JP6904521B2 - アレルゲン低減化組成物 - Google Patents
アレルゲン低減化組成物 Download PDFInfo
- Publication number
- JP6904521B2 JP6904521B2 JP2017024070A JP2017024070A JP6904521B2 JP 6904521 B2 JP6904521 B2 JP 6904521B2 JP 2017024070 A JP2017024070 A JP 2017024070A JP 2017024070 A JP2017024070 A JP 2017024070A JP 6904521 B2 JP6904521 B2 JP 6904521B2
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- Prior art keywords
- allergen
- allergens
- manufactured
- zinc
- reducing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Description
硫酸亜鉛七水和物(和光純薬工業株式会社製)5gをイオン交換水100gに溶解し、この液を撹拌しながら、炭酸ナトリウム十水和物(和光純薬工業株式会社製)5gをイオン交換水100gに溶解した液を徐々に添加し、炭酸亜鉛の白色沈殿を得た。この沈殿をろ別し、ポイズ520(花王株式会社製)0.2gを添加後イオン交換水を加えて20gとし、直径1mmのガラスビーズを用いて湿式粉砕を10分間行い、約10%の炭酸亜鉛分散製剤を得て実施例1とした。
炭酸亜鉛(和光純薬工業株式会社製)20g、ポイズ520(花王株式会社製)1g、イオン交換水79gを混合し、直径1mmのガラスビーズを用いて湿式粉砕を10分間行い、炭酸亜鉛20%の分散製剤を得て実施例2とした。
塩基性炭酸亜鉛(堺化学工業株式会社製)20g、ポイズ520(花王株式会社製)1g、イオン交換水79gを混合し、直径1mmのガラスビーズを用いて湿式粉砕を10分間行い、塩基性炭酸亜鉛20%の分散製剤を得て実施例3とした。
酸化亜鉛(和光純薬工業株式会社製)20g、ポイズ520(花王株式会社製)1g、イオン交換水79gを混合し、直径1mmのガラスビーズを用いて湿式粉砕を10分間行い、酸化亜鉛20%の分散製剤を得て比較例1とした。
微粒子化酸化亜鉛(FINEX 25:堺化学工業株式会社製)20g、ポイズ520(花王株式会社製)1g、イオン交換水79gを混合し、直径1mmのガラスビーズを用いて湿式粉砕を10分間行い、微粒子化酸化亜鉛20%の分散製剤を得て比較例2とした。
塩基性炭酸マグネシウム(和光純薬工業株式会社製)20g、ポイズ520(花王株式会社製)1g、イオン交換水79gを混合し、直径1mmのガラスビーズを用いて湿式粉砕を10分間行い、塩基性炭酸マグネシウム20%の分散製剤を得て比較例3とした。
塩化亜鉛(和光純薬工業株式会社製)10gをイオン交換水90gに溶解した溶液を比較例4とした。
アレルゲン低減化組成物によるダニアレルゲンの低減化効果の測定
ダニアレルゲンDer f2を含有する、タンパク質量として約900ng/1mL{リン酸緩衝液(pH7.2)}のアレルゲン液1mLに対し、実施例1〜3、比較例1〜3をそれぞれ20または40μL反応させた。これら試料について Der f2酵素免疫測定法(ELISA)のサンドイッチ法にてダニアレルゲン低減化効果の測定を行った。まず、リン酸緩衝液(pH7.4)で2μg/mLに希釈した抗Der f2 モノクローナル抗体15E11を、F16 MAXISORP NUNC−IMMUNO MODULEプレート(NUNC社製)の1ウェルあたり100μLずつ添加し、4℃にて3日感作させた。感作後、液を捨て、ブロッキング試薬{1重量%牛血清アルブミン+リン酸緩衝液(pH7.2)}を1ウェルあたり200μLずつ添加し、37℃、60分間反応させた。反応後、リン酸緩衝液(pH7.2)にてプレートを洗浄した。
アレルゲン低減化組成物によるスギ花粉アレルゲンの低減化効果の測定
スギ花粉アレルゲンCry j1として約12.5ng/1mL{リン酸緩衝液(pH7.2)}のアレルゲン液1mLに対し、実施例1〜3、比較例1〜3をそれぞれ20または40μL反応させた。これら試料についてCry j1酵素免疫測定法(ELISA)のサンドイッチ法にてスギ花粉アレルゲン低減化効果の測定を行った。まず、リン酸緩衝液(pH7.4、0.1重量%NaN3含有)で2μg/mLに希釈したCry j1 モノクローナル抗体013を、F16 MAXISORP NUNC−IMMUNO MODULEプレート(NUNC社製)の1ウェルあたり100μLずつ添加し、4℃にて1日感作させた。感作後、液を捨て、ブロッキング試薬{1重量%牛血清アルブミン+リン酸緩衝液(pH7.2、0.1重量%NaN3含有)}を1ウェルあたり200μLずつ添加し、37℃、60分間反応させた。反応後、リン酸緩衝液{pH7.2、0.1重量%ポリオキシエチレン(20)ソルビタンモノラウレート含有}にてプレートを洗浄した。
実施例3を5g、ウレタン系バインダーとしてスーパーフレックス130(第一工業製薬株式会社製)2gを採り、イオン交換水43gを加えて希釈した。この希釈液に27cm×20cmのポリプロピレン製不織布(80g/m2)を浸漬処理し、希釈液6.5gを付着させ、110℃で乾燥させた。(加工量は塩基性炭酸亜鉛として約2.4g/m2)。
比較例1について、加工例1と同様の方法にて27cm×20cmのポリプロピレン製不織布(80g/m2)を浸漬処理を行った(加工量は酸化亜鉛として約2.4g/m2)。
比較例4を10g、ウレタン系バインダーとしてスーパーフレックス130(第一工業製薬株式会社製)2gを採り、イオン交換水38gを加えて希釈した。この希釈液に27cm×20cmのポリプロピレン製不織布(80g/m2)を浸漬処理し、希釈液6.5gを付着させ、110℃で乾燥させた。(加工量は塩化亜鉛として約2.4g/m2)。
加工例1〜3の不織布を等分に切断し(13.5cm×20cm)、一方を4Lのイオン交換水に浸漬して30分間攪拌し、取り出して室温で風乾し水洗後の試料とした。
加工例1〜3の不織布および、これらの水洗を行った不織布を5cm×5cmに切り取り、チャック付きポリ袋に投入し、標準ダニアレルゲン懸濁液(ダニアレルゲンDer f2を含有しタンパク質量として約900ng/1mL)1mLを加え、試料とアレルゲンを接触させた。1時間後にチャック付きポリ袋からアレルゲン液を搾り出し、遠心分離後のこれら試料について Der f2酵素免疫測定法(ELISA)のサンドイッチ法にてダニアレルゲン濃度の測定を[試験例1]と同様の方法を用いて行った。結果を表3に示す。
本発明の、炭酸亜鉛を含有するアレルゲン低減化組成物を使用することにより、ダニや花粉等のアレルゲンを低減させることができ、また不織布、繊維または繊維製品、建築用内装材に耐水性を有するアレルゲンを低減させる機能を付与することができ、さらにアレルゲンを低減できる不織布、繊維または繊維製品、建築用内装材を提供することができる。
Claims (3)
- 炭酸亜鉛を含有することを特徴とするアレルゲン低減化組成物。
- 炭酸亜鉛が塩基性炭酸亜鉛であることを特徴とする請求項1記載のアレルゲン低減化組成物。
- 請求項1または請求項2に記載のアレルゲン低減化組成物を加工したアレルゲン低減化用壁材、壁紙、不織布、フィルター材料、繊維または繊維製品、建築用内装材。
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