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    • 3. 发明申请
    • ARZNEIMITTEL ZUR BEHANDLUNG VON VIRALEN HAUT- UND TUMORERKRANKUNGEN
    • 药物的病毒性皮肤病和肿瘤疾病的治疗
    • WO2003043628A1
    • 2003-05-30
    • PCT/EP2002/012919
    • 2002-11-18
    • MEDIGENE AKTIENGESELLSCHAFTCHANG, YunikLATHROP, RobertBÖHM, ErwinGANDER-MEISTERERNST, IreneGREGER, ReginaHOLLDACK, JohannaMOEBIUS, Ulrich
    • CHANG, YunikLATHROP, RobertBÖHM, ErwinGANDER-MEISTERERNST, IreneGREGER, ReginaHOLLDACK, JohannaMOEBIUS, Ulrich
    • A61K31/23
    • A61K9/0014A61K31/23A61K31/353A61K47/06A61K47/10A61K47/14Y10S514/934Y10S514/947Y10S514/967Y10S514/969A61K2300/00
    • Die vorliegende Erfindung betrifft ein Arzneimittel, enthaltend eine Verbindung der allgemeinen Formel wobei, R 1 unabhängig voneinander ein unverzweigter oder verzweigter, gesättigter, einfach oder mehrfach ungesättigter, gegebenenfalls substituierter C 11 -C 21 Alkyl-, Alkylen- oder Alkinylrest, vorzugsweise ein C 11 -C 15 - Alkyl-, Alkylen- oder Alkinylrest, insbesondere ein C 11 -C 13 Alkyl-, Alkylen- oder Alkinylrest, vor allem ein C 13 -Alkylrest bedeutet, und R2 unabhängig voneinander ein unverzweigter oder verzweigter C 1 -C 8 Alkyl Alkylen- oder Alkinylrest, vorzugsweise ein C 1 -C 6 - Alkyl-, Alkylen- oder Alkinylrest, insbesondere ein C 2 -C 4 Alkyl-, Alkylen- oder Alkinylrest, vor allem ein C 3 Alkylrest, ein -[CH 2 -(CH 2 ) m -O] n H Rest mit n = 1 bis 10, vorzugsweise n = 1 bis 5, m = 1 bis 5, vorzugsweise m = 1 bis 3, einen -CH 2 -[CH-(OH)] p [CH 2 -(R 3 )]-Rest, wobei R 3 unabhängig voneinander ein Wasserstoff oder ein Hydroxylrest, p = 1 bis 7, vorzugsweise p = 1 bis 4, ein Pentose-Rest oder ein Hexose-Rest bedeutet, als therapeutisch aktiven Wirkstoff alleine oder zusammen mit einem oder mehreren weiteren pharmazeutischen Wirkstoffen als Kombinationspräparat zur Behandlung von viralen Hauterkrankungen und/oder Tumorerkrankungen, hervorgerufen insbesondere durch humane Papilloma Viren (HPV) und/oder Herpes Viren, sowie eine topisch wirkende Arzneimittelformulierung und deren Verwendung.
    • 本发明涉及含有通式的化合物的药物,其中,R 1彼此独立地直链或支链的,饱和的,单或多不饱和,任选取代的C11-C21烷基,亚烷基或炔基,优选C11-C15烷基 指亚烷基或亚炔基,特别是C11-C13烷基,亚烷基或炔基,特别是C13-烷基,和R 2独立地为直链或支链的C1-C8烷基亚烷基或亚炔基,优选为C1-C6 - - 烷基,亚烷基或炔基,特别是C 2 -C 4烷基,亚烷基或炔基,特别是C 3烷基, - [CH 2(CH 2)Mo]的NH基团,其中n = 1至10,优选n = 1至5,M = 1至5,优选M = 1至3,一个-CH 2 [CH(OH)] p [CH 2(R 3)] - 基团,其中R 3独立地是氢或羟基,p = 1至7,优选地,p = 1至4,戊糖基团或一个己糖 基团,如单独或与一种或多种另外的药物活性物质,作为病毒性皮肤疾病和/或肿瘤疾病的治疗的组合制剂一起治疗活性成分,由人类乳头状瘤病毒(HPV)和/或疱疹病毒,以及局部作用的药物制剂,并引起了特别 它们的使用。
    • 4. 发明申请
    • INTRAVAGINAL TREATMENT OF VAGINAL INFECTIONS WITH METRONIDAZOLE COMPOSITIONS
    • 甲硝唑组合物阴道内治疗阴道感染
    • WO2006050303A2
    • 2006-05-11
    • PCT/US2005/039349
    • 2005-10-26
    • QLT USA INC.EBMEIER, MathewLATHROP, Robert
    • EBMEIER, MathewLATHROP, Robert
    • A61K9/00A61K31/4164A61P31/04
    • A61K9/0034A61K31/4164
    • The present invention provides a buffered non-flowing composition suitable for the treatment of bacterial vaginosis. The composition includes metronidazole in a concentration of about 0.50% (w/w) to about 1.50% (w/w). The metronidazole is present together with a buffer system in a physiologically tolerable medium. The buffer system provides an acidic buffered pH value for the composition in the range of about 5.0 to about 6.0. The present invention also provides for a method for inhibiting a microorganism. The method includes contacting a microorganism with an effective amount of the composition of the present invention, for a period of time effective to inhibit the microorganism. The present invention also provides for a method for treating bacterial vaginosis in a human patient. The method includes intravaginal administration to a patient in need of such treatment an effective amount of the composition the present invention. The composition is introduced into the vagina at least once a day for a time period of at least one day.
    • 本发明提供适用于治疗细菌性阴道病的缓冲不流动组合物。 该组合物包含浓度为约0.50%(w / w)至约1.50%(w / w)的甲硝哒唑。 甲硝唑与缓冲系统一起存在于生理上可耐受的介质中。 缓冲体系为组合物提供约5.0至约6.0的酸性缓冲pH值。 本发明还提供了一种抑制微生物的方法。 该方法包括使微生物与有效量的本发明组合物接触一段有效抑制微生物的时间。 本发明还提供了治疗人类患者的细菌性阴道病的方法。 该方法包括对需要这种治疗的患者进行阴道内给药有效量的本发明组合物。 该组合物每天至少一次引入阴道至少一天的时间。
    • 6. 发明申请
    • ON-LINE APPARATUS AND METHOD FOR DETERMINING ENDOTOXIN LEVELS
    • 在线装置和确定内毒素水平的方法
    • WO2005047858A2
    • 2005-05-26
    • PCT/US2004/037097
    • 2004-11-08
    • CAMBREX BIO SCIENCE WALKERSVILLE, INC.BONEN, Matthew, RichardBERZOFSKY, Ronald, NormanRICHARDSON, Bruce, J.LATHROP, Robert, L., IIIDEN DULK, Bruce, Rodney
    • BONEN, Matthew, RichardBERZOFSKY, Ronald, NormanRICHARDSON, Bruce, J.LATHROP, Robert, L., IIIDEN DULK, Bruce, Rodney
    • G01N
    • G01N1/18G01N33/5302G01N35/1097G01N2035/103
    • An apparatus and method for on-line testing for the presence of an endotoxin within a fluid sample from a fluid line. The apparatus is positioned in fluid communication with a fluid line to perform the on-line fluid testing for the presence of at least one endotoxin. The apparatus can include a housing and a fluid sampling system positioned in fluid communication with the fluid line. The fluid sampling system can comprise a valve for controlling the fluid flow from the fluid line into the fluid sampling system. A fluid flow well is positioned within the housing and in fluid communication with the fluid sampling system. A removable assembly can also be secured within the housing. The removable assembly comprises a plurality of wells for receiving used and unused fluid carrying members that can receive samples from the fluid flow well, a plurality of fluid sample receiving wells, and a plurality of vessel retention positions comprising recesses for securely receiving portions of respective fluid vessels. A detecting system is provided for testing a control sample and a sample of the fluid from the fluid line. The results of these tests are compared in order to determine if the fluid sample is carrying any endotoxins. In an embodiment, fluorescence testing of the sample is compared to that of the control in order to determine if the sample includes an endotoxin.
    • 用于在线测试来自流体管线的流体样品内存在内毒素的装置和方法。 该装置定位成与流体管线流体连通,以进行在线流体测试以存在至少一种内毒素。 该装置可以包括壳体和定位成与流体管线流体连通的流体采样系统。 流体采样系统可以包括用于控制从流体管线流入流体采样系统的流体流量的阀。 流体流动井位于壳体内并与流体采样系统流体连通。 可拆卸的组件也可以固定在壳体内。 可移除的组件包括多个井,用于接收可以从流体井接收样品的多余的未使用流体承载构件,多个流体样品接收孔,以及多个容器保持位置,其包括用于牢固地接收各个流体的部分的凹部 船只。 提供了一种用于从流体管线测试对照样品和流体样品的检测系统。 比较这些测试的结果以确定流体样品是否携带任何内毒素。 在一个实施方案中,将样品的荧光测试与对照的荧光测试进行比较,以确定样品是否包含内毒素。
    • 7. 发明申请
    • AN AUTOMATED SAMPLE PROCESSING APPARATUS AND A METHOD OF AUTOMATED TREATING OF SAMPLES AND USE OF SUCH APPARATUS
    • 自动样品处理装置和自动处理样品的方法和使用这种装置
    • WO2004057308A1
    • 2004-07-08
    • PCT/DK2003/000911
    • 2003-12-19
    • DAKOCYTOMATION DENMARK A/SLATHROP, RobertKEY, MarcFAVUZZI, John
    • LATHROP, RobertKEY, MarcFAVUZZI, John
    • G01N1/31
    • G01N1/312G01N35/00029G01N35/00871G01N35/0092G01N35/0099G01N35/10G01N35/1002G01N2001/317G01N2035/00138G01N2035/00326G01N2035/00534G01N2035/00881
    • An automated staining apparatus (1) and a method for treating samples arranged on carrier means (7) is disclosed, in which portions of two or more selected reagents from a first station (2) containing the reagents are collected individually by means of a robot arm (20) handling a probe (10) and dispensed in a mixing station (9) of the apparatus. After mixing the reagents in the mixing station (9) , e.g. by shaking or rotating the mixing cup containing the reagents, the reagent mixture is applied to selected samples by means of the robot arm (20) and a probe.(10) .By providing a staining apparatus having an automated mixer integrated therein, staining or treatment processes requiring a mixture of unmixable reagents, such as a water based and an oil based reagent, or insoluble reagents, can be performed automatically instead of requiring human interaction or manual performance of some process steps in a much more automated process, and the quality of the staining process may be improved as a desired degree of mixing of reagents may be provided or an optimal application time window for a deteriorating mixture may be reached.
    • 公开了一种自动染色装置(1)和用于处理载体装置(7)上的样品的方法,其中来自含有试剂的第一工位(2)的两种或更多种所选试剂的部分通过机器人分别收集 臂(20)处理探针(10)并分配在装置的混合站(9)中。 将混合站(9)中的试剂混合后, 通过摇动或旋转含有试剂的混合杯,将试剂混合物通过机器人手臂(20)和探针(10)施加到选定的样品上。(10)通过提供具有整合在其中的自动混合器的染色装置,染色或 可以自动执行需要混合不溶性试剂(如水基和油基试剂)或不溶性试剂的处理方法,而不需要在更加自动化的过程中进行人工交互或手动执行某些工艺步骤,而且质量 可以提供染色过程的可能性,因为可以提供试剂的所需程度,或者可以达到恶化混合物的最佳施用时间窗。
    • 8. 发明申请
    • PHARMACEUTICAL COMPOSITION APPLICABLE TO BODY TISSUE
    • 适用于身体组织的药物组合物
    • WO2006042324A2
    • 2006-04-20
    • PCT/US2005037074
    • 2005-10-12
    • QLT USA INCEBMEIER MATHEWLATHROP ROBERT
    • EBMEIER MATHEWLATHROP ROBERT
    • A61K9/08A61K31/135A61K47/38A61P31/10
    • A61K9/7015A61K9/0014A61K31/045A61K31/125A61K31/137A61K31/496A61K31/717A61K47/08A61K47/10A61K47/38
    • The present invention provides a non-water soluble, film-forming composition which adheres to body tissue and forms a pharmaceutical carrier to provide localized delivery of an antifungal agent to a treatment site. The composition will typically include: (a) an alkyl cellulose; (b) a hydroxyalkyl cellulose; (c) a pharmaceutically acceptable polar protic solvent; (d) an antifungal agent selected from the group of naftifine, ciclopirox, terbinafine, pharmaceutically acceptable salts thereof, and combinations thereof; (e) an glycol ether; (f) an antipruritic agent selected from the group of camphor, menthol, butamben picrate, metacresol, benzyl alcohol, camphorated metacresol, juniper tar, phenol, phenolate sodium, resorcinol, camphorated metacresol, carbolic acid, and combinations,; and (g) a solubility enhancing agent, a surfactant, a wetting agent, or a combination thereof. The present invention also provides for the use of the composition composition of the present invention, in treating a fungal infection (e.g., nail fungus) in a mammal afflicted with such an infection.
    • 本发明提供了一种非水溶性成膜组合物,其粘附于身体组织并形成药物载体以提供抗真菌剂向治疗部位的局部递送。 组合物通常包括:(a)烷基纤维素; (b)羟烷基纤维素; (c)药学上可接受的极性质子溶剂; (d)选自脱头芬,环吡酮,特比萘芬,其药学上可接受的盐及其组合的抗真菌剂; (e)乙二醇醚; (f)选自樟脑,薄荷醇,苦丁酸苦参酸,甲酚,苯甲醇,樟脑甲醇,杜松子焦油,苯酚,苯酚钠,间苯二酚,樟脑甲酚,卡拉酸及其组合的止痒剂。 和(g)增溶溶剂,表面活性剂,润湿剂或其组合。 本发明还提供本发明的组合物组合物在治疗患有这种感染的哺乳动物中的真菌感染(例如指甲真菌)中的用途。
    • 10. 发明申请
    • INTRAVAGINAL TREATMENT OF VAGINAL INFECTIONS WITH METRONIDAZOLE COMPOSITIONS
    • 用METRONIDAZOLE组合物治疗阴道感染的腹腔内治疗
    • WO2006050303A3
    • 2006-10-19
    • PCT/US2005039349
    • 2005-10-26
    • QLT USA INCEBMEIER MATHEWLATHROP ROBERT
    • EBMEIER MATHEWLATHROP ROBERT
    • A61K9/00A61K31/4164A61P31/04
    • A61K9/0034A61K31/4164
    • The present invention provides a buffered non-flowing composition suitable for the treatment of bacterial vaginosis. The composition includes metronidazole in a concentration of about 0.50% (w/w) to about 1.50% (w/w). The metronidazole is present together with a buffer system in a physiologically tolerable medium. The buffer system provides an acidic buffered pH value for the composition in the range of about 5.0 to about 6.0. The present invention also provides for a method for inhibiting a microorganism. The method includes contacting a microorganism with an effective amount of the composition of the present invention, for a period of time effective to inhibit the microorganism. The present invention also provides for a method for treating bacterial vaginosis in a human patient. The method includes intravaginal administration to a patient in need of such treatment an effective amount of the composition the present invention. The composition is introduced into the vagina at least once a day for a time period of at least one day.
    • 本发明提供了适用于治疗细菌性阴道病的缓冲非流动组合物。 组合物包含浓度为约0.50%(w / w)至约1.50%(w / w)的甲硝唑。 甲硝唑与缓冲系统一起存在于生理上可耐受的培养基中。 缓冲系统为组合物提供约5.0至约6.0范围内的酸性缓冲pH值。 本发明还提供了抑制微生物的方法。 该方法包括使微生物与有效量的本发明组合物接触一段有效抑制微生物的时间。 本发明还提供了一种在人类患者中治疗细菌性阴道病的方法。 该方法包括对需要这种治疗的患者的阴道内施用有效量的本发明的组合物。 每天至少一次将组合物引入阴道至少一天的时间。