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Malaria is a global problem, as treatment failure has hampered the efficacy of most anti-malarial medications. The goal of this study was to see if stem bark extract from Zanthoxylum zanthoxyloides had antiplasmodial properties that could be used to treat both susceptible and resistant parasites. The stem bark of Z. zanthoxyloides (500g) was crushed and extracted with ethanol. The extract was tested for antiplasmodial activity in vitro against the chloroquine-sensitive (CQS) strain NF54 and chloroquine-resistant strains (CQR) K1 of P. falciparum, as well as in vivo against the CQS(NK65) strain of P. berghei at 100, 200, and 400 mg/kg bw. Bioassay-guided fractionation of the extract was performed. The crude extract had an in vitro activity of 1076.4 56.4 and 1315.1 121.6 ng/ml against chloroquine sensitive and resistant parasites, respectively while standard drugs (chloroquine and artesunate) were 10.94 nM (3478.92 ng/ml) and 9.24 nM (3215.52ng/ml) for CQS and 310.68 nM (98796 ng/ml) and 10.94 nM (3650.52 ng/ml) for CQR respectively. At Day 7, mice treated with 100, 200, and 400 mg/kg bw crude extract had parasite densities of 1159, 928, and 869 parasites/ µl, respectively (compared to positive control that had 123 parasites /µl). In vitro antiplasmodial activity was best in the K2, K4, and K6 fractions (IC50 were 6670, 6890, and 6480 ng/ml), but in vivo antiplasmodial activity was best in the K4 fraction (1183 parasites/ µl).The stem bark extract of Z. zanthoxyloides have remarkable antiplasmodial activity against both chloroquine sensitive and drug resistant P. falciparum supporting it ethnomedicinal use in malaria treatment.The extract of Z. zanthoxyloides has promising antiplasmodial activity and could be used to generate therapeutic leads against the multidrug-resistant K1 strain of P. falciparum, in addition to providing an alternative allopathic antiplasmodial medication.

Stem bark of Sterculia setigera Delile, family Sterculiaceae, is used in traditional medicine in Sudan and other African countries to treat various diseases. This study aimed to investigate the chemical constituents, antioxidant, enzyme inhibition and antiproliferative activities of stem bark extracts and an isolated compound. Compounds were extracted using hexane and dichloromethane: ethanol (DE) (1:1). Chromatographic techniques were performed to characterize the phenolic compounds. We isolated lupeol as a bioactive compound in S. setigera from DE extract. The antioxidant and enzyme inhibitory properties of each extract were evaluated. The antiproliferative activity of the DE extract was determined. Results showed that five known compounds namely; procyanidins as dimer B, trimer C1 and tetramer, 3,4-dimethoxyphenol s-D-apiofuranosyl (1″→6″)- s -D-glucopyranoside and (+)- catechin were identified or tentatively elucidated, in addition to the isolation and characterization of lupeol. DE extract showed significantly (p

Research on the activity of ?-glucosidase inhibition of Bunga Kupu-Kupu stem bark extract (Bauhinia semibifida Roxb) has been carried out in vitro. This study aims to determine the inhibitory activity of the extracts of B. semibifida Roxb. stem bark against the ?-glucosidase enzyme in vitro. Testing the inhibitory activity of the ?-glucosidase enzyme using extracts of n-hexane, ethyl acetate, and methanol from the stem bark of the Bunga Kupu-Kupu and the Akarbose as a positive control. In vitro testing was carried out using a microplate reader instrument with a wavelength of 410 nm. The results showed that the extract of n-hexane extract of the B. semibifida stem bark had an IC50 value 15,625 µg/mL, ethyl acetate extract had an IC50 value 35,495 µg/mL, and the methanol extract had an IC50 value 34,279 µg/mL. By category, the three B. semibifida stem bark extracts have the active ability to inhibit the ?-glucosidase enzyme, while the Akarbose had an IC50 value 0,384 µg/mL as a positive control has a very active ability as an antidiabetic through the inhibition of the ?-glucosidase enzyme. The results showed that extraction of ?-glucosidase inhibitor compound with n-hexane yielded extract with highest inhibitor activity.

Background: C. arborea belonging to Araliaceae family is used traditionally to cure many alien diseases including gonorrhoeae infection, diarrhea, malaria, and diabetes mellitus. The plant has been examined on the basis of scientific in vitro and in vivo evaluations possessing the major pharmacological activities including antimicrobial, antibacterial, antihyperglycemic, antiplasmodial and anticancer properties. Aim of the study: In the present paper, we reported the isolation and characterization of secondary metabolites from the methanol extract of the stem bark of Cussonia arborea Hochst after a short review of the traditional and pharmacological studies done on this important medicinal plant. Materials and methods: MeOH extract of stem bark of C. arborea was suspended in water and successively extracted with EtOAc and n-BuOH. The EtOAc extract (18 g) was subjected to repeated column chromatography to yield seven (1-7) compounds. Their structures were determined by means of NMR, and published data. Results: The isolated compounds were identified as: protocatechuic acid (1), mixture of 3,23-dihydroxyolean-12-en-28-oic acid (2a) and 3,23-dihydroxyurs-12-en-28-oic acid (2b) in ratio 5/4, 3-O-β-D-xylopyranosylolean-12-en-28-oic acid (3), 3-O-α-L-arabinopyranosylolean-12-en-28-oic acid (4), β-resorcylic acid (5), mixture of 3-O-β-D-glucopyranosyl-23-hydroxyolean-12-en-28-oic acid (6a) and 3-O-β-D-glucopyranosyl-23-hydroxyurs-12-en-28-oic acid (6b) in ration 4/1, 3-O-β-D-glucopyranosyl-(1→2)-α-L-arabinopyranosyl-3β-hydroxyolean-12-en-28-oic acid (7). Compounds 3, 4, 5, 7, 2b and 6b are herein reported for the first time in this plant

Parinari curatellifolia and other Parinari species are used traditionally in many parts of Africa as a remedy for malaria among other diseases. To ascertain this folkloric claim, the antiplasmodial potential of ethanol extract of Parinari curatellifolia stem bark (EEPCSB) and n-hexane extract of Parinari curatellifolia stem bark (HEPCSB) on Plasmodium falciparum was studied. Parasites were grown in a 96-well plate containing Roswell Park Memorial Institute-1640. The wells were grouped into: control (untreated), artemether-treated, EEPCSB-treated and HEPCSBtreated groups. Treatments were administered to the tune of 10, 20, 40 and 80 μg/ml. Parasitemia was observed by microscopy after 24, 48 and 72h of incubation. EEPCSB and HEPCSB elicited dose and duration-dependent reduction (p0.05) in plasmodium lactate dehydrogenase activity of EEPCSB-treated and artemether-treated groups. Findings from this study show that extracts of P. curatellifolia stem bark, especially EEPCSB, demonstrated excellent inhibitory activities against P. falciparum and can be a good source of compounds for the development of novel antimalarial drugs. Keywords: Parinari curatellifolia; Extracts; Plasmodium falciparum; Parasitemia; Antiplasmodial

Objectives: The present study determines the bioactive constituents in the stem bark of Tamarindus indica and also assesses its biological properties against Staphylococcus aureus and Pseudomonas aeruginosa in vitro. Methods: The clinical isolates were collected from wounds of patients and cultivated in a nutrient broth. The extract of stem bark of T. indica was added to the bacteria in Muller Hinton ager to test its biological activity. Results: Crude extracts of T. indica showed potency against S. aureus with the highest zone of inhibition of 19.00 ± 0.60 mm at 200 mg/ml concentration of the extract. The extract showed potency against P. aeruginosa at varying concentrations with a zone of inhibition between 13.5 ± 0.20 mm and 6.25 ± 0.45 mm. However, the extracts of T. indica recorded a minimum inhibitory concentration (MIC) value of 6.25 mg/ml and an minimum bactericidal concentration value of 25 mg/ml against P. aeruginosa and also recorded a MIC value of 3.13 mg/ml against S. aureus. The preliminary analysis of bioactive compounds of the crude extract of T. indica showed that it has a wide range of phytochemical constituents including saponins, alkaloids, flavonoids, tannins, and anthraquinones. Conclusion: The results suggested that the extract of stem bark of T. indica has the potential of being the best alternative antimicrobial agent use to cure infectious diseases caused by S. aureus and P. aeruginosa.

Aim: The aim is to evaluate the toxicological profiles of methanol stem bark extract of E. camaldulensis (MSEEC) on Wister albino rats. Methods: Acute toxicity study was conducted according to OECD, 2001. The rats were grouped into six groups of one rat each and were given single oral dose 5000 mg/kg of the extract. A total of 30 albino rats of both sex were used for the toxicological study. The rats were divided into five (5) groups of six (6) rats. Control group (group 1) received distilled water orally 1 ml/kg. Groups (2-5) received doses of 500, 1000, 1500 and 2000 mg/kg of the extracts. The experiment lasted for 28 days. Data analysis was done using SPSS version 20.0. Results: The LD50 of MSEEC was greater than 5000mg/kg. The sub-chronic doses of 500-2000 mg/kg of the extract shows no significant (P>.05) difference of the hematological parameters when compared to the control. The Serum biochemical parameters were no significant (P>.05) compared to the control. However, there was an increase in creatinine level at doses 500, 1500 and 200 mg/kg. Conclusion: The results from this study indicate that administration of methanol stem bark extract of Eucalyptus camaldulensis did not produce significant toxic effect.

Aim: This study was aimed at examining the antimicrobial and wound healing activities of Gardenia aqualla stem bark methanol extract (GASBME) in order to provide scientific basis for its antimicrobial and wound healing properties. Methodology: Preliminary phytochemical screening was done and antimicrobial activity determined using some pathogenic micro-organisms were evaluated following its wound healing effectiveness in Wistar rats using the model of superficial skin excision wound. Data were analysed using one-way analysis of variance (ANOVA) followed by Dunnet’s t-test. Results: The results of preliminary phytochemical screening revealed the presence of carbohydrate, cardiac glycosides, saponins, flavonoids, triterpenes, tannins, alkaloids with anthraquinones being absent. The extract showed antimicrobial activity on Staphylococcus aureus, Corynebacterium ulcerans, Escherichia coli, Klebsiella pneumonia and Salmonella typhi and significant (p< 0.05, p< 0.001) decrease in wound measurement by the 11th day. Conclusion: This study demonstrated that GASBME possesses antimicrobial activity with wound healing properties that justifies the ethno-medicinal use of the plant in wound/ulcer healings.

A new iso-benzofuranone propanamide: 3-(3-oxo-1, 3-dihydroisobenzofuran-1-yl) propanamide (zenkeramide) (1) along with three known compounds: Trans-N-coumaroyltyramine (2), β-Sitosterol (3) and β-s...

Ximenia americana L. is popularly known as a plum or wild plum, which belongs to the Olacaceae family. Rhipicephalus (Boophilus) microplus represents one of the most important bovine ectoparasites that causes damage to the livestock sector. The objective of this study was to evaluate the acaricide effect of the X. americana stem bark hydroethanolic extract (EHXA) against R. (B.) microplus and its possible modulatory action when in association with cypermethrin, through the adult immersion test. The in vitro acaricide activity of the extract over R. (B.) microplus engorged females was tested using concentrations ranging from 5 to 80 mg mL− 1, which resulted in mortalities between 13.34 and 100 %, with a posture index (PI) between 0.038 and 0.226 and a posture inhibition index (PII) between 0.87 and 83.33 %. The modulatory effect of the EHXA (1.58 mg mL− 1) resulted in mortality between 0 and 46.6 %, with a posture index of 0.221 to 0.139 and a posture inhibition index between 3.01 and 38.49 %. The acaricide activity of the EHXA and its action on oviposition was demonstrated for the first time in this study, demonstrating the potential use of this extract as an auxiliary therapy in R. (B.) microplus control.

Background: Spondias mombin L. belongs to the family Anacardiaceae. Despite its wide ethnomedicinal applications in the management of diverse diseases, there is a paucity of documented reports on its standardization.Objectives: The present study evaluated microscopical characters and some physicochemical properties of different parts of the plant for its identification and standardization.Material and Methods: Epidermal tissue preparation of the leaf of Spondias mombin (SM) was obtained using physical method while thin sections (10-12 μm) of the stem bark and root were obtained using a rotary microtome. Physicochemical parameters were determined for the powdered samples of SM using standard methods.Results: Diagnostic characters from the epidermal tissue of the leaf revealed anomocytic, paracytic stomatal type, non-glandular trichome, smooth to slightly wavy anticlinal walls while sections of the stem bark and root were characterized with abundant sclereids and calcium oxalate crystals. The stomatal number and stomatal index of the abaxial epidermis were 23.70±0.86 and 24.62±0.78 %, respectively. Ethanol had the highest extractive value (17.84±0.50) % in the leaf whereas it was lowest in petroleum ether (1.92±0.08) %. The leaf had the lowest ash value (7.13±0.76) %.Conclusion: The microscopical characterization and some of the physicochemical parameters reported herein could be useful in the compilation of monograph for the correct identification of Spondias mombin, thus contributing to the knowledge of its collection and preservation.

To control the quality of Betula alnoides stem bark (BAS), lupeol, which is a promising compound found in BAS, has been determined by reverse phase high performance liquid chromatography (RP-HPLC) ...

Background: Terminalia macroptera Guill. &Perr. (Combretaceae) is a flowering plant with several ethno-medicinal claims. However, the dearth of information on its analgesic property has necessitated this study.Objectives: to evaluate the anti-nociceptive potential of ethanol extract of Terminalia macroptera stem bark (TMSB) in mice.Materials and Methods: Male and female mice of weight range 22 – 25g were randomly allotted into seven groups (n= 5) and treated as follows: Group I received 0.5 mL distilled water orally (negative control), Groups II-V were orally administered ethanol extract of T. macroptera stem bark (TMSB) at 50, 100, 200, and 400 mg/kg respectively while groups VI-VII received piroxicam 10 mg/kg and pentazocine 2 mg/kg intraperitoneally respectively as standards. The same treatment pattern was adopted for both pain models: tail immersion and acetic acid-induced writhing assays. Data were expressed as mean ± standard error of mean (SEM) using two-way analysis of variance (ANOVA) followed by Tukey’s and Bonferroni's multiple comparisons tests with p < 0.05 taken as significance.Results: The ethanolic extract of Terminalia macroptera stem bark showed significant dose-dependent anti-nociceptive activity at 100 and 400 mg/kg (2.95±0.41 and 2.9±0.31 respectively) 60 min post-treatment compared to the negative control group in the tail immersion test. Significant inhibition of nociception (0.20±0.20) was obtained at 400 mg/kg compared to the negative control group in the acetic acid-induced writhing test.Conclusions: The ethanol extract of Terminalia macroptera stem bark exhibited dose-dependent anti-nociceptive potential in both tail immersion and acetic acid-induced writhing assays in mice.

Background: Depression is one of the most common psychiatric disorders affecting nearly 17% of the world population and the existing antidepressant drugs used in clinical settings are largely associated with serious side effects. Tamarindus indica (Fabaceae) is a plant that has been used ethno-medicinally as a remedy for depression.Objectives: The objective of this study was to determine the antidepressant activity of methanol stem bark extract of Tamarindus indica using mice, also to determine the LD50 and phytoconstituents of same extract.Methods: Fresh leaves of Tamarindus indica were collected, pulverised and extracted using 70% v/v methanol. Phyto-constituents of the extract were screened and Median lethal dose (LD50) was determined using standard protocols. Antidepressant effects of the extract were investigated using Tail suspension test (TST) and forced swimming test (FST) models.Results: The results of median lethal dose revealed the LD50 value of 470 mg/kg body weight and the phytochemical screening showed the presence of saponins, alkaloids and glycosides. The extract at the doses of 75 and 150 mg/kg body weight significantly (p

The present study investigated the antidiabetic and antioxidant capacity of hydromethanol extract from Parkia biglobosa stem bark (PBSBHM) in fructose-streptozotocin induced type 2 diabetic rats af...

Aim: The aim is to evaluate the antioxidant potentials of Eucalyptus camaldulensis methanol stem bark extract (ECMSBE) on Wister albino rats. Methodology: The phytochemical screening of ECMSBE was conducted using standard methods. A total of 36 albino rats were used for the antioxidant studies. The rats were divided into six (6) groups of six rats. Control group received distilled water orally at 2ml/kg. Oxidative stress was induced in groups 2 to group 6 CCl4 (1ml/kg, s.c) at every 72hrs for 10 days. Group 2 was untreated while groups 3 – 6 received doses of 50, 100, 150 and 200mg/kg of ECMSBE respectively. On the 11th day, the rats were sacrificed and the liver was removed and homogenised and oxidative stress parameters were determined. Results: Phytochemical analysis of ECMSBE revealed the presence of saponins, flavonoids, tannins, phenols, glycosides, steroids, terpenoids and resins. There was no significant difference (P.05) in the levels of SOD, CAT and GPx between the group induced with CCl4 only and the group treated with ECMSBE (50mg/kg), however, it these concentrations were significantly higher (P.05) when compared the group that was treated with ECMSBE (200mg/kg) Conclusion: The result suggest that the extract of E. camaldulensis possessed antioxidant properties which can be used as effective protecting agents against oxidative stress and other diseases.

This study presents the fabrication of nanocomposite for the sequestering of Cr(VI) from solution. The nanocomposites were obtained from the molecular sieve and functionalized multiwall carbon nanotubes and further modified with Pentaclethra macrophylla (oil bean tree) stem bark extract. The pristine molecular sieve (MS) and the modified nanocomposite [Pentaclethra macrophylla stem bark extract anchored on molecular sieve (SMP)] adsorbent were characterized by the FTIR, FESEM, XRD, BET, and TGA techniques. The batch adsorption experiment revealed an agitation time of 120 min, 0.02 g dosage, and sorbate pH of 2.0 as optimum conditions for effective use of MS and SMP. Under these conditions a maximum monolayer capacity (qmax) of 135.5 mg g���1 was obtained for SMP, a value that is better compared to many other related absorbent materials. The uptake of Cr(VI) onto MS and SMP was best described by pseudo-first-order and Elovich kinetic models respectively. Meanwhile, the Freundlich model was noticed to sufficiently describe the isotherm data obtained for MS and SMP. The adsorption of Cr(VI) onto MS and SMP was spontaneous, endothermic, and entropy-driven. The reusability of the nanocomposite and its efficient Cr(VI) removal, present SMP as a potent adsorbent for the sequestration Cr(VI) from aqueous solution. nsufficient innovative research on the sequestration of Cr(VI) from the aquatic ecosystem has made Cr(VI) a recalcitrant water contaminant that often affects water sources. In this work, a novel plant anchor-nanocomposite was fabricated from the spent molecular sieve, multi-walled carbon nanotubes, and the extract from the stem bark of Pentaclethra macrophylla. It was envisaged that due to the phytochemical constituent of the modifier, this nanocomposite could also act as potent adsorbents for the treatment of Cr(VI) polluted water. To the best of our knowledge, the application of Pentaclethra macrophylla stem bark extract as a modifier for the green fabrication of nanocomposite has not been reported. The resulting composites showed good uptake capacity for Cr(VI) as well as efficient reusability.

The prominent benefit of granite is owned to its physicochemical property and ubiquitous nature. Vast application of granite which also includes its use as an adsorbent in environmental remediation practice, can also be enhanced. To further enhanced the uptake capacity of granite, nanocomposite consisting of multiwall carbon nanotubes (MWCNTs) and granite was fabricated and further modified using Dialiumguineensestem bark extract. The structure and composition of pristine granite (PG) and modified nanocomposite granite (G) based material were examined and confirmed by the FTIR, Raman, TGA, SEM and XRD. Meanwhile, the specific surface areasof PG (1.268 m2/g) and G (16.57 m2/g) were obtained using the BET surface area analyser. The optimization step revealed that the uptake capacities of PG and G were dependent on solution pH, sorbent dose and contact time. Meanwhile, pseudo-second-order and Elovich kinetic models were noticed to best describe the data for the removal of Cr (VI) by PG and G. Equilibrium isotherm study revealed that Freundlich and Langmuir models fitted well to the experimental data obtained for the uptake of Cr(VI) onto PG and G respectively. Furthermore, electrostaticattraction betweentheDialiumguineense stem bark extract on the surface of G and Cr(VI) influenced the uptake of Cr(VI). On the other hand, the interaction between the plant extract and Cr(VI) may result in the attenuation of Cr(VI) via reduction to Cr(III). Finally, the thermodynamically favoured adsorptive process demonstrated high adsorbent reusability with good stability for Cr(VI) uptake.

The continuous search for new compounds in natural-based plants is a promising strategy for the prevention of diseases. This work examined antiglycation activity compounds isolated from the antidia...

Background: Dryobalanops rappa is a plant species belonging to the family of Dipterocarpaceae. Nevertheless, the active compounds present in D. rappa have never been investigated. Objective: The aim of this research is to isolate and characterize compounds from Dryobalanops rappa and to study its bioactivity against human MCF-7 breast cancer and A549 lung cancer cell lines and several bacterial strains. Methods: The isolation step was carried out using a combination of chromatographic techniques. The structure of the isolated compounds was elucidated mainly using NMR spectroscopy. The cytotoxic activity of isolated compounds was determined with MTT assay, and the antimicrobial was screened using a modified resazurin microtiter-plate assay. Results: Isolation and purification of methanolic extract of D. rappa stem bark yielded 14 known oligomeric resveratrol types of compounds (1-14). Results showed that isolated ampelopsin E (5) and vaticanol C (14) displayed moderate activity against human MCF-7 breast cancer and A549 lung cancer cell lines with IC50 values 14.3 and 10.7 μg/mL, respectively. Interestingly, acetate derivative of isolated laevifonol (2) and ampelopsin F (3) was found to possess potent activities towards MCF-7 cancer cell line with IC50 values 2.8 and 3.3 μg/mL, respectively, in comparison to the parental compounds that demonstrated weak activities (IC50 > 50 μg/mL). For the antibacterial assay, compounds 10 and 12 showed moderate activities towards Gram-positive bacterial strains (MIC ≤ 50 μM). Conclusion: 14 known oligomeric resveratrol types of compounds have been isolated. The activity of 14 against A549 cell line, 5 against MCF-7 cell line, and 10 and 12 against Gram-positive bacterial strains were the most promising results of this study. While the strong cytotoxicity of acetate derivative (2 and 3) against MCF-7 cell line has revealed the potential of resveratrol oligomers to be used as a template for designing new anticancer drugs.

The purpose of this study was to determine the antioxidant activity of crude extract and their fractions, the content of secondary metabolite types of crude extract, and the chemical content and toxicity of the most active fractions as antioxidants from the stem bark of Artocarpus anisophyllus Miq. (Mentawa). The methods used are phytochemical screening, toxicity tests against Artemia salina by the Brine Shrimp Lethality Test (BSLT), antioxidant activity assay with DPPH radical reduction method, and determination of chemical compound by GC-MS analysis. Phytochemical test results showed that crude extract containing alkaloids, triterpenoids, phenolics and flavonoids. The results of the antioxidant activity of the n-hexane, ethyl acetate and methanol fractions obtained IC50 values of 127.69, 28.65 and 79.43ppm, respectively. Ethyl acetate (as the most active fraction) was then fractionated using a vacuum chromatography column and the fractions obtained were E1 (268.8mg), E2 (337.1), E3 (234.3mg) and E4 (431.2mg). The antioxidant activity test showed that E2 was the most active compared to other fractions with an IC50 value of 37.24ppm. While the toxicity test results showed that E2 was very active with an LC50 value of 6.23ppm indicating that E2 was also potentially developed as an anticancer drug. Based on GC-MS spectrum analysis, of the several main compounds, four of which are aromatic compounds that have the potential to be developed as antioxidants, namely 2- (Benzyloxy) phenol (phenolic compound) (3.96%) (51),), 1, 2- Benzenedicarboxylic acid, dinonyl ester (2.44%) (52), Linderazulene (2.43%) (30), p-Nonylphenol (2.36%). Some other aromatic minor compounds can also be active as antioxidants.

The phytochemical study of the CH2Cl2- MeOH (1:1, v/v) extract of the stem bark of Carapa procera DC (Meliaceae) led to the isolation and characterisation of a new natural limonoid 7β-obacunol (6),...

Three new bufadienolides, namely, paulliniogenin A (1), paulliniogenin B (2), and 16β-formyloxybersamagenin 1,3,5-orthoacetate (3), together with two known bufadienolides and six known phenolic substances, were isolated from the stem bark of Bersama abyssinica subsp. abyssinica and B. abyssinica subsp. paullinioides. The structures of the compounds were elucidated based on their NMR and HRMS data analyses. The relative configurations were defined by single-crystal X-ray crystallography and NOESY correlations. Cytotoxicity against the L929 and KB3.1 cancer cell lines of the isolated compounds was investigated using an MTT assay. Paulliniogenin A (1) and 16β-hydroxybersamagenin-1,3,5-orthoacetate (4) showed cytotoxicity against the KB3.1 cell line with IC50 values of 1.4 ± 0.77 and 1.6 ± 0.81 μM, respectively. Moreover, paulliniogenin A (1) and paulliniogenin B (2) demonstrated weak activity against Staphylococcus aureus.

This study aims to determine a suitable artificial neural network (ANN) regression model for quantification of polyphenols from herbal matrices through thin-layer chromatography (TLC) images. Galli...

A low-cost adsorbent (Detarium senegalense stem bark extract coated shale (DSMS)) comprising pristine shale (PSH) coated with D. senegalense stem bark extract was prepared and utilized for the adso...

Introduction Xanthones are metabolites with a variety of biological properties. The Clusiaceae family, which until recently included the genus Calophyllum, is recognised for its production of monohydroxylated and polyhydroxylated xanthones. Presently, C. brasiliense is the only Calophyllum spp. known to occur in the Yucatan peninsula. Objective To use a combination of traditional phytochemical methods and carbon-13 nuclear magnetic resonance (13 C-NMR) dereplication analysis to identify xanthones in the stem bark of C. brasiliense. Material and methods Initial fractionation and purification of the stem bark extract of C. brasiliense produced macluraxanthone (1). Additional xanthones, together with chromanones and terpenoids, were identified using 13 C-NMR dereplication analysis in different semipurified fractions obtained from the low and medium polarity fractions of the stem bark extract of C. brasiliense. Results Initial identification of macluraxanthone (1) was confirmed by 13 C-NMR dereplication analysis; additionally, 13 C-NMR dereplication analysis allowed the identification of a number of monohydroxylated and polyhydroxylated xanthones, together with chromanones and terpenoids. Conclusion This study confirms C. brasiliense as a rich source of xanthones and the 13 C-NMR dereplication analysis as a suitable method to quickly identify the presence of different families of secondary metabolites in semipurified fractions.

Amphimas pterocarpoides is used traditionally for the treatment of oedema, infections, malaria and skin diseases. This study described pharmacognostic and physicochemical parameters of the leaf and stem bark. The carrageenan-induced foot oedema and the baker’s yeast-induced pyrexia were used to assess the anti-inflammatory and antipyretic activities respectively. The leaf of A. pterocarpoides is oddly pinnate compound, oblong in shape with acuminate apex and obtuse base. The stem bark is scaly and rugged and exudes a reddish resin when bruised. Leaf microscopy displayed wavy-walled epidermal cells, paracytic stomata, glandular and clothing trichomes, bean-shaped lignified vascular bundle, prismatic calcium oxalate crystals. The leaf (APL) and stem bark (APSB) extracts (30-300 mg/kg p.o.) significantly inhibited foot oedema in chicks with maximum percentage inhibition of 76.65 ± 6.27% and 77.04 ± 2.53% respectively [ED50 = 225.3± 31.52 mg/kg (APL) and 178.9 ± 29.57 mg/kg (APSB)]. APL, APSB and paracetamol also showed significant antipyretic activity [ED50 = 70.95 ± 9.24 mg/kg (APL), 27.02 ± 1.96 mg/kg (APSB), 32.47 ± 3.03 mg/kg (Paracetamol)]. Tannins, flavonoids, phytosterols, triterpenoids and coumarins were identified in A. pterocarpoides. This study has provided essential diagnostic characteristics for the quality control of A. pterocarpoides and justified its anti-inflammatory and antipyretic effects. Key words: Pharmacognosy, carrageenan, Amphimas pterocarpoides, pyrexia, inflammation.

Aqueous extract of bark of Kigelia pinnata was used as reducing source for the biological green synthesis of AgNPs. The synthesized particles were characterized by UV-Visible spectrum, XRD, SEM, dynamic light scattering (DLS). The anti-fungal activity of AgNPs was evaluated against Aspergillus niger (MTCC:281), Aspergillus flavus (MTCC:277) and Candida albicans (MTCC:227) by agar diffusion method. Particle size of AgNPs was measured as 76.4nm ± 6.3nm and Zeta potential was stable at -43.2mV using DLS analysis. SEM analysis measured the size of AgNPs as ~75nm. XRD analysis confirmed that the synthesized NPs were silver (Ag), based on the JCPDS entry 85-1355 and it is crystalline in nature. The size of the crystal was calculated as 10nm using the Scherrer formula. The AgNPs demonstrated significant anti-fungal activity against C. albicans (MIC:15.6µg/ml), A. niger (MIC:62.4µg/ml) and A. flavus (MIC:31.2µg/ml). These results confirm that AgNPs synthesized using K. pinnata barks could be used as potential antifungal agent against fungal pathogens.

This study assessed the adsorptive uptake of Cr(VI) onto eco-friendly adsorbent fabricated via the surface coating of pristine dolerite (PD) using the extract ofAzadirachta indica stem bark. The ma...

Rauwolfia vomitoria is used in Cameroon in indigenous medicine to treat liver diseases. The present study was carried out on the hepatoprotective and antioxidant effects of the plant aqueous extract. Liver toxicity was induced by oral route administration of CCl4 two times per week for four weeks. Rats were given concomitantly by oral route, aqueous extract at the doses of 100, 200 and 300 mg/kg or silymarin four days a week for four weeks. By the end, bloods were collected for liver functional parameters analyses. Liver tissues were removed, to assess to oxidative stress parameters and histological analyses. The extract (300 mg/kg) decreased enzyme activity of ALT, AST and the level of TG with the percentage 54.23%, 49.63% and 28.74% respectively while it increased the enzyme activity of SOD, CAT and level of MDA at about 67.16%, 71.42% and 43.80% respectively compared to control animals. These results suggested that aqueous extract has strong hepatoprotective effect on CCl4-induced liver damage and increase antioxidant defense system activity.

Introduction: Khaya senegalensis is a genus of seven species of trees in the mahogany family Meliaceae, native to tropical Africa and Madagascar. Mahogany in English, Aganwo in Yoruba, Madachi in Hausa and Ono in Igbo. All species become big trees 30–35m tall, rarely 45m, with a trunk over 1 m trunk diameter, often buttressed at the base. The leaves are pinnate, with 4-6 pairs of leaflets, the terminal leaflet absent; each leaflet is 10–15 cm long abruptly rounded toward the apex but often with an acuminate tip. Aim: The aim of the study was to determine the Toxic effect of prolonged oral administration of the aqueous stem bark of Khaya senegalensis extract on the histology of Kidneys and its biochemical parameters in wistar rats. Methods: This work is an experimental research. A total of 20 wistar rats were randomly divided in to 5 groups each of which consist of 4 rats. Group 1 received distilled water to serve as control while group 2, 3, 4, and 5 received 500 mg/kg bw, 1000 mg/kg bw 2000 mg/kg bw and 4000 mg/kg bw of the aqueous extract respectively for 60 days after which they were sacrificed, processed in Automatic Tissue Processor machine, Sectioned and stained with H &E. Results: There was statistical significant increase in urea and potassium in all the test groups but is not dose dependent. The creatinine was significantly increased in groups 2, 4 and 5. While other parameters such as sodium, chloride and bicarbonate no significant difference when compared to the control group. The kidney sections showed normal structure in group 1 when compared with the test groups. However, there was significant infiltration of inflammatory cell across all the groups which were suggestive of kidney damage or injury. Similarly phenomenon was noticed in group 5 with additional congestion in the glomerulus and more polymorphs seen. Conclusion: The LD50 was found to be greater than 5000 mg/kg bw, therefore, 400 mg/kgbw was used as higher dose in the experimental wistar rats. There were statistical significant increases in some parameters groups while some groups not significant. The kidney section showed significant infiltration of polymorphs across all the groups more marked in group 5 with distension and damaging of the glomerulus indicating renal injury.

Background: Cardiovascular diseases (CVDs) constitute the number one cause of mortality at the global level, representing 30% of all global deaths. Therefore, finding ways to reduce deaths due to CVDs remain an important public health goal. Traditional healers in northern Nigeria use the stem bark of Vitex doniana to treat hypertensive patients. This study was aimed to investigate the cardiocurative potential of Vitex doniana on doxorubicin-induced Cardiotoxicity in rats. Methods: Thirty five (35) adult Albino rats weighing 175 ± 25 g were used, of which 30 were induced with cardiotoxicity by intraperitoneal injection of doxorubicin (10 mg/kg) for three consecutive days. Rats were treated by oral administration of Silymarin (100 mg/kg) and Vitex doniana aqueous or ethanol extract (100 mg/kg and 200 mg/kg) for 14 consecutive days and thereafter were sacrificed on the 15th day. Blood, plasma and serum were analyzed for lipid profile and serum markers for cardiotoxicity. Results: Phytochemical analysis of the extracts showed the presence of alkaloids, tannins, flavonoids, steroids, phenols, saponins, terpenoids and glycosides. Oral treatment with Vitex doniana extracts significantly (p

In the current study, sequential solvents extraction from the stem bark of Garcinia maingayi, a native plant to Malaysia has led to the isolation of four polyisoprenylated benzophenones: 30-epi-cambogin (GB 1), 14-deoxy-30-epi-cambogin (GB 2), guttiferone F (GB 3), and 14-deoxy-guttiferone F (GB 4). The structures were elucidated using IR, optical rotation, and NMR spectral data. The compounds were evaluated for antiproliferative effect using MTT assay, apoptosis using Annexin V/7-AAD flow cytometry, cell cycle progression, and activation of caspases 3/7, 8 and 9 and BCL2 mRNA expression in MCF-7, HeLa, and HepG2 cancer cell lines. Compounds GB 1 to GB 4 exhibited a remarkable antiproliferative effect on HeLa, MCF-7, and HepG2 cells with IC50 values ranging from 5 to 45 µM. Compounds GB 1 to GB 4 induced significant cell cycle arrest in the G1 phase corroborated with the decrease in the number of MCF-7 and HepG2 cells in S and G2/M phases (P

Chloroform, ethyl acetate and methanolic extracts from leaves and stem bark of Buddleja salviifolia were prepared. The phytochemical profiles, total flavonoid contents (TFC), total phenolic contents (TPC) and ferric reducing power of these extracts were studied. The presence of alkaloids, tannins, phlobatannins, saponins, sterols, flavonoids, coumarins, phenolics, terpenoids, quinones and reducing sugars were identified from these extracts. The TFC of these extracts was found to be in the range of 11.36±0.98 to 30.76±1.15 mg QE/g DW, respectively. The TPC of these extracts was found to be in the range of 175.00±0.41 to 465.27±2.65 mg GAE/g DW, respectively. Additionally, these extracts showed a weak to moderate ferric reducing power compared to ascorbic acid. B. salviifolia finds therapeutic applications in traditional medicine. Further studies are required to commercialize products from this plant.

The phytochemical investigation of the dichloromethane/methanol (1:1) extract of the stem bark of Scyphocephalium ochocoa, led to the isolation of one new dibenzofuran derivative, named scyphocephalione A (1), along with three other compounds, including epicatechin (2), gentisic acid (3) and myo-inositol (4). The structures of all the compounds were established with help of spectroscopic data including IR, UV, MS, 1 D- and 2 D-NMR, as well as by comparison with previously reported data in literature, and chemical modification. All the compounds were obtained from the genus Scyphocephalium for the first time. The anti-inflammatory activity (using chemiluminescence technique) of the crude extract and compound 1, together with NO inhibition (using ELISA), TNF-α (using ELISA) and MCF-7 cells cytotoxicity effects (using MTT assay) of compound 1 were assessed. From the results obtained, compound 1 could be considered as a promising chemotherapeutic agent for the treatment of inflammatory diseases.

Nyirih is a plant from the Meliaceae family with the Latin name Xylocarpus granatum J.Koeing, this nyirih spreads in tropical waters and does not cluster in certain areas. This study aims to determine the total phenolic content of the stem bark extract of nyirih (Xylocarpus granatum J.Koeing) using the UV-Vis spectrophotometric method. The stem bark extract of nyirih (Xylocarpus granatum J. Koeing) was obtained with maceration method using 96% ethanol solvent. Determination of total phenolic content based on the Folin-Ciocalteau method, where the addition of 7% sodium carbonate provides an alkaline atmosphere that will produce phenolic ions. Furthermore, it will reduce Follin to form a blue complex. At a maximum wavelength of 755 nm, the results showed that the average total phenolic content of the stem bark extract of nyirih (Xylocarpus granatum J. Koeing) was 6.163 mg GAE / g extract.

This study evaluated the effects of methanol extract of Peltophorum pterocarpum stem bark (MEPTS) on blood glucose level and lipid profile of Plasmodium berghei ANKA 65-parasitized mice. The levels...

Aims: To investigate the anti-inflammatory activity of Picralima nitida stem bark methanol extract (PNSBE). Study Design: The study was carried out using in vivo (carrageenan-induced paw oedema and egg albumin-induced paw oedema) and in vitro (Human red blood cell (HRBC) membrane stabilization assay) models in rat. Place and Duration of Study: Department of Veterinary Physiology and Pharmacology, Michael Okpara University of Agriculture, Umudike, Abia State, Nigeria from March to July, 2020. Methodology: The extract was used at the doses of 100, 200 and 400 mg/kg while diclofenac (20 mg/kg) was used as the standard reference drug for the in vivo study (carrageenan-induced paw oedema and egg albumin). For the in vitro study (red blood cell haemolysis), the extract was used at the concentrations of 25, 50, 100, 200 and 400 µg/ml while diclofenac 250 µg/ml was used. Results: In the carrageenan-induced paw oedema model, the extract at the doses used and the reference drug significantly (p < 0.05) reduced the paw edema in the rats at 1 hour in a dose dependent manner. Also, in the egg albumin model, the paw oedema of treated rats was significantly (P < 0.05) reduced by PNSBE dose dependently reducing the mean rat paw oedema from 0.99 ± 0.12 to 0.61 ± 0.06 at the first hour. There was also a concentration dependent inhibition of red blood cell haemolysis by the extract in the HRBC membrane stabilization assay. Conclusion: Picralma nitida demonstrated a significant anti-inflammatory activity in this study.

Two new compounds, an isoquinoline (1) and caloneuramide (2), a ceramide were isolated from the stem bark of Discoglypremna caloneura together with seven known compounds namely aurantiamide acetate (3), acetylaleuritolic acid (4), 3α-hydroxylaleuritolic acid 2α-p-hydroxybenzoate (5), mixture of stigmasterol (6) and β-sitosterol (7), mixture of 7-oxo-stigmasterol (8) and 7-oxo-β-sitosterol (9). Their structures were determined based on data from literature and spectroscopic methods. Derivatization reactions on the isoquinoline led to two new compounds, the methylated (10) and acetylated (11) derivatives. Some compounds and extracts were evaluated for their cytotoxic and antiproteinase activity. Antiproteinase effect of compounds 1, 10 and 11 exhibited IC50 values of 10.77, 1.19 and 3.61 μg/mL respectively; significantly low compared to the standard drug, acetyl salicylic acid (IC50 = 20.28 μg/mL). Ethyl acetate and methanol extract exhibited moderate cytotoxicity activity on Chang liver cells with CC50 values of 167.90 ± 2.20 and 106.30 ± 2.03 μg/mL compared to the reference drug cucurmin (CC50 = 11.05 ± 1.04 μg/mL).

Background: Carissa edulis is generally used for the treatment of diverse ailments, but little or no interest has been shown on its hepatoprotective properties. This research work was aimed at evaluating the safety and claimed hepatoprotective activity of Carissa edulis.Method: For the intent of data collection, the method of Li et al., 2011 was used. In this method animals were treated with (250,500 and 1000mg/kg) of stem bark extract. The extract was given daily by gavage to the animals for 28 consecutive days. The 50% v/vCCl4 and olive oil was gavaged through gastric tube twice a week. The tests conducted were liver function test, liver antioxidant enzymes test, lipid profile test as well as Histopathological assessment of the liver sections.Results: Results of the study revealed that the markers in the animal treated with CCl4 were significantly higher than the normal control at (P

The present study investigated antioxidant properties, total phenolic and flavonoid contents in methanol extract of the leaf, stem bark, and fruit of Olea ferruginea Royle, Olea europaea L., and Ti...