JP2003533468A5 - - Google Patents

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JP2003533468A5
JP2003533468A5 JP2001583736A JP2001583736A JP2003533468A5 JP 2003533468 A5 JP2003533468 A5 JP 2003533468A5 JP 2001583736 A JP2001583736 A JP 2001583736A JP 2001583736 A JP2001583736 A JP 2001583736A JP 2003533468 A5 JP2003533468 A5 JP 2003533468A5
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matrix material
protein matrix
protein
solvated
compressed
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Priority claimed from PCT/US2001/006502 external-priority patent/WO2001087267A1/en
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【特許請求の範囲】
【請求項1】 塗布可能なフィルムを形成するように1又は複数の生物適合性溶媒と組み合わされた1又は複数の生物適合性タンパク質材料を含んで成る溶媒化され圧縮されたタンパク質マトリックス材料であって、前記の塗布可能なフィルムが部分的に乾燥され、接着体に形成され、そしてバルク水を減少せしめ且つ溶媒化され圧縮されたタンパク質マトリックス材料形成するように圧縮されている、タンパク質マトリックス材料。
【請求項2】 塗布可能なフィルムを形成するように1又は複数の生物適合性溶媒と組み合わされた1又は複数の生物適合性タンパク質材料を含んで成る溶媒化された接着性タンパク質体であって、前記の塗布可能なフィルムが部分的に乾燥され、そして溶媒化された接着体に形成されているタンパク質体。
【請求項3】 溶媒化され、圧縮されたタンパク質マトリックス材料の製造方法において、
(a)1又は複数の生適合性タンパク質材料および1又は複数の生適合性溶媒を含む塗布可能な組成物を調製し、
(b)前記組成物を塗布して皮膜を形成し、
(c)塗布皮膜が接着性体に形成されるまで前記塗布皮膜を部分的に乾燥し、
(d)前記接着性体を形成し、そして前記接着性体を圧縮してタンパク質マトリックス材料を生成する、
ことを含んで成る方法。
【請求項4】 前記生物適合性タンパク質が、エラスチン、コラーゲン、アルブミン、ケラチン、フィブロネクチン、シルク、シルクフィブロイン、アクチン、ミオシン、フィブリノーゲン、トロンビン、アプロチニン、アンチトロンビンIII 、エラスチン様ブロック、シルク様ブロック、コラーゲン様ブロック、ラミニン様ブロック,フィブロネクチン様ブロック、シルク様およびエラスチン様ブロック、コラーゲン−へパリン、及びコラーゲン−コンドロイチンから成る群から選択される、請求項1に記載のタンパク質マトリックス材料、請求項2に記載のタンパク質体又は請求項3に記載の方法。
【請求項5】 前記生適合性溶媒が、水、ジメチルスルホキシド(DMSO)、生体適合性アルコール、生体適合性酸、油および生適合性グリコールから成る群から選択される、請求項1又は4に記載のタンパク質マトリックス材料、請求項2又は4に記載のタンパク質体、或いは請求項3又は4に記載の方法。
【請求項6】 前記タンパク質マトリックス材料が、1または複数の薬理学的活性剤、好ましくは鎮痛薬、麻酔薬、抗精神病薬、ステロイド、抗ステロイド、コルチコステロイド、抗緑内障薬、抗アルコール薬、抗凝固薬、遺伝子物質、抗血栓崩壊薬、抗癌薬、抗パーキンソン薬、鎮痙薬、抗炎症薬、避妊薬、酵素剤、細胞、増殖因子、抗ウイルス薬、抗細菌薬、抗真菌薬、低血糖薬、抗ヒスタミン薬、化学誘引物質、neutraceuticals、抗肥満薬、喫煙停止薬、助産薬および抗喘息薬から成る群から選択される薬理学的活性剤を更に含む、請求項1、4又は5に記載のタンパク質マトリックス材料、請求項2、4又は5に記載のタンパク質体、或いは請求項3、4又は5に記載の方法。
【請求項7】 前記薬理学的活性剤が、二次易移動性薬剤送達装置を含む、請求項6に記載のタンパク質マトリックス材料、タンパク質体、或いは方法。
【請求項8】 1つまたは複数の生物適合性高分子材料をさらに含む、請求項1、4〜7のいずれか1項に記載のタンパク質マトリックス材料、請求項2、4〜7のいずれか1項に記載のタンパク質体、或いは請求項3、4〜7のいずれか1項に記載の方法。
【請求項9】 前記1つまたは複数の生物適合性高分子物質が、エポキシ樹脂、ポリエステル樹脂、アクリル樹脂、ナイロン樹脂、シリコーン樹脂、ポリ無水物、ポリウレタン樹脂、ポリカルボネート、ポリ(テトラフルオロエチレン)、ポリカプロラクトン、ポリエチレンオキシド、ポリエチレングリコール、ポリ(ビニルクロリド)、ポリ乳酸、ポリグリコール酸、ポリプロピレンオキシド、ポリ(アルキレン)グリコール、ポリオキシエチレン、セバシン酸、ポリビニルアルコール、2−ヒドロキシエチルメタクリレート、ポリメチルメタクリレート、1,3−ビス(カルボキシフェノキシ)プロパン、脂質、ホスファチジルコリン、トリグリセリド、ポリヒドロキシブチレート、ポリヒドロキシバレレート、ポリ(エチレンオキシド)、ポリオルトエステル、ポリ(アミノ酸)、ポリシノアクリレート、ポリホスファゼン、ポリスルホン、ポリアミン、ポリ(アミドアミン)、フィブリン、グラファイト、軟質フルオロポリマー、イソブチルベース物質、イソプロピルスチレン、ビニルピロリドン、セルロースアセテートジブチレート、シリコーンゴムおよびこれらのコポリマーから成る群から選択される請求項8記載の、タンパク質マトリックス材料、タンパク質体、或いは方法。
【請求項10】 前記タンパク質マトリックス物質が1つまたは複数の架橋剤により架橋され、当該架橋試薬が、好ましくは、グルタルアルデヒド、p−アジドベンゾイルヒダジド、N−5−アジド−2−ニトロベンゾイルオキシスクシンイミド、N−スクシンイミジル6−[4’アジド−2’ニトロ−フェニルアミノ]ヘキサノエートおよび4−[p−アジドサリチルアミド]ブチルアミンから成る群から選択される、請求項1、4〜9のいずれか1項に記載のタンパク質マトリックス材料、或いは請求項2、4〜9いずれか1項に記載のタンパク質体。
【請求項11】 前記マトリックス材料が、マスキング又はUV光活性化剤を用いて、予め定められたパターンに架橋することによりプリントされる、請求項1、4〜10のいずれか1項に記載のタンパク質マトリックス材料。
【請求項12】 前記タンパク質マトリックス材料が、シリンダー、キューブ、球、挿入材、メッシュ、ストリップ、縫合、プラグ、包帯、ディスク、関節、出口封止材、チューブ、粒子、シート、ウエファー、糸及びパッチからなる群から選択される形態で製造される、請求項1、4〜10のいずれか1項に記載のタンパク質マトリックス材料。
【請求項13】 前記タンパク質マトリックス材料が、タンパク質マトリックス材料の2以上の層を含む、請求項1、4〜10のいずれか1項に記載のタンパク質マトリックス材料。
【請求項14】 前記タンパク質マトリックス材料を1又は複数の架橋剤により架橋する工程を含んで成る、請求項3〜9の何れか1項に記載のタンパク質マトリックス材料の製造方法。
【請求項15】 請求項1、4〜10のいずれか1項に記載の溶媒化され圧縮されたタンパク質マトリックス材料を含んでなる、溶媒化され圧縮された薬剤供給装置。
【請求項16】 シリンダー、キューブ、粒子、シート、ウエファ、糸及びパッチからなる群から選択される形態で製造される、請求項15に記載の溶媒化され圧縮された薬剤供給装置。
【請求項17】 外部刺激との接触の後に前記薬理学的活性剤を放出する放出機構を更に有する、請求項15又は16に記載の薬剤供給装置。
【請求項18】 1又は複数のタンパク質マトリックス材料の1又は複数の層を含む、請求項15〜17のいずれか1項に記載の薬剤供給装置。
【請求項19】 請求項1、4〜10、12及び13のいずれか1項に記載の溶媒化され圧縮されたタンパク質マトリックス材料を含んでなる圧縮されている創傷治癒装置。
【請求項20】 骨挿入物、メッシュ、ストリップ、縫合、歯科用プラグ、皮膚包帯、帯具、組織プラグ、脊椎挿入物、椎間円板、関節、気管支組織挿入物、腹部挿入物、血管挿入物、粒子、生物学的ファッスナー、ステップル、止血材および出入口封止装置から成る群から選択される、請求項19に記載の創傷治癒装置。
【請求項21】 付着性末端に隣接した非付着性ストリップ上に置かれたタンパク質マトリックス物質のセグメントを含む請求項20に記載の創傷治癒装置。
【請求項22】 骨挿入物、メッシュ、ストリップ、縫合、歯科用プラグ、皮膚包帯、帯具、組織プラグ、脊椎挿入物、椎間円板、関節、気管支組織挿入物、腹部挿入物、血管挿入物、粒子、生物学的ファッスナー、ステップル、止血材又は出入口封止装置の後に連結された、追加の医薬活性剤の供給のためのパッチ供給システムを含む、請求項20に記載の創傷治癒装置。
【請求項23】 1又は複数のタンパク質マトリックス材料の1又は複数の層を含む、請求項19又は20に記載の創傷治癒装置。
【請求項24】 請求項1、4〜10、12及び13からなる群から選択される溶媒化され圧縮されたタンパク質マトリックス材料を含んでなる、溶媒化され圧縮された組織移植片。
【請求項25】 血管、管状移植片、気管チューブ、気管支チューブ、カテーテル機能チューブ、肺移植片、胃腸セグメント、透明マトリックス移植片、心臓弁、軟骨、腱、靭帯、皮膚移植片、粒子、骨挿入物、メッシュ、ストリップ、縫合、歯科用プラグ、組織プラグ、脊椎挿入物、椎間円板、関節、気管支組織挿入物、腹部挿入物、血管挿入物、び出入口封止装置及び膵臓移植装置から成る群から選択される請求項24に記載の組織移植片。
【請求項26】 1又は複数のタンパク質マトリックス材料の1又は複数の層を含む、請求項24又は25に記載の組織移植片。
【請求項27】 請求項1、4〜10、12及び13からなる群から選択される溶媒化され圧縮されたタンパク質マトリックス材料を含んでなる、溶媒化され圧縮されたステント被覆。
【請求項28】 1又は複数のタンパク質マトリックス材料の1又は複数の層を含む、請求項27に記載のステント被覆。
【請求項29】 請求項1、4〜10、12及び13からなる群から選択される溶媒化され圧縮されたタンパク質マトリックス材料を含んでなる、溶媒化され圧縮されているタンパク質マトリックスIUD。
【請求項30】 請求項1、4〜10、12及び13からなる群から選択される溶媒化され圧縮されたタンパク質マトリックス材料を含んでなる、溶媒化され圧縮されたイメージマーカー。
[Claims]
1. A solvated, compressed protein matrix material comprising one or more biocompatible protein materials combined with one or more biocompatible solvents to form a coatable film. Wherein said coatable film is partially dried, formed into an adherent, and compressed to reduce bulk water and form a solvated, compressed protein matrix material.
2. A solvated adhesive protein body comprising one or more biocompatible protein materials combined with one or more biocompatible solvents to form a coatable film. A protein body wherein said coatable film has been partially dried and formed into a solvated adhesive.
3. A method for producing a solvated and compressed protein matrix material, comprising:
(A) preparing a coatable composition comprising one or more biocompatible protein materials and one or more biocompatible solvents;
(B) applying the composition to form a film;
(C) partially drying the coating film until the coating film is formed on the adhesive body,
(D) forming the adhesive and compressing the adhesive to produce a protein matrix material;
A method comprising:
4. The method according to claim 1, wherein the biocompatible protein is elastin, collagen, albumin, keratin, fibronectin, silk, silk fibroin, actin, myosin, fibrinogen, thrombin, aprotinin, antithrombin III, elastin-like block, silk-like block, collagen. The protein matrix material according to claim 1, wherein the protein matrix material is selected from the group consisting of block-like blocks, laminin-like blocks, fibronectin-like blocks, silk-like and elastin-like blocks, collagen-heparin, and collagen-chondroitin. 4. The method of claim 3, wherein
5. The method according to claim 1, wherein the biocompatible solvent is selected from the group consisting of water, dimethyl sulfoxide (DMSO), a biocompatible alcohol, a biocompatible acid, an oil and a biocompatible glycol. The protein matrix material according to claim 2, the protein body according to claim 2 or 4, or the method according to claim 3 or 4.
6. The method of claim 1, wherein the protein matrix material comprises one or more pharmacologically active agents, preferably analgesics, anesthetics, antipsychotics, steroids, antisteroids, corticosteroids, antiglaucoma drugs, antialcoholic drugs, Anticoagulants, genetic substances, antithrombolytics, anticancer drugs, antiparkinsonian, antispasmodic, antiinflammatory, contraceptives, enzymatics, cells, growth factors, antivirals, antibacterials, antifungals, 5. The method according to claim 1, further comprising a pharmacologically active agent selected from the group consisting of hypoglycemic drugs, antihistamines, chemoattractants, neutraceuticals, antiobesity drugs, smoking cessation drugs, midwifery drugs and antiasthmatic drugs. The protein matrix material according to claim 5, the protein body according to claim 2, 4 or 5, or the method according to claim 3, 4 or 5.
7. The protein matrix material, protein body, or method of claim 6, wherein the pharmacologically active agent comprises a secondary mobile drug delivery device.
8. The protein matrix material according to claim 1, further comprising one or more biocompatible polymeric materials, and the protein matrix material according to any one of claims 2, 4 to 7. The protein body according to claim or the method according to any one of claims 3, 4 to 7.
9. The method according to claim 1, wherein the one or more biocompatible polymer substances are epoxy resin, polyester resin, acrylic resin, nylon resin, silicone resin, polyanhydride, polyurethane resin, polycarbonate, poly (tetrafluoroethylene). ), Polycaprolactone, polyethylene oxide, polyethylene glycol, poly (vinyl chloride), polylactic acid, polyglycolic acid, polypropylene oxide, poly (alkylene) glycol, polyoxyethylene, sebacic acid, polyvinyl alcohol, 2-hydroxyethyl methacrylate, poly Methyl methacrylate, 1,3-bis (carboxyphenoxy) propane, lipid, phosphatidylcholine, triglyceride, polyhydroxybutyrate, polyhydroxyvalerate, poly (ethylene oxide) , Polyorthoesters, poly (amino acids), polysinoacrylates, polyphosphazenes, polysulfones, polyamines, poly (amidoamines), fibrin, graphite, soft fluoropolymers, isobutyl-based substances, isopropylstyrene, vinylpyrrolidone, cellulose acetate dibutyrate, silicone 9. The protein matrix material, protein body, or method of claim 8, selected from the group consisting of rubber and copolymers thereof.
10. The protein matrix material is cross-linked by one or more cross-linking agents, wherein the cross-linking reagent is preferably glutaraldehyde, p-azidobenzoyl hidazide, N-5-azido-2-nitrobenzoyloxy. The succinimide, N-succinimidyl 6- [4'azido-2'nitro-phenylamino] hexanoate and 4- [p-azidosalicylamido] butylamine are selected from the group consisting of: The protein matrix material according to claim 1 or the protein body according to any one of claims 2, 4 to 9.
11. The method according to claim 1, wherein the matrix material is printed by crosslinking in a predetermined pattern using a masking or UV light activator. Protein matrix material.
12. The protein matrix material may be a cylinder, cube, sphere, insert, mesh, strip, suture, plug, bandage, disk, joint, outlet seal, tube, particle, sheet, wafer, thread, and patch. The protein matrix material according to any one of claims 1, 4 to 10, wherein the protein matrix material is manufactured in a form selected from the group consisting of:
13. The protein matrix material according to claim 1, wherein the protein matrix material comprises two or more layers of the protein matrix material.
14. The method for producing a protein matrix material according to claim 3, comprising a step of crosslinking the protein matrix material with one or more crosslinking agents.
15. A solvated and compressed drug delivery device comprising a solvated and compressed protein matrix material according to any one of claims 1, 4 to 10.
16. The drug delivery device of claim 15, wherein the drug delivery device is manufactured in a form selected from the group consisting of cylinders, cubes, particles, sheets, wafers, threads, and patches.
17. The drug delivery device according to claim 15, further comprising a release mechanism that releases the pharmacologically active agent after contact with an external stimulus.
18. The drug delivery device according to any one of claims 15 to 17, comprising one or more layers of one or more protein matrix materials.
19. A compressed wound healing device comprising a solvated compressed protein matrix material according to any one of claims 1, 4 to 10, 12 and 13.
20. Bone insert, mesh, strip, suture, dental plug, skin bandage, bandage, tissue plug, spinal insert, intervertebral disc, joint, bronchial tissue insert, abdominal insert, vascular insert 20. The wound healing device of claim 19, wherein the wound healing device is selected from the group consisting of an object, a particle, a biological fastener, a stapler, a hemostat, and a port closure device.
21. The wound healing device according to claim 20, comprising a segment of protein matrix material placed on a non-adherent strip adjacent to an adherent end.
22. Bone insert, mesh, strip, suture, dental plug, skin dressing, bandage, tissue plug, spinal insert, intervertebral disc, joint, bronchial tissue insert, abdominal insert, vascular insert 21. The wound healing device of claim 20, comprising a patch delivery system for delivery of an additional pharmaceutically active agent, connected after the object, particle, biological fastener, stapler, hemostat or port closure device.
23. The wound healing device according to claim 19 or 20, comprising one or more layers of one or more protein matrix materials.
24. A solvated and compressed tissue graft comprising a solvated and compressed protein matrix material selected from the group consisting of: 1, 4-10, 12 and 13.
25. Blood vessels, tubular grafts, tracheal tubes, bronchial tubes, catheter function tubes, lung grafts, gastrointestinal segments, transparent matrix grafts, heart valves, cartilage, tendons, ligaments, skin grafts, particles, bone inserts Objects, meshes, strips, sutures, dental plugs, tissue plugs, spinal inserts, intervertebral discs, joints, bronchial tissue inserts, abdominal inserts, vascular inserts, vent seals and pancreas implants 25. The tissue graft of claim 24 selected from the group.
26. The tissue implant of claim 24 or 25, comprising one or more layers of one or more protein matrix materials.
27. A solvated and compressed stent coating comprising a solvated and compressed protein matrix material selected from the group consisting of: 1, 4-10, 12 and 13.
28. The stent coating of claim 27, comprising one or more layers of one or more protein matrix materials.
29. A solvated and compressed protein matrix IUD comprising a solvated and compressed protein matrix material selected from the group consisting of: 1, 4-10, 12 and 13.
30. A solvated and compressed image marker comprising a solvated and compressed protein matrix material selected from the group consisting of: 1, 4-10, 12 and 13.

JP2001583736A 2000-02-28 2001-02-28 Protein matrix materials, production and their production and use Pending JP2003533468A (en)

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US18542000P 2000-02-28 2000-02-28
US60/185,420 2000-02-28
US22276200P 2000-08-03 2000-08-03
US60/222,762 2000-08-03
PCT/US2001/006502 WO2001087267A1 (en) 2000-02-28 2001-02-28 Protein matrix materials, devices and methods of making and using thereof

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JP2003533468A5 true JP2003533468A5 (en) 2008-04-24

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CA (1) CA2401385C (en)
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