Antioxidant and antibacterial activities of Opuntia ficus indica seed oil fractions and their bioactive compounds identification

AbstractAim:The twoMethods:Based on the inhibition concentration at 50 percent (ICResults:Results showed that antioxidant and antibacterial activities considerably varied depending on the fraction. In fact, unsaponifiable fraction has higher biological activities than the glyceridic ones. The unsaponifiable fraction has stronger effects of scavenging 2,2-Diphenyl-1-picrylhydrazyl (DPPH) radical and it is more efficient against bleaching of β-carotene than the saponifiable extract, unlike the experimental results of 2,2′-azino-bis3-ethylbenzthiazoline-6- sulfonic acid (ABTS) scavenging test. Furthermore, the unsaponifiable fraction was more efficient against all pathogenic strains speciallyConclusion:Informations provided through this work are important for the valorization and use of this cactus vegetable oil in cosmetic, pharmaceutical and nutraceutical industries.

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Metabolism of Rhaponticin and Activities of its Metabolite, Rhapontigenin: A Review

Current Medicinal Chemistry ◽

10.2174/0929867326666190121143252 ◽

2020 ◽

Vol 27 (19) ◽

pp. 3168-3186 ◽

Cited By ~ 2

Author(s):

Dan Chen ◽

Jing-Ru Liu ◽

Yanjin Cheng ◽

Hua Cheng ◽

Ping He ◽

...

Keyword(s):

Morphological Changes ◽

Biological Activities ◽

Reference Value ◽

Antibacterial Activities ◽

Therapeutic Drug ◽

Oxygen Species ◽

Dpph Radical ◽

Anticancer Activities ◽

Human Cytochrome ◽

Underlying Mechanisms

Rhaponticin is a stilbenoid glucoside compound, found in medicinal plant of rhubarb rhizomes. Rhapontigenin (RHAG), the stilbene aglycone metabolite of rhaponticin, has shown various biological activities including anticancer activities to act a potential human cytochrome P450 inhibitor, antihyperlipidemic effect, anti-allergic action, antioxidant and antibacterial activities. Moreover, it was reported to scavenge intracellular Reactive Oxygen Species (ROS), the 1,1-Diphenyl-2-Picrylliydrazyl (DPPH) radical, and Hydrogen Peroxide (H2O2). Meanwhile, RHAG exhibited the inhibitory activity for the synthesis of DNA, RNA and protein, and also presented the capacity of inducing morphological changes and apoptosis of C. albicans. Here, the structure, pharmacokinetics, pharmacological effects as well as underlying mechanisms of rhaponticin and its metabolite, RHAG, have been extensively reviewed. This review will provide a certain reference value for developing the therapeutic drug of rhaponticin or RHAG.

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Gas Chromatographic Analysis of Bioactive Compounds in the Seed Oil of Pentaclethra macrophylla (African Oil Bean Tree)

10.53365/nrfhh/143048 ◽

2021 ◽

Author(s):

Abdulrasaq Oyedeji ◽

Luqman Azeez ◽

Bibilomo Odeyemi

Keyword(s):

Liquid Chromatography ◽

Bioactive Compounds ◽

Chromatographic Analysis ◽

Seed Oil ◽

Industrial Applications ◽

Gas Liquid Chromatography ◽

Bioactive Components ◽

Ionization Detector ◽

Flame Ionization ◽

Β Carotene

This study characterized the bioactive components in the seed oil of <i>Pentaclethra macrophylla</i> to establish its usefulness in replacing costly convectional oils in industrial applications. Identification and quantification of the bioactive attributes were performed using gas-liquid chromatography with flame ionization detector (GC-FID) after extraction with n-Hexane. The main bioactive contents per 100 g in the oil were sitosterol (457.58 mg), campesterol (34.54 mg) and stigma-sterol (18.52 mg) been the most abundant sterols. The oil contained per 100 g β-carotene (15.89 mg), xanthophyll (10.32 mg), lutein (9.22 mg), and neo-xanthin (5.46 mg) as the highest carotenoids. The oil has ɣ- tocopherol (43.83 mg) and α-tocopherol (3.35 mg) also per 100 g. The main terpenes per 100 g in the oil were γ-elemene (17.28 mg), α-caryophyllene (13.06 mg), β-elemene (12.43 mg) and D-limonene (6.11 mg). Terpenoids including β-amyrin, α-amyrin and lupeol were found in trace amounts.

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Comparative Analysis of Biological Activity of Artificial and Wild Agarwood

Forests ◽

10.3390/f12111532 ◽

2021 ◽

Vol 12 (11) ◽

pp. 1532

Author(s):

Sheng Ma ◽

Mengji Qiao ◽

Yunlin Fu ◽

Penglian Wei ◽

Yingjian Li ◽

...

Keyword(s):

Sulfonic Acid ◽

Biological Activities ◽

Reducing Power ◽

Acetylcholinesterase Activity ◽

Antioxidant Ability ◽

Dpph Radical ◽

Soluble Extract ◽

Clearance Rates ◽

Activity Inhibition ◽

The Difference

Agarwood is a highly economically important medicinal herb with widespread uses; however, the difference between the biological activities of artificial and wild agarwood is unclear. In this study, the alcohol-soluble extracts of agarwood produced by fungi and natural agarwood were used to determine the differences between the overall biological activities. The antioxidant ability (the clearance rates of 1,1-diphenyl-2-picrylhydrazyl (DPPH) and 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS+) radicals, and total reducing power), anti-acetylcholinesterase, and anti-α-glucosidase activity were determined by ultraviolet-visible spectrophotometry. The results indicated that with 2 mg/mL alcohol-soluble extracts, the scavenging DPPH radical rates of the artificial agarwood samples were 93.74–102.31% of that of the wild agarwood, and the ABTS+ radical clearance rates of the artificial agarwood samples were 75.38–95.52% of that of the natural agarwood. With 3.5 mg/mL alcohol-soluble extracts, the artificial agarwood samples had a total reducing power of 63.07–80.29% of that of the wild agarwood. With 4 mg/mL alcohol-soluble extract, the acetylcholinesterase activity inhibition rates of the artificial agarwood samples were 102.56–109.16% of that of the wild agarwood. With 1 mg/mL alcohol soluble extracts, the α-glucosidase effect inhibitions rates of the artificial agarwood samples were 68.32–100.39% of that of the wild agarwood.

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Pharmacologically potentials of different substituted coumarin derivatives

10.31221/osf.io/w6hdg ◽

2019 ◽

Cited By ~ 1

Author(s):

Chem Int

Keyword(s):

Benzene Ring ◽

Bioactive Compounds ◽

Biological Activities ◽

Pharmacological Properties ◽

Coumarin Derivatives ◽

Wide Range ◽

Anti Oxidant ◽

Anti Inflammatory ◽

Coumarin Compounds

Coumarin and its derivatives are widely spread in nature. Coumarin goes to agroup as benzopyrones, which consists of a benzene ring connected to a pyronemoiety. Coumarins displayed a broad range of pharmacologically useful profile.Coumarins are considered as a promising group of bioactive compounds thatexhibited a wide range of biological activities like anti-microbial, anti-viral,antiparasitic, anti-helmintic, analgesic, anti-inflammatory, anti-diabetic, anticancer,anti-oxidant, anti-proliferative, anti-convulsant, and antihypertensiveactivities etc. The coumarin compounds have immense interest due to theirdiverse pharmacological properties. In particular, these biological activities makecoumarin compounds more attractive and testing as novel therapeuticcompounds.

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Cyanobacteria—From the Oceans to the Potential Biotechnological and Biomedical Applications

Marine Drugs ◽

10.3390/md19050241 ◽

2021 ◽

Vol 19 (5) ◽

pp. 241

Author(s):

Shaden A. M. Khalifa ◽

Eslam S. Shedid ◽

Essa M. Saied ◽

Amir Reza Jassbi ◽

Fatemeh H. Jamebozorgi ◽

...

Keyword(s):

Bioactive Compounds ◽

Biomedical Applications ◽

Large Scale ◽

Biological Activities ◽

Scale Production ◽

Pharmacological Activities ◽

Large Scale Production ◽

Marine Products ◽

Hiv 1 ◽

Successful Phase

Cyanobacteria are photosynthetic prokaryotic organisms which represent a significant source of novel, bioactive, secondary metabolites, and they are also considered an abundant source of bioactive compounds/drugs, such as dolastatin, cryptophycin 1, curacin toyocamycin, phytoalexin, cyanovirin-N and phycocyanin. Some of these compounds have displayed promising results in successful Phase I, II, III and IV clinical trials. Additionally, the cyanobacterial compounds applied to medical research have demonstrated an exciting future with great potential to be developed into new medicines. Most of these compounds have exhibited strong pharmacological activities, including neurotoxicity, cytotoxicity and antiviral activity against HCMV, HSV-1, HHV-6 and HIV-1, so these metabolites could be promising candidates for COVID-19 treatment. Therefore, the effective large-scale production of natural marine products through synthesis is important for resolving the existing issues associated with chemical isolation, including small yields, and may be necessary to better investigate their biological activities. Herein, we highlight the total synthesized and stereochemical determinations of the cyanobacterial bioactive compounds. Furthermore, this review primarily focuses on the biotechnological applications of cyanobacteria, including applications as cosmetics, food supplements, and the nanobiotechnological applications of cyanobacterial bioactive compounds in potential medicinal applications for various human diseases are discussed.

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Pinus Species as Prospective Reserves of Bioactive Compounds with Potential Use in Functional Food—Current State of Knowledge

Plants ◽

10.3390/plants10071306 ◽

2021 ◽

Vol 10 (7) ◽

pp. 1306

Author(s):

Marcin Dziedziński ◽

Joanna Kobus-Cisowska ◽

Barbara Stachowiak

Keyword(s):

Human Health ◽

Bioactive Compounds ◽

Functional Food ◽

Biological Activities ◽

Food Ingredients ◽

Beneficial Effects ◽

Pine Tree ◽

Pine Trees ◽

Health Promoting ◽

Few Data

The pine (Pinus L.) is the largest and most heteromorphic plant genus of the pine family (Pinaceae Lindl.), which grows almost exclusively in the northern hemisphere. The demand for plant-based remedies, supplements and functional food is growing worldwide. Although pine-based products are widely available in many parts of the world, they are almost absent as food ingredients. The literature shows the beneficial effects of pine preparations on human health. Despite the wide geographical distribution of pine trees in the natural environment, there are very few data in the literature on the widespread use of pine in food technology. This study aims to present, characterise and evaluate the content of phytochemicals in pine trees, including shoots, bark and conifer needles, as well as to summarise the available data on their health-promoting and functional properties, and the potential of their use in food and the pharmaceutical industry to support health. Various species of pine tree contain different compositions of bioactive compounds. Regardless of the solvent, method, pine species and plant part used, all pine extracts contain a high number of polyphenols. Pine tree extracts exhibit several described biological activities that may be beneficial to human health. The available examples of the application of pine elements in food are promising. The reuse of residual pine elements is still limited compared to its potential. In this case, it is necessary to conduct more research to find and develop new products and applications of pine residues and by-products.

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Facile Green, Room-Temperature Synthesis of Gold Nanoparticles Using Combretum erythrophyllum Leaf Extract: Antibacterial and Cell Viability Studies against Normal and Cancerous Cells

Antibiotics ◽

10.3390/antibiotics10080893 ◽

2021 ◽

Vol 10 (8) ◽

pp. 893

Author(s):

Olufunto T. Fanoro ◽

Sundararajan Parani ◽

Rodney Maluleke ◽

Thabang C. Lebepe ◽

Jose R. Varghese ◽

...

Keyword(s):

Gold Nanoparticles ◽

Cell Viability ◽

Leaf Extract ◽

Room Temperature ◽

Klebsiella Oxytoca ◽

Cost Effective ◽

Average Diameter ◽

Antibacterial Activities ◽

Inhibition Concentration ◽

First Time

We herein report a facile, green, cost-effective, plant-mediated synthesis of gold nanoparticles (AuNPs) for the first time using Combretum erythrophyllum (CE) plant leaves. The synthesis was conducted at room temperature using CE leaf extract serving as a reducing and capping agent. The as-synthesized AuNPs were found to be crystalline, well dispersed, and spherical in shape with an average diameter of 13.20 nm and an excellent stability of over 60 days. The AuNPs showed broad-spectrum antibacterial activities against both pathogenic Gram-positive (Staphylococcus epidermidis (ATCC14990), Staphylococcus aureus (ATCC 25923), Mycobacterium smegmatis (MC 215)) and Gram-negative bacteria (Proteus mirabilis (ATCC 7002), Escherichia coli (ATCC 25922), Klebsiella pneumoniae (ATCC 13822), Klebsiella oxytoca (ATCC 8724)), with a minimum inhibition concentration of 62.5 µg/mL. In addition, the as-synthesized AuNPs were highly stable with exceptional cell viability towards normal cells (BHK- 21) and cancerous cancer cell lines (cervical and lung cancer).

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