期刊文献+

丙交酯-乙交酯共聚物中残留单体的去除 被引量:2

Removing of Residual Monomers in Poly(lactic-co-glycolic acid)
原文传递
导出
摘要 将丙交酯-乙交酯共聚物(PLGA)溶于二氯甲烷中,用稀盐酸为萃取剂(即稀酸萃取法)或乙醇为沉淀剂(乙醇沉淀法)去除PLGA中残留的乙交酯和丙交酯单体。考察了两种方法的工艺参数对单体残留量的影响。结果表明,稀酸萃取法比乙醇沉淀法的去除效果好,但所用盐酸会破坏PLGA;沉淀法能有效避免PLGA的降解,且工艺简单。上述两法的去除效果均优于真空加热法。 The poly (lactic-co-glycolic acid) (PLGA) was dissolved in dichloromethane, then the solution was treated by extraction method with diluted hydrochloric acid or precipitation method with ethanol as precipitation agent to remove the residual monomers in PLGA. The residual monomer contents of glycolide and lactide in PLGA treated by these methods were determined by GC. The results showed the effects of the two methods were both better than vacuum- heating, and the diluted acid extraction method was better than precipitation method, but PLGA would be degraded by the dilute hydrochloric acid. Therefore, the precipitation method was more suitable.
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2013年第9期904-906,共3页 Chinese Journal of Pharmaceuticals
基金 符合GLP要求的新制剂与新释药系统技术平台建设(2012ZX09304004) 注射用可生物降解药用辅料PLGA的产业化研究(2011ZX09401-403-1) 新型缓控释药用辅料开发与应用的关键技术(2011ZX09501-001-03)
关键词 丙交酯-乙交酯共聚物 萃取 沉淀法 残留单体 poly (lactic-co-glycolic acid) extraction precipitation method residual monomer
  • 相关文献

参考文献5

  • 1Mooney D J, Breuer C, McNamara K, et al. Fabricating tubular devices from polymers of lactic and glycolic Acid for tissue engineering [J]. Tissue Eng, 1995, 1 (2) : 107-118.
  • 2Takada S, Uda Y, Toguchi H, et al. Application of a spray drying technique in the production of TRH-containing injectable sustained-release microparticles of biodegradable polymers [JJ. PDA J Pharm Sci Technol, 1995, 49(4): 180-184.
  • 3赵耀明,黄俊豪,陈军武,麦杭珍.生物降解医用材料——聚乙丙交酯的研究[J].合成纤维工业,1997,20(4):1-4. 被引量:32
  • 4焦剑,雷渭媛.高聚物结构、性能与测试[M].1版,北京:化学工、fE出版社,2003:221-227.
  • 5罗丙红,廖凯荣,全大萍,卢泽俭,陈用烈.丙交酯-乙交酯共聚中的酯交换及共聚物结构和性质研究[J].高分子学报,2003,13(6):803-808. 被引量:8

二级参考文献11

  • 1赵耀明,黄俊豪,陈军武,庄慧卿,黄兹国.生物降解材料—聚乙交酯医用纤维的研究[J].华南理工大学学报(自然科学版),1994,22(6):71-79. 被引量:17
  • 2[1]Athanasiou K A,Niederaner G G,Agrawal C M.Biomaterials,1996,17:93~102
  • 3[2]Lu L,Peter S J,Lyman M D,Lai H L,Leite S M,Tamada J A,Vacanti J P,Langer R,Mikos A G.Biomaterials,2000,21:1595~1605
  • 4[3]Kricheldorf H R,Kreiser-Saunder I.Makromol Chem,1998,199:1081~1087
  • 5[4]Kricheldorf H R,Kreiser I.Makromol Chem,1987,188:1861~1873
  • 6[5]Janusz K.Polymer,1996,37(2):201~203
  • 7[6]Maciej B,Piotr D,Janusz K.Polymer Bulletin,1999,42:131~139
  • 8[7]Piotr D,Janusz K,Maciej B.Macromolecules,1999,32:4735~4737
  • 9[8]Piotr D,Janusz K,Henryk J,Henryk J,Maciej B.Macromolecules,2001,34:5090~5098
  • 10[9]Piotr D,Janusz K,Henryk J,Maciej B.Polymer,2002,43:2595~2601

共引文献37

同被引文献17

引证文献2

二级引证文献7

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