JP5547093B2 - 送達粒子 - Google Patents
送達粒子 Download PDFInfo
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- JP5547093B2 JP5547093B2 JP2010546434A JP2010546434A JP5547093B2 JP 5547093 B2 JP5547093 B2 JP 5547093B2 JP 2010546434 A JP2010546434 A JP 2010546434A JP 2010546434 A JP2010546434 A JP 2010546434A JP 5547093 B2 JP5547093 B2 JP 5547093B2
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Description
本明細書で用いる「消費者製品」は、販売される形態での使用又は消費を意図し、後続する商業的製造又は変性を意図しない、ベビーケア、ビューティケア、衣類及びホームケア、ファミリーケア、フェミニンケア、ヘルスケア、スナック、並びに/又は飲料製品あるいは装置を意味する。このような製品には:おむつ、よだれ掛け、拭き取り用品、漂白、カラーリング、染色、コンディショニング、シャンプー、スタイリング等の、毛髪処理(人、犬、及び/又は猫)用商品及び/又は毛髪処理に関する方法、脱臭剤及び制汗剤、パーソナルクレンジング、化粧品、クリーム、ローション、及び消費者が使用するためのその他の局所的に適用される製品の適用を含むスキンケア、及びシェービング製品、布、硬表面、及び布及びホームケアの分野における任意のその他の表面を処理するための製品及び/又は処理に関する方法、例えば、空気ケア、自動車の手入れ、食器洗い、布地コンディショニング(軟化等)、洗濯洗浄力、洗濯及びすすぎ添加剤及び/又はケア、硬表面洗浄及び/又は処理、及び消費者用又は業務用のその他の洗浄、トイレットペーパー、化粧紙、鼻がみ、及び/又はペーパータオル、タンポン、女性用ナプキン用に関する製品及び/又は方法、練り歯磨き、歯用ゲル、歯のリンス、義歯接着剤、歯のホワイトニング等の口腔ケア製品及び/又は処理に関する方法製品及び/又は処理に関する方法、咳止め薬及び風邪治療薬、痛み止め、RX医薬、ペットの健康及び栄養、並びに浄水等の市販のヘルスケア、主に通常の食事の合間に消費される又は食事の添え物(meal accompaniment)として消費されることが意図されている加工食品(非限定例には、ポテトチップ、トルティーヤチップス、ポップコーン、プレッツェル、コーンチップス、シリアルバー、野菜チップス又はクリスプス、スナックミックス、パーティーミックス、マルチグレインチップス、スナッククラッカー、チーズスナック、ポークラインズ、コーンスナック、ペレットスナック、押出スナック、及びベーグルチップスが挙げられる)、及びコーヒー、に関する商品及び/又は方法、が挙げられるが、これらに限定されない。
1つの態様において、有益剤送達総重量に基づいて、
a.)有益送達組成物の総重量に基づいて、約1%〜約85%、約8%〜約80%、約12%〜約75%、約15%〜約65%、約20%〜約60%、又は更には約25%〜約55%の有益剤を提供するのに十分な量の有益剤を含む、約2%〜約97%、約10%〜約90%、約15%〜約85%、約20%〜約80%、約25%〜約75%、又は更には約30%〜約70%のカプセル化された有益剤と、
b.)約1%〜約50%、約2%〜約45%、約3%〜約40%、約4%〜約37%、約5%〜約35%、又は更には約6%〜約30%の可塑剤と、
c.)約1%〜約50%、約2%〜約45%、約3%〜約35%、約4%〜約30%、約5%〜約25%、又は更には約6%〜約20%の結合剤と、
d.)任意に、約1%〜約50%、約2%〜約45%、約5%〜約40%、約7%〜約35%、約9%〜約30%、又は更には約10%〜約27%のダスティング剤と、を含むことができる凝集体、微粒子、又は押出品であってもよい有益剤送達組成物が開示される。
a.上記カプセル化された有益剤は香料マイクロカプセルを含んでもよく、この香料マイクロカプセルはシェルを含み、このシェルは架橋メラミンホルムアルデヒドを含み、
b.上記可塑剤は水を含んでもよく、
c.上記結合剤は、CMC等のメチルセルロース等のセルロース類及びその誘導体、アルギネート及びその誘導体、でんぷん類、ポリビニルアルコール類、ポリエチレンオキシド、ポリビニルピロリドン、キトサン及び/又はカラギーナン等の天然ゴム類などの多糖類、架橋ポリアクリレート類等のポリアクリレート類、ワックス類、ポリエチレングリコール類、例えば、4000Daを超える分子量(重量平均)を有する、又は更には約4000Da〜約15,000Daの分子量(重量平均)を有するポリエチレングリコール類、アルコールエトキシレート類、界面活性剤類、及びこれらの混合物からなる群から選択されてもよく、並びに
d.上記ダスティング剤は、シリカ類、ゼオライト類、非晶質アルミノケイ酸塩、粘土類、でんぷん類、セルロース類、塩化ナトリウム、硫酸ナトリウム、硫酸マグネシウム及び/又は炭酸ナトリウム等の水溶性塩類、糖類等の多糖類、及びこれらの混合物からなる群から選択されてもよい。
本発明の有益剤送達組成物は、本明細書の実施例に従って、及び/又は以下の方法によって調製されてもよく、前記方法は、
a.)カプセル体と、可塑剤と、結合剤とを混合して、混合物を形成することと、
b.)この混合物をダスティング剤と混合して、材料を形成することと、
c.)この材料から十分な量の上記可塑剤を除去して、製品の総重量に基づいて、約1%〜約50%、約2%〜約45%、3%〜約40%、約4%〜約37%、約5%〜約35%、又は更には約6%〜約30%の可塑剤を含む製品を得ることと、を含む。
出願人らは、組み込み方法の間にカプセル体のシェルが時期尚早に破裂することを含む、カプセル化された有益剤を乾燥製品に組み込むことに付随する問題は、カプセル化された有益剤を更に加工し、かつ、微粒子、粉末、又はその他の本質的に乾燥形態であってもよい乾燥消費者製品等の消費者製品に添加され得る凝集体の中に組み込むと、最小限にできることを発見した。
本明細書において採用されるカプセル化された有益剤は、米国特許第6,592,990 B2号及び/又は米国特許第6,544,926 B1号の教示、並びに本明細書に開示される実施例を介して製造されてもよい。
ニュージャージー州クランバリー(Cranbury))、ベイカー・ヒューズ社(Baker Hughes Corp.)(米国テキサス州ヒューストン(Houston))、ハーキュレス社(Hercules Corp.)(米国デラウェア州ウィルミントン(Wilmington))、アグリウム社(Agrium Inc.)(カナダ、アルバータ州カルガリー(Calgary))、ISP社(米国ニュージャージー州)から入手可能である。
1つの態様において、カプセル化された有益剤はホルムアルデヒドスカベンジャーと組み合わされてもよい。1つの態様において、カプセル化された有益剤は、本発明のカプセル化された有益剤を含んでもよい。好適なホルムアルデヒドスカベンジャーには、亜硫酸水素ナトリウム、尿素、エチレン尿素、システイン、システアミン、リシン、グリシン、セリン、カルノシン、ヒスチジン、グルタチオン、3,4−ジアミノ安息香酸、アラントイン、グリコウリル、アントラニル酸、アントラニル酸メチル、メチル4−アミノベンゾエート、エチルアセトアセテート、アセトアセトアミド、マロンアミド、アスコルビン酸、1,3−ジヒドロキシアセトン二量体、ビウレット、オキサミド、ベンゾグアナミン、ピログルタミン酸、ピロガロール、メチルガラート、エチルガラート、プロピルガラート、トリエタノールアミン、スクシンアミド、チアベンダゾール、ベンゾトリアゾール、トリアゾール、インドリン、スルファニル酸、オキサミド、ソルビトール、グルコース、セルロース、ポリ(ビニルアルコール)、部分的に加水分解されたポリ(ビニルホルムアミド)、ポリ(ビニルアミン)、ポリ(エチレンイミン)、ポリ(オキシアルキレンアミン)、ポリ(ビニルアルコール)−コ−ポリ(ビニルアミン)、ポリ(4−アミノスチレン)、ポリ(L−リシン)、キトサン、ヘキサンジオール、エチレンジアミン−N,N’−ビスアセトアセトアミド、N−(2−エチルヘキシル)アセトアセトアミド、2−ベンゾイルアセトアセトアミド、N−(3−フェニルプロピル)アセトアセトアミド、リリアール、ヘリオナール、メロナール、トリプラール、5,5−ジメチル−1,3−シクロヘキサンジオン、2,4−ジメチル−3−シクロヘキセンカルボキシアルデヒド、2,2−ジメチル−1,3−ジオキサン−4,6−ジオン、2−ペンタノン、ジブチルアミン、トリエチレンテトラミン、水酸化アンモニウム、ベンジルアミン、ヒドロキシシトロネロール、シクロヘキサノン、2−ブタノン、ペンタンジオン、デヒドロ酢酸、又はこれらの混合物からなる群から選択される物質が挙げられる。これらホルムアルデヒドスカベンジャーは、米国ミズーリ州セントルイスのシグマ/アルドリッチ/フルカ(Sigma/Aldrich/Fluka of St. Louis, MO. U.S.A.)、又は米国ペンシルバニア州ウォリントンのポリサイエンス社(PolySciences, Inc. of Warrington, PA U.S.A.)から入手可能である。
本出願人の消費者製品は、本出願に開示される有益剤送達組成物の実施形態を含んでもよい。1つの態様において、この消費者製品は、粉末、顆粒、又はその他の本質的に乾燥した洗剤であってもよい。
本発明の目的には必須ではないが、以下に例示される補助剤の非限定的な一覧は本組成物において使用するのに適しており、例えば、性能を補助若しくは向上させるために、洗浄化される基材の処理のために、又は香料、着色剤、染料などを用いる場合のように組成物の審美性を変化させるために、望ましくは本発明の特定の実施形態に組み込むことができる。こうした補助剤は、本出願人らの凝集体/粒子を介して供給される構成成分に追加されると理解される。これらの追加的構成成分の明確な性質、及びそれを組み込む濃度が、組成物の物理的形態及び使用されるべき作業の性質によって決まる。好適な補助材料には、ポリマー、例えばカチオン性ポリマー、界面活性剤、ビルダー、キレート化剤、移染防止剤、分散剤、酵素及び酵素安定剤、触媒作用性物質、漂白活性化剤、ポリマー分散剤、粘土汚れ除去/再付着防止剤、増白剤、泡抑制剤、染料、追加の香料及び香料送達システム、構造弾性化剤、柔軟仕上げ剤、キャリア、ヒドロトロープ、加工助剤、並びに/又は顔料が挙げられるが、これらに限定されない。下記の開示に加え、このような他の補助剤の好適な例及び使用濃度は、米国特許第5,576,282号、同第6,306,812 B1号、及び同第6,326,348 B1号に記載されており、これらは参照により組み込まれる。
本発明の組成物は、任意の好適な形態に処方されることができ、配合者によって選択される任意の方法によって調製することができるが、その非限定的な具体例は、米国特許第5,879,584号、同第5,691,297号、同第5,574,005号、同第5,569,645号、同第5,565,422号、同第5,516,448号、同第5,489,392号、同第5,486,303号に記載されており、その全てが本明細書に参照により組み込まれる。
本明細書に開示されるカプセル化された有益剤を含有する組成物は、ある部位、とりわけ表面又は布地を洗浄又は処理するのに使用することができる。通常、この場所の少なくとも一部は、希釈されない形態の又は液体に希釈された、本出願人らの組成物の実施形態、例えば洗浄液と接触され、そしてその後、任意に、その場所が洗浄及び/又はすすがれてもよい。1つの態様において、部位は、任意に、洗浄及び/又はすすがれ、本発明の有益剤送達組成物の1種類以上、又は本発明の有益剤送達組成物の1種類以上を含む消費者製品と接触させられ、その後、任意に洗浄及び/又はすすがれる。本発明の目的上、洗浄には、擦ること及び機械的攪拌が挙げられるが、これらに限定されない。布地は、標準的な消費者の使用条件で洗濯又は処理することが可能なほとんどの任意の布地を含み得る。開示される組成物を含み得る液体は、約3〜約11.5のpHを含んでよい。こうした組成物は、典型的に、溶液中で約500ppm〜約15,000ppmの濃度で使用される。洗浄溶媒が水であるとき、水温は、典型的には、約5℃〜約90℃であり、部位が布地を含むとき、水と布地との割合は、典型的には、約1:1〜約30:1である。
本出願の「試験方法」の項で開示される試験方法は、本出願人らの発明が本明細書に記載され及び特許請求されているように、本出願人らの発明のパラメータの各値を求めるために使用されるべきであると理解される。
有益剤送達組成物の粒径分布は、ASTM試験方法E726−01「粒状キャリア及び粒状殺虫剤の粒径分布(Particle Size Distribution of Granular Carriers and Granular Pesticides)」を用いて決定される。具体的には、この方法は、中央に取り付けられたコルクを有する鋳鉄製のシーブスタック蓋(cast iron sieve stack lid)を備えるタイラーロタップ篩振盪器(Tyler RoTap sieve shaker))(W.S.タイラー社(W. S. Tyler Company)(オハイオ州クリーブランド(Cleveland))を使用して実施されなければならない。分析する材料の全ての粒径を網羅するために、少なくとも5種類のふるい寸法が選択されるべきである(工程7.1)。ふるい分けの後に、1つのふるいの上に40重量%を超える試料が見られる場合は、ふるい分けによる選択を変更して、全てのふるいの上に40重量%が見られるまで試料を再試験する。
1)152taps/分
2)285rpm楕円形運動
3)蓋の上のコルクは保持カップの上部から5mm突出する。
4)ハンマーのピーク高さからコルクの上部までのハンマードロップは33mm。
5)ふるい分けの時間は5分。
D50=10∧[Log(Da50)−(Log(Da50)−Log(Db50))*(Qa50−50%)/(Qa50−Qb50)]
(式中、Qa50及びQb50は、それぞれ50番目の百分位数の真上及び真下のデータの累積質量百分位数であり、Da50及びDb50は、これらのデータに相当するマイクロメートルシーブサイズ値である。)本出願の目的上、質量基準の中央粒径は特徴的な寸法であると考慮される。
材料を20℃にした状態でマイクロメータを使用して測定することによって、押出品の直径を求める。平均値を決定するために、試験される試料から5つの代表押出品を選び出し、測定方法の間に押出品を変形させないように注意しながら押出品を測定し、次に、このような測定値の相加平均を計算する。本出願の目的上、かかる相加平均は押出品の特徴的な寸法であると考慮される。
第一の混合物を、水208グラムとアルキルアクリレート−アクリル酸コポリマー[ポリサイエンス社(Polysciences, Inc.)(米国ペンシルバニア州ウォリントン(Warrington))]5グラムを混合することにより調製する。この第一の混合物を酢酸を使用してpH5.0に調整する。
第一の混合物を、水208グラムとアルキルアクリレート−アクリル酸コポリマー(ポリサイエンス社(Polysciences, Inc.)(米国ペンシルバニア州ウォリントン(Warrington)))5グラムを混合することにより調製する。この第一の混合物を酢酸を使用してpH5.0に調整する。
第一の混合物を、水208グラムとアルキルアクリレート−アクリル酸コポリマー(ポリサイエンス社(Polysciences, Inc.)(米国ペンシルバニア州ウォリントン(Warrington)))5グラムを混合することにより調製する。この第一の混合物を酢酸を使用してpH5.0に調整する。
実施例1〜3の香料マイクロカプセルスラリーの9kgアリコートを、R1382を取り付けたユーロスター混合機(Eurostar mixer)(IKA)を使用して、200RPMの一定速度で混合する。香料マイクロカプセルスラリーのそれぞれに、500gのカルボキシメチルセルロース(CPケルコ(Kelco))を混合しながら添加する。これらスラリーを、全部で2時間、又は均一なペーストが形成されるまで、混合する。こうして、3つの個別のペーストが作られる。
1.28kgの沈殿シリカシペルナト(Sipernat)(登録商標)22S(デグサ(Degussa))を、F−20パドルミキサー(フォルベルク(Forberg))に加える。最初にミキサーを5秒間動かして、ミキサーの基部にシリカを均等に分配する。ミキサーを停止し、実施例4に従って作った8.25kgのペーストを、粉末の上に均一に分配する。続いて、ミキサーを120rpmで全部で30秒間動かす。混合の後、ぬれた状態の粒子をミキサーから放出して、2000マイクロメートルのスクリーンを使用してふるい分けて、大きすぎるものを除去する。スクリーンを通過する良好な生成物を、CDT 0.02流動層乾燥機(ニロ(Niro))の中で500gごとのバッチで、カール・フィッシャーで測定した最終含水量が20重量%になるまで乾燥する。乾燥器は、入り口温度140℃及び速度0.68m/sで操作される。実施例4で作られたペーストのそれぞれに関してこの手順を繰り返して、3つの別個の凝集体を得た。
実施例1〜3の香料マイクロカプセルスラリーの800gアリコートを、それぞれ、均一なペーストが形成されるまでスパチュラを使用して、200gのカルボキシメチルセルロース(CPケルコ(Kelco))と共に混合する。こうして、3つの個別のペーストが作られる。次に、各ペーストを、運搬スクリューのみを使用して、APV 19mmバレル2軸押し出し機(ベーカー・パーキンス社(Baker Perkins Ltd.))を通過させる。ダイプレートは直径1mmの穴を有する。押出成形機は、速度100rpm及び周囲温度で運転されて、3組の押出品を作る。
実施例1〜3の香料マイクロカプセルスラリーの1kgアリコートを、それぞれ、離散粒子の湿塊が形成されるまでスパチュラを使用して、100gの架橋ポリアクリレート(アクアリック(Aqualic)CAシリーズ、日本触媒)と共に混合する。濡れた状態の粒子の各組を別個のプラスチックバッグの中に定置して、自由流動凝集体粒子が形成されるまで、300gのゼオライト4A(化学工業株式会社(Industrial Chemicals Ltd))を振りかける。混合の後、2000マイクロメートルのふるいを使用して材料をふるい分けて、大きすぎるものを除去する。
実施例1〜3の香料マイクロカプセルスラリーの250gアリコートを、それぞれ、混合物がペーストを形成するまでスパチュラを使用して、5gの架橋ポリアクリレート(アクアリック(Aqualic)CAシリーズ、日本触媒)と共に混合する。台所用フードプロセッサ(ブラウン(Braun))の中で、各ペースト100gを50gのゼオライト4A(化学工業株式会社(Industrial Chemicals Ltd))と共に個別に混合して、3組の凝集体粒子を形成する。混合の後、凝集体粒子の各組を2000マイクロメートルのスクリーンを使用してふるい分けて、大きすぎるものを除去する。材料の薄層をトレイの上に広げ、凝集体粒子の含水量が20重量%になるまで50℃のオーブンの中に定置することによって、凝集体粒子の各組のスクリーンを通過する良好な生成物を乾燥させる。
アルギン酸ナトリウム粉末(マヌコール(Manucol)DM、インターナショナル・スペシャリティー・プロダクツ(International Speciality Products))を実施例1〜3の香料マイクロカプセルスラリーの3つの個々のアリコートに溶解して1%アルギン酸溶液を作る。ウルトラターラックス(Ultra Turrax)T25混合機(IKA)を速度10000/分で使用してこれら組成物を十分に混合する。次に、PMC/アルギネート混合物を個別のキトサン(プリメックス(Primex))の1%水溶液に滴加する。ビーズは硬化するまで、典型的には10〜45分キトサン溶液の中にとどまる(硬貨時間は使用するキトサンの等級及び濃度によって異なる)。硬貨工程の後、この物質を取り出して含水量12重量%になるまで37℃で乾燥させて、個別の3組のビーズを作る。
アルギン酸ナトリウム粉末(マヌコール(Manucol)DM、インターナショナル・スペシャリティー・プロダクツ(International Speciality Products))を実施例1〜3の香料マイクロカプセルスラリーの3つの個々のアリコートに溶解して1%アルギン酸溶液を作る。ウルトラターラックス(Ultra Turrax)T25混合機(IKA)を速度10000/分で使用してこれら組成物を十分に混合する。次に、PMC/アルギネート混合物を個別の塩化カルシウム(シグマ・アルドリッチ(Sigma-Aldrich))の1%水溶液に滴加する。5分後、この物質を取り出して含水量12重量%になるまで37℃で乾燥させて、個別の3組のビーズを作る。
110gのルパゾール(Lupasol)(登録商標)WF(BASF)をビーカーに加え、水浴を使用して約60℃まで加熱する。この温度に達したら、150gのδダマスコン(delta damascone)(IFF)をルパゾール(Lupasol)(登録商標)WF(BASF)に添加し、均質な反応生成物(典型的にはアミン反応生成物として知られる)が形成されるまで、ウルトラターラックス(Ultra Turrax)T25混合機(IKA)を速度20000/分で使用して混合する。この間、ビーカーは約60℃の水浴の中に入れたままとする。混合の後、この物質を更に12時間この温度で維持する。12時間後、約60℃に予熱した実施例1の香料マイクロカプセルスラリー250gを、約70℃で溶融された425gの溶融ルテンゾール(Lutensol)(登録商標)AT 80粉末(BASF)と一緒に加える。この混合物をIKAウルトラターラックス(Ultra Turrax)T25混合機を速度20000/分で使用して、約60℃で均質になるまでブレンドする。このブレンド混合物100gを167gの軽量炭酸ナトリウム(light sodium carbonate)に添加し、台所用フードプロセッサ(ブラウン(Braun))の中で混合して凝集体を作る。
Claims (13)
- 有益剤送達組成物であって、
a.)有益剤およびシェルを含むカプセル化された有益剤と、可塑剤と、結合剤とを混合して、混合物を形成することと、
b.)前記混合物をダスティング剤と混合して、材料を形成することと、
c.)前記材料から前記可塑剤を除去して、送達組成物の総重量に基づいて、1重量%〜85重量%の前記有益剤および前記シェルを含む2重量%〜97重量%の前記カプセル化された有益剤と、1重量%〜50重量%の可塑剤と、1重量%〜50重量%の前記結合剤と、1重量%〜50重量%の前記ダスティング剤とを含む有益剤送達組成物を得ることと、を含む方法によって形成され、かつ
前記可塑剤が、水、アルコール、グリコール、脂肪酸、パラフィン、ペトロラクタム、鉱油、植物油、及びこれらの混合物からなる群から選択される物質であり、
前記結合剤が、セルロース、アルギネート、でんぷん、ポリビニルアルコール、ポリエチレンオキシド、ポリビニルピロリドン、多糖、ポリアクリレート、ワックス、ポリエチレングリコール、アルコールエトキシレート、界面活性剤、およびこれらの混合物からなる群から選択される物質であり、
前記ダスティング剤が、沈殿シリカまたはゼオライトである、有益剤送達組成物。 - 前記有益剤が、香料、光沢剤、防虫剤、シリコーン、ワックス、香味料、ビタミン、布地柔軟化剤、スキンケア剤、酵素、抗菌剤、漂白剤、およびこれらの混合物からなる群から選択される、請求項1に記載の有益剤送達組成物。
- 前記可塑剤が、水、アルコール、およびこれらの混合物からなる群から選択される物質であり、請求項1又は2に記載の有益剤送達組成物。
- 前記結合剤が、セルロース、アルギネート、でんぷん、ポリビニルアルコール、多糖、ポリアクリレート、4000Daを超える重量平均分子量を有するポリエチレングリコール、およびこれらの混合物からなる群から選択される物質である、請求項1〜3のいずれか一項に記載の有益剤送達組成物。
- 前記ダスティング剤が、沈殿シリカである、請求項1〜4のいずれか一項に記載の有益剤送達組成物。
- 前記有益剤が香料を含み、前記シェルが架橋メラミンホルムアルデヒドを含む、請求項1〜5のいずれか一項に記載の有益剤送達組成物。
- a.)前記有益剤が香料を含み、前記シェルが架橋メラミンホルムアルデヒドを含み、
b.)前記可塑剤が水を含み、
c.)前記結合剤が、セルロース、アルギネート、でんぷん、ポリビニルアルコール、ポリエチレンオキシド、ポリビニルピロリドン、多糖、ポリアクリレート、ワックス、4000Daを超える重量平均分子量を有する、又は更には4000Da〜15,000Daの重量平均分子量を有するポリエチレングリコール、アルコールエトキシレート、界面活性剤、およびこれらの混合物からなる群から選択され、
d.)前記ダスティング剤が、沈殿シリカである、請求項1〜4のいずれか一項に記載の有益剤送達組成物。 - 前記有益剤送達組成物が、凝集体、押出品、又は微粒子であり、前記凝集体、押出品、又は微粒子が、100マイクロメートル〜3000マイクロメートルの特徴的な寸法を有し、前記凝集体及び微粒子に関する前記特徴的な寸法が前記凝集体及び微粒子の中央粒径であり、前記押出品の前記特徴的な寸法が前記押出品の平均直径である、請求項1〜7のいずれか一項に記載の有益剤送達組成物。
- 請求項1〜8のいずれか一項に記載の有益剤送達組成物と、カチオン性ポリマー、界面活性剤、ビルダー、キレート剤、移染防止剤、分散剤、酵素、及び酵素安定剤、触媒物質、漂白活性剤、ポリマー分散剤、粘土汚れ除去/再付着防止剤、光沢剤、抑泡剤、染料、追加の香料及び香料送達システム、構造弾性化剤、柔軟仕上げ剤、キャリア、ヒドロトロープ、加工助剤、及び/又は顔料、並びにこれらの混合物からなる群から選択される消費者製品添加剤と、を含む消費者製品組成物。
- 消費者製品の総重量に基づいて0.1重量%〜20重量%の量の前記有益剤送達組成物を含む、請求項9に記載の消費者製品組成物。
- 請求項1〜7のいずれか一項に記載の有益剤送達組成物と、染料、香料、蛍光増白剤、沈着補助剤、及びこれらの混合物からなる群から選択される物質と、を有する組成物。
- 布地を処理及び/又は洗浄する方法であって、
a.)前記布地を、請求項1〜11のいずれか一項に記載の組成物と接触させることと、
b.)前記布地を洗浄及び/又はすすぐことと、を含む、方法。 - 請求項1〜11のいずれか一項に記載の組成物で処理された布地。
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JP2014196490A (ja) * | 2008-02-15 | 2014-10-16 | ザ プロクター アンド ギャンブルカンパニー | 送達粒子 |
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WO2009101593A2 (en) | 2009-08-20 |
US20090209661A1 (en) | 2009-08-20 |
ES2658822T3 (es) | 2018-03-12 |
CN103860399A (zh) | 2014-06-18 |
CN101945638A (zh) | 2011-01-12 |
EP2247275B1 (en) | 2017-11-29 |
PL2247275T3 (pl) | 2018-05-30 |
MX2010008931A (es) | 2010-09-09 |
JP2011511876A (ja) | 2011-04-14 |
CA2713594C (en) | 2015-03-24 |
MX344613B (es) | 2016-12-20 |
BRPI0907884A2 (pt) | 2015-07-21 |
HUE035721T2 (hu) | 2018-08-28 |
WO2009101593A3 (en) | 2009-10-29 |
JP2014196490A (ja) | 2014-10-16 |
ZA201005524B (en) | 2011-04-28 |
EP2247275A2 (en) | 2010-11-10 |
CA2713594A1 (en) | 2009-08-20 |
US20120010120A1 (en) | 2012-01-12 |
BRPI0907884B1 (pt) | 2019-09-10 |
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