Hydrogel dressing, preparation method thereof, multifunctional nano-composite dressing, and preparation method and application of multifunctional nano-composite dressing
A nanocomposite and hydrogel technology, which is applied in the fields of pharmaceutical formulation, medical science, drug delivery, etc., can solve problems such as difficult to achieve satisfactory results, single functionality, and difficult to cover the full-cycle antibacterial performance of wound repair. Achieve the effect of making up for poor antibacterial effect, overcoming single function, and good biocompatibility
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[0063] The present invention also provides a preparation method of multifunctional nanocomposite dressing, comprising the following steps:
[0064] Step 1, synthesizing photothermal nanomaterials;
[0065] Step 2, loading antibacterial drugs
[0066] Disperse antibacterial drugs and photothermal nanomaterials in deionized water, incubate together in a rotary mixer, and then remove unadsorbed antibacterial drugs by centrifugation and deionized water washing methods to obtain photothermal nanomaterials loaded with antimicrobial drugs ;
[0067] Step 3. Synthesis of multifunctional nanocomposite dressing
[0068] An acetic acid solution of alkylated chitosan and an aqueous solution of aldehyde functionalized polyethylene glycol were prepared respectively;
[0069] The photothermal nanomaterials loaded with antibacterial drugs were mixed with the acetic acid solution of alkylated chitosan, and the aqueous solution of aldehyde-functionalized polyethylene glycol was added, and mi...
Embodiment 1
[0071] Synthesis and performance characterization of embodiment 1 hydrogel dressing
[0072] (1) Synthesis of hydrogel dressing
[0073] The synthetic method of the PEG of step 1, aldehyde group functionalization
[0074] 4-Formylbenzoic acid (0.5 g), PEG 2000 (1.6 g) and 4-dimethylaminopyridine (0.025 g) were dissolved in 50 mL of tetrahydrofuran, dicyclohexylcarbodiimide (0.84 g) was added, and The reaction was stirred overnight at room temperature. The resulting white solid was filtered off. The filtrate was purified three times by dissolving with appropriate amount of tetrahydrofuran and then adding diethyl ether to precipitate. For its H NMR spectrum, see Figure 8 .
[0075] 1 H NMR (500MHz, CDCl 3 ,δ):10.11(s,2H),8.22(d,J=8.3Hz,4H),7.95(d,J=8.3Hz,4H),4.53-4.50(m,4H),3.86-3.84(m, 4H),3.70-3.60(m,172-176H).
[0076] The synthetic method of the chitosan (FCS) of step 2, alkylation
[0077] 1g of chitosan was first dissolved in 50mL of 0.2M acetic acid solution, a...
Embodiment 2
[0090] Synthesis and characterization of embodiment 2 multifunctional nanocomposite dressing
[0091] (1) Synthesis of multifunctional nanocomposite dressings
[0092] Step 1. Synthesize WS 2 Nanosheets
[0093] Add 15 mL of oleylamine to a 100 mL flask, heat to 65 °C, and degas under vacuum for 1 hour. Then continue to heat up to 320°C in an argon-protected environment, and add 500 μL of hexamethyldisilazane. At the same time prepare the precursor solution: 50mg of WCl 6 Completely dissolve in 300 μL oleic acid, add 5 mL of oleylamine, at this time the color of the solution changes from dark brown to yellow. Next, quickly add 240 μL CS 2 , the color of the solution turned orange. Inject the precursor solution into the heated hot oleylamine solution with a syringe pump at a rate of 0.15 mL / min. After the reaction solution was cooled to room temperature, 10 mL of n-hexane and 10 mL of isopropanol were added to the reaction solution to precipitate WS 2 Nanosheets. The nan...
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