@article {1499, title = {Antioxidant and Anticancer Activities of Ocimum basilicum L. cv. Dark Opal (Lamiaceae)}, journal = {Pharmacognosy Journal}, volume = {6}, year = {2014}, month = {3rd Sept, 2014}, pages = {S}, type = {Original Article}, chapter = {32}, abstract = {

Background: Plants used in folk and traditional medicines have been accepted as therapeutic drug development in modern medicine.Although manystudies have been focused on Lamiaceae family,few studies on medical effects of purple basil have been performed until now. Objective: Ocimum basilicum cv. dark opal was chosen for this study as it has been used in Persian traditional medicine and many Iranian dishes. It was considered important to determine the cytotoxicity effect andthe reductive capacity of the purple basil oils and extracts, as this may indicate their potential as antioxidants. Materials and Methods: The reducing power activity of both essential oils of the leaves (before flowering) and the seeds and also methanolic extracts of roots and aerial parts (stem-leaf) (collected prior flowering), and flowers were determined by utilizing of FRAP. Also the MTT assay has been used in order to consider in vitro cytotoxicity of essential oils and extracts on cancerous cell line (MCF-7). Moreover, the extracts were analyzed by HPLC to comprise the rate of some phenolic compounds. Results: The purple basil extracts have more powerful antioxidant activity than the essential oils. MCF-7 revealed to have a meaningful cell death when compared with controls, and the oils were found to be more effective than the extracts. Also the phytochemical analysis of the extracts has led to the identification of 3 phenolic compounds (Rosmarinic acid, p-Coumaric acid and Ferulic acid). Conclusion: Our study tends to validate the traditional use of this medicinal herb as complementary and alternative medicine.

Key Words: purple basil, antioxidant, MCF-7, HPLC.

}, keywords = {3-(4, 4 diphenyltetrazolium bromide assay, 5-dimethylthiazol-2yl)-2, A549 Cell Line, Cytotoxic, Digera muricata, HeLa cell line.}, author = {Mohammadi M and Majd A and Nejadsattari T and Hashemi M} } @article {1500, title = {Antiproliferative activity of crude extract and fractions obtained from Digera muricata on Hela cell lines of human cervix and A549 cell lines of Human Lung.}, journal = {Pharmacognosy Journal}, volume = {6}, year = {2014}, month = {3rd Sept, 2014}, pages = {32-38}, type = {Original Article}, chapter = {32}, abstract = {

Digera muricata (Linn.) of family Amaranthaceae is an ethanobotanically important plant species traditionally used against various disorders. Cytotoxic potential of methanolic extract and its fractions were investigated against Hela and A549 cell lines. Crude extract of Digera muricata was prepared in methanol by Continuous Hot Soxhlation technique. Crude extract was fractionated into two organic and one aqueous fraction by the help of Column Chromatography. MTT assay was used to evaluate the reduction of viability of the cancer cell lines. Cell viability was inhibited by crude extract of Digera muricata in a dose dependent manner ranging from 25\μg/ml to 250\μg/ml. Apoptosis assays using nucleic acid stains namely PI exclusion assay and Hoestch/PI assay were performed by the help of fluorescence microscopy. Morphological analysis was done by calculation of Apoptotic ratio and Percentage apoptosis. Our results suggests that methanolic and aqueous fraction of the extract of Digera muricata can be good source of cytotoxic compounds.

Key words: 3-(4,5-dimethylthiazol-2yl)-2,4 diphenyltetrazolium bromide assay, A549 cell line, cytotoxic, Digera muricata, HeLa cell line.

}, keywords = {3-(4, 4 diphenyltetrazolium bromide assay, 5-dimethylthiazol-2yl)-2, A549 Cell Line, Cytotoxic, Digera muricata, HeLa cell line}, author = {Shazia Usmani and Arshad Hussain and A.H.A Farooqui and Mohd.Arshad and Sahabjada Siddiqui and Mohd.Ahmad and Shadma Wahab} }