期刊文献+

基于聚赖氨酸的星形嵌段共聚物对胰岛素的装载与控制释放研究

Investigation of Poly(L-lysine)-based Star-block Copolymers as pH-responsive Nanocarriers for Insulin
下载PDF
导出
摘要 目的:研究合成的星形嵌段共聚物(PEI-PLL-b-mPEG)对胰岛素的装载以及pH敏感释放。方法:将PEI-PLL-b-mPEG与胰岛素混合体系对水溶液进行充分透析以测定装载量;将PEI-PLL-b-mPEG-胰岛素复合体对不同pH值的缓冲溶液进行透析,测定胰岛素的释放速率。结果:PEI-PLL-b-mPEG可实现对胰岛素的快速有效俘获并显示明显的pH敏感释放,同时能保持胰岛素的结构完整和生物活性。结论:合成的PEI-PLL-b-mPEG可用作酸度敏感释放的胰岛素载体。 Objective:To investigate the encapsulation and pH-responsive releasing properties of the synthesized star-block copolymers(PEI-PLL-b-mPEG)towards insulin.Methods:The PEI-PLL-b-mPEG-insulin mixture was dialyzed against PB buffer thoroughly to determine the loading capacities of insulin.The PEI-PLLb-mPEG-insulin complex was dialyzed against buffer solutions with different pH to determine the releasing profiles of the encapsulated insulin.Results:PEI-PLL-b-mPEG showed fast amd efficient encapsulation towards insulin,as well as pH-responsive releasing properties.The insulin released from PEI-PLLb-mPEG demonstrated retained chemical integrity and bioactivity.Conclusion: PEI-PLL-b-mPEG might have potential applications for controlled drug delivery.
出处 《汕头大学医学院学报》 2011年第2期72-74,共3页 Journal of Shantou University Medical College
基金 国家自然科学基金资助项目(50973058)
关键词 星形共聚物 pH敏感释放 胰岛素 star-block copolymer pH-responsive release insulin
  • 相关文献

参考文献9

  • 1BRANCO M C, POCHAN D J, WAGNER N J, et al. The ef- fect of protein structure on their controlled release from an in- jectable peptide hydrogel[J]. Biomaterials, 2010, 31 (35) : 9527 - 9534.
  • 2CHAN A W, NEI.JFEEI.D R J. Tunable semi-synthetic network alginate for absorptiove encapsulation and controned release of protein therapeufics[J]. Biornaterials, 2010, 31 ( 34 ) : 9040 - 9047.
  • 3YE M, KIM S, PARK K. Issues in long-term protein delivery using biodegradable microparticles[J]. J Controlled Release, 2010, 145(3) : 241 - 260.
  • 4KAKIZAWA Y, NISHIO R, HIRANO T, et al. Controlled re- lease of protein drugs from newly developed amphiphilie poly- mer-based micropartieles composed d nanopartieles[J]. J Controlled Release, 2010, 142(1): 8- 13.
  • 5AKAGI T, KANEKO T, KIDA T, et al. Preparation and char- acterizmion of biodegradable nanoparticles based on poly (γ-glutamic acid)with L-phenylalanine as a protein carrier[J]. J Controlled Release, 2005, 108(2- 3): 226- 236.
  • 6SONG Y, ZHOU J, I2 Q, et al. Preparation and characteriza- tion d novel quatemized cellulose nanopartides as protein car- riers[J]. Macromol Biosci, 2009, 9(9): 857-863.
  • 7GAO X, HANG X, WU Z, et al. Synthesis and physicoche- mical characterization of a novel amphlphilic polylactic acid- hyperbranched polyglycerol conjugate for protein delivery[J]. J Controlled Release, 2009, 140(2): 141 - 147.
  • 8CROMMEL1N D J A, DAEMEN T, ACHERPHOF G L, et al. Liposoraes: vehicles for the targeted and controlled delivery of peptides and proteins[J]. J Controlled Release, 1997, 46( 1 - 2) : 165 - 175.
  • 9RODRIGUEZ H J, LECOMMANIDOUX S. Reversible insideout micellizationon of pH-responsive and water-soluble vesicles based on polypepfide dibloek eopolymers[J]. J Am Chem Soe, 2005, 127(7) : 2026 - 2027.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部