Vitamin c-containing polycaprolactone microsphere filler and preparation method therefor
A technology of polycaprolactone and vitamins, applied in medical preparations containing active ingredients, skin care preparations, microcapsules, etc., can solve the problems of vitamin C instability and easy oxidation and decomposition
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[0029]As a specific example of the preparation method of polycaprolactone microspheres containing vitamin C in the present disclosure, such a preparation method includes the following steps: (a) by dissolving polycaprolactone in the first solvent and dissolving vitamin C in a second solvent to prepare respective solutions, and then uniformly mix the two solutions to prepare a single solution to prepare a dispersed phase; (b) prepare an emulsion by mixing said dispersed phase with an aqueous solution (continuous phase) containing a surfactant (c) forming microspheres by extracting an organic solvent from the dispersed phase in said emulsion prepared in step (b) into a continuous phase and evaporating; and (d) said continuous phase from step (c) phase recovery of the microspheres to prepare vitamin C-containing polycaprolactone microspheres.
[0030] In step (a), the polycaprolactone preferably has an intrinsic viscosity in the range of 0.16 to 1.90 dL / g.
[0031] The first sol...
Embodiment 1
[0050] Example 1: Preparation of polycaprolactone microspheres encapsulated with ascorbic acid
[0051] By dissolving 4.9975 g of biocompatible polymer Purasorb PC 04 (manufacturer: Corbion, Netherlands) and 0.0025 g of ascorbic acid (manufacturer: Tokyo Chemical Industries, Japan) in 19.99 g of dichloromethane (manufacturer: JT Baker, USA) and 1.70 mL of dimethyl sulfoxide (manufacturer: Sigma Aldrich, USA), and then mix the two solutions to prepare a dispersed phase.
[0052] A 1 w / v% polyvinyl alcohol aqueous solution (viscosity: 4.8 to 5.8 mPa·s) was used as the continuous phase, and 1200 mL of the continuous phase was supplied to an emulsification device equipped with a 10 μm diameter porous membrane while injecting the prepared dispersion phase to prepare microspheres. The prepared microsphere suspension was placed in a preparation container and stirred at a speed of 150 rpm. The temperature of the membrane emulsification device and the preparation vessel was maintai...
Embodiment 1-1
[0054] Example 1-1: Preparation of polycaprolactone microspheres encapsulated with ascorbic acid
[0055] By dissolving 4.985 g of biocompatible polymer Purasorb PC 04 (manufacturer: Corbion, Netherlands) and 0.015 g of ascorbic acid (manufacturer: Tokyo Chemical Industries, Japan) in 19.94 g of dichloromethane (manufacturer: JT Baker, USA) and 1.70 mL of dimethyl sulfoxide (manufacturer: Sigma Aldrich, USA), and then mix the two solutions to prepare a dispersed phase.
[0056] A 1 w / v% polyvinyl alcohol aqueous solution (viscosity: 4.8 to 5.8 mPa·s) was used as the continuous phase, and 1200 mL of the continuous phase was supplied to an emulsification device equipped with a 10 μm diameter porous membrane while injecting the prepared dispersion phase to prepare microspheres. The prepared microsphere suspension was placed in a preparation container and stirred at a speed of 150 rpm. The temperature of the membrane emulsification device and the preparation vessel was maintai...
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