JP5050851B2 - 疼痛治療剤 - Google Patents
疼痛治療剤 Download PDFInfo
- Publication number
- JP5050851B2 JP5050851B2 JP2007523928A JP2007523928A JP5050851B2 JP 5050851 B2 JP5050851 B2 JP 5050851B2 JP 2007523928 A JP2007523928 A JP 2007523928A JP 2007523928 A JP2007523928 A JP 2007523928A JP 5050851 B2 JP5050851 B2 JP 5050851B2
- Authority
- JP
- Japan
- Prior art keywords
- pain
- administration
- salt
- propyloctanoic acid
- analgesic
- 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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- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
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- UZBODILCSLUHQR-JLMRSGIVSA-N zenvia Chemical compound C([C@@H]12)CCC[C@]11CCN(C)[C@H]2CC2=CC=C(OC)C=C21.C1C([C@H](C2)C=C)CCN2[C@H]1[C@@H](O)C1=CC=NC2=CC=C(OC)C=C21 UZBODILCSLUHQR-JLMRSGIVSA-N 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
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Classifications
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/36—Opioid-abuse
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- Pain & Pain Management (AREA)
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- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Description
しかしながら、(2R)−2−プロピルオクタン酸が疼痛、特に神経因性疼痛に有用である旨の記載はどこにもない。
[1](2R)−2−プロピルオクタン酸、その塩、またはそのプロドラッグを含有してなる疼痛の予防、治療、症状進展抑制および/または鎮痛薬の調節剤;
[2]1回あたりの投与量が10mg乃至5000mgである前記[1]記載の剤;
[3]経口投与用である前記[2]記載の剤;
[4]1回あたりの経口投与量が100mg乃至5000mgである前記[3]記載の剤;
[5]非経口投与用である前記[2]記載の剤;
[6]非経口投与が静脈内投与である前記[5]記載の剤;
[7]1回あたりの静脈内投与量が100mg乃至2000mgである前記[6]記載の剤;
[8]1回あたりの静脈内投与量が体重1kgあたり2mg乃至20mgである前記[6]記載の剤;
[9]静脈内投与が点滴静注である前記[6]記載の剤;
[10]疼痛が神経因性疼痛である前記[1]記載の剤;
[11]神経因性疼痛が、癌性疼痛、帯状疱疹後疼痛、糖尿病性疼痛、HIV関連神経因性疼痛、結石誘発疼痛、神経痛、口腔顔面痛、または痛覚過敏である前記[10]記載の剤;
[12]さらに、速効性鎮痛薬を組み合わせてなる前記[1]記載の剤;
[13]さらに、オピオイド鎮痛薬、非オピオイド鎮痛薬、神経因性疼痛鎮痛薬、非ステロイド系抗炎症薬、抗うつ薬、抗てんかん薬、中枢性筋弛緩薬、制吐薬、および局所麻酔薬から選択される一種以上を組み合わせてなる前記[1]記載の剤;
[14]鎮痛薬の調節が、鎮痛薬の依存性および/または耐性の低減である前記[1]記載の剤;
[15]哺乳動物に対し、1回あたり10mg乃至5000mgの(2R)−2−プロピルオクタン酸、その塩、またはそのプロドラッグを投与することを特徴とする疼痛の予防、治療、症状進展抑制および/または鎮痛薬の調節方法;
[16]1回あたりの投与量が10mg乃至5000mgであることを特徴とする(2R)−2−プロピルオクタン酸、その塩、またはそのプロドラッグを含有してなる疼痛の予防、治療、症状進展抑制および/または鎮痛薬の調節剤を製造するための(2R)−2−プロピルオクタン酸、その塩、またはそのプロドラッグの使用;および
[17]哺乳動物に対し、神経ブロック、脊髄刺激療法、無痙攣性通電、イオントフォレシス、鍼灸、指圧、マッサージ、電気治療、温熱療法、光線治療、温泉治療、高圧酸素療法、アロマセラピー、バイオフィードバック、リラクゼーション訓練、催眠療法、注意そらし技法、および心理カウンセリングから選択される一種以上の方法と、(2R)−2−プロピルオクタン酸、その塩、またはそのプロドラッグを含有する医薬組成物の投与を組み合わせて行うことを特徴とする疼痛の予防、治療および/または症状進展抑制方法等に関する。
(2R)−2−プロピルオクタン酸、その塩、またはそのプロドラッグの毒性は非常に低いものであり、医薬として使用するために十分安全であると判断できる。例えば、イヌを用いた単回静脈内投与では、(2R)−2−プロピルオクタン酸は、100mg/kgで死亡例が見られなかった。
本発明は、疼痛の予防、治療および/または症状進展抑制を目的として、或いは鎮痛薬の調節を目的として、(2R)−2−プロピルオクタン酸、その塩、またはそのプロドラッグの有効量、好ましくは、1回あたり1mg乃至5000mgの、より好ましくは、1回あたり10mg乃至5000mgの(2R)−2−プロピルオクタン酸、その塩、またはそのプロドラッグを投与することを特徴とするものである。本発明に用いられる(2R)−2−プロピルオクタン酸、その塩、またはそのプロドラッグを含有してなる医薬組成物は、有効成分として(2R)−2−プロピルオクタン酸、その塩、またはそのプロドラッグを含有しており、哺乳動物(例えば、ヒト、非ヒト動物、例えば、サル、ヒツジ、ウシ、ウマ、イヌ、ネコ、ウサギ、ラット、マウス等)において前記の目的のために使用することができる。特に本発明で開示する好ましい用法・用量で、哺乳動物(例えば、ヒトや非ヒト動物等、好ましくはヒト、特に好ましくは患者)に、経口的または非経口的に全身投与することによって、また髄腔内投与や経皮投与のように局所投与することによって、疼痛、とりわけ神経因性疼痛を予防、治療および/または症状進展抑制したり、鎮痛薬(とりわけオピオイド鎮痛薬)の依存性や耐性を低減したり、或いは使用量を減じたり使用開始時期を遅らせたり副作用を減ずる等の好ましい効果を得ることができる。
(2R)−2−プロピルオクタン酸、その塩、またはそのプロドラッグが、疼痛に対して抑制作用(鎮痛作用)を有することは、例えば、以下の実験によって証明された。また、(2R)−2−プロピルオクタン酸、その塩、またはそのプロドラッグを評価する測定方法は、測定精度および/または測定感度の向上をはかるために、以下のように改良を加えたものである。以下に詳細な実験方法を示す。
ラット脊髄神経結紮モデルでの(2R)−2−プロピルオクタン酸の有効性評価
(1)脊髄神経結紮モデルラットの作成
実験には、雄性ラットを使用した。脊髄神経結紮モデルは、Kim & Chungの方法(Kim, S. H. & Vhung, J. M. An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat. Pain, 50, 355-363, 1992)に準じて行った。すなわち、片側の第5腰髄神経を絹糸で強く結紮することで作成した。
具体的には、以下の手順で行った。
ラットに40mg/kg(液量0.8mL/kg)のペントバルビタール(ネンブタール注射液(商品名)、大日本製薬株式会社)を腹腔内投与し、麻酔下で背位に固定し、正中線に沿って腹部を剪刀で開腹した。滅菌ガーゼを用いて腸等を片側に寄せ、腹部大動脈と腹部大静脈を確認し、腸腰静脈直下の筋肉をピンセットで裂いた。筋肉中の第4腰髄神経と第5腰髄神経を確認し、第5腰髄神経(L5)を6-0の絹糸で結紮した。その後、片側に寄せた腸を元の位置に戻し、アンピシリンナトリウム(注射用ビクシリン(商品名)、明治製菓株式会社)を添加した生理食塩液(株式会社大塚製薬工場)(アンピシリン濃度:20mg/mL)を5mL腹腔内に貯留させ、腹部の筋肉および皮膚をナイロン糸で縫合した。
(2R)−2−プロピルオクタン酸は、30mg/kgの投与量で、脊髄神経結紮直後から14日間、1日1回の経口投与(計14回)を行った。また、媒体対照についても同様の投与を行った。
(3−1)疼痛反応潜時(熱刺激潜時)の測定(熱痛覚過敏の評価)
最終投与の翌日に、熱刺激潜時を測定した。すなわち、左右の足蹠に下方からハロゲンランプにより赤外線を照射し、逃避反応を起こすまでの時間(疼痛反応潜時:秒)を計測した。
(3−2)触刺激逃避閾値の測定(触覚アロディニアの評価)
最終投与の翌日に触刺激逃避閾値を測定した。すなわち、左右の足蹠に下方からフィラメント(von Frey filaments : VFF)を押し当て、逃避反応を起こしたときのVFFの表示値を記録し、重さ(g)に換算した。
疼痛反応潜時(熱刺激潜時)の測定(熱痛覚過敏の評価)
脊髄神経結紮モデルラットに(2R)−2−プロピルオクタン酸または媒体を投与し、疼痛反応潜時(熱刺激潜時)の測定を行うことにより、熱痛覚過敏に対する(2R)−2−プロピルオクタン酸の効果を検討した結果を以下の表1に示す。
脊髄神経結紮モデルラットに(2R)−2−プロピルオクタン酸または媒体を投与し、触刺激逃避閾値の測定を行うことにより、触覚アロディニアに対する(2R)−2−プロピルオクタン酸の効果を検討した結果を以下の表2に示す。
製剤例1
(2R)−2−プロピルオクタン酸含有注射剤の製造
注射用水に、(2R)−2−プロピルオクタン酸(2.0kg)およびリン酸三ナトリウム・12水和物(3.54kg)を加え、注射用水を用いて40Lとした。均一な溶液とした後、無菌フィルター(デュラポア0.22μmメンブレン)で濾過し、2mLずつプラスチックアンプルに充填し、高圧蒸気滅菌(123℃、15分間)することで、1アンプル中100mgの活性成分を含有するアンプル2万本を得た。
(2R)−2−プロピルオクタン酸含有ソフトカプセルの製造
ゼラチン(20kg)および濃グリセリン(6kg)を、精製水(20kg)の存在下、70℃で混和し、均一な溶液を得た。この溶液および(2R)−2−プロピルオクタン酸(0.9kg)を、ソフトカプセル充填機(ロータリー式軟カプセル成型機H−1型;カマタ)に投入し、(2R)−2−プロピルオクタン酸を充填したソフトカプセルの生球を得た。得られた生球を、タンブラ乾燥および棚乾燥に順次付すことにより、1カプセル中に300mgの(2R)−2−プロピルオクタン酸を含有するソフトカプセル(2200カプセル)を得た。
Claims (8)
- (2R)−2−プロピルオクタン酸、またはその塩を含有してなり、1回あたりの経口投与量が100mg乃至5000mgである経口投与用か、または、1回あたりの静脈内投与量が100mg乃至2000mgである非経口投与用である、神経因性疼痛の予防、治療、症状進展抑制および/または鎮痛薬の調節剤。
- 1回あたりの静脈内投与量が体重1kgあたり2mg乃至20mgである請求の範囲1記載の剤。
- 静脈内投与が点滴静注である請求の範囲1記載の剤。
- 神経因性疼痛が、癌性疼痛、帯状疱疹後疼痛、糖尿病性疼痛、HIV関連神経因性疼痛、結石誘発疼痛、神経痛、口腔顔面痛、または痛覚過敏である請求の範囲1記載の剤。
- さらに、速効性鎮痛薬を組み合わせてなる請求の範囲1記載の剤。
- さらに、オピオイド鎮痛薬、非オピオイド鎮痛薬、神経因性疼痛鎮痛薬、非ステロイド系抗炎症薬、抗うつ薬、抗てんかん薬、中枢性筋弛緩薬、制吐薬、および局所麻酔薬から選択される一種以上を組み合わせてなる請求の範囲1記載の剤。
- 鎮痛薬の調節が、鎮痛薬の依存性および/または耐性の低減である請求の範囲1記載の剤。
- (2R)−2−プロピルオクタン酸、またはその塩を含有してなり、1回あたりの経口投与量が100mg乃至5000mgである経口投与用か、または、1回あたりの静脈内投与量が100mg乃至2000mgである非経口投与用である、神経因性疼痛の予防、治療、症状進展抑制および/または鎮痛薬の調節剤を製造するための(2R)−2−プロピルオクタン酸、またはその塩の使用。
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PCT/JP2006/312712 WO2007000970A1 (ja) | 2005-06-27 | 2006-06-26 | 疼痛治療剤 |
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WO2023214547A1 (ja) * | 2022-05-02 | 2023-11-09 | 日本臓器製薬株式会社 | プログラム、情報処理装置及び情報処理方法 |
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JPH07316092A (ja) * | 1993-06-01 | 1995-12-05 | Ono Pharmaceut Co Ltd | ペンタン酸誘導体、その製造方法およびそれらを含有する薬剤 |
JP2001509500A (ja) * | 1997-07-09 | 2001-07-24 | ディ − ファーム リミテッド | 分岐鎖脂肪酸、それらの誘導体、および中枢神経系障害の処置における使用 |
JP2005500305A (ja) * | 2001-06-25 | 2005-01-06 | ディ − ファーム リミテッド | 分枝鎖状脂肪酸およびその誘導体の痛み処置における使用 |
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JPS59120427A (ja) | 1982-12-28 | 1984-07-12 | Katashi Aoki | 射出延伸吹込成形機における2層プリフオ−ム成形装置 |
JP3084345B2 (ja) | 1995-04-26 | 2000-09-04 | 小野薬品工業株式会社 | 光学活性な2−プロピルオクタン酸の製造方法 |
WO1998007447A1 (en) * | 1996-08-23 | 1998-02-26 | Algos Pharmaceutical Corporation | Anticonvulsant containing composition for treating neuropathic pain |
US7582678B2 (en) * | 1997-07-09 | 2009-09-01 | D-Pharm Limited | Use of branched-chain fatty acids and derivatives thereof for the treatment of pain |
TW509672B (en) | 1998-05-12 | 2002-11-11 | Ono Pharmaceutical Co | Novel intermediate compounds and processes for the production of optical active octanoic acid derivatives |
TWI268921B (en) | 1999-02-18 | 2006-12-21 | Ono Pharmaceutical Co | A process for preparing (2R)-2-propyloctanoic acid |
JP2005298334A (ja) | 2001-12-19 | 2005-10-27 | Ono Pharmaceut Co Ltd | 新規な中間体化合物およびそれを用いる化合物の製造方法 |
AU2003231465A1 (en) | 2002-05-15 | 2003-12-02 | Ono Pharmaceutical Co., Ltd. | Process for producing optically active alkylcarboxylic acid derivative |
WO2004110972A1 (ja) | 2003-06-10 | 2004-12-23 | Ono Pharmaceutical Co., Ltd. | (2r)−2−プロピルオクタン酸の製造方法、その中間体 |
JP5485497B2 (ja) * | 2003-10-03 | 2014-05-07 | 小野薬品工業株式会社 | 神経変性疾患の予防および/または治療方法 |
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JPH07316092A (ja) * | 1993-06-01 | 1995-12-05 | Ono Pharmaceut Co Ltd | ペンタン酸誘導体、その製造方法およびそれらを含有する薬剤 |
JP2001509500A (ja) * | 1997-07-09 | 2001-07-24 | ディ − ファーム リミテッド | 分岐鎖脂肪酸、それらの誘導体、および中枢神経系障害の処置における使用 |
JP2005500305A (ja) * | 2001-06-25 | 2005-01-06 | ディ − ファーム リミテッド | 分枝鎖状脂肪酸およびその誘導体の痛み処置における使用 |
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EP1900363A4 (en) | 2010-01-13 |
EP2465499A2 (en) | 2012-06-20 |
JPWO2007000970A1 (ja) | 2009-01-22 |
US8975298B2 (en) | 2015-03-10 |
US20090030078A1 (en) | 2009-01-29 |
EP2465499A3 (en) | 2013-02-13 |
WO2007000970A1 (ja) | 2007-01-04 |
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