Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
  • A61L33/00—Antithrombogenic treatment of surgical articles, e.g. sutures, catheters, prostheses, or of articles for the manipulation or conditioning of blood; Materials for such treatment
  • A61L33/04—Use of organic materials, e.g. acetylsalicylic acid
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
  • A61L31/00—Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
  • A61L31/14—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
  • A61L31/16—Biologically active materials, e.g. therapeutic substances
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
  • A61L33/00—Antithrombogenic treatment of surgical articles, e.g. sutures, catheters, prostheses, or of articles for the manipulation or conditioning of blood; Materials for such treatment
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
  • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors

Definitions

• the present invention relates to stents containing blood coagulation factor Xa, processes for producing these stents and their use, in particular for the treatment and / or prophylaxis of thromboses and / or restenoses.
• Atherosclerotic coronary diseases are treated, among other things, with the now common method of percutaneous transluminal coronary angioplasty (PTCA).
• PTCA percutaneous transluminal coronary angioplasty
• a balloon catheter is inserted into the narrowed or closed
• the risk of acute restenosis can be reduced by adding platelet aggregation inhibitors.
• the coronary wall can be mechanically supported by a usually cylindrical and expandable braid (stent) which is introduced into the diseased vessel and deployed at the site of the stenosis in order to open the narrowed area and to keep it open by supporting the blood vessel wall , Even if this method can slightly reduce the risk of restenosis, there is currently no convincing therapy available for subacute restenosis.
• Anticoagulants such as heparin are currently used; Platelet aggregation inhibitors such as, for example, aspirin, clopidogrel (Plavix) or ticlopidine (ticlid); or glycoprotein III / ⁇ ia antagonists such as, for example, abciximab, are used systemically in stent treatment.
• Platelet aggregation inhibitors such as, for example, aspirin, clopidogrel (Plavix) or ticlopidine (ticlid); or glycoprotein III / ⁇ ia antagonists such as, for example, abciximab, are used systemically in stent treatment.
• a more recent option for treating restenosis is to administer the active ingredient locally by means of a stent which releases the active ingredient.
• the combination of Active ingredient and stent enable drug treatment and mechanical stabilization in one application.
• stents with anticoagulants enables a high local concentration of active ingredient without the undesirable systemic side effects (e.g. bleeding or stroke).
• stents can be coated with coating materials containing active ingredient.
• the active ingredient is released by diffusion from the paint or by degradation of the paint when using biodegradable paint systems.
• drug-containing stents can be melted by embedding the drug in a polymeric carrier e.g. with the help of injection molding processes.
• the active ingredient is usually released by diffusion.
• Blood coagulation factor Xa inhibitors are particularly suitable as active substances for the treatment and / or prophylaxis of thromboses and restenoses after the PTCA.
• the blood coagulation factor Xa plays a role in the proliferation of vascular smooth muscle cells (VSMC, vascular s ooth muscle cells).
• VSMC vascular smooth muscle cells
• the migration and proliferation of VSMC due to an injury to the endothelium and the resulting formation of a neointima mainly contribute to the formation of restenosis and atherosclerosis in. Platelets, thrombi and other components of the thrombotic process are important factors in the formation of neointima.
• the serine protease thrombin the formation of which is modulated by the blood coagulation factor Xa, has, in addition to its effect in the plasma coagulation system, further cell effects via its specific receptor. Through this mechanism, it activates platelets and acts as a strong mitogen for endothelial cells, VSMC, connective tissue cells and macrophages.
• the mitogenic effect of the blood coagulation factor Xa occurs indirectly via the platelet-based growth factor (PDGF)
• Receptor tyrosine kinase pathway and leads to the activation of the mitogen-activated protein kinases (MAPK, mitogen-activated protein kinases), which are intracellular mediators of cell proliferation.
• MAPK mitogen-activated protein kinases
• VSMC proliferation modulated by the blood coagulation factor Xa influences the reclosure of vessels and the restenosis after angioplasty.
• intimal hyperplasia after vascular endothelial damage and thus the restenosis rate after successful angioplasty can be reduced by reducing the mitogenic effects of blood coagulation factor Xa itself and / or by reducing the formation of the potent mitogen thrombin ( MM Samama, JM Walenga, B. Kaiser, J. Fareed, Specific Factor Xa Inhibitors, in: M. Verstraete, V. Fuster, EJ Topol (ed.), Cardiovascular Thrombosis: Thrombocardiology and Thromboneurology, Philadelphia 1998, pp. 175- 176).
• oxazolidinones of the formula (I) are suitable for this type of treatment, they act in particular as anticoagulants and as selective inhibitors of the blood coagulation factor Xa and are described in detail in WO 01/47919.
• the compounds in general there and especially the compounds specifically mentioned therein are an express part of the description of the present invention.
• the present invention thus relates to stents containing one or more compounds of the formula (I)
• R 1 represents optionally benzo-condensed thiophene (thienyl), which may optionally be substituted one or more times;
• R 2 represents any organic radical
• R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are the same or different and stand for hydrogen or for (-CC 6 ) alkyl
• R 2 represents one of the following groups: A-,
• radical "A” stands for (C 6 -C 1 ) aryl, preferably for (C 6 -C 1 o) aryl, in particular for phenyl or naphthyl, very particularly preferably for phenyl;
• the radical "B” represents a 5- or 6-membered aromatic heterocycle which contains up to 3 heteroatoms and / or hetero chain links, in particular up to 2 heteroatoms and / or hetero chain links, from the series S, N, NO ( Contains N-oxide) and O;
• radical “D” stands for a saturated or partially unsaturated, mono- or bicyclic, optionally benzo-fused 4- to 9-membered heterocycle which has up to three heteroatoms and / or hetero chain links from the series S, SO, SO 2 , N,
• v means either 0 or 1
• R, R and R are identical or different and independently of one another are hydrogen, (C 1 -C 4 ) -alkyl, (C 3 -C 7 ) -cycloalkyl, (CC 4 ) -alkanoyl,
• R 33 (C, -C 6) alkoxy, (C ⁇ -C4) alkoxy- (C ⁇ -C4) alkyl, (C ⁇ -C 4) -Alkoxycar- bonyl- (C ⁇ -C4) alkyl, (-C-C 4 ) -Aminoa_kyl, (C ⁇ -C 4 ) -alkoxycarbonyl, (C 1 -C 4 ) -alkanoyl- (C 1 -C 4 ) -alkyl, (C 3 -C 7 ) -cycloalkyl, (C 2 -C 6 ) alkenyl,
• (-CC 8 ) alkyl which can optionally be substituted by phenyl or acetyl, (C 6 -C 14 ) aryl, (C 5 -C 1 o) heteroaryl, trifluoromethyl, tetrahydrofuranyl or butyrolactone,
• R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are the same or different and are for hydrogen or for
• R 1 represents thiophene (thienyl), in particular 2-thiophene, which may optionally be mono- or polysubstituted by halogen, preferably chlorine or bromine, amino, aminomethyl or (C 1 -C 8 ) -alkyl, preferably methyl, where the (C 1 -C 8 ) -alkyl radical can in turn optionally be substituted one or more times by halogen, preferably fluorine,
• R> 2 represents one of the following groups:
• radical "A” is (C 6 -C 14) -aryl, preferably (C 6 -C 1 o) aryl, in particular phenyl or naphthyl, very particularly preferably phenyl;
• the radical "B” represents a 5- or 6-membered aromatic heterocycle which contains up to 3 heteroatoms and / or hetero chain links, in particular up to 2 heteroatoms and / or hetero chain links, from the series S, N, NO ( NT
• Oxide and contains O
• radical "D” stands for a saturated or partially unsaturated 4- to 7-membered heterocycle which has up to three heteroatoms and or hetero chain links from the series S, SO, SO 2 , N, NO (N-oxide) and O contains;
• the groups “A”, “B” and “D” defined above can each be optionally substituted one or more times with a radical from the group consisting of halogen; trifluoromethyl; oxo; cyano; nitro; carbamoyl; pyridyl; (-C 6
• alkanoyl (C 3 -C 7 ) cycloalkanoyl; (C 6 -C 4 ) -axylcarbonyl; (C 5 -C 10 ) hetero- arylcarbonyl; (CC 6 ) alkanoyloxymethyloxy; -COOR 27 ; -SO 2 R 27 ;
• -C (NR 27 R 28 ) NR 29 ; -CONR 28 R 29 ; -SO 2 NR 28 R 29 ; -OR 30 ; -NR 30 R 31 , (C, -C 6 ) ⁇ alkyl and (C 3 -C 7 ) cycloalkyl,
• v means either 0 or 1
• R 27 , R 28 and R 29 are the same or different and independently of one another are hydrogen, (-CC 4 ) -alkyl or (C 3 -C 7 ) -cycloalkyl,
• R 27 and R 28 or R 27 and R 29 together with the nitrogen atom to which they are attached form a saturated or partially unsaturated 5- to 7-membered heterocycle with up to three, preferably up to two identical or different heteroatoms from the Form group of N, O and S, and
• R 30 and R 31 are the same or different and are, independently of one another, hydrogen, (C 1 -C 4 ) -alkyl, (C 3 -C 7 ) cycloalkyl, (C 1 -C 4 ) alkylsulfonyl,
• -CH 2 C (NR 27 R 28 ) NR 29 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are the same or different and stand for hydrogen or for (-CC 6 ) alkyl
• R 1 stands for thiophene (thienyl), in particular 2-thiophene, which may optionally be mono- or polysubstituted by halogen, preferably chlorine or bromine, or (C 1 -C 8 ) -alkyl, preferably methyl, the (dC ⁇ -Alkyl may optionally be substituted one or more times by halogen, preferably fluorine,
• R 2 stands for one of the following groups: A, AM, DMA, BMA,
• radical "A” represents phenyl or naphthyl, in particular phenyl
• the radical "B” stands for a 5- or 6-membered aromatic heterocycle which contains up to 2 heteroatoms from the series S, N, NO (N-oxide) and O
• the radical “D” stands for a saturated or partially unsaturated 5- or 6-membered heterocycle which contains up to two heteroatoms and or hetero-chain links from the series S, SO, SO 2 , N, NO (N-oxide) and O;
• v is either 0 or 1, preferably 0, and
• R 27 , R 28 and R 29 are the same or different and are independently hydrogen, (-CC 4 ) alkyl or cyclopropyl, cyclopentyl or cyclohexyl
• R and R or R and R together with the nitrogen atom to which they are attached can form a saturated or partially unsaturated 5- to 7-membered heterocycle with up to two identical or different heteroatoms from the group of N, O and S. , and
• R 30 and R 31 are identical or different and independently of one another hydrogen, (dC) alkyl, cyclopropyl, cyclopentyl, cyclohexyl, (dC 4 ) alkylsulfonyl, (C 1 -C 4 ) hydroxyalkyl, (C 1 -C 4 ) aminoalkyl , Di- (C 1 -C 4 ) -alkylamino- (C 1 -C 4 ) -alkyl, (-C-C 3 ) -alkanoyl or phenylcarbonyl,
• R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are the same or different and stand for hydrogen or for (dC 6 ) alkyl
• R 1 represents 2-thiophene, which may optionally be substituted in the 5-position by a radical from the group chlorine, bromine, methyl or trifluoromethyl,
• R represents one of the following groups:
• radical "A” represents phenyl or naphthyl, in particular phenyl
• radical "B” stands for a 5- or 6-membered aromatic heterocycle which contains up to 2 heteroatoms from the series S, N, NO (N-oxide) and O;
• radical “D” stands for a saturated or partially unsaturated 5- or 6-membered heterocycle which has a nitrogen atom and optionally a further heteroatom and / or hetero chain link from the series S, SO, SO 2 and O; or bis to two heteroatoms and / or hetero chain links from the
• arylcarbonyl (C 5 -C 6 ) heteroarylcarbonyl; (C 1 -C 3 ) alkanoyloxymethyloxy; -CONR 28 R 29 ; -SO 2 NR 28 R 29 ; -OH; -NR 30 R 31 ; (dC 4 ) alkyl; and cyclopropyl, cyclopentyl or cyclohexyl,
• v is either 0 or 1, preferably 0, and
• R 27 , R 28 and R 29 are identical or different and independently of one another are hydrogen, (dC 4 ) -A_kyl or else cyclopropyl, cyclopentyl or cyclohexyl
• R and R or R and R together with the nitrogen atom to which they are attached can form a saturated or partially unsaturated 5- to 7-membered heterocycle with up to two identical or different heteroatoms from the group of N, O and S. , and
• R 30 and R 31 are identical or different and independently of one another are hydrogen, (C 1 -C 4 ) alkyl, cyclopropyl, cyclopentyl, cyclohexyl, (dC) alkylsulfonyl, (C 1 -C 4 ) hydroxyalkyl, (C 1 -C 4 ) -Aminoalkyl, di- (dC) -alkylamino- (-C-C 4 ) -alkyl, (C ⁇ -C 3 ) -alkanoyl or phenylcarbonyl,
• R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are the same or different and represent hydrogen or (dC 4 ) alkyl
• Stents containing compounds of the formula (I) are very particularly preferred.
• R 1 represents 2-thiophene which is substituted in the 5-position by a radical from the group chlorine, bromine, methyl or trifluoromethyl,
• R 2 stands for DA-:
• radical "A” represents phenylene
• radical "D” represents a saturated 5- or 6-membered heterocycle
• a ring carbon member in which a ring carbon member can be replaced by a hetero atom from the series S, N and O;
• the previously defined group "A" in the meta position with respect to the linkage to the oxazohdinone can optionally be mono- or disubstituted with a radical from the group of fluorine, chlorine, nitro, amino, trifluoromethyl, methyl or cyano,
• R 3 , R 4 , R 5 , R 6 , R 7 and R 8 represent hydrogen and their pharmaceutically acceptable salts and / or hydrates.
• a stent containing the compound from Example 44 of WO 01/47919 with the following formula is also very particularly preferred
• the present invention describes the use of one or more compounds of the formula (I), optionally in combination with one or more other active ingredients, for the production of a drug-containing release system, in particular of a drug-containing stent.
• the present invention describes a release system, in particular a stent, which contains one or more compounds of the formula (I), if appropriate in combination with one or more other active compounds, which has a targeted release of one or more compounds of the formula (I ) and any other active substances that may be present at the site of action (drug targeting) and are therefore suitable for the prophylaxis and / or treatment of restenosis and / or thromboses, in particular according to PTCA.
• the present invention also describes a method for the treatment and / or prophylaxis of thromboses and / or restenosis, one or more compounds of the formula (I) being used in combination with a stent.
• the compounds of the formula (I) can be used either systemically or preferably in the form of a stent containing compounds of the formula (I).
• the new combination of compounds of the formula (I) with a stent enables more effective treatment and / or prophylaxis of thromboses and / or restenosis.
• Local application of compounds of the formula (I) in combination with a stent makes it possible to reduce the dose of the medicament required to prevent thrombosis and / or restenosis. Undesired systemic effects can be minimized.
• the local concentration can be increased and thus the effectiveness can be increased.
• Thromboses and / or restenosis suitable active ingredients such as, for example and preferably, abciximab, eptifibatide, tirofiban, acetylsalicylic acid, ticlopidine or clopidogrel.
• suitable active ingredients such as, for example and preferably, abciximab, eptifibatide, tirofiban, acetylsalicylic acid, ticlopidine or clopidogrel.
• An additional systemic treatment with compounds of the formula (I) is preferred, in particular by oral administration.
• the stent base body either consisting of metals or non-degradable plastics such as, for example and preferably, polyethylene, polypropylene, polycarbonate, polyurethane and / or polytetrafluoroethylene (PTFE).
• PTFE polytetrafluoroethylene
• stents are coated and / or filled with the compounds of the formula (I).
• compounds of formula (I) in the case of nonmetallic stents can be incorporated directly into the material used to produce the stents.
• carrier materials are mixed with the compounds of the formula (I).
• the carrier materials used are preferably polymeric carriers, in particular biocompatible, non-biodegradable polymers or polymer mixtures, such as, for example and preferably, polyacrylates and their copolymers, for example and preferably poly (hydroxyethyl) methyl methacrylates; Polyvinyl pyrrolidones; Cellulose esters and ethers; fluorinated polymers such as, for example, and preferably PTFE; Polyvinyl acetates and their copolymers; cross-linked and uncross-linked polyurethanes, polyethers or polyesters; polycarbonates; Polydimethylsiloxanes.
• biocompatible, biodegradable polymers or polymer mixtures such as, for example and preferably, polymers or copolymers of lactide and glycolide, or of caprolactone and glycolide; other polyester; polyorthoesters; polyanhydrides; polyaminoacids; Polysacchari.de; polyiminocarbonates; Polyphosphazenes and poly (ether-ester) copolymers are used as polymeric carriers.
• Mixtures of biodegradable and / or non-biodegradable polymers are also suitable as polymeric carriers. These mixtures optimally set the release rate of the active ingredient.
• the mixtures of compounds of the formula (I) and carrier are dissolved, preferably in suitable solvents. These solutions are then applied to the stent using various techniques, such as spraying, dipping or brushing. After subsequent or simultaneous removal of the solvent, the stent with the active ingredient-containing lacquer is formed. Alternatively, mixtures of compounds can also be used of formula (I) and carrier are melted and applied by the same application methods.
• the stents are preferably pretreated in order to enlarge the outer and / or inner stent surface. This increases the loading potential and larger amounts of lacquer (active ingredient / polymer) can be applied.
• lacquer active ingredient / polymer
• For the pretreatment of the stents for example, different etching techniques but also treatments with ionized radiation are used. Likewise, micro-pores or cavities can be created in the stents using various techniques.
• the active substance contents of the stents coated or filled with compounds of the formula (I) are generally from 0.001% by weight to 50% by weight, preferably from 0.01% by weight to 30% by weight, particularly preferably 0.1% to 15% by weight.
• the compounds of the formula (I) can also be incorporated directly, for example as melt embedding, into the stent base body.
• active substance-containing polymeric carrier compositions are processed to the final active substance-containing form by customary processes, for example by injection molding.
• the active ingredient is usually released by diffusion.
• the active substance contents of stents with embedded compounds of the formula (I) are generally from 0.001% by weight to 70% by weight, preferably from 0.01% by weight to 50% by weight, particularly preferably 0.1 % By weight to 30% by weight.
• the compounds of the formula (I) containing stents are optionally additionally coated with a membrane.
• This membrane serves as an example and preferably to control the drug release and / or to protect the active ingredient-containing stents from external influences.

Landscapes

• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Veterinary Medicine (AREA)
• Public Health (AREA)
• General Health & Medical Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• Engineering & Computer Science (AREA)
• Epidemiology (AREA)
• Chemical & Material Sciences (AREA)
• Surgery (AREA)
• Hematology (AREA)
• Medicinal Chemistry (AREA)
• Vascular Medicine (AREA)
• Biomedical Technology (AREA)
• Heart & Thoracic Surgery (AREA)
• Molecular Biology (AREA)
• General Chemical & Material Sciences (AREA)
• Pharmacology & Pharmacy (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Diabetes (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Materials Engineering (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Materials For Medical Uses (AREA)
• Plural Heterocyclic Compounds (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Applications Claiming Priority (3)

Publications (1)

Family

ID=7703557

Family Applications (1)

Country Status (22)

Families Citing this family (15)

Family Cites Families (6)

• 2001
  • 2001-10-24 DE DE10152460A patent/DE10152460A1/de not_active Withdrawn
• 2002
  • 2002-02-11 IL IL16144502A patent/IL161445A0/xx unknown
  • 2002-10-11 CA CA002464290A patent/CA2464290A1/en not_active Abandoned
  • 2002-10-11 EE EEP200400080A patent/EE200400080A/xx unknown
  • 2002-10-11 RU RU2004115757/15A patent/RU2004115757A/ru not_active Application Discontinuation
  • 2002-10-11 AU AU2002340549A patent/AU2002340549B2/en not_active Ceased
  • 2002-10-11 CN CNA028210034A patent/CN1575189A/zh active Pending
  • 2002-10-11 EP EP02774699A patent/EP1439869A1/de not_active Withdrawn
  • 2002-10-11 MX MXPA04003755A patent/MXPA04003755A/es not_active Application Discontinuation
  • 2002-10-11 PL PL02367968A patent/PL367968A1/xx not_active Application Discontinuation
  • 2002-10-11 JP JP2003537695A patent/JP2005506151A/ja active Pending
  • 2002-10-11 US US10/493,552 patent/US20050064006A1/en not_active Abandoned
  • 2002-10-11 WO PCT/EP2002/011402 patent/WO2003035133A1/de active IP Right Grant
  • 2002-10-11 HU HU0401760A patent/HUP0401760A3/hu unknown
  • 2002-10-11 BR BR0213481-0A patent/BR0213481A/pt not_active IP Right Cessation
  • 2002-10-11 KR KR10-2004-7006051A patent/KR20040074977A/ko not_active Application Discontinuation
  • 2002-10-11 NZ NZ532443A patent/NZ532443A/en unknown
• 2004
  • 2004-04-20 ZA ZA200402989A patent/ZA200402989B/en unknown
  • 2004-04-22 EC EC2004005075A patent/ECSP045075A/es unknown
  • 2004-04-23 MA MA27648A patent/MA26341A1/fr unknown
  • 2004-05-13 NO NO20041984A patent/NO20041984L/no not_active Application Discontinuation
  • 2004-05-21 HR HR20040456A patent/HRP20040456A2/hr not_active Application Discontinuation

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events