wangqian Pokročilý
Počet príspevkov : 115 Registration date : 28.11.2013
| Predmet: The anaplastic lymphoma kinase gene encodes a receptor tyrosine kinase that has Št december 26, 2013 8:59 am | |
| e. aprotic sol vents such as chloroform, the spectrum displays vibronic structure with max near 420 nm. This feature corresponds to the fully conjugated form of the protonated enol, In polar protic solvents such as DMSO, the vibronic features are no longer resolved, MAPK 経路 癌 and hence, the molar absorptivity decreases as solvent polarity increases resulting in max shifts to nearly 430 nm, In agreement with this, the UV vis spectrum of CurcuEmulsomes dis played the same max as curcumin in chloroform, and differed from max of curcumin dissolved in DMSO, Hence, curcumin incorporated in CurcuEmul somes is evidently in its fully conjugated protonated enol form. Like the absorbance spectrum, the emission spectrum of CurcuEmulsomes pursued that of curcumin in chloroform and showed a max at 500 nm, Excitated at 420 nm, free curcumin in DMSO showed an emission peak centered at 520 nm and curcumin in water did not fluoresce.<br><br> Curcumin composition inside CurcuEmulsomes Since turmeric as a mixture was demonstrated to have the same inhibitory effect as pure curcumin, curcu min was used as purchased without any further purifica tion. Therefore, the turmeric fed to the system contained all three analogues, i. e. curcumin, DMC and BDMC. HPLC analysis オーダー MK-1775 showed that the turmeric extract consisted of 78. 1% curcumin, 17. 7% DMC and 4. 1% BDMC, whereas CurcuEmulsomes comprised of 40. 8% curcumin, 40. 3% DMC and 16.<br><br> 8% BDMC, As curcumin analogues were the only substances in Cur cuEmulsomes raising a peak at 420 nm, empty emulsomes did not show any peak in HPLC analysis, Effect of CurcuEmulsomes on HepG2 cell viability Previous studies demonstrated that supplier MS-275 10 50 curcumin induces cell death primarily through apoptosis, Within this range, HepG2 cells were treated with CurcuEmulsomes and free curcumin of the same concentrations, respectively. After treatment for 6, 24 and 48 hours, the cell viability was determined with CellTiter Blue assay. As shown in Figure 6, CurcuEmulsomes showed no significant cytotoxicity until 24 hours, in contrast to free curcumin which demonstrated significant toxicity especially in the early stage, i. e. after 6 hours. Nonetheless, on the long terms, incorporated curcumin preserved its biological ac tivity, and thus, acted as efficient as free curcumin.<br><br> Ac cordingly, after 48 hours 30 CurcuEmulsome lowered the viability of HepG2 to approximately 70%, 40 CurcuEmulsome to approximately 50%, same percentages as observed with free curcumin, In contrary, empty emulsomes showed no significant effect on HepG2 cell viability. It is also important to mention that the viabilities re corded over 100% might be due to the phys ical interference of the CurcuEmulsomes, as well as due to the changes in cellular activities involved in redox reac tions in response to curcumin and CurcuEmulsomes, as CellTiter Blue is a fluorescent assay used to measure cell viability via non specific redox enzyme activity, Therefore, although the latter hypothesis is likely to be the case, the complete clarification merits further study. | |
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