South Asian Research Journal of Natural Products http://journalsarjnp.com/index.php/SARJNP <p style="text-align: justify;"><strong>South Asian Research Journal of Natural&nbsp;Products</strong>&nbsp;aims to publish&nbsp;high-quality&nbsp;papers (<a href="/index.php/SARJNP/general-guideline-for-authors">Click here for Types of paper</a>) covering all aspects of research&nbsp;of naturally occurring compounds or the biology of living systems from which they are obtained.</p> en-US contact@journalsarjnp.com (South Asian Research Journal of Natural Products) contact@journalsarjnp.com (South Asian Research Journal of Natural Products) Tue, 25 Feb 2020 06:13:09 +0000 OJS 3.1.1.4 http://blogs.law.harvard.edu/tech/rss 60 Antibiotics Sensitivity Profile of Wounds’ Bacterial Isolates and Antibacterial Assessment of Chromolaena odorata Aqueous and Ethyl Acetate Extracts http://journalsarjnp.com/index.php/SARJNP/article/view/30095 <p><strong>Aim:</strong> To study the <em>in vitro</em> inhibitory effect of <em>C. odorata</em> extracts on bacterial isolates from wound swab samples.</p> <p><strong>Place of Study:</strong> University of Medical Sciences Teaching Hospital, Akure, Ondo State, Nigeria, between January and June 2019.</p> <p><strong>Methodology:</strong> Wound swabs were collected from patients of University of Medical Sciences Teaching Hospital, Akure. Air-dried and powdered <em>C. odorata</em> leaves were extracted using distilled water and ethyl acetate and concentrated using a rotary evaporator. Qualitative phytochemical screening of <em>C. odorata</em> extracts was done by standard methods. Antibiotics susceptibility pattern of bacterial isolates to a panel of ten (10) conventional antibiotics was determined by disc diffusion method. Antibacterial activity of <em>C. odorata</em> extracts were determined using agar diffusion&nbsp; method.</p> <p><strong>Results:</strong> <em>Pseudomonas aeruginosa</em> was the most abundant bacteria isolated (40.30%) in this study. <em>Chromolaena odorata</em> aqueous extract had higher extraction yield (24.1%) than ethyl acetate extract. Phytochemical screening revealed the presence of saponin, flavonoids, terpenoids, steroids, tannin, glycoside and phenol of <em>C. odorata</em> extracts. <em>Proteus vulgaris</em> exhibited 100% resistance against augmentin. The highest zone of inhibition observed with the <em>C. odorata</em> ethyl acetate extract was against <em>P. aeruginosa </em>(18.67±0.67 mm).</p> <p><strong>Conclusion:</strong> This study reveals the <em>in vitro</em> inhibitory effect of <em>C. odorata</em> extracts on bacteria isolated from wounds thus presenting them as potential antibacterial agents.</p> Mercy Adewumi Alabi ##submission.copyrightStatement## http://journalsarjnp.com/index.php/SARJNP/article/view/30095 Wed, 25 Dec 2019 00:00:00 +0000 Phytochemical Screening, Antimicrobial and Antioxidant Activity of Lepidium sativum Seeds Extract http://journalsarjnp.com/index.php/SARJNP/article/view/30096 <p>Plants play a significant role in drug discovery and development of pharmaceuticals process. In many countries, medicinal plants consider the main source of primary health care.</p> <p><strong>Aims:</strong> This study aimed to investigate the phytochemical screening, antimicrobial and antioxidant activities of <em>Lepidium sativum</em> seeds extracts and fractions.</p> <p><strong>Methodology:</strong> Seeds of <em>L. sativum</em> were collected and extracted by maceration in methanol and the extract was fractionated using hexane, chloroform, ethyl acetate and an aqueous solvent. Phytochemical screening of crude extract was performed using standard methods. The crude extracts and the fractions were tested against <em>Staphylococcus aureus</em>, <em>Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa, Aspergillus niger and Candida albicans</em>. The radical scavenging (DPPH) was determined according to the standard methods.</p> <p><strong>Results:</strong> The phytochemical screening result of the crude extract showed the presence of flavonoids, alkaloids, tannins, saponins, phenols, glycosides and terpenoids. Antimicrobial activities results were showed variation in the inhibition zones from 8-20 mm; the best activity was in <em>A. niger</em> 20 mm at concentration 100 mg/mL of crude extract, however in <em>S. Aureus</em> 16 mm at the same concentration of ethyl acetate fraction. The results of free radical scavenging activity results obtained were higher at ethyl acetate fraction (76±0.02%), chloroform fraction (74±0.01%) and aqueous fraction (70±0.09%), while moderate at the crude extracts (46±0.07%) and low at hexane fraction (21±0.04%).</p> <p><strong>Conclusion:</strong> It could be concluded that the crude extracts and fractions of <em>L. sativum </em>had high potential as an antibacterial and antioxidant agent, which can be used for medicinal purposes.</p> Awdalla B. Omer, Azhari H. Nour, Mahmoud M. Ali, Omer Adam Omer Ishag, Ibrahim Yaagoub Erwa, Mohammed Abdelwahhab Ali ##submission.copyrightStatement## http://journalsarjnp.com/index.php/SARJNP/article/view/30096 Fri, 20 Mar 2020 00:00:00 +0000 Use of Polyphenol Extracts from Dioscorea steriscus and Plecranthus esculentus N.E.Br Tubers to Curb Oxidative Deterioration of Sunflower Oil http://journalsarjnp.com/index.php/SARJNP/article/view/30097 <p><strong>Aim:</strong> The aim of the present study was to determine the possibility of using polyphenol extracts from <em>Dioscorea steriscus</em> and <em>Plecranthus esculentus N.E.Br </em>tubers of Zimbabwe as preservatives for sunflower oil under oven and kitchen storage conditions.</p> <p><strong>Methodology:</strong> Polyphenols were extracted from <em>Dioscorea steriscus</em> and <em>Plecranthus esculentus</em> tubers, screened using polyphenol screening assays and added to virgin sunflower oil at 100 ppm dose.&nbsp; Oxidative stability was determined using peroxide values and UV-Vis absorbances a 232 nm.</p> <p><strong>Results:</strong> Polyphenol screening assays of aqueous acetone extracts from <em>Dioscorea steriscus </em>and<em> Plecranthus esculentus</em> tubers revealed the presence of flavonoids, phenolic acids, tannins, lignans and anthocyanins. Oxidative stability of sunflower oil under kitchen storage conditions (room temperature) and oven storage conditions (65°C) as measured by peroxide values and UV-Vis absorbances at 232 nm followed the order <em>D. steriscus</em> fortified ˃ BHT fortified ˃ <em>P. esculentus</em> fortified ˃ unfortified. The lowest mean peroxide value (17.72±0.05 mEq/kg oil) over a 5 week storage duration under kitchen storage conditions was recorded in <em>D.steriscus</em> fortified sunflower oil and the highest (31.17±0.16 mEq/kg oil) was recorded in unfortified sunflower oil.</p> <p><strong>Conclusion:</strong> Polyphenol extracts from <em>Dioscorea steriscus</em> and <em>Plecranthus esculentus</em> tubers showed high preservative potential on virgin sunflower oil under both kitchen and oven storage conditions. Polyphenol extracts from <em>D. steriscus</em> and <em>P. esculentus</em> tubers may be used as alternative sources of antioxidants for the preservation of sunflower oil.</p> Masimba Tapera, Ruth Wanjau, Alex K. Machocho, Pamhidzai Dzomba ##submission.copyrightStatement## http://journalsarjnp.com/index.php/SARJNP/article/view/30097 Wed, 25 Mar 2020 00:00:00 +0000