Nikouei Nazila Safaei, Ghasemi Nasim, Lavasanifar Afsaneh
Faculty of Pharmacy and Pharmaceutical Sciences, University of Alberta, Edmonton, Alberta, T6G 2E1, Canada.
Department of Chemical and Materials Engineering, University of Alberta, Edmonton, Alberta, T6G 2V4, Canada.
Pharm Res. 2016 Feb;33(2):358-66. doi: 10.1007/s11095-015-1794-z. Epub 2015 Sep 28.
To assess the potential of triblock copolymers based on poly(ethylene glycol) (PEG) and functionalized poly(ε-caprolactone) as temperature/pH responsive gels for controlled delivery of macromolecules.
Poly(α-carboxylate-co-α-benzylcarboxylate-ε-caprolactone)-PEG-poly(α-carboxylate-co-α-benzylcarboxylate-ε-caprolactone) (PCBCL-PEG-PCBCL) was synthesized through ring opening polymerization of α-benzyl carboxylate-ε-caprolactone by PEG, followed by 30% debenzylation of the lateral blocks. The effect of Tris buffer and pH on the sol-gel transition temperature of PCBCL-PEG-PCBCL was assessed. The temperature/pH responsive release of tetramethylrhodamine-dextran (TMR-D) (10 and 40 kDa) from PCBCL-PEG-PCBCL was investigated.
Replacement of water with Tris buffer reduced PCBCL-PEG-PCBCL sol-gel transition temperature. Thermo-reversible hydrogels were only formed at pHs ≥ 5.0, but PCBCL-PEG-PCBCL transition temperature was not affected by pH above pH 5.0. In contrast to Pluronic F127 that released 100% of TMR-D within 2 h, PCBCL-PEG-PCBCL hydrogel controlled TMR-D release efficiently at pH = 7.4 and 37°C (~27 and 11% TMRD 10 and 40 kDa release within 150 h, respectively). At 50°C or pH = 9.0, TMR-D release was increased slightly, while at room temperature or pH = 5.0, no control over TMR-D release was observed by PCBCL-PEG-PCBCL hydrogel.
PCBCL-PEG-PCBCL hydrogel provides depot release of macromolecules at physiological conditions. This release can be triggered through changes in the temperature or pH.
评估基于聚乙二醇(PEG)和功能化聚己内酯的三嵌段共聚物作为温度/pH响应性凝胶用于大分子药物控释的潜力。
通过聚乙二醇引发α-苄基羧酸己内酯的开环聚合反应合成聚(α-羧酸-co-α-苄基羧酸-ε-己内酯)-PEG-聚(α-羧酸-co-α-苄基羧酸-ε-己内酯)(PCBCL-PEG-PCBCL),随后对侧链进行30%的脱苄基反应。评估了Tris缓冲液和pH对PCBCL-PEG-PCBCL溶胶-凝胶转变温度的影响。研究了PCBCL-PEG-PCBCL对四甲基罗丹明-葡聚糖(TMR-D)(10和40 kDa)的温度/pH响应释放情况。
用Tris缓冲液代替水可降低PCBCL-PEG-PCBCL的溶胶-凝胶转变温度。热可逆水凝胶仅在pH≥5.0时形成,但pH高于5.0时PCBCL-PEG-PCBCL的转变温度不受影响。与在2小时内释放100% TMR-D的普朗尼克F127不同,PCBCL-PEG-PCBCL水凝胶在pH = 7.4和37°C时能有效控制TMR-D的释放(10和40 kDa的TMRD分别在150小时内释放约27%和11%)。在50°C或pH = 9.0时,TMR-D的释放略有增加,而在室温或pH = 5.0时,PCBCL-PEG-PCBCL水凝胶对TMR-D的释放没有控制作用。
PCBCL-PEG-PCBCL水凝胶在生理条件下可实现大分子药物的长效释放。这种释放可通过温度或pH的变化来触发。