首页> 外文期刊>Biomaterials >Biodegradability and biocompatibility of a pH- and thermo-sensitive hydrogel formed from a sulfonamide-modified poly(epsilon-caprolactone-co-lactide)-poly(ethylene glycol)-poly(epsilon-caprolactone-co-lactide) block copolymer
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Biodegradability and biocompatibility of a pH- and thermo-sensitive hydrogel formed from a sulfonamide-modified poly(epsilon-caprolactone-co-lactide)-poly(ethylene glycol)-poly(epsilon-caprolactone-co-lactide) block copolymer

机译:由磺酰胺改性的聚(ε-己内酯-丙交酯)-聚乙二醇-聚(ε-己内酯-丙交酯)嵌段共聚物形成的pH和热敏水凝胶的生物降解性和生物相容性

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A pH- and thermo-sensitive block copolymer was synthesized by adding pH-sensitive sulfamethazine oligomers (SMOs) to either end of a thermo-sensitive poly(epsilon-caprolactone-co-lactide)-poly(ethylene glycol)-poly(epsilon-caprolactone-co-lactide) (PCLA-PEG-PCLA) block copolymer. The resulting pH- and thermo-sensitive SMO-PCLA-PEG-PCLA-SMO block copolymer solution did not form a gel at high pH (pH 8.0) or at increased temperatures (ca. 70 degrees C), but did form a stable gel under physiological conditions (pH 7.4 and 37 degrees C). The degradation rate of the pH- and thermo-sensitive block copolymer decreased substantially compared with the control block copolymer of PCLA-PEG-PCLA, due to the buffering effect of the SMO-PCLA-PEG PCLA-SMO sulfonamide groups on the acidic monomer-induced rapid degradation of PCLA-PEG-PCLA. This suitable sol-gel transition and sustained biodegradability of the pH- dand thermo-sensitive SMO-PCLA-PEG-PCLA-SMO block copolymers resolves two of the major drawbacks associated with thermo-sensitive block copolymers, namely premature gelation and rapid degradation. interestingly, SMO-PCLA-PEG PCLA-SMO showed no evidence of cytotoxicity in vitro. However, subcutaneous injection of the pH- and thermo-sensitive block copolymer solution (20 wt% in PBS at pH 8.0) into Sprague-Dawley (SD) rats resulted in rapid, stable gel formation, with the injected hydrogel being completely degraded in vivo in just 6 weeks. The injected hydrogel in vivo presented a typical acute inflammation within 2 weeks, although chronic inflammation was not observed during the first 6-week period. As such, the pH- and thermo-sensitive hydrogel of the SMO-PCLA-PEG-PCLA-SMO block copolymer is a suitable candidate for use in drug delivery systems and cell therapy. (c) 2006 Elsevier Ltd. All rights reserved.
机译:通过将pH敏感的磺胺二甲嘧啶低聚物(SMO)添加到热敏感的聚(ε-己内酯-丙交酯)-聚(乙二醇)-聚(ε-己内酯-共-丙交酯(PCLA-PEG-PCLA)嵌段共聚物。所得的对pH和热敏感的SMO-PCLA-PEG-PCLA-SMO嵌段共聚物溶液在高pH(pH 8.0)或升高的温度(约70摄氏度)下均未形成凝胶,但形成了稳定的凝胶在生理条件下(pH 7.4和37摄氏度)。与PCLA-PEG-PCLA的对照嵌段共聚物相比,pH和热敏嵌段共聚物的降解速率大大降低,这是由于SMO-PCLA-PEG PCLA-SMO磺酰胺基团对酸性单体-诱导PCLA-PEG-PCLA迅速降解。 pH值和热敏SMO-PCLA-PEG-PCLA-SMO嵌段共聚物的这种合适的溶胶-凝胶转变和持续的生物降解性解决了与热敏嵌段共聚物相关的两个主要缺点,即过早胶凝和快速降解。有趣的是,SMO-PCLA-PEG PCLA-SMO没有显示出体外细胞毒性的证据。但是,向Sprague-Dawley(SD)大鼠皮下注射pH敏感的热敏嵌段共聚物溶液(pH 8.0的PBS中20 wt%的PBS)导致快速,稳定的凝胶形成,并且注射的水凝胶在体内完全降解在短短6周内。尽管在最初的6周内未观察到慢性炎症,但体内注射的水凝胶在2周内呈现出典型的急性炎症。这样,SMO-PCLA-PEG-PCLA-SMO嵌段共聚物的pH敏感和热敏感的水凝胶是用于药物递送系统和细胞疗法的合适候选者。 (c)2006 Elsevier Ltd.保留所有权利。

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