Sciences of Phytochemistry
Volume 4 Issue 1
Showing 8 Articles
RESEARCH ARTICLE
- research article
Phytochemistry and GCMS Analysis of Ethanol and Aqueous Stembark Extracts of Detarium microcarpum Guill. & Perr. Fabaceae
Mubarak Muhammad Dahiru, Neksumi Musa, Enoch Buba Badgal
The therapeutic applications of medicinal plants in the treatment of various diseases can be attributed to their diverse phytochemical constituents. This study aimed to investigate the phytochemical composition of aqueous and ethanol stem bark extracts of Detarium microcarpum. Qualitative and quantitative analyses were conducted to determine the presence and concentrations of phytochemicals, followed by the identification of phytoconstituents using gas chromatography-mass spectrometry (GC-MS). The aqueous extract was found to contain saponins (27.11 ± 0.22%) and flavonoids (47.33 ± 0.70% ), with alkaloids, steroids, glycosides, and terpenoids absent. In contrast, the ethanol extract contained alkaloids (10.78 ± 0.59%), saponins (45.11 ± 0.48%), glycosides (5.44 ± 0.48%), and flavonoids (11.00 ± 0.77%), while steroids and terpenoids were not detected. GC-MS analysis revealed 14 compounds in the aqueous extract and 20 in the ethanol extract. The major constituents of the aqueous extract included hydroperoxide, 1,4-dioxan-2-yl (58.32%), 1,2,3-benzenetriol (16.44%), and cis-p-coumaric acid (11.05%). In the ethanol extract, the predominant compounds were coumarin (29.41%), benzofuran (17.23%), and catechol (9.23%). The identified compounds may serve as potential synthetic templates for the development of novel therapeutic agents targeting various diseases. This study supports the ethnomedicinal use of D. microcarpum and provides a scientific basis for its role in traditional medical practices.
Sciences of Phytochemistry
9 Jan 202511 pages - research article
GC-MS Profiling, In Vitro Antimalarial, and Antimicrobial activity of Ricinodendron heudelotii Seed Extracts
Vincent Oghenerobo Imieje, Lilian Nneoma Amafili
Malaria remains a significant public health challenge, particularly in sub-Saharan Africa, where the emergence of Plasmodium falciparum strains resistant to artemisinin-based combination therapies (ACTs) exacerbates the situation. This underscores the urgent need to identify novel, less toxic antimalarial compounds, particularly from natural sources. This study evaluated the in vitro antimalarial and antimicrobial activities of Ricinodendron heudelotii (RHD) seed extracts against Plasmodium falciparum (P. falciparum) and select pathogenic microorganisms using standard protocols. Seeds (250 g) were dried, ground, and extracted with n-hexane and dichloromethane, yielding RHD-HEX and RHD-DCM extracts, respectively. The oily extract (RHD-HEX) was analyzed via gas chromatography-mass spectrometry (GC-MS), revealing 26 phytoconstituents, including monoterpenes, fatty acids, and phytosterols. Antimalarial assays showed that RHD-HEX and RHD-DCM exhibited moderate activity (> 200 µg/mL) against the chloroquine-sensitive P. falciparum (D6 strain). Both extracts demonstrated stronger activity against the chloroquine-resistant W2 strain, with IC50 values of 30.29 and 33.48 µg/mL, respectively. Antimicrobial screening indicated moderate activity against tested pathogenic fungi and bacteria (IC50 > 200 µg/mL) compared to fluconazole and cefotaxime controls. Cytotoxicity against VERO cell lines was also assessed. The findings suggest that the phytoconstituents in RHD extracts may contribute to the observed antimalarial and antimicrobial effects, warranting further investigation.
Sciences of Phytochemistry
9 Jan 20258 pages - research article
In Vitro Bactericidal Activity of Bacopa Monnieri Leaf Extracts on Human Pathogenic Bacteria
Subba Tata Sape
The increasing resistance of bacteria to conventional antibiotics poses a global health challenge, emphasizing the urgent need to discover new antibacterial compounds to combat hard-to-treat infections. This study aims to evaluate the bactericidal activity of crude leaf extracts from the multi-medicinal plant Bacopa monnieri against six bacterial strains. The crude extracts, prepared at different concentrations (100, 200, and 300 µg/mL), were tested for efficacy using the agar well diffusion method. Among the tested extracts, the ethanol extract exhibited the highest bactericidal activity, followed by chloroform and hexane extracts. Notably, all three solvent extracts at 300 µg/mL were most effective against Staphylococcus aureus, with inhibition zones of 21.5 mm (ethanol), 16.12 mm (chloroform), and 10.3 mm (hexane). In contrast, the lowest antibacterial activity was observed against Proteus vulgaris, with inhibition zones of 15.3 mm (ethanol), 10.2 mm (chloroform), and 5.6 mm (hexane). These findings suggest that the ethanol extract of B. monnieri is a promising candidate for the development of novel antibacterial compounds.
Sciences of Phytochemistry
10 Feb 20256 pages 
research articlePhenolic Content and Antioxidant Activity of Colocasia esculenta in Commercial Herbal Products
Gumilar Adhi Nugroho, Yesi Desmiaty, Yati Sumiyati, Sandra Loretta Suherman, Helsa Lim
Taro (Colocasia esculenta L.) is a plant with a long history of use in traditional medicine in several countries worldwide. The corm of taro and two commercial products were analysed due to total phenolic, flavonoid, luteolin, and antioxidant properties. Taro corm was extracted with water and analysed for phytochemical screening, total flavonoids, total phenolic, luteolin, and antioxidant properties. The phytochemical screening of taro showed that it contains secondary metabolites of flavonoids, tannins, saponins, triterpenoids, and quinones. The results of the determination of total flavonoid content of taro extract, Product 1, and Product 2 capsule obtained 19.34 ± 0.26 mg QE/g extract, 18.58 ± 0.18 mg QE/g extract, and 16.29 ± 0.23 mg QE/g extract. The results of determining the total phenolic content of taro, Product 1, and Product 2 capsules obtained 39.75 ± 0.95 mg GAE/g extract, 38.46 ± 0.46 mg GAE/g extract, and 35.91 mg GAE/g extract. ± 0.82 mg GAE/g extract. The results of the determination of luteolin from taro, Product 1, and Product 2 capsules obtained 0.83 ± 0.05 %, 0.39 ± 0.04 %, and 0.18 ± 0.08 %. The results of the antioxidant activity test obtained IC50 of vitamin C of 4.6780 ± 0.0319 ppm, corm dry extract and ginger rhizome 141.2383 ± 3.4995 ppm and 97.6685 ± 7.8760 ppm, respectively, and capsule products 2; 126.0724 ± 1.3672 ppm. The water extract of corm and available products containing CE extract have met the quality standard parameters required for non-specific parameters, luteolin content, and antioxidant properties.
Sciences of Phytochemistry
14 Mar 20257 pages
research articleAntimicrobial Activity of Triterpenoid and Steroidal Cinnamates from Vitellaria paradoxa
Olusesan Ojo, Mokgadi P. Mphahlele, Edwin M. Mmutlane, Derek T. Ndinteh
Antimicrobial resistance (AMR) remains a global threat to human health, and its recent burden has necessitated an urgent need for new antibiotics to fight the growing negative impacts of AMR. Vitellaria paradoxa Gaertn. is a medicinal plant used to treat bacterial infections, including diarrhea, tuberculosis (TB), and other respiratory infections in Africa. This study, therefore, assessed the antimicrobial effect and the cytotoxicity of isolated secondary metabolites from the hexane extract of V. paradoxa stem-bark against a panel of bacterial pathogens. After cold maceration, the resulting extract was purified using column chromatography on silica gel. The resazurin-based 96-well plate micro-dilution method was used to assess the antimicrobial activity of the isolated compounds. On further assay, the MTT assay was used to evaluate the cytotoxic effect of compounds on the cervical cancer cell line (HeLa). The column fractionation led to the isolation of 11-hydroxy β-amyrin cinnamate (compound 1), α-amyrin cinnamate (compound 2), and sitosterol cinnamate (compound 3). All the compounds exhibited antibacterial activity against the tested pathogens, with minimum inhibitory concentration (MIC) ranging from 0.0625-1.0 mg/mL. Compound 3 showed the highest antibacterial activity against all bacterial strains (MICs; 0.0625-0.25 mg/mL). The compounds showed no remarkable cytotoxic properties (IC₅₀; 77.82 ± 10.5-82.53 ± 4.07). As far as we know, the results described the antimicrobial activities of compounds 1-3 for the first time. These results provide scientific justification for the traditional uses of V. paradoxa in treating bacterial infections. The highest antibacterial effect of compound 3 highlights its potential as a lead compound.
Sciences of Phytochemistry
13 Mar 20257 pages- research article
Phytochemical Composition and Antioxidant Properties of Dissotis erecta (Guill. & Perr.) Dandy Flowers
Basil Nse Ita, Godwin Ndarake Enin, Itoro Esiet Udo
Dissotis erecta is a shrubby herb belonging to the Melastomataceae family, commonly found in Nigeria. It is widely recognized for its diverse ethnomedicinal applications, including treating edema, diarrhea, stomach discomfort, and rheumatism. Alongside other plant parts, its flowers, rich in biologically active compounds, are valued for their aesthetic appeal and potential health benefits. This study assessed the antioxidant properties, total phenolic, total flavonoid, and bioactive contents of the methanolic extract of D. erecta flowers. The antioxidant properties were determined by the DPPH radical scavenging activity, ABTS radical scavenging activity, ferric reducing activity, and metal chelating assay. The extract demonstrated strong DPPH radical scavenging activity, ABTS radical scavenging activity, metal chelating ability, and reducing power, with IC50 values of 79.84 ± 0.64 µg/mL, 125.77 ± 2.64 µg/mL, 87.89 ± 0.91 µg/mL, and 71.71 ± 0.55 µg/mL, respectively. Phytocompounds such as alkaloids, sterols, and terpenoids were present in the flower extract, while phlobatanins and glycosides were absent. Total phenolic content was 57.47 ± 0.21 mg GAE/g, while total flavonoid content was 83.52 ± 0.31 mg QE/g. Gas chromatography-mass spectroscopy (GC-MS) analysis identified α-terpineol (86.53%), nerolidol (7.44%), campesterol (1.12%), and neocurdione (1.29%) as the predominant components. These findings indicate that D. erecta flowers contain a significant amount of phytocompounds with antioxidative properties that could potentially be useful in managing diseases related to oxidative stress.
Sciences of Phytochemistry
25 Apr 20259 pages - research article
Analgesic and Anti-Inflammatory Effects of Ethanol Leaf Extract of Guiera Senegalensis in Murine Models
Umar Abdulkadir Hassan, Jalilah Ibrahim Tahir, Comfort Foluwake Akanji, Abdulmutalib Adamu, Albashir Tahir
Pain and inflammation are global public health challenges, often requiring safer and more effective treatments. Medicinal plants like Guiera senegalensis have been traditionally used for pain and inflammatory conditions, but scientific validation of their therapeutic potential is limited. This study aimed to evaluate the analgesic and anti-inflammatory properties of ethanol leaf extract of G. senegalensis in murine models. Fresh G. senegalensis leaves were collected, authenticated, and subjected to ethanol extraction. Phytochemical analysis was conducted to identify bioactive compounds. Acute toxicity studies were performed following OECD guidelines. Analgesic effects were evaluated using the acetic acid-induced writhing test and the hot plate test, while the anti-inflammatory activity was assessed using the formalin-induced paw edema model. Phytochemical analysis revealed the presence of tannins, saponins, and flavonoids. Acute toxicity tests showed no mortality or severe adverse effects at 2000 mg/kg. The extract demonstrated dose-dependent analgesic activity, with 84% inhibition of writhing at doses of 25 mg/kg and 50 mg/kg, outperforming Diclofenac (59%). In the hot plate test, moderate central analgesic effects were observed. Anti-inflammatory tests showed significant reductions in paw edema at doses of 12.5 and 25 mg/kg, comparable to Diclofenac. Ethanol leaf extract of G. senegalensis exhibits significant analgesic and anti-inflammatory activities, likely mediated by its flavonoid, saponin, and tannin content. These findings support its traditional use and highlight its potential as a natural alternative for managing pain and inflammation.
Sciences of Phytochemistry
25 Apr 20256 pages - research article
Phytochemical and Antiplasmodial Studies of Methanol Extract from Aerial Parts of Scadoxus multiflorus
Akeem Ayodele Olaiya, Tawakaltu Omolara Tijani, Dauda Garba, Sakynah Musa Abdullahi, Ibrahim Mohammed Sule
Scadoxus multiflorus, a fleshy herbaceous plant with a large bulb, is traditionally used in ethno-medicine for managing malaria, treating ulcers, cardiotonic activity and stimulant in debility. This study aimed to conduct phytochemical screening and evaluate the antiplasmodial activity of its aerial parts. The plant material was extracted with methanol using maceration process, and the crude extract was partitioned into hexane, chloroform, ethyl acetate, and butanol fractions. Qualitative phytochemical screening revealed the presence of tannins, flavonoids, alkaloids, terpenoids, steroids, saponins, phenols, and cardiac glycosides in the crude extract and fractions. Quantitative analysis revealed that phenolic compounds were the most abundant in the crude extract (198.32 mg/g), while alkaloids were the least (51.14 mg/g). The n-hexane fraction, however, had the highest tannin content (215 mg/g). Acute toxicity testing, following OECD 2008 guidelines, showed that the median lethal dose (LD₅₀) was greater than 5000 mg/kg, indicating the extract's safety. Antiplasmodial activity was evaluated using both suppressive and curative models in Plasmodium berghei-infected albino mice. The extract at 1000 mg/kg significantly suppressed parasitemia by 58.8% in the early infection (suppressive test) and reduced parasitemia by 61.8% in the established infection (curative test). Chloroquine, the standard drug at 5 mg/kg, produced higher parasite suppression (84.52%) and curative effects (84.50%) compared to the extract. The results suggest that the methanol extract of S. multiflorus aerial parts possesses antiplasmodial activity, supporting its traditional use in malaria management.
Sciences of Phytochemistry
26 May 20257 pages
Journal Key Facts
Publishing Fee (APC)
No Charge
Open Access License
CC BY 4.0
Language
English
Overview
Sciences of Phytochemistry (Sci. Phytochem.) is an international, peer-reviewed journal published by ETFLIN, dedicated to advancing research in all aspects of phytochemistry and plant-derived bioactive compounds. The journal provides a platform for the dissemination of original research, reviews, and scientific communications that explore the chemistry, biological activities, and applications of natural products derived from plants. We welcome contributions that deepen the understanding of the chemical diversity of plants and their potential in pharmaceuticals, nutraceuticals, agriculture, cosmetics, and environmental sustainability.
Latest Articles
Recently published research articles, review papers, and technical notes from the current volume of the journal.
- research article
Phytochemical Screening and Antioxidant Activity of Mimosa tenuiflora (Willd. ) Poir Root Extracts.
Victor Wagner Barajas-Carrillo, Carlos Eduardo Covantes-Rosales, Valeria Estefanía Castrejón-Medina, Alexander Manuel Mendoza-Martínez, Saul Toledo, Adela Yolanda Bueno-Durán, Mercedes Zambrano-Soria, Karina Janice Guadalupe Díaz-Resendiz, Laura Janeth Díaz-Rubio, Iván Córdova-Guerrero
This study evaluated the phytochemical profile and antioxidant activity of extracts and partitions derived from the root of Mimosa tenuiflora (Willd. ) Poir. , also known as tepezcohuite. Three extracts were prepared through hydroalcoholic maceration, total alkaloid extraction, and Soxhlet extraction. Additionally, four partitions were obtained from the ethanolic extract using the modified Kupchan technique: n-hexane, dichloromethane, n-butanol, and water. Qualitative phytochemical screening showed the presence of alkaloids, tannins, flavonoids, saponins, steroids, triterpenoids, reducing sugars, coumarins, and cardiac glycosides in various several fractions, while no anthraquinone glycosides were detected. Antioxidant activity was assessed using DPPH and ABTS assays. In the DPPH assay, the most active fractions were the butanolic (EC50 = 2.20 ± 0.45 µg/mL) and the ethanolic (EC50 = 2.25 ± 0.01 µg/mL). While, in the ABTS assay, the ethanolic extract and butanol partition were the most active fractions with EC50 values of 4.87 ± 1.11 µg/mL and 5.43 ± 0.21 µg/mL respectively. The less polar fractions (n-hexane, Soxhlet) exhibited lower activity. This study expands the phytochemical knowledge of M. tenuiflora, focusing on its roots, an organ less extensively characterized than the bark regarding its comprehensive phytochemical and antioxidant profile. The results show that this organ is a promising source of bioactive metabolites with antioxidant capacity. This finding justifies further investigation into the pharmacological and therapeutic applications of these compounds, which is particularly relevant given that while previous research has systematically favored the bark, and existing root studies have focused primarily on specific alkaloids, comprehensive profiling remains limited.
Sciences of Phytochemistry
6 Apr 202612 pages - research article
A Computational Investigation of Cathinone, the Major Psychotropic Alkaloid from Muguka (a Cultivar of Catha edulis), Co-administered with Diazepam
Mohamed Said Rajab
Muguka, a high-cathinone cultivar of Catha edulis consumed widely in East Africa, presents a growing health risk when co-administered with diazepam. This theoretical study represents one of the first integrated computational investigations focusing on the interaction between Muguka derived cathinone and diazepam, combining molecular docking, ADMET profiling, and physiologically based pharmacokinetic (PBPK) modeling. The in silico analysis identified overlapping CYP2D6 and CYP2C19 pathways, supporting potential mutual metabolic inhibition. The predictive PBPK models suggest moderate CYP2D6/CYP2C19-mediated drug-drug interactions based on a simulated oral dose of 100 mg cathinone and 30 mg diazepam in a human adult population. Co-administration is predicted to increase cathinone systemic exposure by 1.5-fold (AUC ↑50%) and reduce clearance by 33%, while diazepam exposure is projected to rise by 1.3-fold (AUC ↑30%) with 24% clearance reduction. Molecular docking revealed high-affinity binding of cathinone (-6.4 kcal/mol) at the dopamine transporter (DAT) and diazepam (-6.8 kcal/mol) at the γ-aminobutyric acid-A (GABA-A) receptor, indicating distinct yet potentially complementary CNS targets. Collectively, these computational predictions suggest that co-use may prolong CNS exposure and theoretically enhance neurotoxicity, and dependence risk. This integrated computational framework provides a hypothetical mechanistic evidence for stimulant-benzodiazepine interactions and underscores the need for clinical monitoring and validation.
Sciences of Phytochemistry
25 Feb 20269 pages - research article
Phytochemical Analysis, Antinociceptive and Anti-inflammatory Activities of Mimusops elengi Bojer Leaf Extract-loaded Chitosan Nanoparticles in Albino Mice
Cletus Anes Ukwubile, Chidi Kaosi Clement
The present study evaluated the antinociceptive and anti-inflammatory activities of Mimusops elengi Bojer leaf extract encapsulated in chitosan nanoparticles (CS-NPs) using murine models, to determine whether nanoparticle formulation enhances the biological effects of a methanolic plant extract. Preliminary phytochemical screening was conducted using established qualitative colorimetric assays, which indicated the presence of major secondary metabolite classes, including phenolics and flavonoids; these tests were intended for compositional inference rather than definitive compound identification. Total phenolic and flavonoid contents were subsequently quantified using spectrophotometric methods, yielding 806.12 mg gallic acid equivalents (GAE)/g and 103.08 mg quercetin equivalents (QE)/g of extract, respectively. Antinociceptive activity was assessed using acetic acid–induced writhing and hot-plate assays, while anti-inflammatory effects were evaluated via the carrageenan-induced paw edema model. Animals treated with M. elengi–loaded CS-NPs exhibited statistically significant reductions in writhing responses, prolonged pain reaction latency, and decreased paw edema when compared with untreated controls and animals receiving the crude extract (p < 0.05). Inflammatory mediator analysis further demonstrated significant downregulation of pro-inflammatory cytokines (TNF-α, IL-1β, and PGE₂) alongside upregulation of anti-inflammatory cytokines (IL-10 and IL-22). Oxidative stress assessment showed reduced malondialdehyde (MDA) levels, indicating attenuation of lipid peroxidation. All experiments were conducted with appropriate replication, and data were subjected to statistical analysis to ensure reproducibility. While the phytochemical screening provides preliminary compositional insights, the observed pharmacological effects are attributed to the combined action of extract constituents and improved delivery via chitosan nanoparticles. Overall, the findings support the hypothesis that nanoparticle-based formulation can enhance the antinociceptive and anti-inflammatory efficacy of M. elengi leaf extract, highlighting its potential as a complementary therapeutic approach while underscoring the need for further compound-level characterization and safety evaluation.
Sciences of Phytochemistry
22 Jan 202613 pages - research article
Phytochemical Characterization and Evaluation of Antioxidant Activity in Sorghum bicolor Leaves Extracts
Poro David Clark, Gloria Ihuoma Ndukwe, Kehinde Jonathan Awatefe
This study investigated the phytochemical composition and in-vitro antioxidant potential of leaves extracts from Sorghum bicolor, which were obtained through sequential maceration with solvents of different polarities (n-hexane and methanol). The extraction yields revealed a predominance of polar compounds, with methanol extract (12.5% w/w) significantly higher than the n-hexane extract (1.7% w/w). Gas chromatography–mass spectrometry (GC–MS) profiling, using NIST library matching (similarity scores > 80%) without reference standards, showed distinct patterns based on solvent use: the n-hexane extract contained nine primarily lipophilic compounds, mainly consisting of Z-2-octadecen-1-ol and octadecenoic acid derivatives, whereas the methanol extract yielded fifteen characterized by polar fatty acids and oxygenated derivatives. Identifications were tentative; those with lower match scores or inconsistent retention times required confirmation through alternative methods. Antioxidant capacity was evaluated via 2, 2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging, hydroxyl radical inhibitory activity (HRIA), and ferric reducing antioxidant power (FRAP) assays. The methanol extract demonstrated concentration-dependent DPPH scavenging (IC₅₀ = 0.1402 mg/L), comparable to vitamin C (0.1369 mg/L) in this assay, while the n-hexane extract showed weaker activity (IC₅₀ 3.22 mg/L). In HRIA and FRAP assays, vitamin C consistently showed greater activity than either extract, with n-hexane IC50 estimates constrained by poor curve fits (R2< 0.9). Overall, the methanol extract surpassed the n-hexane extract across all assays but did not match the effectiveness of vitamin C. These in-vitro results suggest that S. bicolor leaves contain polar phytochemicals that merit further fractionation, compound-level characterization, and evaluation in biologically relevant models to elucidate their potential as sources of natural antioxidants.
Sciences of Phytochemistry
17 Feb 202612 pages - research article
Ethnobotany, Phytochemistry, Pharmacology, and Toxicology of Cycas revoluta Thunb.: An Updated Review
Abdul Jaleel K, Prakash PS, Nakshathra KV, Devika V
Cycas revoluta Thunb. (sago palm), a cycad native to southern Japan, is widely cultivated and has a long history of ethnobotanical use, including as a famine food and in traditional medicine, but is also well known for its pronounced toxicity to humans and animals. This review critically synthesizes literature published between 1958–2025 on the ethnobotany, phytochemistry, pharmacology, and toxicology of C. revoluta from ScienceDirect, PubMed, Scopus, and Google Scholar. Presented as a structured narrative review, the study highlights diverse phytochemicals, including biflavonoids, cycasin, β-N-methylamino-L-alanine (BMAA), and reported antimicrobial peptides, noting variability in compound verification and reproducibility. Reported pharmacological activities are derived mainly from in vitro and preclinical studies, with limited in vivo validation and no established clinical relevance, whereas toxicological evidence for neurotoxicity, genotoxicity, and hepatotoxicity is robust. This imbalance underscores the need for caution in extrapolating therapeutic potential. Key gaps include inadequate extract standardization, limited bioavailability and safety data, and overreliance on single-study findings. Future research should prioritize rigorous toxicological assessment and reproducible validation before any translational application is considered. In addition, the review emphasizes the importance of distinguishing traditional knowledge from experimentally validated evidence and separating descriptive phytochemical inventories from mechanistic and translational insights. Particular attention is given to methodological limitations, including inconsistent extraction protocols, insufficient structural confirmation of reported compounds, and the frequent absence of dose–response, pharmacokinetic, and long-term safety evaluations. By adopting a critical and balanced perspective, this review aims to guide future studies toward scientifically rigorous, ethically responsible, and clinically relevant research directions.
Sciences of Phytochemistry
28 Jan 202610 pages