Preparation method for constructing electrochemical immunosensor based on imitation mussel chemistry
An immunosensor and electrochemical technology, applied in the field of functional polymers, can solve the problems of inability to load signal molecules to provide enough effective sites, expand detection signals, etc., and achieve the effect of expanding the detection range and reducing the detection limit.
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Embodiment 1
[0040] Example 1: Preparation of mussel-like chemically modified multi-walled carbon nanotubes (MWCNTs@PDA)
[0041] MWCNTs (100 mg) were dissolved in a mixed solution of ethanol (40 mL) and distilled water (30 mL), ultrasonically dispersed for 30 min, and then dopamine hydrochloride (80 mg) was added under magnetic stirring. After 10 minutes, Tris buffer (pH = 8.5, 50 ml) was added dropwise to the reaction system and reacted at room temperature for 24 hours. Finally, the product was obtained by washing with ethanol and distilled water and centrifuging.
Embodiment 2
[0042] Example 2: Preparation of Macroinitiator (MWCNTs@PDA-Br)
[0043] Dried MWCNTs@PDA (100 mg) was dissolved in anhydrous dichloromethane (DCM) (20 mL) and sonicated for 30 min. Dimethylaminopyridine (DMAP) (20 mg) and bromophenylacetic acid (BPA) (340 mg) were then added. Under stirring in an ice bath, dicyclohexylcarbodiimide (DCC) (330 mg) was dissolved in DCM (10 ml), and added dropwise to a round-bottomed flask with a constant pressure dropping funnel, and the temperature of the reaction system was gradually raised. to room temperature. After 24 hours, it was collected by centrifugation and washed several times with ethanol and distilled water, and finally the product was dried.
Embodiment 3
[0044] Example 3: Preparation of surface-initiated PET-ATRP functional polymer brushes (MWCNTs@PDA-PGMA)
[0045] GMA (6.04 ml, 45.6 mmol), MWCNTs@PDA-Br (50 mg), EY (15.8 mg, 0.0228 mmol), TEA (95 μl, 0.684 mmol), EBPA ( 40 μl, 0.228 mmol) and DMF (20 ml) in the reaction mixture. By filling the reactant with N 2 to achieve oxygen-free N 2 atmosphere. The mixture was then transferred to a magnetically driven stirring device containing LED flexible strips for LED irradiation (λ max = 460 nm), the reaction was carried out overnight at room temperature. The reaction was exposed to air and quenched in the dark. The reaction mixture was then dissolved in DMF and precipitated into a large amount of methanol solution. The lower precipitate was collected by centrifugation, washed with DMF and water, then dialyzed, and then freeze-dried to obtain the product.
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