http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2019109065-A1

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filingDate 2018-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_09ba0faadac4eb0aad2b6cc44ce67e07
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0bf1e841d6e13c68ae1a5dd8ed7c545e
publicationDate 2019-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2019109065-A1
titleOfInvention Covalent anesthetic-polymer conjugates for prolonged local anesthesia
abstract Anesthetics covalently conjugated onto biodegradable and biocompatible hydrophilic polymers via hydrolysable linkages provide controlled release of local anesthetics in vivo in an effective amount for nerve blockade with reduced toxicity relative to the unconjugated anesthetic agent. The rate of anesthetic release can be tuned by changing the hydrophilicity of the polymer. Exemplary formulations of Poly (glycerol sebacate) (PGS), optionally including Poly ethylene glycol (PEG) polymers conjugated to Tetrodotoxin (TTX) (PGS-PEG-TTX and PGS-TTX), and methods of use thereof are provided Nerve blockade from PGS-PEG-TTX and PGS-TTX was associated with minimal systemic and local toxicity to the muscle and the peripheral nerves. TDP-TTX conjugates homogeneously dispersed into PEG200 are also described. PEG200 not only worked as a medium, but also worked as a chemical permeation enhancer (CPE) to enhance the effectiveness of TTX.
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