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两亲性嵌段共聚物PLA-b-PDMAEMA的合成及性能研究 被引量:2

Synthesis and Properties of Amphiphilic Poly-Lactide-b-Poly ( N , N-dimethylamino-2-ethyl methacrylate ) Copolymer
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摘要 以2-苄基三硫代碳酸酯基乙醇为引发剂,在辛酸亚锡催化下引发丙交酯(LA)开环聚合,合成大分子链转移剂PLA macro-CTA,加入第二单体聚甲基丙烯酸N,N-二甲氨基乙酯(DMAEMA),通过可逆-加成-断裂链转移(RAFT)自由基聚合,得到两亲性嵌段共聚物PLA-b-PDMAEMA。采用核磁共振光谱(1 HNMR和13 CNMR)、红外光谱(FT-IR)及凝胶色谱(GPC)对合成的共聚物化学结构进行表征,并通过接触角测试和热重分析(TGA)对其进行性能测试。结果表明成功合成了嵌段共聚物且分子量分布指数较窄;引入PDMAEMA链段后聚乳酸的热稳定性和亲水性得到提高。 A macro-chain transfer agent(PI.A macro CTA) was synthesized by the ring opening polymerization of lactide(LA) in the presence of stannous octoate as catalyst and 2-(ben-zylsulfanylthiocarbonylsulfanyI) ethanol as initator, then chain extension of PLA via reversible iaddition-fragmentation chain transfer (RAFE') radical polymeriza- tion of N, N-dimethylamino-2 ethyl methacrylate(DMAEMA) resulted in the formation of amphiphilic PLA-b-PD- MAEMA copolymer. The nuclear magnetic resonance spectroscopy(l HNMR and 13CNMR), fourier transform infra- red spectroscopy(FT-IR) and gel permeation chromatography(GPC) were employed to characterize the structure of the polymers, and performance test was carried out by contact angle meter and thermogravimetric analysis (TGA). The results showed that the copolymer with narrow molecular mass distribution was successfully synthesized. The hy- drophilicity and thermal stability of polylactide were improved due to the influence of PDMAEMA.
出处 《材料导报》 EI CAS CSCD 北大核心 2013年第8期74-77,共4页 Materials Reports
基金 安徽省教育厅自然科学重点研究项目(KJ2012A018) 安徽大学科研训练计划项目(KYXL20110024)
关键词 两亲性嵌段共聚物 RAFT聚合 性能 amphiphilic block eopolymer, RAFT polymerization, property
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  • 1AliTuncel Ender Unsal Hüseyin Cicek.pH-sensitive uniform gel beads for DNA adsorption[J].Journal of Applied Polymer Science,2000,(14):3154-3161.
  • 2Naiwa HS. Handbook of Nanostructured Material and Nanotechnology [M]. Vol 5, Austrilia: Academic Press, 2000.577-626.
  • 3Kataoka K, Harada A, Nagasaki Y. Block copolymer micelles for drug delivery: design, characterization and biological significance [J]. Adv Drug Deliv Rev, 2001, 47 (1): 113-131.
  • 4Torchilin VP. Structure and design of polymeric surfactantbased drug delivery systems [J]. J Controlled Relaese, 2001,73 (2-3): 137-172.
  • 5Kabanov AV, Batrakova EV, Alakhov VY. Pluronic block copolymers as novel polymer therapeutics for drug and gene delivery [J]. J Controlled Release, 2002, 82 (2-3): 189-212.
  • 6Inoue T, Chen G, Nakamae K, et al. An AB block copolymer of oligo (methyl methacrylate) and poly (acrylic acid) for micellar delivery of hydrophobic drugs [J]. J Controlled Release, 1998, 51 (2-3): 221-229.
  • 7Harada A, Kataoka K. Chain length recognition: core-shell supramolecular assembly from oppositely charged block copolymers [J]. Science, 1999, 283 (5398): 65-67.
  • 8Lemieux P, Guerin N, Paradis G, et al. A combination of poloxamers increase gene expression of plasmid DNA in skeletal muscle[J]. Gene Ther, 2000, 7 (11): 986-991.
  • 9Yamamoto Y, Nagasaki Y, Kato Y, et al. Long-circulating poly(ethylene glycol) -poly (DL-lactide) block copolymer micelles with modulated surface charge [J]. J Controlled Release, 2001,77 (1-2): 27-38.
  • 10Lavasanifar A, Samuel J, Kwon GS. Micelles self-assembled from poly (ethylene oxide) -block-poly (N-hexyl stearate L-aspartamide) by a solvent evaporation method: effect on the solubilization and heamolytic activity of amphotericin B[J]. J Controlled Rele

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  • 1Hiekey R J, Haynes A S, Kikkawa J M, eta[. Controliing the selassembly structure of magnetic nanoparticles and amphiphilic block-copolymers: From micelles to vesicles [J]. J Am Chem Soc,2002,133:1517.
  • 2Ezhilarasi P N, Karthik P, Chhanwal N, et al. Nanoencap- sulation techniques for food bioactive components: A review [J]. Food Bioprocess Techn, 2012,6 (3) : 628.
  • 3Gref R, Domb A, Quellec P. The controlled intravenous de- livery of drugs using PEG-coated sterically stabilized nanospheres[J].AdvDrugDeliverRev,2012,64:316.
  • 4Gaucher G, Dufresne M H, Sant V P, et al. Block copoly- mer micelles: Preparation, characterization and application in drug delivery[J]. J Controlled Release, 2005,109 : 169.
  • 5Martina M S, Fortin J P, Mnager C, et al. Generation of superparamagnetic liposomes revealed as highly efficient MRI contrast agents for in vivo imaging. [J]. J Am Chem Soc, 2005,127 : 10676.
  • 6Ai H, Flask C, Weinberg B, et al. Magnetite-loaded poly meric micelles as ultrasensitive magnetic-resonance probes [J]. Adv Mater, 2005,17.. 1949.
  • 7Khemtong C, Kessinger C W, Ren J, et al. In vivo off-reso- nance saturation magnetic resonance imaging of alphavbeta3- targeted superparamagnetic nanoparticles. [J]. Cancer Res, 2009,69(4):1651.
  • 8Park J H, Maltzahn G V, Ruoslahti E, et al. Supporting in- formation for: Micellar hybrid nanopartieles for simultane- ous magneto-fluorescent imaging and drug delivery[J]. An ew (;hem Int Ed, 2008,120 (38) : 7394.
  • 9Gong C Y, Shi S, Dong P W, et al. Synthesis and charac- terization of PEG-PCL-PEG thermosensitive hydrogel[J]. Int J Pharm, 2009,365 (1-2) .. 89.
  • 10田浤,姚文兵.聚乙二醇化技术在药物转运系统中的研究进展[J].中国药科大学学报,2008,39(4):379-384. 被引量:7

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