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JP2007518805A5
JP2007518805A5 JP2006551208A JP2006551208A JP2007518805A5 JP 2007518805 A5 JP2007518805 A5 JP 2007518805A5 JP 2006551208 A JP2006551208 A JP 2006551208A JP 2006551208 A JP2006551208 A JP 2006551208A JP 2007518805 A5 JP2007518805 A5 JP 2007518805A5
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pharmaceutical composition
coenzyme
tumor
cells
tumor cells
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CoQ10組成物
好ましい1実施形態では、本発明は、がんを治療するためのCoQ10組成物を提供する。好ましくは、組成物は、少なくとも約1%〜約25%(w/w)のCoQ10、より好ましくは約1%〜約20%(w/w)のCoQ10を含んでなる。以下の実施例において記載する代表的な実施形態では、CoQ10の局所用製剤を担がん動物の皮膚に施用して腫瘍の増殖速度を低下させる。CoQ10はピュアプレスクリプションズ(Pure Prescriptions)[米国カリフォルニア州サンディエゴ(San Diego)所在]から、任意の適切な量(例えば1キログラム)の粉末形態で得ることが可能である。CoQ10含有組成物を送達するために、任意の適切な担体を使用することが可能である。例えば、リポソームを担体として使用してもよい。例示的なリポソームの製剤は、Phospholipon(登録商標)90G(アメリカン・レシチン(American Lechitin))[米国コネチカット州スタンフォード(Stanford)所在]、Phospholipon90H(アメリカン・レシチン(American Lechitin))[米国コネチカット州スタンフォード(Stanford)所在]、グリセロール、ブチル化ヒドロキシトルエン(BHT)、エタノール、中鎖トリグリセリド(MCT)、ラベンダー(シグマ−アルドリッチ(Sigma−Aldrich))[米国ミズーリ州セントルイス(St.Louis)所在]、およびコエンザイムQ10(ピュアプレスクリプションズ(Pure Prescriptions))[米国カリフォルニア州サンディエゴ(San Diego)所在]からなる。この製剤を調製するためのプロトコールの例は、最初にPhospholipon(登録商標)90H 0g、Phospholipon(登録商標)90G 5gを、MCT 1.5g、BHT
0.3g、およびエタノール9mlと75℃で溶解することを必要とする。次に、コエンザイムQ10 12gを混合物中に溶解する。窒素飽和水で調製した1mMリン酸バッファー(pH8.2)65ml、グリセロール13.3g、およびラベンダー50μLを加える。上記の混合物を、高速ブレンダー中12000RPMでブレンドしてクリームを形成する。このクリームを、使用するまで4℃で貯蔵する。
マウスのSK−MEL28腫瘍に及ぼすコエンザイムQ10局所用製剤の効果
SK−MEL28を皮下層へ注射して、マウスにおいてメラノーマ腫瘍を誘発した。動
物実験は、各4匹のマウスを含む対照群および投与群より構成した。マウスに2つの腫瘍を接種した。図14のグラフは、各マウスにおいて接種の結果生じた腫瘍の平均の大きさを示す。投与群では、コエンザイムQ10の局所用製剤(10%)を腫瘍に30日間、毎日塗布した。その後、腫瘍を摘出して大きさを測定した。投与群の総合的な平均の大きさの差異は対照群と比較して有意であった(P<0.05)。

Claims (10)

  1. がん患者を治療するための薬剤組成物であって、
    %〜20%(w/w)のコエンザイムQ10を含み、
    局所投与用であ前記がんは、扁平上皮がんまたはメラノーマである、薬剤組成物。
  2. 腫瘍細胞の溶解をもたらす、請求項1に記載の薬剤組成物。
  3. 前記コエンザイムQ10を含んでなる組成物が局所用クリーム剤として調合される、請求項1に記載の薬剤組成物。
  4. 治療上有効な量のコエンザイムQ10組成物が1つまたは複数の化学療法剤とともに投与される、請求項1に記載の薬剤組成物。
  5. 前記化学療法剤を、治療上有効な量のコエンザイムQ10を含んでなる組成物と同時に投与するか、同組成物の前に投与するか、または同組成物の後に投与することができる、請求項に記載の薬剤組成物。
  6. 前記化学療法剤が、シクロホスファミド(CTX、25mg/kg/日、経口投与)、タキサン(パクリタキセルまたはドセタキセル)、ブスルファン、シスプラチン、シクロホスファミド、メトトレキセート、ダウノルビシン、ドキソルビシン、メルファラン、クラドリビン、ビンクリスチン、ビンブラスチン、およびクロラムブシルからなる群から選択される、請求項に記載の薬剤組成物。
  7. 治療の結果腫瘍細胞の増殖が阻害される、請求項1に記載の薬剤組成物。
  8. 対象における腫瘍細胞の増殖を阻害するための薬剤組成物であって、
    %〜20%(w/w)のコエンザイムQ10を含み、
    局所投与用であ前記腫瘍細胞は、扁平上皮がん細胞またはメラノーマ細胞である、薬剤組成物。
  9. 腫瘍細胞にアポトーシスを引き起こすための薬剤組成物であって、
    %〜20%(w/w)のコエンザイムQ10を含み、
    局所投与用であ前記腫瘍細胞は、扁平上皮がん細胞またはメラノーマ細胞である、薬剤組成物。
  10. 腫瘍における血管形成を阻害するための薬剤組成物であって、
    前記薬剤組成物は腫瘍と接触され、
    %〜20%(w/w)のコエンザイムQ10を含み、
    局所投与用であ前記腫瘍は、扁平上皮がんまたはメラノーマである、薬剤組成物。
JP2006551208A 2004-01-22 2005-01-21 局所用コエンザイムq10製剤 Expired - Fee Related JP5247031B2 (ja)

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US53831904P 2004-01-22 2004-01-22
US60/538,319 2004-01-22
PCT/US2005/001581 WO2005069916A2 (en) 2004-01-22 2005-01-21 Topical co-enzyme q10 formulations and methods of use

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JP2007518805A JP2007518805A (ja) 2007-07-12
JP2007518805A5 true JP2007518805A5 (ja) 2013-02-21
JP5247031B2 JP5247031B2 (ja) 2013-07-24

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JP2015139948A Pending JP2015187167A (ja) 2004-01-22 2015-07-13 コエンザイムq10製剤
JP2016228189A Active JP6670738B2 (ja) 2004-01-22 2016-11-24 コエンザイムq10製剤
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US (8) US8147825B2 (ja)
EP (4) EP2371363B1 (ja)
JP (5) JP5247031B2 (ja)
KR (11) KR101372783B1 (ja)
CN (4) CN1953743B (ja)
AU (2) AU2005206953B2 (ja)
BR (1) BRPI0507039A8 (ja)
CA (3) CA2553690C (ja)
CY (1) CY1114006T1 (ja)
DK (1) DK1718283T3 (ja)
ES (4) ES2410587T3 (ja)
HK (1) HK1098062A1 (ja)
HR (1) HRP20130459T1 (ja)
IL (5) IL176995A (ja)
ME (1) ME01881B (ja)
MX (1) MXPA06008293A (ja)
NO (3) NO337809B1 (ja)
PL (1) PL1718283T3 (ja)
PT (1) PT1718283E (ja)
RS (1) RS52792B (ja)
SI (1) SI1718283T1 (ja)
WO (1) WO2005069916A2 (ja)

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