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Fluorescent probe for marking and tracking cytoplasmic membranes and preparation method of fluorescent probe

A fluorescent probe and cytoplasmic membrane technology, applied in the field of fluorescent probes and their preparation, can solve the problems of difficult observation by scientists, poor stability of cell membrane labeling, complicated synthesis and preparation process, etc. The effect of improving the signal-to-noise ratio

Active Publication Date: 2014-03-26
DALIAN UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Currently, fluorophores for labeling and tracking cell membranes are mainly commercially available (Invitrogen TM ) FM series and Dil series, however, its stability to cell membrane markers is poor, which is not conducive to application, its own low photostability is not conducive to user operation, and its synthesis and preparation process is cumbersome, and it is difficult to store for a long time , resulting in high cost and high price, which is not conducive to widespread use
[0004] Although there have been corresponding studies and reports on some activity mechanisms of cells, it is still difficult for scientists to observe the more detailed activity mechanisms intuitively and in real time

Method used

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  • Fluorescent probe for marking and tracking cytoplasmic membranes and preparation method of fluorescent probe
  • Fluorescent probe for marking and tracking cytoplasmic membranes and preparation method of fluorescent probe
  • Fluorescent probe for marking and tracking cytoplasmic membranes and preparation method of fluorescent probe

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022]

[0023] Add 324 mg of fluoroborate dipyrrole and 420 mg of carbazole aldehyde into a two-necked reaction flask, then add 8.5 mg of piperidine as a catalyst, and 4? After removing toluene, silica gel column separation (eluent: dichloromethane:methanol=30:1) gave 234mg of purple solid, yield 40%.

[0024]

[0025] Dissolve 234 mg of the product obtained in the previous step in dichloromethane, add 568 mg of iodomethane, react at 25 ° C for 24 hours, filter with suction, and retain the filter cake to obtain 262 mg of purple-black solid fluorescent probe A-1, with a yield of 90%.

[0026]

[0027] Dissolve 586mg of fluorescent probe A-1 in methanol, add 940mg of potassium bromide, and stir at 50°C for 24h. Press and spin dry to obtain 646 mg purple-black solid fluorescent probe B-1 with a yield of 95%.

Embodiment 2

[0029]

[0030] Add 482 mg of fluoroborate dipyrrole and 584 mg of carbazole aldehyde into a two-necked reaction flask, then add 25.5 mg of piperidine as a catalyst, and 4? Spin to dry under reduced pressure, remove toluene, and separate on silica gel column (eluent: dichloromethane:methanol=20:1) to obtain 824 mg of green solid with a yield of 80%.

[0031]

[0032] Dissolve 824 mg of the product obtained in the previous step in dichloromethane, add 269 mg of acrolein and an appropriate amount of HCl, react at 25°C for 24 hours, filter with suction, and retain the filter cake to obtain 923 mg of dark green solid fluorescent probe A-2 with a yield of 95 %.

[0033]

[0034] Dissolve 1214mg of fluorescent probe A-2 in methanol, 2300mg of potassium periodate, and stir at 50°C for 24h. After the reaction is completed, the reaction solution is spin-dried under reduced pressure, dissolved in dichloromethane, filtered, and the filtrate is kept and reduced again. Press and ...

Embodiment 3

[0036]

[0037] Add 376 mg of fluoroborate dipyrrole and 672 mg of carbazole aldehyde into a two-necked reaction flask, then add 25.5 mg of piperidine as a catalyst, and 4? Spin to dry under reduced pressure, remove toluene, and separate on silica gel column (eluent: dichloromethane:methanol=15:1) to obtain 760 mg of green solid with a yield of 75%.

[0038]

[0039] Dissolve 760 mg of the product obtained in the previous step in dichloromethane, add 488 mg of propane sultone and an appropriate amount of HCl, react at 25°C for 24 hours, add an appropriate amount of ether, filter with suction, and retain the filter cake to obtain 898 mg of dark green solid fluorescent probe A -3, 90% yield.

[0040]

[0041]Dissolve 1,330 mg of fluorescent probe A-3 in methanol, add 1,030 mg of sodium bromide, and stir at 50°C for 24 hours. After the reaction is complete, the reaction solution is spin-dried under reduced pressure, dissolved in dichloromethane, filtered, and the filtrat...

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Abstract

A fluorescent probe for marking and tracking cytoplasmic membranes and a preparation method of the fluorescent probe belong to the field of fine chemical engineering. According to the fluorescent probe, BODIPY is adopted as a substrate to react with carbazole aldehyde under nitrogen or argon protection, piperidine is adopted as a catalyst, and a 4-angstrom molecular sieve is adopted as a dehydrating agent; the reaction product reacts with a quaternization reagent to obtain fluorescent probe molecules. The fluorescent probe has a large emission wave length ranging from 600 to 700 nm, avoids the interference of autofluorescence of cells and reduces the optical damage on cells; the fluorescent probe has a bipolar structure, fluorescence quenching is caused when the fluorescent probe congregates in water, and the fluorescence is obviously improved when the fluorescent probe is embedded in the cytoplasmic membranes; the probe participates in biological processes together when positioned in the cytoplasmic membrane, and being free from toxic and side effects, the probe is suitable for microscopic observation of cellular processes related to the cytoplasmic membranes; the fluorescent probe has high synthesis efficiency and stable properties, is easy to preserve for a long term, and provides a visual and concise low-cost detection reagent for studying relevant processes of the cytoplasmic membranes.

Description

technical field [0001] The invention relates to a fluorescent probe for marking and tracking cell plasma membrane and a preparation method thereof, belonging to the field of fine chemical industry. Background technique [0002] The cell membrane is a barrier that prevents extracellular substances from freely entering the cell. It ensures the relative stability of the intracellular environment and enables various biochemical reactions to run in an orderly manner. It is also a channel for the exchange of information, matter and energy between cells and the surrounding environment, helping cells obtain the required substances and discharge metabolic waste. Fluidity is a basic characteristic of cell membranes, based on which cells perform a variety of physiological functions, such as the absorption, digestion and efflux of cell membranes through pinocytosis, phagocytosis or exocytosis , The substance inside. Therefore, real-time, dynamic, and long-term visual tracking of the ...

Claims

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Application Information

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IPC IPC(8): C09K11/06C07F5/02G01N33/52
Inventor 肖义张新富
Owner DALIAN UNIV OF TECH
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