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Arsenic trioxide-loaded CalliSpheres: In vitro study of drug release and antitumor activity, and in vivo study of pharmacokinetics, treatment efficacy and safety in liver cancer

  • Authors:
    • Xuhua Duan
    • Guorui Zhao
    • Xinwei Han
    • Jianzhuang Ren
    • Hao Li
    • Pengfei Chen
    • Manzhou Wang
    • Shuguang Ju
  • View Affiliations / Copyright

    Affiliations: Department of Interventional Radiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, P.R. China
    Copyright: © Duan et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Article Number: 124
    |
    Published online on: May 7, 2021
       https://doi.org/10.3892/or.2021.8075
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Abstract

The aim of the present study was to investigate the arsenic trioxide (ATO) loading/releasing efficiency of CalliSphere beads (CBs), as well as the in vitro anticancer activity, in vivo pharmacokinetics, treatment efficacy and safety of ATO-eluting CBs in liver cancer. The ATO loading and releasing efficiencies in CBs were evaluated. Furthermore, cell viability, invasion, apoptosis, VEGF expression and MMP9 expression were determined in liver cancer cells treated with ATO-eluting CBs or ATO solution. Rabbit liver models were established and underwent TACE with ATO-eluting CBs or ATO/lipiodol emulsion. Subsequently, their ATO pharmacokinetics were determined and macroscopic/microscopic examinations were conducted. In vitro, CB-loaded ATO increased during 40 min with an optimal loading efficiency of 23.0±2.5%, and released ATO rapidly within the first 30 min (31.40±10.0%) then slowed down within the latter 48 h (47.20±4.70%). ATO-eluting CBs exhibited decreased cell viability to some extent and similar invasive cell count, apoptosis rate, VEGF and MMP9 levels compared with ATO solution at various concentrations and time-points. In vivo, ATO concentration was lower in plasma, but higher in tumor tissues, and necrosis was more complete in tumor tissue while milder in normal liver parenchyma after rabbit liver was embolized with ATO-eluting CBs compared with ATO/lipiodol emulsion. ATO-eluting CBs may be a novel and promising therapeutic option in treating liver cancer.
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Copy and paste a formatted citation
Spandidos Publications style
Duan X, Zhao G, Han X, Ren J, Li H, Chen P, Wang M and Ju S: Arsenic trioxide-loaded CalliSpheres: <em>In vitro</em> study of drug release and antitumor activity, and <em>in vivo</em> study of pharmacokinetics, treatment efficacy and safety in liver cancer. Oncol Rep 46: 124, 2021.
APA
Duan, X., Zhao, G., Han, X., Ren, J., Li, H., Chen, P. ... Ju, S. (2021). Arsenic trioxide-loaded CalliSpheres: <em>In vitro</em> study of drug release and antitumor activity, and <em>in vivo</em> study of pharmacokinetics, treatment efficacy and safety in liver cancer. Oncology Reports, 46, 124. https://doi.org/10.3892/or.2021.8075
MLA
Duan, X., Zhao, G., Han, X., Ren, J., Li, H., Chen, P., Wang, M., Ju, S."Arsenic trioxide-loaded CalliSpheres: <em>In vitro</em> study of drug release and antitumor activity, and <em>in vivo</em> study of pharmacokinetics, treatment efficacy and safety in liver cancer". Oncology Reports 46.1 (2021): 124.
Chicago
Duan, X., Zhao, G., Han, X., Ren, J., Li, H., Chen, P., Wang, M., Ju, S."Arsenic trioxide-loaded CalliSpheres: <em>In vitro</em> study of drug release and antitumor activity, and <em>in vivo</em> study of pharmacokinetics, treatment efficacy and safety in liver cancer". Oncology Reports 46, no. 1 (2021): 124. https://doi.org/10.3892/or.2021.8075
Copy and paste a formatted citation
x
Spandidos Publications style
Duan X, Zhao G, Han X, Ren J, Li H, Chen P, Wang M and Ju S: Arsenic trioxide-loaded CalliSpheres: <em>In vitro</em> study of drug release and antitumor activity, and <em>in vivo</em> study of pharmacokinetics, treatment efficacy and safety in liver cancer. Oncol Rep 46: 124, 2021.
APA
Duan, X., Zhao, G., Han, X., Ren, J., Li, H., Chen, P. ... Ju, S. (2021). Arsenic trioxide-loaded CalliSpheres: <em>In vitro</em> study of drug release and antitumor activity, and <em>in vivo</em> study of pharmacokinetics, treatment efficacy and safety in liver cancer. Oncology Reports, 46, 124. https://doi.org/10.3892/or.2021.8075
MLA
Duan, X., Zhao, G., Han, X., Ren, J., Li, H., Chen, P., Wang, M., Ju, S."Arsenic trioxide-loaded CalliSpheres: <em>In vitro</em> study of drug release and antitumor activity, and <em>in vivo</em> study of pharmacokinetics, treatment efficacy and safety in liver cancer". Oncology Reports 46.1 (2021): 124.
Chicago
Duan, X., Zhao, G., Han, X., Ren, J., Li, H., Chen, P., Wang, M., Ju, S."Arsenic trioxide-loaded CalliSpheres: <em>In vitro</em> study of drug release and antitumor activity, and <em>in vivo</em> study of pharmacokinetics, treatment efficacy and safety in liver cancer". Oncology Reports 46, no. 1 (2021): 124. https://doi.org/10.3892/or.2021.8075
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