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Polysaccharide arabinogalactan from larchLarix sibiricaas carrier for molecules of salicylic and acetylsalicylic acid: preparation, physicochemical and pharmacological study
- Source :
- Drug Delivery. 22:400-407
- Publication Year :
- 2014
- Publisher :
- Informa UK Limited, 2014.
-
Abstract
- Inclusion complexes of salicylic acid (SA) and acetylsalicylic acid (aspirin, ASA) with polysaccharide arabinogalactan (AG) from larch wood Larix sibirica and Larix gmelinii were synthesized using mechanochemical technology. In the present study, we have investigated physicochemical properties of the synthesized complexes in solid state and in aqueous solutions as well as their anti-aggregation and ulcerogenic activity. The evidence of the complexes formation was obtained by nuclear magnetic resonance (NMR) relaxation technique. It was shown that in aqueous solution the molecules of SA and ASA are in fast exchange between the complex with AG macromolecules and solution. The stability constant of aspirin complex was calculated. It was shown that mechanochemically synthesized complexes are more stable when compared to the complex obtained by mixing solutions of the components. Complexes of ASA show two-fold increase of anti-platelet effect. It allows to reduce the dose of the antithrombotic drug and its ulcerogenic activity. These results substantiate the possibility to design new preparations on the basis of ASA with increased activity and safety.
- Subjects :
- Male
Larix gmelinii
Platelet Aggregation
Surface Properties
Administration, Oral
Pharmaceutical Science
Larix
Polysaccharide
Galactans
Phase Transition
chemistry.chemical_compound
Arabinogalactan
Animals
Organic chemistry
Rats, Wistar
chemistry.chemical_classification
Drug Carriers
Aqueous solution
Aspirin
biology
General Medicine
biology.organism_classification
Solutions
Solubility
chemistry
Larix sibirica
Stability constants of complexes
Salicylic Acid
Platelet Aggregation Inhibitors
Salicylic acid
Macromolecule
Subjects
Details
- ISSN :
- 15210464 and 10717544
- Volume :
- 22
- Database :
- OpenAIRE
- Journal :
- Drug Delivery
- Accession number :
- edsair.doi.dedup.....9de3faf8b76cb37a5409d0273028434a
- Full Text :
- https://doi.org/10.3109/10717544.2014.884655