JP2010144315A - METHOD FOR LIGHT STABILIZING gamma-ORYZANOL AND ATTACHING IT TO FIBER AND FIBER PRODUCT WITH SUCH METHOD PROCESSED - Google Patents
METHOD FOR LIGHT STABILIZING gamma-ORYZANOL AND ATTACHING IT TO FIBER AND FIBER PRODUCT WITH SUCH METHOD PROCESSED Download PDFInfo
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Abstract
Description
本発明は、γ−オリザノールにビタミンE類を併用し、油剤に溶解させ、繊維に加工することにより、光による分解を抑制することが出来、肌着やシャツ等の衣料分野に利用できる。 In the present invention, vitamin E is used in combination with γ-oryzanol, dissolved in an oil agent, and processed into a fiber, whereby decomposition by light can be suppressed, and can be used in the field of clothing such as underwear and shirts.
γ−オリザノールは米胚芽に含まれているオイルに溶ける性質の生理活性成分であり、血液の循環促進、加齢による皮膚の機能低下を防ぐ効果が知られ、スキンケア加工等に注目されている薬剤であるが、そのままでは光により分解してしまい生理活性効果が持続しないという問題がある。 γ-Oryzanol is a physiologically active ingredient that dissolves in oil contained in rice germ, and is known to have effects of promoting blood circulation and preventing skin function deterioration due to aging However, there is a problem that if it is used as it is, it is decomposed by light and the physiologically active effect is not sustained.
本発明は、γ−オリザノールを繊維に付着せしめ、生理活性効果を持続させる事を目的とするものである。 An object of the present invention is to adhere γ-oryzanol to fibers and maintain a physiologically active effect.
本発明は、γ−オリザノールをビタミンE類と共に油剤に溶解しエマルジョン化して繊維に付着せしめることに基づくものであり、このことにより前記課題を解決する事が判明した。 The present invention is based on dissolving γ-oryzanol in an oil together with vitamin E, emulsifying it, and adhering it to the fiber, and it has been found that this problem can be solved.
本発明は、繊維に、γ−オリザノールと酢酸α−トコフェロールを油剤に溶解させ繊維に付着させることにより、優れた光安定性を与えることが出来る効果がある。 INDUSTRIAL APPLICABILITY The present invention has an effect that excellent light stability can be imparted by dissolving γ-oryzanol and α-tocopherol acetate in an oil and adhering them to the fiber.
本発明に用いる繊維とは、綿、羊毛、絹等の天然繊維、レーヨン、ポリノジック、アセテート等の再生繊維、ポリエステル、ナイロン、アクリル等の合成繊維で、これらを1種または2種以上を混紡したものであってもよい。 The fibers used in the present invention are natural fibers such as cotton, wool, and silk, regenerated fibers such as rayon, polynosic, and acetate, and synthetic fibers such as polyester, nylon, and acrylic, and these are mixed in one kind or two or more kinds. It may be a thing.
上記γ−オリザノールを水に乳化させる界面活性剤は、非イオン系界面活性剤またはアニオン系界面活性剤を用いることが好ましいが、特に制限されるものではない。 The surfactant for emulsifying γ-oryzanol in water is preferably a nonionic surfactant or an anionic surfactant, but is not particularly limited.
本発明の機能性繊維の製造方法としては、まずγ−オリザノールおよび酢酸α−トコフェロールを油剤に溶解させ、次に界面活性剤を配合し、80℃に加熱し溶解させた後、同じく80℃の水を加え乳化液を作成し、繊維を浸漬、乾燥処理すればよい。 As a method for producing the functional fiber of the present invention, first, γ-oryzanol and α-tocopherol acetate are dissolved in an oil agent, then a surfactant is blended, heated to 80 ° C. and dissolved, and then at 80 ° C. Water may be added to prepare an emulsion, and the fibers may be immersed and dried.
また、油剤の濃度は特に限定されないが、γ−オリザノールおよび酢酸α−トコフェロールと同量またはそれ以上が好ましい。 Further, the concentration of the oil agent is not particularly limited, but the same amount or more as that of γ-oryzanol and α-tocopherol acetate is preferable.
洗濯耐久性を向上させる為には各種併用バインダー、例えばポリエステル樹脂、ウレタン樹脂、塩化ビニル樹脂、酢酸ビニル樹脂、シリコン樹脂、アクリル樹脂等を使用すればよい。 In order to improve the washing durability, various combined binders such as polyester resin, urethane resin, vinyl chloride resin, vinyl acetate resin, silicon resin, acrylic resin and the like may be used.
本発明で得られた機能性繊維に付着したγ−オリザノールは、酢酸α−トコフェロールを使用しないときに比べて飛躍的に光安定性があがり、繊維加工後、2ヶ月間、暴露試験を行なっても、残存が認められる。 The γ-oryzanol adhering to the functional fiber obtained in the present invention is dramatically more photostable than when α-tocopherol acetate is not used, and an exposure test is conducted for 2 months after the fiber processing. Is also observed.
以下の実施例により本発明を具体的に報告する。尚、γ−オリザノールの生理活性効果の測定方法としては、各加工試料をアセトンで3回抽出した後、エバポレーターで濃縮し、DPPHラジカル消去法にて紫色の退色により確認した。 The invention is specifically reported by the following examples. In addition, as a measuring method of the physiological activity effect of γ-oryzanol, each processed sample was extracted three times with acetone, then concentrated with an evaporator, and confirmed by purple fading by the DPPH radical elimination method.
(実施例1)γ−オリザノール(15部)および酢酸α−トコフェロール(15部)を流動パラフィン(170部)に溶解させ、ノニオン系界面活性剤(100部)(NIKKOL(日光ケミカルズ))、グリセリン(50部)を混合し、80℃で加熱溶解し、同じく80℃の水(650部)を加えていき、乳化液(1000部)を得た。 (Example 1) γ-oryzanol (15 parts) and α-tocopherol acetate (15 parts) are dissolved in liquid paraffin (170 parts), nonionic surfactant (100 parts) (NIKKOL (Nikko Chemicals)), glycerin (50 parts) was mixed, heated and dissolved at 80 ° C., and water (650 parts) at 80 ° C. was added to obtain an emulsion (1000 parts).
(実施例2)実施例1の酢酸α−トコフェロールの量を1.5部に変えた他は実施例1と同じ方法で乳化物を得た。 (Example 2) An emulsion was obtained in the same manner as in Example 1 except that the amount of α-tocopherol acetate in Example 1 was changed to 1.5 parts.
(実施例3)実施例1の酢酸α−トコフェロールをα−トコフェロールに変えた他は実施例1と同じ方法で乳化物を得た。 Example 3 An emulsion was obtained in the same manner as in Example 1 except that α-tocopherol acetate in Example 1 was changed to α-tocopherol.
(比較例1)実施例1から酢酸α−トコフェノールを抜いた他は実施例1と同じ方法で乳化物を得た。 (Comparative Example 1) An emulsion was obtained in the same manner as in Example 1 except that α-tocophenol acetate was omitted from Example 1.
(比較例2)実施例1からγ−オリザノールを抜いた他は、実施例1と同じ方法で乳化物を得た。 Comparative Example 2 An emulsion was obtained in the same manner as in Example 1 except that γ-oryzanol was omitted from Example 1.
(比較例3)実施例1からγ−オリザノール、酢酸α−トコフェノールを抜いた他は、実施例1と同じ方法で乳化物を得た。 (Comparative Example 3) An emulsion was obtained in the same manner as in Example 1, except that γ-oryzanol and α-tocophenol acetate were omitted from Example 1.
各配合割合を表1に示した。
綿ニットを表1に示す乳化物の10%水溶液に浸漬し、絞り率90%で較った後、110℃で10分間熱処理し、各試料を得た。 The cotton knit was immersed in a 10% aqueous solution of the emulsion shown in Table 1 and compared with a drawing ratio of 90%, and then heat treated at 110 ° C. for 10 minutes to obtain each sample.
各試料を屋外で暴露し、DPPHラジカル消去能力を測定した。 Each sample was exposed outdoors to measure DPPH radical scavenging ability.
各試験結果を表2に示した。
表2よりγ−オリザノールに酢酸α−トコフェロールを加えて乳化させた試料は抗酸化効果が認められ、長期間の光安定性が向上したことは明らかである。 From Table 2, it is clear that the sample obtained by emulsifying γ-oryzanol with α-tocopherol acetate showed an antioxidant effect and improved long-term light stability.
本発明は、γ−オリザノールを光安定化させ、繊維に付着させる事が出来るので、持続性のある生理活性効果を付与した繊維製品を提供することが可能である。 In the present invention, since γ-oryzanol can be light-stabilized and adhered to the fiber, it is possible to provide a fiber product imparted with a sustained physiological activity effect.
Claims (5)
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2012052281A (en) * | 2010-08-03 | 2012-03-15 | Suzuki Kutsushita:Kk | Chemical fiber containing polyhydric alcohol derivative, and textile product comprising the same |
Citations (12)
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JPH02300301A (en) * | 1989-02-17 | 1990-12-12 | Toray Ind Inc | Clothing |
JPH06272172A (en) * | 1993-03-23 | 1994-09-27 | Toray Ind Inc | Modified textile structure and its production |
JPH06299467A (en) * | 1993-04-12 | 1994-10-25 | Toray Ind Inc | Modified fiber structure and its production |
JPH10235171A (en) * | 1996-12-25 | 1998-09-08 | Terumo Corp | Manufacture of hollow fiber membrane, hollow fiber membrane, and hollow fiber membrane type dialyser |
JP2000178878A (en) * | 1998-10-09 | 2000-06-27 | Canon Inc | Cloth-treating agent, cloth-treating liquid, cloth, printing method, printed material and method for providing high quality printed material stably |
JP2002240848A (en) * | 2001-02-13 | 2002-08-28 | Ci Sanplus Kk | Wrap film for packaging food |
JP2004076188A (en) * | 2002-08-15 | 2004-03-11 | Bayer Ltd | Textile finishing agent |
JP2004324026A (en) * | 2003-04-28 | 2004-11-18 | Ohara Palladium Kagaku Kk | Function-imparting agent and method for producing fibrous product having functionality by using the same |
JP2004346466A (en) * | 2003-05-26 | 2004-12-09 | Nisshinbo Ind Inc | Fiber structure having sebaceous gland activation substance fixed thereto |
JP2005113304A (en) * | 2003-10-07 | 2005-04-28 | Toray Ind Inc | Textile structure |
JP2006276744A (en) * | 2005-03-30 | 2006-10-12 | Toshiba Corp | Photoreceptor sheet and image forming apparatus |
JP2008038258A (en) * | 2006-08-01 | 2008-02-21 | Gunze Ltd | Method for processing fibrous product and processed fiber |
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Patent Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
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JPH02300301A (en) * | 1989-02-17 | 1990-12-12 | Toray Ind Inc | Clothing |
JPH06272172A (en) * | 1993-03-23 | 1994-09-27 | Toray Ind Inc | Modified textile structure and its production |
JPH06299467A (en) * | 1993-04-12 | 1994-10-25 | Toray Ind Inc | Modified fiber structure and its production |
JPH10235171A (en) * | 1996-12-25 | 1998-09-08 | Terumo Corp | Manufacture of hollow fiber membrane, hollow fiber membrane, and hollow fiber membrane type dialyser |
JP2000178878A (en) * | 1998-10-09 | 2000-06-27 | Canon Inc | Cloth-treating agent, cloth-treating liquid, cloth, printing method, printed material and method for providing high quality printed material stably |
JP2002240848A (en) * | 2001-02-13 | 2002-08-28 | Ci Sanplus Kk | Wrap film for packaging food |
JP2004076188A (en) * | 2002-08-15 | 2004-03-11 | Bayer Ltd | Textile finishing agent |
JP2004324026A (en) * | 2003-04-28 | 2004-11-18 | Ohara Palladium Kagaku Kk | Function-imparting agent and method for producing fibrous product having functionality by using the same |
JP2004346466A (en) * | 2003-05-26 | 2004-12-09 | Nisshinbo Ind Inc | Fiber structure having sebaceous gland activation substance fixed thereto |
JP2005113304A (en) * | 2003-10-07 | 2005-04-28 | Toray Ind Inc | Textile structure |
JP2006276744A (en) * | 2005-03-30 | 2006-10-12 | Toshiba Corp | Photoreceptor sheet and image forming apparatus |
JP2008038258A (en) * | 2006-08-01 | 2008-02-21 | Gunze Ltd | Method for processing fibrous product and processed fiber |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2012052281A (en) * | 2010-08-03 | 2012-03-15 | Suzuki Kutsushita:Kk | Chemical fiber containing polyhydric alcohol derivative, and textile product comprising the same |
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