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Nanoscaled polyion complex micelles for targeted delivery of recombinant hirudin to platelets based on cationic copolymer
- Source :
- Molecular pharmaceutics. 7(3)
- Publication Year :
- 2010
-
Abstract
- Polyion complex (PIC) micelles based on methoxy poly(ethylene glycol)-grafted-chitosan (mPEG-g-chitosan) and Arg-Gly-Asp conjugated poly(ethylene glycol)-grafted-chitosan (RGD-PEG-g-chitosan) were designed as carriers for platelet-targeted delivery of recombinant hirudin variant-2 (rHV2). The rHV2-loaded plain PIC micelles (mPIC micelles) and RGD conjugated PIC micelles (RGD-PIC micelles) were successfully prepared with mean size of 30.9 +/- 0.5 nm and 41.9 +/- 1.8 nm, and their encapsulation efficiencies were 76.90 +/- 0.84% and 81.08 +/- 0.85%, respectively. The pharmacokinetics experiments showed that the mean retention time (MRT) of rHV2 encapsulated in both kinds of micelles was significantly prolonged, especially for mPIC micelles. The confocal laser scanning microscopy intuitively proved the specific binding of RGD-PIC micelles to platelets. The efficacies of rHV2-loaded RGD-PIC micelles were greatly better than those of rHV2-loaded mPIC micelles and rHV2 solution in aspect of anticoagulation and inhibition of platelet aggregation. These results suggested platelet-targeting specificity of RGD-PIC micelles and that RGD-PIC micelles could potentially be used as a carrier for platelet-targeted delivery and long circulation of rHV2.
- Subjects :
- Blood Platelets
Male
endocrine system
Platelet Aggregation
Polymers
Pharmaceutical Science
Conjugated system
Micelle
Polyethylene Glycols
Rats, Sprague-Dawley
chemistry.chemical_compound
Hirudin Therapy
Cations
Drug Discovery
Polymer chemistry
Copolymer
Molecule
Animals
Platelet
Micelles
Chitosan
Microscopy, Confocal
Molecular Structure
Cationic polymerization
Anticoagulants
biochemical phenomena, metabolism, and nutrition
Hirudins
Recombinant Proteins
Rats
Recombinant Hirudin
chemistry
Molecular Medicine
Ethylene glycol
Oligopeptides
Subjects
Details
- ISSN :
- 15438392
- Volume :
- 7
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Molecular pharmaceutics
- Accession number :
- edsair.doi.dedup.....41c5b5013cff78edd8c34c1bf80ba5dd