Isocyanate-terminated lactic acid oligomers as a new means to conjugate functional drugs or polymers with bioresorbable hydrophobic segments

Journal of Bioactive and Compatible Polymers

Volumn 22, Issue 6, 2007, Pages 637-650

  Van Den Berghe, Hélène ^a   Coudane, Jean ^a   Vert, Michel ^a  

^a UNIV MONTPELLIER   (France)

Author keywords

Bioresorbable polymeric synthon; Carbamate derivative; Curtius rearrangement; Lactic acid polymers; Polymer drug conjugates; Urea derivative

Indexed keywords

CONJUGATE FUNCTIONAL DRUGS; HYDROPHOBIC SEGMENTS; POLYLACTIC ACID; POLYMERIZING LACTIDES;

AMINES; DRUG PRODUCTS; LACTIC ACID; POLYMERIZATION; POLYMERS; UREA;

OLIGOMERS;

ACID ANHYDRIDE; AZIDE; CARBAMIC ACID; ISOCYANATE; LACTIC ACID; OLIGOMER; POLY(ALPHA HYDROXY ACID); POLYMER; UNCLASSIFIED DRUG; UREA;

ARTICLE; CHEMICAL REACTION; CURTIUS REARRANGEMENT; DIODE; DRUG BINDING; DRUG DELIVERY SYSTEM; DRUG SOLUBILITY; FLUOROMETRY; HYDROPHOBICITY; POLYMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; REFRACTOMETRY; SPECTROMETRY;

EID: 36348998579     PISSN: 08839115     EISSN: 15308030     Source Type: Journal    
DOI: 10.1177/0883911507084413     Document Type: Article

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