BODIPY@Ir(Ⅲ) Complexes Assembling Organic Nanoparticles for Enhanced Photodynamic Therapy

Yang Liu ,  Nan Song ,  Li Chen ,  Zhi-Gang Xie

Citation:  Yang Liu, Nan Song, Li Chen, Zhi-Gang Xie. BODIPY@Ir(Ⅲ) Complexes Assembling Organic Nanoparticles for Enhanced Photodynamic Therapy[J]. Chinese Journal of Polymer Science, 2018, 36(3): 417-424. doi: 10.1007/s10118-018-2096-9 shu

BODIPY@Ir(Ⅲ) Complexes Assembling Organic Nanoparticles for Enhanced Photodynamic Therapy

English


    1. [1]

      Li H., Wang P., Deng Y., Zeng M., Tang Y., Zhu W. H., Cheng Y.. Combination of active targeting, enzyme-triggered release and fluorescent dye into gold nanoclusters for endomicroscopy-guided photothermal/photodynamic therapy to pancreatic ductal adenocarcinoma[J]. Biomaterials, 2017, 139:  30-38. doi: 10.1016/j.biomaterials.2017.05.030

    2. [2]

      Li X., Gao M., Xin K., Zhang L., Ding D., Kong D., Wang Z., Shi Y., Kiessling F., Lammers T., Cheng J., Zhao Y.. Singlet oxygen-responsive micelles for enhanced photodynamic therapy[J]. J. Control. Release, 2017, 260:  12-21. doi: 10.1016/j.jconrel.2017.05.025

    3. [3]

      Linares I. A. P., de Oliveira K. T., Perussi J. R.. Chlorin derivatives sterically-prevented from self-aggregation with high antitumor activity for photodynamic therapy[J]. Dyes Pigm., 2017, 145:  518-527. doi: 10.1016/j.dyepig.2017.06.011

    4. [4]

      Xiong H., Zhou D., Zheng X., Qi Y., Wang Y., Jing X., Huang Y.. Stable amphiphilic supramolecular self-assembly based on cyclodextrin and carborane for the efficient photodynamic therapy[J]. Chem. Commun., 2017, 53:  3422-3425. doi: 10.1039/C6CC10059G

    5. [5]

      Du E., Hu X., Roy S., Wang P., Deasy K., Mochizuki T., Zhang Y.. Taurine-modified Ru(ii)-complex targets cancerous brain cells for photodynamic therapy[J]. Chem. Commun., 2017, 53:  6033-6036. doi: 10.1039/C7CC03337K

    6. [6]

      Gu B., Wu W., Xu G., Feng G., Yin F., Chong P. H. J., Qu J., Yong K. T., Liu B.. Precise two-photon photodynamic therapy using an efficient photosensitizer with aggregationinduced emission characteristics[J]. Adv. Mater., 2017, 29(28):  . doi: 10.1002/adma.201701076

    7. [7]

      Huang L., Li Z., Zhao Y., Yang J., Yang Y., Pendharkar A. I., Zhang Y., Kelmar S., Chen L., Wu W., Zhao J., Han G.. Enhancing photodynamic therapy through resonance energy transfer constructed near-Infrared photosensitized nanoparticles[J]. Adv. Mater., 2017, 29(28):  . doi: 10.1002/adma.201604789

    8. [8]

      Yue C., Yang Y., Song J., Alfranca G., Zhang C., Zhang Q., Yin T., Pan F., de la Fuente J. M., Cui D.. Mitochondriatargeting near-infrared light-triggered thermosensitive liposomes for localized photothermal and photodynamic ablation of tumors combined with chemotherapy[J]. Nanoscale, 2017, 9:  11103-11118. doi: 10.1039/C7NR02193C

    9. [9]

      Zheng Y., Lu H., Jiang Z., Guan Y., Zou J., Wang X., Cheng R., Gao H.. Low-power white light triggered AIE polymer nanoparticles with high ROS quantum yield for mitochondria-targeted and image-guided photodynamic therapy[J]. J. Mater. Chem. B, 2017, 5:  6277-6281.

    10. [10]

      Li Y., Zheng X., Zhang X., Liu S., Pei Q., Zheng M., Xie Z.. Porphyrin-based carbon dots for photodynamic therapy of hepatoma[J]. Adv. Healthc. Mater., 2017, 6(1):  . doi: 10.1002/adhm.201600924

    11. [11]

      Liu W., Wang Y. M., Li Y. H., Cai S. J., Yin X. B., He X. W., Zhang Y. K.. Fluorescent imaging-guided chemotherapyand-photodynamic dual therapy with nanoscale porphyrin metal-organic framework[J]. Small, 2017, 13(17):  . doi: 10.1002/smll.201603459

    12. [12]

      Rui L., Xue Y., Wang Y., Gao Y., Zhang W.. A mitochondria-targeting supramolecular photosensitizer based on pillararene for photodynamic therapy[J]. Chem. Commun., 2017, 53:  3126-3129. doi: 10.1039/C7CC00950J

    13. [13]

      Zhang W., Lin W., Zheng X., He S., Xie Z.. Comparing effects of redox sensitivity of organic nanoparticles to photodynamic activity[J]. Chem. Mater., 2017, 29:  1856-1863. doi: 10.1021/acs.chemmater.7b00207

    14. [14]

      Zheng X., Wang L., Pei Q., He S., Liu S., Xie Z.. Metal-organic framework@porous organic polymer nanocomposite for photodynamic therapy[J]. Chem. Mater., 2017, 29:  2374-2381. doi: 10.1021/acs.chemmater.7b00228

    15. [15]

      Isik M., Guliyev R., Kolemen S., Altay Y., Senturk B., Tekinay T., Akkaya E. U.. Designing an intracellular fluorescent probe for glutathione:two modulation sites for selective signal transduction[J]. Org. Lett., 2014, 16:  3260-3263. doi: 10.1021/ol501272z

    16. [16]

      Isik M., Ozdemir T., Turan I. S., Kolemen S., Akkaya E. U.. Chromogenic and fluorogenic sensing of biological thiols in aqueous solutions using BODIPY-based reagents[J]. Org. Lett., 2013, 15:  216-219. doi: 10.1021/ol303306s

    17. [17]

      Göl C., Malkoç M., Yeşilot S., Durmuş M.. Novel zinc(Ⅱ) phthalocyanine conjugates bearing different numbers of BODIPY and iodine groups as substituents on the periphery[J]. Dyes Pigm., 2014, 111:  81-90. doi: 10.1016/j.dyepig.2014.06.003

    18. [18]

      Kim B., Sui B., Yue X., Tang S., Tichy M. G., Belfield K. D.. In vitro photodynamic studies of a BODIPY-based photosensitizer[J]. Eur. J. Org. Chem., 2017, (1):  25-28.

    19. [19]

      Wang W., Wang L., Li Z., Xie Z.. BODIPY-containing nanoscale metal-organic frameworks for photodynamic therapy[J]. Chem. Commun., 2016, 52:  5402-5405. doi: 10.1039/C6CC01048B

    20. [20]

      Guo Z., Zou Y., He H., Rao J., Ji S., Cui X., Ke H., Deng Y., Yang H., Chen C., Zhao Y., Chen H.. Bifunctional platinated nanoparticles for photoinduced tumor ablation[J]. Adv. Mater., 2016, 46(28):  10155-10164.

    21. [21]

      Liu Y., Li Z., Chen L., Xie Z.. Near infrared BODIPY-platinum conjugates for imaging, photodynamic therapy and chemotherapy[J]. Dyes Pigm., 2017, 141:  5-12. doi: 10.1016/j.dyepig.2017.01.075

    22. [22]

      Cakmak Y., Kolemen S., Duman S., Dede Y., Dolen Y., Kilic B., Kostereli Z., Yildirim L. T., Dogan A. L., Guc D., Akkaya E. U.. Designing excited states:theory-guided access to efficient photosensitizers for photodynamic action[J]. Angew. Chem., 2011, 50:  11937-11941. doi: 10.1002/anie.v50.50

    23. [23]

      Epelde-Elezcano N., Palao E., Manzano H., PrietoCastaneda A., Agarrabeitia A. R., Tabero A., Villanueva A., de la Moya S., Lopez-Arbeloa I., Martinez-Martinez V., Ortiz M. J.. Rational design of advanced photosensitizers based on orthogonal BODIPY dimers to finely modulate singlet oxygen generation[J]. Chem. Eur. J., 2017, 23:  4837-4848. doi: 10.1002/chem.v23.20

    24. [24]

      Ozdemir T., Bila J. L., Sozmen F., Yildirim L. T., Akkaya E. U.. Orthogonal Bodipy trimers as photosensitizers for photodynamic action[J]. Org. Lett., 2016, 18:  4821-4823. doi: 10.1021/acs.orglett.6b02418

    25. [25]

      Wu W., Cui X., Zhao J.. Hetero BODIPY-dimers as heavy atom-free triplet photosensitizers showing a long-lived triplet excited state for triplet-triplet annihilation upconversion[J]. Chem. Commun., 2013, 49:  9009-9011. doi: 10.1039/c3cc45470c

    26. [26]

      Zhang X. F., Yang X.. Photosensitizer that selectively generates singlet oxygen in nonpolar environments:photophysical mechanism and efficiency for a covalent BODIPY dimer[J]. J. Phys. Chem. B, 2013, 117:  9050-9055. doi: 10.1021/jp405102m

    27. [27]

      Mari C., Huang H., Rubbiani R., Schulze M., Würthner F., Chao H., Gasser G.. Evaluation of perylene bisimide-based RuⅡand IrⅢ complexes as photosensitizers for photodynamic therapy[J]. Eur. J. Inorg. Chem., 2017, 2017:  1745-1752.

    28. [28]

      Wang L., Yin H., Cui P., Hetu M., Wang C., Monro S., Schaller R. D., Cameron C. G., Liu B., Kilina S., McFarland S. A., Sun W.. Near-infrared-emitting heteroleptic cationic iridium complexes derived from 2, 3-diphenylbenzo[g]quinoxaline as in vitro theranostic photodynamic therapy agents[J]. Dalton Trans, 2017, 46:  8091-8103. doi: 10.1039/C7DT00913E

    29. [29]

      Xiang H., Chen H., Tham H. P., Phua S. Z. F., Liu J. G., Zhao Y.. Cyclometalated iridium(Ⅲ)-complex-based micelles for glutathione-responsive targeted chemotherapy and photodynamic therapy[J]. ACS Appl. Mater. Interfaces, 2017, 9:  27553-27562. doi: 10.1021/acsami.7b09506

    30. [30]

      Zheng Y., He L., Zhang D. Y., Tan C. P., Ji L. N., Mao Z. W.. Mixed-ligand iridium(Ⅲ) complexes as photodynamic anticancer agents[J]. Dalton Trans., 2017, 46:  11395-11407. doi: 10.1039/C7DT02273E

    31. [31]

      Liu J., Jin C., Yuan B., Liu X., Chen Y., Ji L., Chao H.. Selectively lighting up two-photon photodynamic activity in mitochondria with AIE-active iridium(Ⅲ) complexes[J]. Chem. Commun., 2017, 53:  2052-2055. doi: 10.1039/C6CC10015E

    32. [32]

      McKenzie L. K., Sazanovich I. V., Baggaley E., Bonneau M., Guerchais V., Williams J. A., Weinstein J. A., Bryant H. E.. Metal complexes for two-photon photodynamic therapy:a cyclometallated iridium complex induces two-photon photosensitization of cancer cells under near-IR light[J]. Chem. Eur. J., 2017, 23:  234-238. doi: 10.1002/chem.v23.2

    33. [33]

      Nam J. S., Kang M. G., Kang J., Park S. Y., Lee S. J., Kim H. T., Seo J. K., Kwon O. H., Lim M. H., Rhee H. W., Kwon T. H.. Endoplasmic reticulum-localized iridium(Ⅲ) complexes as efficient photodynamic therapy agents via protein modifications[J]. J. Am. Chem. Soc., 2016, 138:  10968-10977. doi: 10.1021/jacs.6b05302

    34. [34]

      Qiu K., Ouyang M., Liu Y., Huang H., Liu C., Chen Y., Ji L., Chao H.. Two-photon photodynamic ablation of tumor cells by mitochondria-targeted iridium(Ⅲ) complexes in aggregate states[J]. J. Mater. Chem. B, 2017, 5:  5488-5498. doi: 10.1039/C7TB00731K

    35. [35]

      Tian X., Zhu Y., Zhang M., Luo L., Wu J., Zhou H., Guan L., Battaglia G., Tian Y.. Localization matters:a nuclear targeting two-photon absorption iridium complex in photodynamic therapy[J]. Chem. Commun., 2017, 53:  3303-3306. doi: 10.1039/C6CC09470H

    36. [36]

      Deligonul N., Browne A. R., Golen J. A., Rheingold A. L., Gray T. G.. Cyclometalated iridium(Ⅲ) complexes of azadipyrromethene chromophores[J]. Organometallics, 2014, 33:  637-643. doi: 10.1021/om4007032

    37. [37]

      Zhou J., Gai L., Zhou Z., Mack J., Xu K., Zhao J., Qiu H., Chan K. S., Shen Z.. Highly efficient near IR photosensitizers based on Ir-C bonded porphyrin-aza-BODIPY conjugates[J]. RSC Adv., 2016, 6:  72115-72120. doi: 10.1039/C6RA10131C

    38. [38]

      Majumdar P., Yuan X., Li S., Le Guennic B., Ma J., Zhang C., Jacquemin D., Zhao J.. Cyclometalated Ir(Ⅲ) complexes with styryl-BODIPY ligands showing near IR absorption/emission:preparation, study of photophysical properties and application as photodynamic/luminescence imaging materials[J]. J. Mater. Chem. B, 2014, 2:  2838-2854. doi: 10.1039/C4TB00284A

    39. [39]

      Palao E., Sola-Llano R., Tabero A., Manzano H., Agarrabeitia A. R., Villanueva A., Lopez-Arbeloa I., Martinez-Martinez V., Ortiz M. J.. Acetylacetonate BODIPY-biscyclometalated iridium(Ⅲ) complexes:effective strategy towards smarter fluorescent photosensitizer agents[J]. Chem. Eur. J., 2017, 23:  10139-10147. doi: 10.1002/chem.v23.42

    40. [40]

      Sun J., Zhong F., Yi X., Zhao J.. Efficient enhancement of the visible-light absorption of cyclometalated Ir(Ⅲ) complexes triplet photosensitizers with BODIPY and applications in photooxidation and triplet-triplet annihilation upconversion[J]. Inorg. Chem., 2013, 52:  6299-6310. doi: 10.1021/ic302210b

    41. [41]

      Tabrizi L., Chiniforoshan H.. New cyclometalated Ir(Ⅲ) complexes with NCN pincer and meso-phenylcyanamide BODIPY ligands as efficient photodynamic therapy agents[J]. RSC Adv., 2017, 7:  34160-34169. doi: 10.1039/C7RA05579J

    42. [42]

      Khairoutdinov R. F., Doubova L. V., Haddon R. C., Saraf L.. Persistent photoconductivity in chemically modified single-wall carbon nanotubes[J]. J. Phys. Chem. B, 2004, 108:  19976-19981. doi: 10.1021/jp046495m

    43. [43]

      Li Z., Zheng M., Guan X., Xie Z., Huang Y., Jing X.. Unadulterated BODIPY-dimer nanoparticles with high stability and good biocompatibility for cellular imaging[J]. Nanoscale, 2014, 6:  5662-5665. doi: 10.1039/C4NR00521J

    44. [44]

      Liu Y., Song N., Chen L., Xie Z.. Triple-BODIPY organic nanoparticles with particular fluorescence emission[J]. Dyes Pigm., 2017, 147:  241-245. doi: 10.1016/j.dyepig.2017.08.026

  • 加载中
计量
  • PDF下载量:  0
  • 文章访问数:  2197
  • HTML全文浏览量:  87
文章相关
  • 发布日期:  2018-03-05
  • 收稿日期:  2017-09-27
  • 接受日期:  2017-11-23
  • 网络出版日期:  2017-12-27
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

/

返回文章