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超支化聚乙烯亚胺-聚天冬氨酸苄酯共聚物的制备及性能 被引量:3

Synthesis,Self-assembly and Gene Transfection Hyperbranched Polyethylenimine-poly (β-benzyl-L-aspartate) Copolymer
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摘要 以超支化聚合物聚乙烯亚胺为引发剂,天冬氨酸苄酯-NCA为单体,利用热开环聚合法合成了超支化聚乙烯亚胺-聚天冬氨酸苄酯共聚物(PEI-PBLA).用核磁共振波谱对PEI-PBLA的化学结构进行了表征.研究了PEI-PBLA在水溶液及有机溶液中的自组装行为.以芘为荧光探针测定了共聚物在水中形成胶束的临界胶束浓度.以甲基橙为客体分子,研究了共聚物胶束的包覆能力,结果表明,共聚物对客体分子的吸附与溶液的pH值有关.研究了共聚物与质粒DNA的复合发现,PEI-PBLA能够很好地与质粒DNA复合,并且可以避免DNA酶的降解,对其起到一定的保护作用.此聚合物在药物传输、可控释放及基因载体等方面都有着潜在的应用价值. A novel amphiphilic and biodegradable copolymer of hyperbranched polyethylenimine-poly(β-benzyl-L-aspartate)(PEI-PBLA) was synthesized by ring opening polymerization of the N-carboxyanhydride of β-benzyl-L-aspartate(BLA-NCA) with hyperbranched polyethylenimine(PEI) as initiator and characterized by 1H NMR.PEI-PBLA copolymers could form micelles in both organic solvent and water.The micelle formation of PEI-PBLA in CH2Cl2 was displayed by extraction of methyl orange indicator from aqueous solutions.As for PEI-PBLA micelle in water,the critical micelle concentration(cmc) was determined by fluorescence probe method and corresponding morphology was observed by TEM.Meanwhile,the complexation of PEI-PBLA with DNA was explored by gel retardation.The studies imply that PEI-PBLA has great potential in many applications,such as drug delivery,gene transfection and so on.
机构地区 东北大学理学院
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2010年第6期1280-1284,共5页 Chemical Journal of Chinese Universities
基金 国家自然科学基金(批准号:20704003) 超分子结构与材料国家重点实验室开放课题(批准号:SKLSSM200906)资助
关键词 超支化聚乙烯亚胺(PEI) 聚天冬氨酸苄酯 高分子胶束 基因载体 Hyperbranched polyethylenimine(PEI) Poly(β-benzyl-L-aspartate) Polymer micelle Gene vector
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参考文献11

  • 1Xu S.,Luo Y.,Haag R..Macromolecular Bioscience[J],2007,7:968-974.
  • 2Neu M.,Fischer D.,Kissel T..Journal of Gene Medicine[J],2005,7:992-1009.
  • 3Tansey W.,Ke S.,Cao X.Y.,Pasuelo M.J.,Wallace S.,Li C..Journal of Controlled Release[J],2004,94:39-51.
  • 4Tian H.,Chen X.,Lin H.,Deng C.,Zhang P.,Wei Y.,Jing X..Chem.Eur.J.[J],2006,12:4305 -4312.
  • 5Tian H.,Xiong W.,Wei J.,Wang Y.,Chen X.,Jing X.,Zhu Q..Biomaterials[J],2007,28:2899-2907.
  • 6田华雨,夏加亮,林浩,陈磊,陈学思,李悦生,景遐斌.两亲性线性-超支化多臂共聚物在水溶液中自组装为阳离子囊泡的研究[J].高等学校化学学报,2006,27(9):1771-1774. 被引量:5
  • 7Masataka Nakanishi,Joon-Sik Park,Woo-Dong Jang,Makoto Oba.Reactive & Functional Polymers[J],2007,67:1361-1372.
  • 8Masayuki Yokoyama,Ayumi Satoh,Yasuhisa Sakurai,Teruo Okano,Yasuhiro Matsumura,Tadao Kakizoe,Kataoka Kazunori.Journal of Controlled Release[J],1998,55:219-229.
  • 9Li Y.,Kwon G.S..Colloids and Surfaces B:Biointerfaces[J],1999,16:217-226.
  • 10Fuller W.D.,Verlander M.S.,Goodaman M..Biopolymers[J],1976,15:1869-1971.

二级参考文献14

  • 1李丽颖,孙平川,要旸,陈铁红,李宝会,金庆华,丁大同.聚(L-丙氨酸)-聚羟乙基谷氨酰胺双嵌段两亲性共聚多肽的合成及其在水溶液中的自组装[J].高等学校化学学报,2005,26(8):1548-1551. 被引量:7
  • 2Xiong X. Y., Tam K. C., Gan L. H.. Macromolecules[J], 2003, 36(26): 9979-9985
  • 3Yu Y. , Zhang L. , Eisenberg A.. Macromolecules[J] , 1998, 31(4) : 1144-1154
  • 4Johnson J. M. , Ha T. , Chu S. et al. Biophysical Journal[J] , 2002, 83(6) : 3371-3379
  • 5Kataoka K. , Harada A. , Nagasaki Y.. Advanced Drug Delivery Reviews[ J ] , 2001 , 47 (1) : 113--131
  • 6Yokoyama M. , Fukushima S. , Uehara R. et al.. Journal of Controlled Release[J] , 1998, 50(1-3) : 79-92
  • 7Brannan A. K., Bates F. S.. Macromolecules[J] , 2004, 37(24): 8816-8819
  • 8Vriezema D. M., Hoogboom J., Velonia K. et al.. Angewandte Chemie-Intemational Edition[J], 2003, 42(7) : 772-776
  • 9Yan D. Y , Zhou Y. F. , Hou J.. Science[J] , 2004, 303(5654) : 65-67
  • 10Zhou Y. F., Yan D. Y.. Angewandte Chemie-International Edition[J], 2004, 43(37): 4896-4899

共引文献4

同被引文献72

  • 1尉继征,林磊,熊伟,祝庆余.新型阳离子基因传递载体PEI-PBLG的细胞转染研究[J].生物工程学报,2007,23(2):229-234. 被引量:6
  • 2Collins SA, Guinn BA, Harrison PT, et al. Viral vector in caner immunotherapy : which vector for which strategy [ J ]. Curr Gene Ther,2008,8(2) :66.
  • 3Merdan T,Kopeeek J, Kissel T. Prospects for cationic polymers in gene and oligonucleotide therapy against cancer [ J ]. Adv Drug Deliv Rev,2002,54 (5) :715.
  • 4Ogris M, Walker G, Blessing L, et al. Tumor - targeted gene therapy : strategies for the preparation of ligand - polyeth) lene glycol- polyethylenimine/DNA complexes [ J]. J Controlled Release, 2003,91(1 -2) :173.
  • 5Wolsehek MF, Thallinger C, Kursa M, et al. Specific systemic nonviral gene delivery to hmnan hepatocellular carcinoma xenografts in SCID mice[ J ]. Hepatology,2002,36 (5) :1006.
  • 6Ogris M, Brunner S, Schuller S, et al. PEGylated DNA/ transferrin. PEI complexes:reduced interaction with blood components, extended circulation in blood and potential for systemic gene delivery [ J ]. Gene Ther, 1999,6 (4):595.
  • 7Blessing L, Kursa M, Holzhauser R, et al. Diferent strategiesfor formation of pegylated EGF - COnjugated PEI/DNA complexes for targeted gene delivery [ J]. Bioconjug Chem, 2001,12 (4) :529.
  • 8Kursa M, Walker GF, Roessler V, et al. Novel shielded transferrin - polyethylene glycol - polyethylenimine/DNA complexes for systemic tumortargeted gene transfer [ J ]. Bioconjug Chem,2003,14( 1 ) :222.
  • 9Kim EM,Jeong HI,Park IK,et al. Monitoring the effect of PEGylation on polyethylenimine /n vivo using nuclear Imaging teehniqu[ J]. Nucl Med Biol,2004,31 (6):781.
  • 10Kichler A, Chillon M, Leborgne C, et al. Intranasal gene delivery with a polyethylenimine - PEG conjugate [ J ]. J Controlled Release,2002,81 ( 3 ) : 379.

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