Multifunctional croconaine nanoparticles for efficient optoacoustic imaging of deep tumors and photothermal therapy

Research output: Contribution to journalArticleResearchpeer review

Authors

  • Nian Liu
  • Patrick O'Connor
  • Vipul Gujrati
  • Pia Anzenhofer
  • Uwe Klemm
  • Karin Kleigrewe
  • Michael Sattler
  • Oliver Plettenburg
  • Vasilis Ntziachristos

External Research Organisations

  • Helmholtz Zentrum München - German Research Center for Environmental Health
  • Technical University of Munich (TUM)
  • Zhejiang University
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Details

Original languageEnglish
Pages (from-to)4637-4647
Number of pages11
JournalNanophotonics
Volume11
Issue number21
Early online date26 Sept 2022
Publication statusPublished - Dec 2022

Abstract

The proper design of near-infrared light-absorbing agents enables efficient optoacoustic imaging-guided phototherapy. In particular, several croconaine-based organic agents with excellent optical properties have been recently reported for this purpose. However, most of them absorb light below 800 nm, limiting deep-tissue imaging applications. To this end, we utilized a recently described novel croconaine derivative (CR880) to develop CR880-based nanoparticles (CR880-NPs) for effective in vivo delivery, deep tissue optoacoustic imaging and photothermal therapy applications. Radicals and strong π-πstacking in CR880 result in an 880 nm absorption peak with no blue-shift upon condensing to the solid phase. DSPE-PEG2000-formulated CR880-NPs exhibited high optoacoustic generation efficiency and photostability, and could be visualized in the tumors of three different mouse tumor models (breast, brain, and colon tumor) with high image contrast. The high photothermal conversion efficiency of CR880-NPs (∼58%) subsequently enabled efficient in vivo tumor elimination using a low energy laser, while remaining biocompatible and well-tolerated. This work introduces a promising novel agent for cancer theranostics of challenging deep-seated tumors.

Keywords

    880 nm, croconaine, deep tumors, nanoparticles, optoacoustics, photothermal therapy

ASJC Scopus subject areas

Sustainable Development Goals

Cite this

Multifunctional croconaine nanoparticles for efficient optoacoustic imaging of deep tumors and photothermal therapy. / Liu, Nian; O'Connor, Patrick; Gujrati, Vipul et al.
In: Nanophotonics, Vol. 11, No. 21, 12.2022, p. 4637-4647.

Research output: Contribution to journalArticleResearchpeer review

Liu, N, O'Connor, P, Gujrati, V, Anzenhofer, P, Klemm, U, Kleigrewe, K, Sattler, M, Plettenburg, O & Ntziachristos, V 2022, 'Multifunctional croconaine nanoparticles for efficient optoacoustic imaging of deep tumors and photothermal therapy', Nanophotonics, vol. 11, no. 21, pp. 4637-4647. https://doi.org/10.1515/nanoph-2022-0469
Liu, N., O'Connor, P., Gujrati, V., Anzenhofer, P., Klemm, U., Kleigrewe, K., Sattler, M., Plettenburg, O., & Ntziachristos, V. (2022). Multifunctional croconaine nanoparticles for efficient optoacoustic imaging of deep tumors and photothermal therapy. Nanophotonics, 11(21), 4637-4647. https://doi.org/10.1515/nanoph-2022-0469
Liu N, O'Connor P, Gujrati V, Anzenhofer P, Klemm U, Kleigrewe K et al. Multifunctional croconaine nanoparticles for efficient optoacoustic imaging of deep tumors and photothermal therapy. Nanophotonics. 2022 Dec;11(21):4637-4647. Epub 2022 Sept 26. doi: 10.1515/nanoph-2022-0469
Liu, Nian ; O'Connor, Patrick ; Gujrati, Vipul et al. / Multifunctional croconaine nanoparticles for efficient optoacoustic imaging of deep tumors and photothermal therapy. In: Nanophotonics. 2022 ; Vol. 11, No. 21. pp. 4637-4647.
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title = "Multifunctional croconaine nanoparticles for efficient optoacoustic imaging of deep tumors and photothermal therapy",
abstract = "The proper design of near-infrared light-absorbing agents enables efficient optoacoustic imaging-guided phototherapy. In particular, several croconaine-based organic agents with excellent optical properties have been recently reported for this purpose. However, most of them absorb light below 800 nm, limiting deep-tissue imaging applications. To this end, we utilized a recently described novel croconaine derivative (CR880) to develop CR880-based nanoparticles (CR880-NPs) for effective in vivo delivery, deep tissue optoacoustic imaging and photothermal therapy applications. Radicals and strong π-πstacking in CR880 result in an 880 nm absorption peak with no blue-shift upon condensing to the solid phase. DSPE-PEG2000-formulated CR880-NPs exhibited high optoacoustic generation efficiency and photostability, and could be visualized in the tumors of three different mouse tumor models (breast, brain, and colon tumor) with high image contrast. The high photothermal conversion efficiency of CR880-NPs (∼58%) subsequently enabled efficient in vivo tumor elimination using a low energy laser, while remaining biocompatible and well-tolerated. This work introduces a promising novel agent for cancer theranostics of challenging deep-seated tumors.",
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note = "Funding Information: Research funding: This project has received funding from the European Research Council (ERC) under the European Union{\textquoteright}s Horizon 2020 research and innovation programme under grant agreement no. 694968 (PREMSOT). The research leading to these results was supported by the Deutsche Forschungsgemeinschaft (DFG), Germany (Gottfried Wilhelm Leibniz Prize 2013, NT 3/10–1) as well as by the DFG as part of the CRC 1123 (Z1). Dr. Nian Liu acknowledges support from the China Scholarship Council. Dr. Patrick O{\textquoteright}Connor acknowledges support by the Helmholtz Association and the BMBF (16GW0251K). We wish to thank Carsten Peters (Department of Chemistry, Technical University of Munuch) for the TEM measurement, Dr. Juan Antonio Aguilar-Pimentel (German Mouse Clinic/Institute of Experimental Genetics, Helmholtz Zentrum M{\"u}nchen) for providing the thermal camera, Mohammed Azeem for assisting phantom preparation, and Dr. Doris Bengel for assisting with experimental procedures. We also wish to thank Dr. Sergey Sulima and Dr. Robert Wilson for helpful suggestions on the manuscript.",
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AU - Liu, Nian

AU - O'Connor, Patrick

AU - Gujrati, Vipul

AU - Anzenhofer, Pia

AU - Klemm, Uwe

AU - Kleigrewe, Karin

AU - Sattler, Michael

AU - Plettenburg, Oliver

AU - Ntziachristos, Vasilis

N1 - Funding Information: Research funding: This project has received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme under grant agreement no. 694968 (PREMSOT). The research leading to these results was supported by the Deutsche Forschungsgemeinschaft (DFG), Germany (Gottfried Wilhelm Leibniz Prize 2013, NT 3/10–1) as well as by the DFG as part of the CRC 1123 (Z1). Dr. Nian Liu acknowledges support from the China Scholarship Council. Dr. Patrick O’Connor acknowledges support by the Helmholtz Association and the BMBF (16GW0251K). We wish to thank Carsten Peters (Department of Chemistry, Technical University of Munuch) for the TEM measurement, Dr. Juan Antonio Aguilar-Pimentel (German Mouse Clinic/Institute of Experimental Genetics, Helmholtz Zentrum München) for providing the thermal camera, Mohammed Azeem for assisting phantom preparation, and Dr. Doris Bengel for assisting with experimental procedures. We also wish to thank Dr. Sergey Sulima and Dr. Robert Wilson for helpful suggestions on the manuscript.

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