Screening Of Antimicrobial Activity Research Articles

Methods for screening and evaluation of antimicrobial activity: A review of protocols, advantages, and limitations.

Infectious diseases pose a formidable global challenge, compounded by the emergence of antimicrobial resistance. Consequently, researchers are actively exploring novel antimicrobial compounds as potential solutions. This endeavor underscores the pivotal role of methods employed for screening and evaluating antimicrobial activity-a critical step in discovery and characterization of antimicrobial agents. While traditional techniques such as well-diffusion, disk-diffusion, and broth-dilution are commonly utilized in antimicrobial assays, they may encounter limitations concerning reproducibility and speed. Additionally, a diverse array of antimicrobial assays including cross-streaking, poisoned-food, co-culture, time-kill kinetics, resazurin assay, bioautography, etc., are routinely employed in antimicrobial evaluations. Advanced techniques such as flow-cytometry, impedance analysis, and bioluminescent technique may offer rapid and sensitive results, providing deeper insights into the impact of antimicrobials on cellular integrity. However, their higher cost and limited accessibility in certain laboratory settings may present challenges. This article provides a comprehensive overview of assays designed to characterize antimicrobial activity, elucidating their underlying principles, protocols, advantages, and limitations. The primary objective is to enhance understanding of the methodologies designed for evaluating antimicrobial agents in our relentless battle against infectious diseases. By selecting the appropriate antimicrobial testing method, researchers can discern suitable conditions and streamline the identification of effective antimicrobial agents.

Phyto-extract-mediated Synthesis of Silver Nanoparticles using Blumea lacera Leaf Extract and Antimicrobial Activity Screening

Phyto-extract-mediated Synthesis of Silver Nanoparticles using Blumea lacera Leaf Extract and Antimicrobial Activity Screening

Screening of Antimicrobial Activity of Murraya koenigii Leaf Extracts Against Pathogenic Bacterial Strains Staphylococcus aureus and Escherichia coli Isolated from Contaminated Water

Aim: Murraya koenigii is a widely used plant both as a potential medicinal agent and also for common cooking purposes. Aim of this present study was to determine the antimicrobial activity of Murraya koenigii leaf extracts on Staphylococcus aureus and Escherichia coli. 
 Study Design: Screening and isolation of pathogenic bacterial strains from contaminated water. Preparation of Murraya koenigii leaf extracts using petroleum ether, acetone and ethyl acetate by using serial extraction method with Soxhlet apparatus.
 Place and Duration of Study: Department of microbiology, Agro biotec research centre Ltd, Poovanthuruthu, Kottayam, Kerala, India, between 2014 January to 2014 May.
 Methodology:  Staphylococcus aureus and Escherichia coli were the bacterial strains used in this study. Morphological and biochemical analysis of microorganisms were conducted to identify the strains. Leaf extracts (petroleum ether, acetone and ethyl acetate) of Murraya koenigii were screened using MHA disc diffusion methods.
 Results: Various concentration of plant extracts were used to check its activity against isolated pathogens. Acetone extract of curry leaves exhibit maximum zone of inhibition against Staphylococcus aureus and petroleum ether extracts shown maximum inhibition against Escherichia coli.

The synthesis, characterization, antioxidant and antimicrobial activity of some novel amides of the esters of substituted 1,4-dihydropyridines

The esters of substituted 1,4-dihydropyirdines (1,4-DHP) are formed in the reaction of an appropriate aldehyde and ethyl acetoacetate in the presence of concentrated water solution of ammonia. The esters form the amides by the reaction with primary amines. The series of the amides has been synthesized with the aim to analyze their chemical characteristics, antioxidant and antimicrobial activity. The amine used in this research is 2-aminothiazole. The antioxidant activity is analysed by 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2'-Azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) methods and the antimicrobial activity screening was performed by broth microdilution method, using different microbial strains. The characterization of the obtained amides was done by melting points, FTIR, NMR and elemental analysis. The possibilities for further research was suggested, which could lead to the application of selected compounds.

Screening and Evaluation of Antimicrobial Activity of Medicinal Plants Collected from Lalitpur District

Objectives: To screen and evaluate antimicrobial activity of crude ethanol extracts of medicinal plants against various bacteria. Methods: The study was conducted from February - August 2018 in Pinnacle college, Lalitpur with plan to collect Seven different herbs species; Acorus calamus (Bojho), Aloe vera (Ghiu Kumari), Artermisia indica (Titepate), Azadirachta indica (Neem), Mentha arvensis (Pudhina), Zanthoxylum armatum (Timur) and Zingiber officinale (Ginger) were subjected to 70% ethanol soxhlet extraction, then extract then heated at 78.37°C to remove ethanol, working solution was prepared in DMSO. Test organisms included mainly enteric isolates i.e. Escherichia coli, Pseudomonas aeruginosa, Klebsiella oxytoca, Salmonella Typhi and Staphylococcus aureus were selected. The Antibiotic Susceptibility tests of isolates were done by of Modified Kirby Bauer disc diffusion method. The antimicrobial activities of the extracts were determined by Agar well diffusion technique. Minimum Bactericidal Concentration (MBC) was determined by dilution technique. Results: Among 7 plants that were tested, 6 plants were found to have activity against test bacteria. Acorus calamus 3/5(60%) was effective against test bacteria. Azadirachta indica and Menthe arvensis inhibited 2/5 (40%). Aloevera and Artermisia indica were effective against S aureus only 1/5(20%) and Zingiber officinale had no antibacterial effects over any tested bacteria. S. aureus was the most susceptible Gram positive bacteria meanwhile K. oxytoca stood among Gram negative, emerged as the most resistant species. S. aureus showed ZOI with 6 plant extracts excluding ginger P. aeruginosa was inhibited by Acorus calamus, Azadirachta indica and Mentha arvensis. The largest ZOI of 15 mm was obtained with Zanthoxylum armatum acting upon S. aureus. While, the smallest diameter of 8 mm was showed by Acorus calamus against S. Typhi. The lowest MBC was given 15.63 mg/ml by Mentha arvensis and Azadirachta indica against Pseudomonas aeruginosa while, Artermisia indica against S. aureus. Conclusion: Medicinal plants should be possible medication in the future to combat pathogens.  

Antimicrobial Activity and Phytochemical Screening of Traditional Medicinal Plants

In Nepal, traditional medicinal plants and herbs have long been relied upon for treating various diseases. This study was aimed to explore the antimicrobial properties of commonly used traditional medicinal plants. This study was conducted from December 2022 to June 2023 at the Department of Microbiology, St. Xavier's College, Maitighar, Kathmandu. In this study, antimicrobial property of 12 plants were tested against four ATCC cultures of bacteria- Staphylococcus aureus (ATCC 6538P), Staphylococcus epidermidis (ATCC 12228), Escherichia coli (ATCC 8739) and Pseudomonas aeruginosa (ATCC 9027). The extracts were prepared using Soxhlet's apparatus with ethanol and distilled water as solvents. The ethanolic extract of S. aromaticum had the highest percentage yield The ethanolic extract of O. sanctum showed highest potential against S. aureus with a zone of inhibition of 21mm. The ethanolic extract of S. aromaticum demonstrated antimicrobial activity against S. aureus, E. coli, P. aeruginosa, and S. epidermidis, with respective zones of inhibition of 18mm, 16mm, 18mm, and 20mm. The distilled water extract of A. marmelos displayed the highest antimicrobial activity against E. coli, with a zone of inhibition of 18mm. Phytochemical screening revealed that both extracts of S. aromaticum had the highest presence of phytochemicals. The ethanol extract of Z. armatum exhibited the highest antibacterial activity, with a minimum inhibitory concentration (MIC) value of 2mg/ml against S. aureus. The study of the selected plants extracts confirmed their efficacy as natural antimicrobials against the tested organisms, suggesting their potential for novel drug development in treating infectious diseases. Int. J. Appl. Sci. Biotechnol. Vol 11(4): 186-196.

Screening of antimicrobial, antibiofilm and cytotoxic activities of some medicinal plants from Balıkesir province, Türkiye: pointing to the potential effects of Allium paniculatum flower

Screening of antimicrobial, antibiofilm and cytotoxic activities of some medicinal plants from Balıkesir province, Türkiye: pointing to the potential effects of Allium paniculatum flower

Antimicrobial Activity Screening of Bacteria Isolated from Tasik Cermin

Introduction: With the emergence of the multi-drug resistant bacteria that threaten the human health, novel antimicrobial compounds from natural environment have been increasingly explored. Tasik Cermin is a lake completely covered by karst towers and hills and lacks any inflow or outflow of water making it an oligotrophic environment with limited nutrient availability. Increased competition among microorganisms leads to production of antimicrobial compounds that can inhibit the growth of its competitor. Thus, the aim of this study is to assess antimicrobial activity of bacterial isolates from Tasik Cermin and identify the most resistant isolate. Methods: The isolates were tested against five test bacteria: Staphylococcus aureus, Bacillus subtilis, Streptococcus pneumoniae, Escherichia coli, and Proteus vulgaris by primary screening through perpendicular streak method, secondary screening followed by MIC and MBC and the most resistant bacteria was identified by molecular identification. Results: The result indicates that only one isolate (Isolate TC1A) was able to show potential antimicrobial activity against P. vulgaris and S. pneumoniae. This isolate was further tested by secondary screening through agar well diffusion method and inhibition zone were observed on P. vulgaris (14.97 ± 0.05), E. coli (9.23 ± 0.25) and S. pneumoniae (14.93 ± 0.12). Statistical analysis by One-Way ANOVA and Tukey test method indicates that inhibition zone of E. coli is significantly different as compared to S. pneumoniae and P. vulgaris. Molecular identification revealed that the isolate TC1A was identified as Achromobacter sp. with 97.68% similarity percentage. Conclusion: This finding shows that bacterial isolates from under-explored areas have the potential of producing novel antimicrobial compounds.

Design, Synthesis, and In Vitro and In Vivo Bioactivity Studies of Hydrazide-Hydrazones of 2,4-Dihydroxybenzoic Acid.

In this research, twenty-four hydrazide-hydrazones of 2,4-dihydroxybenzoic acid were designed, synthesized, and subjected to in vitro and in vivo bioactivity studies. The chemical structure of the obtained compounds was confirmed by spectral methods. Antimicrobial activity screening was performed against a panel of microorganisms for all synthesized hydrazide-hydrazones. The performed assays revealed the interesting antibacterial activity of a few substances against Gram-positive bacterial strains including MRSA-Staphylococcus aureus ATCC 43300 (compound 18: 2,4-dihydroxy-N-[(2-hydroxy-3,5-diiodophenyl)methylidene]benzohydrazide-Minimal Inhibitory Concentration, MIC = 3.91 µg/mL). In addition, we performed the in vitro screening of antiproliferative activity and also assessed the acute toxicity of six hydrazide-hydrazones. The following human cancer cell lines were used: 769-P, HepG2, H1563, and LN-229, and the viability of the cells was assessed using the MTT method. The HEK-293 cell line was used as a reference line. The toxicity was tested in vivo on Danio rerio embryos using the Fish Embryo Acute Toxicity (FET) test procedure according to OECD No. 236. The inhibitory concentration values obtained in the in vitro test showed that N-[(4-nitrophenyl)methylidene]-2,4-dihydroxybenzhydrazide (21) inhibited cancer cell proliferation the most, with an extremely low IC50 (Inhibitory Concentration) value, estimated at 0.77 µM for LN-229. In addition, each of the compounds tested was selective against cancer cell lines. The compounds with a nitrophenyl substituent were the most promising in terms of inhibition cancer cell proliferation. The toxicity against zebrafish embryos and larvae was also very low or moderate.

The clove essential oil and its combination with galangal oil exhibit antibacterial activity, potential as antiseptic agent

Essential oils are known and have been tested for their antimicrobial properties. Previous studies have tested the antimicrobial activity of clove and galangal essential oils alone. Thus, the purpose of this study was to determine the antimicrobial activity of clove and galangal essential oils alone as well as their combinations. The screening of antimicrobial activity was performed by disc diffusion assay against Gram-positive bacteria and Gram-negative bacteria. Both essential oils showed antimicrobial activity against Escherichia coli at 10% (v/v) concentration. Furthermore, five combinations of clove and galangal essential oils were made and tested at 1:1, 7:3, 9:1, 3:7, and 1:9 ratio. Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) of three combinations with the highest activity were performed against Escherichia coli. The MIC and MBC of clove oil is at 2.5% (v/v) and 5% (v/v) while the MIC and MBC of Galangal oil is at 5% (v/v) and 10% (v/v). All three combinations showed MIC and MBC value is at 5% (v/v) and 10% (v/v) respectively. In addition, based on SNI EN 1276:2019 assay, the clove and galangal essential oil as well as their combinations meet the requirement as antiseptic agent against E. coli.

In Vitro Screening of Antimicrobial and Anti-Coagulant Activities, ADME Profiling, and Molecular Docking Study of Citrus limon L. and Citrus paradisi L. Cold-Pressed Volatile Oils.

Citrus, which belongs to the Rutaceae family, is a very widespread genus in the Mediterranean Basin. In Tunisia, various parts of these spontaneous or cultivated plants are used in common dishes or in traditional medicine. The purpose of this work was to investigate C. limon and C. paradisi essential oil (EO). The samples were studied for their chemical composition using SPME/MS, as well as their antibacterial and antifungal activities. Prothrombin time (PT) and activated partial thromboplastin time (aPTT) methods were used to evaluate the anticoagulant potentialities. The obtained results show that both essential oils are rich in monoterpenes hydrocarbons, whereby limonene is the main compound in C. paradisi EO (86.8%) and C. limon EO (60.6%). Moreover, C. paradisi EO contains β-pinene (13.3%), sabinene (2.2%) and α-pinene (2.1%). The antibacterial assay of the essential oils showed important bactericidal and fungicidal effects against all strains tested. In fact, the MICs values of C. limon EO ranged from 0.625 to 2.5 mg/mL against all Gram-positive and Gram-negative bacteria, and from 6.25 to 12.5 mg/mL for Candida spp. strains, while C. paradisi EO was more active against all bacteria with low MICs values ranging from 0.192 to 0.786 mg/mL, and about 1.5 mg/mL against Candida species. Both tested Citrus EOs exhibited interesting anticoagulant activities as compared to heparin. The molecular docking approach was used to study the binding affinity and molecular interactions of all identified compounds with active sites of cytidine deaminase from Klebsiella pneumoniae (PDB: 6K63) and the C (30) carotenoid dehydrosqualene synthase from Staphylococcus aureus (PDB: 2ZCQ). The obtained results show that limonene had the highest binding score of -4.6 kcal.mol-1 with 6K63 enzyme, and -6.7 kcal.mol-1 with 2ZCQ receptor. The ADME profiling of the major constituents confirmed their important pharmacokinetic and drug-like properties. Hence, the obtained results highlight the potential use of both C. limon and C. paradisi essential oils as sources of bioactive compounds with antibacterial, antifungal, and anti-coagulant activities.

Phytochemical screening and evaluation of antimicrobial activity of Pterolobium stellatum root extract

Phytochemical screening and evaluation of antimicrobial activity of Pterolobium stellatum root extract

Antimicrobial and Antioxidant Activity Screening of Mushrooms Growing in the Leningrad Region

Introduction. The emergence of new strains of microorganisms that are multidrug resistant (MDR) in relation to the antimicrobial drugs used is one of the pressing problems of modern medicine. To prevent an increase in MDR-related deaths, the search for new antibiotics and their introduction into medical practice must be continuously ongoing. Infectious diseases are also accompanied by cell damage and the development of free radical oxidation processes, therefore the search for new antioxidants is also an important task. Considering the powerful biosynthetic potential of basidiomycetes, this group of fungi has every prospect of becoming a new source of biologically active substances in general, as well as antibiotics and antioxidants in particular. Cap mushrooms, represented mainly by basidiomycetes, number about 14,000 species and are an accessible source of raw materials for the search for promising antimicrobial compounds and antioxidants.Aim. Study of the antioxidant and antimicrobial activity of total extracts obtained from cap mushrooms against Escherichia coli, Staphylococcus aureus and Candida albicans and assessment of the suitability of cap mushrooms as a natural source of substances with antimicrobial and antioxidant activity.Materials and methods. The antifungal and antibacterial activity of the extracts was determined by the micromethod of two-fold serial dilutions in a liquid nutrient medium in 96-well plates in duplicate. The study of this type of biological activity was carried out against reference (type) strains Staphylococcus aureus ATCC 6538-P, Escherichia coli ATCC 25922, Candida albicans NCTC 885-653. To study antioxidant activity using DPPH, we used alcoholic extracts from the fruiting bodies of mushrooms obtained by maceration with 96 % ethanol at a ratio of raw materials to extractant of 1 to 8 for 24 hours, an aqueous solution of ascorbic acid (vitamin C) and an ethanol solution of Trolox.Result and discussion. In relation to S. aureus, a representative of gram-positive flora, the studied extracts of cap mushrooms showed low activity, on average about 2500 or 5000 μg/ml. In relation to E. coli, a representative of gram-negative flora, 8 % of the studied cap mushroom extracts showed an average activity of about 1250 μg/ml. The largest number of cap mushroom extracts – 19% of all studied species – showed activity against the yeast micromycete C. albicans. The highest activity against C. albicans was observed in extracts of the mushrooms Cantharellula umbonata with an MIC of 625 μg/ml, Cortinarius olivaceofuscus with an MIC of 625 μg/ml, and Hypomyces chrysospermus with an MIC of 312 μg/ml. During screening of antioxidant activity, the studied extracts were divided into three groups: with high (more than 50 % PPR), medium (from 15 to 50 % PPR) and low (less than 15 %) antioxidant activity. It was shown that the sum of phenolic compounds significantly correlates with the level of antioxidant activity in all three groups, but in the groups with medium and low antioxidant activity there are also other non-phenolic groups of compounds that make a significant contribution to the total antioxidant activity.Conclusion. Cap mushrooms are a promising source of biologically active substances with antifungal and antioxidant activity.

Fe3O4 Nanoparticles Catalyzed Tandem Synthesis of Fluorescent 3‐(4,5‐diaryl‐1H‐imidazol‐2‐yl) quinoline‐2‐amines: Solvatochromic, DFT and Biological Studies

AbstractIn the present work, Fe3O4 nanoparticles were prepared by the co‐precipitation method and employed as effective nanocatalysts in the tandem synthesis of 3‐(4,5‐diaryl‐1H‐imidazol‐2‐yl)quinolin‐2‐amines. An effective multicomponent reaction is plighted for 2‐chloroquinoline‐3‐carbaldehydes and substituted benzils to obtain novel heterocycles 3‐(4,5‐diaryl‐1H‐imidazol‐2‐yl)quinolin‐2‐amines. These molecules are fluorescent and hence for proper understanding of optical behaviour, solvatochromic and DFT studies were carried out. Also, the optical and energy bandgaps were calculated. Molecular docking studies manifested the strong binding affinities by these compounds at the active site of the Candida albicans dihydrofolate reductase enzyme (PDB ID: 1AI9) and Novobiocin (PDB ID: 4URO) with excellent C‐score values. Antimicrobial activity screening results have shown remarkable activity against Escherichia coli with appreciable MIC values and hence noteworthy action has been demonstrated against this bacterium. The zones of inhibition for some of the target compounds are also good against gram positive Staphylococcus aureus exhibiting excellent activity.

Antimicrobial activity and phytoconstituents screening of noxious invasive alien plants, Ageratina adenophora and Chromolaena odorata from Mizoram, a part of Indo-Burma biodiversity hotspot in India

Antimicrobial activity and phytoconstituents screening of noxious invasive alien plants, Ageratina adenophora and Chromolaena odorata from Mizoram, a part of Indo-Burma biodiversity hotspot in India

New Evidence for Artemisia absinthium as an Alternative to Classical Antibiotics: Chemical Analysis of Phenolic Compounds, Screening for Antimicrobial Activity.

Artemisia absinthium, an important herb of the Artemisia genus, was evaluated in this study for its potential as an alternative to classical antibiotics. The antimicrobial activity of methanol extracts of A. absinthium (MEAA) was evaluated using the broth microdilution method, revealing that A. absinthium exhibited broad-spectrum antibacterial and antifungal activity. Ultra-performance liquid chromatography-quadrupole-time of flight mass spectrometry (UPLC-Q-TOF-MS) was used to analyze the chemical profile of the MEAA, with a focus on flavonoids, quinic acids, and glucaric acids. A total of 90 compounds were identified, 69 of which were described for the first time in A. absinthium. Additionally, a new class of caffeoyl methyl glucaric acids was identified. The main active compounds were quantified and screened for antimicrobial activity. A. absinthium was found to be rich in quinic acids and flavonoids. The screening for antimicrobial activity also revealed that salicylic acid, caffeic acid, casticin, and 3,4-dicaffeoylquinic acid had varying degrees of antimicrobial activity. The acute toxicity of MEAA was examined following OECD guidelines. The administration of 5000 mg/kg bw of MEAA did not result in mortality in male and female mice. Furthermore, there were no observed effects on the visceral organs or general behavior of the mice, demonstrating the good safety of MEAA. This study provides new evidence for the use of A. absinthium as an alternative to classical antibiotics in addressing the problem of bacterial resistance.

Streptomyces marispadix sp. nov., isolated from marine beach sediment.

A novel actinomycetal strain, designated M600PL45_2T, was isolated from marine sediments obtained from Ingleses beach, Porto, on the Northern Coast of Portugal and was subjected to a polyphasic taxonomic characterisation study. The here described Gram-reaction-positive strain is characterised by the production of a brown pigment in both solid and liquid medium and forms typical helical hyphae that differentiate into smooth spores. The results of a phylogenetic analysis based on the 16S rRNA gene sequence indicated that M600PL45_2T has a high similarity to two members of the genus Streptomyces, Streptomyces bathyalis ASO4wetT (98.51 %) and Streptomyces daqingensis NEAU ZJC8T (98.44 %). The genome of M600PL45_2T has a size of 6 695 159 bp, a DNA G+C content of 70.71 mol% and 5538 coding sequences. M600PL45_2T grows at 15-37 °C and with a maximal growth rate between 25 °C and 30 °C. Growth at pH 6.0 to 9.0 with the optimal range between 6.0 and 7.5 was observed. M600PL45_2T showed a high salinity tolerance, growing with 0-10 % (w/v) NaCl, with best growth with 1-3% (w/v) NaCl. Major cellular fatty acids are iso-C15:0 (25.03 %), anteiso-C15:0 (17.70) and iso-C16:0 (26.90 %). The novel isolate was able to grow in media containing a variety of nitrogen and carbon sources. An antimicrobial activity screening indicated that an extract of M600PL45_2T has inhibitory activity against Staphylococcus aureus. On the basis of the polyphasic data, M600PL45_2T (= CECT 30365T = DSM 114036T) is introduced as the type strain of a novel species, that we named Streptomyces marispadix sp. nov.

Screening for Antimicrobial Activities and Enzymatic Activities Production of Some Actinomycetes spp. Isolated from different Soil Samples from Hilla Province

One hundered and fifty soil samples were collected from different city of Babylon /Iraq. Thirty-three Actinomycetes isolates were obtained, purified and identified according to morphological properties and biochemical tests. All isolates were tested for their antimicrobial activities and screened for production of some important enzymes such as amylase, catalase, protease, cellulase and lipase. The results obtained that 13 isolated have such potential and all 13 isolates have amylase activity. The most active isolates in production of study enzymes were KO-AG18, HI-SA24 and KO-RS27. Most 13 Actinomycetes isolates were showed antimicrobial against some Gram -positive bacteria (Staphylococcus albus, Staphylococcus aureus and Streptococcus pyogenes) and Gram- negative (Klebsella pneumoniae, Escherichia coli, , Serratia marcescens, Pseudomonas aeruginosa and Aeromonas hydrophila due to inhibition zone diameter (mm) ranged from 4-37 against gram negative and from 6- 37 against gram positive bacteria.

Synthesis of novel glycosyl thiadiazole triazines and screening for antimicrobial activity

Synthesis of novel glycosyl thiadiazole triazines and screening for antimicrobial activity

Phytochemical screening and evaluation of antioxidant, anti-inflammatory, antimicrobial, and membrane-stabilizing activities of different fractional extracts of Grewia nervosa (Lour.) Panigrahi

BackgroundGrewia nervosa (Lour.) Panigrahi, a medicinal herb native to the steep forested region of Bangladesh, is utilized as a treatment for a variety of diseases or conditions, including dysmenorrhea, paratyphoid, bone fractures, jaundice, kidney stones, dyspepsia, heat stroke, cold, fever, diarrhea, hepatitis B, ingestion, and anthelmintic medication. This research aims to investigate the phyto-pharmacological qualities of this herb. MethodsThe herb was extracted using absolute ethanol followed by fractionation with n-hexane and chloroform. Following an initial investigation of phytochemicals, antioxidant, anti-inflammatory, antimicrobial, and membrane stabilization activities were assessed using the DPPH, egg albumin model, disc diffusion method, and erythrocyte hemolysis model, respectively. ResultsA preliminary phytochemical report suggests that G. nervosa contains reducing sugars, gums, amides, alkaloids, glycosides, flavonoids, steroids, tannins, flavonoids, and saponins. In a concentration-dependent approach, its fractional extracts displayed promising antioxidant, anti-inflammatory, antimicrobial, and membrane-stabilizing activity. It was seen that all fractions had a statistically significant capacity to prevent RBCs from hemolyzing, which suggests a potent membrane stabilizing function in-vitro. ConclusionTaken together, G. nervosa possesses important secondary metabolites and exhibits in-vitro antioxidant, anti-inflammatory, antimicrobial, and membrane stabilizing capacities. This endorses the conventional usage of G. nervosa, although additional study is needed on this potentially beneficial plant.