Fullerene micro-nano material with effects of prevention and/or treatment on myelosuppression and use thereof
A fullerene micro-nano, bone marrow suppression technology, applied in the field of biomedicine, can solve problems such as easy to cause gastrointestinal reactions, not widely used, low absorption rate, etc., achieve excellent bone marrow suppression, efficiently scavenge free radicals, prevent and treat bone marrow inhibitory effect
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Embodiment 1
[0039] Embodiment 1, water-soluble gadolinium hydroxylated metal fullerene (GFNC) scavenging free radical effect in vitro
[0040] 1) Electron paramagnetic resonance (ESR) detection of free radical intensity experiment:
[0041] The method of producing hydroxyl radicals induced by ultraviolet rays was used. The control group was: 50 μL of hydrogen peroxide with a mass concentration of 37%, 50 μL of PBS buffer (pH=7.4) and a small amount (0.133 mM) of lutidine N-oxide (DMPO, Free radical scavenger) solutions were mixed, irradiated with 280nm ultraviolet light for 8min, and the signal of hydroxyl radicals could be produced at this time; the experimental group was: 50 μL of hydrogen peroxide with a mass concentration of 37%, 50 μL of PBS buffer (pH=7.4) and A small amount (0.133mM) of lutidine N-oxide (DMPO, free radical scavenger) solution was mixed, and 10μL of 20μM water-soluble gadolinium hydroxylated metal fullerene aqueous solution was immediately added, and 280nm ultraviol...
Embodiment 2
[0043] Embodiment 2, the free radical scavenging effect of water-soluble hydroxylated hollow fullerene in vitro
[0044] 1) Electron paramagnetic resonance (ESR) detection of free radical intensity experiment:
[0045] The method of producing hydroxyl radicals induced by ultraviolet rays was used. The control group was: 50 μL of hydrogen peroxide with a mass concentration of 37%, 50 μL of PBS buffer (pH=7.4) and a small amount (0.133 mM) of lutidine N-oxide (DMPO, Free radical scavenger) solutions were mixed, irradiated with 280nm ultraviolet light for 8min, and the signal of hydroxyl radicals could be produced at this time; the experimental group was: 50 μL of hydrogen peroxide with a mass concentration of 37%, 50 μL of PBS buffer (pH=7.4) and A small amount (0.133mM) of lutidine N-oxide (DMPO, free radical scavenger) solution was mixed, and 10 μL of 20 μM water-soluble hydroxylated hollow fullerene aqueous solution was immediately added, and 280nm ultraviolet light was irrad...
Embodiment 3
[0047] Example 3. Myelosuppressive Protection of Water-Soluble Gadolinium Hydroxylated Metallofullerenes in Vivo Levels
[0048] Animal model: 4-5 week old ICR mice were selected and randomly divided into 4 groups, 6 mice in each group, corresponding to blank control group, GFNC experimental group, X-ray irradiation experimental group and X-ray + GFNC experimental group respectively. Inoculate 10 on the right thigh of mice 6 A mouse hepatoma cell (H22 cell) was inoculated 5-7 days later, when the tumor diameter reached about 5 mm, the experiment was carried out.
[0049] Blank control group: the drugs injected in the experimental group were replaced by the same volume of normal saline, and the same volume of normal saline was injected intravenously.
[0050] GFNC experimental group: mice were injected with GFNC aqueous solution (1 mM) through the tail vein, and the drug dosage was 0.004 mmol GFNC / kg mouse body weight.
[0051] X-ray irradiation experiment group: the whole bo...
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