Preparation method of human hair melanosomes derivative and application of human hair melanosomes derivative in antibiosis and tissue repair
A derivative and human technology, applied in the field of biochemistry, can solve the problems of no photothermal therapy, achieve excellent biodegradability and biocompatibility, promote tissue repair, and simple operation
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Embodiment 1
[0041] The preparation method of HHMs,
[0042] Pretreatment: Break human hair to a length less than 3cm, ultrasonically clean it with deionized water for 15min, the ultrasonic frequency is 100Hz, and the time is 15min, repeat washing three times, and dry naturally at room temperature;
[0043] Hydrothermal reaction: In a high-pressure hydrothermal kettle, the pretreated human hair is subjected to a hydrothermal reaction in a NaOH solution, the concentration of the NaOH solution is 0.5mol / L, and the amount of the solution is 30 times the mass of the human hair, The temperature of the hydrothermal reaction is 50°C, and the reaction time is 12h;
[0044] Separation: The material obtained after the hydrothermal reaction is completed is subjected to centrifugation, and the centrifugation speed is 9500pm, and the time is 15min. After centrifugation, remove the supernatant, wash with deionized water, and centrifuge again, repeating three times. Then the sample was vacuum-dried at ...
Embodiment 2
[0047] Determine the maximum amount of lysozyme (Lyso) loaded on HHMs via electrostatic interactions:
[0048] Specifically, 4 mg of the prepared HHM powder was uniformly dispersed in 5 mL of deionized water. Meanwhile, 4, 8, 16, 32, 64 mg of Lyso powder were dissolved in 5 mL of deionized water, and then mixed with the above HHMs solution. The mixed solution was stirred at room temperature for 6 hours and centrifuged at 9500 rpm for 15 minutes to obtain supernatant and HHMs-Lyso. HHMs-Lyso was ultrasonically washed with deionized water and centrifuged at 9500 rpm for 15 min, repeated three times. The corresponding supernatant was collected, and the free Lyso content in the supernatant was measured by a spectrophotometer at 281 nm using a UV-Vis spectrophotometer (UV-3600, Shimadu, JP). Therefore, the Lyso loading on HHMs can be calculated from the initial Lyso content and the final free Lyso content to be 1:0.63 (HHM:Lyso, mass ratio).
Embodiment 3
[0050] Preparation of HHMs-Lyso composites:
[0051] The prepared 30 mg HHMs powder was uniformly dispersed in 10 mL deionized water. Meanwhile, 10 mg of Lyso powder was dissolved in 10 mL of deionized water, and then mixed with the above HHMs solution to obtain a HHMs-Lyso solution (2 mg / mL). The HHMs-Lyso solution was stirred at room temperature for 6 hours, ready to use without storage.
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