摘要:
Procede de creation d'un composant optique pour générer, a partir d'une source d'eclairage donnée, un eclairage en champ proche donne L'invention porte sur un procédé de fabrication d'un composant optique (Cnf) configuré pour générer sur une cible d'éclairage (T) en champ proche un éclairage ayant un motif déterminé selon lequel chaque point (i) de la cible d'éclairage (T) reçoit une quantité de lumière (alpha_i) par un éclairage issu d'une source de lumière d'éclairage (S) incident sur le composant optique (Cnf) placé entre la source de lumière d'éclairage (S) et la cible d'éclairage (T).
摘要:
The present invention relates to an isolated humanized protein binding to human Glycoprotein VI (hGPVI ) for treating a GPVI-related condition in a subject in need thereof, wherein said isolated humanized protein is to be administered during at least 2 hours to the subject, preferably during at least 4 to 6 hours.
摘要:
The present invention relates to a method for diagnosing renal cell carcinoma (RCC) in a subject comprising the steps of: i) measuring the expression level of soluble SEMA7A in a fluid sample; ii) comparing the expression measured at step i) with its predetermined reference value, and iii) concluding that the subject suffers from RCC when the expression level of SEMA7A is higher than its predetermined reference value. Inventors found that SEMA7A was detected in all patients despite the disease ontogeny. SEMA7A levels were significantly reduced in patients one month after nephrectomy, and almost inexistent in healthy donors. This reinforces the specific correlation of SEMA7A to renal cell carcinoma. More importantly, SEMA7A was detected in all grades IV of RCC at similar levels, suggesting that it could be an early stage biomarker. Taken altogether, these data define SEMA7A as an early circulating biomarker of renal cell carcinoma, allowing early diagnosis in a non-invasive manner.
摘要:
The present invention relates to a peptide comprising the amino acid sequence QGLIGDIALPRWGALWGDSV (SEQ ID NO: 1). Inventors have tested in wild-type mice a single domain antibody directed against VWF and tagged with an albumin-binding peptide. After giving a single dose intravenously (50 microgram/mouse), VWF levels were increased 8-15 fold for at least 7 days, knowing that the half-life of VWF is about 2-3 hours in a mouse. Moreover, intravenous administration of VWF together with a sdAb fused to an albumin-binding peptide resulted in detectable levels of VWF at 48 and 72 hours after injection, whereas no VWF could be detected when injected in the absence of such sdAb fused to an albumin-binding peptide. Thus, these results show a very long-lasting effect of this new approach.
摘要:
The present invention relates to anti-inflammatory drug formulation. Especially, this invention relates to corticosteroid prodrug nanoparticle. In a first aspect, this invention relates to a nanoparticle comprising a therapeutic agent and a surface coating material. The invention also relates to a process of manufacturing at least one nanoparticle of invention. The invention also relates to pharmaceutical composition and pharmaceutical kits.
摘要:
The present invention relates to isolated single-domain antibodies (sdAb) directed against Antithrombin (AT) to prolong the half-life of the proteins. Inventors have generated isolated single domain antibodies (sdAbs) directed against antithrombin. They observed that in amidolytic assays, sdAbs are incapable of blocking the inhibitory antithrombin activity towards thrombin and factor Xa in the presence of heparin. The different combinations of sdAb were able to block the inhibitory antithrombin activity towards thrombin and factor Xa in mice. Thus, the inventors propose to use different combinations of sdAb to block the inhibitory function of antithrombin in order to promote thrombin generation and thus treat haemophilia and other conditions that are associated with bleeding. Accordingly, the invention relates also to a method of preventing or treating bleeding disorders in a subject in need thereof, comprising administering to said subject a therapeutically effective amount of the single domain antibodies or the drug conjugate of the invention.
摘要:
The present invention relates to an N-Methyl-D-aspartate (NMDA) receptor antagonist, for use in the treatment of diseases associated with angiogenesis such as tumor angiogenesis, ocular neovascular disease, Age-related macular degeneration (AMD).
摘要:
The object of the present invention is an injection device (1) of curing cement (12) for percutaneous vertebroplasty, said device(l) comprising a system (7,8) for generating volumetric flow of said cement (12), and a pipe (17) connecting said injection device (1) to a percutaneous needle (14), said injection device (1) further comprises at least one active heat exchanger (13) located on the pipe (17) for dynamic controlled heating and/or cooling of said cement (12) during the injection, and a passive heat exchanger on the syringe (7).
摘要:
The present invention concerns a combination of (i) a DNA methylation inhibitor, and (ii) a Vitamin D receptor agonist, for simultaneous or sequential use in the treatment of a drug resistant cancer and/or in prevention of tumor relapse in a patient suffering from cancer. The present invention also relates to a combination of (i) a DNA methylation inhibitor, and (ii) a Vitamin D receptor agonist, for increasing, restoring or enhancing sensitivity of a patient suffering from cancer to a chemotherapeutic drug in a patient suffering from cancer.
摘要:
La présente invention concerne des compositions pharmaceutiques comprenant du thiosulfate de sodium dispersé dans une émulsion hydrophile-dans-lipophile, et leur utilisation pour une administration topique pour le traitement d'une calcification ectopique et/ou de ses conséquences chez un individu, le thiosulfate de sodium étant sous la forme d'une composition pharmaceutique comprenant en outre une émulsion hydrophile-dans- lipophile. L'invention concerne également un procédé de préparation de ces compositions pharmaceutiques.