4.7 Article

Indocyanine Green-Based Theranostic Nanoplatform for NIR Fluorescence Image-Guided Chemo/Photothermal Therapy of Cervical Cancer

Journal

INTERNATIONAL JOURNAL OF NANOMEDICINE
Volume 16, Issue -, Pages 4847-4861

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IJN.S318678

Keywords

cervical cancer; indocyanine green; chemo/photothermal therapy; nanoparticles; near-infrared fluorescence imaging

Funding

  1. Fundamental Research Funds for the Central Universities
  2. State Key Laboratory of Pathogenesis, Prevention and Treatment of High IncidenceDiseases in Central Asia Fund [SKLHIDCA20195, SKLHIDCA20193, SKLHIDCA20206]
  3. Xinjiang Autonomous Region Health Commission
  4. Young Scientific and Technological Talents Project [WJWJ202012]
  5. Xinjiang Autonomous Region Collaborative Innovation Program [2019E0282]
  6. Graduate Student Innovation Program of the Hospital [330104006]
  7. National Natural Science Foundation of China [82060326]
  8. First Affiliated Hospital of Xinjiang Medical University

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Indocyanine green (ICG) is a favorable fluorescence nanoprobe known for its strong NIR-I fluorescence emission and good photothermal capabilities. To enhance its therapeutic efficiency, ICG was encapsulated with bovine serum albumin (BSA) and loaded with the chemotherapeutic drug doxorubicin (DOX) to form the BSA@ICG-DOX theranostic nanoplatform. The resulting nanoplatform showed strong NIR-I fluorescence emission, excellent photothermal properties, biocompatibility, and tumor targeting ability, making it a promising tool for combined diagnosis and therapy of subcutaneous cervical tumors.
Purpose: Indocyanine green (ICG) is a favorable fluorescence nanoprobe for its strong NIR-I fluorescence emission and good photothermal capabilities. However, the stability and tumor targeting ability of ICG is poor, which limits its further applications. To further improve the photothermal and therapeutic efficiency of ICG, bovine serum albumin (BSA) was utilized to encapsulate the ICG and the chemotherapeutic drug doxorubicin (DOX) was loaded to form the BSA@ICG-DOX theranostic nanoplatform. Methods: In this study, ICG-loaded BSA nanoparticles (NPs) and the BSA@ICG-DOX NPs were fabricated using reprecipitation methods. Next, the tumour inhibition ability and biocompatibility of the NPs were evaluated. A subcutaneous xenografted nude mice model was established and imaging guided synergetic therapy was performed with the assistance of BSA@ICG-DOX NPs under 808 nm laser irradiation. Results: The BSA@ICG NPs exhibited strong NIR-I fluorescence emission, excellent photothermal properties, biocompatibility, and tumor targeting ability. To further improve the therapeutic efficiency, the chemotherapeutic drug doxorubicin (DOX) was loaded into the BSA@ICG NPs to form the BSA@ICG-DOX theranostic nanoplatform. The BSA@ICG-DOX NPs were spherical with an average size of similar to 194.7 nm. The NPs had high encapsula-tion efficiency (DOX: 19.96% and ICG: 60.57%), and drug loading content (DOX: 0.95% and ICG: 3.03%). Next, excellent NIR-I fluorescence and low toxicity of the BSA@ICG-DOX NPs were verified. Targeted NIR-I fluorescence images were obtained after intravenous injection of the NPs into the subcutaneous cervical tumors of the mice. Conclusion: To improve the anti-tumor efficiency of the ICG@BSA NPs, the chemothera-peutic drug DOX was loaded into the BSA@ICG NPs. The NIR excitation/emission and targeted BSA@ICG-DOX NPs enables high-performance diagnosis and chemo/photothermal therapy of subcutaneous cervical tumors, providing a promising approach for further biomedical applications.

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