Fluorescent carbon dot nanoprobe for detecting hydrogen sulfide and imaging hydrogen sulfide in living cells based on inner filter effect and its application method
A technology of fluorescent carbon dots and nanoprobes, which is applied in the field of biochemical analysis, can solve the problems of continuous detection of hydrogen sulfide content and achieve high selectivity and low cost
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Embodiment 1
[0033] Preparation method of fluorescent carbon dot nanoprobes based on inner filter effect detection of hydrogen sulfide and hydrogen sulfide imaging in living cells:
[0034] 1. Synthesis of Fluorescent Carbon Nanodots
[0035] Fluorescent nano-carbon dots (CDs) were prepared by pyrolyzing tomatoes, as follows: Weigh 5.0 g of fresh tomatoes in a mortar, grind them thoroughly and filter them through a 150-mesh filter membrane, take 3 mL of the filtrate in a hydrothermal reaction kettle, and then add 20mL of ultrapure water was heated to 250°C and stirred. After 10 hours, stop heating and naturally cool to room temperature, filter, and take the filtrate in a dialysis bag (MWCO: 1 kDa, pore size: ca. 1.0 nm) under the environment of ultrapure water Dialyze for 24 hours in the dark, and store the supernatant at 4°C in the dark. figure 1 The transmission electron micrograph and particle size distribution diagram of the synthesized green carbon quantum dots are given. It can be s...
Embodiment 2
[0043] 1. Synthesis of Fluorescent Carbon Nanodots
[0044] Fluorescent nano-carbon dots (CDs) were prepared by pyrolyzing tomatoes, as follows: Weigh 5.0 g of fresh tomatoes in a mortar, grind them thoroughly and filter them through a 150-mesh filter membrane, take 3 mL of the filtrate in a hydrothermal reaction kettle, and then add 21mL of ultrapure water was heated to 250°C and stirred. After 10 hours, stop heating and naturally cool to room temperature, filter, and take the filtrate in a dialysis bag (MWCO: 1 kDa, pore size: ca. 1.0 nm) under the environment of ultrapure water Dialyze for 24 hours in the dark, and store the supernatant at 4°C in the dark.
[0045] 2. Synthesis of DMI
[0046] 2,3,3-Trimethyl-3H-indole (1.6g, 10mmoL) and iodomethane (2.84g, 20mmoL) were mixed and dissolved in 10mL of acetonitrile, refluxed at 60°C for 11h under the protection of argon, and naturally cooled to room temperature , a light pink precipitate was obtained, filtered, washed three...
Embodiment 3
[0052] 1. Synthesis of Fluorescent Carbon Nanodots
[0053] Fluorescent nano-carbon dots (CDs) were prepared by pyrolyzing tomatoes, as follows: Weigh 5.0 g of fresh tomatoes in a mortar, grind them thoroughly and filter them through a 150-mesh filter membrane, take 3 mL of the filtrate in a hydrothermal reaction kettle, and then add 22mL of ultrapure water was heated to 250°C and stirred. After 10 hours, stop heating and naturally cool to room temperature, filter, and take the filtrate in a dialysis bag (MWCO: 1 kDa, pore size: ca. 1.0 nm) under the environment of ultrapure water Dialyze for 24 hours in the dark, and store the supernatant at 4°C in the dark.
[0054] 2. Synthesis of DMI
[0055] 2,3,3-Trimethyl-3H-indole (4.8g, 30mmoL) and iodomethane (8.52g, 60mmoL) were mixed and dissolved in 10mL of acetonitrile, refluxed at 60°C for 11h under the protection of argon, and naturally cooled to room temperature , a light pink precipitate was obtained, filtered, washed three...
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