JP2001521561A - ホスフェートによって鎖延長化された生分解性ポリマー、組成物、物品、並びにその製造及び使用方法 - Google Patents
ホスフェートによって鎖延長化された生分解性ポリマー、組成物、物品、並びにその製造及び使用方法Info
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- JP2001521561A JP2001521561A JP54194898A JP54194898A JP2001521561A JP 2001521561 A JP2001521561 A JP 2001521561A JP 54194898 A JP54194898 A JP 54194898A JP 54194898 A JP54194898 A JP 54194898A JP 2001521561 A JP2001521561 A JP 2001521561A
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Landscapes
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Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.式IまたはII 式中、 Xは−O−またはR'がHまたはアルキルである−NR'−であり、 M1およびM2はそれぞれ独立して(1)炭素原子数1〜20を有する分岐鎖また は直鎖の脂肪族基または(2)炭素原子数1〜20を有する分岐鎖または直鎖のオキ シ−、カルボキシ−またはアミノ−脂肪族基であり、 Yは−O−、−S−または−NR'−であり、 Lは炭素原子数1〜20を有する分岐鎖または直鎖の脂肪族基であり、 RはH、アルキル、アルコキシ、アリール、アリーロキシ、複素環式基また はヘテロシクロキシであり、 x:yのモル比は約1であり、 n:(xまたはy)のモル比は約200:1と1:200の間であり、そして、 q:rのモル比は約1:99と99:1の間である。 にて示される繰返しモノマー単位よりなる、生分解前および生分解時に生体適合 性を有する生分解性ポリマー。 2.M1およびLの各々が分岐鎖または直鎖のアルキレン基である請求の範囲 第1項のポリマー。 3.M1およびLの各々が1〜7の炭素原子数を有する請求の範囲第1項のポ リマー。 4.M1がエチレン基またはメチル置換メチレン基であり、そしてLがエチレ ン基である請求の範囲第1項のポリマー。 5.Rがアルキル基、アルコキシ基、フェニル基、フェノキシ基またはヘテロ シクロキシ基である請求の範囲第1項のポリマー。 6.Rが1から7の炭素原子数を有するアルコキシ基である請求の範囲第1項 のポリマー。 7.Rがエトキシ基である請求の範囲第1項のポリマー。 8.M1およびM2の各々が分岐鎖または直鎖のアルキレン基である請求の範囲 第1項のポリマー。 9.M1およびM2のうちの少なくとも一つが、aおよびbの各々が1から7で ある、−(CH2)a−、−(CH2)a−O−および−O−(CH2)a−O−(CH2)b− からなる群から選ばれた式を有するアルキレン基またはアリコキシレン基である 請求の範囲第1項のポリマー。 10.M1およびM2のうちの少なくとも一つが、式 −CHR2−CO−O−CHR3− 式中、R2およびR3はそれぞれ独立してH、アルキル、アルコキシ、アリール 、アリーロキシ、複素環式基またはヘテロシクロキシである。 を有する請求の範囲第1項のポリマー。 11.M1およびM2の各々が1〜7の炭素原子数を有する請求の範囲第1項のポ リマー。 12.Xが−O−である請求の範囲第1項のポリマー。 13.Xが−NR'−である請求の範囲第1項のポリマー。 14.M1およびM2の各々がアルキレン基またはアリコキシレン基であり、Lが アルキレン基であり、Xが−O−であり、そしてRがアルコキシ基である請求の 範囲第1項のポリマー。 15.x:yのモル比が約1である請求の範囲第1項のポリマー。 16.q:rのモル比が約1:99および99:1である請求の範囲第1項のポリマ ー。 17.xおよびyの各々が約1乃至1000である請求の範囲第1項のポリマー。 18.n:(xまたはy)のモル比が約100:1と1:100の間ある請求の範囲第 1項のポリマー。 19.該ポリマーが融解重合によって製造されたものである請求の範囲第1項の ポリマー。 20.該ポリマーが付加的な生体適合性を有するモノマー単位よりなる請求の範 囲第1項のポリマー。 21.該ポリマーがアセトン、ジメチレンクロライド、クロロホルム、酢酸エチ ル、DMAC、N−メチルピロリドン、ジメチルホルムアミドおよびジメチルス ルホキシドよりなる群から選ばれた少なくとも1種の溶媒に可溶である請求の範 囲第1項のポリマー。 22.式IまたはII 式中: Xは−O−またはR'がHまたはアルキルである−NR'−であり、 M1およびM2はそれぞれ独立して(1)炭素原子数1〜20を有する分 岐鎖または直鎖の脂肪族基または(2)炭素原子数1〜20を有する分岐鎖または 直鎖のオキシ−、カルボキシ−またはアミノ−脂肪族基であり、 Yは−O−、−S−または−NR'−であり、 Lは炭素原子数1〜20を有する分岐鎖または直鎖の脂肪族基であり、 RはH、アルキル、アルコキシ、アリール、アリーロキシ、複素環式基また はヘテロシクロキシであり、 x:yのモル比は約1であり、 n:(xまたはy)のモル比は約200:1と1:200の間であり、そして、 q:rのモル比は約1:99と99:1の間である。 にて示される繰返しモノマー単位よりなる、生分解前および生分解中、生体適合 性を有する生分解ポリマー、生分解前および生分解時に生体適合性を有する生分 解性ポリマーの製造方法であって、 (a)式III、IVまたはV 式中、M1、M2およびXは上記に定義したとおりである。 を有する複素環式化合物のうちの少なくとも1種と、式 H−Y−L−Y−H 式中、YおよびLは上記に定義したとおりである。 を有する開始剤とを反応させて下記に示した式VIまたはVIIのプレポリマーを 生成させ、 式中、X、M1、M2、Y、L、x、y、qおよびrは上記に定義したとおりで ある。 (b)さらに式III、IVまたはVの該プレポリマーを式VIII 「haro」はBr、ClまたはIであり、Rは上記に定義したとおりである。 を有するホスホロジハリデートを反応させて式IまたはIIの該ポリマー を生成させる工程かるなる前記生分解性ポリマーの製造方法。 23.M1およびLの各々が分岐鎖または直鎖のアルキレン基である請求の範囲 第22項の方法。 24.M1がエチレン基またはメチル置換メチレン基であり、そしてLがエチレ ン基である請求の範囲第22項の方法。 25.Rが1から7の炭素原子数を有するアルコキシ基である請求の範囲第22項 の方法。 26.Rがエトキシ基である請求の範囲第22項の方法。 27.M1およびM2の各々が分岐鎖または直鎖のアルキレン基である請求の範囲 第22項の方法。 28.M1およびM2のうちの少なくとも一つが、aおよびbの各々が1から7で ある、−(CH2)a−、−(CH2)a−O−および−O−(CH2)a−O−(CH2)b− からなる群から選ばれた式を有するアルキレン基またはアリコキシレン基である 請求の範囲第22項の方法。 29.M1およびM2のうちの少なくとも一つが、式 −CHR2−CO−O−CHR3− 式中、R2およびR3はそれぞれ独立してH、アルキル、アルコキシ、アリール 、アリーロキシ、複素環式基またはヘテロシクロキシである。 を有する請求の範囲第22項の方法。 30.M1およびM2の各々が1〜7の炭素原子数を有する請求の範囲第22項の方 法。 31.Xが−O−である請求の範囲第22項の方法。 32.Xが−NR'−である請求の範囲第22項の方法。 33.M1およびM2の各々がアルキレン基またはアリコキシレン基であり、Lが アルキレン基であり、Xが−O−であり、そしてRがアルコキシ基である請求の 範囲第22項の方法。 34.x:yのモル比が約1である請求の範囲第22項の方法。 35.q:rのモル比が約1:99および99:1である請求の範囲第22項の方法。 36.xおよびyの各々が約1乃至1000である請求の範囲第22項の方法。 37.n:(xまたはy)のモル比が約100:1から約1:100までである請求の 範囲第22項の方法。 38.反応ステップ(a)が約0から約+235℃で行われる請求の範囲第22項の方法 。 39.反応ステップ(a)が約1時間と7日との間の期間中で行われる請求の範囲 第22項の方法。 40.該開始剤におけるLが、1以上の付加的なY−H−含有置換基ここのYは 上記に定義したとおりである、で置換されている請求の範囲第22項の方法。 41.触媒が反応ステップ(a)中に存在する請求の範囲第22項の方法。 42.酸受容体が重合ステップ(b)中に存在する請求の範囲第22項の方法。 43.該重合ステップ(b)が約−40℃と+150℃との間の温度で行われる請求の範 囲第22項の方法。 44.該重合ステップ(b)が約30分から24時間までの時間中で行なわれる請求の 範囲第22項の方法。 45.式IまたはIIの該ポリマーは、該ポリマーの非溶媒あるいは部分溶媒を用 いて該ポリマーの溶液をクエンチすることによって精製される請求の範囲第22項 の方法。 46.請求の範囲第1項のポリマーからなる生体吸収性縫合剤。 47.請求の範囲第1項のポリマーからなる骨および結合組織の傷をなおすため の整形外科器具、骨セメントまたは骨ワックス。 48.請求の範囲第1項のポリマーからなる分解性または非分解性織物用の積層 物。 49.請求の範囲第1項のポリマーからなる移植可能な器具用のコーティング材 。 50.次の成分からなる生分解性ポリマー組成物: (a)少なくとも一つの生物学的に活性な物質および (b)式IまたはII 式中、 Xは−O−またはR'がHまたはアルキルである−NR'−であり、 M1およびM2はそれぞれ独立して(1)炭素原子数1〜20を有する分岐鎖また は直鎖の脂肪族基または(2)炭素原子数1〜20を有する分岐鎖または直鎖のオキ シ−、カルボキシ−またはアミノ−脂肪族基であり、 Yは−O−、−S−または−NR'−であり、 Lは炭素原子数1〜20を有する分岐鎖または直鎖の脂肪族基であり、 RはH、アルキル、アルコキシ、アリール、アリーロキシ、複素環式基また はヘテロシクロキシであり、 x:yのモル比は約1であり、 n:(xまたはy)のモル比は約200:1と1:200の間であり、そして、 q:rのモル比は約1:99と99:1の間である。 にて示される繰返しモノマー単位よりなる、生分解前および生分解時に生体適合 性を有する生分解性ポリマー。 51.M1およびLの各々が分岐鎖または直鎖のアルキレン基である請求の範囲 第50項のポリマー組成物。 52.M1がエチレン基またはメチル置換メチレン基であり、そしてLがエチレ ン基である請求の範囲第50項のポリマー組成物。 53.Rがアルキル基、アルコキシ基、フェニル基、フェノキシ基またはヘテロ シクロキシ基である請求の範囲第50項のポリマー組成物。 54.Rがアルコキシ基である請求の範囲第50項のポリマー組成物。 55.M1およびM2の各々が分岐鎖または直鎖のアルキレン基である請求の範囲 第50項のポリマー組成物。 56.M1およびM2のうちの少なくとも一つが、aおよびbの各々が1から7で ある、−(CH2)a−、−(CH2)a−O−および−O−(CH2)a−O−(CH2)b− からなる群から選ばれた式を有するアルキレン基またはアリコキシレン基である 請求の範囲第50項ののポリマー組成物。 57.M1およびM2のうちの少なくとも一つが、式 −CHR2−CO−O−CHR3− 式中、R2およびR3はそれぞれ独立してH、アルキル、アルコキシ、アリール 、アリーロキシ、複素環式基またはヘテロシクロキシである。 を有する請求の範囲第50項のポリマー組成物。 58.M1およびM2の各々が1〜7の炭素原子数を有する請求の範囲第50項のポ リマー組成物。 59.Xが−O−である請求の範囲第50項のポリマー組成物。 60.Xが−NR'−である請求の範囲第50項のポリマー組成物。 61.M1およびM2は各々アルキレン基またはアリコキシレン基であり、Lがア ルキレン基であり、Xが−O−であり、そしてRがアルコキシ基である請求の範 囲第50項のポリマー組成物。 62.x:yのモル比が約1である請求の範囲第50項のポリマー組成物。 63.q:rのモル比が約1:99および99:1である請求の範囲第50項のポリマ ー組成物。 64.xおよびyの各々が約1乃至1000である請求の範囲第50項のポリマー組成 物。 65.n:(xまたはy)のモル比が約100:1から約1:100まである請求の範 囲第50項のポリマー組成物。 66.該ポリマーが融解重合によって製造されたものである請求の範囲第50項の ポリマー組成物。 67.該ポリマーが付加的な生体適合性を有するモノマー単位からなる請求の範 囲第50項のポリマー組成物。 68.該ポリマーがアセトン、ジメチレンクロライド、クロロホルム、酢酸エチ ル、DMAC、N−メチルピロリドン、ジメチルホルムアミドおよびジメチルス ルホキシドよりなる群から選ばれた少なくとも1種の溶媒に可溶である請求の範 囲第50項のポリマー組成物。 69.生物学的に活性な物質が多糖類、発育因子、ホルモン、抗脈管形成因子、 インターフェロン又はサイトカイン及びこれら物質のプロ医薬よりなる群から選 ばれる請求の範囲第50項のポリマー組成物。 70.生物学的に活性な物質が治療薬またはプロ医薬である請求の範囲第50項の ポリマー組成物。 71.該医薬が抗新生物剤、抗生物質、抗ウイルス剤、抗黴剤、抗炎症剤及び抗 凝固剤からなる群より選ばれる請求の範囲第70項のポリマー組成物。 72.抗新生物剤がパクリタキセルである請求の範囲第71項のポリマー組成物。 73.該生物学的に活性な物質と該ポリマーは均一なマトリックスを形成する請 求の範囲第50項のポリマー組成物。 74.該ポリマーが生分解時にこのポリマーのホスホエステル結合の加水分解の 機能として少なくとも部分的に生物学的に活性な物質がインビボでのコントロー ルされた放出速度によって特徴づけられる請求の範囲第50項のポリマー組成物。 75.移植、注入あるいは別の手段によって体内に全体的にまたは部分的に配置 されるのに有用な物品であって、次の成分からなる生分解性ポリマー組成物から なる物品: (a)少なくとも一つの生物学的に活性な物質および (b)式IまたはII 式中、 Xは−O−またはR'がHまたはアルキルである−NR'−であり、 M1およびM2はそれぞれ独立して(1)炭素原子数1〜20を有する分岐鎖また は直鎖の脂肪族基または(2)炭素原子数1〜20を有する分岐鎖または直鎖のオキ シ−、カルボキシ−またはアミノ−脂肪族基であり、 Yは−O−、−S−または−NR'−であり、 Lは炭素原子数1〜20を有する分岐鎖または直鎖の脂肪族基であり、 RはH、アルキル、アルコキシ、アリール、アリーロキシ、複素環式基また はヘテロシクロキシであり、 x:yのモル比は約1であり、 n:(xまたはy)のモル比は約200:1と1:200の間であり、そして、 q:rのモル比は約1:99と99:1の間である。 にて示される繰返しモノマー単位よりなる、生分解前および生分解時に生体適合 性を有する生分解性ポリマー。 76.M1およびLの各々が分岐鎖または直鎖のアルキレン基である請求の範囲 第75項の物品。 77.M1およびLの各々が1から7の炭素原子数を有する請求の範囲第75項の 物品。 78.Rがアルキル基、アルコキシ基、フェニル基、フェノキシ基またはヘテロ シクロキシ基である請求の範囲第75項の物品。 79.Rがアルコキシ基である請求の範囲第75項の物品。 80.M1およびM2の各々が分岐鎖または直鎖のアルキレン基である請求の範囲 第75項の物品。 81.M1およびM2のうちの少なくとも一つが、aおよびbの各々が1〜7であ る、−(CH2)a−、−(CH2)a−O−および−O−(CH2)a−O−(CH2)b−か らなる群から選ばれた式を有するアルキレン基またはアリコキシレン基である請 求の範囲第75項の物品。 82.M1およびM2のうちの少なくとも一つが、式 −CHR2−CO−O−CHR3− 式中、R2およびR3はそれぞれ独立してH、アルキル、アルコキシ、アリール 、アリーロキシ、複素環式基またはヘテロシクロキシである。 を有する請求の範囲第75項の物品。 83.M1およびM2の各々が1から7までの炭素原子数を有する請求の範囲第75 項の物品。 84.Xが−O−である請求の範囲第75項の物品。 85.Xが−NR'−である請求の範囲第75項の物品。 86.M1およびM2は各々アルキレン基またはアリコキシレン基であり、Lがア ルキレン基であり、Xが−O−であり、そしてRがアルコキシ基である請求の範 囲第75項の物品。 87.x:yのモル比が約1である請求の範囲第75項の物品。 88.q:rのモル比が約1:99および99:1である請求の範囲第75項の物品。 89.xおよびyの各々が約1乃至1000である請求の範囲第75項の物品。 90.n:(xまたはy)のモル比が約100:1から約1:100まである請求の範 囲第75項の物品。 91.該ポリマーが融解重合によって製造される請求の範囲第75項の物 品。 92.該ポリマーが付加的な生体適合性を有するモノマー単位からなる請求の範 囲第75項の物品。 93.該ポリマーがアセトン、ジメチレンクロライド、クロロホルム、酢酸エチ ル、DMAC、N−メチルピロリドン、ジメチルホルムアミドおよびジメチルス ルホキシドよりなる群から選ばれた少なくとも1種の溶媒に可溶である請求の範 囲第75項の物品。 94.生物学的に活性な物質が多糖類、発育因子、ホルモン、抗脈管形成因子、 インターフェロンまたはサイトカイン及びこれら物質のプロ医薬よりなる群から 選ばれる請求の範囲第75項の物品。 95.生物学的に活性な物質が治療薬またはプロ医薬である請求の範囲第75項の 物品。 96.該医薬が抗新生物剤、抗生物質、抗ウイルス剤、抗黴剤、抗炎症剤、抗凝 固剤及びこれら物質のプロ医薬からなる群より選ばれる請求の範囲第75項の物品 。 97.抗新生物剤がパクリタキセルである請求の範囲第75項の物品。 98.該生物学的に活性な物質と該ポリマーは均一なマトリックスを形成する請 求の範囲第75項の物品。 99.該生物学的に活性な物質が該ポリマー内でカプセル化されている請求の範 囲第75項の物品。 100.該ポリマーが生分解時にこのポリマーのホスホエステル結合の加水分解 の機能として少なくとも部分的に生物学的に活性な物質のインビボでのコントロ ールされた放出速度によって特徴づけられる請求の範囲第75項の物品。 101.該物品が動物の体内への移植または注入用に適用される請求の範囲第75 項の物品。 102.該物品が微小球である請求の範囲第75項の物品。 103.該物品が血管の多い組織に移植または注入されたときに組織刺激が最小 限になる請求の範囲第75項の物品。 104.該物品が分解性織物の積層物に形成している請求の範囲第75項 の物品。 105.該物品が吸収性の縫合剤、骨障害の修復用材料または移植器具の被覆材 に形成している範囲第75項の物品。 106.(a)生物学的に活性な物質と、式IまたはII 式中: Xは−O−またはR'がHまたはアルキルである−NR'−であり、 M1およびM2はそれぞれ独立して(1)炭素原子数1〜20を有する分岐鎖また は直鎖の脂肪族基または(2)炭素原子数1〜20を有する分岐鎖または直鎖のオキ シ−、カルボキシ−またはアミノ−脂肪族基であり、 Yは−O−、−S−または−NR'−であり、 Lは炭素原子数1〜20を有する分岐鎖または直鎖の脂肪族基であり、 RはH、アルキル、アルコキシ、アリール、アリーロキシ、複素環式基また はヘテロシクロキシであり、 x:yのモル比は約1であり、 n:(xまたはy)のモル比は約200:1と1:200の間であり、そして、 q:rのモル比は約1:99と99:1の間である。 にて示される繰返しモノマー単位よりなる、生分解前および生分解時に 生体適合性を有する生分解性ポリマーを配合して混合物を形成させ、 (b)該混合物を成形固形物品または微小球に形成させ、そして (c)移植した固形物品または注入したマトリックスが生物学的液体と少なくと も部分接触するように予め選択された場所に該固形物品または微小球をインビボ で移植または注入してなる生物学的に活性な物質のコントロールされた放出方法 。 107.M1およびLの各々が分岐鎖または直鎖のアルキレン基である請求の範囲 第106項の方法。 108.Rがアルコキシ基である請求の範囲第106項の方法。 109.M1およびM2の各々が分岐鎖または直鎖のアルキレン基である請求の範 囲第106項の方法。 110.M1およびM2のうちの少なくとも一つが、aおよびbの各々は1〜7で ある、−(CH2)a−、−(CH2)a−O−および−O−(CH2)a−O−(CH2)b− からなる群から選ばれた式を有するアルキレン基またはアリコキシレン基である 請求の範囲第106項の方法。 111.M1およびM2のうちの少なくとも一つが、式 −CHR2−CO−O−CHR3− 式中、R2およびR3はそれぞれ独立してH、アルキル、アルコキシ、アリール 、アリーロキシ、複素環式基またはヘテロシクロキシである。 を有する請求の範囲第106項の方法。 112.M1およびM2の各々が1から7までの炭素原子数を有する請求の範囲第1 06項の方法。 113.Xが−O−である請求の範囲第106項の方法。 114.Xが−NR'−である請求の範囲第106項の方法。 115.M1およびM2は各々アルキレン基またはアリコキシレン基であり、Lが アルキレン基であり、Xが−O−であり、そしてRがアルコキシ基である請求の 範囲第106項の方法。 116.x:yのモル比が約1である請求の範囲第106項の方法。 117.q:rのモル比が約1:99および99:1である請求の範囲第106項の方法 。 118.xおよびyの各々が約1乃至1000である請求の範囲第106項の方法。 119.n:(xまたはy)のモル比が約100:1から約1:100まである請求の 範囲第106項の方法。 120.該ポリマーが付加的な生体適合性を有するモノマー単位からなる請求の 範囲第106項の方法。 121.生物学的に活性な物質が多糖類、発育因子、ホルモン、抗脈管形成因子 及び他の抗新生物剤、インターフェロン又はサイトカイン及びこれら物質のプロ 医薬よりなる群から選ばれる請求の範囲第106項の方法。 122.抗新生物剤がパクリタキセル請求の範囲第106項の方法。 123.生物学的に活性な物質が治療薬またはプロ医薬である請求の範囲第106項 の方法。 124.該医薬が化学療法薬、抗生物質、抗ウイルス剤、抗黴剤、抗炎症剤及び 抗凝固剤からなる群より選ばれる請求の範囲第106項の方法。 125.該生物学的に活性な物質と該ポリマーは均一なマトリックスを形成する 請求の範囲第106項の方法。 126.該生物学的に活性な物質が該ポリマー内でカプセル化されている請求の 範囲第106項の方法。 127.該ポリマーが生分解時にこのポリマーのホスホエステル結合の加水分解 の機能として少なくとも部分的に生物学的に活性な物質のインビボでのコントロ ールされた放出速度によって特徴づけられる請求の範囲第106項の方法。 128.該物品が無毒性であり、血管の多い組織に移植または注入されたときに 組織刺激が最小限になる請求の範囲第106項の方法。 129.該物品が微小球の形態になっている請求の範囲第106項の方法。 130.該物品が分解性織物の積層物に形成している請求の範囲第106項の方法。 131.該ポリマー組成物が移植用被覆材として使用される請求の範囲第106項の 方法。 132.該ポリマー組成物が癒着防止用バリヤとして使用される請求の範囲第106 項の方法。 133.該ポリマー組成物が神経発生用管として成形される請求の範囲第106項の 方法。
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1998
- 1998-02-04 UA UA99105931A patent/UA54505C2/uk unknown
- 1998-04-02 CA CA002285909A patent/CA2285909C/en not_active Expired - Fee Related
- 1998-04-02 JP JP54194898A patent/JP4170399B2/ja not_active Expired - Fee Related
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- 1998-04-02 CN CN98805196A patent/CN1107687C/zh not_active Expired - Fee Related
- 1998-04-02 KR KR1019997009119A patent/KR20010006041A/ko active IP Right Grant
- 1998-04-02 AU AU69449/98A patent/AU742110B2/en not_active Ceased
- 1998-04-02 HU HU0001412A patent/HUP0001412A2/hu unknown
- 1998-04-02 DE DE69825040T patent/DE69825040T2/de not_active Expired - Lifetime
- 1998-04-02 EP EP98915207A patent/EP0971969B1/en not_active Expired - Lifetime
- 1998-04-02 BR BR9809390-8A patent/BR9809390A/pt not_active Application Discontinuation
- 1998-04-02 RU RU99123428/04A patent/RU2207350C2/ru not_active IP Right Cessation
- 1998-04-02 AT AT98915207T patent/ATE271084T1/de not_active IP Right Cessation
- 1998-04-02 IL IL13212298A patent/IL132122A0/xx unknown
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1999
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2000
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- 2000-10-10 HK HK00106411A patent/HK1027366A1/xx not_active IP Right Cessation
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2008138051A (ja) * | 2006-11-30 | 2008-06-19 | Terumo Corp | α−ヒドロキシ酸重合体組成物およびそれを用いた成形品の製造方法 |
JP2009096720A (ja) * | 2007-10-12 | 2009-05-07 | Idemitsu Kosan Co Ltd | 生分解性液状エステル化合物 |
Also Published As
Publication number | Publication date |
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CA2285909A1 (en) | 1998-10-08 |
EP0971969B1 (en) | 2004-07-14 |
DE69825040D1 (de) | 2004-08-19 |
HUP0001412A2 (hu) | 2000-08-28 |
CN1107687C (zh) | 2003-05-07 |
BR9809390A (pt) | 2000-06-13 |
NZ500674A (en) | 2002-02-01 |
IL132122A0 (en) | 2001-03-19 |
UA54505C2 (uk) | 2003-03-17 |
JP4170399B2 (ja) | 2008-10-22 |
AU742110B2 (en) | 2001-12-20 |
CN1256701A (zh) | 2000-06-14 |
WO1998044020A1 (en) | 1998-10-08 |
NO994803D0 (no) | 1999-10-01 |
HK1027366A1 (en) | 2001-01-12 |
DE69825040T2 (de) | 2005-09-08 |
US20020151617A1 (en) | 2002-10-17 |
US6166173A (en) | 2000-12-26 |
AU6944998A (en) | 1998-10-22 |
NO994803L (no) | 1999-12-03 |
ATE271084T1 (de) | 2004-07-15 |
EP0971969A1 (en) | 2000-01-19 |
US6376644B1 (en) | 2002-04-23 |
KR20010006041A (ko) | 2001-01-15 |
RU2207350C2 (ru) | 2003-06-27 |
CA2285909C (en) | 2008-07-29 |
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