Polyaphron topical composition with vitamin D and corticosteroid, application and manufacturing method thereof

A technology of corticosteroids and compositions, applied in the field of topical compositions, which can solve the problems of poor diffusion, unfavorable, unacceptable to patients, etc., and achieve the effect of happy application, enhanced skin permeability, and reduced possibility

Inactive Publication Date: 2015-08-05
MC2 THERAPEUTICS LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

This is undesirable and may lead to poor patient acceptance
[0016] Another disadvantage of the composition of US-B-6,753,013 is that in order for the composition to provide beneficial results in topical treatments, high levels of vitamin D or vitamin D analogs are required in order to have sufficient vitamin D or vitamin D analogs penetrating into the skin
This is because the composition exhibits poor diffusion through the skin
This is disadvantageous since vitamin D and vitamin D analogs are known skin irritants

Method used

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  • Polyaphron topical composition with vitamin D and corticosteroid, application and manufacturing method thereof
  • Polyaphron topical composition with vitamin D and corticosteroid, application and manufacturing method thereof
  • Polyaphron topical composition with vitamin D and corticosteroid, application and manufacturing method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0122] Three gel polyaphron dispersions with the compositions described below were prepared by the following methods.

[0123]

[0124]

[0125] Gel polymicrobubble dispersion 3

oil phase

weight%

Squalane (from Olive - A&E Connock)

9.00

Polydimethylsiloxane (Q7-1920, 100CP-Dow Corning)

44.10

Cyclomethicone (STb5NF-Dow Corning)

36.00

Laureth-4 (Volpo L4-Croda)

0.90

water box

Poloxamer 188 (Pluronic F68-BASF)

1.00

[0126] softened water

9.00

[0127] Final product

weight%

Gel polymicrobubble dispersion 1

7.20

Gel polymicrobubble dispersion 2

18.60

Gel polymicrobubble dispersion 3

74.20

[0128] * The content of calcipotriol in the final formulation was 50 μg / g.

[0129] ** The content of betamethasone dipropionate in the final formulation was 643 μg / g (equivalent to 500 μg / g of b...

Embodiment 2

[0158]

[0159]

[0160]

[0161] Gel polymicrobubble dispersion 3

oil phase

weight%

Squalane (from Olive - A&E Connock)

9.00

Polydimethylsiloxane (Q7-9120, 100CP-Dow Corning)

44.10

Cyclomethicone (STb5NF-Dow Corning)

36.00

Laureth-4 (Volpo L4-Croda)

0.90

water box

Poloxamer 188 (Pluronic F68-BASF)

1.00

softened water

9.00

[0162] water gel

weight%

Polyacrylic acid (Ultrez 10-Noveon)

1.00

Triethanolamine (TEA)

reach pH 7.50

softened water

Make up to 100%

[0163] Final product

weight%

Gel polymicrobubble dispersion 1

9.19

Gel polymicrobubble dispersion 2

23.61

Gel polymicrobubble dispersion 3

47.27

Propylene Glycol

10.05

water gel

9.88

[0164] * The final calcipotriol level was 55.4 μg / g.

[016...

Embodiment 3

[0175] Three gel polyaphron dispersions and aqueous gels of the compositions described below were prepared by the following methods.

[0176]

[0177]

[0178] Gel polymicrobubble dispersion 3

oil phase

weight%

Squalane (from Olive - A&E Connock)

9.00

[0179] Polydimethylsiloxane (Q7-9120, 100CP-Dow Corning)

44.10

Cyclomethicone (STb5NF-Dow Corning)

36.00

Laureth-4 (Volpo L4-Croda)

0.90

water box

Poloxamer 188 (Pluronic F68-BASF)

1.00

softened water

9.00

[0180] water gel

weight%

Polyacrylic acid (Ultrez 10-Noveon)

1.00

Triethanolamine (TEA)

reach pH 7.50

softened water

Make up to 100%

[0181] Final product

weight%

Gel polymicrobubble dispersion 1

12.95

Gel polymicrobubble dispersion 2

20.18

Gel polymicrobubble dispersion...

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PUM

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Abstract

A composition suitable for topical application comprising a continuous phase and at least one discontinuous phase, said composition comprising at least one polyaphron dispersion, at least one vitamin D or vitamin D analogue and at least one corticosteroid.

Description

[0001] This application is a divisional application, the international application number of the original application is PCT / GB2008 / 000894, the international application date is March 14, 2008, the Chinese national application number is 200880008496.X, and the entry date for entering the Chinese national phase is 2009 September 15, 2009, the title of the invention is "Multi-microbubble topical composition with vitamin D and corticosteroid". technical field [0002] The present invention relates to compositions for topical application comprising at least one vitamin D or vitamin D analogue and at least one corticosteroid. Background technique [0003] It is known that compositions comprising vitamin D or vitamin D analogs are useful in the treatment of a variety of skin conditions. [0004] For example, EP-B-474,517 discloses the use of compositions containing one or more 1α-hydroxylated-19-nor-vitamin D compounds having a triple bond in the side chain for the treatment of ps...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K45/06A61K31/59A61K31/593A61K9/00A61P17/06A61K31/573A61K31/58A61K31/56
CPCA61K31/59A61K45/06A61K47/10A61K47/44A61K9/0014A61K47/06A61K31/573A61K9/06A61K9/10A61K9/1075A61K31/00A61K31/56A61K47/14A61K47/24A61K47/34A61P17/00A61P17/06A61K2300/00
Inventor 德里克·阿尔佛雷德·惠勒大卫·弗拉泽·斯蒂尔米歇尔·乔治乌斯蒂恩·欣德特-派得森
Owner MC2 THERAPEUTICS LTD
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