Surface-modified ultraviolet blocking powder and ultraviolet blocking composition including same

a technology of ultraviolet blocking powder and composition, which is applied in the field of surface-modified ultraviolet blocking powder and ultraviolet blocking composition, can solve the problems of skin irritation, difficult to enhance biocompatibility, and decrease in titer, and achieves superior stability and uniformity, high biocompatibility, and superior biocompatibility

Inactive Publication Date: 2014-09-25
KCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention provides a way to modify surfaces of UV blocked powders without adding too much materials that could harm their properties. By using a modified UV blocking powder, they can block UV rays effectively without causing damage on human tissues. Additionally, the use of a specific type of binder called phospholipid monomers helps stabilize the UV blocking powder during storage. Overall, these technical results lead to improved performance and cost efficiency in producing UV blocking compositions.

Problems solved by technology

This patent describes various technical problem addressed in this patent text: The current method of adding titania to sunscreen compositions can cause skin irritations, while reducing the amount of titania needed may result in decreased tissue compatibility. To address this issue, there is a desire to develop a new type of sunscreen composition without containing titania.

Method used

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  • Surface-modified ultraviolet blocking powder and ultraviolet blocking composition including same
  • Surface-modified ultraviolet blocking powder and ultraviolet blocking composition including same
  • Surface-modified ultraviolet blocking powder and ultraviolet blocking composition including same

Examples

Experimental program
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Effect test

example 1

(1) Preparation of UV blocking powder having trichloroacetyl group

[0053]20 g of titanium dioxide (after drying), 600 g of toluene, and 2.0 g of trichloroacetyl isocyanate were placed in a 1 L flask, stirred under reflux at 50˜100° C. for 5˜10 hr, and then cooled to room temperature. The mixture was centrifuged to remove the supernatant (the solvent layer), dispersed in THF and then centrifuged again. These procedures were repeated until the unreacted trichloroacetyl isocyanate was completely removed, followed by drying in a vacuum to remove the residual THF solvent and then drying in a vacuum, thus obtaining a UV blocking powder having a trichloroacetyl group.

(2) Preparation of Surface-Modified UV Blocking Powder

[0054]20 g of the UV blocking powder having a trichloroacetyl group, 4 g of MPC (Methacryloyloxyethyl phosphorylcholine), 0.04 g of Mo(CO)6, and 200 g of ethanol were placed in a 500 L flask, and maintained at 50˜90° C. for 1˜4 hr and thus polymerized. Cooling to room temperatu

example 2

(1) Preparation of UV Blocking Powder Having Trichloroacetyl Group

[0056]The present example was carried out in the same manner as in Example 1, with the exception that, before reaction between titanium dioxide (after drying) and trichloroacetyl isocyanate, titanium dioxide was reacted with tetraethoxysilane (TEOS) and then with trichloroacetyl isocyanate.

[0057]20 g of titanium dioxide (after drying), 600 g of toluene, and 30 g of tetraethoxysilane (TEOS) were placed in a 1 L flask, stirred under reflux at 70˜120° C. for 5˜10 hr and then cooled to room temperature. Subsequently, centrifugation to remove the supernatant (the solvent layer), dispersion in THF, centrifugation and drying in a vacuum were performed, thus obtaining a powder comprising titanium dioxide and tetraethoxysilane.

[0058]20 g of the powder comprising titanium dioxide and tetraethoxysilane, 200 g of methanol, and 20 g of 0.01M HCl were placed in a 1 L flask, stirred at 20˜70° C. for 30 min˜hr, centrifuged to remove the

example 3

(1) Preparation of UV Blocking Powder Having Chloroacetyl Group

[0062]20 g of titanium dioxide (after drying), 600 g of toluene, and 2.0 g of chloroacetyl isocyanate were placed in a 1 L flask, stirred under reflux at 50˜100° C. for 5˜10 hr and then cooled to room temperature. Subsequently, centrifugation to remove the supernatant (the solvent layer), dispersion in THF and centrifugation were performed. These procedures were repeated until the unreacted chloroacetyl isocyanate was completely removed, followed by drying in a vacuum to remove the residual THF solvent and then further drying in a vacuum, thus obtaining a UV blocking powder having a trichloroacetyl group.

(2) Preparation of Surface-Modified UV Blocking Powder

[0063]20 g of the UV blocking powder having a chloroacetyl group, 4 g of MPC (Methacryloyloxyethyl phosphorylcholine), 0.04 g of Mo(CO)6, and 200 g of ethanol were placed in a 500 L flask, and maintained at 50˜90° C. for 1˜4 hr and thus polymerized. Subsequently, cooling

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Abstract

The present invention relates to a surface-modified ultraviolet blocking powder obtained by reacting an ultraviolet blocking powder including a chloroacetyl group, a phospholipid monomer including an unsaturated bonding, and a catalyst inducing the reaction of the chloroacetyl group and the unsaturated bonding. According to the surface-modified ultraviolet blocking powder of the present invention, the surface may be modified using an effective method, and through chemical bonding (covalent bonding) and as a result of surface modification, the stability of the powder is high. In addition, since the surface modification is performed by using a biocompatible component, the ultraviolet blocking composition including the surface-modified ultraviolet blocking powder may provide ultraviolet blocking properties and biocompatibility at the same time.

Description

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Claims

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Application Information

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Owner KCI
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