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Frontiers of Materials Science

ISSN 2095-025X

ISSN 2095-0268(Online)

CN 11-5985/TB

邮发代号 80-974

2019 Impact Factor: 1.747

Frontiers of Materials Science  2022, Vol. 16 Issue (3): 220614   https://doi.org/10.1007/s11706-022-0614-8
  本期目录
Electroactive chitosan-aniline pentamer hydrogel for peripheral nerve regeneration
Deqiang MIAO, Ya LI, Zhongbing HUANG(), Yulin WANG, Min DENG, Xiaohui LI
College of Biomedical Engineering, Sichuan University, Chengdu 610065, China
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Abstract

Electroactive hydrogels could guide the regeneration of nerves and promote their functional recovery. An aniline pentamer-crosslinked chitosan (CS-AP) hydrogel with better electroactivity and degradation was fabricated by the carbodiimide method, and then injected into the repair site of sciatic nerve damage, with its gelation time, tensile strength, and conductivity reaching 35 min, 5.026.69 MPa, and from 2.97 × 10−4 to 3.25 × 10−4 S·cm−1, respectively, due to the cross-linkage and well-distribution of AP. There was better cytocompativility of CS-AP hydrogel on nerve cells. The results of the in vivo repair indicated that CS-AP10 hydrogel induced the capillaries formation and the repair of sciatic nerve defect, and re-innervated gastrocnemius muscle in the CS-AP10 group were obviously better than other experimental groups, due to the electroactivity of CS-AP and its degradation into fragments. These results indicated the potential application of CS-AP hydrogel in the regeneration and function recovery of peripheral nerve injury.

Key wordsperipheral nerve regeneration    chitosan    aniline pentamer    electroactive hydrogel    capillary formation
收稿日期: 2022-04-10      出版日期: 2022-07-28
Corresponding Author(s): Zhongbing HUANG   
 引用本文:   
. [J]. Frontiers of Materials Science, 2022, 16(3): 220614.
Deqiang MIAO, Ya LI, Zhongbing HUANG, Yulin WANG, Min DENG, Xiaohui LI. Electroactive chitosan-aniline pentamer hydrogel for peripheral nerve regeneration. Front. Mater. Sci., 2022, 16(3): 220614.
 链接本文:  
https://academic.hep.com.cn/foms/CN/10.1007/s11706-022-0614-8
https://academic.hep.com.cn/foms/CN/Y2022/V16/I3/220614
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1 M, Siemionow G Brzezicki . Chapter 8: Current techniques and concepts in peripheral nerve repair. International Review of Neurobiology, 2009, 87 : 141– 172
https://doi.org/10.1016/S0074-7742(09)87008-6 pmid: 19682637
2 H, Zhu L, Shen M, Yang , et al.. Progress in facial reinnervation. Journal of Neurorestoratology, 2021, 9( 3): 177– 185
https://doi.org/10.26599/JNR.2021.9040016
3 C E, Schmidt J B Leach . Neural tissue engineering: strategies for repair and regeneration. Annual Review of Biomedical Engineering, 2003, 5( 1): 293– 347
https://doi.org/10.1146/annurev.bioeng.5.011303.120731 pmid: 14527315
4 Y, Wang Y, Zhang X, Li , et al.. The progress of biomaterials in peripheral nerve repair and regeneration. Journal of Neurorestoratology, 2020, 8( 4): 252– 269
https://doi.org/10.26599/JNR.2020.9040022
5 R, Javed Q Ao . Nanoparticles in peripheral nerve regeneration: a mini review. Journal of Neurorestoratology, 2022, 10( 1): 1– 12
https://doi.org/10.26599/JNR.2022.9040001
6 B, Guo P X Ma . Conducting polymers for tissue engineering. Biomacromolecules, 2018, 19( 6): 1764– 1782
https://doi.org/10.1021/acs.biomac.8b00276 pmid: 29684268
7 R, Ravichandran S, Sundarrajan J R, Venugopal , et al.. Applications of conducting polymers and their issues in biomedical engineering. Journal of the Royal Society Interface, 2010, 7( Suppl 5): S559– S579
https://doi.org/10.1098/rsif.2010.0120.focus pmid: 20610422
8 A D, Bendrea L, Cianga I Cianga . Review paper: progress in the field of conducting polymers for tissue engineering applications. Journal of Biomaterials Applications, 2011, 26( 1): 3– 84
https://doi.org/10.1177/0885328211402704 pmid: 21680608
9 Q, Wu C, Pan Y, Hu , et al.. Neuroprotective effects of adipose-derived stem cells on ferrous sulfate-induced neurotoxicity. Brain Science Advances, 2021, 7( 3): 172– 183
https://doi.org/10.26599/BSA.2021.9050008
10 P, Zarrintaj E, Zangene S, Manouchehri , et al.. Conductive biomaterials as nerve conduits: recent advances and future challenges. Applied Materials Today, 2020, 20 : 100784
https://doi.org/10.1016/j.apmt.2020.100784
11 E N, Zare P, Makvandi B, Ashtari , et al.. Progress in conductive polyaniline-based nanocomposites for biomedical applications: a review. Journal of Medicinal Chemistry, 2020, 63( 1): 1– 22
https://doi.org/10.1021/acs.jmedchem.9b00803 pmid: 31502840
12 J, Liu Y S, Kim C E, Richardson , et al.. Genetically targeted chemical assembly of functional materials in living cells, tissues, and animals. Science, 2020, 367( 6484): 1372– 1376
https://doi.org/10.1126/science.aay4866 pmid: 32193327
13 X, Ma J, Ge Y, Li , et al.. Nanofibrous electroactive scaffolds from a chitosan-grafted-aniline tetramer by electrospinning for tissue engineering. RSC Advances, 2014, 4( 26): 13652– 13661
https://doi.org/10.1039/c4ra00083h
14 B L, Guo A, Finne-Wistrand A C Albertsson . Simple route to size-tunable degradable and electroactive nanoparticles from the self-assembly of conducting coil–rod–coil triblock copolymers. Chemistry of Materials, 2011, 23( 17): 4045– 4055
https://doi.org/10.1021/cm201782v
15 P, Zarrintaj B, Bakhshandeh M R F, Saeb , et al.. Oligoaniline-based conductive biomaterials for tissue engineering. Acta Biomaterialia, 2018, 72 : 16– 34
https://doi.org/10.1016/j.actbio.2018.03.042 pmid: 29625254
16 R, Dong X, Zhao B, Guo , et al.. Biocompatible elastic conductive films significantly enhanced myogenic differentiation of myoblast for skeletal muscle regeneration. Biomacromolecules, 2017, 18( 9): 2808– 2819
https://doi.org/10.1021/acs.biomac.7b00749 pmid: 28792734
17 J, Chen M, Yu B, Guo , et al.. Conductive nanofibrous composite scaffolds based on in-situ formed polyaniline nanoparticle and polylactide for bone regeneration. Journal of Colloid and Interface Science, 2018, 514 : 517– 527
https://doi.org/10.1016/j.jcis.2017.12.062 pmid: 29289734
18 B L, Guo A, Finne-Wistrand A C Albertsson . Enhanced electrical conductivity by macromolecular architecture: hyperbranched electroactive and degradable block copolymers based on poly(ε-caprolactone) and aniline pentamer. Macromolecules, 2010, 43( 10): 4472– 4480
https://doi.org/10.1021/ma100530k
19 L, Zhang L, Wang B, Guo , et al.. Cytocompatible injectable carboxymethyl chitosan/N-isopropylacrylamide hydrogels for localized drug delivery. Carbohydrate Polymers, 2014, 103 : 110– 118
https://doi.org/10.1016/j.carbpol.2013.12.017 pmid: 24528707
20 P, Li Y F, Poon W, Li , et al.. A polycationic antimicrobial and biocompatible hydrogel with microbe membrane suctioning ability. Nature Materials, 2011, 10( 2): 149– 156
https://doi.org/10.1038/nmat2915 pmid: 21151166
21 J R, Bain S E, Mackinnon D A Hunter . Functional evaluation of complete sciatic, peroneal, and posterior tibial nerve lesions in the rat. Plastic and Reconstructive Surgery, 1989, 83( 1): 129– 136
https://doi.org/10.1097/00006534-198901000-00024 pmid: 2909054
22 H, Guan Z, Xie P, Zhang , et al.. Synthesis and characterization of biodegradable amphiphilic triblock copolymers containing L-glutamic acid units. Biomacromolecules, 2005, 6( 4): 1954– 1960
https://doi.org/10.1021/bm0492069 pmid: 16004433
23 Y Y, Feng S, Bai G G, Li , et al.. Reprogramming rat astrocytes into neurons using small molecules for cell replacement following intracerebral hemorrhage. Brain Science Advances, 2021, 7( 3): 184– 198
https://doi.org/10.26599/BSA.2021.9050009
24 Medinaceli L, de W J, Freed R J Wyatt . An index of the functional condition of rat sciatic nerve based on measurements made from walking tracks. Experimental Neurology, 1982, 77( 3): 634– 643
https://doi.org/10.1016/0014-4886(82)90234-5 pmid: 7117467
25 Z, Zong Y, Kimura M, Takahashi , et al.. Characterization of chemical and solid state structures of acylated chitosans. Polymer, 2000, 41( 3): 899– 906
https://doi.org/10.1016/S0032-3861(99)00270-0
26 J, Hu L, Huang X, Zhuang , et al.. Electroactive aniline pentamer cross-linking chitosan for stimulation growth of electrically sensitive cells. Biomacromolecules, 2008, 9( 10): 2637– 2644
https://doi.org/10.1021/bm800705t pmid: 18698845
27 X, Wang T, Sun C, Wang , et al.. 1H NMR determination of the doping level of doped polyaniline. Macromolecular Chemistry and Physics, 2010, 211( 16): 1814– 1819
https://doi.org/10.1002/macp.201000194
28 Y, Liu J, Hu X, Zhuang , et al.. Synthesis and characterization of novel biodegradable and electroactive hydrogel based on aniline oligomer and gelatin. Macromolecular Bioscience, 2012, 12( 2): 241– 250
https://doi.org/10.1002/mabi.201100227 pmid: 22028067
29 D, Chao X, Ma X, Lu , et al.. Design, synthesis and characterization of novel electroactive polyamide with amine-capped aniline pentamer in the main chain via oxidative coupling polymerization. Journal of Applied Polymer Science, 2007, 104( 3): 1603– 1608
https://doi.org/10.1002/app.25749
30 T H, Qazi R, Rai D, Dippold , et al.. Development and characterization of novel electrically conductive PANI‒PGS composites for cardiac tissue engineering applications. Acta Biomaterialia, 2014, 10( 6): 2434– 2445
https://doi.org/10.1016/j.actbio.2014.02.023 pmid: 24561709
31 B, Bagheri P, Zarrintaj A, Samadi , et al.. Tissue engineering with electrospun electro-responsive chitosan-aniline oligomer/polyvinyl alcohol. International Journal of Biological Macromolecules, 2020, 147 : 160– 169
https://doi.org/10.1016/j.ijbiomac.2019.12.264 pmid: 31904459
32 Z, Bagher Z, Atoufi R, Alizadeh , et al.. Conductive hydrogel based on chitosan-aniline pentamer/gelatin/agarose significantly promoted motor neuron-like cells differentiation of human olfactory ecto-mesenchymal stem cells. Materials Science and Engineering C, 2019, 101 : 243– 253
https://doi.org/10.1016/j.msec.2019.03.068 pmid: 31029317
33 S, Liu J, Wang D, Zhang , et al.. Investigation on cell biocompatible behaviors of polyaniline film fabricated via electroless surface polymerization. Applied Surface Science, 2010, 256( 11): 3427– 3431
https://doi.org/10.1016/j.apsusc.2009.12.046
34 G, Stoll S, Jander R R Myers . Degeneration and regeneration of the peripheral nervous system: from Augustus Waller’s observations to neuroinflammation. Journal of the Peripheral Nervous System, 2002, 7( 1): 13– 27
https://doi.org/10.1046/j.1529-8027.2002.02002.x pmid: 11939348
35 X, Tang C, Xue Y, Wang , et al.. Bridging peripheral nerve defects with a tissue engineered nerve graft composed of an in vitro cultured nerve equivalent and a silk fibroin-based scaffold. Biomaterials, 2012, 33( 15): 3860– 3867
https://doi.org/10.1016/j.biomaterials.2012.02.008 pmid: 22364696
36 G, Kaur R, Adhikari P, Cass , et al.. Electrically conductive polymers and composites for biomedical applications. RSC Advances, 2015, 5( 47): 37553– 37567
https://doi.org/10.1039/C5RA01851J
37 P M, Richardson U M, McGuinness A J Aguayo . Axons from CNS neurons regenerate into PNS grafts. Nature, 1980, 284( 5753): 264– 265
https://doi.org/10.1038/284264a0 pmid: 7360259
38 C E, Schmidt V R, Shastri J P, Vacanti , et al.. Stimulation of neurite outgrowth using an electrically conducting polymer. Proceedings of the National Academy of Sciences of the United States of America, 1997, 94( 17): 8948– 8953
https://doi.org/10.1073/pnas.94.17.8948 pmid: 9256415
39 A, Domínguez-Bajo A, González-Mayorga C R, Guerrero , et al.. Myelinated axons and functional blood vessels populate mechanically compliant rGO foams in chronic cervical hemisected rats. Biomaterials, 2019, 192 : 461– 474
https://doi.org/10.1016/j.biomaterials.2018.11.024 pmid: 30502723
40 P, Carmeliet M Tessier-Lavigne . Common mechanisms of nerve and blood vessel wiring. Nature, 2005, 436( 7048): 193– 200
https://doi.org/10.1038/nature03875 pmid: 16015319
41 B, Xia Y Lv . Dual-delivery of VEGF and NGF by emulsion electrospun nanofibrous scaffold for peripheral nerve regeneration. Materials Science and Engineering C, 2018, 82 : 253– 264
https://doi.org/10.1016/j.msec.2017.08.030 pmid: 29025656
42 X, Zhang H, Qi S, Wang , et al.. Cellular responses of aniline oligomers: a preliminary study. Toxicology Research, 2012, 1( 3): 201– 205
https://doi.org/10.1039/c2tx20035j
43 Y, Zhao Y, Wang J, Gong , et al.. Chitosan degradation products facilitate peripheral nerve regeneration by improving macrophage-constructed microenvironments. Biomaterials, 2017, 134 : 64– 77
https://doi.org/10.1016/j.biomaterials.2017.02.026 pmid: 28456077
44 X, Chen C, Liu Z, Huang , et al.. Preparation of carboxylic graphene oxide-composited polypyrrole conduits and their effect on sciatic nerve repair under electrical stimulation. Journal of Biomedical Materials Research Part A, 2019, 107( 12): 2784– 2795
https://doi.org/10.1002/jbm.a.36781 pmid: 31408274
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