6533b834fe1ef96bd129de56
RESEARCH PRODUCT
ALTMET Polymerization of Amino Acid-Based Monomers Targeting Controlled Drug Release
Luana Becker PeresLuana Becker PeresFrederik R. WurmClaudia SayerRafael Muñoz-espíRafael Muñoz-espíManfred WagnerKatharina LandfesterPedro Henrique Hermes De AraújoLaura Preisssubject
Molar massPolymers and PlasticsDieneOrganic Chemistrychemistry.chemical_element02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesRutheniumInorganic ChemistryMiniemulsionchemistry.chemical_compoundMonomerchemistryPolymerizationAmidePolymer chemistryMaterials ChemistryCopolymer0210 nano-technologydescription
Giving the imminent necessity of a new generation of biodegradable and biocompatible polymers prepared from feedstock, the synthesis of a potentially biodegradable amino acid-based copolymer by the alternating diene metathesis (ALTMET) strategy is herein presented. The reaction was tailored to minimize isomerization and deactivation of ruthenium catalysts by intramolecular coordination with the amide carbonyl group of the amino-acid-based monomer. Alternated l-lysine–phosphoester copolymers with molar masses higher than 18 000 g/mol were obtained using Hoveyda–Grubbs second-generation and Umicore M2 catalysts. The copolymer was further used to prepare nanoparticles loaded with rifampicin (up to 50 wt %) by the miniemulsion/solvent evaporation technique. The l-lysine-based copolymer is shown to be a promising material for biomedical applications, such as controlled drug delivery system.
year | journal | country | edition | language |
---|---|---|---|---|
2016-09-07 | Macromolecules |