Citation: Hong Jiajin, Liu Yong, Chen Jialiang, Ma Kefeng. Progress in Ionic Liquids of Biological Engineering[J]. Chemistry, ;2018, 81(12): 1072-1077. shu

Progress in Ionic Liquids of Biological Engineering

  • Corresponding author: Ma Kefeng, makefeng@njust.edu.cn
  • Received Date: 8 May 2018
    Accepted Date: 19 September 2018

Figures(5)

  • Ionic liquids (ILs) have many excellent properties such as non-volatility, nonflammability, high ionic conductivity, physicochemical stability, wide electrochemical window, structural diversity and designability. In recent years, they have played a vital role in electrochemistry, biology, green chemistry, etc. This article mainly reviews some applications of ILs in biology. Firstly, the target gene or drug is expected to be delivered by ILs as an ideal carrier to target cells for therapeutic purposes. Secondly, the toxicity effects of ILs on organisms have been explored on purpose for killing cancer cells and other special cells or green degradation. Thirdly, the good electrocatalytic activity and high sensitivity of ILs can lead to preparations of biosensors for electrochemical detections. Finally, ILs can be used as the carrier for separations of nucleic acids, simplifying the separation process and improving the efficiency.
  • 加载中
    1. [1]

    2. [2]

      K R Seddon. J. Chem. Technol. Biotechnol., 1997, 68(4):351~356. 

    3. [3]

      A García, R González, A H Battez et al. Tribol. Int., 2014, 72(4):42~50.

    4. [4]

    5. [5]

      C P Mehnert. Chem. Eur. J., 2005, 11(1):50~56. 

    6. [6]

      P J Dyson. Biphasic Chemistry Utilising Ionic Liquids//Fall Meeting of the Swiss-Chemical-Society. 2005: 66~71.

    7. [7]

       

    8. [8]

       

    9. [9]

      P J Dyson. Transit. Met. Chem., 2002, 27(4):353~358. 

    10. [10]

      P Y Teo, W Cheng, J L Hedrick et al. Adv. Drug Deliv. Rev., 2016, 98:41~63. 

    11. [11]

      L Naldini. Nature, 2015, 526(7573):351~360. 

    12. [12]

      T G Park, J H Jeong, S W Kim. Adv. Drug Deliv. Rev., 2006, 58(4):467~486.

    13. [13]

      Y Yue, C Wu. Biomater. Sci., 2013, 1(2):152~170. 

    14. [14]

      D Schaffert, E Wagner. Gene Ther., 2008, 15(16):1131~1138. 

    15. [15]

      M A Mintzer, E E Simanek. Chem. Rev., 2008, 109(2):259~302.

    16. [16]

      S K Samal, M Dash, V S Van et al. Chem. Soc. Rev., 2012, 41(21):7147~7194. 

    17. [17]

      K Manojkumar, K T Prabhu Charan, A Sivaramakrishna et al. Biomacromolecules, 2015, 16(3):894~903. 

    18. [18]

      R R Mazid, A Cooper, Y Zhang et al. RSC Adv., 2015, 5(54):43839~43844. 

    19. [19]

      M Isik, M Agirre, J Zarate et al. J. Polym. Sci. A, 2017, 55(2):280~287. 

    20. [20]

      M H Allen Jr, M D Green, H K Getaneh et al. Biomacromolecules, 2011, 12(6):2243~2250. 

    21. [21]

      Y Wang, L Wang, M Yan et al. ACS Appl. Mater. Interf., 2017, 9(34):28185~28194. 

    22. [22]

      S Pandey. Anal. Chim. Acta, 2006, 556(1):38~45.

    23. [23]

      M Opallo, A Lesniewski. J. Electroanal. Chem., 2011, 656(1/2):2~16.

    24. [24]

      B Jagannath, S Muthukumar, S Prasad. Anal. Chim. Acta, 2018, 1016:29~39. 

    25. [25]

      R D Munje, S Muthukumar, B Jagannath et al. Sci. Rep., 2017, 7(1):1950.

    26. [26]

      C Y Xue, K L Yang. Langmuir, 2008, 24(2):563~567. 

    27. [27]

      H Tan, S Yang, G Shen et al. Angew. Chem., 2010, 122(46):8790~8793. 

    28. [28]

      D Zhao, Y Peng, L Xu et al. ACS Appl. Mater. Interf., 2015, 7(42):23418~23422. 

    29. [29]

      N Maleki, A Safavi, F Tajabadi. Anal. Chem., 2006, 78(11):3820~3826. 

    30. [30]

      W Sun, D Wang, G Li et al. Electrochim. Acta, 2008, 53(28):8217~8221. 

    31. [31]

      W Sun, P Qin, R Zhao et al. Talanta, 2010, 80(5):2177~2181. 

    32. [32]

      K Liu, J Zhang, G Yang et al. Electrochem. Commun., 2010, 12(3):402~405. 

    33. [33]

      W Sun, X Qi, Y Zhang et al. Electrochim. Acta, 2012, 85(4):145~151.

    34. [34]

      Q Zhu, F Gao, Y Yang et al. Sens. Actuat. B, 2015, 207:819~826. 

    35. [35]

      W Zhang. Sens. Actuat. B, 2013, 176:386~389. 

    36. [36]

      W Sun, X Wang, W Wang et al. J. Solid State Electrochem., 2015, 19(8):2431~2438. 

    37. [37]

      X Lu, J Hu, X Yao et al. Biomacromolecules, 2006, 7(3):975~980. 

    38. [38]

      X Lu, Q Zhang, L Zhang et al. Electrochem. Commun., 2006, 8(5):874~878. 

    39. [39]

      G Bolat, S Abaci. Sensors, 2018, 18(3):773. 

    40. [40]

      A Safavi, F Farjami. Biosens. Bioelectron., 2011, 26(5):2547~2552. 

    41. [41]

      A I Gopalan, K P Lee, D Ragupathy. Biosens. Bioelectron., 2009, 24(7):2211~2217. 

    42. [42]

      Z Zhu, L Qu, X Li et al. Electrochim. Acta, 2010, 55(20):5959~5965. 

    43. [43]

      E Eksin, M Muti, A Erdem. Electroanalysis, 2013, 25(10):2321~2329.

    44. [44]

      C Sengiz, G Congur, A Erdem. Sensors, 2015, 15(9):22737~22749. 

    45. [45]

      J Deng, W Liang, J Fang. ACS Appl. Mater. Interf., 2016, 8(6):3928~3932. 

    46. [46]

      D Chen, L Tang, J Li. Chem. Soc. Rev., 2010, 39(8):3157~3180. 

    47. [47]

      J Zhao, G Chen, L Zhu et al. Electrochem. Commun., 2011, 13(1):31~33. 

    48. [48]

      Y Zhang, L Huang. Microchim. Acta, 2012, 176(3/4):463~470.

    49. [49]

      A Erdem, M Muti, F Mese et al. Colloids Surf. B, 2014, 114:261~268. 

    50. [50]

      H Kazerooni, B Nasernejad. J. Appl. Electrochem., 2015, 45(12):1289~1298. 

    51. [51]

      J Y Huang, L Zhao, W Lei et al. Biosens. Bioelectron., 2018, 99:28~33. 

    52. [52]

      H Schwarzenbach, D S Hoon, K Pantel. Nat. Rev. Cancer, 2011, 11(6):426~437. 

    53. [53]

      J I Cutler, E Auyeung, C A Mirkin. J. Am. Chem. Soc., 2012, 134(3):1376~1391. 

    54. [54]

      Z Guo, Q L Liu. Nat. Biotechnol., 1997, 15(4):331~335. 

    55. [55]

      S Hayashi, H Hamaguchi. Chem. Lett., 2004, 33(12):1590~1591. 

    56. [56]

      B Mallick, B Balke, C Felser et al. Angew. Chem. Int. Ed., 2008, 47(40):7635~7638. 

    57. [57]

      K D Clark, M Varona, J L Anderson. Angew. Chem. Int. Ed., 2017, 56(26):7630~7633. 

    58. [58]

      O Nacham, K D Clark, J L Anderson. Anal. Chem., 2016, 88(15):7813~7820. 

    59. [59]

      D L Kim, H Vovusha, U Schwingenschlögl et al. J. Membrane Sci., 2017, 539:161~171. 

    60. [60]

      O Nacham, K D Clark, M Varona et al. Anal. Chem., 2017, 89(20):10661~10666. 

    61. [61]

      R F M Frade, A A Rosatella, C S Marques et al. Green Chem., 2009, 11(10):1660~1665. 

    62. [62]

      J Ranke, K Mölter, F Stock et al. Ecotoxicol. Environ. Safety, 2004, 58(3):396~404. 

    63. [63]

      R A Kumar, N Papaïconomou, J M Lee et al. Environ. Toxicol., 2009, 24(4):388~395. 

    64. [64]

      B Jastorff, K Mölter, P Behrend et al. Green Chem., 2005, 7(5):362~372. 

    65. [65]

      Z Du, L Zhu, M Dong et al. Aquat. Toxicol., 2012, 124:91~93.

    66. [66]

      Z Zhang, J Liu, X Cai et al. Environ. Sci. Technol., 2011, 45(4):1688~1694. 

    67. [67]

      K M Docherty, C F Kulpa Jr. Green Chem., 2005, 7(4):185~189. 

    68. [68]

      P Nan, S Yan, Y Wang et al. Environ. Toxicol., 2017, 32(2):404~416. 

    69. [69]

      C Robert, F L Barnes, I Hue et al. Mol. Reprod. Dev., 2000, 57(2):167~175. 

    70. [70]

      H Akbas, A Karadag, A Aydin et al. J. Mol. Liq., 2017, 230:482~495. 

    71. [71]

      E M Siedlecka, W Mrozik, Z Kaczyński et al. J. Hazard. Mater., 2008, 154(1/3):893~900.

    72. [72]

      E M Siedlecka, P Stepnowski. Environ. Sci. Pollut. Res., 2009, 16(4):453~458. 

    73. [73]

      C Zhang, S V Malhotra, A J Francis. Chemosphere, 2011, 82(11):1690~1695. 

    74. [74]

      N Gathergood, P J Scammells, M T Garcia. Green Chem., 2006, 8(2):156~160. 

    75. [75]

      V R Thamke, K M Kodam. J. Hazard. Mater., 2016, 320:408~416. 

  • 加载中
    1. [1]

      Jianfeng Yan Yating Xiao Xin Zuo Caixia Lin Yaofeng Yuan . Comprehensive Chemistry Experimental Design of Ferrocenylphenyl Derivatives. University Chemistry, 2024, 39(4): 329-337. doi: 10.3866/PKU.DXHX202310005

    2. [2]

      Yajun Hou Jinxin Liu Tao Chen Yi Zhang Lei Zhou . Sonogashira coupling reaction in ionic liquids: a detailed exploration of experiment 4.4D in the “101 Plan” synthetic chemistry curriculum. University Chemistry, 2026, 41(6): 136-144. doi: 10.12461/PKU.DXHX202510101

    3. [3]

      Kuaibing Wang Feifei Mao Weihua Zhang Bo Lv . Design and Practice of a Comprehensive Teaching Experiment for Preparing Biomass Carbon Dots from Rice Husk. University Chemistry, 2025, 40(5): 342-350. doi: 10.12461/PKU.DXHX202407042

    4. [4]

      Yongming Zhu Huili Hu Yuanchun Yu Xudong Li Peng Gao . Construction and Practice on New Form Stereoscopic Textbook of Electrochemistry for Energy Storage Science and Engineering: Taking Basic Course of Electrochemistry as an Example. University Chemistry, 2024, 39(8): 44-47. doi: 10.3866/PKU.DXHX202312086

    5. [5]

      Yameen AhmedXiangxiang FengYuanji GaoYang DingCaoyu LongMustafa HaiderHengyue LiZhuan LiShicheng HuangMakhsud I. SaidaminovJunliang Yang . Interface Modification by Ionic Liquid for Efficient and Stable FAPbI3 Perovskite Solar Cells. Acta Physico-Chimica Sinica, 2024, 40(6): 2303057-0. doi: 10.3866/PKU.WHXB202303057

    6. [6]

      Hua YuDingdu ChenXuan WangLijun YangGeming WangPu Hu . MOF-encapsulated phosphorus/nitrogen ionic liquid as a multifunctional flame-retardant additive for high-safety lithium-ion batteries. Acta Physico-Chimica Sinica, 2026, 42(7): 100201-0. doi: 10.1016/j.actphy.2025.100201

    7. [7]

      Zihan Lin Wanzhen Lin Fa-Jie Chen . Electrochemical Modifications of Native Peptides. University Chemistry, 2025, 40(3): 318-327. doi: 10.12461/PKU.DXHX202406089

    8. [8]

      Cen Zhou Biqiong Hong Yiting Chen . Application of Electrochemical Techniques in Supramolecular Chemistry. University Chemistry, 2025, 40(3): 308-317. doi: 10.12461/PKU.DXHX202406086

    9. [9]

      Zeqiu ChenLimiao CaiJie GuanZhanyang LiHao WangYaoguang GuoXingtao XuLikun Pan . Advanced electrode materials in capacitive deionization for efficient lithium extraction. Acta Physico-Chimica Sinica, 2025, 41(8): 100089-0. doi: 10.1016/j.actphy.2025.100089

    10. [10]

      Yongjian Zhang Fangling Gao Hong Yan Keyin Ye . Electrochemical Transformation of Organosulfur Compounds. University Chemistry, 2025, 40(5): 311-317. doi: 10.12461/PKU.DXHX202407035

    11. [11]

      Tinghui ANDong XIANGJiaqi LIJiawei WANGShuming YUNan WANGKedi CAI . Research progress on the application of laser synthesis technology for electrochemical functional materials. Chinese Journal of Inorganic Chemistry, 2025, 41(9): 1731-1754. doi: 10.11862/CJIC.20240412

    12. [12]

      Xinyi ZhangKai RenYanning LiuZhenyi GuZhixiong HuangShuohang ZhengXiaotong WangJinzhi GuoIgor V. ZatovskyJunming CaoXinglong Wu . Progress on Entropy Production Engineering for Electrochemical Catalysis. Acta Physico-Chimica Sinica, 2024, 40(7): 2307057-0. doi: 10.3866/PKU.WHXB202307057

    13. [13]

      Yanqin Wang Kang Wang Chen Sun Zhexi Yang . Comprehensive Experiment of Materials Chemistry: Directional Conversion of Urea to Nitrite by Electrochemical Method. University Chemistry, 2026, 41(6): 415-424. doi: 10.12461/PKU.DXHX202603025

    14. [14]

      Linbao Zhang Weisi Guo Shuwen Wang Ran Song Ming Li . Electrochemical Oxidation of Sulfides to Sulfoxides. University Chemistry, 2024, 39(11): 204-209. doi: 10.3866/PKU.DXHX202401009

    15. [15]

      Zhaoyu WenNa HanYanguang Li . Recent Progress towards the Production of H2O2 by Electrochemical Two-Electron Oxygen Reduction Reaction. Acta Physico-Chimica Sinica, 2024, 40(2): 2304001-0. doi: 10.3866/PKU.WHXB202304001

    16. [16]

      Feng Lin Zhongxin Jin Caiying Li Cheng Shao Yang Xu Fangze Li Siqi Liu Ruining Gu . Preparation and Electrochemical Properties of Nickel Foam-Supported Ni(OH)2-NiMoO4 Electrode Material. University Chemistry, 2025, 40(10): 225-232. doi: 10.12461/PKU.DXHX202412017

    17. [17]

      Yanqin Wang Pengfei Liu Jiaqi Cai Wenbin Su . Electrochemical method for directional conversion of nitrate in wastewater into high-value ammonia: a comprehensive experimental case study for materials chemistry undergraduates. University Chemistry, 2026, 41(7): 351-363. doi: 10.12461/PKU.DXHX202604110

    18. [18]

      Shuhui Li Rongxiuyuan Huang Yingming Pan . Electrochemical Synthesis of 2,5-Diphenyl-1,3,4-Oxadiazole: A Recommended Comprehensive Organic Chemistry Experiment. University Chemistry, 2025, 40(5): 357-365. doi: 10.12461/PKU.DXHX202407028

    19. [19]

      Hongyi LIAimin WULiuyang ZHAOXinpeng LIUFengqin CHENAikui LIHao HUANG . Effect of Y(PO3)3 double-coating modification on the electrochemical properties of Li[Ni0.8Co0.15Al0.05]O2. Chinese Journal of Inorganic Chemistry, 2024, 40(7): 1320-1328. doi: 10.11862/CJIC.20230480

    20. [20]

      Yu Wang Xianyu Liu Tianming Lv Miao Cui Shoulei Zhang Changgong Meng . Chemistry “101 Plan” synthetic chemistry experiment course construction: study on the preparation and identification of potassium persulfate. University Chemistry, 2026, 41(6): 145-151. doi: 10.12461/PKU.DXHX202511028

Metrics
  • PDF Downloads(5)
  • Abstract views(495)
  • HTML views(43)

通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索
Address:Zhongguancun North First Street 2,100190 Beijing, PR China Tel: +86-010-82449177-888
Powered By info@rhhz.net

/

DownLoad:  Full-Size Img  PowerPoint
Return