JP2020026405A - アセナピン含有貼付剤 - Google Patents
アセナピン含有貼付剤 Download PDFInfo
- Publication number
- JP2020026405A JP2020026405A JP2018151923A JP2018151923A JP2020026405A JP 2020026405 A JP2020026405 A JP 2020026405A JP 2018151923 A JP2018151923 A JP 2018151923A JP 2018151923 A JP2018151923 A JP 2018151923A JP 2020026405 A JP2020026405 A JP 2020026405A
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- JP
- Japan
- Prior art keywords
- patch
- sensitive adhesive
- asenapine
- pressure
- acid
- 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.)
- Granted
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Abstract
Description
[1] 支持体上に粘着剤層を備える貼付剤であって、粘着剤層がアセナピンマレイン酸塩、スチレン系粘着剤、及び、吸収促進剤を含有し、アセナピンマレイン酸塩の含有量が、遊離体換算で0.05〜0.34mg/kg体重であり、16〜26時間に1回の間隔でヒトの皮膚に貼付することによりアセナピンを投与するための貼付剤。
[2] 統合失調症を治療するための貼付剤である、[1]に記載の貼付剤。
[3] スチレン系粘着剤が、スチレン−イソプレン−スチレンブロック共重合体を含む、[1]又は[2]に記載の貼付剤。
[4] 吸収促進剤が、パルミチン酸イソプロピル、ソルビタンモノオレエート、プロピレングリコールモノラウレート、スクワラン、及びイソステアリルアルコールから選択される、[1]又は[2]に記載の貼付剤。
[5] アセナピンマレイン酸塩の含有量が、遊離体換算で6.4mgであるとき、アセナピンの最大血漿中濃度(Cmax)が0.5〜6.0ng/mLであり、Tmaxが8〜28時間である、[1]〜[3]のいずれかに記載の貼付剤。
[6] 支持体上に粘着剤層を備える貼付剤であって、粘着剤層がアセナピンマレイン酸塩、スチレン系粘着剤、及び、吸収促進剤を含有し、アセナピンマレイン酸塩の含有量が、遊離体換算で3〜20mgであり、16〜26時間に1回の間隔でヒトの皮膚に貼付することによりアセナピンを投与するための貼付剤。
[7] 統合失調症を治療するための貼付剤である、[6]に記載の貼付剤。
[8] スチレン系粘着剤が、スチレン−イソプレン−スチレンブロック共重合体を含む、[6]又は[7]に記載の貼付剤。
[9] 吸収促進剤が、パルミチン酸イソプロピル、ソルビタンモノオレエート、プロピレングリコールモノラウレート、スクワラン、及びイソステアリルアルコールから選択される、[6]〜[8]のいずれかに記載の貼付剤。
[10] アセナピンマレイン酸塩の含有量が、遊離体換算で6.4mgであるとき、アセナピンの最大血漿中濃度(Cmax)が0.5〜6.0ng/mLであり、Tmaxが8〜28時間である、[6]〜[9]のいずれかに記載の貼付剤。
表1に示す成分を混合し、膏体液を調製した。得られた膏体液をプラスチックフィルム(支持体)上に展延し、粘着剤層を形成させた。粘着剤層の上に更にプラスチックフィルム(剥離ライナー)を積層し、貼付剤を得た。粘着剤層の単位面積あたりの質量は、100g/m2である。表1中、数値は、質量%を意味する。
(1)製剤
得られた貼付剤を貼付面積が10cm2(アセナピンマレイン酸塩の含有量:4.5mg)、20cm2(アセナピンマレイン酸塩の含有量:9.0mg)、30cm2(アセナピンマレイン酸塩の含有量:13.5mg)、40cm2(アセナピンマレイン酸塩の含有量:18.0mg)となるように、それぞれ裁断した。実施例1〜4の貼付剤の貼付面積、各貼付剤中のアセナピンマレイン酸の含有量は、表2のとおりである。
実施例2の貼付剤を、健康成人の腹部、臀部、上腕部、上背部、上胸部の皮膚に24時間適用し、経時的に採血を行い、アセナピンの血漿中濃度を測定した。採血した時間は、適用してから0、2、4、8、12、16、20、24、26、28、32、36、48、60、72、96、及び120時間後である。液体クロマトグラフィータンデム質量分析装置(LC−MS/MS)を用いて、採取した各血液サンプルを分析し、アセナピン及びN−デスメチルアセナピンの血漿中濃度を算出した。得られたデータに基づき、横軸に採取時間[単位:hr]を、縦軸に血漿中濃度[単位:ng/mL]をプロットして、血漿中濃度−時間曲線を作成し、各パラメータを以下の式に基づき算出した。
Cmax[ng/mL]=観察された血漿中濃度の最大値(「最大血漿中濃度」ともいう。)
tmax[hr]=最大血漿中濃度(Cmax)に達するまでに要する時間
AUC0−t[ng・hr/mL]=台形則により計算された、0〜t時間までの血漿中濃度−時間曲線の曲線下面積
AUC0−inf[ng・hr/mL]=AUC0−t+Ct/λZとして計算された、0〜無限大時間までの血漿中濃度−時間曲線の曲線下面積
λZ=血漿中濃度−時間曲線に基づく回帰分析により決定された、見かけの終末相の消失速度定数
t1/2[hr]=ln2/λZの式に基づき計算された、見かけの消失半減期
代謝率(Cmax)[%]=(N−デスメチルアセナピンのCmax)/(アセナピンのCmax)×100
代謝率(AUC)[%]=(N−デスメチルアセナピンのAUC0−inf)/(アセナピンのAUC0−inf)×100
実施例1〜4に示すように、貼付剤をヒトの皮膚に貼付し、ドパミンD2受容体の占有率を算出した。具体的には、貼付剤を適用する2日前に、20名の被験者にPETトレーサー([11C]−(+)−4−プロピル−9−ヒドロキシナフトキサゾリン、D2/3受容体刺激薬)を静脈注射し、MRI測定により脳内のリガンドの分布状況を画像解析した。その後、比較例1及び実施例1〜3に示すように、貼付剤を被験者の皮膚に7日間適用した。各被験者において、24時間ごとに貼付剤を剥離し、新たな貼付剤を適用した。比較例1投与群及び実施例1〜3投与群の対象者数がそれぞれ、5名、5名、4名、6名となるように被験者を分類した。最初に貼付剤を適用した日をDay1とし、Day7が終了した段階(合計6回の経皮投与した段階)で、再度、PETトレーサーを投与し、MRI測定を行った。D2受容体の占有率は、PETトレーサーの受容体結合能(BP:Binding Potential)を指標にして、以下の式にしたがい、算出した。
D2受容体の占有率(%)=(貼付前のBP−貼付後のBP)/(貼付前のBP)×100
一群あたり204名の被験者(統合失調症患者)に対して、実施例2及び4の貼付剤を24時間ごとに貼り替えながら、6週間にわたって適用した。プラセボ群として、206名の被験者(統合失調症患者)に対して、アセナピンマレイン酸塩を含有しない貼付剤を同様にして適用した。統合失調症の治療効果は、Day0及びDay42(Week6)の時点で、PANSS(Positive and Negative Syndrome Scale)評価基準にしたがい、評価した。PANSS評価基準は、「The positive and negative syndrome scale(PANSS) for schizophrenia」(Kay,S.R et al.Schizophr. Bull.13(2):261−276)に基づくものであり、30項目を7段階のスコアで評価し、その合計を被験者数で除した値を算出した。スコアの数値が大きいほど、重症度が高いことを意味する。
表6に示す成分を混合し、膏体液を調製した。得られた膏体液をプラスチックフィルム(支持体)上に展延し、粘着剤層を形成させた。粘着剤層の上に更にプラスチックフィルム(剥離ライナー)を積層し、比較例1、実施例5〜18の貼付剤を得た。粘着剤層の単位面積あたりの質量は、100g/m2である。表6中、数値は、質量%を意味する。実施例6〜23の貼付剤の調製では、吸収促進剤として表7に記載の成分を使用した。架橋型ポリビニルピロリドンとは、N−ビニルピロリドンをポップコーン重合して得られるポリマーである。
所定時間における皮膚透過量(μg/cm2)=[アセナピン濃度(μg/mL)×流量(mL)]/貼付剤の面積(cm2)
Claims (5)
- 支持体上に粘着剤層を備える貼付剤であって、
前記粘着剤層がアセナピンマレイン酸塩、スチレン系粘着剤、及び、吸収促進剤を含有し、
前記アセナピンマレイン酸塩の含有量が、遊離体換算で0.05〜0.34mg/kg体重であり、
16〜26時間に1回の間隔でヒトの皮膚に貼付することによりアセナピンを投与するための貼付剤。 - 統合失調症を治療するための貼付剤である、請求項1に記載の貼付剤。
- 前記スチレン系粘着剤が、スチレン−イソプレン−スチレンブロック共重合体を含む、請求項1又は2に記載の貼付剤。
- 前記吸収促進剤が、パルミチン酸イソプロピル、ソルビタンモノオレエート、プロピレングリコールモノラウレート、スクワラン、及びイソステアリルアルコールから選択される、請求項1〜3のいずれか一項に記載の貼付剤。
- 前記アセナピンマレイン酸塩の含有量が、遊離体換算で6.4mgであるとき、アセナピンの最大血漿中濃度が0.5〜6.0ng/mLであり、最大血漿中濃度に達するまでに要する時間が8〜28時間である、請求項1〜4のいずれか一項に記載の貼付剤。
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JP7337287B2 (ja) | 2020-11-16 | 2023-09-01 | 久光製薬株式会社 | アセナピンの分解を抑制する方法 |
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