Mary Aubrey Zamayla Sumagaysay, Stephany Abrio, Hazrat Ayna Tomawis Balindong, Norhussien Hadji ali Calandada, Daniella Tongco Cemine, Jumaima Sidic Hadji Assim, Janz Kyle Abonitalia Magdales, Mikaella Abrigo Mercado, Christle Joyce Barte Taripe, Madeleine Cabeltes Zamayla, Jevie Lyn Peralta-Tan Nery, Eugene Marc Daguio Cera III, Mylene Sevilla AndalJustin Dave Magracia, Justin Dave Magracia Manantan, Jan Karlo Tiongson Ecalne
{"title":"评估肉桂树皮乙醇提取物的抗氧化活性","authors":"Mary Aubrey Zamayla Sumagaysay, Stephany Abrio, Hazrat Ayna Tomawis Balindong, Norhussien Hadji ali Calandada, Daniella Tongco Cemine, Jumaima Sidic Hadji Assim, Janz Kyle Abonitalia Magdales, Mikaella Abrigo Mercado, Christle Joyce Barte Taripe, Madeleine Cabeltes Zamayla, Jevie Lyn Peralta-Tan Nery, Eugene Marc Daguio Cera III, Mylene Sevilla AndalJustin Dave Magracia, Justin Dave Magracia Manantan, Jan Karlo Tiongson Ecalne","doi":"10.30574/gscbps.2024.28.1.0272","DOIUrl":null,"url":null,"abstract":"Kalingag (Cinnamomum mercadoi) is a native plant of the Philippines that has long been used in traditional medicine. Because of its indigenous nature, research on this plant remains limited. This research evaluated the phytochemical content and antioxidant properties of a crude ethanolic extract from Cinnamomum mercadoi bark. The plant bark collected from Davao Occidental was thoroughly cleaned with distilled water to remove any adhering dirt, air-dried for a week in the shade, and then pulverized with a Wiley mill. The bark was then subjected to Soxhlet extraction for 6 hours, and the pooled extracts were concentrated for 5 hours at 60°C in a rotary evaporator to yield a green, syrupy substance. The extract was tested for phytochemical content, followed by Fourier Transform Infrared Spectroscopy (FTIR) for confirmation of the subsequent results by determining the functional groups that comprise their structure, before being assessed using the DPPH assay for free radical scavenging. The phytochemical screening and subsequent FTIR analysis revealed important metabolites such as tannins, glycosides, phytosterols, and terpenoids, all of which contribute to the antioxidant activity of the crude ethanolic extract. In the DPPH assay, the extract demonstrated concentration-dependent activity (IC50 = 85.7627 µg/mL) compared to the gallic acid (IC50 = 4.1818 µg/mL). Such findings highlight the importance of purifying and isolating specific compounds to boost the plant's antioxidant activity. To maximize its value, further study into other parts of the plant is recommended.","PeriodicalId":12808,"journal":{"name":"GSC Biological and Pharmaceutical Sciences","volume":"1 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluation of antioxidant activity of the crude ethanolic extract from the bark of Cinnamomum mercadoi\",\"authors\":\"Mary Aubrey Zamayla Sumagaysay, Stephany Abrio, Hazrat Ayna Tomawis Balindong, Norhussien Hadji ali Calandada, Daniella Tongco Cemine, Jumaima Sidic Hadji Assim, Janz Kyle Abonitalia Magdales, Mikaella Abrigo Mercado, Christle Joyce Barte Taripe, Madeleine Cabeltes Zamayla, Jevie Lyn Peralta-Tan Nery, Eugene Marc Daguio Cera III, Mylene Sevilla AndalJustin Dave Magracia, Justin Dave Magracia Manantan, Jan Karlo Tiongson Ecalne\",\"doi\":\"10.30574/gscbps.2024.28.1.0272\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Kalingag (Cinnamomum mercadoi) is a native plant of the Philippines that has long been used in traditional medicine. Because of its indigenous nature, research on this plant remains limited. This research evaluated the phytochemical content and antioxidant properties of a crude ethanolic extract from Cinnamomum mercadoi bark. The plant bark collected from Davao Occidental was thoroughly cleaned with distilled water to remove any adhering dirt, air-dried for a week in the shade, and then pulverized with a Wiley mill. The bark was then subjected to Soxhlet extraction for 6 hours, and the pooled extracts were concentrated for 5 hours at 60°C in a rotary evaporator to yield a green, syrupy substance. The extract was tested for phytochemical content, followed by Fourier Transform Infrared Spectroscopy (FTIR) for confirmation of the subsequent results by determining the functional groups that comprise their structure, before being assessed using the DPPH assay for free radical scavenging. The phytochemical screening and subsequent FTIR analysis revealed important metabolites such as tannins, glycosides, phytosterols, and terpenoids, all of which contribute to the antioxidant activity of the crude ethanolic extract. In the DPPH assay, the extract demonstrated concentration-dependent activity (IC50 = 85.7627 µg/mL) compared to the gallic acid (IC50 = 4.1818 µg/mL). Such findings highlight the importance of purifying and isolating specific compounds to boost the plant's antioxidant activity. To maximize its value, further study into other parts of the plant is recommended.\",\"PeriodicalId\":12808,\"journal\":{\"name\":\"GSC Biological and Pharmaceutical Sciences\",\"volume\":\"1 3\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-07-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"GSC Biological and Pharmaceutical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.30574/gscbps.2024.28.1.0272\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"GSC Biological and Pharmaceutical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.30574/gscbps.2024.28.1.0272","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Evaluation of antioxidant activity of the crude ethanolic extract from the bark of Cinnamomum mercadoi
Kalingag (Cinnamomum mercadoi) is a native plant of the Philippines that has long been used in traditional medicine. Because of its indigenous nature, research on this plant remains limited. This research evaluated the phytochemical content and antioxidant properties of a crude ethanolic extract from Cinnamomum mercadoi bark. The plant bark collected from Davao Occidental was thoroughly cleaned with distilled water to remove any adhering dirt, air-dried for a week in the shade, and then pulverized with a Wiley mill. The bark was then subjected to Soxhlet extraction for 6 hours, and the pooled extracts were concentrated for 5 hours at 60°C in a rotary evaporator to yield a green, syrupy substance. The extract was tested for phytochemical content, followed by Fourier Transform Infrared Spectroscopy (FTIR) for confirmation of the subsequent results by determining the functional groups that comprise their structure, before being assessed using the DPPH assay for free radical scavenging. The phytochemical screening and subsequent FTIR analysis revealed important metabolites such as tannins, glycosides, phytosterols, and terpenoids, all of which contribute to the antioxidant activity of the crude ethanolic extract. In the DPPH assay, the extract demonstrated concentration-dependent activity (IC50 = 85.7627 µg/mL) compared to the gallic acid (IC50 = 4.1818 µg/mL). Such findings highlight the importance of purifying and isolating specific compounds to boost the plant's antioxidant activity. To maximize its value, further study into other parts of the plant is recommended.