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The cooperation between doxorubicin and ALTSPC make a better effect in killing cancer cells Yan-Li Qin, Xiao-Huang and Ji-Yao Chen a 5 abs dox 5 abs a dox 5 5 abs dox 10 abs a dox 5 10 abs 0.30 0.28 0.26 Altspc 5 dox 10 a:dox 5:10 250 Dox (positive) 350 200 0.22 250 0.20 0.18 ALTSPC (negative) a 5 excit dox 10 feng1 excit dox 10 feng2 excit a dox 5 10 feng1 excit a dox 5 10 feng2 excit a dox 5 10 feng3 excit 300 0.24 150 200 0.16 0.14 B B B samples Abstract: Aluminium tetrasulfonated phthalocyanine(AlTSPc) is a nontoxic PDT drug, which is FDA approved for clinical trials against tumors. But the time of it entering cancer cells is long, and its fluorescence is not strong enough to detect. Doxorubicin is another medicine that cure cancer cells, it enters cells must faster than ALTSPC and it has much strong fluorescence. We let the two samples work together. As a result, their cooperation get a better effect in killing cancer cells. 100 0.12 0.10 150 100 0.08 50 0.06 electrop horesis 50 0.04 0.02 0 0 0.00 300 400 500 600 A 700 400 450 500 550 600 650 700 750 800 850 A Abs spectrum Fl spectrum 300 320 340 360 380 400 420 440 460 480 500 520 A Ex spectrum They connect with each other because of electric force The spectrums above tell that there are interaction between the two samples Cell livability MTT C: control A: ALTSPC D: doxorubicin L: light Samples Fl of dox in RBL cells DIC pictures of RBL cells Fl of ALTSPC in RBL cells Given more time ,the effect will be more clear Conclusions ALTSPC is negative charged, doxorubicin is positive charged. We mix their solution together. The electricphoresis tells us that they connect with each other because of their electric force. From the spectrums we know that there are FRET effect between them. By the MTT assay, we know more cancer cells are killed just because of their cooperation. So we hope that they will cooperate together to kill more cancer cells with a faster speed. References: (1) Ying-jun chen, xiu-ping Yan, SMALL.2009,5,NO. 17, 2012-2018. (2) Sharman, W. M.; Allen, C. M.; van Lier, J. E. Drug Discovery Today 1999, 4,507–517