JP2021525110A - 注射デバイス向けの圧力センサアセンブリおよび方法 - Google Patents
注射デバイス向けの圧力センサアセンブリおよび方法 Download PDFInfo
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Abstract
Description
Claims (15)
- 薬物送達デバイスであって:
ハウジングと;
薬物送達デバイス(100)のハウジング(110)内に収容されるように構成された薬物容器(114)であって、該薬物容器(114)内に薬剤(40)を収容するように構成されたストッパ(200)を含む薬物容器(114)と;
薬物送達動作中に薬物容器(114)のストッパ(200)に力をかけて該ストッパ(200)を薬物容器(114)内へ駆動し、薬剤(40)の用量を薬物送達デバイス(100)から排出するように構成された駆動機構(106)と;
プロセッサ(343)と;
駆動機構(106)によって印加される力を測定し、測定信号をプロセッサ(343、810)へ出力するように配置されたセンサ(341)と;
プロセッサに動作を実行させるように動作可能な命令を記憶する少なくとも1つの非一時的なコンピュータ可読媒体(344)であって、該動作は:
薬物送達動作中に圧力センサ(341)を起動すること、
薬物送達動作中に測定信号を受信すること、および
受信した測定信号に基づいて、薬剤(40)の用量が薬物送達デバイス(100)から排出されたかどうかを判定することを含む、少なくとも1つの非一時的なコンピュータ可読媒体(344)と;
可聴、触覚、または可視の警報(542)を薬物送達デバイス(100)の使用者に提供するように構成された警報機構(541)とを含み、該動作は:
薬剤(40)の用量が薬物送達デバイス(100)から排出されたかどうかを判定したことに基づいて、薬物送達標示を生成することと、
該薬物送達標示に基づいて警報機構(541)を起動することとを含む、前記薬物送達デバイス。 - 非一時的なコンピュータ可読媒体(344)は、用量に対する基準測定信号を記憶し、
薬剤(40)の用量が排出されたかどうかを判定することは、受信した測定信号を基準測定信号と比較することを含む、請求項1に記載の薬物送達デバイス。 - 薬物送達デバイス(100)は、用量を設定し、設定された用量に対応する用量信号をプロセッサ(343)へ出力するように構成された用量選択機構(112)を含み、
動作は、用量信号を受信することと、用量に対する基準測定信号を計算することとを含み、
薬剤(40)の用量が排出されたかどうかを判定することは、受信した測定信号を基準測定信号と比較することを含む、請求項1に記載の薬物送達デバイス。 - 命令は、測定信号によって表される力または圧力を予期の最大の力または圧力と比較することを含み、
薬剤(40)の用量が薬物送達デバイス(100)から排出されたかどうかを判定することは、比較に基づいて流体経路閉塞状態を検出することを含む、請求項1〜3のいずれか1項に記載の薬物送達デバイス。 - 動作は:
薬物送達動作の開始と測定信号によって表される圧力または力の増大との間の時間遅延を計算することを含み、
薬剤(40)の用量が薬物送達デバイス(100)から排出されたかどうかを判定することは、時間遅延に基づいて、薬物容器(114)と駆動機構(106)との間のプライミング間隙を検出することを含む、請求項1〜4のいずれか1項に記載の薬物送達デバイス。 - 動作は、薬物送達動作の終了時に、測定信号によって表される圧力または力を予期の最小の圧力または力と比較することを含み、
薬剤(40)の用量が薬物送達デバイス(100)から排出されたかどうかを判定することは、比較に基づいて、駆動機構(106)内の内部の力が正常化したときを判定することを含む、請求項1〜5のいずれか1項に記載の薬物送達デバイス。 - 無線信号(482)を外部デバイス(480)へ伝送するように構成された無線モジュール(345)を含み、命令は:
薬剤(40)の用量が薬物送達デバイス(100)から排出されたかどうかを判定したことに基づいて、薬物送達標示を生成することと、
薬物送達標示を外部デバイスへ伝送することとを含む、請求項1〜6のいずれか1項に記載の薬物送達デバイス。 - 警報機構(541)は、感知された圧力に基づいて、薬物送達動作の成功および/または薬物送達動作中に検出された問題を使用者に警報するように構成される、請求項1〜7のいずれか1項に記載の薬物送達デバイス。
- ストッパ(200)および駆動機構(106)のうちの1つまたはそれ以上の位置を検出し、位置信号をプロセッサへ出力するように構成された位置センサ(342)を含み:
命令は、薬物送達動作前、薬物送達動作中、および薬物送達動作後のうちの少なくとも1つで位置信号を受信することを含み、
薬剤(40)の用量が薬物送達デバイス(100)から排出されたかどうかを判定することは、受信した測定信号および受信した位置信号に基づいて行われる、
請求項1〜8のいずれか1項に記載の薬物送達デバイス。 - 薬物送達デバイス内で使用するための電子アセンブリであって:
プロセッサ(343)と;
カートリッジ(114)内の圧力または薬物送達デバイス(100)の駆動機構(106)によって印加される力を測定し、測定信号をプロセッサ(343)へ出力するように配置されたセンサ(341)と;
プロセッサ(343)に動作を実行させるように動作可能な命令を記憶する少なくとも1つの非一時的なコンピュータ可読媒体(344)とを含み、該動作は:
薬物送達動作中にセンサ(341)を起動し、薬物送達動作中に圧力または力測定信号を受信することと、
受信した測定信号に基づいて、薬剤(40)の用量が薬物送達デバイス(100)から排出されたかどうかを判定することとを含む、前記電子アセンブリ。 - 圧力または力センサを使用して薬物送達デバイス(100)からの薬剤(40)の用量の薬物送達動作を分析する方法であって:
薬物送達動作中にセンサ(341)を起動し、薬物送達動作中に測定信号を受信することと、
受信した測定信号に基づいて、薬剤(40)の用量が薬物送達デバイス(100)から排出されたかどうかを判定することとを含む、前記方法。 - 薬物送達デバイス(100)の用量選択機構から用量信号を受信し、用量信号に対する基準測定信号を計算することを含み:
薬剤(40)の用量が排出されたかどうかを判定することは、受信した測定信号を基準測定信号と比較することを含む、
請求項11に記載の方法。 - 測定信号時間によって表される圧力を予期の最大の圧力または力と比較することを含み:
薬剤(40)の用量が薬物送達デバイス(100)から排出されたかどうかを判定することは、比較に基づいて、流体経路閉塞状態を検出することを含む、
請求項11または12に記載の方法。 - 薬物送達動作の開始と測定信号によって表される圧力または力の増大との間の時間遅延を計算することを含み:
薬剤(40)の用量が薬物送達デバイス(100)から排出されたかどうかを判定することは、時間遅延に基づいて、薬物容器(114)と駆動機構との間のプライミング間隙を検出することを含む、
請求項11〜13のいずれか1項に記載の方法。 - 薬物送達動作の終了時に、測定信号によって表される圧力または力を予期の最小の圧力または力と比較することを含み:
薬剤(40)の用量が薬物送達デバイス(100)から排出されたかどうかを判定することは、比較に基づいて、駆動機構が正常化したことを検出することを含む、
請求項11〜14のいずれか1項に記載の方法。
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