Method for quickly, simply and conveniently evaluating potential toxicity of molecules with planar structures
A planar structure and molecular technology, which is applied in the field of quick and easy evaluation of the potential toxicity of planar structure molecules, and can solve problems such as cumbersome operation, toxicity, and cumbersome detection operations
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Embodiment 1
[0035] Example 1: Determination of the saturation value of EB (ethidium bromide) binding to DNA.
[0036] Take 6 10mL colorimetric tubes (sequentially numbered ①②③④⑤⑥), add 1mL BR buffer solution, 0.1mL 1.00×10 -3 mol / L EB solution, then add 0, 0.1, 0.13, 0.15, 0.18, 0.21mL 3.78×10 -5 mol / L DNA solution, take another 10mL colorimetric tube, add 1mL BR buffer solution and 0.15mL 3.78×10 -5 mol / L DNA solution. Then dilute the 7 colorimetric tubes with water to the scale of 5mL, eliminate the bubbles and mix them with a vortex mixer, place them in a 37°C water bath for 60 minutes, and perform synchronous scanning on a fluorescence spectrophotometer to obtain RLS spectra (resonance scattering spectra), emission and The excitation slit is 15nm, and the scanning range is 220-700nm. Through the measurement of resonance scattering spectroscopy, it can be seen that the colorimetric tube numbered ⑤ has the strongest resonance scattering signal. The DNA concentration at this time is the sat...
Embodiment 2
[0037] Example 2: Determination of the saturation value of doxorubicin and DNA binding.
[0038] Take 6 10mL colorimetric tubes (sequentially numbered ①②③④⑤⑥), add 1mL BR buffer, 0.1mL 2.00×10 -4 mol / L doxorubicin solution, add 0, 0.3, 0.4, 0.5, 0.6, 0.7mL 3.78×10 -6 mol / L DNA solution, take another 10mL colorimetric tube, add 1mL BR buffer solution and 0.4mL 3.78×10 -6 mol / L DNA solution. Then dilute 7 colorimetric tubes with water to the scale of 5mL, eliminate bubbles and mix them with a vortex mixer, place them in a 37°C water bath for 60 minutes, and perform synchronous scanning on a fluorescence spectrophotometer to obtain RLS spectra. The emission and excitation slits are 15nm. The scanning range is 220-700nm. Through resonance scattering spectroscopy, it can be seen that the colorimetric tube numbered ④ has the strongest resonance scattering signal. At this time, the DNA concentration is the saturation concentration of doxorubicin molecule and DNA binding. At this time, t...
Embodiment 3
[0039] Example 3: Determination of the saturation value of mitoxantrone and DNA binding.
[0040] Take 6 10mL colorimetric tubes (sequentially numbered ①②③④⑤⑥), add 1mL BR buffer, 0.1mL 1.00×10 -4 mol / L Mitoxantrone solution, add 0, 0.2, 0.4, 0.6, 0.8, 1mL 3.78×10 -6 mol / L DNA solution, take another 10mL colorimetric tube, add 1mL BR buffer solution and 0.4mL 3.78×10 -6 mol / L DNA solution. Then dilute 7 colorimetric tubes with water to the scale of 5mL, eliminate bubbles and mix them with a vortex mixer, place them in a 37°C water bath for 60 minutes, and perform synchronous scanning on a fluorescence spectrophotometer to obtain RLS spectra. The emission and excitation slits are 15nm. The scanning range is 220-700nm. Through resonance scattering spectroscopy, it can be seen that the resonance scattering signal of the colorimetric tube number ⑤ is the strongest. The DNA concentration at this time is the saturation concentration of mitoxantrone molecules and DNA binding. At this ti...
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