Babinot Julien, Renard Estelle, Langlois Valérie
Institut de Chimie et des Matériaux Paris-Est (ICMPE), Systèmes Polymères Complexes, UMR-CNRS 7182, 2-8 rue Henri Dunant, 94320 Thiais, France.
Macromol Rapid Commun. 2010 Apr 6;31(7):619-24. doi: 10.1002/marc.200900803. Epub 2010 Feb 3.
A new synthesis of amphiphilic biodegradable copolymers consisting of hydrophobic poly(3-hydroxyalkanoate) (PHA) backbone and hydrophilic poly(ethylene glycol) (PEG) units as side chains is described. Poly[(3-hydroxyoctanoate)-co-(3-hydroxyundecenoate)] (PHOU) was first methanolyzed and its unsaturated side chains were quantitatively oxidized to carboxylic acid. Esterification with propargyl alcohol led to an alkyne-containing "clickable" PHA in 71% conversion. Its reactivity was successfully demonstrated by grafting azide-terminated PEG chains of 550 and 5 000 g · mol(-1) , respectively. All products were fully characterized using GPC, (1) H, and COSY NMR.
本文描述了一种新型两亲性可生物降解共聚物的合成方法,该共聚物由疏水性聚(3-羟基链烷酸酯)(PHA)主链和亲水性聚(乙二醇)(PEG)单元作为侧链组成。聚[(3-羟基辛酸酯)-共-(3-羟基十一碳烯酸酯)](PHOU)首先进行甲醇解,其不饱和侧链被定量氧化为羧酸。与炔丙醇酯化得到转化率为71%的含炔基“可点击”PHA。通过分别接枝550和5000 g·mol⁻¹的叠氮基封端的PEG链,成功证明了其反应活性。所有产物均使用凝胶渗透色谱法(GPC)、¹H和COSY核磁共振进行了全面表征。