JP2019524774A - 炎症性皮膚疾患及び皮膚病変を処置するための酸素化コレステロール硫酸(ocs)の使用 - Google Patents
炎症性皮膚疾患及び皮膚病変を処置するための酸素化コレステロール硫酸(ocs)の使用 Download PDFInfo
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Abstract
Description
多くの炎症性皮膚疾患、例えば、皮膚炎(接触性皮膚炎、アトピー性皮膚炎、及び湿疹を含む)に対して現在利用可能な有効な処置は限られている。皮膚炎は、皮膚に炎症を起こし、並びに発赤、腫脹、水疱形成、痂皮形成、鱗屑化、滲出、及び/又はかゆみを特徴とする、いくつかの皮膚状態を指す。いくつかの種類の皮膚炎は、アレルギーによって引き起こされるが、それらの大部分は、公知の原因を有しない。時々皮膚炎を引き起こすことが知られている一般的な刺激物は、石鹸、唾液、様々な食品、洗剤、ベビーローション、及び香水を含む。植物(特に、ツタウルシ(poison ivy)、オーク、及びスマック(sumac))、及び金属(例えば、ニッケル、クロム、及び水銀)、化粧品、及び特定の薬品も、接触性皮膚炎を引き起こし得る。接触性皮膚炎を処置するための1つの選択肢は、抗ヒスタミン薬、例えば、ジフェンヒドラミン(Benadryl(登録商標))及びヒドロキシジン(Atarax(登録商標))である。しかし、これらの薬品は、眠気を引き起こす可能性があり、常に有効とは限らない。もう1つの選択肢は、ステロイドクリームであり、これは、皮膚炎症、かゆみ、及び腫脹を低下させるのを助ける。しかし、ステロイドの過剰使用は、皮膚を損傷し得る。さらに、他の多くの種類の皮膚炎症、例えば、UV紅斑、乾癬、及び赤芽球性プロトポルフィリン症(EPP)があり、それらに対する処置の選択肢は限られており、グルココルチコイド及び抗TNF抗体が通常の選択である。しかし、しばしば、これらの薬剤は、有効性を欠いているか、又は全身的に投与される必要があり、したがって望ましくない副作用を引き起こし得るかのいずれかである。特に、乾癬は、管理又は治癒が非常に困難である。
本開示は、これらの必要性に対処し、炎症性皮膚疾患及び皮膚病変の処置及び/又は予防的な処置を必要とする対象に、1つ以上の酸素化コレステロール硫酸(OCS)を投与することによって、炎症性皮膚疾患及び皮膚病変を処置及び/又は予防的に処置する方法を提供する。
炎症性皮膚疾患又は皮膚病変を処置又は予防的に処置するのに十分な量の1つ以上の酸素化コレステロール硫酸(OCS)を対象に投与すること
を含む、方法。
皮膚浸透促進剤; 及び
増粘剤
を含む、組成物。
皮膚浸透促進剤; 及び
皮膚浸透促進剤とは異なる溶媒
を含む、組成物。
炎症性皮膚疾患又は皮膚病変を処置又は予防的に処置するのに十分な量の、態様67〜124のいずれか1つに記載の組成物を対象に投与すること
を含む、方法。
ヒドロキシプロピルβ-シクロデキストリン(HPbCD); 及び
リン酸緩衝生理食塩水
を含む、組成物。
ポリエチレングリコール3350;
ポリソルベート80;
塩化ナトリウム; 及び
リン酸緩衝生理食塩水
を含む、組成物。
炎症性皮膚疾患及び皮膚病変の処置及び/又は予防的な処置を必要とする対象において、炎症性皮膚疾患及び皮膚病変を処置及び/又は予防的に処置する方法が本明細書に記載され、同様に、炎症性皮膚疾患に至る、これを引き起こす、又はこれによって引き起こされる、又はこれに関連する状態を処置及び/又は予防的に処置する方法が本明細書に記載される。本方法は、一般に、罹患した皮膚、又は罹患している可能性がある皮膚を、疾患/状態を処置及び/又は予防的に処置するのに有効又は十分な量の、少なくとも1つの酸素化コレステロール硫酸(OCS)と接触させることを含む。本方法は、一般に、そのような処置を必要とする対象、例えば、炎症性皮膚疾患に罹患しやすいこと、又は炎症性皮膚疾患の少なくとも1つの徴候若しくは症状を既に示していることに起因して、そのような処置から利益を得るであろう対象を、特定又は診断することを含む。例えば、対象は、特定の患者集団、例えば、急性の傷害(例えば、皮膚損傷剤への曝露又は曝露の疑い)に起因する皮膚疾患を有するもの、又は慢性状態(例えば、皮膚損傷剤への長期曝露、炎症性皮膚疾患への遺伝的素因など)を有するもの、又は皮膚障害の素因を作る他の状態(例えば、糖尿病)及び/若しくは他の原因に由来する他の状態を有するもののメンバーであってもよい。
以下の定義は、全体を通して使用される:
本明細書で使用される場合、「予防的に処置する(prophylactically treat)」(「予防的処置(prophylactic treatment)」、「予防的に処置すること(prophylactically treating)」など)及び「予防する(prevent)」(「予防(prevention)」、「予防すること(preventing)」など)は、それを必要とする対象への少なくとも1つのOCSの予防的投与によって、炎症性皮膚疾患又は皮膚病変の少なくとも1つの症状の発生を避ける又は回避することを互換的に指す。一般に、「予防的」又は「予防」は、患者が障害を発症する可能性の低減に関する。典型的には、対象は、疾患又は望ましくない状態の少なくとも1つの症状を発症する危険性があるか、又は発症しやすいと当業者によって見なされるか、あるいは医学的介入がない場合、疾患/状態の少なくとも1つの症状を発症する可能性があると見なされる。しかし、一般に、「予防」又は「予防的処置」について、投与は、対象が疾患の症状(状態、障害、症候群など; 別段の指示がない限り、これらの用語は、本明細書では互換的に使用される)を有する、又は有することが知られるか若しくは確認される前に行われる。言い換えれば、症状は、まだ明白又は観察可能ではなくてもよい。対象は、様々な要因、例えば、以下に限定されないが、遺伝的素因; 最近の特定の、若しくは疑わしい、若しくは避けられない将来の毒性物質(例えば、毒性化学物質又は薬品、放射線など)への曝露; 又は、予防されている疾患/状態の発症と結びつく若しくはこれに関連する別のストレッサー若しくはストレッサーの組み合わせへの曝露又はこの経験、に起因して危険性があると見なされてもよい。炎症性皮膚疾患又は皮膚病変の予防のいくつかの態様では、対象は、炎症性皮膚疾患又は皮膚病変の潜在的な前兆の症状、例えば、紅斑を既に示していてもよい。そのような態様では、対象の処置は、前兆状態の不快な又は有害な影響又はアウトカム(結果)を予防する。疾患又は状態の「予防」又は「予防的処置」は、検出可能な症状の発生を完全に防止することを含み得るか、あるいは、本明細書で提供される医学的介入がない場合、すなわち、1つ以上のOCSが投与されない場合に起こるであろう、炎症性皮膚疾患の少なくとも1つの症状の程度、重症度、又は持続期間を軽減又は減弱することを含み得る。あるいは、対象は、初期症状を経験していてもよく、予防されるのは、重篤期の疾患への進行である。
本明細書に記載の組成物及び方法で処置される対象は、一般に、「炎症性皮膚疾患」若しくは「炎症性皮膚障害」と診断されており、及び/又は1つ以上の皮膚病変で苦しんでいる。いくつかの態様では、炎症は、非感染性の炎症であり、例えば、炎症は、感染性物質に関連しないか又はそれによって引き起こされない。炎症性皮膚疾患又は皮膚病変の症状は、対象の単一の部位(位置)に生じてもよく、又は複数の部位に生じてもよい。いくつかの態様では、1つ以上の炎症性皮膚障害及び1つ以上の皮膚病変は、両方とも、皮膚若しくは膜の隣接する区画、又は個体の別々の部位のいずれかで、対象に生じ得る。
いくつかの態様では、処置される患者は、ヘルペスウイルスを有する。全てのヘルペスウイルスのうち、ヘルペスウイルス・ホミニス(Herpesvirus hominis)の作用は、群を抜いて最も一般に経験される。ヘルペスウイルス・ホミニスは、単純ヘルペスの原因であり、I型及びII型という2つの異なる型を有する。I型は、コールドソア(cold sore)の形態の口唇ヘルペス(口腔ヘルペス)、並びに口唇若しくは鼻の周りの見苦しい病変を引き起こす。II型は、ウエストより下、主に性器領域に現れる、ただれの形態の性器ヘルペス(Herpes genitalis)(性器ヘルペス(genital herpes))を引き起こす。2つの型は、それらの挙動の性質に関してほとんど変わらず、どちらか一方が他方の代わりをすることができる。したがって、II型は、コールドソアを引き起こすことができ、一方、I型はまた、性器に感染することができる。それにもかかわらず、II型は、性器ヘルペスの少なくとも約80パーセント(80%)の原因である。
本明細書に記載の方法及び組成物に使用されるOCSの例としては、以下に限定されないが、5-コレステン-3,25-ジオール,3-サルフェート(25HC3S); 5-コレステン-3,25-ジオール,ジサルフェート(25HCDS); 5-コレステン,3,27-ジオール,3-サルフェート; 5-コレステン,3,27-ジオール,3,27-ジサルフェート; 5-コレステン,3,7-ジオール,3-サルフェート; 5-コレステン,3,7-ジオール,3,7-ジサルフェート; 5-コレステン,3,24-ジオール,3-サルフェート; 5-コレステン,3,24-ジオール,3,24-ジサルフェート; 5-コレステン,3-オール,24,25-エポキシ3-サルフェート; 及びそれらの塩、特にそれらの薬学的に許容可能な塩が挙げられる。25HC3Sの開示は、例えば、米国特許第8,399,441号(その全体が参照により本明細書に組み込まれる)に見出される。25HCDSの開示は、例えば、米国特許出願公開第20150072962号(その全体が参照により組み込まれる)に見出される。特定の態様では、OCSは、5-コレステン-3,25-ジオール,3-サルフェート(25HC3S)及び5-コレステン-3,25-ジオール,ジサルフェート(25HCDS)(単独で又は組み合わせてのいずれか)から選択される。さらなる態様では、OCSは、5-コレステン-3,25-ジオール,3-サルフェート(25HC3S)である。OCSは、典型的には、体内で天然に生じるOCSの合成版である。
メチルパラベン0.25g
プロピルパラベン0.15g
ラウリル硫酸ナトリウム10g
プロピレングリコール120g
ステアリルアルコール250g
白色ワセリン250g
精製水370g
本方法の実施は、一般に、炎症性皮膚疾患若しくは皮膚病変、又は炎症性皮膚疾患若しくは皮膚病変に関連する状態に罹患しているか又はそれを発症する危険性がある患者を同定すること、及び許容可能な形態の1つ以上のOCSを適切な経路によって投与することを含む。予防的処置もまた包含され、例えば、病因物質(例えば、ツタウルシ)への公知の若しくは疑わしい曝露後の、及び/又は疾患の非常に初期の段階での投与; あるいは、消散したが再発の可能性がある疾患の症状を有している対象、又は公知の危険因子(例えば、遺伝的素因、皮膚炎症、皮膚病変などを引き起こす有害物質への過去の曝露)などを有する対象におけるものを含む。
皮膚炎症を示すことに加えて、いくつかの態様では、本明細書に記載の方法によって処置される対象の集団は、高レベルのコレステロール(高コレステロール血症、例えば、約200mg/dl以上の範囲の血清中のコレステロールレベル)、又は高レベルのコレステロールに関連する状態、例えば、高脂血症、アテローム性動脈硬化症、心疾患、卒中、アルツハイマー病、胆石症、胆汁うっ滞性肝疾患などの症状を有しても若しくは有しなくてもよく、並びに/又はそれと診断されていても若しくは診断されていなくてもよい。いくつかの態様では、本明細書に記載の方法によって処置される対象の集団は、高レベルのコレステロール(高コレステロール血症、例えば、約200mg/dl以上の範囲の血清中のコレステロールレベル)、又は高レベルのコレステロールに関連する状態、例えば、高脂血症、アテローム性動脈硬化症、心疾患、卒中、アルツハイマー病、胆石症、胆汁うっ滞性肝疾患などの症状を有せず、及び/又はそれと診断されていない。
実施例1. 注射研究
注射研究は、以下のように実施した: I. ラットにおける急性(単回投与)筋肉内(IM)注射研究; II. ラットにおける2週間の皮下(SC)注射研究; 及びIII. イヌにおける2週間のSC注射研究。
急性単回投与研究のために、ハノーバーウィスターラット(n=5/性別/用量群)は単回IM注射を受け、次いで、2及び14日の観察期間が続いた。試験した溶液は、ビヒクル(滅菌水中の10mMリン酸ナトリウム緩衝液中の250mg/mLのヒドロキシプロピル-β-シクロデキストリン)中の30mg/mLの25HC3Sナトリウム塩を含んだ。0(ビヒクル)、3、10、及び30mg/kgの25HC3Sナトリウム塩の用量レベルを、1.0、0.1、0.3、及び1.0mL/kgの用量体積で投与した。結果は、ビヒクルラット及び薬物処置ラットにおいて同様の発生率及び重症度の、注射された筋肉における、最小から中程度の筋肉の変性/再生、出血、及び炎症を示した。14日後の変化の激しさはより小さく(最小のみ)、これは、部分的な回復を示した; 25HC3S又はビヒクル体積の存在の明らかな効果は観察されなかった。25HC3S溶液は忍容性良好であり、局部的変化は注射(針)外傷及び/又はビヒクルの影響による可能性が高いと結論付けられた。
別の研究において、ハノーバーウィスターラット(n=12/性別/用量群)は、ビヒクル(滅菌水中の10mMリン酸ナトリウム緩衝液中の250mg/mLのヒドロキシプロピル-β-シクロデキストリン)中の30mg/mLの25HC3Sナトリウム塩の溶液の1日1回のSC注射を2週間受けた。0(ビヒクル)、15、45、及び150mg/kgの25HC3Sナトリウム塩の用量レベルを、5.0、0.5、1.5、及び5.0mL/kgの用量体積で投与した。14日の用量投与後、全てのラットを安楽死させ剖検した。
別の研究において、ビーグル犬(n=4/性別/用量群)は、1日1回のSC注射を2週間受けた。試験した溶液は、ビヒクル(10mMリン酸ナトリウム緩衝液中の250mg/mLのヒドロキシプロピル-β-シクロデキストリン)中の30mg/mLの25HC3Sナトリウム塩を含んだ。0(ビヒクル)、3、10、及び30mg/kgの25HC3Sの用量レベルを、1.0、0.1、0.33、及び1.0mL/kgの用量体積で投与した。14日の用量投与後、全てのイヌを安楽死させ剖検した。結果は、ビヒクル及び薬物処置注射部位における線維増殖、出血、炎症、及び壊死を示した; 発生率及び重症度は、一般に、薬物処置したイヌと比較して、ビヒクル対照においてより高かった(図1B参照)。さらに、注射部位の腫脹は、ビヒクルのみを受けたイヌと比較して、25HC3Sを受けたイヌにおいて著しく減少した(図1C)。
材料及び方法
動物
研究の対象は、40匹の雄のBalb/Cマウス(18〜22g)であった。72時間の検疫期間中に臨床的苦痛、疾患、又は傷害の徴候を示さない動物は、研究のために受け入れられ、全体を通して日常的な動物の世話を受けた。全てのマウスの背部を1.5cm×2cmの面積について剃毛した。
25HC3Sの2つの製剤である製剤A及び製剤Bを、研究のために使用した。
6日間(0〜5日目)乾癬様状態を誘導するために、IMQを、各マウスの剃毛した背部の皮膚(50mg)及び右耳(25mg)に午前中1日1回局所的に適用した。
マウスを苦痛の徴候についてモニタリングし、毎日、背部病変の写真を撮った。背部皮膚の紅斑、鱗屑化、及び厚さを、独立した採点者(盲目的)によって0〜4のスケール(0=無し; 1=わずか; 2=中程度; 3=著しい; 及び4=非常に著しい)で毎日採点した。累積スコア(紅斑+鱗屑化+肥厚)を、炎症の重症度の指標として計算した(0〜12のスケールで)。浮腫の指標として、背部皮膚の厚さを電子カリパスによって測定した。
研究中の全てのマウスを麻酔し放血させた。血液を回収し、血清に処理し、分析的使用のために-80℃で保存した。
ELISAによるサイトカインTNFα及びIL-17の測定のために、背部皮膚の半分をホモジナイズした。
この研究の結果を、図2及び3A及び3Bに提示する。図2に見られるように、製剤B懸濁液で処置したマウスでは、背部皮膚の紅斑(発赤)が有意に低減した。背部皮膚の紅斑は、製剤Aで処置したマウスでは有意に低減せず、右耳の紅斑は、製剤A又はBで処置したマウスでは有意に低減しなかった。
(局所用クリーム中5mg/mlの25HC3Sナトリウム塩、外用)
症例報告: ボランティアの男性(60歳)は、2年前にツタウルシ攻撃後に、激しいかゆみを伴う慢性皮膚炎に罹患していた。罹患領域を、ボディローション(Cococare(登録商標)、ビタミンEクリーム)中の5mg/mlの25HC3Sナトリウム塩0.5mlで、3日に1回、合計3回の適用について外的に処置した。2日以内に、かゆみは治まり、発赤及び腫脹は減少した。皮膚は10日でほぼ完全に回復した。
市販のビヒクル及び特注組成物を使用して、25HC3Sの局所用製剤を調製した。
列挙した組成物を、相分離の徴候をモニタリングすることによって、室温、すなわち25℃での質感、均質性、及び物理的安定性について評価した。
PLO20(商標)、PLO20 Flowable(商標)、SaltStable L0(商標)、及びHRT(ホルモン補充療法)ボタニカルベースは、HUMCO(商標)由来であった。ビタミンEクリームは、12,000I.U.のビタミンEを含有するCococare(登録商標)由来であった。
製剤を、25HC3Sをビヒクルに添加することによって調製し、ロッド又はホモジナイゼーションを使用して混合した。表1は、25HC3S薬物負荷、外観、及び物理的安定性を示す。
材料:
Carbopol(登録商標)971P NF及びCarbopol(登録商標)974P NFは、Lubrizolから得た。Pluronic(登録商標)F68、オレイン酸、Tween(登録商標)80、Tween 60、オレイルアルコール(Novol(商標))、Span(登録商標)20は、CRODAから得た。Lauroglcol(登録商標)90、Transcutol(登録商標)、Labrasol(登録商標)、Plurol(登録商標)Oleique、Labrafil(登録商標)2125csは、Gattefosseから得た。DMSOは、Gaylord Chemical Companyから、ジプロピルグリコールは、DOW Chemical Companyから、乳酸ラウリル(Ceraphyl(商標)31)は、Ashlandから、Kolliphore(登録商標)P407(Lutrol(登録商標)F127)は、Mutcher Inc.から得た。他の全ての添加剤は、Spectrumから購入した。
全ての製剤は水性の(o/wエマルジョン)、ゲル、及び1つのマイクロエマルジョンであった。Carbopol(登録商標)、Lutrol(登録商標)F127、及び/又はPluronic(登録商標)F68を増粘剤として使用した。エタノール、Lauroglcol(商標)90、Transcutol(登録商標)、Labrasol(登録商標)、Plurol(登録商標)Oleique、Labrafil(登録商標)2125cs、オレイン酸、HPbCD、プロピレングリコール(PG)、レシチンイソプロピルパルミテート溶液ベース(LIPS)を、皮膚浸透促進剤として使用した。Tween(登録商標)及びSpan(登録商標)を界面活性剤として使用した。トロラミンを用いて、製剤のpHを調整した。
約5%の25HC3Sを含有する製剤の化学的安定性を、25℃及び40℃でモニタリングした。サンプルを、秤量した約0.5gの製剤を2mLのガラスバイアル中に入れることによって調製し、栓をして密封した。各温度及び時点について二重のサンプルを使用した。化学的安定性試験に用いた組成物及び結果を、表11に列挙する。2つのサンプルの平均効力を報告する。
材料及び方法
この研究の目的は次のとおりである:
●マイクロプラークアッセイによって評価した場合の、乾癬患者における病変内注射された25HC3Sの有効性に関する予備的証拠を確立すること。
●乾癬患者における25HC3Sの安全性を評価すること。
●病変内注射された25HC3Sの異なる製剤の有効性に関する証拠を比較する。
●この試験は、二重盲検の、参加者内の、無作為化した、ビヒクル及び実対照薬(active comparator)を対照とした、単回投与研究であった。参加者は、投与の28日以内にスクリーニング訪問に参加した。乾癬の標的プラーク(複数可)を選択した。
○0日目: 各参加者を、研究薬物の2つの異なる製剤、2つのビヒクル製剤、1つの実対照薬、及び1つの未処置領域(合計6個の処置)で処置した。未処置領域を除いて、各処置を、病変内注射として各参加者に施した。
○参加者は、1日目、2日目、7日目、及び14日目に、マイクロプラーク評価のために外来診察に戻るように求められた。
軽度から重度の乾癬を有する10人の患者を、スクリーニング後にこの臨床試験に登録した。参加者が研究に適格となるために、全ての標的プラークは、局部乾癬重症度指数(LPSI)スコア≧6を有していた。0日目: 各参加者を、研究薬物の2つの異なる製剤、2つのビヒクル製剤、1つの実対照薬、及び1つの未処置領域(合計6個の処置)で処置した。
乾癬における25HC3Sの効果を、ビヒクル又はこのマイクロプラークアッセイにおける未処置と比較した、LPSIスコアの変化によって評価した。対象の標的プラーク内の各製剤について、研究訪問によってLPSIスコアの変化の差及びその95%信頼区間(CI)を導き出すことによって、薬物対ビヒクルの比較を行った。
注射用25HC3Sは、注射溶液用の滅菌粉末である。10mLガラスバイアル、及びFluroTec(登録商標)でコーティングされた栓を使用した場合の25HC3S安定性を、2〜8℃で12ヶ月、25℃/60%RHで6ヶ月、及び40℃/75%RHで6ヶ月まで、バイアルを逆さ向きに保存して研究した。これらの安定性データに基づいて、以下に示すように、25HC3Sと容器閉鎖システムとの間には良好な適合性があると結論付けられた。
ビヒクルで構成した後、30mg/mLの25HC3S生成物を、100mLの5%デキストロース注射液(USP)又は0.9%塩化ナトリウム注射液(USP)に希釈し、30mg〜150mgの25HC3Sの用量範囲のIV注入として対象に投与した。これは、30mg/mLの25HC3S生成物の1.0mL(30mg用量について)又は5.0mL(150mg用量について)、又はその間の任意の体積を、100mLデキストロース又は塩化ナトリウム注入バッグに添加することによって達成された。注入バッグ中の全混合内容物を、約2時間かけて50mL/時の速度で対象に注入した。
方法
以下の表20及び21に示す製剤を、以下のように作製した。25HC3Sを、水を除く溶媒/浸透促進剤/界面活性剤の混合物に溶解した。Carbopol(登録商標)ポリマーを、別に水に溶解し、トロラミンを添加してゲルを形成した。次いで、25HC3Sの溶液を、Carbopolゲルに添加して、混合した。最終製剤は、典型的には、クリーム又はゲルであった。
得られた製剤の外観を、以下の表20及び21に示す。製剤のほとんどを、室温で4ヶ月間置いておいた。それらの物理的安定性を、以下の表20及び21に示すように記録した。
目的
●皮膚に透過する薬物含有量を増加させる
●局所用製剤の安定性を改善する
●製剤中の薬物溶解度を増加させる
●市販のビヒクル
●CococareのビタミンEクリーム
●他の4つのビヒクル
●インハウスで開発し評価したビヒクル(クリーム又はゲルに焦点を合わせて)
●全てのビヒクルは水性であった(W/Oエマルジョン及びゲル)。
●増粘剤: Carbopol974(架橋ポリアクリル酸ポリマー)、Pluronic F68
●乳化剤: Tween 80、Span 20
●皮膚透過促進剤
EtOH、プロピレングリコール、DiPG、乳酸ラウリル、オレイン酸、オレイルアルコール、脂質賦形剤(labrafil M2125、Lauroglycol)、レシチンイソプロピルパルミテート溶液(LIPS)
以下の表22に示す製剤を作製した。Carbopolベースのクリーム又はゲルで達成された最大薬物負荷は、1wt%であったので、薬物を含有する以下の製剤のそれぞれは、1wt%の非放射性標識25HC3Sを含んでいた。陽性対照C1では、20wt%のDMSOをEtOH中に含ませて、1wt%の薬物負荷を達成した。
上記のように、この研究は、ドナー当たり3つの透過実験を有する4つの皮膚ドナーを含んだ。非常に微量の薬物がレセプター液中に見出された。結果を、以下の表23及び24に示す。
●C1: EtOH(80%)、DMSO(20%)
●F9: オレイルアルコール(10%)、diPG(20%)、H2O(57%)
●F5: PG(40%)、H2O(54%)
●F6: PG(15%)、オレイン酸(10%)、H2O(62%)
●F8: PG(20%)、EtOH(10%)、DMSO(20%)、H2O(47%)
●F4: 乳酸ラウリル(2.5%)、H2O(87%)
●F7: PEG400(40%)、H2O(57%)
●C1対F8
●EtOH: 高PE
●F9対F5
●PGよりも優れたOAlc+diDP
●F5対F7
●PEG400より優れたPG
●F5対F6
●PGは、OAとほぼ同じであり得る。
●F5対F4
●LLは、PGよりも有効であり得る(濃度単位当たりの拡散)。
実施例8からの製剤F4、F5、F6、及びF9を、表25に示すように、化学的安定性について試験した。製剤を以下に示す温度で3週間保存した後、残っている薬物の量をHPLCによってアッセイした。
方法
以下の表26及び27に示す製剤を、製剤44、46、48、及び50を除いて、実施例7に記載の手順を用いて作製した。最終製剤は、典型的には、クリーム又はゲルであった。
1)薬物を水中のHPbCDの溶液に溶解した。
2)パルミチン酸イソプロピル及びTween 60を、溶融セチルアルコールと60℃で混合した。
3)薬物溶液を、セチルアルコール/IPM及びTween 60の混合物に添加し、均一なクリームが形成されるまで混合した。
1)薬物を、溶媒/浸透促進剤の混合物に溶解した。
2)次いで、二酸化ケイ素を添加し、ゲルが形成されるまで混合した。
得られた製剤の外観を、以下の表26及び27に示す。製剤の一部を、室温で2ヶ月間置いておいた。それらの物理的安定性を、以下の表26に示すように記録した。
目的
●皮膚に透過する薬物含有量を最大化する
●F9及びF5/F6に基づく
●透過能力を増加させる
●薬物負荷を最大化する
●相乗効果のために、複数の透過促進剤を使用する
●水を減らして、薬物溶解度を増加させる(増粘剤としてCarbopolを使用しない)
●PG(優れた透過促進剤及び適度な可溶化剤)を増加させる(約30mg/mL)
●EtOH(優れた透過促進剤であるが、それほど良くはない可溶化剤)を追加/保持する(約3mg/mL)
●少量のPEG400(不十分な透過促進剤であるが、優れた可溶化剤)を添加する(約130mg/mL)
●SiO2を、水を必要としない増粘剤として使用する
以下の表28に示す製剤を、実施例8に記載の手順を用いて作製した。
この研究は、5つの透過実験を有する1つの皮膚ドナーを含んだ。非常に微量の薬物がレセプター液中に見出された。結果を、以下の表29に示す。
●製剤F14及び対照は、深部皮膚に透過した最も多量の薬物を有した。
実施例11からの製剤F14を、表30に示すように、化学的安定性について試験した。製剤を以下に示す温度及び湿度で1週間保存した後、残っている薬物の量をHPLCによってアッセイした。
方法
以下の表31及び32に示す製剤を、実施例10に記載の手順を用いて作製した。
得られた製剤の外観を、以下の表31及び32に示す。6wt%25HC3Sは全て、調製された組成物中に溶解していた。表32の製剤を室温で1ヶ月間置いておき、それらの物理的安定性を記録した。
目的
尋常性乾癬(すなわち、プラーク乾癬)患者における活性化合物の有効性を調べること。
活性化合物25HC3Sを、以下の表34に示すように、2つの製剤において調製する。プラセボは、活性化合物なしで同じ賦形剤を含有する。
これは、無作為化した、研究者盲検の、プラセボを対照とした、探索的臨床研究である。
Claims (38)
- 炎症性皮膚疾患又は皮膚病変の処置又は予防的な処置を必要とする対象において、炎症性皮膚疾患又は皮膚病変を処置又は予防的に処置する方法であって、
炎症性皮膚疾患又は皮膚病変を処置又は予防的に処置するのに十分な量の1つ以上の酸素化コレステロール硫酸(OCS)を対象に投与すること
を含む、方法。 - 炎症性皮膚疾患が、乾癬、皮膚炎、赤芽球性プロトポルフィリン症(EPP)、及び紫外線(UV)紅斑のうちの少なくとも1つを含む、請求項1に記載の方法。
- 炎症性皮膚疾患が、乾癬を含む、請求項1に記載の方法。
- 炎症性皮膚疾患が、皮膚炎を含む、請求項1に記載の方法。
- 1つ以上のOCSが、5-コレステン-3,25-ジオール,3-サルフェート(25HC3S)又はその薬学的に許容可能な塩を含む、請求項1〜4のいずれか一項に記載の方法。
- 1つ以上のOCSが、約0.001mg/kg/日〜約100mg/kg/日の範囲の用量で対象に投与される、請求項1〜5のいずれか一項に記載の方法。
- 1つ以上のOCSが、1日に1回から1年に1回の範囲の頻度で投与される、請求項1〜6のいずれか一項に記載の方法。
- 投与が、局部的及び全身的のうちの少なくとも1つによって行われる、請求項1〜7のいずれか一項に記載の方法。
- 投与が、局所的、経口的、及び注射によってのうちの少なくとも1つによって行われる、請求項1〜8のいずれか一項に記載の方法。
- 投与が、局所的に行われる、請求項1〜9のいずれか一項に記載の方法。
- 投与が、注射によって行われる、請求項1〜10のいずれか一項に記載の方法。
- 投与が、経口的に行われる、請求項1〜9のいずれか一項に記載の方法。
- 1つ以上のOCSが、医薬製剤として投与され、医薬製剤は、少なくとも1つの薬学的に許容可能な賦形剤を含む、請求項1〜12のいずれか一項に記載の方法。
- 医薬製剤が、ローション又はクリームである、請求項13に記載の方法。
- 炎症性皮膚疾患又は皮膚病変を処置又は予防的に処置する方法に使用するための、請求項1又は5に定義される1つ以上の酸素化コレステロール硫酸(OCS)であって、前記方法は、請求項1〜14のいずれか一項に定義される方法である、酸素化コレステロール硫酸。
- 炎症性皮膚疾患又は皮膚病変を処置又は予防的に処置する方法に使用するための医薬の製造のための、請求項1及び5のいずか一項に定義される1つ以上の酸素化コレステロール硫酸(OCS)の使用であって、前記方法は、請求項1〜14のいずれか一項に定義される方法である、使用。
- 酸素化コレステロール硫酸(OCS);
皮膚浸透促進剤; 及び
増粘剤
を含む、組成物。 - OCSが、5-コレステン-3,25-ジオール,3-サルフェート(25HC3S)又はその薬学的に許容可能な塩を含む、請求項17に記載の組成物。
- OCSが、組成物の重量に基づいて、約0.1wt%〜約50wt%の範囲の量で存在する、請求項17〜18のいずれか一項に記載の組成物。
- OCSが、組成物の重量に基づいて、約0.5wt%〜約10wt%の範囲の量で存在する、請求項17〜19のいずれか一項に記載の組成物。
- 皮膚浸透促進剤が、アルカノール、脂肪アルコール、脂肪酸、脂肪酸エステル、及びポリオールから選択される少なくとも1つのメンバーを含む、請求項17〜20のいずれか一項に記載の組成物。
- 皮膚浸透促進剤が、エタノール、セチルアルコール、ポリソルベート、モノラウリン酸プロピレングリコール、ラウリン酸ソルビタン、2-(2-エトキシエトキシ)エタノール、カプリロカプロイルポリオキシル-8グリセリド、オレイン酸ポリグリセリル、ポリオキシエチル化グリコール化グリセリド、オレイン酸、シクロデキストリン若しくはシクロデキストリン誘導体、プロピレングリコール、ジプロピレングリコール、ポリエチレングリコール、PEG化カプリル酸/カプリン酸グリセリド、及びレシチンイソプロピルパルミテートから選択される少なくとも1つのメンバーを含む、請求項17〜21のいずれか一項に記載の組成物。
- 皮膚浸透促進剤が、組成物の重量に基づいて、約1wt%〜約98wt%の範囲の量で組成物中に存在する、請求項17〜22のいずれか一項に記載の組成物。
- 皮膚浸透促進剤が、組成物の重量に基づいて、約5wt%〜約50wt%の範囲の量で組成物中に存在する、請求項17〜23のいずれか一項に記載の組成物。
- 増粘剤が、ポリアクリル酸、アリルスクロースで架橋されたポリアクリル酸、アリルペンタエリスリトールで架橋されたポリアクリル酸、アリルペンタエリスリトールで架橋されたポリアクリル酸及びC10〜C30アルキルアクリレート、ポリ(エチレングリコール)-ブロック-ポリ(プロピレングリコール)-ブロック-ポリ(エチレングリコール)、ポロキサマー、セルロース誘導体、メチルセルロース、カルボキシメチルセルロース、及びカルボマーから選択される少なくとも1つのメンバーを含む、請求項17〜24のいずれか一項に記載の組成物。
- 増粘剤が、組成物の重量に基づいて、約0.2wt%〜約40wt%の範囲の量で組成物中に存在する、請求項17〜25のいずれか一項に記載の組成物。
- 酸素化コレステロール硫酸(OCS);
皮膚浸透促進剤; 及び
皮膚浸透促進剤とは異なる溶媒
を含む、組成物。 - OCSが、5-コレステン-3,25-ジオール,3-サルフェート(25HC3S)又はその薬学的に許容可能な塩を含む、請求項27に記載の組成物。
- OCSが、組成物の重量に基づいて、約0.1wt%〜約50wt%の範囲の量で存在する、請求項27〜28のいずれか一項に記載の組成物。
- 皮膚浸透促進剤が、アルカノール、脂肪アルコール、脂肪酸、脂肪酸エステル、及びポリオールから選択される少なくとも1つのメンバーを含む、請求項27〜29のいずれか一項に記載の組成物。
- 皮膚浸透促進剤が、エタノール、セチルアルコール、ポリソルベート、モノラウリン酸プロピレングリコール、ラウリン酸ソルビタン、2-(2-エトキシエトキシ)エタノール、カプリロカプロイルポリオキシル-8グリセリド、オレイン酸ポリグリセリル、ポリオキシエチル化グリコール化グリセリド、オレイン酸、シクロデキストリン若しくはシクロデキストリン誘導体、プロピレングリコール、ジプロピレングリコール、ポリエチレングリコール、PEG化カプリル酸/カプリン酸グリセリド、及びレシチンイソプロピルパルミテートから選択される少なくとも1つのメンバーを含む、請求項27〜30のいずれか一項に記載の組成物。
- 皮膚浸透促進剤が、組成物の重量に基づいて、約1wt%〜約98wt%の範囲の量で組成物中に存在する、請求項27〜31のいずれか一項に記載の組成物。
- 溶媒が、プロピレンカーボネート、ジメチルスルホキシド、ポリエチレングリコール、N-メチル-ピロリドン、及び鉱油から選択される少なくとも1つのメンバーを含む、請求項27〜32のいずれか一項に記載の組成物。
- 溶媒が、組成物の重量に基づいて、約1wt%〜約98wt%の範囲の量で組成物中に存在する、請求項27〜33のいずれか一項に記載の組成物。
- 炎症性皮膚疾患又は皮膚病変の処置又は予防的な処置を必要とする対象において、炎症性皮膚疾患又は皮膚病変を処置又は予防的に処置する方法であって、
炎症性皮膚疾患又は皮膚病変を処置又は予防的に処置するのに十分な量の、請求項17〜34のいずれか一項に記載の組成物を対象に投与すること
を含む、方法。 - 炎症性皮膚疾患が、乾癬、皮膚炎、赤芽球性プロトポルフィリン症(EPP)、及び紫外線(UV)紅斑のうちの少なくとも1つを含む、請求項35に記載の方法。
- 前記の1つ以上の酸素化コレステロール硫酸(OCS)の量を対象に投与することが、請求項17〜34のいずれか一項に定義される組成物を対象に投与することを含む、請求項15に記載の使用のための1つ以上の酸素化コレステロール硫酸(OCS)。
- 前記の1つ以上の酸素化コレステロール硫酸(OCS)の量を対象に投与することが、請求項17〜34のいずれか一項に定義される組成物を対象に投与することを含む、請求項16に記載の使用。
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WO2006047022A1 (en) | 2004-10-25 | 2006-05-04 | Virginia Commonwealth University | Nuclear sulfated oxysterol, potent regulator of cholesterol homeostasis, for therapy of hypercholesterolemia, hyperlipidemia, and atherosclerosis |
TWI816417B (zh) | 2013-12-24 | 2023-09-21 | 維吉尼亞聯邦大學 | 氧化膽固醇硫酸鹽(ocs)之用途 |
KR20230152787A (ko) | 2016-08-02 | 2023-11-03 | 버지니아 커먼웰스 유니버시티 | 5-콜레스텐-3, 25-디올, 3-술페이트 (25hc3s) 또는 이의 약학적으로 허용 가능한 염, 및 적어도 하나의 시클릭 올리고당을 포함하는 조성물 |
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