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化学进展 2010, Vol. 22 Issue (04): 669-676 前一篇   后一篇

• 综述与评论 •

基于环糊精的高度支化聚合物*

田威;范晓东**;孔杰;刘郁杨;张卫红   

  1. (西北工业大学理学院应用化学系 西安 710072)
  • 收稿日期:2009-04-21 修回日期:2009-06-02 出版日期:2010-04-24 发布日期:2010-03-30
  • 通讯作者: 范晓东 E-mail:xfand@126.com
  • 基金资助:

    高载药智能型超支化环糊精高分子的设计、合成及药控释放研究

Cyclodextrin-Based Highly Branched Polymers

Tian Wei; Fan Xiaodong**; Kong Jie; Liu Yuyang; Zhang Weihong   

  1. (Department of Applied Chemistry, School of Science, Northwestern Polytechnical University, Xi’an 710072, China)
  • Received:2009-04-21 Revised:2009-06-02 Online:2010-04-24 Published:2010-03-30
  • Contact: Fan Xiaodong E-mail:xfand@126.com

环糊精(CD)与高度支化聚合物都存在空腔结构,若将两者结合起来可构筑出含有两种不同疏水空腔且具有特异物理化学功能的高分子体系,并有望在分子包合与识别、药物控释、基因传输等领域得到新的应用。本文根据高度支化聚合物与环糊精结合方式的不同,从以环糊精为核的高度支化聚合物、外端悬挂环糊精的高度支化聚合物、高度支化聚合物的结构单元与环糊精包合、环糊精与客体分子包合后自组装成高度支化聚合物,以及用功能化的环糊精单体合成超支化聚合物等5个方面对其研究进展进行了总结和评述,并在此基础上展望了该类聚合物的研究方向和发展趋势。

Both of cyclodextrins (CDs) and highly branched polymers including hyperbranched and dendrimers possess molecule cavities in their architectures. Therefore, if the combination of two types of molecular cavities can be obtained in a common polymer structure, it will not only possess some interesting characters in the research of relationship between properties and structure, but also may endow some important applications in various fields, such as inclusion technologies, drug delivery system and gene delivery. In this paper, the investigations and applications on the combination of CDs and highly branched polymers are summarized according to the different combination types. The main content includes five aspects as follow: (1) highly branched polymers with a cyclodextrin core; (2) highly branched polymers carrying cyclodextrins as the pendent groups; (3) inclusion complexation between the interior core, terminal Group or monomer of highly branched polymers and cyclodextrins; (4) highly branched polymers from the self-assembly of cyclodextrins; (5) hyperbranched polymers based on the functional cyclodextrin monomers. In addition, new research trends are expected based on the progress of this kind of polymer.

Contents
1 Introduction
2 Highly branched polymers with a cyclodextrin core
3 Highly branched polymers carrying cyclodextrins as the pendent groups
4 Inclusion complexation between the interior core, terminal group or monomer of highly branched polymers and cyclodextrins
5 Highly branched polymers from the self-assembly of cyclodextrins
6 Hyperbranched polymers based on the functional cyclodextrin monomers
7 Conclusion and outlook

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[1 ] D′Souza V T,Lipkowitz K B. Chem. Rev. ,1998,98: 1741—1742
[2 ] Szejtli J. Chem. Rev. ,1998,98: 1743—1754
[3 ] Breslow R,Yang Z,Ching R. J. Am. Chem. Soc. ,1998,120: 3536—3537
[4 ] David C B,Nigel M D,Ian G T. Int. J. Pharm. ,2000,197:1—11
[5 ] 刘琼( Liu Q) ,范晓东( Fan X D ) . 高分子通报( Chinese Polymer Bulletin) ,2002,(5) : 41—48
[6 ] Mamata S,Rohit S,Banerjee U C. Biotechnol. Adv. ,2002,20: 341—359
[7 ] Martin D V. Proc. Biochem. ,2004,39: 1033—1046
[8 ] Jikei M,Kakimoto M. Prog. Polym. Sci. ,2001,26: 1233—1285
[9 ] Gao C,Yan D. Prog. Poly. Sci. ,2004,29: 183—275
[10] Hirao A,Sugiyama K,Matsuo A,et al. Polym. Int. ,2008,57: 554—570
[11] Dermody D L,Peez R F,Bergbreiter D E,et al. Langmuir,1999,15: 885—890
[12] Schwarz M A,Hauser P C. Anal. Chem. ,2003,75: 4691—4695
[13] Uekama K, Hirayama F, Arima H. J. Incl. Phenom.Macrocycl. Chem. ,2006,56: 3—8
[14] Arkas M, Allabashi R, Tsiourvas D, et al. Environ. Sci.Technol. ,2006,40: 2771—2777
[15] Allabashi R,Arkas M,Hrmann G,et al. Water Research,2007,41: 476—486
[16] Vyas A, Saraf S, Saraf S. J. Incl. Phenom. Macrocycl.Chem. ,2008,62: 23—42
[17] Niederhafner P,ebestk J,Jeek J. J. Pept. Sci. ,2008,14:2—43
[18] Niederhafner P,ebestk J,Jeek J. J. Pept. Sci. ,2008,14:44—65
[19] Hattori K, Imata H, Kubota K, et al. J. Incl. Phenom.Macrocycl. Chem. ,1996,25: 69—72
[20] García-López J J,Santoyo-González F,Vargas-Berenguel A,et al. Chem. Eur. J. ,1999,5: 1775—1784
[21] Ortega-Caballero F,Giménez-Martínez J J,García-Fuentes L,et al. J. Org. Chem. ,2001,66: 7786—7795
[22] Vargas-Berenguel A,Ortega-Caballero F,Santoyo-González F,et al. Chem. Eur. J. ,2002,8: 814—827
[23] Abe H,Kenmoku A,Yamaguch N,et al. J. Incl. Phenom.Macrocycl. Chem. ,2002,44: 39—47
[24] Muhanna A M A,Ortiz-Salmerón E,García-Fuentes L,et al.Tetrahedron Lett. ,2003,44: 6125—6128
[25] Chen L,Zhu X Y,Yan D Y,et al. Polym. Prepr. ,2003,44:669—670
[26] Benito J M,Gómez-García M,Mellet C O,et al. J. Am. Chem.Soc. ,2004,126: 10355—10363
[27] Amir R J,Shabat D. Domino Dendrimers. Adv. Polym. Sci. ,2006,192: 59—93
[28] Suh J,Hah S S,Lee S H. Bioorg. Chem. ,1997,25: 63—75
[29] Roessler B J, Bielinska A U, Janczak K, et al. Biochem.Biophys. Res. Commun. ,2001,283: 124—129
[30] Arima H,Kihara F,Hirayama F,et al. Bioconjugate Chem. ,2001,12: 476—484
[31] Arima H, Wada K, Kihara F, et al. J. Incl. Phenom.Macrocycl. Chem. ,2002,44: 361—364
[32] Kihara F,Arima H,Tsutsumi T,et al. Bioconjugate Chem. ,2002,13: 1211—1219
[33] Kihara F,Arima H,Tsutsumi T,et al. Bioconjugate Chem. ,2003,14: 342—350
[34] Wadaa K,Arimaa H,Tsutsumi T,et al. J. Controlled Release,2005,104: 397—413
[35] Tsutsumi T,Arima H,Hirayama F,et al. J. Incl. Phenom.Macrocycl. Chem. ,2006,56: 81—84
[36] Chihara Y,Arima H,Arizono M, et al. J. Incl. Phenom.Macrocycl. Chem. ,2006,56: 89—93
[37] Arima H,Chihara Y,Arizono M,et al. J. Controlled Release,2006,116: 64—74
[38] Tsutsumi T, Hirayama F, Uekama K, et al. J. Controlled Release,2007,119: 349—359
[39] 曹中林( Cao Z L) ,范晓东( Fan X D) ,孙乐( Sun L) . 高分子材料科学与工程( Polymeric Materials Science and Engineering) ,2007,23: 53—56
[40] Tian W,Fan X D,Liu Y Y,et al. J. Polym. Sci. Part A:Polym. Chem. ,2008,46: 5036—5052
[41] 田威( Tian W) ,范晓东( Fan X D) ,刘涛( Liu T) 等. 高等学校化学学报( J. Chem. Chinese U. ) ,2009,30: 632—637
[42] Tian W,Fan X D,Kong J,et al. Macromol. Chem. Phys. ,2009,210: 2107—2117
[43] Cardona C M,Alvarez J,Kaifer A E,et al. J. Am. Chem.Soc. ,2000,122: 6139—6144
[44] Cardona C M,McCarley T D,Kaifer A E. J. Org. Chem. ,2000,65: 1857—1864
[45] van Bommel K J C,Metselaar G A,Verboom W,et al. J. Org.Chem. ,2001,66: 5405—5412
[46] Dodziuka H,Demchukb O M,Schilf W,et al. J. Mol. Struct. ,2004,693: 145—151
[47] Newkome G R,Kim H J,Choi K H,et al. Macromolecules,2004,37: 6268—6274
[48] Zhu X Y,Chen L,Yan D Y,et al. Langmuir,2004,20:484—490
[49] Mahalingam V,Onclin S,Péter M,et al. Langmuir,2004,20:11756—11762
[50] Nijhuis C A,Yu F,Knoll W,et al. Langmuir,2005,21:7866—7876
[51] Crespo-Biel O,Dordi B,Maury P,et al. Chem. Mater. ,2006,18: 2545—2551
[52] Arai T,Ogawa J,Mouri E,et al. Macromolecules,2006,39:1607—1613
[53] Nijhuis C A,Sinha J K,Wittstock G,et al. Langmuir,2006,22: 9770—9775
[54] Sadhu V B,Perl A,Péter M,et al. Langmuir,2007,23:6850—6855
[55] Thompson D. Langmuir,2007,23: 8441—8451
[56] Kobata K,Ogawa J,Pandey S S,et al. Synth. Met. ,2007,157: 311—317
[57] Nijhuis C A,Boukamp B A,Ravoo B J,et al. J. Phys. Chem.C,2007,111: 9799—9810
[58] Thompson D. J. Phys. Chem. B,2008,112: 4994—4999
[59] Kojima C,Toi Y,Harada A,et al. Bioconjugate Chem. ,2008,19: 2280—2284
[60] Wan H S,Chen Y,Chen L,et al. Macromolecules,2008,41:465—470
[61] Chen L,Zhu X Y,Yan D Y,et al. Angew. Chem. Int. Ed. ,2006,45: 87—90
[62] Topchieva I N, Sorokina E M, Efremova N V, et al.Bioconjugate Chem. ,2000,11: 22—29
[63] Alvarez-Parrilla E,Cabrer P R,Al-Soufi W,et al. Angew.Chem. Int. Ed. ,2000,39: 2856—2858
[64] Tellini V H S,Jover A,García J C,et al. J. Am. Chem. Soc. ,2006,128: 5728—5734
[65] Galantini L,Jover A,Leggio C,et al. J. Phys. Chem. B,2008,112: 8536—8541
[66] Miyawaki A,Takashima Y,Yamaguchi H,et al. Tetrahedron,2008,64: 8355—8361
[67] Tian W,Fan X D,Kong J,et al. Macromolecules,2009,42:640—651

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摘要

基于环糊精的高度支化聚合物*