Research article

Antimicrobial activity of Ziziphus mauritiana and Acacia nilotica against multidrug-resistant Escherichia coli and Klebsiella pneumoniae

  • Received: 07 May 2025 Revised: 12 July 2025 Accepted: 21 July 2025 Published: 04 August 2025
  • Multidrug-resistant (MDR) strains such as Escherichia coli and Klebsiella pneumoniae, resistant to broad-spectrum antibiotics, are a modern global issue. Plant extracts offer promising antimicrobial activity for such pathogens. This study evaluated the efficacy of aqueous and hydro-ethanolic extracts from leaves and bark of two cheaply and easily available plants, i.e., Ziziphus mauritiana (ber) and Acacia nilotica (gum Arabic or Kikar), against MDR E. coli and K. pneumoniae. Antibiotic susceptibility testing confirmed resistance in both strains to all tested antibiotics (ampicillin, ciprofloxacin, streptomycin, and tetracycline), with inhibition zones ≤ 10 mm. Antimicrobial assays revealed that hydro-ethanolic extracts of Z. mauritiana leaves exhibited the highest activity, with inhibition zones of 20 mm (E. coli) and 19 mm (K. pneumoniae) at 100 mg/mL, outperforming aqueous extracts. The minimum inhibitory concentration (MIC) for all the tested extracts was notably low (6 mg/mL for E. coli and K. pneumoniae). Growth curve analysis demonstrated significant suppression of bacterial proliferation by all extracts at MIC, with optical density (OD600) values remaining below 0.25 over 24 h compared to controls (OD600 ≥ 2.20). Additionally, biofilm formation was completely inhibited at MIC as well as sub-inhibitory concentrations (sub-MIC) of ½ MIC, highlighting that the antibiofilm activity of these extracts is not due to antimicrobial activity. Findings highlight the efficacy of extracts from different parts and solvents against MDR pathogens, suggesting their potential as an adjunct therapy. Findings suggest that hydro-ethanolic extracts perform significantly better than aqueous extracts, while no significant difference in antimicrobial activity was found in extracts from different parts of plants. Lastly, it was found that Z. mauritiana extracts have greater antimicrobial potential than A. nilotica extracts.

    Citation: Abdul Rafay Rafiq, Areeba Ameen. Antimicrobial activity of Ziziphus mauritiana and Acacia nilotica against multidrug-resistant Escherichia coli and Klebsiella pneumoniae[J]. AIMS Molecular Science, 2025, 12(3): 234-254. doi: 10.3934/molsci.2025015

    Related Papers:

  • Multidrug-resistant (MDR) strains such as Escherichia coli and Klebsiella pneumoniae, resistant to broad-spectrum antibiotics, are a modern global issue. Plant extracts offer promising antimicrobial activity for such pathogens. This study evaluated the efficacy of aqueous and hydro-ethanolic extracts from leaves and bark of two cheaply and easily available plants, i.e., Ziziphus mauritiana (ber) and Acacia nilotica (gum Arabic or Kikar), against MDR E. coli and K. pneumoniae. Antibiotic susceptibility testing confirmed resistance in both strains to all tested antibiotics (ampicillin, ciprofloxacin, streptomycin, and tetracycline), with inhibition zones ≤ 10 mm. Antimicrobial assays revealed that hydro-ethanolic extracts of Z. mauritiana leaves exhibited the highest activity, with inhibition zones of 20 mm (E. coli) and 19 mm (K. pneumoniae) at 100 mg/mL, outperforming aqueous extracts. The minimum inhibitory concentration (MIC) for all the tested extracts was notably low (6 mg/mL for E. coli and K. pneumoniae). Growth curve analysis demonstrated significant suppression of bacterial proliferation by all extracts at MIC, with optical density (OD600) values remaining below 0.25 over 24 h compared to controls (OD600 ≥ 2.20). Additionally, biofilm formation was completely inhibited at MIC as well as sub-inhibitory concentrations (sub-MIC) of ½ MIC, highlighting that the antibiofilm activity of these extracts is not due to antimicrobial activity. Findings highlight the efficacy of extracts from different parts and solvents against MDR pathogens, suggesting their potential as an adjunct therapy. Findings suggest that hydro-ethanolic extracts perform significantly better than aqueous extracts, while no significant difference in antimicrobial activity was found in extracts from different parts of plants. Lastly, it was found that Z. mauritiana extracts have greater antimicrobial potential than A. nilotica extracts.



    加载中

    Acknowledgments



    The authors received no funding for this research. However, equipment was provided by the laboratories of the given affiliations.

    Conflict of interest



    The authors declare they have no conflict interest in this paper.

    [1] Azwanida NN (2015) A Review on the Extraction Methods Use in Medicinal Plants, Principle, Strength and Limitation. Med Aromat Plants 4.
    [2] Manning SD, Motiwala AS, Springman AC, et al. (2008) Variation in virulence among clades of Escherichia coli O157:H7 associated with disease outbreaks. Proc Natl Acad Sci USA 105: 4868-4873. https://doi.org/10.1073/pnas.0710834105
    [3] Malabadi RB, Sadiya MR, Kolkar KP, et al. (2024) Pathogenic Escherichia coli (E. coli) food borne outbreak: Detection methods and controlling measures. Magna Sci Adv Res Rev 10: 052-085. https://doi.org/10.30574/msarr.2024.10.1.0003
    [4] Kathayat D, Lokesh D, Ranjit S, et al. (2021) Avian pathogenic Escherichia coli (APEC): An overview of virulence and pathogenesis factors, zoonotic potential, and control strategies. Pathogens 10: 467. https://doi.org/10.3390/pathogens10040467
    [5] Li Y, Li J, Hu T, et al. (2020) Five-year change of prevalence and risk factors for infection and mortality of carbapenem-resistant Klebsiella pneumoniae bloodstream infection in a tertiary hospital in North China. Antimicrob Resist Infect Control 9. https://doi.org/10.1186/s13756-020-00728-3
    [6] Di Domenico EG, Cavallo I, Sivori F, et al. (2020) Biofilm production by carbapenem-resistant Klebsiella pneumoniae significantly increases the risk of death in oncological patients. Front Cell Infect Microbiol 10: 561741. https://doi.org/10.3389/fcimb.2020.561741
    [7] Chassagne F, Samarakoon T, Porras G, et al. (2021) A systematic review of plants with antibacterial activities: A taxonomic and phylogenetic perspective. Front Pharmacol 11: 586548. https://doi.org/10.3389/fphar.2020.586548
    [8] O'Brien CJ, Campbell S, Young A, et al. (2023) Chinee apple (Ziziphus mauritiana): A comprehensive review of its weediness, ecological impacts and management approaches. Plants 12: 3213. https://doi.org/10.3390/plants12183213
    [9] Nigussie D, Davey G, Legesse BA, et al. (2021) Antibacterial activity of methanol extracts of the leaves of three medicinal plants against selected bacteria isolated from wounds of lymphoedema patients. BMC Complement Med Ther 21: 2. https://doi.org/10.1186/s12906-020-03183-0
    [10] Hussain SZ, Naseer B, Qadri T, et al. (2021) Ber/Jujube (Ziziphus mauritiana): Morphology, taxonomy, vomposition and health benefits. Fruits grown in highland regions of the Himalayas . Cham: Springer 157-168. https://doi.org/10.1007/978-3-030-75502-7_12
    [11] Astari RY, Winarsih S, Handayani D, et al. (2025) In silico analysis of Ziziphus mauritiana Lam. bioactive compounds targeting GABA receptor and ADMET profiles for potential postpartum depression treatment. J Pharm Pharmacogn Res 13: S118-S128. https://doi.org/10.56499/jppres24.2239_13.s1.118
    [12] San AMM, Thongpraditchote S, Sithisarn P, et al. (2013) Total phenolics and total flavonoids contents and hypnotic effect in mice of Ziziphus mauritiana Lam. seed extract. Evid-Based Compl Altern Med 2013: 1-4. https://doi.org/10.1155/2013/835854
    [13] Hafez LO, Brito-Casillas Y, Abdelmageed N, et al. (2024) The Acacia (Vachellia nilotica (L.) P.J.H. Hurter & Mabb.): Traditional uses and recent advances on its pharmacological attributes and potential activities. Nutrients 16: 4278-4278. https://doi.org/10.3390/nu16244278
    [14] Omer Abdalla K (2021) Biochemistry, medicinal properties & toxicity of Acacia nilotica fruits. Biomed Res Clin Rev 3: 1-6. https://doi.org/10.31579/2692-9406/040
    [15] Abbasian K, Asgarpanah J, Ziarati P (2015) Chemical composition profile of Acacia Nilotica seed growing wild in south of Iran. Orient J Chem 31: 2. http://doi.org/10.13005/ojc/310251
    [16] Aliero AA, Musa I, Manga SS (2023) Antimicrobial activities of bioactive compounds isolated from Acacia nilotica against multi-drug resistant bacteria. Microbes and Infectious Diseases . In press
    [17] Kumari S, Swer TL (2025) Acacia nilotica Linn: A comprehensive review of its nutritional profile, pharmacological activities, and food applications. Phytochem Rev . http://doi.org/10.1007/s11101-025-10128-3
    [18] Nawaz Z, Zahoor MK, et al. (2019) Molecular identification of blaCTX-M and blaTEM genes among multi-drug resistant Enteropathogenic Escherichia coli isolated from children. Pak J Pharm Sci 32: 1215-1218.
    [19] Siddique MH, Aslam B, Imran M, et al. (2020) Effect of silver nanoparticles on biofilm formation and EPS production of multidrug-resistant Klebsiella pneumoniae. BioMed Res Int 2020: 6398165. https://doi.org/10.1155/2020/6398165
    [20] Macwilliams MP, Liao M (2006) Luria Broth (LB) and Luria Agar (LA) media and their uses protocol. American Society for Microbiology : 1-4. Available from: https://asm.org/getattachment/5d82aa34-b514-4d85-8af3-aeabe6402874/LB-Luria-Agar-protocol-
    [21] Alarjani KM, Skalicky M (2021) Antimicrobial resistance profile of Staphylococcus aureus and its in-vitro potential inhibition efficiency. J Infect Public Heal 14: 1796-1801. https://doi.org/10.1016/j.jiph.2021.10.018
    [22] Lonsway DR (2023) Preparation of routine media and reagents used in antimicrobial susceptibility testing. ClinMicroNow . https://doi.org/10.1002/9781683670438.cmph0082
    [23] Åhman J, Matuschek E, Kahlmeter G (2022) Evaluation of ten brands of pre-poured Mueller-Hinton agar plates for EUCAST disc diffusion testing. Clin Microbiol Infec 28: 1499.e1-1499.e5. https://doi.org/10.1016/j.cmi.2022.05.030
    [24] Tamma PD, Harris PNA, Mathers AJ, et al. (2022) Breaking down the breakpoints: Rationale for the 2022 clinical and laboratory standards institute revised piperacillin-tazobactam breakpoints against Enterobacterales. Clin Infect Dis 77: 1585-1590. https://doi.org/10.1093/cid/ciac688
    [25] Sampath Kumar NS, Sarbon NM, Rana SS, et al. (2021) Extraction of bioactive compounds from Psidium guajava leaves and its utilization in preparation of jellies. AMB Expr 11: 36. https://doi.org/10.1186/s13568-021-01194-9
    [26] Farjana A, Zerin N, Kabir MS (2014) Antimicrobial activity of medicinal plant leaf extracts against pathogenic bacteria. Asian Pac J Trop Dis 4: S920-S923. https://doi.org/10.1016/s2222-1808(14)60758-1
    [27] Huang Y, Flint SH, Palmer JS (2021) The heat resistance of spores from biofilms of Bacillus cereus grown in tryptic soy broth and milk. Int Dairy J 123: 105169. https://doi.org/10.1016/j.idairyj.2021.105169
    [28] Klančnik A, Piskernik S, Jeršek B, et al. (2010) Evaluation of diffusion and dilution methods to determine the antibacterial activity of plant extracts. J Microbiol Meth 81: 121-126. https://doi.org/10.1016/j.mimet.2010.02.004
    [29] Liu L, Yu B, Sun W, et al. (2020) Calcineurin signaling pathway influences Aspergillus niger biofilm formation by affecting hydrophobicity and cell wall integrity. Biotechnol Biofuels 13: 54. https://doi.org/10.1186/s13068-020-01692-1
    [30] Wang L, Fan D, Chen W, et al. (2015) Bacterial growth, detachment and cell size control on polyethylene terephthalate surfaces. Sci Rep 5: 15159. https://doi.org/10.1038/srep15159
    [31] Haque MA, Imamura R, Brown GA, et al. (2017) An experiment-based model quantifying antimicrobial activity of silver nanoparticles on Escherichia coli. RSC Adv 7: 56173-56182. https://doi.org/10.1039/C7RA10495B
    [32] Welch BL (1947) The generalization of ‘student's’ problem when several different population varlances are involved. Biometrika 34: 28-35. https://doi.org/10.1093/biomet/34.1-2.28
    [33] Rai A, Tripathi AM, Saha S, et al. (2020) Comparison of antimicrobial efficacy of four different plant extracts against cariogenic bacteria: An in vitro study. Int J Clin Pediatr Dent 13: 361-367. https://doi.org/10.5005/jp-journals-10005-1796
    [34] Mehmood A, Javid S, Khan MF, et al. (2022) In vitro total phenolics, total flavonoids, antioxidant and antibacterial activities of selected medicinal plants using different solvent systems. BMC Chem 16: 64. https://doi.org/10.1186/s13065-022-00858-2
    [35] Okla MK, Alatar AA, Al-amri SS, et al. (2021) Antibacterial and antifungal activity of the extracts of different parts of Avicennia marina (Forssk.) Vierh. Plants 10: 252. https://doi.org/10.3390/plants10020252
    [36] Molehin OR, Adefegha SA (2014) Comparative study of the aqueous and ethanolic extract of Momordica foetida on the phenolic content and antioxidant properties. Int Food Res J 21: 401-405.
    [37] Rather LJ, Shahid-ul-Islam, Mohammad F (2015) Acacia nilotica (L.): A review of its traditional uses, phytochemistry, and pharmacology. Sustain Chem Pharm 2: 12-30. https://doi.org/10.1016/j.scp.2015.08.002
    [38] Riaz S, Faisal M, Hasnain S, et al. (2011) Antibacterial and cytotoxic activities of Acacia nilotica Lam (Mimosaceae) methanol extracts against extended spectrum beta-lactamase producing Escherichia coli and Klebsiella species. Trop J Pharm Res 10: 785-791. https://doi.org/10.4314/tjpr.v10i6.12
    [39] Yahia Y, Benabderrahim MA, Tlili N, et al. (2020) Bioactive compounds, antioxidant and antimicrobial activities of extracts from different plant parts of two Ziziphus Mill. species. PLOS ONE 15: e0232599. https://doi.org/10.1371/journal.pone.0232599
    [40] Abdelgader LMA, Zain THKM, Mahjaf GM (2024) Detection of antimicrobial activity of Acacia nilotica extract on gram-negative bacteria isolated from clinical specimens in Shendi Town, Sudan. Saudi J Pathol Microbiol 9: 254-259. https://doi.org/10.36348/sjpm.2024.v09i12.001
    [41] Sadiq MB, Tarning J, Cho TZA, et al. (2017) Antibacterial activities and possible modes of action of Acacia nilotica (L.) Del. against multidrug-resistant Escherichia coli and Salmonella. Molecules 22: 47. https://doi.org/10.3390/molecules22010047
    [42] Sharma AK, Kumar A, Yadav SK, et al. (2014) Studies on antimicrobial and immunomodulatory effects of hot aqueous extract of Acacia nilotica L. leaves against common veterinary pathogens. Vet Med Int 2014: 747042. https://doi.org/10.1155/2014/747042
    [43] Azhari N, Arbab MH, Khidir A, et al. (2024) Antibacterial activity of some medicinal plants against extended spectrum beta lactamase (ESBL) producing Escherichia coli and Klebsiella pneumonia in Khartoum State–Sudan. SVOA Microbiol 5: 136-142. https://doi.org/10.58624/svoamb.2024.05.051
    [44] Said Gulam Khan HB, Mohd Sarmin NI, Arzmi MH, et al. (2020) Antifungal activities of Ziziphus mauritiana against Candida albicans: In vitro study. Compend Oral Sci 7: 1-12. https://doi.org/10.24191/cos.v7i0.17489
    [45] Abalaka ME, Daniyan SY, Mann A (2010) Evaluation of the antimicrobial activities of two Ziziphus species (Ziziphus mauritiana L. and Ziziphus spinachristi L.) on some microbial pathogens. Afri J Pharm Pharmaco 4: 135-139.
    [46] Priyanka C, Kumar P, Bankar SP, et al. (2015) In vitro antibacterial activity and gas chromatography–mass spectroscopy analysis of Acacia karoo and Ziziphus mauritiana extracts. J Taibah Univ Sci 9: 13-19. https://doi.org/10.1016/j.jtusci.2014.06.007
    [47] Khairani H, Priyanto JA, Prastya ME, et al. (2025) Antibacterial activity of endophytic actinobacteria isolated from Ziziphus mauritiana against multidrug-resistant strains. Makara Journal of Science Makara Journal of Science 29: 10. https://doi.org/10.7454/mss.v29i1.2574
    [48] Ibrahim NL, Habibu UA, Idris AM (2024) Antibacterial efficacy of frozen and unfrozen Ziziphus mauritiana leaf extracts on selected clinical bacteria. Bayero J Pure Appl Sci 17: 94-102. http://doi.org/10.4314/bajopas.v17i1.13
    [49] Hammi KM, Essid R, Khadraoui N, et al. (2022) Antimicrobial, antioxidant and antileishmanial activities of Ziziphus lotus leaves. Arch Microbiol 204: 119. https://doi.org/10.1007/s00203-021-02733-5
    [50] Eslami G, Hashemi A, Yazdi MMK, et al. (2016) Antibacterial effects of Zataria multiflora, Ziziphus, Chamomile and Myrtus communis methanolic extracts on IMP-type metallo-beta-lactamase-producing Pseudomonas aeruginosa. Arch Clin Infect Dis 11: e32413. https://doi.org/10.5812/archcid.32413
    [51] Perović T, Lazović B, Adakalić M, et al. (2024) Insights into bioactivity guided chemical profiling of Ziziphus jujuba Mill. fruits wild-growing in Montenegro. Heliyon 11: e41361. https://doi.org/10.1016/j.heliyon.2024.e41361
    [52] Daneshmand F, H Zare-Zardini, B Tolueinia, et al. (2013) Crude extract from Ziziphus jujuba fruits, a weapon against pediatric infectious disease. Iran J Ped Hematol Oncol 3: 216-221.
    [53] Ambrin, Dastagir G, Bakht J, et al. (2020) Antimicrobial and phytochemical evaluation of Ziziphus mauritiana var. spontanea Edgew. and Oenothera biennis L. Pak J Zool 52. https://doi.org/10.17582/journal.pjz/20190428160433
    [54] Usman A, Ahmad M, Hamza MM, et al. (2023) Antimicrobial activity of Acacia nilotica and Ziziphus mauritiana against clinical isolates of Escherichia coli and Klebsiella a erogenes. UMYU J Microbiol Res 8: 1-7. https://doi.org/10.47430/ujmr.2382.001
    [55] Zou W, Hassan I, Akram B, et al. (2023) Validating interactions of pathogenic proteins of Staphylococcus aureus and E. coli with phytochemicals of Ziziphus jujube and Acacia nilotica. Microorganisms 11: 2450. https://doi.org/10.3390/microorganisms11102450
    [56] Abubakar AL, Dandare A, Abubakar IH, et al. (2018) Antimicrobial activities of Acacia nilotica, Ziziphus Jujube Linn and Lawsonia Inermis. Nigerian J Basic Appl Sci 26: 1-8. https://doi.org/10.5455/njbas.299969
    [57] Saidu Y, Muhammad SA, Abbas AY, et al. (2016) In vitro screening for protein tyrosine phosphatase 1B and dipeptidyl peptidase IV inhibitors from Nigerian medicinal plants. J Intercult Ethnopharmacol 6: 154-157. https://doi.org/10.5455/jice.20161219011346
    [58] Joshi T, Deepa PR, Joshi M, et al. (2023) Matters of the desert: A perspective on achieving food and nutrition security through plants of the (semi) arid regions. J Agric Food Res 14: 100725. https://doi.org/10.1016/j.jafr.2023.100725
    [59] Elamary RB, Albarakaty FM, Salem WM (2020) Efficacy of Acacia nilotica aqueous extract in treating biofilm-forming and multidrug resistant uropathogens isolated from patients with UTI syndrome. Sci Rep 10: 1125. https://doi.org/10.1038/s41598-020-67732-w
    [60] Moktan N, Gajbhiye RL, Sahithi TVVS, et al. (2024) Antibacterial and antibiofilm activities of extract and bioactive compounds from Bergenia ciliata (Haw.) Sternb. flowers against Streptococcus mutans through cell membrane damage. J Ethnopharmacol 339: 119144. https://doi.org/10.1016/j.jep.2024.119144
    [61] Yadav G, Meena M (2021) Bioprospecting of endophytes in medicinal plants of Thar Desert: An attractive resource for biopharmaceuticals. Biotechnol Rep 30: e00629. https://doi.org/10.1016/j.btre.2021.e00629
    [62] Febriza A, Faradiana S, Abdullah MF (2023) Antibacterial effects of Ziziphus mauritiana (Lam) leaf extract against Vibrio cholerae. Herb-Med J Terbitan Berkala Ilmiah Herbal Kedokteran dan Kesehatan 5: 3. https://doi.org/10.30595/hmj.v5i3.14307
    [63] Syafriza D, Hasanah U, Hidayatullah T, et al. (2024) Antibacterial assessment of Ziziphus mauritiana Lam on inhibition of the growth and biofilm of Streptococcus mutans. Dent J 57: 189-194. https://doi.org/10.20473/j.djmkg.v57.i3.p189-194
    [64] Li J, Shi Y, Song X, et al. (2025) Mechanisms of antimicrobial resistance in Klebsiella: Advances in detection methods and clinical implications. Infect Drug Resist : 1339-1354. https://doi.org/10.2147/idr.s509016
    [65] Rodríguez B, Pacheco L, Bernal I, et al. (2023) Mechanisms of action of flavonoids: Antioxidant, antibacterial and antifungal properties. Ciencia Ambiente y Clima 6: 33-66. https://doi.org/10.22206/cac.2023.v6i2.3021
    [66] Mulat M, Banicod RJS, Tabassum N, et al. (2025) Multiple strategies for the application of medicinal plant-derived bioactive compounds in controlling microbial biofilm and virulence properties. Antibiotics 14: 555. https://doi.org/10.3390/antibiotics14060555
    [67] Arip M, Selvaraja M, Mogana R, et al. (2022) Review on plant-based management in combating antimicrobial resistance—Mechanistic perspective. Front pharmacol 13: 879495. https://doi.org/10.3389/fphar.2022.879495
    [68] Barfour AF, Mensah AY, Asante-Kwatia E, et al. (2021) Antibacterial, antibiofilm, and efflux pump inhibitory properties of the crude extract and fractions from Acacia macrostachya stem bark. Sci World J 2021: 5381993. https://doi.org/10.1155/2021/5381993
    [69] Datta S, Singh V, Nag S, et al. (2024) Marine-derived cytosine arabinoside (Ara-C) inhibits biofilm formation by inhibiting PEL operon proteins (Pel A and Pel B) of Pseudomonas aeruginosa: An in-silico approach. Mol Biotechnol 67: 1924-1938. https://doi.org/10.1007/s12033-024-01169-8
    [70] Moulick S, Bera R, Roy DN (2025) Bactericidal action of ginger (Zingiber officinale Roscoe) extract against Escherichia coli through synergistic modulation of the AcrAB-TolC efflux pump and inhibition of peptidoglycan synthesis: In vitro and in silico approaches. Microb Pathogenesis 204: 107624. https://doi.org/10.1016/j.micpath.2025.107624
    [71] Samreen, Ahmad I (2025) Anti-infective synergy of Acacia nilotica bioactive fraction and methyl gallate with meropenem against pathogenicity of Pseudomonas aeruginosa. 3 Biotech 15: 209. https://doi.org/10.1007/s13205-025-04372-9
    [72] Owolarafe T, Lhegboro G, Salawu K, et al. (2022) Toxicological investigation of aqueous extract Zizphus mauritiana leaf on Wistar rat. Int J Tradit Complement Med Res 3: 91-100. https://doi.org/10.53811/ijtcmr.1056770
    [73] Alli LA, Adesokan AA, Salawu OA, et al. (2015) Toxicological studies of aqueous extract of Acacia nilotica root. Interdisciplinary Toxicol 8: 48-54. https://doi.org/10.1515/intox-2015-0005
    [74] Moulick S, Roy DN (2024) Bioflavonoid baicalein modulates tetracycline resistance by inhibiting efflux pump in Staphylococcus aureus. Micro Drug Resist 30: 363-371. https://doi.org/10.1089/mdr.2024.0099
    [75] Kumar P, Sharma DK, Farooqui NA (2024) Ziziphus mauritiana: A comprehensive review on ethnopharmacological, phytochemical and pharmacological properties. Int J Pharm Sci Rev Res 84: 62-70. https://doi.org/10.47583/ijpsrr.2024.v84i01.010
    [76] Ur Rehman N, Ansari MN, Ahmad W, et al. (2022) GC–MS analysis and in vivo and ex vivo antidiarrheal and antispasmodic effects of the methanolic extract of Acacia nilotica. Molecules 27: 2107. https://doi.org/10.3390/molecules27072107
    [77] Eiki N, Manyelo TG, Hassan ZM, et al. (2022) Phenolic composition of ten plants species used as ethnoveterinary medicines in Omusati and Kunene regions of Namibia. Sci Rep 12: 21135. https://doi.org/10.1038/s41598-022-25948-y
    [78] Gupta RC, Doss RB, Lall R, et al. (2019) Babool (Acacia nilotica). Nutraceuticals in veterinary medicine : 103-111. https://doi.org/10.1007/978-3-030-04624-8_8
    [79] El-Saber Batiha G, Akhtar N, Alsayegh AA, et al. (2022) Bioactive compounds, pharmacological actions, and pharmacokinetics of genus Acacia. Molecules 27: 7340. https://doi.org/10.3390/molecules27217340
  • molsci-12-03-015-s001.pdf
  • Reader Comments
  • © 2025 the Author(s), licensee AIMS Press. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0)
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

Metrics

Article views(1239) PDF downloads(59) Cited by(0)

Article outline

Figures and Tables

Figures(5)  /  Tables(3)

Other Articles By Authors

/

DownLoad:  Full-Size Img  PowerPoint
Return
Return

Catalog