Abstract:In the present investigation, we examined the cytotoxic effect of methanolic extract from Origanum vulgare on HCT-116 and MDA-MB-231 cell line in vitro. In order to determine the cytotoxic effects we used an MTT viability assay. The results showed that cell growth is significantly lower in extract treated cells compared to untreated control. The effect of inhibition of cell growth was higher in the treatment of HCT-116 cell line than in MDA-MB-231. Based on the results it is determined that O. vulgare is a sig… Show more
“…majoranum (Hussain and Markham, ) as well as O . vulgare (Grbović et al ., ; Martins et al ., ). Peaks 42 and 44 were characterised as isoorientin and orientin, with ions at m / z 447, showing the same fragmentation pattern at m / z 357 and 327, which correspond to [M−H−90] − and [M−H−120] − , respectively, from the main fragment.…”
Section: Resultsmentioning
confidence: 98%
“…It exhibited a fragment at m/z 473, which corresponds to the loss of the [MÀHÀ90À120] À ion from the precursor ion. Vicenin-2 was reported to occur in O. majoranum (Hussain and Markham, 1981) as well as O. vulgare (Grbović et al, 2013;Martins et al, 2014). Peaks 42 and 44 were characterised as isoorientin and orientin, with ions at m/z 447, showing the same fragmentation pattern at m/z 357 and 327, which correspond to [MÀHÀ90] À and [MÀHÀ120] À , respectively, from the main fragment.…”
Section: Characterisation Of the Phenolic Compounds And Other Phytochmentioning
The distribution of phenolic compounds in the methanolic extract showed a variation among studied plants. Mentha pulegium can be considered as a source of gallocatechin.
“…majoranum (Hussain and Markham, ) as well as O . vulgare (Grbović et al ., ; Martins et al ., ). Peaks 42 and 44 were characterised as isoorientin and orientin, with ions at m / z 447, showing the same fragmentation pattern at m / z 357 and 327, which correspond to [M−H−90] − and [M−H−120] − , respectively, from the main fragment.…”
Section: Resultsmentioning
confidence: 98%
“…It exhibited a fragment at m/z 473, which corresponds to the loss of the [MÀHÀ90À120] À ion from the precursor ion. Vicenin-2 was reported to occur in O. majoranum (Hussain and Markham, 1981) as well as O. vulgare (Grbović et al, 2013;Martins et al, 2014). Peaks 42 and 44 were characterised as isoorientin and orientin, with ions at m/z 447, showing the same fragmentation pattern at m/z 357 and 327, which correspond to [MÀHÀ90] À and [MÀHÀ120] À , respectively, from the main fragment.…”
Section: Characterisation Of the Phenolic Compounds And Other Phytochmentioning
The distribution of phenolic compounds in the methanolic extract showed a variation among studied plants. Mentha pulegium can be considered as a source of gallocatechin.
“…There is a great need to examine reliable and inexhaustible sources of natural substances. In addition, it is important to understand the mechanisms of anticancer agents for future application in cancer therapy [15]. Carcinogenesis is one of the most important phenomena that could be attributed to free radicals/reactive oxygen species.…”
This study was conducted to evaluate antitumor effects of roesmarinus (Rosmarinus officinalis) extracts (aqueous and methanol) on Rhabdomyosarcoma; RD cell line and a normal cell line; mouse embryo fibroblast; MEF). Chemical detections of Rosemary extracts revealed that the aqueous and methanol extracts were positive for flavonoids, alkaloids, phenol, terpenes, saponine, glycosides, steroids and tannins. The percentage growth inhibition (PGI) of five leaf extract concentrations 50, 100, 250, 500 and 1000 (µg/ml) were assessed in vitro using RD and MEF. The results revealed that the five concentrations of the plant extracts showed anti-tumor properties in a concentrationdependent manner, and the methanol extract recorded better values of PGI than aqueous extract in RD cell lines, while, less PGI values were recorded in the MEF cell line. This experiment investigated the cytotoxic activity of the methanolic and aqueous extracts of Rosemary at concentrations (50 -100 -250 -500 -1000 μg/mL) on RD cell lines. A dose-dependent reduction was observed in treated cell line after 24 hrs. of treatment, but lower concentrations exhibited lower cytotoxic effects. Maximum inhibition of proliferation was achieved at the highest concentration (1000 μg/mL).
“…Based on National Cancer Institute Standard (IC50>100), P. frainifolia and O. vulgare extracts can be considered as "non-toxic" to cells [30]. According to the published reports about the cytotoxicity of O. vulgare extract and also the minor difference between IC50 (107.6 µg/ml) and the toxicity threshold level for P. frainifolia obtained in this study, extreme caution should be taken before using these plants as natural antioxidants [31,32].…”
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