Introduction
Foodborne diseases resulting from bacterial contamination during food processing or consumption of spoilt food are a common cause of illness and death especially in developing countries [
1,
2]. Common foodborne pathogenic bacteria such as
Escherichia coli, Bacillus cereus, Listeria monocytogenes Salmonella Typhi, and
Staphylococcus aureus among others have been well-documented to produce toxins that result in a diverse range of disease conditions [
3]. Incidences of community foodborne disease outbreaks are frequently reported in low and middle-income countries, with children being the most vulnerable [
4]. Food preservation plays a critical role in the control of foodborne diseases. However, the conventional use of chemicals as preservatives has been faulted as possessing a harmful effect on human health [
5,
6,
7]. Likewise, the treatment of infectious disease conditions with a commercial antibiotic has proven less effective due to the increasing incidence of antimicrobial resistance [
8]. Conventional medications are also relatively expensive for treatment in low and medium-income economies [
9]. These combined concerns have prompted the intense research and development of alternatives for food preservation and treatment of foodborne diseases. Several emerging methods have been developed. Of these, the traditional plant-based approach to foodborne disease treatments, food preservation, and packaging has received great attention for safety, antimicrobial efficiency, and biodegradability [
2,
10,
11]. In addition to its inexpensive cost and accessibility, it, therefore, remains plausible to consider ethnomedicinal plants as a potential source of antimicrobials for food preservation and treatment of foodborne diseases.
Guava (
Psidium guajava L.) is a common fruit tree that grows in several tropical and subtropical parts of the world. It is widely valued because of its edible fruit and its leaves [
12,
13]. Guava leaves are used traditionally for the treatment of several ailments around the world. In West Africa, the leaves are utilised as a key recipe in herbal preparation for the treatment of malaria which is endemic to the region. It is reported to contain phytochemicals such as flavonoids, carotenoids, and polyphenols among others [
14]. Quercetin has been isolated as one of the major compounds in the leaves [
15]. The ethnobotanical use and bioactivity of Guava leaves include but are not limited to wound healing, antidiabetic, as cough sedative, anti-inflammatory etc. [
16]. The twig of the Guava plant is popularly used as a chewing stick in Western Nigeria which is used in cleaning by brushing against the teeth and gum [
17]. The use of this local chewing stick and extracts has been reported to reduce the presence of tartar/dental plaque formation on the tooth. Hence the investigation of the extracts for its antibacterial activities, especially it pertains to oral health [
18]. As a result of the potentials of the different Guava parts, the leaves
, and stem bark have been the focus of several antimicrobial studies. Due to its relative antibacterial activity, the Guava plant has the potential to serve as a plant-based alternative for food preservation and the treatment of disease conditions resulting from food poisoning. However, there is yet to be an exhaustive study comparing the bioactivity of the plant extract based on polarity. It has been documented that most parts of a plant can contain natural bioactive constituents, likewise, the polarity of extracts could significantly influence its activity. The constituent of some plant phytochemicals can complicate and buffer the activity of others. Therefore, the aim of this study was to employ the use of liquid-liquid fractionation to investigate the comparative antibacterial activity of the crude extracts of Guava leaves and bark against selected food isolates;
Escherichia coli, Pseudomonas aeruginosa, Streptococcus pneumonia,
Bacillus cereus and
Staphylococcus aureus.
Materials and Methods
Plant Material
Psidium guajava leaves and stem bark were harvested from Guava trees at the Orchard Garden, Landmark University, Omu-aran, Kwara State (8°07’30.9”N; 5°04’53.8”E). The plant samples were rinsed under running tap water. Part of the collected fresh leaves were stored at 4°C and the remaining plant sample air dried. The dried materials were pulverised with an electric blender and stored in a labelled air-tight container priorl use.
Qualitative Phytochemical Screening
Test for phytochemicals in crude
Psidium guajava leaves and stem bark extract was analysed for saponins, tannins, phenols, flavonoids, terpenoids and steroids using standard protocols [
21,
22] as guide to the procedure adopted.
Organisms Used in Study
The test bacteria used in this experimental study were isolated from food samples. They were identified by morphological, cultural, and biochemical characteristics. The list of isolates include; two strains of Gram negative (Escherichia coli, and Pseudomonas aeruginosa) and three strains of Gram positive (Staphylococcus aureus, Streptococcus pneumonia and Bacillus cereus) bacteria. Fresh culture of each isolates was utilized in assessing antibacterial activity of the Guava leaf and stem bark crude extracts.
Statistical Analysis
Result of zones of inhibition was analysed using IBM-SPSS Statistics version 26 (IBM Corp., USA) software and reported as mean ± standard deviation (p < 0.05).
Results
The results of qualitative phytochemical screening analysis of Guava leaf and stem bark extracts are presented in
Table 1. All the extracts were present for Tannin, Phenol, Flavonoid, and Terpenoids. Saponin was present in the aqueous leaf extract and the stem bark aqueous and acetone extract but was absent in the leaf ethanol and acetone extracts. The stem bark showed the absence of Steroids. However, steroids was present in the leaf extracts excluding acetone leaf extract.
The antibacterial activity of the fractions from
Psidium guajava leaves and stem bark against
E. coli (29.0 ± 1.0 mm to 14.0 ± 1.0 mm) is shown in
Table 2 compared to the standard antibiotics Ciprofloxacin (53.0 ± 1.0mm). Based on zone of inhibition, the widest inhibition diameter was reported for Ethyl Acetate fraction of Stem bark acetone extract at 29.0 ± 1.0 mm, followed by 23.5 ± 1.5 mm in n-Hexane fraction of Fresh leaf aqueous extract and 21.0 ± 1.0 mm in Ethyl Acetate faction of Dried Leave ethanol extract. The least activity was reported for Ethyl Acetate fraction Fresh leaf aqueous extract (14.0 ± 1.0 mm).
Test of fractionated crude extract from
Psidium guajava leaves and stem bark against
P. aeruginosa is shown in
Table 3, with activity ranging from 34.0 ± 1.0 mm to 13.5 ± 1.5 mm. n-Hexane fraction of dried leaf acetone extract had the largest zone of inhibition (34.0 ± 1.0 mm). Stem bark acetone extract had activity at 27.5 ± 2.5 mm for its aqueous fraction and 26.1 ± 1.00 mm for ethyl acetate fraction. The water fraction of the dried leave aqueous extract was least in zone of inhibition at 13.5 ± 1.5 mm.
Results of inhibitory activity of fractions from Guava (
Psidium guajava) leaves and stem bark crude extracts and against
Streptococcus pneumonia ranged from 27.5 ± 1.5 mm to 11.5 ± 0.5 mm, where the control Ciproflaxin was 41.5 ± 1.5 mm. Ethyl Acetate fraction of Dried leaf ethanol extract and Stem bark acetone extract showed antibacterial activity against
Streptococcus pneumonia at 27.5 ± 1.5 mm and 27.0 ± 1.0 mm respectively (
Table 4). The ethyl acetate and aqueous fractions for dried leaf acetone extract both exhibited activity at 21.0 ± 1.0 mm against
Streptococcus pneumonia. The least activity (11.5 ± 0.5 mm) was recorded for the n-Hexane fraction of Fresh leaf aqueous extract.
The antibacterial activity of the fraction of crude extracts from
Psidium guajava against
Bacillus cereus ranged from 29.0 ± 1.0 mm to 12.0 ± 1.0 mm, with the control (Ciprofloxain) 59.0 ± 1.0 mm (
Table 5). Ethyl acetate fraction from Stem bark acetone extract showed the highest inhibition against
Bacillus cereus at 29.0 ± 1.0 mm. Stem bark aqueous extract was 24.5 ± 0.5 mm and fractions of dried leaf ethanol extract at 24.0 ± 1.0 mm. The lowest activity was in the aqueous fraction of fresh leave aqueous extract (12.0 ± 1.0 mm).
The range of inhibition of fractions from
Psidium guajava leaves and stem bark crude extracts was from 19.5 ± 0.5 mm to 30.0 ± 1.0 mm against
Staphylococcus aureus. The control antibiotic was 43.5 ± 0.5 mm in zone of inhibition (
Table 6). The widest zone of inhibition was observed in the aqueous fraction of Stem bark acetone extract (30.0 ± 1.0 mm). Aqueous fractions of dried leaf Ethanol and acetone extract show inhibition at 29.5 ± 0.5 mm and 26.5 ± 0.5 mm respectively. The lowest activity was reported for the aqueous fraction of dried leaf aqueous extract at 19.5 ± 0.5 mm.
Discussion
According to the WHO, Traditional Medicine Strategy (2014-2023), traditional medicine has continued to play a vital role in the treatment and management of diseases, especially in primary health care [
24,
25]. Therefore medicinal plants are continuously being sourced from the environment and prepared into herbal products. Different techniques are employed in this preparation, which includes but not limited to maceration, infusion, decoction, hot steam extraction among others [
26]. For efficiency in plant extraction and yield; increasing the surface area of solvent and sample is important. The solvent type also has a complementary effect on the combination of active ingredients to be extracted [
27].
This study reports on the presence of phytochemicals containing the active component of the plant extract. The choice of extraction solvent was based on availability, sustainable utilisation and report of prior antibacterial activity from other studies [
28,
29,
30]. Water is polar and is commonly used in traditional settings for the extraction of plant bioactive components in the treatment of disease conditions. Ethanol and Acetone are solvents of mid-polarity. While ethanol is cheap and likewise commonly used similarly as water in folk medicine, studies have reported acetone to be capable of isolating antimicrobial compounds with high activity. Acetone as a solvent also has an advantage of easy removal from solution compared to water and ethanol [
31,
32]. Likewise
, acetone has been reported to be nontoxic to bioassay systems and generally have high antimicrobial activities in several studies, [
33]. Results from this study’s qualitative phytochemical screening showed a wide range of compounds present in both
Psidium guajava leaf and stem bark (
Table 1). This included Tanin, Phenol, Flavonoid and Terpenoid, this is consistent to other reports [
34]. However, absence of Saponin in Leaf ethanol and acetone extract shows effect of solvent polarity on the type of phytocompound extracted. Likewise, both extracts from the stem bark for aqueous and acetone was absent for Steroids. Liquid-liquid fraction is a technique for partitioning the range of compounds in a mixture based on polarity [
35]. During the fractions of the crude extracts from
Psidium guajava leaf and stem bark, choice of solvent was based on polarity. n-Hexane is a non polar solvent, regularly used for the defatting process of plant extracts. Ethyl acetate is a mid polar solvent and has the capacity to elute compounds in its mid polarity range. The liquid liquid fractionation process therefore resulted in varying amount of fractions except in the stem bark aqueous extract, where the n-Hexane and ethyl acetate fraction did not result in any yield.
Food contamination may pose a great threat to the human population, especially in cases resulting from infectious diseases and food poisoning [
36]. In this study the antibacterial potential of different fractions of
Psidium guajava leaf and stem bark extracts was assessed against five (5) isolates from food sources. The isolates included
Escherichia coli, Pseudomonas aeruginosa, Streptococcus pneumonia,
Bacillus cereus and
Staphylococcus aureus. The ethyl acetate and aqueous fractions from the stem bark of acetone extract generally showed better antimicrobial activity compared with other extracts from leaves. For
Bacillus cereus and Streptococcus pneumonia which are both gram positive bacteria and
Escherichia coli (gram positive), the ethyl acetate fraction of the stem bark of acetone extract showed the most potent activity. While the aqueous fraction of acetone extract was most inhibitory for
Staphylococcus aureus (gram positive). This shows that phytocompounds in the stem bark has a validated potential mechanisms of antimicrobial activity against both gram positive and negative bacteria. In the leaf extracts, n-Hexane fraction from dried leaf acetone extract showed highest activity for
Pseudomonas aeruginosa (gram negative). In this study, acetone extracts generally gave a higher anti-microbial activity. Nevertheless, all fractions of the extracts showed considerable bioactivity against the test bacteria isolates. The present study in addition has demonstrated the importance of the extratcted fractions in optimising bioactivity.
Conclusions
This study shows the potential of identifying novel antibacterial agent from
Psidium guajava leaf and stem bark, while optimising its potential application for treatment in traditional medicine. In the light of latest trends in plant natural products research and development, green synthesis of nanoparticles from guava stem and leaves could aid increase antibacterial activity, for food security, sustainable agriculture and in treatment regimen, [
37,
38,
39]. Following the Sixty-second
World Health Assembly-WHA resolution on Traditional Medicine (WHA62.13) for safety purposes; it is advocated that toxicological analysis be performed on the extraced fractions in dose dependent manner. Further work is suggested to isolate antibacterial compounds and characterize them from the fractions especially the stem bark and analyse same for their therapeutic and optimal development into food and pharmaceutical products.
Funding
There was no specific grant received for this research work.
Conflicts of Interest
The authors declare that no conflict of interest exists in respect of this study.
References
- Dawwam, G.E.; Al-Shemy, M.T.; El-Demerdash, A.S. Green synthesis of cellulose nanocrystal/ZnO bio-nanocomposites exerting antibacterial activity and downregulating virulence toxigenic genes of food-poisoning bacteria. Sci Rep 2022, 12, 16848. [Google Scholar] [CrossRef] [PubMed]
- Yassin, M.T.; Abdel-Fattah Mostafa, A.; Al-Askar, A.A.; Alkhelaif, A.S. In vitro antimicrobial potency of Elettaria cardamomum ethanolic extract against multidrug resistant of food poisoning bacterial strains. J King Saud Univ - Sci 2022, 34, 102167. [Google Scholar] [CrossRef]
- Takó, M.; Kerekes, E.B.; Zambrano, C.; Kotogán, A.; Papp, T.; et al. Plant Phenolics and Phenolic-Enriched Extracts as Antimicrobial Agents against Food-Contaminating Microorganisms. Antioxidants 2020, 9, 165. [Google Scholar] [CrossRef] [PubMed]
- Cissé, G. Food-borne and water-borne diseases under climate change in low- and middle-income countries: Further efforts needed for reducing environmental health exposure risks. Acta Trop 2019, 194, 181–188. [Google Scholar] [CrossRef]
- Abd El-Hack, M.E.; El-Shall, N.A.; El-Kasrawy, N.I.; El-Saadony, M.T.; Shafi, M.E.; et al. The use of black pepper (Piper guineense) as an ecofriendly antimicrobial agent to fight foodborne microorganisms. Environ Sci Pollut Res 2022, 29, 10894–10907. [Google Scholar] [CrossRef]
- Petrova, P.; Arsov, A.; Tsvetanova, F.; Parvanova-Mancheva, T.; Vasileva, E.; et al. The Complex Role of Lactic Acid Bacteria in Food Detoxification. Nutrients 2022, 14, 2038. [Google Scholar] [CrossRef] [PubMed]
- Wu, F.; Rodricks, J.V. Forty Years of Food Safety Risk Assessment: A History and Analysis. Risk Anal 2020, 40, 2218–2230. [Google Scholar] [CrossRef] [PubMed]
- Laxminarayan, R.; Van Boeckel, T.; Frost, I.; Kariuki, S.; Khan, E.A.; et al. The Lancet Infectious Diseases Commission on antimicrobial resistance: 6 years later. Lancet Infect Dis 2020, 20, e51–e60. [Google Scholar] [CrossRef] [PubMed]
- Cameron, A.; Ewen, M.; Ross-Degnan, D.; Ball, D.; Laing, R. Medicine prices, availability, and affordability in 36 developing and middle-income countries: a secondary analysis. The Lancet 2009, 373, 240–249. [Google Scholar] [CrossRef] [PubMed]
- Jafarzadeh, S.; Jafari, S.M.; Salehabadi, A.; Nafchi, A.M.; Uthaya Kumar, U.S.; et al. Biodegradable green packaging with antimicrobial functions based on the bioactive compounds from tropical plants and their by-products. Trends Food Sci Technol 2020, 100, 262–277. [Google Scholar] [CrossRef]
- Salanță, L.C.; Cropotova, J. An Update on Effectiveness and Practicability of Plant Essential Oils in the Food Industry. Plants 2022, 11, 2488. [Google Scholar] [CrossRef]
- Angulo-López, J.E.; Flores-Gallegos, A.C.; Torres-León, C.; Ramírez-Guzmán, K.N.; Martínez, G.A.; et al. Guava (Psidium guajava L.) Fruit and Valorization of Industrialization By-Products. Processes 2021, 9, 1075. [Google Scholar] [CrossRef]
- Rajan, S.; Hudedamani, U. Genetic Resources of Guava: Importance, Uses and Prospects. In: Rajasekharan PE, Rao VR (editors). Conservation and Utilization of Horticultural Genetic Resources. Singapore: Springer. pp. 363–383. [CrossRef]
- Akkawi, M.; Abu-Lafi, S.; Abouremeleh, Q.; Lutgen, P. Screening of guava (Psidium guajava) leaves extracts against β-hematin formation. 9. Epub ahead of print 4 February 2021. [CrossRef]
- Naseer, S.; Hussain, S.; Naeem, N.; Pervaiz, M.; Rahman, M. The phytochemistry and medicinal value of Psidium guajava (guava). Clin Phytoscience 2018, 4, 32. [Google Scholar] [CrossRef]
- Kumar, M.; Tomar, M.; Amarowicz, R.; Saurabh, V.; Maheshwari, C.; et al. Guava (Psidium guajava L.) Leaves: Nutritional Composition, Phytochemical Profile, and Health-Promoting Bioactivities. Foods. Epub ahead of print 1 April 2021. [CrossRef]
- Kapoor, S.; Gandhi, N.; Kapoor, A. Guava (Psidium guajava). In: Nayik GA, Gull A (editors). Antioxidants in Fruits: Properties and Health Benefits. Singapore: Springer. pp. 227–249. [CrossRef]
- Hassan, S.A.; Metwalli, N.E.; Ibrahim, G.G.; Aly, M.A. Comparison of the efficacy of mouth rinses camellia sinensis extract, guava leaves extract and sodium fluoride solution, on Streptococcus mutans and Lactobacillus in children (an in vivo study). Future Dent J. Epub ahead of print 27 November 2018. [CrossRef]
- Dada, E.O.; Ekundayo, F.O.; Makanjuola, O.O. Antibacterial Activities of Jatropha curcas (LINN) on Coliforms Isolated from Surface Waters in Akure, Nigeria. Int J Biomed Sci IJBS 2014, 10, 25–30. [Google Scholar] [PubMed]
- Quintanilla-Licea, R.; Gomez-Flores, R.; Samaniego-Escamilla, M.Á.; Hernández-Martínez, H.C.; Tamez-Guerra, P.; et al. Cytotoxic Effect of Methanol Extracts and Partitions of Two Mexican Desert Plants against the Murine Lymphoma L5178Y-R. Am J Plant Sci 2016, 7, 1521–1530. [Google Scholar] [CrossRef]
- Izuegbuna, O.; Otunola, G.; Bradley, G. Chemical composition, antioxidant, anti-inflammatory, and cytotoxic activities of Opuntia stricta cladodes. PLOS ONE 2019, 14, e0209682. [Google Scholar] [CrossRef] [PubMed]
- Owolabi, A.; Ndako, J.; Owa, S.; Oluyori, A.; Oludipe, E.; et al. Antibacterial and Phytochemical Potentials of Ficus capensis Leaf Extracts Against Some Pathogenic Bacteria. Epub ahead of print 5 April 2022. [CrossRef]
- Noel, D.; Wain, J.; Lar, P. Use of Vitex doniana (black plum) and Abutilon hirtum (Florida keys) extracts as an integral part of phytomedicine in tackling multidrug-resistant Salmonella. J Infect Dev Ctries 2022, 16, 1323–1328. [Google Scholar] [CrossRef] [PubMed]
- Liu, C. Overview on development of ASEAN traditional and herbal medicines. Chin Herb Med 2021, 13, 441–450. [Google Scholar] [CrossRef]
- Savatagi, S.B.; Srinivas, P.N.; Payyappallimana, U. Factors influencing the emergence of self-reliance in primary health care using traditional medicine: A scoping review. Indian J Public Health 2022, 66, 214. [Google Scholar] [CrossRef]
- Manousi, N.; Sarakatsianos, I.; Samanidou, V. 10 - Extraction Techniques of Phenolic Compounds and Other Bioactive Compounds From Medicinal and Aromatic Plants. In: Grumezescu AM, Holban AM (editors). Engineering Tools in the Beverage Industry. Woodhead Publishing. pp. 283–314. [CrossRef]
- Chuo, S.C.; Nasir, H.M.; Mohd-Setapar, S.H.; Mohamed, S.F.; Ahmad, A.; et al. A Glimpse into the Extraction Methods of Active Compounds from Plants. Crit Rev Anal Chem 2022, 52, 667–696. [Google Scholar] [CrossRef] [PubMed]
- Mehmood, A.; Javid, S.; Khan, M.F.; Ahmad, K.S.; Mustafa, A. In vitro total phenolics, total flavonoids, antioxidant and antibacterial activities of selected medicinal plants using different solvent systems. BMC Chem 2022, 16, 64. [Google Scholar] [CrossRef] [PubMed]
- Patra, A.; Abdullah, S.; Pradhan, R.C. Review on the extraction of bioactive compounds and characterization of fruit industry by-products. Bioresour Bioprocess 2022, 9, 14. [Google Scholar] [CrossRef]
- Rezaei, M.; Ghasemi Pirbalouti, A. Phytochemical, antioxidant and antibacterial properties of extracts from two spice herbs under different extraction solvents. J Food Meas Charact 2019, 13, 2470–2480. [Google Scholar] [CrossRef]
- Eloff, J.N. Avoiding pitfalls in determining antimicrobial activity of plant extracts and publishing the results. BMC Complement Altern Med 2019, 19, 106. [Google Scholar] [CrossRef]
- Karaaslan, M.A.; Cho, M.; Liu, L.-Y.; Wang, H.; Renneckar, S. Refining the Properties of Softwood Kraft Lignin with Acetone: Effect of Solvent Fractionation on the Thermomechanical Behavior of Electrospun Fibers. ACS Sustain Chem Eng 2021, 9, 458–470. [Google Scholar] [CrossRef]
- Famuyide, I.M.; Aro, A.O.; Fasina, F.O.; Eloff, J.N.; McGaw, L.J. Antibacterial and antibiofilm activity of acetone leaf extracts of nine under-investigated south African Eugenia and Syzygium (Myrtaceae) species and their selectivity indices. BMC Complement Altern Med 2019, 19, 141. [Google Scholar] [CrossRef]
- Yahaya, A.; Ali, M.; EL-Hassan, F.I.; Jido, B.A. Antibacterial activity of guava (Psidium guajava l.) extracts on Staphylococcus aureus isolated from patients with urinary tract infections attending a tertiary-care hospital. Sci World J 2019, 14, 47–51. [Google Scholar]
- Ho, K.L.; Tan, C.G.; Yong, P.H.; Wang, C.W.; Lim, S.H.; et al. Extraction of phytochemicals with health benefit from Peperomia pellucida (L.) Kunth through liquid-liquid partitioning. J Appl Res Med Aromat Plants 2022, 30, 100392. [Google Scholar] [CrossRef]
- Garvey, M. Food pollution: a comprehensive review of chemical and biological sources of food contamination and impact on human health. Nutrire 2019, 44, 1. [Google Scholar] [CrossRef]
- Jiang, Y.; Zhou, P.; Zhang, P.; Adeel, M.; Shakoor, N.; et al. Green synthesis of metal-based nanoparticles for sustainable agriculture. Environ Pollut 2022, 309, 119755. [Google Scholar] [CrossRef] [PubMed]
- Qamer, S.; Romli, M.H.; Che-Hamzah, F.; Misni, N.; Joseph, N.M.S.; et al. Systematic Review on Biosynthesis of Silver Nanoparticles and Antibacterial Activities: Application and Theoretical Perspectives. Molecules 2021, 26, 5057. [Google Scholar] [CrossRef] [PubMed]
- Vieira, I.R.S.; de Carvalho, A.P.A.; de Conte-Junior, C.A. Recent advances in biobased and biodegradable polymer nanocomposites, nanoparticles, and natural antioxidants for antibacterial and antioxidant food packaging applications. Compr Rev Food Sci Food Saf 2022, 21, 3673–3716. [Google Scholar] [CrossRef] [PubMed]
Table 1.
Qualitative analysis of Guava (Psidium guajava) leaf and stem bark extracts.
Table 1.
Qualitative analysis of Guava (Psidium guajava) leaf and stem bark extracts.
Phytochemicals |
Leaf extract |
Stem bark extract |
Aq |
EtOH |
Ace |
Aq |
Ace |
Saponin |
+ |
- |
- |
+ |
+ |
Tannin |
+ |
+ |
+ |
+ |
+ |
Phenol |
+ |
+ |
+ |
+ |
+ |
Flavonoid |
+ |
+ |
+ |
+ |
+ |
Terpenoid |
+ |
+ |
+ |
+ |
+ |
Steroids |
+ |
+ |
- |
- |
- |
Table 2.
Antibacterial activity of Fractions from Guava (Psidium guajava) leaves and stem bark crude extracts and against Escherichia coli.
Table 2.
Antibacterial activity of Fractions from Guava (Psidium guajava) leaves and stem bark crude extracts and against Escherichia coli.
Crude Extract |
Fractions (100 mg/mL) |
n-Hexane |
Ethyl Acetate |
Water |
Dried Leaves |
Aq |
16.5 ± 1.5 |
18.0 ± 1.0 |
19.5 ± 0.5 |
EtOH |
20.0 ± 2.0 |
21.0 ± 1.0 |
15.5 ± 0.5 |
Ace |
20.5 ± 1.5 |
19.5 ± 0.5 |
17.0 ± 1.0 |
Fresh Leaves |
Aq |
23.5 ± 1.5 |
14.0 ± 1.0 |
16.5 ± 1.5 |
Stem Bark |
Aq |
- |
- |
17.0 ± 1.0 |
Ace |
16.5 ± 1.5 |
29.0 ± 1.0 |
17.0 ± 1.0 |
Ciprofloxacin (Control) |
53.0 ± 1.0 |
53.0 ± 1.0 |
53.0 ± 1.0 |
Table 3.
Antibacterial activity of Fractions from Guava (Psidium guajava) leaves and stem bark crude extracts and against Pseudomonas aeruginosa.
Table 3.
Antibacterial activity of Fractions from Guava (Psidium guajava) leaves and stem bark crude extracts and against Pseudomonas aeruginosa.
Crude Extract |
Fractions (100 mg/mL) |
n-Hexane |
Ethyl Acetate |
Water |
Dried Leaves |
Aq |
20.0 ± 0.0 |
15.5 ± 1.5 |
13.5 ± 1.5 |
EtOH |
19.0 ± 1.0 |
24.0 ± 1.0 |
17.0 ± 0.0 |
Ace |
34.0 ± 1.0 |
24.0 ± 1.0 |
16.5 ± 1.5 |
Fresh Leaves |
Aq |
23.5 ± 1.5 |
11.5 ± 0.5 |
14.0 ± 1.0 |
Stem Bark |
Aq |
- |
- |
19.0 ± 1.0 |
Ace |
15.0 ± 1.0 |
26.0 ± 1.0 |
27.5 ± 2.5 |
Ciprofloxacin (Control) |
51.0 ± 1.5 |
51.0 ± 1.5 |
51.0 ± 1.5 |
Table 4.
Antibacterial activity of Fractions from Guava (Psidium guajava) leaves and stem bark crude extracts and against Streptococcus pneumonia.
Table 4.
Antibacterial activity of Fractions from Guava (Psidium guajava) leaves and stem bark crude extracts and against Streptococcus pneumonia.
Crude Extract |
Fractions (100 mg/mL) |
n-Hexane |
Ethyl Acetate |
Water |
Dried Leaves |
Aq |
12.0 ± 1.0 |
16.5 ± 1.5 |
21.0 ± 1.0 |
EtOH |
13.5 ± 0.5 |
27.5 ± 1.5 |
25.5 ± 3.5 |
Ace |
16.5 ± 0.5 |
26.0 ± 1.0 |
26.0 ± 1.0 |
Fresh Leaves |
Aq |
11.5 ± 0.5 |
21.0 ± 1.0 |
24.0 ± 0.0 |
Stem Bark |
Aq |
- |
- |
22.5 ± 0.5 |
Ace |
19.5 ± 0.5 |
27.0 ± 1.0 |
24.5 ± 0.5 |
Ciprofloxacin (Control) |
41.5 ± 1.5 |
41.5 ± 1.5 |
41.5 ± 1.5 |
Table 5.
Antibacterial activity of Fractions from Guava (Psidium guajava) leaves and stem bark crude extracts and against Bacillus cereus.
Table 5.
Antibacterial activity of Fractions from Guava (Psidium guajava) leaves and stem bark crude extracts and against Bacillus cereus.
Crude Extract |
Fractions (100 mg/mL) |
n-Hexane |
Ethyl Acetate |
Water |
Dried Leaves |
Aq |
13.0 ± 1.0 |
23.0 ± 1.0 |
17.0 ± 1.0 |
EtOH |
23.0 ± 1.5 |
20.5 ± 0.5 |
24.0 ± 1.0 |
Ace |
16.0 ± 1.0 |
19.5 ± 0.5 |
23.0 ± 1.0 |
Fresh Leaves |
Aq |
19.5 ± 0.5 |
20.0 ± 2.0 |
12.0 ± 1.0 |
Stem Bark |
Aq |
- |
- |
24.5 ± 0.5 |
Ace |
16.5 ± 1.5 |
29.0 ± 1.0 |
23.5 ± 1.5 |
Ciprofloxacin (Control) |
59.0 ± 1.0 |
59.0 ± 1.0 |
59.0 ± 1.0 |
Table 6.
Antibacterial activity of Fractions from Guava (Psidium guajava) leaves and stem bark crude extracts and against Staphylococcus aureus.
Table 6.
Antibacterial activity of Fractions from Guava (Psidium guajava) leaves and stem bark crude extracts and against Staphylococcus aureus.
Crude Extract |
Fractions (100 mg/mL) |
n-Hexane |
Ethyl Acetate |
Water |
Dried Leaves |
Aq |
22.0 ± 1.0 |
21.5 ± 1.5 |
19.5 ± 0.5 |
EtOH |
20.5 ± 0.5 |
25.0 ± 1.0 |
29.5 ± 0.5 |
Ace |
22.0 ± 1.0 |
23.0 ± 0.0 |
26.5 ± 0.5 |
Fresh Leaves |
Aq |
24.5 ± 0.5 |
21.0 ± 2.0 |
23.0 ± 2.0 |
Stem Bark |
Aq |
- |
- |
20.5 ± 0.5 |
Ace |
22.0 ± 2.0 |
26.0 ± 1.0 |
30.0 ± 1.0 |
Ciprofloxacin (Control) |
43.5 ± 0.5 |
43.5 ± 0.5 |
43.5 ± 0.5 |
|
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).