Dental implant and production method for said implant
    2.
    发明授权
    Dental implant and production method for said implant 有权
    用于所述植入物的牙种植体和生产方法

    公开(公告)号:US08940320B2

    公开(公告)日:2015-01-27

    申请号:US12091925

    申请日:2006-10-17

    CPC分类号: A61C8/0013 A61C8/0016

    摘要: The invention relates to a dental implant, which comprises a coating at least in those surface areas that come into contact with hard and/or soft tissue when implanted. To ensure that the active ingredient contained in the coating (bisphosphonate) is released into the surrounding tissue or can act in the latter in a controlled manner at the correct speed, the coating is characterized in that it contains bisphosphonate, the respective pharmaceutically compatible salts or esters of the latter, in addition to at least one amphiphilic component, selected from the group containing branched or linear, substituted or unsubstituted, saturated or partially unsaturated C10-C30 alkyl-, alkenyl, alkylaryl-, aryl-, cycloalkyl-, alkylcycloalkyl-, alkylcycloaryl-carboxylates, -phosphates or -sulfates or mixtures thereof and/or a water-soluble ionic polymer component. The invention also relates to a method for producing a dental implant of this type and to a specific composition, which can be used to produce a coating of this type.

    摘要翻译: 本发明涉及一种牙科植入物,其包括至少在植入时与硬组织和/或软组织接触的表面区域中的涂层。 为了确保涂层(二膦酸盐)中包含的活性成分被释放到周围组织中,或者以适当的速度以可控的方式在后者中起作用,其特征在于其包含双膦酸盐,各自的药学上相容的盐或 除了至少一种选自含有支链或直链,取代或未取代的饱和或部分不饱和或不饱和的C 10 -C 30烷基 - ,烯基,烷基芳基 - ,芳基 - ,环烷基 - ,烷基环烷基 - 烷基环芳基羧酸盐,磷酸盐或硫酸盐或其混合物和/或水溶性离子聚合物组分。 本发明还涉及这种类型的牙科植入物的制造方法以及可用于制造这种类型的涂层的特定组合物。

    Bioabsorbable composite material
    3.
    发明授权
    Bioabsorbable composite material 有权
    生物可吸收复合材料

    公开(公告)号:US08642064B2

    公开(公告)日:2014-02-04

    申请号:US10580549

    申请日:2004-11-25

    IPC分类号: A61F2/00 A61F13/00 C09K3/00

    摘要: A method of producing a self-hardening, bioabsorbable composite material, the material produced and its areas of application are described. The method is based on the principal method steps (I) immobilisation of a polymerisation initiator in a microporous pore system of a first partial amount of a bioabsorbable calcium phosphate used in producing the self-hardening, bioabsorbable composite material, (II) immobilisation of a polymerisation activator in the microporous pore system of a second partial amount of the bioabsorbable calcium phosphate used in producing the self-hardening, bioabsorbable composite material and (III) homogeneous mixing of the components according to (I) and (II) with a liquid or paste-form, multi-functional monomer capable of forming a biocompatible, bioabsorbable polymer network or a corresponding monomer mixture and, optionally, with further constituents which modify the properties of the monomer or monomer mixture. The described self-hardening, bioabsorbable composite materials can be used as bone adhesives for the fixing of bone fractures, as shaped pieces of standardised dimensions and as implants that are individual to a patient in the context of regenerative bone healing in humans and animals.

    摘要翻译: 描述了生产自硬化生物可吸收复合材料的方法,所生产的材料及其应用领域。 该方法基于主要方法步骤(I)将聚合引发剂固定在用于生产自硬化生物可吸收复合材料的第一部分量的生物可吸收磷酸钙的微孔孔系统中,(II)固定化 用于生产自硬化生物可吸收复合材料的第二部分量的生物可吸收磷酸钙的微孔孔体系中的聚合活化剂和(III)根据(I)和(II)的组分与液体或 糊状的多功能单体,其能够形成生物相容的生物可吸收的聚合物网络或相应的单体混合物,并且任选地具有改变单体或单体混合物的性质的其它组分。 所描述的自硬化生物可吸收复合材料可用作固定骨折的骨粘合剂,​​作为标准尺寸的成形件,以及在人和动物的再生骨愈合背景下对患者个体的植入物。

    IMPLANT AND METHOD FOR THE MANUFACTURE THEREOF
    4.
    发明申请
    IMPLANT AND METHOD FOR THE MANUFACTURE THEREOF 有权
    其制造方法及其制造方法

    公开(公告)号:US20110053113A1

    公开(公告)日:2011-03-03

    申请号:US12919678

    申请日:2009-02-23

    摘要: What is described is an implant that comprises a coating, at least in areas, in the implanted state in the surface areas that are at least directly in contact with skin and/or soft tissue. The implant is preferably characterized in that the coating comprises both a statin, such as simvastatin, in the hydrolyzed or unhydrolyzed form, or pharmaceutically compatible salts thereof, as well as at least one other component selected from the group consisting of branched or linear, substituted or unsubstituted, saturated or partially unsaturated C10-C30 alkyl, alkenyl, alkylaryl, aryl, cycloalkyl, alkylcycloalkyl, alkylcycloaryl amines or mixtures thereof and/or at least one water-soluble ionic polymer component. A method for production such an implant is also described as well as a composition that can be used in such a method.

    摘要翻译: 描述的是植入物,其至少在表面区域中至少在植入状态的区域中至少直接与皮肤和/或软组织接触的涂层。 优选的植入物的特征在于,所述涂层包含水解或未水解形式的他汀类药物,例如辛伐他汀,或其药学上相容的盐,以及至少一种选自支链或直链,取代的其它组分 或未取代的饱和或部分不饱和的C 10 -C 30烷基,烯基,烷基芳基,芳基,环烷基,烷基环烷基,烷基环芳基胺或其混合物和/或至少一种水溶性离子聚合物组分。 还描述了用于生产这种植入物的方法以及可以在这种方法中使用的组合物。

    Pharmaceutical preparation, method for its production as well as its use
    5.
    发明授权
    Pharmaceutical preparation, method for its production as well as its use 有权
    药物制剂,其生产方法及其用途

    公开(公告)号:US07345024B2

    公开(公告)日:2008-03-18

    申请号:US10600556

    申请日:2003-06-20

    IPC分类号: A61K31/65 A61K31/70

    摘要: The invention relates to hardly soluble antiphlogistic salts and antiphlogistic-antibiotic pharmaceutical preparations and their use. The hardly water soluble antiphlogistic antibiotics salts have as their cationic component one of the antibiotics gentamicin, clindamycin, neomycin, streptomycin, tetracycline, doxicyline, oxytetracycline and rolitetracycline and as their anionic component one of the antiphlogistics ibuprofen, naproxen, indomethacin, dexamethasone-21-phosphate, dexamethasone-21-sulfate, triamcinolone-21-phosphate and triamcinolone-21-sulfate. The antiphlogistic antibiotics salts are used in pharmaceutical preparations as controlled-release antibiotic/antibiotics drugs. The invention describes antiphlogistic-antibiotic pharmaceutical preparations for which mixtures in the solid state of aggregation are used, which are composed of an easily water soluble salt of gentamicin, clindamycin, neomycin, streptomycin, tetracycline, doxicycline, oxytetracycline and/or rolitetracycline and at least one easily water soluble salt of ibuprofen, naproxen, indomethacin, dexamethasone-21-phosphate, dexamethasone-21-sulfate, triamcinolone-21-phosphate and/or triamcinolone-21-sulfate and at least one inorganic and/or organic pharmaceutical adjuvant and which are used as permanent or temporary implants in the form of tablets and/or molded bodies.

    摘要翻译: 本发明涉及难溶性消炎盐和消炎抗生素药物制剂及其应用。 难溶水性消炎抗生素盐作为其阳离子成分,其中一种抗生素是庆大霉素,克林霉素,新霉素,链霉素,四环素,多西环素,土霉素和四环素,作为其阴离子组分之一布洛芬,萘普生,吲哚美辛,地塞米松21- 磷酸盐,地塞米松21-硫酸盐,曲安西龙21-磷酸盐和曲安奈德21-硫酸盐。 消炎抗生素盐用作药物制剂作为控释抗生素/抗生素药物。 本发明描述了使用固体状态的混合物的消炎抗生素药物制剂,其由庆大霉素,克林霉素,新霉素,链霉素,四环素,多西环素,土霉素和/或四环素的易水溶性盐组成,至少 布洛芬,萘普生,吲哚美辛,地塞米松21-磷酸盐,地塞米松21-硫酸盐,曲安西龙21-磷酸盐和/或曲安奈德21-硫酸盐和至少一种无机和/或有机药物佐剂的一种易溶于水的盐, 用作片剂和/或成型体形式的永久或临时植入物。

    ANTIBIOTIC(S)-POLYMER COMBINATION
    6.
    发明申请
    ANTIBIOTIC(S)-POLYMER COMBINATION 审中-公开
    抗生素(S) - 聚合物组合

    公开(公告)号:US20080058733A1

    公开(公告)日:2008-03-06

    申请号:US11931895

    申请日:2007-10-31

    摘要: The present invention relates to an antibiotic(s)-polymer combination, which under physiological conditions guarantees the continuous release of antibiotics over a period of several days and can be used in human and veterinary medicine. The invented antibiotic(s)-polymer combination is wherein in a homogeneous polymer mixture, consisting of one or more hydrophobic polymers from the groups of poly(methacrylic acid esters), the poly(acrylic acid esters) and the poly(methacrylic acid ester-co-acrylic acid esters) and one or more hydrophilic polymers from the group of polyethers, one or more slightly water-soluble antibiotics from the groups of aminoglycoside antibiotics, the lincosamide antibiotics, the tetracycline antibiotics and quinolone antibiotics, possibly an easily water-soluble antibiotic from the groups of aminoglycoside antibiotics, the lincosamide antibiotics and the tetracycline antibiotics, and possibly one or more organic adjuvants are suspended, and that this suspension forms a composite.

    摘要翻译: 本发明涉及抗生素 - 聚合物组合,其在生理条件下保证抗生素在数天内持续释放并可用于人和兽医学。 本发明的抗生素聚合物组合是在由聚(甲基丙烯酸酯),聚(丙烯酸酯)和聚(甲基丙烯酸酯 - 酯)组成的一组或多种疏水聚合物组成的均匀聚合物混合物中, 共聚丙烯酸酯)和一种或多种来自聚醚组的亲水性聚合物,一种或多种来自氨基糖苷类抗生素的轻微水溶性抗生素,氯胺素抗生素,四环素抗生素和喹诺酮类抗生素,可能是易溶于水的 来自氨基糖苷类抗生素组的抗生素,林可素类抗生素和四环素抗生素,以及可能的一种或多种有机助剂悬浮,并且该悬浮液形成复合物。

    Implant and production method for said implant
    8.
    发明授权
    Implant and production method for said implant 有权
    所述植入物的种植体和生产方法

    公开(公告)号:US09050391B2

    公开(公告)日:2015-06-09

    申请号:US12091902

    申请日:2006-10-17

    IPC分类号: A61L27/54 A61F2/00 A61L27/32

    摘要: The invention relates to an implant, e.g. a stent, bone replacement material, a prosthesis, a scaffold or similar, which comprises a coating at least in those surface areas that come into contact with hard and/or soft tissue when implanted. To ensure that the active ingredient contained in the coating (bisphosphonate) is released into the surrounding tissue or can act in the latter in a controlled manner at the correct speed, the coating is characterized in that it contains bisphosphonate, the respective pharmaceutically compatible salts or esters of the latter, in addition to at least one amphiphilic component, selected from the group containing branched or linear, substituted or unsubstituted, saturated or partially unsaturated C10-C30 alkyl-, alkenyl, alkylaryl-, aryl-, cycloalkyl-, alkylcycloalkyl-, alkylcycloaryl-carboxylates, -phosphates or -sulfates or mixtures thereof and/or a water-soluble ionic polymer component. The invention also relates to a method for producing an implant of this type and to a specific composition, which can be used to produce a coating of this type.

    摘要翻译: 本发明涉及植入物,例如 支架,骨置换材料,假体,支架或类似物,其包括至少在植入时与硬组织和/或软组织接触的那些表面区域中的涂层。 为了确保涂层(二膦酸盐)中包含的活性成分被释放到周围组织中,或者以适当的速度以可控的方式在后者中起作用,其特征在于其包含双膦酸盐,各自的药学上相容的盐或 除了至少一种选自含有支链或直链,取代或未取代的饱和或部分不饱和或不饱和的C 10 -C 30烷基 - ,烯基,烷基芳基 - ,芳基 - ,环烷基 - ,烷基环烷基 - 烷基环芳基羧酸盐,磷酸盐或硫酸盐或其混合物和/或水溶性离子聚合物组分。 本发明还涉及一种用于生产这种类型的植入物和特定组合物的方法,其可用于制备这种类型的涂层。

    Implant and method for the manufacture thereof
    9.
    发明授权
    Implant and method for the manufacture thereof 有权
    种植体及其制造方法

    公开(公告)号:US08414958B2

    公开(公告)日:2013-04-09

    申请号:US12919678

    申请日:2009-02-23

    IPC分类号: A61L33/00

    摘要: What is described is an implant that comprises a coating, at least in areas, in the implanted state in the surface areas that are at least directly in contact with skin and/or soft tissue. The implant is preferably characterized in that the coating comprises both a statin, such as simvastatin, in the hydrolyzed or unhydrolyzed form, or pharmaceutically compatible salts thereof, as well as at least one other component selected from the group consisting of branched or linear, substituted or unsubstituted, saturated or partially unsaturated C10-C30 alkyl, alkenyl, alkylaryl, aryl, cycloalkyl, alkylcycloalkyl, alkylcycloaryl amines or mixtures thereof and/or at least one water-soluble ionic polymer component. A method for production such an implant is also described as well as a composition that can be used in such a method.

    摘要翻译: 描述的是植入物,其至少在表面区域中至少在植入状态的区域中至少直接与皮肤和/或软组织接触的涂层。 优选的植入物的特征在于,所述涂层包含水解或未水解形式的他汀类药物,例如辛伐他汀,或其药学上相容的盐,以及至少一种选自支链或直链,取代的其它组分 或未取代的饱和或部分不饱和的C 10 -C 30烷基,烯基,烷基芳基,芳基,环烷基,烷基环烷基,烷基环芳基胺或其混合物和/或至少一种水溶性离子聚合物组分。 还描述了用于生产这种植入物的方法以及可以在这种方法中使用的组合物。

    Bone Formation Agent and Method of Production
    10.
    发明申请
    Bone Formation Agent and Method of Production 有权
    骨形成剂及其生产方法

    公开(公告)号:US20070254011A1

    公开(公告)日:2007-11-01

    申请号:US10580549

    申请日:2004-11-25

    IPC分类号: A61L24/00 A61L27/42 A61L27/46

    摘要: A method of producing a self-hardening, bioabsorbable composite material, the material produced and its areas of application are described. The method is based on the principal method steps (I) immobilisation of a polymerisation initiator in a microporous pore system of a first partial amount of a bioabsorbable calcium phosphate used in producing the self-hardening, bioabsorbable composite material, (II) immobilisation of a polymerisation activator in the microporous pore system of a second partial amount of the bioabsorbable calcium phosphate used in producing the self-hardening, bioabsorbable composite material and (III) homogeneous mixing of the components according to (I) and (II) with a liquid or paste-form, multi-functional monomer capable of forming a biocompatible, bioabsorbable polymer network or a corresponding monomer mixture and, optionally, with further constituents which modify the properties of the monomer or monomer mixture. The described self-hardening, bioabsorbable composite materials can be used as bone adhesives for the fixing of bone fractures, as shaped pieces of standardised dimensions and as implants that are individual to a patient in the context of regenerative bone healing in humans and animals.

    摘要翻译: 描述了生产自硬化生物可吸收复合材料的方法,所生产的材料及其应用领域。 该方法基于主要方法步骤(I)将聚合引发剂固定在用于生产自硬化生物可吸收复合材料的第一部分量的生物可吸收磷酸钙的微孔孔系统中,(II)固定化 用于生产自硬化生物可吸收复合材料的第二部分量的生物可吸收磷酸钙的微孔孔体系中的聚合活化剂和(III)根据(I)和(II)的组分与液体或 糊状的多功能单体,其能够形成生物相容的生物可吸收的聚合物网络或相应的单体混合物,并且任选地具有改变单体或单体混合物的性质的其它组分。 所描述的自硬化生物可吸收复合材料可用作固定骨折的骨粘合剂,​​作为标准尺寸的成形件,以及在人和动物的再生骨愈合背景下对患者个体的植入物。