Phytochemical Screening, Antimicrobial and Antioxidant Activities of Aloe buettneri, Mitracarpus scaber and Hannoa undulata used in Togolese Cosmetopoeia
Abstract
Background: Aloe buettneri, Mitracarpus scaber and Hannoa undulata are three plants species used in the Togolese traditional medicine to cure dermatosis. This study aims at assessing their anti-oxidant and anti-microbial activities on acne-developing micro-organisms.
Methods: Six micro-organisms including Cutibacterium acnes ATCC 6919, Pseudomonas aeruginosa ATCC 27853; Escherichia coli ATCC 25922; Klebsiella pneumoniae ATCC 700603; Staphylococcus aureus ATCC 29213; and Candida albicans ATCC 35659 were used. Inhibition diameter was assessed using the agar well diffusion method. Minimum inhibitory and minimum microbicidal concentrations have been achieved through the liquid dilution method. Anti-oxidant activities were evaluated by DPPH antiradical scaving and FRAP methods. Phytochemical screening was also realized.
Results: All the microorganism’s strains tested, excepted Candida albicans and Escherichia coli, were susceptible to plants extracts at 250 mg/mL in the agar well diffusion assay with inhibition diameters ranging from 12.10 ± 0.07 to 18.20 ± 0.10 mm. The MICs values were comprised between 15.625 mg/mL and 62.5 mg/mL, when MMCs ranged from 31.25 to 125 mg/mL. At the concentration of 500 µg/mL, the scavenging properties on DPPH radicals were 49.20 ± 0.15% for H. undulata, 41.29 ± 0.51% for A. buettneri, 59.57 ± 0.41% for M. scaber and 87.22 ± 0.03% for Quercetin. For FRAP assay, the effective concentration (EC50) of A. buettneri, M. scaber and H. undulata extracts were 977.44 ± 1.13 µg/mL; 267.74 ± 10.13 µg/mL and, 272.54 ± 12.87 µg/mL respectively while quercetin presented the EC50 of 48.63 ± 2.00 µg/mL. The antimicrobial and antioxidant activities of these species might be required to the presence of polyphenols, tannins, flavonoids, triterpenes, saponoside and alkaloids identified by phytochemical screening.
Conclusion: The three plants extracts are all potential natural antimicrobial and antioxidant candidates for treating acne vulgaris.
Keywords: Aloe buettneri, Mitracarpus scaber, Hannoa undulata, antimicrobial activity, antioxidant activity, phytochemical screening, Acne vulgaris
Keywords:
Aloe buettneri, Mitracarpus scaber, Hannoa undulata, antimicrobial activity, antioxidant activity, phytochemical screening, Acne vulgarisDOI
https://doi.org/10.22270/jddt.v12i2-S.5409References
Vos T, Flaxman AD, Naghavi M, et al. Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. The lancet. 2012; 380(9859):2163-2196. https://doi.org/10.1016/S0140-6736(12)61729-2
Sevimli Dikicier B. Topical treatment of acne vulgaris: efficiency, side effects, and adherence rate. Journal of International Medical Research. 2019; 47(7):2987-2992. https://doi.org/10.1177/0300060519847367
Zouboulis CC. Endocrinology and immunology of acne: Two sides of the same coin. Experimental Dermatology. 2020; 29(9):840-859. https://doi.org/10.1111/exd.14172
Sarici G, Cinar S, Armutcu F, Altınyazar C, Koca R, Tekin N. Oxidative stress in acne vulgaris. Journal of the European Academy of Dermatology and Venereology. 2010; 24(7):763-767. https://doi.org/10.1111/j.1468-3083.2009.03505.x
Sahib AS, Al-Anbari HH, Raghif ARA. Oxidative stress in acne vulgaris: an important therapeutic target. Journal of Molecular Pathophysiology. 2013; 2(1):27-31. https://doi.org/10.5455/jmp.20130127102901
Grange PA, Chéreau C, Raingeaud J, et al. Production of superoxide anions by keratinocytes initiates P. acnes-induced inflammation of the skin. PLoS Pathog. 2009; 5(7): e1000527. https://doi.org/10.1371/journal.ppat.1000527
Aubin G, Portillo M, Trampuz A, Corvec S. Propionibacterium acnes, an emerging pathogen: from acne to implant-infections, from phylotype to resistance. Medecine et maladies infectieuses. 2014; 44(6):241-250. https://doi.org/10.1016/j.medmal.2014.02.004
Varghese A. Acne vulgaris and antimicrobial resistance: a review. Reviews in Medical Microbiology. 2020; 31(3):150-154. https://doi.org/10.1097/MRM.0000000000000209
Kistowska M, Gehrke S, Jankovic D, et al. IL-1β drives inflammatory responses to propionibacterium acnes in vitro and in vivo. Journal of Investigative Dermatology. 2014; 134(3):677-685. https://doi.org/10.1038/jid.2013.438
Zouboulis C, Eady A, Philpott M, et al. What is the pathogenesis of acne? Experimental dermatology. 2005; 14(2):143-143. https://doi.org/10.1111/j.0906-6705.2005.0285a.x
Li Cx, You Zx, Lin Yx, Liu Hy, Su J. Skin microbiome differences relate to the grade of acne vulgaris. The Journal of dermatology. 2019; 46(9):787-790. https://doi.org/10.1111/1346-8138.14952
Kumar B, Pathak R, Mary PB, Jha D, Sardana K, Gautam HK. New insights into acne pathogenesis: exploring the role of acne-associated microbial populations. Dermatologica sinica. 2016; 34(2):67-73. https://doi.org/10.1016/j.dsi.2015.12.004
Hall JB, Cong Z, Imamura-Kawasawa Y, et al. Isolation and identification of the follicular microbiome: implications for acne research. Journal of Investigative Dermatology. 2018; 138(9):2033-2040. https://doi.org/10.1016/j.jid.2018.02.038
Chanda S, Baravalia Y. Screening of some plant extracts against some skin diseases caused by oxidative stress and microorganisms. African Journal of Biotechnology. 2010; 9(21):3210-3217.
de Rodriguez DJ, Angulo-Sanchez JL, da Silva JAT, Aguilar-Gonzalez CN. Review of Aloe species' medicinal properties and bioactive compounds. Floriculture, ornamental and plant biotechnology. 2006; 460-471.
Metowogo K, Amégnona A, Messanvi G, Kwashie E-G. Antioxidant and gastric antisecretory properties of hydoalcoholic extract of Aloe buettneri A. Berger (Lilliaceae). Pharmacopée et médecine traditionnelle africaine. 2012; 16.
Metowogo K, Agbonon A, Eklu-Gadegbeku K, Aklikokou A, Gbeassor M. Anti-ulcer and anti-inflammatory effects of hydroalcohol extract of Aloe buettneri A. Berger (Lilliaceae). Tropical journal of pharmaceutical research. 2008; 7(1):907-912. https://doi.org/10.4314/tjpr.v7i1.14676
Metowogo K, Eklu-Gadegbeku K, Agbonon A, Aklikokou KA, Gbeassor M. Gastroprotective effect of hydroalcoholic extract of Aloe buettneri. Iranian journal of pharmaceutical research: IJPR. 2011; 10(1):69.
Ouadja B, Anani K, Djeri B, Ameyapoh Y, Karou D. Evaluation of the phytochemical composition, antimicrobial and anti-radical activities of Mitracarpus scaber (Rubiaceae). Journal of Medicinal Plants Research. 2018; 12(28):493-499. https://doi.org/10.5897/JMPR2018.6631
Tettegah M, Eklu-Kadegbeku K, Aklikokou AK, Agbonon A, De Souza C, Gbeassor M. Infected wound healing and antimicrobial effects of Chenopodium ambrosioides and Mitracarpus scaber. International Journal of Biological and Chemical Sciences. 2009; 3(3). https://doi.org/10.4314/ijbcs.v3i3.45329
Adesanwo J, Aiyelaagbe O, Moronkola D. Antimicrobial and cytotoxic activity of the stem and root bark extracts of Quassia undulata and isolated constituents. Toxicological & Environmental Chemistry. 2009; 91(5):999-1003. https://doi.org/10.1080/02772240802614606
Fankibe N, Metowogo K, Kantati YT, et al. Phytochemical screening and antimicrobial activities of hydroethanolic extracts from leaves and roots of Cochlospermum planchonii (Bixaceae). Journal of Pharmacognosy and Phytotherapy. 2020; 12(4):94-101. https://doi.org/10.5897/JPP2020.0591
Motto AE, Lawson-Evi P, Bakoma B, Eklu-Gadegbeku K, Aklikokou K. Antihyperlipidemic and antioxidant properties of hydro-alcoholic extracts from Anogeissus leiocarpus (Combretaceae). Heliyon. 2021; 7(4): e06648. https://doi.org/10.1016/j.heliyon.2021.e06648
Kpemissi M, Eklu-Gadegbeku K, Veerapur VP, et al. Nephroprotective activity of Combretum micranthum G. Don in cisplatin induced nephrotoxicity in rats: In-vitro, in-vivo and in-silico experiments. Biomedicine & Pharmacotherapy. 2019; 116:108961 https://doi.org/10.1016/j.biopha.2019.108961
Karou D, Dicko MH, Simpore J, Traore AS. Antioxidant and antibacterial activities of polyphenols from ethnomedicinal plants of Burkina Faso. African journal of biotechnology. 2005; 4(8):823-828.
De Souza C, Ameganvi K, Koumaglo K, Gbeassor M. Etude de l'activité antimicrobienne des extraits aqueux totaux de dix plantes médicinales. Revue de Médecines et Pharmacopées Africaines. 1993; 2(7):107-115.
Mohammed MJ, Anand U, Altemimi AB, Tripathi V, Guo Y, Pratap-Singh A. Phenolic Composition, Antioxidant Capacity and Antibacterial Activity of White Wormwood (Artemisia herba-alba). Plants. 2021; 10(1):164. https://doi.org/10.3390/plants10010164
Basak PY, Gultekin F, Kilinc I. The role of the antioxidative defense system in papulopustular acne. The Journal of dermatology. 2001; 28(3):123-127. https://doi.org/10.1111/j.1346-8138.2001.tb00105.x
Baghel SS, Shrivastava N, Baghel RS, Agrawal P, Rajput S. A review of quercetin: antioxidant and anticancer properties. World J Pharm Pharmaceutical Sci. 2012; 1(1):146-160.
Olszowy M. What is responsible for antioxidant properties of polyphenolic compounds from plants? Plant Physiology and Biochemistry. 2019; 144:135-143. https://doi.org/10.1016/j.plaphy.2019.09.039
Otlewska A, Baran W, Batycka-Baran A. Adverse events related to topical drug treatments for acne vulgaris. Expert Opinion on Drug Safety. 2020/04/02 2020; 19(4):513-521. https://doi.org/10.1080/14740338.2020.1757646
Patel DJ, Bhatia N. Oral Antibiotics for Acne. American Journal of Clinical Dermatology. 2020; 1-12.
Qin M, Landriscina A, Rosen JM, et al. Nitric oxide-releasing nanoparticles prevent Propionibacterium acnes-induced inflammation by both clearing the organism and inhibiting microbial stimulation of the innate immune response. Journal of Investigative Dermatology. 2015; 135(11):2723-2731. https://doi.org/10.1038/jid.2015.277
Bouarab Chibane L, Degraeve P, Ferhout H, Bouajila J, Oulahal N. Plant antimicrobial polyphenols as potential natural food preservatives. Journal of the Science of Food and Agriculture. 2019; 99(4):1457-1474. https://doi.org/10.1002/jsfa.9357
Daglia M. Polyphenols as antimicrobial agents. Current opinion in biotechnology. 2012; 23(2):174-181. https://doi.org/10.1016/j.copbio.2011.08.007
Cristani M, D'Arrigo M, Mandalari G, et al. Interaction of four monoterpenes contained in essential oils with model membranes: implications for their antibacterial activity. Journal of agricultural and food chemistry. 2007; 55(15):6300-6308. https://doi.org/10.1021/jf070094x
O'Rourke A, Beyhan S, Choi Y, et al. Mechanism-of-action classification of antibiotics by global transcriptome profiling. Antimicrobial agents and chemotherapy. 2020; 64(3). https://doi.org/10.1128/AAC.01207-19
Published
Abstract Display: 792
PDF Downloads: 777
PDF Downloads: 64 How to Cite
Issue
Section
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0). that allows others to share the work with an acknowledgment of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgment of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).

.