Chitosan-amphiphilic ion/quaternary ammonium salt natural dressing and its preparation method and application
A technology of chitin and quaternary ammonium salts, applied in medical science, bandages, etc., can solve problems such as high crystallinity, limitation, and poor solubility, and achieve strong antibacterial activity, reduced surface energy, and high antibacterial activity.
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[0040] The invention discloses a preparation method of a chitin-amphiphide ion / quaternary ammonium salt natural dressing, which comprises the following steps:
[0041] Step 1, pretreatment: immerse the shells in an HCl solution with a mass percentage of 3%-8% for 3 days to prepare the pretreated shells;
[0042] Step 2, synthesis of antibacterial monomer: N-(2-(acryloyloxy) ethyl)-N,N-dimethyl is dissolved in acetonitrile (MeCN) to obtain N- (2-(acryloyloxy)ethyl)-N,N-dimethyl acetonitrile solution, and then to N-(2-(acryloyloxy)ethyl)-N,N-dimethyl acetonitrile Hexyl bromide (molar ratio: N-(2-(acryloyloxy) ethyl)-N, N-dimethylhexyl bromide = 1:1-1:1.5) was added to the solution, and the mixture was heated at 75-85°C React under vigorous stirring for 12-20 hours; the stirring speed is 50-80r / min; after the reaction is completed, use vacuum filtration to filter the mixture, and finally obtain a white solid (a) after freeze-drying, which is the antibacterial monomer N-( 2-(acr...
Embodiment 1
[0052] A preparation method of chitin-amphiphilic ion / quaternary ammonium salt natural dressing, comprising the following steps:
[0053] Step 1. Pretreatment: immerse the shells in a 5% HCl solution by mass for 3 days to prepare the pretreated shells;
[0054] Step 2, synthetic antibacterial monomer:
[0055] Dissolve N-(2-(acryloyloxy)ethyl)-N,N-dimethyl in acetonitrile (MeCN) to obtain N-(2-(acryloyloxy)ethyl) with a mass concentration of 15%. )-N, N-dimethyl acetonitrile solution, then to N-(2-(acryloyloxy) ethyl)-N, N-dimethyl acetonitrile solution, add hexyl bromide (molar ratio: N- (2-(acryloyloxy)ethyl)-N,N-dimethylhexyl bromide=1:1.2), the mixture was reacted under vigorous stirring at 80°C for 16 hours, and the stirring speed was 65r / min; the reaction was completed Afterwards, the mixture was filtered using vacuum filtration (37°C, 1 hour), and finally after freeze-drying (-20°C, 1 hour), a white solid (a) was obtained, which was the antibacterial monomer N-(2-(acr...
Embodiment 2
[0064] A preparation method of chitin-amphiphilic ion / quaternary ammonium salt natural dressing, comprising the following steps:
[0065] Step 1. Pretreatment: immerse the shells in a 3% HCl solution by mass for 3 days to prepare the pretreated shells;
[0066] Step 2, synthesis of antibacterial monomer: N-(2-(acryloyloxy) ethyl)-N,N-dimethyl is dissolved in acetonitrile (MeCN) to obtain N-(2- (Acryloyloxy)ethyl)-N,N-dimethyl in acetonitrile solution, then add N-(2-(acryloyloxy)ethyl)-N,N-dimethyl in acetonitrile solution Hexyl bromide (molar ratio: N-(2-(acryloyloxy) ethyl)-N, N-dimethylhexyl bromide = 1:1), reacted under vigorous stirring at 75°C for 20 hours, stirred The rotation speed is 50r / min; after the reaction is completed, the mixture is filtered by vacuum filtration, and finally a white solid (a) is obtained after freeze-drying, which is the antibacterial monomer N-(2-(acryloyloxy)ethyl)-N , N-dimethylhexyl-1-ammonium (ADMHA, a); the vacuum filtration temperature ...
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