Resorbable thin membranes
    1.
    发明授权
    Resorbable thin membranes 有权
    可再吸收的薄膜

    公开(公告)号:US07592017B2

    公开(公告)日:2009-09-22

    申请号:US10631980

    申请日:2003-07-31

    IPC分类号: A61K2/00 A01N37/18

    摘要: Resorbable lactide polymer thin membranes are disclosed. The thin membranes are constructed of polylactide resorbable polymers, which are engineered to be absorbed into the body relatively slowly over time in order to reduce potential negative side effects. The membranes are formed to have very thin thicknesses, for example, thicknesses between about 0.010 mm and about 0.300 mm. The membranes can be extruded from polylactide polymers having a relatively high viscosity property, can be preshaped with relatively thick portions, and can be stored in sterile packages.

    摘要翻译: 公开了可再吸收的丙交酯聚合物薄膜。 薄膜由聚丙交酯可吸收聚合物构成,其被设计成随时间相对缓慢地吸收到身体中以减少潜在的负面副作用。 膜形成为具有非常薄的厚度,例如厚度在约0.010mm和约0.300mm之间。 膜可以从具有相对高粘度性质的聚丙交酯聚合物挤出,可以用相对较厚的部分预成型,并且可以储存在无菌包装中。

    Radiation sterilizable antimicrobial ointment and process to manufacture
    2.
    发明授权
    Radiation sterilizable antimicrobial ointment and process to manufacture 失效
    辐射灭菌抗菌软膏及其制造工艺

    公开(公告)号:US5609866A

    公开(公告)日:1997-03-11

    申请号:US163609

    申请日:1993-12-06

    摘要: Sterilized povidone-iodine (polyvinylpyrrolidone-iodine) in an ointment form is obtained by preparation of a mixture of purified water, povidone-iodine, a non-ionic gelling agent, and a non-ionic low suds surfactant. The ointment is a liquid in the temperature range of about 2.degree. C. to 9.degree. C. because of the influence of the non-ionic gelling agent. At room temperature, the mixture forms a free standing ointment which can be sterilized by gamma radiation without degradation of its antimicrobial efficacy, viscosity or shelf life. The ointment is easily prepared by using chilled purified water which maintains the mixture as a liquid while all of the ingredients are mixed together. At room temperature the mixture becomes a free standing ointment.

    摘要翻译: 通过制备纯化水,聚维酮碘,非离子胶凝剂和非离子低泡表面活性剂的混合物,得到软膏形式的灭活聚维酮碘(聚乙烯吡咯烷酮 - 碘)。 由于非离子胶凝剂的影响,软膏是在约2℃至9℃的温度范围内的液体。 在室温下,混合物形成自立式软膏,其可以通过γ辐射灭菌而不降低其抗菌效力,粘度或保质期。 通过使用冷冻纯化水容易地制备软膏,其将混合物保持为液体,同时将所有成分混合在一起。 在室温下,混合物成为独立软膏。

    Method of augmenting soft tissue in mammals
    4.
    发明授权
    Method of augmenting soft tissue in mammals 失效
    增加哺乳动物软组织的方法

    公开(公告)号:US5712252A

    公开(公告)日:1998-01-27

    申请号:US611613

    申请日:1996-03-08

    IPC分类号: A61K38/17 A61K38/00 A61K2/00

    CPC分类号: A61K38/1709

    摘要: The present invention relates to a method of augmenting soft tissue in a mammal which includes injecting keratin into the soft tissue. The method of the present invention may be used to treat incontinence and vesicoureteral reflux.

    摘要翻译: 本发明涉及一种增加哺乳动物软组织的方法,包括将角蛋白注入软组织。 本发明的方法可用于治疗失禁和膀胱输尿管反流。

    Surface treated metallic implant and blasting material
    7.
    发明授权
    Surface treated metallic implant and blasting material 失效
    表面处理金属植入物和爆破材料

    公开(公告)号:US07377943B2

    公开(公告)日:2008-05-27

    申请号:US10480918

    申请日:2002-06-14

    摘要: The invention relates to a metallic implant, which has vitreous-crystalline bioactive material on the surface thereof. According to the invention, a metallic implant base body arranged on the surface of the particles has a bioactive, vitreous-crystalline material consisting of 15-45 wt. % CaO, 40-45 wt. % P2O5, 10-40 wt. % ZrO2 and 0.7-3.5 wt. % fluoride, having apatite and calcium zirconium phosphate as main crystalline and a glass phase as an auxiliary component. Said vitreous crystalline material contains at least 35 wt. % main crystal phases and at least 5-15 wt. % auxiliary compounds. All of the percentage data is expressed in relation to the total weight of the vitreous crystalline material and the particle size of the vitreous crystalline material is between 60-350 μm.

    摘要翻译: 本发明涉及一种在其表面上具有玻璃态生物活性物质的金属植入物。 根据本发明,布置在颗粒表面上的金属植入物基体具有生物活性的玻璃状结晶材料,其由15-45wt。 %CaO,40-45wt。 %P 2 O 5,10-40重量% %ZrO 2和0.7-3.5wt。 %氟化物,磷灰石和磷酸钙锆为主晶,玻璃相为辅助成分。 所述玻璃态结晶材料含有至少35wt。 %主晶相和至少5-15wt。 %辅助化合物。 所有百分比数据都以玻璃态结晶材料的总重量表示,玻璃状结晶材料的粒径在60-350μm之间。

    Preparation-at-use device comprising pre-formed hydrogel product
    9.
    发明授权
    Preparation-at-use device comprising pre-formed hydrogel product 有权
    准备使用的装置包括预先形成的水凝胶产品

    公开(公告)号:US08353399B2

    公开(公告)日:2013-01-15

    申请号:US13282568

    申请日:2011-10-27

    IPC分类号: B65D25/08 A61K2/00

    摘要: Disclosed is a preparation-at-use device comprising: (1) a pre-formed hydrogel component packaged in a first compartment; the pre-formed hydrogel component comprising a gelling agent and a solvent; and (2) a benefit component packaged in a second compartment; the benefit component comprising at least one compound that is unstable when contacted with the pre-formed hydrogel component; wherein the first and second compartments are separately packaged prior to use, and wherein the device comprises means for contacting the pre-formed hydrogel component and benefit component upon use.

    摘要翻译: 公开了一种制备用途装置,包括:(1)预先形成的包封在第一隔室中的水凝胶组分; 预形成的水凝胶组分包含胶凝剂和溶剂; 和(2)包装在第二隔室中的益处组件; 所述有益成分包含至少一种当与预形成的水凝胶组分接触时不稳定的化合物; 其中所述第一和第二隔室在使用之前被分开包装,并且其中所述装置包括用于在使用时接触预先形成的水凝胶组分和有益成分的装置。

    Sphingomyelin detecting probe
    10.
    发明授权

    公开(公告)号:US06995236B2

    公开(公告)日:2006-02-07

    申请号:US10138634

    申请日:2002-05-06

    IPC分类号: A61K2/00 C12N15/09 C12N7/00

    CPC分类号: G01N33/92 C07K14/43536

    摘要: An object of the present invention is to provide a protein useful as a sphingomyelin detecting probe, which specifically recognizes sphingomyelin and has low cytotoxicity. The present invention provides a protein which has an amino acid sequence having, as the amino acid sequence from the 1st to the 48th amino acid, the amino acid sequence from the 1st to the 48th amino acid in Lysenin 1, and as the amino acid sequence from the 49th to the 298th amino acid, the amino acid sequence from the 51st to the 300th amino acid in Lysenin 3; and a protein which is obtained by deleting N terminal and/or C terminal from earthworm toxins Lysenin 1 or 3, and which specifically recognizes sphingomyelin.