FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to pharmaceutics. There are developed agent for forming a biogel, biogels for hemostasis, wound closure, tissue engineering and targeted drug delivery. The agent contains a soluble carrier whereon a number of fibrinogen-binding groups is immobilised. The biogel that contains fibrinogen molecules and a number of soluble carriers applicable for intravenous and/or local administration; each carrier comprises a number of fibrinogen-binding groups immobilised on the carrier, and each fibrinogen molecule is bound to at least two fibrinogen-binding groups so that the fibrinogen molecules occurs to be bound to each other through the carriers by non-covalent bonds between the fibrinogen-binding groups and the fibrinogen molecules. The biogel containing fibrin monomers and a number of soluble carriers applicable for intravenous and/or local administration, wherein each carrier comprises a number of fibrinogen-binding groups immobilised on the carrier, while the fibrin monomers are bound to each other through the carriers by non-covalent bonds between the fibrinogen-binding groups and the fibrinogen monomers. The biogel containing fibrin and a number of soluble carriers applicable for intravenous and/or local administration, wherein each carrier comprises a number of fibrinogen-binding groups immobilised on the carrier with the fibrin monomers in fibrin are covalently bound to each other by peptide bonds, and the fibrin monomers in fibrin are bound to each other through the carriers by non-covalent bonds between the fibrinogen-binding groups and the fibrinogen monomers. A method for forming the biogel involving a contact of the fibrinogen molecules with a number of soluble carriers. A method for hemostasis by topical administration of the biogel at a haemorrhage or a wound. Using a number of soluble carriers applicable for intravenous and/or local administration. A pharmaceutical formulation for topical administration containing the biogel, agent or a number of soluble carriers.
EFFECT: using the declared invention enables preparing the agents requiring no toxic reagents to be used, have a minimal risk of allergic reactions, and are easy to prepare and use.
2 tbl, 4 dwg, 5 ex
Title | Year | Author | Number |
---|---|---|---|
PEPTIDE DENDRIMERS CONTAINING FIBRINOGEN-BINDING PEPTIDES | 2015 |
|
RU2719562C2 |
HEMOSTATIC COMPOSITIONS | 2016 |
|
RU2744694C2 |
HAEMOSTATIC WOUND DRESSING | 2013 |
|
RU2661036C2 |
FIBRIN/FIBRINOGEN-BINDING CONJUGATE | 2001 |
|
RU2279890C2 |
COMPLEMENTED MATRIXES FOR TREATING BONE FRACTURES | 2006 |
|
RU2422172C2 |
ANTIFIBRIN ANTIBODY FOR USE AS ANTITHROMBOTIC AGENT | 1995 |
|
RU2152801C2 |
IMMUNOASSAY OF SOLUBLE FIBRIN POLYMERS | 1994 |
|
RU2173347C2 |
METHOD FOR PRODUCING EX VIVO SOLUBLE FIBRINOGEN | 2014 |
|
RU2571288C1 |
FIBRINOGEN CONTENT ANALYSIS | 2012 |
|
RU2619256C2 |
COLLAGEN-BASED HEMOSTATIC SPONGE, METHOD FOR ITS OBTAINING, BANDAGE FOR WOUNDS INCLUDING SUCH A SPONGE AND KIT FOR PREPARING BANDAGE FOR WOUNDS | 1997 |
|
RU2193897C2 |
Authors
Dates
2014-01-10—Published
2007-11-27—Filed