4.8 Article

Iridium Complex-Loaded Sorafenib Nanocomposites for Synergistic Chemo-photodynamic Therapy of Hepatocellular Carcinoma

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 14, Issue 33, Pages 37356-37368

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c07247

Keywords

sorafenib; photodynamic therapy; iridium-based photosensitizer; hepatocellular carcinoma; reactive oxygen species

Funding

  1. National Natural Science Foundation of China [81472673, 81672720, 81672334, 21501121]
  2. Natural Science Foundation of Shanghai [19ZR1434700, 22ZR1411800]

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The study fabricated a nano-chemo-phototherapy drug by combining an iridium-based photosensitizer with sorafenib (IPS) via a self-assembly process. The IPS exhibited significantly improved therapeutic efficacy against tumor cells by inducing apoptosis and necrosis, inhibiting HCC cell proliferation, and promoting cell apoptosis.
Although sorafenib, a multi-kinase inhibitor, has provided noteworthy benefits in patients with hepatocellular carcinoma (HCC), the inevitable side effects, narrow therapeutic window, and low bioavailability seriously affect its clinical application. To be clinically distinctive, innovative drugs must meet the needs of reaching tumor tissues and cause limited side effects to normal organs and tissues. Recently, photodynamic therapy, utilizing a combination of a photosensitizer and light irradiation, was selectively accumulated at the tumor site and taken up effectively via inducing apoptosis or necrosis of cancer cells. In this study, a nano-chemo-phototherapy drug was fabricated to compose an iridium-based photosensitizer combined with sorafenib (IPS) via a self-assembly process. Compared to the free iridium photosensitizer or sorafenib, the IPS exhibited significantly improved therapeutic efficacy against tumor cells because of the increased cellular uptake and the subsequent simultaneous release of sorafenib and generation of reactive oxygen species production upon 532 nm laser irradiation. To evaluate the effect of synergistic treatment, cytotoxicity detection, live/ dead staining, cell proliferative and apoptotic assay, and Western blot were performed. The IPS exhibited sufficient biocompatibility by hemolysis and serum biochemical tests. Also, the results suggested that IPS significantly inhibited HCC cell proliferation and promoted cell apoptosis. More importantly, marked anti-tumor growth effects via inhibiting cell proliferation and promoting tumor cell death were observed in an orthotopic xenograft HCC model. Therefore, our newly proposed nanotheranostic agent for combined chemotherapeutic and photodynamic therapy notably improves the therapeutic effect of sorafenib and has the potential to be a new alternative option for HCC treatment.

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