Efficient Combination Chemo-Sonodynamic Cancer Therapy Using Mitochondria-Targeting Sonosensitizer-Loaded Polysorbate-Based Micelles

• Published in: International journal of molecular sciences 2024-03, Vol.25 (6), p.3474
• Main Authors: Kang, Hyeon Ju, Truong Hoang, Quan, Min, Jun, Son, Min Soo, Tram, Le Thi Hong, Kim, Byoung Choul, Song, Youngjun, Shim, Min Suk
• Format: Article
• Language: English
• Subjects: Antimitotic agents; Antineoplastic agents; Bioavailability; Cancer; Cancer therapies; Care and treatment; Cell death; Cell Line, Tumor; Chemotherapy; Communication; Health aspects; Humans; Micelles; Microscopy; Mitochondria; Mitochondria - metabolism; Morphology; Nanoparticles; Neoplasms - drug therapy; Organophosphorus Compounds; Permeability; Physiology; Polysorbates; Porphyrins - metabolism; Proteins; Reactive oxygen species; Reactive Oxygen Species - metabolism; Spectrum analysis; Surface active agents; Tumors
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25063474

Sonodynamic therapy (SDT), utilizing ultrasound (US) and sonosensitizers, holds immense potential as a noninvasive and targeted treatment for a variety of deep-seated tumors. However, the clinical translation of SDT is hampered by several key limitations in sonosensitizers, especially their low aqueous stability and poor cellular uptake. In this study, non-ionic polysorbate (Tween 80, T80) was adopted to formulate effective nanocarriers for the safe and efficient delivery of sonosensitizers to cancer cells. Mitochondria-targeting triphenylphosphonium (TPP)-conjugated chlorin e6 (Ce6) sonosensitizer was loaded into T80-based micelles for efficient SDT. Pro-oxidant piperlongumine (PL) was co-encapsulated with TPP-conjugated Ce6 (T-Ce6) in T80 micelles to enable combination chemo-SDT. T80 micelles substantially enhanced the cellular internalization of T-Ce6. As a result, T80 micelles loaded with T-Ce6 and PL [T80(T-Ce6/PL)] significantly elevated intracellular reactive oxygen species (ROS) generation in MCF-7 human breast cancer cells upon US exposure. Moreover, T-Ce6 exhibited selective accumulation within the mitochondria, leading to efficient cell death under US irradiation. Importantly, T80(T-Ce6/PL) micelles caused cancer-specific cell death by selectively triggering apoptosis in cancer cells through PL. This study demonstrated the feasibility of using T80(T-Ce6/PL) micelles for efficient and cancer-specific combination chemo-SDT.