摘要:
The present invention relates to pharmaceutical compositions in form of solid lipidic nanospheres able to fast penetrate into the cells, comprising as an active substance a lipidic substance consisting of an ester of α-tocopherol or δ-tocopherol or of cholesterol or of glycerol with a carboxylic acid selected from acetic acid, propionic acid, butyric acid and succinic acid, useful in the treatment of tumoral pathologies and of Mediterranean anaemia.
摘要:
A novel method for the mucosal administration of a substance to a mammal is provided. The method comprises contacting a mucosal surface of the mammal with the substance in combination with a Biovector. The Biovector has a core that comprises a natural polymer, or a derivative or a hydrolysate of a natural polymer, or a mixture thereof. A preferred natural polymer is a polysaccharide or an oligosaccharide. The core is optionally coated with an amphiphilic compound, such as a lipid.
摘要:
The present invention relates to pharmaceutical compositions in form of solid lipidic nanospheres able to fast penetrate into the cells, comprising as an active substance a lipidic substance consisting of an ester of α-tocopherol or δ-tocopherol or of cholesterol or of glycerol with a carboxylic acid selected from acetic acid, propionic acid, butyric acid and succinic acid, useful in the treatment of tumoral pathologies and of Mediterranean anaemia.
摘要:
A self-assembling nanoparticle drug delivery system for the delivery of drugs including peptides, proteins, nucleic acids or synthetic chemical drugs is provided. The self-assembling nanoparticle drug delivery system described herein includes viral capsid proteins, such as Hepatitis B Virus core protein, encapsulating the drug, a lipid bi-layer envelope and targeting or facilitating molecules anchored in the lipid bilayer. A method for construction of the self-assembling nanocparticle drug delivery system is also provided.
摘要:
This invention relates to a 2-acylaminopropanol compound represented by the formula (I): (wherein R 1 represents a phenyl group which may be substituted by 1 to 3 same or different substituents selected from alkyl, alkoxy, hydroxyl, hydroxyalkyl and nitro, R 2 represents the following formula (II), (III), (IV), (V) or (VI), (wherein R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , m and p are those defined in the specification) R 11 represents a hydrogen atom or a hydroxyl group, and n represents an integer of 3 to 15) or a pharmaceutically acceptable salt thereof.
摘要:
A novel method for the mucosal administration of a substance to a mammal is provided. The method comprises contacting a mucosal surface of the mammal with the substance in combination with a Biovector. The Biovector has a core that comprises a natural polymer, or a derivative or a hydrolysate of a natural polymer, or a mixture thereof. A preferred natural polymer is a polysaccharide or an oligosaccharide. The core is optionally coated with an amphiphilic compound, such as a lipid.
摘要:
A 2-acylaminopropanol compound represented by general formula (I) or a pharmaceutically acceptable salt thereof, and a medicinal composition containing the same as the active ingredient and being efficacious as an antiviral agent and a remedy for nervous diseases, wherein R1 represents phenyl which may be substituted by one to three same or different substituents selected from among alkyl, alkoxy, hydroxy, hydroxyalkyl and nitro; R2 represents a group represented by any of general formulae (II) through (VI) wherein, R?3, R4, R5, R6, R7, R8, R9¿, m and p are each as defined in the specification; R11 represents hydrogen or hydroxy; and n represents an integer of 3 to 15.