Synthesis and characterization of novel poly(γ-benzyl-L-glutamate) derivatives tailored for the preparation of nanoparticles of pharmaceutical interest
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作者:
Barbosa, Ma Elisa Martinez
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机构:Univ Paris Sud, CNRS, UMR 8612, Lab Pharm & Biopharm,Fac Pharm, F-92290 Chatenay Malabry, France
Barbosa, Ma Elisa Martinez
Montembault, Veronique
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机构:Univ Paris Sud, CNRS, UMR 8612, Lab Pharm & Biopharm,Fac Pharm, F-92290 Chatenay Malabry, France
Montembault, Veronique
Cammas-Marion, Sandrine
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机构:Univ Paris Sud, CNRS, UMR 8612, Lab Pharm & Biopharm,Fac Pharm, F-92290 Chatenay Malabry, France
Cammas-Marion, Sandrine
Ponchel, Gilles
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机构:Univ Paris Sud, CNRS, UMR 8612, Lab Pharm & Biopharm,Fac Pharm, F-92290 Chatenay Malabry, France
Ponchel, Gilles
Fontaine, Laurent
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机构:Univ Paris Sud, CNRS, UMR 8612, Lab Pharm & Biopharm,Fac Pharm, F-92290 Chatenay Malabry, France
Fontaine, Laurent
机构:
[1] Univ Paris Sud, CNRS, UMR 8612, Lab Pharm & Biopharm,Fac Pharm, F-92290 Chatenay Malabry, France
[2] Univ Maine, LCOM Chim Polymeres, UCOM2, UMR 6011,CNRS, F-72085 Le Mans 9, France
Four poly(gamma-benzyl-L-glutamate) (PBLG) derivatives bearing at one end specific groups were synthesized by ring-opening polymerization of the corresponding gamma-benzyl-L-glutamate N-carboxyanhydride using different amine-terminated initiators. These moieties were chosen to introduce, on demand, specific functionalities in nanoparticles of pharmaceutical interest. The PBLG and PBLG derivatives were characterized by H-1 NMR, viscosimetry, Fourier transform infrared spectroscopy and differential scanning calorimetry. Nanoparticles smaller than 100 mn in diameter could be easily prepared from these PBLG derivatives by slight modification of a known nanoprecipitation technique. (c) 2006 Society of Chemical Industry.