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《材料导报》期刊社  2018, Vol. 32 Issue (5): 755-764    https://doi.org/10.11896/j.issn.1005-023X.2018.05.011
  材料综述 |
基于植物多酚构筑新型功能材料
崔可建1, 2, 蔡超2, 朱才镇1
1 深圳大学化学与环境工程学院,深圳 518060;
2 中国科学院化学研究所,北京 100190
Creating Novel Functional Materials Based on Plant Polyphenols: a Review
CUI Kejian1,2, CAI Chao2, ZHU Caizhen1
1 College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen 518060;
2 Institute of Chemistry, Chinese Academy of Science, Beijing 100190
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摘要 植物多酚是一类来源广泛的生物质材料,具有典型的生物活性和抗氧化性,还具有可吸收紫外线、可与金属离子螯合及可在化学反应中用作亲核试剂等多种功能与性质。植物多酚特殊的分子结构使其可以通过氢键、共价键、配位键、π-π堆叠等多种相互作用与其他分子结合,作为载体用于构筑各种功能材料。本文系统介绍了植物多酚的各种功能,讨论了近年来基于其功能性及化学反应性所开展的功能材料制备方面的研究进展,并展望了植物多酚这一类环境友好型生物质在功能材料制备方面的应用前景。
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崔可建
蔡超
朱才镇
关键词:  植物多酚  功能性  化学反应性  功能载体  结构载体    
Abstract: As biomass materials, plant polyphenols derive from a wealth of sources. Plant polyphenols possess typical bio-activity and anti-oxidation, as well as the abilities of ultraviolet absorption, metal chelation and nucleophilicity in the chemical reaction. Based on its particular molecular structure, plant polyphenol can potentially interact with other molecules by hydrogen bond, covalent bond, coordinate bond and π-π stacking,therefore plant polyphenols can be used for functional materials construction. Here, we introduce the various functionality, discuss the application progress of plant polyphenol based on its functionality and chemical reactivity, and provide new insights into applications of the environment-friendly plant polyphenols to functional materials construction.
Key words:  plant polyphenol    functionality    chemical reactivity    function carrier    construction carrier
               出版日期:  2018-03-10      发布日期:  2018-03-10
ZTFLH:  O636.9  
基金资助: 国家自然科学基金(51673117);深圳市科技创新委员会资助(JSGG20160226201833790;JCYJ20160520163535684;JCYJ20160422144936457)
通讯作者:  朱才镇:通信作者,男,1983年生,博士,研究员,主要从事高性能纤维及新能源材料制备研究 E-mail:czzhu@szu.edu.cn   
作者简介:  崔可建:男,1987年生,博士,主要从事高分子物理与化学研究 E-mail:cuikejian@iccas.ac.cn
引用本文:    
崔可建, 蔡超, 朱才镇. 基于植物多酚构筑新型功能材料[J]. 《材料导报》期刊社, 2018, 32(5): 755-764.
CUI Kejian, CAI Chao, ZHU Caizhen. Creating Novel Functional Materials Based on Plant Polyphenols: a Review. Materials Reports, 2018, 32(5): 755-764.
链接本文:  
http://www.mater-rep.com/CN/10.11896/j.issn.1005-023X.2018.05.011  或          http://www.mater-rep.com/CN/Y2018/V32/I5/755
1 Driel-Murray C V. Ancient egyptian materials and technology[M].Cambridge:Cambridge University Press,2000:299.
2 Haslam E. Practical polyphenolics—From structure to molecular re-cognition and physiological action[M].Cambridge:Cambridge University Press,1998.
3 Ferreira D, Slade D. Flavanoids—Chemistry, biochemistry and applications[M].Boca Raton:CRC/Taylor & Francis,2006:553.
4 Ferreira D, Slade D. Oligomeric proanthocyanidins: Naturally occurring o-heterocycles[J].Natural Product Reports,2002,19(5):517.
5 Ferreira D, Nel R J, Bekker R. Compehensive natural products chemistry[M].Oxford:Pergamon,1999:747.
6 Ferreira D, Bekker R. Oligomeric proanthocyanidins: Naturally occurring o-heterocycles[J].Natural Product Reports,1996,13(5):411.
7 Okuda T, Yoshida T, Hatano T, et al. Chemistry and biology of ellagitannins—An underestimated class of bioactive plant polyphenols[M].Singapore:World Scientific,2009:1.
8 Quideau S, Feldman K S. Ellagitannin chemistry[J].Chemical Reviews,1996,96(1):475.
9 Sailler B, Glombitza K W. Phlorethols and fucophlorethols from the brown alga cystophora retroflexa[J].Phytochemistry,1999,50(5):869.
10 Glombitza K W, Schmidt A. Nonhalogenated and halogenated phlorotannins from the brown alga carpophyllum angustifolium[J].Journal of Natural Products,1999,62(9):1238.
11 Okuda T, Yoshida T, Hatano T, et al. Economic and medicinal plant research[M].London:Academic Press,1991:129.
12 Haslam E. Natural polyphenols (vegetable tannins) as drugs: Possible modes of action[J].Journal of Natural Products,1996,59(2):205.
13 Simon C, Barathieu K, Laguerre M, et al. Three-dimensional structure and dynamics of wine tannin saliva protein complexes[J].A Multitechnique Approach.Biochemistry,2003,42(35):10385.
14 Hagerman A E, Rice M E, Ritchard N T, Mechanisms of protein precipitation for two tannins, pentagalloyl glucose and epicatechin catechin (procyanidin)[J].Journal of Agricultu-ral and Food Chemistry,1998,46(7):2590.
15 Pascal C, Poncet-Legrand C, Imberty A, et al. Interactions between a non glycosylated human proline-rich protein and flavan-3-ols are affected by protein concentration and polyphenol/protein ratio[J].Journal of Agricultural and Food Chemistry,2007,55(12):4895.
16 Poncet-Legrand C, Gautier C, Cheynier V, et al. Interactions between flavan-3-ols and poly(l-proline) studied by isothermal titration calorimetry: Effect of the tannin structure[J].Journal of Agricultural and Food Chemistry,2007,55(22):9235.
17 Kawamoto H, Nakatsubo F, Murakami K. Stoichiometric studies of tannin-protein co-precipitation[J].Phytochemistry,1996,41(5):1427.
18 Feldman K S, Sambandam A, Lemon S T, et al. Binding affinities of gallotannin analogs with bovine serum albumin: Ramifications for polyphenol-protein molecular recognition[J].Phytochemistry,1999,44(7):867.
19 Haslam E, Lilley T H, Cai Y, et al. Traditional herbal medicines—the role of polyphenols[J].Planta Medica,1989,55(1):1.
20 Andjelkovic' M, Van Camp J, De Meulenaer B, et al. Iron-chelation properties of phenolic acids bearing catechol and galloyl groups[J].Food Chemistry,2006,98(1):23.
21 Mira L, Tereza Fernandez M, Santos M, et al. Interactions of flavonoids with iron and copper ions: A mechanism for their antioxidant activity[J].Free Radical Research,2002,36(11):1199.
22 Yoshida K, Mori M, Kondo T. Blue flower color development by anthocyanins: From chemical structure to cell physiology[J].Natural Product Reports,2009,26(7):884.
23 de Freitas V, Mateus N. Chemical transformations of anthocyanins yielding a variety of colours[J].Environmental Chemistry Letters,2006,4(3):175.
24 Northup R R, Dahlgren R A, McColl J G. Polyphenols as regulators of plant-litter-soil interactions in northern california’s pygmy forest: A positive feedback?[J].Biogeochemistry,1998,42(1):189.
25 Hatier J H B, Gould K S. Anthocyanins—biosynthesis, functions, and applications[M].New York:Springer,2008:1.
26 Harborne J B, Williams C A. Advances in flavonoid research since 1992[J].Phytochemistry,2000,55(6):481.
27 Mulder P, Korth H G, Pratt D A, et al. Critical re-evaluation of the O-H bond dissociation enthalpy in phenol[J].The Journal of Physical Chemistry A,2005,109(11):2647.
28 Neudrffer A, Desvergne J P, Bonnefont-Rousselot D, et al. Protective effects of 4-hydroxycinnamic ethyl ester derivatives and related dehydrodimers against oxidation of ldl: Radical scavengers or metal chelators?[J].Journal of Agricultural and Food Chemistry,2006,54(5):1898.
29 Vaya J, Mahmood S, Goldblum A, et al. Inhibition of ldl oxidation by flavonoids in relation to their structure and calculated enthalpy[J].Phytochemistry,2003,62(1):89.
30 Li A S H, Bandy B, Tsang S S. DNA-breaking versus DNA-protecting activity of four phenolic compounds in vitro[J].Free Radical Research,2000,33(5):551.
31 Shi X, Ye J, Leonard S, et al. Antioxidant properties of (-)-epicatechin-3-gallate and its inhibition of Cr (vi)-induced DNA damage and Cr (iv)- or tpa-stimulated NF-κB activation[J].Molecular and Cellular Biochemistry,2000,202(1):125.
32 Aromal S A, Philip D. Facile one-pot synthesis of gold nanoparticles using tannic acid and its application in catalysis[J].Physica E:Low-dimensional Systems & Nanostructures,2012,44(7-8):1692.
33 Dutta A, Dolui S K. Tannic acid assisted one step synthesis route for stable colloidal dispersion of nickel nanostructures[J].Applied Surface Science,2011,257(15):6889.
34 Xiao L S, Mertens M, Wortmann L, et al. Enhanced in vitro and in vivo cellular imaging with green tea coated water-soluble iron oxide nanocrystals[J].ACS Applied Materials & Interfaces,2015,7(12):6530.
35 Aguirre F M A, Becerra R H. New synthesis of bismuth oxide nanoparticles Bi2O3 assisted by tannic acid[J].Applied Physics A:Mate-rials Science & Processing,2015,119(3):909.
36 Cao Y, Zheng R, Ji X, Liu H, et al. Syntheses and characterization of nearly monodispersed, size-tunable silver nanoparticles over a wide size range of 7-200 nm by tannic acid reduction[J].Langmuir,2014,30(13):3876.
37 Fei J, Zhao J, Du C, et al. One-pot ultrafast self-assembly of autofluorescent polyphenol-based core@shell nanostructures and their selective antibacterial applicationsp[J].ACS Nano,2014,8(8):8529.
38 Lim M Y, Shin H, Shin D M, et al. Poly(vinyl alcohol) nanocomposites containing reduced graphene oxide coated with tannic acid for humidity sensor[J].Polymer,2016,(84):89.
39 Huang Q, Hao L, Xie J, et al. Tea polyphenol-functionalized graphene/chitosan as an experimental platform with improved mechanical behavior and bioactivity[J].ACS Applied Materials & Interfaces,2015,7(37):20893.
40 Liao R J, Tang Z H, Lei Y D, et al. Polyphenol-reduced graphene oxide: Mechanism and derivatization[J].Journal of Physical Chemistry C,2011,115(42):20740.
41 Ignat I, Radu D G, Volf I, et al. Antioxidant and antibacterial acti-vities of some natural polyphenols[J].Cellulose Chemistry and Technology,2013,47(5):387.
42 Limmatvapirat C, Charoenteeraboon J, Wetwitayaklung P, et al. In Stability and antioxidant activity of polyphenols in methanolic extracts of sonneratia caseolaris seeds[M].Advances in Superalloys,2011:1062.
43 Fu J, Shen J, Gao G, et al. Natural polyphenol-stabilised highly crosslinked UHMWPE with high mechanical properties and low wear for joint implants[J].Journal of Materials Chemistry B,2013,37(1):4727.
44 Beart J E, Lilley T H, Haslam E. Plant polyphenols—secondary metabolism and chemical defence: Some observations[J].Phytochemistry,1985,24(1):33.
45 Sinha A K, Pathre U, Sane P V. Purification and characterization of sucrose-phosphate synthase from prosopis juliflora[J].Phytochemistry,1997,46(3):441.
46 Yang C S, Wang X, Lu G, et al. Cancer prevention by tea: Animal studies, molecular mechanisms and human relevance[J].Nature Reviews Cancer,2009,9(6):429.
47 Spencer J P E. The impact of flavonoids on memory: Physiological and molecular considerations[J].Chemical Society Reviews,2009,38(4):1152.
48 Di Lorenzo A, Bloise N, Meneghini S, et al. Effect of winemaking on the composition of red wine as a source of polyphenols for anti-infective biomaterials[J].Materials,2016,9(5):doi:10.3390/ma9050316.
49 Siddiqui M F, Oh H S, Rzechowicz M, et al. Biofouling control potential of tannic acid, ellagic acid, and epigallocatechin against pseudomonas aeruginosa and reverse osmosis membrane multispecies community[J].Journal of Industrial and Engineering Chemistry,2015,30:204.
50 Debnath K, Shekhar S, Kumar V, et al. Efficient inhibition of protein aggregation, disintegration of aggregates, and lowering of cytotoxicity by green tea polyphenol-based self-assembled polymer nanoparticles[J].ACS Applied Materials & Interfaces,2016,8(31):20310.
51 Sylla T, Pouységu L, Da Costa G, et al. Gallotannins and tannic acid: First chemical syntheses and in vitro inhibitory activity on alzheimer’s amyloid β-peptide aggregation[J].Angewandte Chemie International Edition,2015,54(28):8217.
52 Ehrnhoefer D E, Bieschke J, Boeddrich A, et al. Egcg redirects amyloidogenic polypeptides into unstructured, off-pathway oligomers[J].Nature Structure Mole Biology,2008,15(6):558.
53 Polya G M, Wang B H, Foo L Y. Inhibition of signal-regulated protein kinases by plant-derived hydrolysable tannins[J].Phytochemistry,1995,38(2):307.
54 Kashiwada Y, Nonaka G, Nishioka I, et al. Tannins as selective inhibitors of protein kinase C[J].Bioorganic & Medicinal Chemistry Letters,1992,2(3):239.
55 Maloney D J, Deng J Z, Starck S R, et al. (+)-Myristinin A, a na-turally occurring DNA polymerase β inhibitor and potent DNA-damaging agent[J].Journal of the American Chemical Society,2005,127(12):4140.
56 Jankun J, Selman S H, Swiercz R, et al. Why drinking green tea could prevent cancer[J].Nature,1997,387(6633):561.
57 Oliver S, Thomas D S, Kavallaris M, et al. Efficient functionalisa-tion of dextran-aldehyde with catechin: Potential applications in the treatment of cancer[J].Polymer Chemistry,2016,7(14):2542.
58 Chen J, Peng Y, Zheng Z, et al. Silver-releasing and antibacterial activities of polyphenol-based polyurethanes[J].Journal of Applied Polymer Science,2015,132(4):41349.
59 Lee F, Lim J, Reithofer M R, et al. Synthesis and bioactivity of a conjugate composed of green tea catechins and hyaluronic acid[J].Polymer Chemistry,2015,6(24):4462.
60 Lee F, Chung J E, Xu K M, et al. Injectable degradation-resistant hyaluronic acid hydrogels cross-linked via the oxidative coupling of green tea catechin[J].ACS Macro Letters,2015,4(9):957.
61 Hegab H M, ElMekawy A, Barclay T G, et al. Single-step assembly of multifunctional poly(tannic acid)-graphene oxide coating to reduce biofouling of forward osmosis membranes[J].ACS Applied Materials & Interfaces,2016,8(27):17519.
62 Liu R, Zhu J, Luo J, et al. Synthesis and application of novel uv-curable hyperbranched methacrylates from renewable natural tannic acid[J].Progress in Organic Coatings,2014,77(1):30.
63 Chen Z H, Wang C H, Chen J Z, et al. Biocompatible, functional spheres based on oxidative coupling assembly of green tea polyphenols[J].Journal of the American Chemical Society,2013,135(11):4179.
64 Fathy N A, Rizk M S, Awad R M S. Pore structure and adsorption properties of carbon xerogels derived from carbonization of tannic acid resorcinol formaldehyde resin[J].Journal of Analytical and Applied Pyrolysis,2016,119:60.
65 Szczurek A, Amaral Labat G, Fierro V, et al. The use of tannin to prepare carbon gels. Part ii. Carbon cryogels[J].Carbon,2011,49(8):2785.
66 Szczurek A, Amaral-Labat G, Fierro V, et al. The use of tannin to prepare carbon gels. Part i: Carbon aerogels[J].Carbon,2011,49(8):2773.
67 Amaral-Labat G, Grishechko L, Szczurek A, et al. Highly mesoporous organic aerogels derived from soy and tannin[J].Green Che-mistry,2012,14(11):3099.
68 Yen K C, Woo E M. Formation of dendrite crystals in poly(ethylene oxide) interacting with bioresourceful tannin[J].Polymer Bulletin,2008,62(2):225.
69 Whittaker J L, Subianto S, Dutta N K, et al. Induced insolubility of electrospun poly(n-vinylcaprolactam) fibres through hydrogen bon-ding with tannic acid[J].Polymer,2016,87:194.
70 Xu W N, Steinschulte A A, Plamper F A, et al. Hierarchical assembly of star polymer polymersomes into responsive multicompartmental microcapsules[J].Chemistry of Materials,2016,28(3):975.
71 Zhao Y N, Gu J, Jia S, et al. Zero-order release of polyphenolic drugs from dynamic, hydrogen-bonded lbl films[J].Soft Matter,2016,12(4):1085.
72 Kim K, Shin M, Koh M Y, et al. Tape: A medical adhesive inspired by a ubiquitous compound in plants[J].Advanced Functional Mate-rials,2015,25(16):2402.
73 Patel A R, Nijsse J, Velikov K P. Novel polymer-polyphenol beads for encapsulation and microreactor applications[J].Soft Matter,2011,7(9):4294.
74 Patel A R, ten-Hoorn J S, Hazekamp J, et al. Colloidal comple-xation of a macromolecule with a small molecular weight natural polyphenol: Implications in modulating polymer functionalities[J].Soft Matter,2013,9(5):1428.
75 Lomova M V, Brichkina A I, Kiryukhin M V, et al. Multilayer capsules of bovine serum albumin and tannic acid for controlled release by enzymatic degradation[J].ACS Applied Materials & Interfaces,2015,7(22):11732.
76 Shin M, Ryu J H, Park J P, et al. DNA/tannic acid hybrid gel exhibiting biodegradability, extensibility, tissue adhesiveness, and hemostatic ability[J].Advanced Functional Materials,2015,25(8):1270.
77 Ejima H, Richardson J J, Liang K, et al. One-step assembly of coordination complexes for versatile film and particle engineering[J].Science,2013,341(6142):154.
78 Guo J, Ping Y, Ejima H, et al. Engineering multifunctional capsules through the assembly of metal-phenolic networks[J].Angewandte Chemie International Edition,2014,53(22):5546.
79 Guo J L, Wang X W, Henstridge D C, et al. Nanoporous metal-phenolic particles as ultrasound imaging probes for hydrogen pero-xide[J].Advanced Healthcare Materials,2015,4(14):2170.
80 Ping Y, Guo J, Ejima H, et al. Ph-responsive capsules engineered from metal-phenolic networks for anticancer drug delivery[J].Small,2015,11(17):2032.
81 Ju Y, Cui J W, Sun H L, et al. Engineered metal-phenolic capsules show tunable targeted delivery to cancer cells[J].Biomacromolecules,2016,17(6):2268.
82 Ju Y, Cui J, Muellner M, et al. Engineering low-fouling and pH-degradable capsules through the assembly of metal-phenolic networks[J].Biomacromolecules,2015,16(3):807.
83 Zeng T, Zhang X, Guo Y, et al. Enhanced catalytic application of Au@polyphenol-metal nanocomposites synthesized by a facile and green method[J].Journal of Materials Chemistry A,2014,2(36):14807.
84 Shen H, Duan C, Guo J, et al. Facile in situ synthesis of silver nanoparticles on boron nitride nanosheets with enhanced catalytic performance[J].Journal of Materials Chemistry A,2015,32(3):16663.
85 Copello G J, Pesenti M P, Raineri M, et al. Polyphenol-SiO2 hybrid biosorbent for heavy metal removal. Yerba mate waste (ilex paraguariensis) as polyphenol source: Kinetics and isotherm studies[J].Colloids and Surfaces B:Biointerfaces,2013,102:218.
86 Lee J, Cho H, Choi J, et al. Chemical sporulation and germination: Cytoprotective nanocoating of individual mammalian cells with a degradable tannic acid-Fe (iii) complex[J].Nanoscale,2015,7(45):18918.
87 Kim S, Kwak S, Lee S, et al. One-step functionalization of zwitte-rionic poly[(3-(methacryloylamino)propyl)dimethyl(3-sulfopropyl)ammonium hydroxide] surfaces by metal-polyphenol coating[J].Chemical Communications,2015,51(25):5340.
88 Lee H, Dellatore S M, Miller W M, et al. Mussel-inspired surface chemistry for multifunctional coatings[J].Science,2007,318(5849):426.
89 Sileika T S, Barrett D G, Zhang R, et al. Colorless multifunctional coatings inspired by polyphenols found in tea, chocolate, and wine[J].Angewandte Chemie International Edition.2013,52(41):10766.
90 Barrett D G, Sileika T S, Messersmith P B. Molecular diversity in phenolic and polyphenolic precursors of tannin-inspired nanocoatings[J].Chemical Communications,2014,50(55):7265.
91 Geissler S, Barrantes A, Tengvall P, et al. Deposition kinetics of bioinspired phenolic coatings on titanium surfaces[J].Langmuir,2016,32:8050.
92 Zhang S, Jiang Z, Wang X, et al. Facile method to prepare microcapsules inspired by polyphenol chemistry for efficient enzyme immobilization[J].ACS Applied Materials & Interfaces,2015,7(35):19570.
93 Pranantyo D, Xu L Q, Neoh K G, et al. Tea stains-inspired initiator primer for surface grafting of antifouling and antimicrobial polymer brush coatings[J].Biomacromolecules,2015,16(3):723.
94 Han P P, Shi J F, Nie T, et al. Conferring natural-derived porous microspheres with surface multifunctionality through facile coordination-enabled self-assembly process[J].ACS Applied Materials & Interfaces,2016,8(12):8076.
95 Krogsgaard M, Andersen A, Birkedal H. Gels and threads: Mussel-inspired one-pot route to advanced responsive materials[J].Chemical Communications,2014,50(87):13278.
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