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公开(公告)号:US5002930A
公开(公告)日:1991-03-26
申请号:US19564
申请日:1987-02-27
IPC分类号: A61K31/13 , A61K31/415 , A61K31/66 , A61K33/02 , A61K38/38 , A61K38/43 , A61K38/44 , A61K38/49 , A61K47/18 , A61M5/19 , A61M5/20 , A61N1/36
CPC分类号: A61K31/66 , A61K31/13 , A61K31/415 , A61K33/02 , A61K38/49 , A61K47/18 , A61K9/0019 , C12Y304/21068
摘要: The absorption rate of proteins with medicinal properties in the blood is enhanced by administering the protein intramuscularly together with an absorption enhancing agent, e.g. hydroxylamine or a salt thereof.
摘要翻译: 通过与吸收促进剂肌内注射蛋白质来增强血液中具有药用性质的蛋白质的吸收速率,例如, 羟胺或其盐。
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公开(公告)号:US4772585A
公开(公告)日:1988-09-20
申请号:US782441
申请日:1985-10-01
IPC分类号: A61K38/00 , A61K31/13 , A61K31/15 , A61K31/155 , A61K31/17 , A61K31/415 , A61K31/66 , A61K31/80 , A61K38/38 , A61K38/44 , A61K38/49 , A61K45/06 , A61K47/00 , A61K47/18 , A61M5/19 , A61M5/20 , A61N1/375 , A61K37/00
CPC分类号: A61K38/38 , A61K31/13 , A61K31/415 , A61K38/446 , A61K38/49 , A61K47/18 , A61K9/0019 , A61M5/2066 , A61M5/19
摘要: The absorption rate of protein-thrombolytic agents with medicinal properties in the blood is enhanced by administering the protein intramuscularly together with an absorption enhancing agent, e.g. hydroxylamine or a salt thereof.
摘要翻译: 血液中药物性质的蛋白质溶解剂的吸收速率通过与吸收促进剂肌内注射蛋白质而增强。 羟胺或其盐。
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公开(公告)号:US20090270420A1
公开(公告)日:2009-10-29
申请号:US12302721
申请日:2007-06-01
申请人: Burton E. Sobel
发明人: Burton E. Sobel
IPC分类号: A61K31/4965 , A61K31/4439 , A61K31/155
CPC分类号: A61K31/47 , A61K45/06 , A61K2300/00
摘要: The invention relates to methods of inhibiting cardiac PAI-1 by administering a PAI-1 antagonist.
摘要翻译: 本发明涉及通过施用PAI-1拮抗剂来抑制心脏PAI-1的方法。
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4.
公开(公告)号:US06391568B1
公开(公告)日:2002-05-21
申请号:US09115992
申请日:1998-07-15
申请人: David J. Schneider , Burton E. Sobel , Paula B. Tracy , Paul G. Held , Paul D. Hale , Norman R. Alpert
发明人: David J. Schneider , Burton E. Sobel , Paula B. Tracy , Paul G. Held , Paul D. Hale , Norman R. Alpert
IPC分类号: G01N33533
CPC分类号: G01N33/80 , G01N33/86 , G01N2333/7056 , G01N2333/75 , Y10S435/971
摘要: The present invention provides a method for the quantification and assessment of platelet activation in whole blood samples and monitoring of antiplatelet pharmacologic agents. The method for quantifying platelet activation includes exposing platelets to a physiological concentration of an agonist that activates some of the platelets, resulting in the formation of at least one binding site on the surface of the activated platelets, and measuring the activated platelets. The present invention provides a method of assessing specific components of platelet activation.
摘要翻译: 本发明提供了一种定量和评估全血样品中血小板活化和监测抗血小板药理剂的方法。 用于定量血小板活化的方法包括将血小板暴露于激活一些血小板的激动剂的生理浓度,导致在活化血小板的表面上形成至少一个结合位点,并测量活化的血小板。 本发明提供评估血小板活化的特定成分的方法。
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公开(公告)号:US4680708A
公开(公告)日:1987-07-14
申请号:US668245
申请日:1984-11-05
申请人: Hans D. Ambos , Michael E. Cain , Burton E. Sobel
发明人: Hans D. Ambos , Michael E. Cain , Burton E. Sobel
IPC分类号: A61B5/0452 , G06F17/00 , A61B5/04 , G06F15/42
CPC分类号: A61B5/04525 , A61B5/7257
摘要: ECG signals are digitized and a template representative of an arrhythmia free interval for a particular patient is formed. Subsequent ECG signals which match the template are averaged to form averaged ECG signals to reduce noise. A fast Fourier transform (FET) is performed on the terminal 40 millisecond portion of the QRS complex and the ST segment. The 60 db area and 40 Hz intercept of the resultant spectral output are used as a figure of merit in predicting the liklihood of a particular patient experiencing ventricular tachycardia. Alternatively, the FET magnitude is squared to form energy spectra of the ECG signals and a measure of the energy in a first preselected portion such as the 20-50 Hz region is compared with a second preselected portion such as the entire spectra to form a figure of merit for predicting ventricular tachycardia.
摘要翻译: ECG信号被数字化,并且形成代表特定患者的无心律失常区间的模板。 将与模板匹配的后续ECG信号平均以形成平均的ECG信号以减少噪声。 在QRS复合体和ST段的终端40毫秒部分执行快速傅里叶变换(FET)。 将所得光谱输出的60分贝区域和40赫兹截距用作预测患有心室心动过速的特定患者的可能性的品质因数。 或者,FET幅度被平方以形成ECG信号的能谱,并且将第一预选部分(例如20-50Hz区域)中的能量的量度与诸如整个光谱的第二预选部分进行比较以形成图 预测室性心动过速的优点。
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公开(公告)号:US4839170A
公开(公告)日:1989-06-13
申请号:US54898
申请日:1987-05-28
申请人: Stanley Sarnoff , Burton E. Sobel
发明人: Stanley Sarnoff , Burton E. Sobel
CPC分类号: A61K31/415 , A61K38/38 , A61K38/49 , A61K47/18 , A61K9/0019
摘要: A package containing (1) t-PA, (2) methylamine or a non-toxic salt thereof and (3) hydroxylamine or a non-toxic salt thereof, the amount of hydroxylamine or non-toxic salt thereof being sufficient to increase the absorption in the blood of the t-PA when it is administered non-intravascularly to a mammal and the amount of methylamine or non-toxic salt thereof being sufficient to reduce the amount of hydroxylamine or non-toxic salt thereof required to obtain the increased absorption of t-PA and a method for intramuscularly administering the same.
摘要翻译: 包含(1)t-PA,(2)甲胺或其无毒盐和(3)羟胺或其无毒盐的包装,其羟胺或无毒盐的量足以增加吸收 在t-PA的血液中,当其非血管内施用于哺乳动物时,甲胺或其无毒盐的量足以减少获得增加的吸收所需的羟胺或无毒盐的量 t-PA及其肌内给药方法。
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