4.8 Article

Cancer cell membrane-coated C-TiO2 hollow nanoshells for combined sonodynamic and hypoxia-activated chemotherapy

期刊

ACTA BIOMATERIALIA
卷 152, 期 -, 页码 562-574

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2022.08.067

关键词

C-TiO 2 hollow nanoshells; Sonodynamic therapy; Chemotherapy; Combination therapy; Hypoxia

资金

  1. National Natural Science Foundation of China [52202343]
  2. Basic and Clinical Cooperative Research and Promotion Program of Anhui Medical University [2021xkjT028]
  3. Anhui Provincial Natural Science Foundation [2208085QC81, 2208085MH251]
  4. Anhui Medical University [1406012201]
  5. Guangdong Provincial Key Laboratory of Precision Medicine for Gastrointestinal Cancer [2020B121201004]
  6. Youth talent lift project of Jiangsu Association for Science and Technology [TJ-2021-075]
  7. Outstanding Youths Development Scheme of Nanfang Hospital, Southern Medical University [2021J008]

向作者/读者索取更多资源

In this study, a biomimetic drug delivery system was synthesized for combined sonodynamic therapy and hypoxia-activated chemotherapy. The system showed good tumor targeting and biocompatibility, and improved the therapeutic effect by exploiting tumor hypoxia.
Sonodynamic therapy (SDT) is a promising strategy for tumor treatment that satisfies all requirements of penetrating deep-seated tissues without causing additional trauma. However, the hypoxic tumor mi-croenvironment impairs the therapeutic effect of SDT. The synergistic treatment of oxygen concentration-dependent SDT and bio-reductive therapy has been proven to be an effective approach to improve the therapeutic efficiency of SDT by exploiting tumor hypoxia. Herein, a biomimetic drug delivery system (C-TiO2/TPZ@CM) was successfully synthesized for combined SDT and hypoxia-activated chemotherapy, which was composed of tirapazamine (TPZ)-loaded C-TiO2 hollow nanoshells (HNSs) as the inner cores and cancer cell membrane (CM) as the outer shells. C-TiO2 HNSs coated with CM achieved tumor target-ing via homologous binding. C-TiO2 @CM as a nanocarrier loaded with TPZ in the presence of the trapping ability of CM and the special cavity structure of C-TiO2 HNSs. Moreover, C-TiO2 HNSs as sonosensitizers killed cancer cells under ultrasound (US) irradiation. Oxygen depletion during SDT induced a hypoxic environment in the tumor to activate the killing effect of co-delivered TPZ, thereby obtaining satisfac-tory synergistic therapeutic effects. In addition, C-TiO2 @CM exhibited remarkable biocompatibility with-out manifest damage and toxicity to the blood and major organs of the mice. The study highlighted that C-TiO2/TPZ@CM served as a powerful biomimetic drug delivery system for effective SDT by exploiting tumor hypoxia.Statement of significance center dot C-TiO2 @CM achieved tumor targeting via homologous binding.center dot C-TiO2 hollow nanoshells could be used as a sonosensitizer and drug carrier for synergistic SDT and hypoxia-activated chemotherapy.center dot C-TiO2/TPZ@CM showed no obvious toxicity under the injection dose.(c) 2022 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

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