Background: Plants are able to deliver a huge number of differing bioactive compounds which may supplement the requirements of the human body by acting as natural antioxidants. Antioxidants are mindful for the defense component of the life form against the pathologies related to the assault of free radicals. The main purpose of this study was to investigate the qualitative phytochemical composition of Vernonia amygdalina leaf extract and its antioxidant activity. Method: The powdered plant sample was successively extracted with aqueous, methanol and ethanol solvents using Soxhlet apparatus. The antioxidant activities of the crude leaf extract were determined using 1, 1- diphenyl-2-picryl hydrazyl (DPPH) radical, 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid (ABTS) radical, phosphomolybdate (PM) and hydrogen peroxide (H₂O₂) scavenging assay. All the examinations were drained triplicates and average values of each test were taken. Results: Phytochemical investigation of the plant revealed that the three solvent extracts contained numerous bioactive compounds namely alkaloids, tannins, saponins, phenols, terpenoids, steroids, glycosides and sugars. The result showed that, the leaf extracts of V. amygdalina obtained from methanol extract exhibit the maximum antioxidant activity compared ethanol and aqueous extracts. The IC50 values of DPPH assay for the H₂O, MeOH and EtOH extracts were 111.4, 94.92 and 94.83 μg/ml; of ABTS assay were 334.3, 179.8 and 256.9 μg/ml; of H₂O₂ assay were 141.6, 156 and 180.6 μg/ml, respectively. The maximum radical scavenging activity was obtained in DPPH assay while the lowest scavenging activity was obtained in ABTS assay method. The data obtained in the in vitro models clearly suggest that methanol extract has higher antioxidant activity due to a higher presence of phenolic constituents in the extract. Conclusion: This study revealed that V. amygdalina leaf has a noteworthy antioxidant and free radical scavenging activity mitigating the traditional use of the plant for different aliments.

Background and Aim: Echinops kebericho, an endemic plant to Ethiopia, traditionally used to treat infectious as well as noninfectious diseases. The primary objective of this study was isolating dehydrocostus lactone (DHCL) from E. kebericho and evaluating antibacterial activities on selected human pathogenic bacteria.Methods: Extraction method used in this study was maceration. Based on the bioassay information methanol extract of the root of E. kebericho was subjected to column chromatography on silica gel by increasing solvent gradients to isolate DHCL. Optimized amount isolation of DHCL was done by dissolving methanol crude extract by hexane followed by recrystallization at room temperature in the dark place. Different concentrations of the extract were subjected by disc diffusion method against tested bacterial species and antioxidant activity test.Results: The phytochemical analysis of E. kebericho revealed a high presence of terpenoids, which are diverse natural compounds known for their antimicrobial and antioxidant properties. This suggests that terpenoids contribute significantly to the pharmacological effects of E. kebericho. In antibacterial testing, Escherichia coli was the most sensitive bacterium among all extracts and concentrations. The methanol extract displayed higher antioxidant activity compared to ethyl acetate and hexane extracts, indicating a higher concentration of antioxidant compounds. Notably, the isolated compound DHCL showed promising activity against tested pathogens and significant antioxidant activity. The higher activity of DHCL compared to the crude extracts suggests its responsibility for the observed effects, indicating that the isolation and purification process may have concentrated its beneficial properties. These findings highlight the potential of E. kebericho and DHCL as sources of bioactive compounds for therapeutic applications.Conclusion: All tested extracts and pure compound showed higher inhibition than positive controls in both bioassay. DHCL the principal bioactive component in the root extract of the plant and it displayed potent antibacterial and antioxidant activity.

This study investigated the anti‐inflammatory properties of Ajuga integrifolia, an herbal preparation. Qualitative and quantitative phytochemical analyses were conducted to identify active compounds in the preparation. The researchers also assessed its ability to inhibit the production of pro‐inflammatory enzymes, cyclooxygenases (COX‐1, COX‐2), and lipoxygenase (5‐LOX) in vitro. The extracts demonstrated dose‐dependent inhibition of these enzymes, with some extracts showing IC₅₀ values comparable to standard anti‐inflammatory drugs. The ethanol extract exhibited significant inhibition of 5‐LOX (52.99 μg/mL), compared to the standard drug zileuton (32.41 μg/mL), while the inhibition of COX‐1 (66.00 μg/mL) and COX‐2 (71.62 μg/mL) was comparable to the standard drug indomethacin (40.57 and 54.39 μg/mL, respectively). These findings suggest that A. integrifolia has the potential to be used as a herbal remedy for treating inflammatory conditions. By inhibiting pro‐inflammatory enzymes, the extracts may effectively reduce inflammation and promote tissue healing or repair. The inhibition potential of extract of this plant can be taken as a good candidate of anti‐inflammatory agent.

The success in discovering natural therapeutic agents relies on bioassay‐guided fractionation and purification techniques. Active ingredients from herbal medicines are beneficial due to their compatibility with various other active substances. To evaluate the antibacterial activities of sesquiterpenoid compound isolated from the leaves of Laggera tomentosa endemic to Ethiopia. The crude extract was obtained using the maceration technique from the leaves of Laggera tomentosa. Hexane, ethyl acetate, and methanol were used to fractionate crude extract for phytochemical and antibacterial evaluation. The phytochemical screening of the crude was done to test the presence or absence of alkaloids, phenols, saponins, flavonoids, tannins, steroids, and glycosides. Methanol extract was subjected to silica gel column chromatography to isolate the pure compound. Structural elucidation of the isolated compound was done via IR and NMR. The fractions and the isolated compound were used to assess the antibacterial activity potentials of this plant material using disc diffusion assay against E. coli, S. aureus, and L. monocytogen. The crude extract (48 g) obtained from 300 g leaves powder was subjected to column separation and pure compound (65 mg) was isolated. The phytochemical screening of the crude indicates the presence of alkaloids, phenols, saponins, flavonoids, and tannins and the absence of steroids and glycosides. Spectral analysis results revealed that the compound isolated was identified as 3‐O‐(3′‐acetoxy‐2′‐hydroxy‐2′‐methylbutyryl)‐cuauhtemone. Regarding the antibacterial activities, the highest (15.56 ± 1.96 mm) and lowest (6.5 ± 0.01 mm) inhibition zone diameters were recorded against S. aureus at concentrations of 100 and 10 mg/mL, respectively, by the methanol soluble fraction. The antibacterial assay revealed that the methanol‐soluble portion of the extract exhibited promising antibacterial activities warranting further studies.

Sedimentary rocks are produced by the weathering of preexisting rocks and the subsequent transportation and deposition of the weathering products. Among the sedimentary rocks, especially limestone is a crucial raw material for cement production. The purpose of this study was to characterize the valuable industrial raw materials, limestone, gypsum, clay, coal, and iron ore, along with the Nile River basin. For sample collection, a random sampling method was applied. Different analytical methods were carried out for complete oxide analysis such as LiBO₂ fusion, HF attack, and gravimetric, calorimetric, and atomic absorption spectroscopy (AAS). The percentages of oxides detected in this study are in the range of acceptable values (high content of CaO ranging from 47.3 to 50.4 and less content of SiO₂ ranging from 8.72 to 11.24) for good proposal as a potential raw material for cement production. The most dominant and wide-range coverage of limestone along with the Nile basin, particularly near Arsema Monastery, was found as matured limestone. The petrographic analysis of gypsum, sandstone, and clay samples indicated that all the samples taken from Wegidi revealed that the high percentage of gypsum ranges from 90 to 95. Sandstone is dominantly preset in Kelala to Jamma road along with Beto River with high content of SiO₂ ranging from 61 to 95. The results of this study indicate that the treated coal samples are relative to high calorific value, fixed carbon, and low ash content. Coal and iron ore from Jamma revealed that high calorific value is 4929.24 and hematite content is 52.2, respectively. The result of this study revealed that a huge amount of limestone reservoir is detected in Borena Wereda, Amhara, Ethiopia.