Sharanya Sundaramoorthy, Anusha Dakshinamoorthi, Chithra K
{"title":"Evaluation of anti-oxidant and anticancer effect of marine algae <i>Cladophora glomerata</i> in HT29 colon cancer cell lines- an <i>in-vitro</i> study.","authors":"Sharanya Sundaramoorthy, Anusha Dakshinamoorthi, Chithra K","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Marine algae are a huge Pandora's box of rich nutrients and huge medicinal compounds. These therapeutic compounds are investigated widely for their anticancer, antioxidant, and anti-diabetic properties.</p><p><strong>Objectives: </strong>This study aims to evaluate the antioxidant and anticancer effect of the marine algae <i>Cladophora glomerata</i> (collected from Hare Island-Tuticorin region) on HT-29 colon cancer cell lines.</p><p><strong>Methodology: </strong>The marine algae, <i>Cladophora glomerata</i>, was collected, processed, and authenticated. Methanol, Ethyl acetate, Chloroform, and Hexane extracts were prepared using a hot solvent extraction process. These extracts were subjected to SOD assay and MTT assay. 5 Fluorouracil was used as the positive control.</p><p><strong>Results: </strong>The antioxidant activity of the SOD assay was found to be 85.66±0.81, 80.10±1.25, and 98±0.93 U/mg protein for methanol, ethyl acetate, chloroform, and hexane extracts, respectively. L-Ascorbic acid was used as the positive control whose SOD antioxidant value was found to be 139±1.24 U/mg protein. The IC50 value of methanol, ethyl acetate, chloroform, hexane algae extracts, and 5 Fluorouracil against HT29 cell lines was calculated to be 28.46±0.65, 48.56±1.19, 93.7±0.91, 88.53±0.83, and 8.2±1.3 μg/ml, respectively.</p><p><strong>Conclusion: </strong>From the above study, we can infer that the methanol extracts of the algae <i>Cladophora glomerata</i> have excellent anticancer activity. Therefore, these compounds can be purified and analyzed further for a potential lead as an anticancer molecule.</p>","PeriodicalId":14352,"journal":{"name":"International journal of physiology, pathophysiology and pharmacology","volume":"14 6","pages":"332-339"},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890206/pdf/ijppp0014-0332.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of physiology, pathophysiology and pharmacology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Marine algae are a huge Pandora's box of rich nutrients and huge medicinal compounds. These therapeutic compounds are investigated widely for their anticancer, antioxidant, and anti-diabetic properties.
Objectives: This study aims to evaluate the antioxidant and anticancer effect of the marine algae Cladophora glomerata (collected from Hare Island-Tuticorin region) on HT-29 colon cancer cell lines.
Methodology: The marine algae, Cladophora glomerata, was collected, processed, and authenticated. Methanol, Ethyl acetate, Chloroform, and Hexane extracts were prepared using a hot solvent extraction process. These extracts were subjected to SOD assay and MTT assay. 5 Fluorouracil was used as the positive control.
Results: The antioxidant activity of the SOD assay was found to be 85.66±0.81, 80.10±1.25, and 98±0.93 U/mg protein for methanol, ethyl acetate, chloroform, and hexane extracts, respectively. L-Ascorbic acid was used as the positive control whose SOD antioxidant value was found to be 139±1.24 U/mg protein. The IC50 value of methanol, ethyl acetate, chloroform, hexane algae extracts, and 5 Fluorouracil against HT29 cell lines was calculated to be 28.46±0.65, 48.56±1.19, 93.7±0.91, 88.53±0.83, and 8.2±1.3 μg/ml, respectively.
Conclusion: From the above study, we can infer that the methanol extracts of the algae Cladophora glomerata have excellent anticancer activity. Therefore, these compounds can be purified and analyzed further for a potential lead as an anticancer molecule.