Silk fibroin/manganese dioxide composite micro-sphere drug carrier with core-shell structure and preparation method
A technology of silk fibroin and manganese dioxide, which is applied in the direction of non-active ingredients of polymer compounds, drug combinations, and pharmaceutical formulations, can solve problems such as unstable properties of nanoparticles, harsh reaction conditions, and complicated nanoparticle synthesis technology, and achieve The effect of excellent singlet oxygen generation ability, simple process, and controllable drug release ability
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Embodiment 1
[0040] The preparation method of the silk fibroin / manganese dioxide composite microsphere drug carrier of the core-shell structure in this embodiment sequentially includes the following steps:
[0041] (1) Take an appropriate amount of silkworm cocoon shells, wash and air dry, and use the existing method for degumming. Subsequently, the degummed silk fibers are sequentially subjected to the existing steps of dissolution, dialysis, and concentration to obtain the silk fibroin aqueous solution;
[0042] (2) Adjust the silk fibroin concentration in step (1) to 2 mg / mL (the solvent is water, the same as in other embodiments), and place 10 mL in the reaction vessel. Slowly add 1 mL of isopropanol dropwise to the silk protein solution, and continue to stir for 30 min to make it uniform.
[0043] (3) Place the mixed solution of step (2) in a -80°C refrigerator, freeze for 12 hours, and then allow it to thaw naturally at room temperature to obtain a milky white silk protein suspension. The...
Embodiment 2
[0049] The preparation method of the silk fibroin / manganese dioxide composite microsphere drug carrier of the core-shell structure in this embodiment sequentially includes the following steps:
[0050] (1) Take an appropriate amount of silkworm cocoon shells, wash and dry, and then degummed them. Subsequently, the degummed silk fibers are successively subjected to the steps of dissolution, dialysis, and concentration to obtain the silk fibroin aqueous solution;
[0051] (2) Adjust the silk fibroin concentration in step (1) to 2%, take 5 mL and place in the reaction vessel, add 2 mL of absolute ethanol and stir evenly.
[0052] (3) Place the mixed solution of step (2) in a refrigerator at -20°C, freeze for 24 hours, and naturally thaw at room temperature to obtain a silk protein suspension. The silk protein suspension was centrifuged, washed and ultrasonically processed to obtain silk protein microspheres with a diameter in the range of 200-500 nm, and resuspended with 10 mL of deion...
Embodiment 3
[0055] Example 3 (In situ drug loading)
[0056] The preparation method of the silk fibroin / manganese dioxide composite microsphere drug carrier of the core-shell structure in this embodiment sequentially includes the following steps:
[0057] (1) Take an appropriate amount of silkworm cocoon shells, wash and dry, and then degummed them. Subsequently, the degummed silk fibers are successively subjected to the steps of dissolution, dialysis, and concentration to obtain the silk fibroin aqueous solution;
[0058] (2) Adjust the silk fibroin concentration in step (1) to 2mg / mL, take 10mL and place it in the reaction vessel, add 2mg of doxorubicin hydrochloride (DOX) to the silk fibroin solution, and ultrasonically disperse it with the silk The protein protein is mixed uniformly, and then 1 mL of isopropanol is slowly added dropwise to the reaction solution, and stirring is continued for 30 minutes to make it uniform.
[0059] (3) Place the mixed solution of step (2) in a -80°C refrigera...
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