Hua Shou-Hu, Li Yong-Yong, Liu Yun, Xiao Wang, Li Cao, Huang Fu-Wei, Zhang Xian-Zheng, Zhuo Ren-Xi
Key Laboratory of Biomedical Polymers of Ministry of Education & Department of Chemistry, Wuhan University, Wuhan 430072, P. R. China.
Macromol Rapid Commun. 2010 Jan 4;31(1):81-6. doi: 10.1002/marc.200900473. Epub 2009 Sep 24.
A series of amphiphilic poly(L-leucine)-block-poly(ethylene glycol)-block-poly(L-leucine) (PLL-PEG-PLL) hybrid triblock copolymers have been synthesized. All the blocks in this system have good biocompatibility and low toxicity. The PLL-PEG-PLL copolymers could self-assemble into micelles with PLL blocks as the hydrophobic core and PEG blocks as the hydrophilic shell, which were characterized by FT-IR, (1) H NMR, and transmission electron microscopy analysis. The critical micellar concentration of the copolymer was 95.0 mg · L(-1) . The circular dichroism spectrum shows that the PLL segments adopt a unique α-helical conformation, which is found to play an important role in controlling the drug release rate. The drug release could be effectively sustained by encapsulation in the micelles. The copolymers may have potential applications in drug delivery.
一系列两亲性聚(L-亮氨酸)-嵌段-聚(乙二醇)-嵌段-聚(L-亮氨酸)(PLL-PEG-PLL)杂化三嵌段共聚物已被合成。该体系中的所有嵌段都具有良好的生物相容性和低毒性。PLL-PEG-PLL共聚物能够自组装成胶束,其中PLL嵌段作为疏水核心,PEG嵌段作为亲水外壳,通过傅里叶变换红外光谱(FT-IR)、氢核磁共振(¹H NMR)和透射电子显微镜分析对其进行了表征。该共聚物的临界胶束浓度为95.0 mg·L⁻¹。圆二色光谱表明,PLL链段呈现独特的α-螺旋构象,发现其在控制药物释放速率方面起着重要作用。通过包封在胶束中可以有效地实现药物的缓释。这些共聚物在药物递送方面可能具有潜在应用。