Temperature-responsive polymer compound and process for producing the same

a technology of temperature-responsive polymer and temperature-responsive polymer, which is applied in the direction of other chemical processes, separation processes, instruments, etc., can solve the problems of poor hydrophobic nature or hydrogen bonding properties of alkylacrylamides, the inability to synthesize a heat-responsive polymer of the alkylamide type, and the inability to provide a sufficient polarity in separating any protein

Inactive Publication Date: 2005-10-13
GE HEALTHCARE BIO SCI CORP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0017] Further, the present inventors have conducted intensive studies and consequently found that a temperature-responsive polymer compound, the temperature-responsiveness of which can be controlled, can be synthesized by introducing a hydrogen-bonding functional group and a hydrophobic group into a monomer followed by polymerizat

Problems solved by technology

It is therefore impossible to synthesize a heat-responsive polymer of the alkylamide type having a side chain with a large carbon atom number.
In the case of an ester-bond type polymer or an alkylamide polymer, it is also difficult to provide a sufficient polarity in separating any protein.
Owing to this characteristic, these alkylacrylamides are poor in the hydrophobic nature or the hydrogen bonding properties, which makes it difficult to efficiently separate, adsorb and release all biological components or organic matters by using the these kinds of polymers.
Although hydrogen-bonding groups can be in

Method used

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  • Temperature-responsive polymer compound and process for producing the same
  • Temperature-responsive polymer compound and process for producing the same
  • Temperature-responsive polymer compound and process for producing the same

Examples

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examples

[0166] The present invention will be described in greater detail by reference to the following Examples, but it should be understood that the invention is not construed as being limited thereto.

example a1

Synthesis of poly-acetamide-propyl methacrylate

[0167] 0.9 g of 2-N-aminoethyl methacrylate hydrochloride was dissolved in a methanol solvent and 1.0 g of propionic anhydride and 0.9 g of triethylamine (TEA) were added thereto. The resultant mixture was stirred under ice-cooling for 4 hours. After the completion of the reaction, the solvent was distilled off with an evaporator and the precipitate was filtered off. The filtrate was recovered and introduced into a silica column. Thus, the eluate fraction containing the target product was taken up and subjected to recrystallization to thereby purify a precursor of the target product acetamide-propyl methacrylate (CH3CONH—(CH2)3—O—CO—C(CH3)═CH2) (yield: 75%). 0.3 g of this precursor was dissolved in 5 ml of n-propanol and 6.2 mg of 2,2-azobisisobutyronitrile (AIBN) was added thereto. Then, the mixture was polymerized at 75° C. for 12 hours under a nitrogen atmosphere. After the completion of the polymerization, the reaction mixture was ...

example a2

Synthesis of poly-propionamide-propyl acrylate

[0168] 4 g of 3-aminopropyl alcohol was dissolved in 100 ml of a dichloromethane solvent and 10 g of propionic anhydride and 0.9 g of triethylamine (TEA) were added thereto. The resultant mixture was stirred at 50° C. for 4 hours. After the completion of the reaction, the solvent was distilled off with an evaporator and the precipitate was filtered off. The filtrate was recovered and introduced into a silica column. Thus, the eluate fraction containing the target product was taken up and subjected to recrystallization to thereby purify a precursor of the target product propionamide-propyl acrylate (CH3CH2CONH—(CH2)3—O—CO—CH═CH2). 1.0 g of this precursor and 8 mg of 2,2-azobis(2-amidinopropane)dihydrochloride were dissolved in 10 ml of ethanol and polymerized at 70° C. for 3 hours. After the completion of the polymerization, an adequate amount of the solvent was removed with an evaporator. The residue was reprecipitated from an alcohol / e...

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Abstract

A temperature-responsive polymer and polymer material which has ester bond(s) and/or acid amide bond(s) respectively at one or more sites in the side chain and can be arbitrarily controlled by varying the side chain is provided. The process for production thereof and the use thereof are also provided.

Description

TECHNICAL FIELD [0001] This invention relates to a novel polymer compound which undergoes stretching and cohesion with a change in the polarity of the polymer per se due to a temperature change, a process for producing this polymer compound, a heat-responsive polymer material containing this compound, a separation method with the use of a material containing this heat-responsive polymer material, and a method for separating chemicals, biological polymers (proteins, peptides, etc.) and biological samples (cells, etc.) by using this material. [0002] In addition, this invention relates to a temperature-responsive polymer compound a change in the characteristics of which can be controlled depending on temperature. Furthermore, the present invention relates to a temperature-responsive polymer compound which is usable, by taking advantage of the temperature-depending change in the characteristics thereof, in adsorption and separation materials, drug carriers, dielectric and magnetic mater...

Claims

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Application Information

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IPC IPC(8): B01J20/26C08F20/28C08F20/36C08F20/58C08F20/60G01N30/54
CPCB01D15/20B01D15/3876B01J20/261B01J20/265B01J20/285B01J2220/54C08F20/28G01N30/54C08F20/36C08F20/58C08F20/60C08F220/60
Inventor AKIYAMA, YOSHIKATSUYOSHIZAKO, KIMIHIROHASEGAWA, YUKIOOKANO, TERUO
Owner GE HEALTHCARE BIO SCI CORP
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