Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Nonaqueous pressure-sensitive adhesive for medicinal tape preparation for percutaneous absorption, medicinal tape preparation for percutaneous absorption, and process for producing the same

a technology of pressure-sensitive adhesive and tape preparation, which is applied in the field of non-aqueous pressure-sensitive adhesive for can solve the problems of not finding a patent document or non-patent document, the pressure-sensitive adhesive layer lacks cohesive strength, and cannot be used in a tape preparation for percutaneous absorption, etc., to achieve excellent adhesive and cohesive strength, not irritated, and high safety with low skin irritation

Inactive Publication Date: 2009-11-05
NIPRO PATCH
View PDF8 Cites 11 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0019]In the step of heat drying the nonaqueous pressure-sensitive adhesive copolymer comprising a (meth)acrylic monomer having an acetoacetyl group as a constituent monomer according to the invention, a network structure is formed by self-crosslinking of the acetoacetyl groups as the solvent evaporates, so that large amounts of oily substances such as the plasticizer can be included in the network structure. The pressure-sensitive adhesive of the invention uses no polyamine derivatives, isocyanate compounds or polyvalent metal chelate compounds as crosslinking agents, and therefore since toxicity is not a concern and the skin is not irritated, the adhesive is suitable for medical use. The medicinal tape preparation for percutaneous absorption of the invention has excellent adhesive and cohesive strength, and is highly safe with low skin irritation. Its properties of drug release and percutaneous absorption are also excellent.

Problems solved by technology

However, no patent document or non-patent document can be found which describes the use of a nonaqueous pressure-sensitive adhesive comprising a copolymer obtained by copolymerization of a (meth)acrylic monomer having an acetoacetyl group, and one or more monomers selected from among other (meth)acrylic monomers and copolymerizable vinyl monomers, as the pressure-sensitive adhesive used in a medicinal tape preparation for percutaneous absorption.
However, no description is found of a tape preparation for percutaneous absorption having a pressure-sensitive adhesive comprising a copolymer with an acetoacetyl group.
However, this preparation for percutaneous absorption employs a crosslinking agent, and it is stated that without a crosslinking agent the pressure-sensitive adhesive layer lacks cohesive strength and cannot be used in a preparation for percutaneous absorption.
In addition, Patent documents 3 and 4 do not provide examples of tape preparations for percutaneous absorption with pressure-sensitive adhesives comprising copolymers with acetoacetyl groups.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Nonaqueous pressure-sensitive adhesive for medicinal tape preparation for percutaneous absorption, medicinal tape preparation for percutaneous absorption, and process for producing the same

Examples

Experimental program
Comparison scheme
Effect test

example 1

Production of Nonaqueous Pressure-Sensitive Adhesive 1

[0046]After charging 157.5 g of 2-ethylhexyl acrylate (hereinafter abbreviated as 2EHA), 35 g of 2-acetoacetoxyethyl methacrylate (hereinafter abbreviated as AAEM), 80.5 g of diacetoneacrylamide (hereinafter abbreviated as DAAM) and 76 g of methyl methacrylate (hereinafter abbreviated as MMA) in a 2-liter four-necked flask equipped with a Dimroth condenser, thermometer, nitrogen gas blow-in tube and stirrer, 525 g of ethyl acetate was added as a solvent and the mixture was dissolved to uniformity. The temperature was raised to 75° C. while blowing in nitrogen gas at flow rate of 100 ml / min. After holding at 75° C. for 30 minutes, a solution of 0.21 g of benzoyl peroxide as an initiator in 5 g of ethyl acetate was added, and the external temperature was set to 85° C. Subsequently, 300 g of toluene was loaded in portions of 100 g at a time at 3, 5 and 7 hours after adding the initiator. During the polymerization, nitrogen gas was c...

example 2

Production of Nonaqueous Pressure-Sensitive Adhesive 2

[0049]A monomer solution was prepared by uniformly pre-dissolving 78.8 g of 2EHA, 78.8 g of n-butyl acrylate (hereinafter abbreviated as BA), 105 g of AAEM, 87.5 g of MMA and 1.05 g of diethyleneglycol dimethacrylate (hereinafter abbreviated as DEGMA). After adding 100 g of the monomer solution in a 2-liter four-necked flask equipped with a Dimroth condenser, thermometer, nitrogen gas blow-in tube and stirrer, 350 g of ethyl acetate was added as a solvent. The temperature was raised to 75° C. while blowing in nitrogen gas at flow rate of 100 ml / min, and after holding at 75° C. for 30 minutes, a solution of 0.35 g of benzoyl peroxide as an initiator in 5 g of ethyl acetate was added, and the external temperature was set to 85° C. Upon confirming reflux of the solvent, the remaining monomer solution was loaded continuously for 3 hours. Next, one hour after the initial continuous loading of the monomer solution, 500 g of ethyl aceta...

example 11

Production of Tape Preparation for Percutaneous Absorption 11

[0082]A 36.2 g portion of pressure-sensitive adhesive 7, and then 1.5 g of ketoprofen, were placed in a screw-cap bottle and stirred for more than an hour in the bottle. A coating tester (LTE-S, Wener Mathis AG) was used for coating and drying of the solution onto a support (polyester film) to a dried coating weight of 140 mg / 10 cm2, and then a liner (silicon-treated polyester film) was used to cover it with the silicon side contacting the pressure-sensitive to obtain tape preparation for percutaneous absorption 11. The ketoprofen content of the obtained preparation was 10 w / w %.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
Tgaaaaaaaaaa
Tgaaaaaaaaaa
temperatureaaaaaaaaaa
Login to View More

Abstract

A nonaqueous pressure-sensitive adhesive for a medicinal tape preparation for percutaneous absorption comprising (a) a support, (b) a pressure-sensitive adhesive layer containing a drug and a nonaqueous pressure-sensitive adhesive and (c) a release film laminated in that order, and a medicinal tape preparation for percutaneous absorption comprising the adhesive. The nonaqueous pressure-sensitive adhesive may comprise a copolymer obtained by copolymerization of a (meth)acrylic monomer having an acetoacetyl group in the molecule and one or more monomers from among other (meth)acrylic monomers without acetoacetyl groups and copolymerizable vinyl monomers, in a nonaqueous solvent. Suitable (meth)acrylic monomers having an acetoacetyl group in the molecule are acetoacetoxyalkyl methacrylates, and especially 2-acetoacetoxyethyl methacrylate. The copolymer nonaqueous pressure-sensitive adhesive of the invention, comprising a (meth)acrylic monomer having an acetoacetyl group as a constituent monomer, is capable of containing large amounts of lipophilic oily substances in the pressure-sensitive adhesive layer, and during heat drying, the acetoacetyl groups undergo self-crosslinking to form a network structure as the solvent evaporates off, so that large amounts of oily substances such as the plasticizer can be included in the network structure. The pressure-sensitive adhesive of the invention uses no polyamine derivatives, isocyanate compounds, polyvalent metal chelate compounds, etc., as crosslinking agents, and therefore toxicity is not a concern and skin is not irritated. A medicinal tape preparation for percutaneous absorption of the invention has superior adhesive strength and cohesive strength, and is highly safe with low skin irritation. It also has excellent drug release and percutaneous absorption properties.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]The present application is a Continuation application of, and claims benefit of, U.S. patent application Ser. No. 10 / 561,751, filed on Dec. 21, 2005, which was the National Stage of, and claims benefit of, International Application PCT / JP2004 / 008544, filed on Jun. 17, 2004, which claims benefit of, and priority to, Japanese Patent Application No. 2003-179162, filed on Jun. 24, 2003, all of which are herein incorporated by reference.TECHNICAL FIELD[0002]The present invention relates to a nonaqueous pressure-sensitive adhesive for a medicinal tape preparation for percutaneous absorption, comprising a copolymer obtained by copolymerization of a (meth)acrylic monomer having an acetoacetyl group in the molecule and one or more monomers selected from among other (meth)acrylic monomers with no acetoacetyl group and copolymerizable vinyl monomers, in a nonaqueous solvent, as well as to a medicinal tape preparation for percutaneous absorption prod...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(United States)
IPC IPC(8): A61K9/70A61K47/32
CPCA61K9/7061A61K47/32Y10T156/1052A61F2013/00663A61L24/046A61P9/12A61P19/00A61P37/08A61K9/70
Inventor KAWAMURA, NAOHISASAWADA, HIDENORIKOBAYASHI, TAKAYUKI
Owner NIPRO PATCH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com