DPPH Free Radical Scavenging Assay Research Articles

In vitro anticancer activity studies of Aspergillus terreus on uterine cervix Cancer cells

The exploration of new anticancer agents is in high demand owing to limitations of conventional therapies. This study was designed to evaluate the cytotoxic potential of Aspergillus terreus ethyl acetate extract on uterine cervix cancer cells. Secondary metabolites were extracted from broth cultures and total phenolic content was determined using the Folin-Ciocaltiu method. Antioxidant activity was evaluated using DPPH and ABTS free radical scavenging assays. The cytotoxic activity of the fungal extract was assessed using Methyl ThaizolylTetazolium bromide (MTT) assay on HeLa cells. Morphological changes in HeLa cells upon treatment with the extract were determined. The effect of the fungal extract on cell cycle arrest was evaluated using flow cytometry. The extract showed a significant free radical scavenging activity. The total phenolic content was found to be 16.76 mg of gallic acid equivalents (GAE) per gram dry weight of the extract. The extract exhibited a cytotoxic effect on the HeLa cells with an IC50 value of 92.68 μg/mL. Cell cycle analysis revealed that A. terreus induced G0/G1 arrest confirming its anticancer activity. Results of the present investigation revealed that crude extract of the A. terreus possesses potential anticancer properties.

The Anti-leukemic Potential of Cyclea peltata as Validated by Phytochemical and Cell Line Studies

Hematological malignancies for a very large percentage of cancers occurring the world over and lead to a very large number of deaths each year. It is not just the disease but also the currently available cure which are equally responsible for the side effects and discomfort experienced by the patients. The side effects of the current chemotherapeutic agents' available range from mouth ulcers, diarrhea, temporary hair loss, rashes, nausea, vomiting, and fatigue to low blood cell counts, increased risk of infections, graft versus host disease, tumor lysis syndrome, differentiation syndrome, and difficulty in conceiving. Due to these myriad side effects researchers and on a continuous lookout for newer treatment alternatives. For most developing countries one of the most attractive options is offered by herbals or plant-based medicines. One such herb is Cyclea peltata. It is a climbing shrub found aplenty in southern and eastern India. It has been used traditionally to cure lots of minor ailments. This paper explores the possibility of using the root extract for the treatment of leukemia. To do this, the extracts of the roots were prepared in different organic solvents to ensure complete extraction of all phytoconstituents fractions. The extracts were then tested on 3 different human cell lines. The potential cause of the antileukemic potential of the plant was also hypothesized and proven by carrying out antioxidant studies using the DPPH free radical scavenging assay. The probable active constituents were identified using the liquid chromatography-mass spectrometry assessment, wherein the responsible fractions were successfully identified. The studies showed that the alkaloid and phenolic phytoconstituents were responsible for the antileukemic potential via their antioxidant activity. This lays down the groundwork of offering a new and safer treatment option that could be further explored to be made into one having actual clinical outreach.

Isolation of Enteromorpha species and analyzing its crude extract for the determination of in vitro antioxidant and antibacterial activities.

The extract of green algae (Enteromorpha species) was prepared by the cold extraction technique. The prepared algal extract exhibits a high antioxidant potential due to the presence of sulfated polysaccharides (SPs). The extract of Enteromorpha species was analyzed to identify the presence of significant biochemical composition. The extract of Enteromorpha species was evaluated to assess the DPPH-free radical scavenging activity, total antioxidant activity by phosphomolybdenum assay, in vitro anti-bacterial by agar diffusion method, and cell viability by MTT assay. It was found that the extract of Enteromorpha species contains the various chemical composition such as carbohydrates (0.13 g/ml), xylose (0.0819 g/ml), sulfate (0.0153 g/ml), and proteins (0.0363 g/ml). Phytochemicals such as flavonoids and phenolic compounds were found in the extract. The antioxidant potential of the crude extract was investigated by the total antioxidant assay (400 µl/ml) and DPPH-free radical scavenging assay (5 µl/ml). The prepared green algal extract produced the highest inhibitory zone up to 18 mm, 13 mm, and 18 mm at 200 µl/ml concentrations against Pseudomonas aeruginosa, Staphylococcus aureus, and Escherichia coli, respectively. The above results revealed that the extract of Enteromorpha species exhibited strong antioxidant and anti-bacterial activities due to the presence of sulfated polysaccharides.

Comparative Analysis of the Antioxidant and Antidiabetic Potential of Nelumbo nucifera Gaertn. and Nymphaea lotus L. var. pubescens (Willd.)

Background. Nelumbo nucifera Gaertn. and Nymphaea lotus L. var. pubescens (Willd.) are both aquatic rhizomatous perennial plants mostly found in the tropical region of Nepal, India, Bangladesh, China, and Eastern Asia. Nymphaea pubescens and Nelumbo nucifera plants are famous for their different biological activities such as antidiabetic, antioxidant, hepatoprotective, antidiarrheal, and anti-inflammatory properties. Objective. The present study majorly focused on the determination of in vitro antioxidant and antidiabetic properties of Nelumbo nucifera and Nymphaea pubescens. Methods. In vitro α-glucosidase inhibition was performed using PNPG as a substrate. Antioxidant property of the plant extract was determined by DPPH free radical scavenging assay. The aluminium trichloride method was done for the estimation of total flavonoid content. Likewise, Folin–Ciocalteu reagent was used for determining total phenolic content. Results. The total phenolic content of N. nucifera and N. pubescens was found to be 172.827 ± 0.41 and 194.87 ± 0.93 mg GAE/g, respectively, while the total flavonoid content was reported 17.12 ± 1.04 and 34.59 ± 1.73 mg QE/g, respectively. The IC50 values of the crude extract and its fractions of N. nucifera against the DPPH free radical ranged from 33.46 ± 0.6 to 3.52 ± 0.09 μg/mL, while that of the N. pubescens ranged from 14.30 ± 0.43 to 1.43 ± 0.08 μg/mL. Similarly, for the in vitro α-glucosidase inhibition activity, the IC50 of the crude extract and its fractions of N. nucifera varied from 349.86 ± 2.91 to 29.06 ± 0.24 μg/mL and that of N. pubescens ranged from 224.4 ± 6.85 to 5.29 ± 0.39 μg/mL. Conclusion. Both aquatic plants N. nucifera and N. pubescens show antioxidant properties and can inhibit α-glucosidase in in vitro. Further research is required to identify the inhibiting compounds.

Chemical constituents from fruits of Cnestis ferruginea Vahl ex. DC (Connaraceae) and evaluation of their anticholinesterase and antiradical activities

The phytochemical investigation of the DCM/MeOH (1:1) extract of the fruits of Cnestis ferruginea led to the isolation and characterization of one new quinic acid derivative, ferruginoic acid (1), together with six known compounds 2–7. Compounds 3–7 were reported for the first time from this species. The structures of compounds 1–7 were elucidated on the basis of 1 D and 2 D NMR spectroscopic data, mass spectrometry and by comparison of spectroscopic data with those from the literature. The anticholinesterase (AChE and BChE) activity and DPPH free radical scavenging assay of compounds 1, 3, 4 and 7 were evaluated. Ferruginoic acid (1) exhibited moderate anticholinesterase activity with IC50 value of 36.18 ± 1.78 µg/mL against AChE. Compounds 3, 4 and 7 showed high activity against free radical (DPPH•) scavenging assay (DPPH) with IC50 values 40.09 ± 0.96 µg/mL, 61.70 ± 0.78 µg/mL and 41.87 ± 0.62 µg/mL respectively. These results indicate that C. ferruginea and its constituents could be employed in the management of Alzheimer’s disease.

Chenopodium album extract ameliorates carbon tetrachloride induced hepatotoxicity in rat model

Major objective of this study was to explore the protective effect of the methanolic extract of Chenopodium albumagainst carbon tetrachloride induced hepatotoxicity in rats. Chenopodium album has locally been used for multiple medicinal proposes. Methanolic extract of Chenopodium album (whole plant) was prepared with Soxhlet extractor and rotatory evaporator. Antioxidant activity of Chenopodium album was determined by DPPH free radical scavenging assay. Thirty Wister (albino) rats (150–200 g) were divided into six groups for the evaluation of hepatoprotective potential of different concentrations of Chenopodium album against carbon tetrachloride (1:1 CCl4: Olive oil) under the controlled laboratory conditions. Group-I rats were administrated with olive oil (Normal control), Group-II with CCl4 only, Group-III with Silymarin (positive control), Group-IV with Chenopodium album (100 mg/kg), Group-V with Chenopodium album (200 mg/kg) and Group-VI rats with Chenopodium album (300 mg/kg) for the period of 28 days. Serum was taken to determine the levels of alanine transaminase, aspartate transaminase, alkaline phosphatase, cholesterol, triglyceride, creatinine and urea in the blood. Formalin stored tissues were examined for histopathological analysis. DPPH assay showed that Chenopodium album has the potential for reduction of oxidative stress. Chenopodium album minimized the levels of ALT (70 ± 8.68 U/L, 68.75 ± 8.38 U/L & 73.5 ± 10.28 U/L), AST (219.5 ± 19.16 U/L, 140.75 ± 13.35 U/L & 221.25 ± 13.33 U/L) and ALP (289.5 ± 28.21 U/L, 258 ± 11.12 U/L & 248.25 ± 4.03 U/L) at different concentrations (100 mg/kg, 200 mg/kg, 300 mg/kg respectively). Chenopodium album enhanced triglyceride level (64.75 ± 12.66 mg/dl at 200 mg/kg) as compared to CCl4 treated group (33.25 ± 1.26 mg/dl). Carbon tetrachloride elevated urea level (43.25 ± 6.6) was decreased by high dose of Chenopodium album (18 ± 8.17). Moreover, Chenopodium album also improved WBC level (9.69 × 103 /Cu.mr & 10.59 × 103 /Cu.mr at low and medium doses respectively), RBCs level (6.97 × 103 /Cu.mr) and hemoglobin level (13.95 G/dL, 13.467 G/dL & 14.05 G/dL at low, medium and high doses). In vivo study of Chenopodium album methanolic extract demonstrates the potential for protection of liver and after pre-clinical studies the plant can be used as a safe alternative of commercially available hepatoprotective medicines.

Phyto-Mediated Copper Oxide Nanoparticles for Antibacterial, Antioxidant and Photocatalytic Performances.

The greatest challenge of the current generation and generations to come is antimicrobial resistance, as different pathogenic bacteria have continuously evolved to become resistant to even the most recently synthesized antibiotics such as carbapenems. Resistance to carbapenems limits the therapeutic options of MDR infections as they are the only safe and effective drugs recommended to treat such infections. This scenario has complicated treatment outcomes, even to the commonest bacterial infections. Repeated attempts to develop other approaches have been made. The most promising novel therapeutic option is the use of nanomaterials as antimicrobial agents. Thus, this study examined the efficacy of Camellia sinensis extract (CSE) and Prunus africana bark extract (PAE) green synthesized Copper oxide nanoparticles (CuONPs) against carbapenem-resistant bacteria. Furthermore, the photocatalytic and antioxidant activities of CuONPs were evaluated to determine the potential of using them in a wide range of applications. CuONPs were biosynthesized by CSE and PAE. UV vis spectroscopy, X-ray Diffraction (XRD), Dynamic light scattering (DLS), Fourier Transform Infrared spectroscopy (FTIR), and Scanning Electron Microscopy (SEM) were used to characterize the nanoparticles. CuONPs susceptibility tests were carried out by the agar well diffusion method. The photocatalytic and antioxidant activities of the CuONPs were determined by the methylene blue and DPPH free radical scavenging assays, respectively. UV vis absorbance spectra registered surface plasmon resonance peaks between 272 and 286 nm, confirming the presence of CuONPs. The XRD array had nine strong peaks at 2θ values typical of CuONPs. FTIR spectra exhibited bands associated with organic functional groups confirming capping and functionalization of the CuONPs by the phytochemicals. DLS analysis registered a net zeta potential of +12.5 mV. SEM analysis revealed that the nanoparticles were spherical and clustered with a mean diameter of 6 nm. Phytosynthesized CuONPs exhibited the highest growth suppression zones of 30 mm with MIC ranging from 30 to 125 μg/ml against MDR bacteria. Furthermore, the CuONPs achieved a methylene blue dye photocatalysis degradation efficiency of 85.5% and a free radical scavenging activity of 28.8%. PAE and CSE successfully bio-reduced copper ions to the nanoscale level with potent antimicrobial, photocatalysis, and antioxidant activities.

Assessment of Antioxidant, Antimicrobial, Cytotoxicity and Thrombolytic Potential of Erythrina fusca Lour Grown in Bangladesh

The current study was conducted to assess the antioxidant, antimicrobial, cytotoxicity and thrombolytic potential of the leaves and stem bark of Erythrina fusca Lour grown in Bangladesh. For the assessment of antioxidant properties, DPPH scavenging and phosphomolybdenum assays were used. In the DPPH free radical scavenging assay, the chloroform soluble fraction of a methanol extract of leaves of E. fusca exhibited the highest free radical scavenging activity with an IC50 value of 5.5 ± 0.60 μg/ml, while the reference standard (ascorbic acid) showed an IC50 value of 5.8 ± 0.18 μg/ml. All the test samples and the standard BHT demonstrated good linear relationship in the phosphomolybdenum assay. It was observed that the test samples contained considerable number of bioactive compounds including total phenolics in the aqueous soluble fraction of the leaves giving the highest 94.02 ± 1.004 GAE/100g of dried sample. All test samples exhibited moderate antimicrobial activity against 13 Gram-positive and Gram-negative bacterial strains and 3 fungi, where the chloroform soluble fraction of the stem bark demonstrated the highest inhibition of growth with zone of inhibition of 19.3 ± 0.21 mm against Bacillus cereus. All the test samples displayed cytotoxic activity against brine shrimp nauplii having significant LC50 and LC90 values. The chloroform soluble materials demonstrated highest lethality with LC50 value of 1.55 ± 0.30 μg/ml and LC90 65.68 ± 0.23 μg/ml. On the other hand, the carbon tetrachloride soluble fraction of the stem bark showed the highest clot lysis (22.75 ± 0.59%) as compared to that (66.77 ± 0.61%) revealed by reference standard, streptokinase. The findings of this study revealed that the leaves and stem bark of E. fusca growing in Bangladesh possesses bioactive compounds but further studies are required to purify and identify them. Bangladesh Pharmaceutical Journal 25(1): 1-8, 2022 (January)

In vitro Analysis Provides New Insights into the Pharmacological Actions of Methanol Extract of Seeds of Tamarindus indica L. and its Kupchan Fractions

Tamarind or Tamarindus indica L. is a multipurpose plant distributed throughout the tropics including Bangladesh. The present study was conducted to establish the preliminary antioxidant, antimicrobial, anti-inflammatory and thrombolytic activities of methanol extract of T. indica seeds along with its Kupchan fractions. To evaluate the antioxidant properties, the total phenolic content of T. indica was determined and expressed in gallic acid equivalent (GAE). Alongside, DPPH free radical scavenging assay was performed to ensure the antioxidant properties of the seeds where the methanolic crude extract revealed the maximum activity having IC50 value of 9.43 μg/ml. In the antimicrobial assay by disk diffusion method, only non-polar fractions of the extract showed mild antimicrobial activity against the test organisms tested while the polar crude methanol extract exhibited the maximum inhibition (58.16%, p < 0.001) of hypotonic solution-induced erythrocyte rupture in anti-inflammatory investigation among all the partitionates. During evaluation of thrombolytic activity in terms of percent of clot lysis, the methanol soluble fraction exhibited the highest percent of thrombolysis (23.5%) as compared to the reference standard, streptokinase (64.25%). The findings of the current study rationalize some of the traditional uses of T. indica and preliminarily ascertain its bioactive potential, which may act as a base for phytochemical and mechanism-based pharmacological studies of the plant in future. Bangladesh Pharmaceutical Journal 25(1): 9-15, 2022 (January)

A Study on Aphanamixis polystachya for evaluation of phytochemical and pharmacological properties

The present study was conducted to detect possible chemicals (phytoconstituents), and investigate antioxidant, antimicrobial and thrombolytic activities of the extract of Aphanamixis polystachya (stem bark). Phytochemical screening was carried out using the standard test methods of different chemical group. For investigating the antioxidant activity, two complementary test methods namely DPPH free radical scavenging assay and total phenolic content determination were carried out. For the evaluation of in Vitro antimicrobial activity, disc diffusion method, and to determine the thrombolytic activity, the method of Prasad et al., 2007 with minor modifications were used. The bark extracts were a rich source of phytochemicals. In DPPH free radical scavenging test, the Carbon tetra chloride soluble fraction showed the highest free radical scavenging activity with IC50 value 19.86 µg/ml. while compared to that of the reference standards ascorbic acid. Aphanamixis polystachya was also found as a good source of total phenolic contents. Moreover, the extracts revealed broad spectrum antimicrobial activity at the concentration of 400 µg/disc. By comparing with the negative control the mean clot lysis % was significant (p value <0.0009). Therefore, further studies are suggested to determine the active compounds responsible for the biological activities of the plant extracts.

Characterization of phytochemicals and determination of antioxidant, antimicrobial and cytotoxic properties of the medicinal plant Ardisia solanacea

The present study was conducted to detect possible phytochemicals and evaluate antioxidant, antimicrobial and cytotoxic activities of the extract of Ardisia solanacea. Phytochemical screening was carried out using the standard test methods of different chemical group. For investigating the antioxidant activity, two complementary test methods namely DPPH free radical scavenging assay and total phenolic content determination were carried out. For the evaluation of in vitro antimicrobial activity, disc diffusion method was used. Evaluation of cytotoxic activity was done using the brine shrimp lethality bioassay. In DPPH free radical scavenging test, the petroleum ether soluble fraction showed the highest free radical scavenging activity with IC50 value 40.04 μg/ml. while compared to that of the reference standards ascorbic acid. Ardisia solanacea was also found as a good source of total phenolic contents. Moreover, the extracts revealed moderate antimicrobial activity at the concentration of 400 μg/disc. In cytotoxic activity test, the petroleum ether soluble fraction showed significant cytotoxic potential (LC50 value of 0.703 μg/ml) among all the fractions comparing with that of standard vincristine (0.544 μg/ml). Therefore, further studies are suggested to determine the active compounds responsible for the pharmacological activities of the plant extracts.

Evaluation of antioxidant activity of Mimosa pudica L. extracts

Antioxidant activity of petroleum ether, chloroform, ethyl acetate and methanol extracts of leaf, stem and root of Mimosa pudica L. was observed through DPPH (2,2-diphenyl-1-picrylhydrazyl) free radical scavenging assay. Five concentrations (12.5, 25.0, 50.0, 100.0 and 200.0µg/ml) were taken for each extract as well as the standard and the absorbances were measured at 517nm using a spectrophotometer against methanol blank. The activity was increased by the increment of concentrations of the extracts. In case of leaf, the highest scavenging percentage was found in chloroform extract (86.40%) at 200.0µg/ml concentration. But for stem and root, the highest scavenging percentages were found in ethyl acetate extracts (73.72% and 83.79% respectively) at same concentration. The ethyl acetate extracts showed the highest activity among all the extracts where the IC50 values were 65.152µg/ml, 76.036µg/ml and 65.000µg/ml and the lowest was found in petroleum ether extracts where the IC50 values were 130.129µg/ml, 147.891µg/ml and 186.449µg/ml for leaf, stem and root respectively and that was for ascorbic acid (standard) was 18.012µg/ml.

TOTAL PHENOLIC, FLAVONOID CONTENT, AND ANTIOXIDANT ACTIVITY OF JUSTICIA TRANQUEBARIENSIS L.F. AND CYCAS BEDDOMEI DYER. LEAVES

Polyphenolics such as tannins and flavonoids are proved as powerful antioxidants to resolve cellular stress, sustain homeostasis in the body and prevent stress-associated disorders. Plant-based medicine gained importance due to its safety margin and multiple benefits. Regular intake of antioxidants is an alternative to avoid serious illness. The current investigation is aimed to measure the phenolic, flavonoid content, the antioxidant activity of Justicia tranquebariensis L.f. and Cycas beddomei leaves. The selected plants are used by tribes and traditional medicine to cure various diseases. Total phenolic content was estimated using the Folin–Ciocalteu colorimetric method, taking gallic acid as standard. At the same time, total flavonoid content was determined by aluminum chloride colorimetric assay using Rutin as standard. The absorbance was measured at 760 nm and 510 nm, respectively. Antioxidant activity was measured by two In vitro methods (DPPH and NO free radical scavenging assay) using standard protocols, where Ascorbic acid served as a reference standard. Results disclosed that the total phenolic content for the methanolic extracts of C. beddomei (36.14 ± 1.72) and J. tranquebariensis (28.57 ± 0.91) was found to be higher than petroleum ether extracts. Similarly, C. beddomei (28.13 ± 2.48) is richer in flavonoids than J tranquebariensis (20.32 ± 1.24). In DPPH assay, methanolic extract C. beddomei (78.21%) is more effective to inhibit the free radicals than J. tranquebariensis (73.05%) with IC50 values 41.55μg/ml & 59.52 μg/ml respectively at higher doses that are comparable to standard ascorbic acid (84.34%, IC50 =63.27 μg/ml). Similarly, in NO free radical scavenging assay, methanolic extract of C. beddomei (72.54%) stood best among all to scavenge the free radicals with IC50 values 50.06 μg/ml, whereas ascorbic acid is found to inhibit 83.26% with IC50 values 39.75μg/ml. The presence of various secondary metabolites such as alkaloids, carbohydrates, phenols, steroids, terpenoids, glycosides, saponins, especially tannins and flavonoids, either alone or in combination, may be responsible for the observed scavenging property. The quantity of the phenolic compounds and flavonoids can be directly correlated to the exhibited activity.

Biological Properties and Phytonutrient Profile of Beans: Vigna angularis, Vigna radiata, and Glycine max

The consumption of specific plant foods in distinct diets reduces chronic illnesses, cardiovascular diseases, diabetes, and even cancer. This offers an interesting platform to study the various phytonutrients claimed by numerous studies for providing different physiological and pharmacological effects in the human body. This study has focused on the analysis of phytonutrients in three leguminous plants, namely Vigna angularis (VA), Vigna radiata (VR), and Glycine max (GM). Chemical constituents evaluated include polyphenols, flavonoids, condensed tannins, and polysaccharides, while DPPH free radical scavenging and ferric reducing antioxidant power (FRAP) assays were utilized for in vitro antioxidant activities. The findings showed that the beans contain a professed number of condensed tannins and polyphenols, while they also contain flavonoids and polysaccharides. The 95% ethanol extract of VA showed the highest level of extracted total polyphenols and total condensed tannin content than other extracts. VA 95% EtOH extract exhibited a phytochemical profile consistent with the obtained biological activities such as antioxidant, anti-inflammatory, and cell viability. Our study has successfully determined the phytonutrient profiles of the bean extracts and their associated biological activities.

Synthesis, characterization, and biological evaluation of novel selenium-containing chitosan derivatives

Though great efforts have been made to develop selenium polysaccharides with unique properties using HNO3-Na2SeO3 methods, the Se content is still low due to the poor esterification efficiency of H2SeO3. Herein, selenodiacetic acid (SA) was introduced into chitosan (CS) to synthesize O-selenodiacetyl chitosan (OSAC) and chitosan-ammonium selenodiacetate (CASA) by covalent and non-covalent interaction, respectively. The obtained CS derivatives were characterized by UV–vis, FTIR, 1H NMR, XPS, TGA, and XRD spectra, and the OSAC and CASA showed high Se content up to 15,720 ± 475 and 26,363 ± 698 μg/g. The OSAC and CASA demonstrated increased antioxidant activities compared to the CS in DPPH and ABTS free radical scavenging assays. Moreover, they exhibited a potent anticancer effect on HepG2 cells with the IC50 values of 0.918 and 1.459 μg/mL. Taken together, this study provides a promising strategy for the design of novel selenium polysaccharides with high Se content and greater biological activity.

Effect of milk-derived bioactive peptides on the lipid stability and functional properties of beef nuggets

The present study was conducted to ascertain the beneficial effects of bioactive peptides on the oxidative stability and functional properties of beef nuggets. In this study, milk casein protein hydrolysates were extracted and incorporated into beef nuggets which were then subjected to different assessment parameters including oxidative stability, functional capability as well as microbial and physico-chemical quality tests were performed for determining the meat quality at different storage periods. The casein protein hydrolysate powder (CPH) was added at different concentrations in nuggets CPH 2%, 4%, 6% and 8%, with reference to storage period of 0, 5, 10 and 15 days at 4 °C. The results regarding total phenolic contents (TPC) and DPPH free radical scavenging assay showed a significant increased with respect to CPH powder and significantly decreased with respect to storage interval. The TVBN, TBARS and POV of the CPH powder incorporated raw beef nuggets also differed significantly within groups with storage time. Higher POV and TBARS were noticed in the CPH 8% incorporated beef nuggets. However, the raw beef nuggets that were made by the incorporation 8% CPH powder, maintained significantly lower level of TBARS at the end of the storage period in contrast with the levels of the control (CPH 0%). The results of the pH and Hunter color test also showed a significant difference with respect to different groups. The microbiological analysis of beef nuggets showed a significant decrease in the level of both the total aerobic and coliform counts and also indicated a decreasing trend in the level of contamination by these bacteria within the groups. This depicted that the casein protein hydrolysate powder (CPH) or simply, the peptide powder has the strong ability to decrease lipid oxidation and related shelf-life retarding natural processes occurring in the meat. It can also greatly enhance the functional properties of the raw meat (beef) and meat products. Thus, it is seen that the bioactive peptides (BAP’s) are a key factor in improving the oxidative stability and functional properties of beef nuggets.

Synthesis, spectroscopic characterization (FT-IR, NMR, UV-Vis), DFT study, antibacterial and antioxidant in vitro investigations of 4,6-bis((E)-1-((3-(1H-imidazol-1-yl)propyl)imino)ethyl)benzene-1,3-diol

A new bis-Schiff base derived from N-(3-Aminopropyl)imidazole and 4, 6-diacetylresorcinol was obtained. The bis Schiff base RS was characterized through mass spectrometry, elemental analysis, infrared, UV-Vis, 1H and 13C NMR spectroscopy. The B3LYP method was used to calculate the optimized structure of the molecule through density functional of theory (DFT) using the 6-31G (d, p) basis set. The 1H and 13C NMR chemical shifts with respect to TMS were calculated using the (GIAO) method in DMSO‑d6 and compared with the experimental data. In addition, the frontier molecular orbitals, electronic properties and the molecular electrostatic potential (MEP) of RS were investigated using DFT calculations. The compound showed significant antibacterial activity against Staphylococcus aureus. The DPPH free radical scavenging assay was used to evaluate the antioxidant activity. The effective concentration (EC50) showed that the compound has a good antioxidant activity.

Screening of the antioxidant and antibacterial effects of extracted essential oils from Thunbergia coccinea, Acacia polyacantha, Polygonum micrpcephallum, Abies spectabilis and Clerodendrum colebrookianum.

During the previous few decades, it has been seen that there is a rapid emergence of pathogens resistant to multiple antibiotics. This has now become a global crisis. Some unexplored or less explored plants also provide some antibacterial, bactericidal and antioxidant properties. The antibacterial, bactericidal effects of extracted essential oils (EEOs) of Thunbergia coccinea, Acacia polyacantha, Polygonum micrpcephallum, Abies spectabilis and Clerodendrum colebrookianum was tested in comparison with standard antibiotics. The methods chosen were disc diffusion and deduction of minimum inhibitory concentration (MIC) by microbroth dilution assays of the EEOs against the bacterial strains.The antioxidant activity was found out utilizing DPPH free radical scavenging assay, MDA, Hydrogen peroxide radical inhibition assay and Superoxide radical inhibition assay (O 2 -). Some commonly used standard antibiotics (metronidazole, amoxicillin, clarithromycin, rifampicin, clindamycin and oxacillin,) were utilized to compare the EEO antibacterial action. Clerodendrum colebrookianum (85.17 ± 3.06 µg MDA/g extract) had a reasonable MDA. Acacia polyacantha in MIC had values of 3.86 ± 0.25 to 6.20 ± 0.16. Polygonum micrpcephallum had excessive H2O2 (48.27 ± 2.4 5%). The antibacterial actions determined by the paper disc‑diffusion technique of the EEO extracted from these plants showed that most had some antibacterial actions. Also, it was seen that the bactericidal action of the EEO extracted from E. alba was most potent against S. pyogenes (4.06 ± 0.15). The extract of the plant at varying concentrations (20, 40, 60, 80 and100 mg/mL) demonstrated noteworthy (P< 0.001) anthelmintic action in an effective change when the dose was adjusted. In conclusion, most of the tested plants contain a medicinal value, which can be utilized in the future to supplement artificial medicines and cure emerging diseases that create havoc for mankind.

Antifungal, antiradical, anti-inflammatory and antineoplastic activities of essential oils of some medicinal plants of the Annonaceae family of Chad and Cameroon

Yeasts infections, cancer and other diseases associated with free radical generation and inflammation are currently a critical public health issue that needs innovative control measures. In order to search for solutions, this study was designed to assess the antifungal, radical scavenging, anti-inflammatory, and antineoplastic activities of essential oils from four Annonaceae plants (Monodora myristica, Xylopia aethiopica, and Xylopia parviflora) collected in Chad and Cameroon. Essential oils were extracted by hydrodistillation. The antifungal activity of the oils was determined using the microdilution method; and their antiradical activity was determined using the DPPH free radical scavenging assay. The anti-inflammatory activity was assessed using the inhibitory effect of oils against the 5-lipoxigenase. Flow cytometry was used to assess the effect of essential oils on cell cycle. The essential oils of X. aethiopica, X. parviflora, and M. myristica inhibited the growth of Candida albicans ATCC24433, Candida parapsilosis ATCC22019, and Cryptococcus neoformans IP95026 with MIC values ranging from 5 to 10 mg/mL. Essential oils of X. aethiopica, X. parviflora, and M. myristica showed free radical scavenging potential with SC50­ values between 8.9 and 11.74 g/L. The oils samples at 100 μg/mL from both origins significantly inhibited cancer cell (MCF-7) and normal epithelial cells of the eye (ARPE-19) growth, with a notable cell cycle arrest at phases G0/G1 and S at 72h respectively. According to the findings of this study, essential oils from Annonaceae plants contain bioactive secondary metabolites that have the potential to inhibit pathogenic yeasts, free radicals, inflammatory and cancer cells. Further research is needed to confirm these findings and formalize their eventual application to control the targeted affections.

Screening revealed the strong cytotoxic activity of &lt;i&gt;Alchemilla smirnovii&lt;/i&gt; and &lt;i&gt;Hypericum alpestre&lt;/i&gt; ethanol extracts on different cancer cell lines

&lt;abstract&gt; &lt;p&gt;Compounds of plant origin are considered promising alternative approaches in the development of medicines for the prevention and treatment of cancer. The large diversity of herbal species still requires careful exploration as a source for new anticancer compounds. The goal of the study was to screen different herbal extracts traditionally used in Armenian folk medicine for their cytotoxic effect against some cancer cell lines, and to find the prospective plant species among them. The cytotoxicity of the plant ethanol extracts was evaluated with MTT test against HeLa (human cervical carcinoma) and A549 (human lung adenocarcinoma) cells. Antioxidant properties were assessed with DPPH free radical scavenging assay. Five of the tested ten herbal extracts exhibited significant growth-inhibiting activity on HeLa cells. Moreover, &lt;italic&gt;Alchemilla smirnovii&lt;/italic&gt; and &lt;italic&gt;Hypericum alpestre&lt;/italic&gt; extracts also showed potent cytotoxicity on human lung adenocarcinoma cells. These two plants possessed high antiradical activity as well. Their DPPH stoichiometric values were 0.4234 and 0.14437 respectively, meaning that 1 µg of plant extract brought the reduction of DPPH equal to the respective stoichiometric values in µg. Thus, &lt;italic&gt;A. smirnovii&lt;/italic&gt; and &lt;italic&gt;H. alpestre&lt;/italic&gt; extracts expressed themselves as potent cytotoxic and antioxidant agents and could have promising anticancer potential. Further evaluation of their &lt;italic&gt;in vivo&lt;/italic&gt; anticancer properties has much interest.&lt;/p&gt; &lt;/abstract&gt;