Journal of Natural Products Discovery (LJMU)
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    38 research outputs found

    3D Printing of Multilayered Hydrogel containing Hyaluronic acid and Linalool

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    This study presents the 3D printing and the development of multilayered hydrogel formulations containing hyaluronic acid (HA) and linalool (LN) for potential use as a personalised moisturising and anti-acne product. Various shapes were printed via 3D printing for personalised application; however, material characterisation was conducted primarily on the first layer. The average film weight was 2.11 ± 0.20 g, with optimal storage conditions identified as placement on a covered plate at 25 °C. Films containing 10% LN demonstrated a higher linalool release profile (maximum 22.66% of the nominal dose) compared to the 5% LN films, correlating with stronger antibacterial activity against Staphylococcus aureus. FT-IR analysis revealed the absence of C=C and C–H peaks in blank and 5% LN films due to water interference, while 10% LN films displayed characteristic LN peaks. Texture analysis showed that the 5% LN film exhibited greater tensile resistance, with the highest force recorded at 27.500 g. LN played an important role in the transformation of hydrogel ink to a liquid-like state under high strain. In conclusion, these findings highlight the potential of 3D-printed HA–LN hydrogels for customisable skincare applications with dual functionality in moisturising and antimicrobial effects

    APOPTOTIC ACTIVITY OF BOSWELLIA CARTERII EXTRACT ON HUMAN NEUTROPHILS.

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    Neutrophil activation is required for the initiation of the defence mechanisms which include phagocytosis. Paradoxically, neutrophils also represent one of the main mediators of tissue injury in various human diseases. The resolution of inflammation requires getting rid of excess inflammatory cells through natural cell death and phagocyte clearance. Frankincense, an oleogum resin of different species of the genus Boswellia (Burseraceae), has long been used in eastern countries\u27 traditional medicine to alleviate pain and inflammation. Although it was demonstrated that boswellic acids are potent activators of polymorphonuclear cells, little is known about the effects of the total extract on the human phagocytes’ apoptosis. We here undertake a characterization of the Boswellia carteri resin extract (BCE) effects on human neutrophils activity and viability in vitro. Oxidative burst after stimulation with BCE was evaluated by reduction of nitroblue tetrazolium (NBT) colorimetric method for superoxide anion radical in the the presence of different compounds (N-ethyl maleimide, diltiazem, chelerythrine and wortmannin). Neutrophils viability was assessed by MTT. Flow analyses were performed with propidium iodide (PI) and annexin V-FITC. Our results show that BCE induces the release reactive species of oxygen in human neutrophils in a dose dependent manner. The superoxide anion radical is principally produced via NADPH oxidase since inhibitors of the enzyme may prevent it. Ca+2 depletion reduce the magnitude of activation and PKC and PI3-K are also apparently involved in the process. The BCE has also cytotoxic activity revealed by the MTT assay. This effect seems to be produced by an apoptotic process as shown by the exclusion of the dye propidium iodide and the annexin V-FITC binding. The capacity of the Boswellia carterii extract to accelerate the cellular death by an apoptotic process suggest that either the extract or its active compounds could have applications for the resolution of some inflammatory conditions

    Antimicrobial Activities, phytochemical composition and thin layer chromatography profile of Gossypium hirsutum and Abelmoschus esculentus leaves extracts

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    Background: This study evaluates the antimicrobial activities, phytochemical composition, and thin layer chromatography (TLC) profile of ethanolic and aqueous leaf extracts of Gossypium hirsutum L. and Abelmoschus esculentus (L.) Moench. Aims: The objective is to investigate the phytochemical constituents and assess the antimicrobial efficacy of these plant extracts against various pathogenic microorganisms. Methods: Leaves were collected, identified, air-dried, and powdered. Ethanolic and aqueous extracts were prepared and subjected to TLC analysis using silica gel plates and a mobile phase of ethanol, methanol, and ethyl acetate (5:3:2). Phytochemical screening was conducted using standard protocols. Antimicrobial activity was evaluated using the agar well diffusion method against pathogens including Escherichia coli, Staphylococcus aureus, Klebsiella pneumoniae, Salmonella typhi, Proteus, Streptococcus pneumoniae and Candida spp. Results: TLC analysis revealed seven compounds in G. hirsutum and six in Abelmoschus esculentus with distinct Rf values. Phytochemical screening identified phenols/tannins, saponins, flavonoids, reducing sugars, terpenoids, and anthraquinones in G. hirsutum, while A. esculentus contained all tested phytochemicals except phytosterol and essential oil. The antimicrobial assay indicated that ethanolic extracts of both plants exhibited significant antibacterial activity, with G. hirsutum showing higher efficacy. Ethanolic extracts of G. hirsutum inhibited S. aureus and S. typhi effectively, while aqueous extracts showed limited activity. Extracts of A. esculentus leaves inhibited all tested organisms except Proteus, with ethanol extracts also ineffective against S. pneumoniae. Conclusion: The study demonstrates that ethanolic extracts of G. hirsutum and A. esculentus possess antimicrobial properties. These findings support the potential use of these plant extracts in developing natural antimicrobial agents

    PHYTOCHEMICAL, ELEMENTAL ANALYSIS AND ANTIFUNGAL ACTIVITY OF ERIGERON FLORIBUNDUS (BILBAO FLEABANE) LEAF EXTRACT AGAINST MALASSEZIA FURFUR

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    Background: Elemental composition and phytochemical content of plants viz; saponins, flavonoids, alkaloids, tannins, polyphenols, terpenoids and their concentrations are potentials for their antifungal or antimicrobial activity. Aim: This study is aimed at evaluating the phytochemical, elemental composition and antifungal activity of the essential oil and dichloromethane extract of E. floribundus, against Malassezia furfur - the fungi that causes Pityriasis versicolor (eczema). Method: Assays for the antifungal activity of were performed using the agar dilution method at serial concentrations ranging from 2 to 0.06 mg/ml. Phytochemicals were determined using the suitable Official Analytical (AOAC) methods. Results: The essential oil of E. floribundus was the most potent, inhibiting the fungi at 0.25 mg/ml (IZD = 27 mm), while the dichloromethane extract inhibited the organism at 0.5 mg/ml (IZD = 25 mm), showing a better activity than the control antifungal, clotrimazole which showed an MIC of 1 mg/ml and an inhibition zone diameter (IZD) of 18 mm. Saponins showed the highest concentration of 900 mg per 5 g in the phytochemicals analyzed; with tannins showing the lowest of 56.6 mg per 5 g.  The concentrations of carbon, nitrogen, magnesium, sodium and Sulphur were 68.7 mg per 100 g, 49.4 mg per 100 g, 324.5 ppm, 78.50 ppm and nil respectively. Conclusion: The essential oil and dichloromethane extract of E. floribundus revealed a good potential as an antifungal agent against M. furfur based on their minimum inhibition concentration, which is better than the conventional antifungal agent used as control in this study. Concentrations of phytochemicals in the plant also suggest that it has potentials for the traditional treatment of eczema/skin disorders

    FORMULATION OF AN ANTIOXIDANT HYDROGEL FACE MASK USING AN ORGANIC, SUSTAINABLY SOURCED, STANDARDISED WATER EXTRACT OF YERBA MATE (ILEX PARAGUARIENSIS) AS ACTIVE INGREDIENT.

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    Background: The use of natural products in cosmetics has become increasingly popular in recent years. One such natural product that has shown promise as a cosmetic ingredient is Ilex paraguariensis, also known as yerba mate. Aim: to formulate an antioxidant hydrogel face mask using an organic, sustainably sourced, standardised water extract of yerba mate (Ilex paraguariensis) as active ingredient. Methods: Organic yerba mate was water-extracted at 40°C and 80°C. Theobromine, theophylline, caffeine, and various phenolic acids were quantified using RP-HPLC-UV analysis. Extracts were then evaluated for antioxidant activity (DPPH assay). A commercially available mask-making machines for home use was used to produce hydrogel masks based on marine collagen and these were analysed for active ingredient distribution (homogeneity). Results: The differences between 40°C and 80°C water extracts of yerba mate. The content in phytochemicals ranged 0.02-1 mg/ml. The extract equivalence in chlorogenic acid (CA) according to the DPPH assay was 0.25 mgCA / mgextract. The hydrogel facial mask was successfully formulated with 0.1 mg/mL of standardised yerba mate extract. The content in phytochemicals within the gel varied most for caffeic acid and theobromine (approx. 20%) but was <10% for theophylline, caffeine, chlorogenic acid, ferulic acid, rutin, quercitrin, and quercetin. Conclusion: Face masks “home” machines can deliver hydrogel face masks based on marine collagen can incorporate yerba mate (Ilex paraguariensis) water extracts as active ingredient without detriment of the consistency, texture and sensory characteristics with relatively homogenous concentrations of the active principles

    Soxhlet extraction cycle-dependent diversity in phenolic profile and antioxidant potency of red cabbage (Brassica oleracea var. capitata F. rubra)

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    Introduction: The Brassicaceae vegetables are a rich source of secondary metabolites that exhibit several health benefits and protection against numerous degenerative diseases. Objectives: The current study was performed to investigate the effect of Soxhlet extraction cycles on the phenolic profile of red cabbage (Brassica oleracea var. capitata F. rubra) and its biological activities. Materials and Methods: The red cabbage sample was harvested from the research fields of Ayub Agricultural Research Institute Faisalabad, Pakistan. The ethanol extracts were prepared using 1-, 2-, 4-, and 8-cycles Soxhlet extraction technique. The antioxidant potential of red cabbage extracts was estimated by evaluation of total phenolic contents (TPC), total flavonoid contents (TFC), DPPH radical scavenging capacity and reducing power. The identification and quantification of polyphenols were carried out by RP-HPLC. The antibacterial activity of red cabbage extracts was determined against Escherichia coli and Staphylococcus aureus and the antiproliferative activity was carried out by MTT mitochondrial viability assay against the human A549 cancer cell line. Results: Gallic acid, p-hydroxyl benzoic acid, chlorogenic acid, and p-coumaric acid were the major phenolic acids, whereas catechin and quercetin were the major flavonoids detected in the red cabbage extracts. The extraction cycles were found to have significant (p ≤ 0.05) effects on the phenolic profile of the red cabbage extracts.  TPC of extracts ranged from 5.22-11.72 mg/g dry matter, measured as gallic acid equivalent, while the TFC ranged from 1.64-5.19 mg/g dry matter; measured as catechin equivalent. The 4-cycles extract of red cabbage exhibited the maximum TPC, TFC, and DPPH free-radical scavenging and reducing activity. Conclusion: The study concluded that the Soxhlet extraction cycles could exert a considerable effect on the yield and polyphenol composition of red cabbage extracts as well as their antioxidant potential. Antibacterial and antiproliferative activities were observed by all the extracts of red cabbage

    IN VITRO EVALUATION OF THE ANTIMICROBIAL, TOXIC, ANTI-ARTHRITIC AND THROMBOLYTIC PROPERTIES OF DIFFERENT PARTS OF PLANT ORCHID RHYNCHOSTYLIS RETUSA (L.) BLUME.

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    Background: Infection due to microbes, trauma, cancer, arthritis and thrombosis are the most common problems worldwide. Traditionally, a large number of herbal extracts are used for the treatment of those disorders. Aim: Ethanolic extracts from leaves, roots and stems of Rhynchostylis retusa (L.) Blume were phytochemically characterised and then tested for their antibacterial, toxicity, anti-arthritic, and thrombolytic properties in-vitro. Methods and Results: Disk diffusion inhibition tests with a panel of fourteen different microorganisms was used as the antimicrobial assays. Antimicrobial activity of the stem extract found to be higher (10-11 mm, 400 µg/disk) than that of root extract whereas leaf showed no activity with ciprofloxacin (43-46 mm, 5 µg/disc) serving as reference standard. Toxicity of the plant extracts in terms of their LC50 values against the brine shrimp (A. salina) was assessed. The toxic potential of leaf extract was 6.7 μg/ml, which is higher than that of stem and root extract (c.a. 8.5 μg/ml). Thrombolytic properties were tested in vitro using streptokinase as reference (%Clot lysis after 1.5h & 24h was 76.15±1.94 & 92.59±2.35, 30000iu). The leaf extract exhibited higher activity. Leaf extract (1000 ppm) lysed of 33.08±1.24% of the clot and 60.47±2.33 after 1.5 h and 24 h of incubation, respectively. Anti-arthritic effects measured as albumin denaturation using diclofenac sodium as reference (IC50=60.25 ppm) revealed the stem extract as more active. Conclusion: our research will help to provide evidence for some of the traditional uses of this medicinal plant

    How specific is Crispr-Cas9?

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    RESEARCH ACTIVITIES IN THE CENTRE FOR NATURAL PRODUCTS DISCOVERY IN 2023

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    In 2023, the Centre for Natural Products Discovery (CNPD) made significant strides in the scientific community through a series of impactful research initiatives. These efforts underscore our commitment to harnessing the world’s natural resources to advance health. The fertile research environment at the CNPD has given rise to various sections, each contributing innovative and practical applications. Our goal here is to provide a concise overview of our research activities for the year. While this summary is not exhaustive, it focuses on the work of our section leaders, which in turn encompasses the contributions of numerous other researchers both within and outside the CNPD

    THE 4th Annual CNPD (Centre for Natural Products Discovery) Conference

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    The 4th Annual CNPD (Centre for Natural Products Discovery) Conference held on 19-22 June 2023 at the John Lennon Arts and Design Building, has been a remarkable success. The feedback from the participants from all over the world (e.g., Bangladesh, Czech Republic, China, Pakistan, India, Italy, Nepal, Romania, South Korea, Switzerland, The Philippines, Turkey and USA), as well as from our home participants, was simply excellent. Many commented that our conference is one of the best conferences they have ever attended. Prof Laura Bishop, PVC Science opened the conference, and welcomed the participants on behalf of the Faculty and LJMU. Prof Satya Sarker, Director of School of Pharmacy and Biomolecular Sciences, and the Founding Head of the Centre for Natural Products Discovery, presented an overview of the centre and welcomed everybody on behalf of the School and the Centre. During the conference, several outstanding invited talks were presented and the quality of the short 10 min presentations was also excellent. The poster session was lively and highly interactive, the extended tea/coffee breaks and lunch breaks provided a fantastic opportunity for networking. There was a lively panel discussion on the contemporary issues in natural products research, and the impact of AI on natural products research and scientific publications dominated the discussion. There were three prizes sponsored by Goss Scientific, and Perkin Elmer, given to the best poster, the best short oral presentation and the best overall performance, selected by a panel of four judges, two internal and two externals. We are absolutely delighted to see our PhD student Waed Alsheikh won the best oral and overall best performance prizes. It can be mentioned that Waed is the Faculty Winner of the 3 min thesis presentation, and the LJMU winner through popular votes. The conference concluded with my ‘vote of thanks’, and a declaration that the 5th Annual CNPD conference will be held online over Teams in 2024, and 6th Annual CNPD conference will be held face-to-face in Liverpool in 2025