Described herein are nanoparticles that are coated with a bilayer of molecules formed from surface binding molecules and amphiphatic molecules. The bilayer coating self assembles on the nanoparticles from readily available materials/molecules. The modular design of the bilayer coated nanoparticles provides a means for readily and efficiently optimizing the properties of the bilayer coated nanoparticle compositions. Also described herein are uses of such nanoparticles in medicine, laboratory techniques, industrial and commerical applications.
COMPOSITIONS AND METHODS COMPRISING CAPURAMYCIN ANALOGUES
申请人:Reddy Venkata
公开号:US20090281054A1
公开(公告)日:2009-11-12
Methods and compositions for treating disease caused by infectious agents, particularly tuberculosis are provided. In particular, methods and compositions comprising substituted derivatives of capuramycin analogs for the treatment of infectious diseases are provided. Also provided are capuramycin analogue formulations comprising PEGylated compounds, including a PEGylated vitamin E derivative, liposomes and nanoparticle carriers. The invention provides methods and compositions comprising a capuramycin analogue and capuramycin analogues in combination with one or more other active agents.
NOVEL 2'-METHYLIDENENUCLEOTIDE COMPOUND, PROCESS FOR PRODUCING THE SAME, AND PHARMACEUTICAL USE THEREOF
申请人:Matsuda, Akira
公开号:EP0690068A1
公开(公告)日:1996-01-03
A novel 2'-methylidenenucleotide compound represented by general formula (I) or a salt thereof, a process for producing the same, and a pharmaceutical use thereof. In said formula, R represents hydrogen or halogen; R¹ and R² represent each independently a fatty acid residue or a hydrocarbon residue; and R³ and R⁴ represent each independently hydrogen, halogen or alkyl. The compound and salts thereof have an excellent antitumor activity against mammals. More specifically, they have a remarkable activity of inhibiting growth of mouse tumors, cultured human tumor cells or human tumors transplanted to nude mice, and hence are efficacious in curing or inhibiting the recurrence of mammalian pulmonary cancer, digestive cancer, mamary cancer, head and neck cancers, gynecologic cancer, urologic cancer, leukemia, melanoma, lymphatic metastatic tumor, and so forth. Also they are useful as an antitumor drug because they have an increased bioavailability and are lowly toxic. Further they have the effects of persistent and increased activities.
PHOTOSENSIBILISATOR-DISPERSION UND VERWENDUNG DERSELBEN
申请人:Universitätsklinikum Regensburg
公开号:EP3225112A1
公开(公告)日:2017-10-04
Die vorliegende Erfindung betrifft eine Photosensibilisator-haltige Dispersion sowie deren Verwendung.
本发明涉及一种含光敏剂的分散体及其用途。
NUCLEIC-ACID-CONTAINING LIPID NANOPARTICLES
申请人:Kyowa Kirin Co., Ltd.
公开号:EP3662913A1
公开(公告)日:2020-06-10
The present invention provides a nucleic acid-containing lipid nanoparticle comprising an analog of a fatty acid ester of glycerol, and a nucleic acid, wherein the analog is not hydrolyzable by a lipase.