulatum (65.80±0.02 mg BSE/g dw). Followed by it was Tannin which was highest in G. micropterum (49.20±0.56 mg CE/g dw) and C. acicularis (32.01±0.24 mg CE/g dw), whereas G. lithophila showed consistently lower concentrations in Phenols (0.19±0.01 mg GAE/g dw), Tannins (9.43±1.59 mg CE/g dw), and Steroids (3.69±0.01 mg BSE/g dw). To the best of our Knowing the current Quantitative analysis of phytochemicals in Red seaweeds is the pioneering work done in the following study areas: Kappad, Elathur, and Beypore. This phytochemical screening with reference to past studies on the same domain confirms that a lot of work needs to be done yet.