Simultaneous Imaging and Photodynamic‐Enhanced Photothermal Inhibition of Cancer Cells Using a Multifunctional System Combining Indocyanine Green and Polydopamine‐Preloaded Upconversion Luminescent Nanoparticles

Author:

Ye Sihao1,Zhang Wenjing1,Shen Yao2,Han Shuai1,Hu Hai1,Liang Yuexiang1,Lin Zijian2,Jin Yuepeng3,Lawson Tom4,Liu Yong1ORCID,Cai Zhenzhai2

Affiliation:

1. Laboratory of Nanoscale Biosensing and Bioimaging (NBAB) School of Ophthalmology and Optometry School of Biomedical Engineering Wenzhou Medical University Wenzhou Zhejiang 325027 China

2. Department of Gastroenterology the Second Affiliated Hospital of Wenzhou Medical University Wenzhou Medical University Wenzhou Zhejiang 325027 China

3. National Key Clinical Specialty (General Surgery) the First Affiliated Hospital of Wenzhou Medical University Wenzhou Medical University Wenzhou Zhejiang 325000 China

4. School of Mathematical and Physical Sciences ARC Centre of Excellence for Nanoscale Biophotonics (CNBP) Macquarie University Sydney NSW 2109 Australia

Abstract

AbstractThis work introduces a novel multifunctional system called UPIPF (upconversion‐polydopamine‐indocyanine‐polyethylene‐folic) for upconversion luminescent (UCL) imaging of cancer cells using near‐infrared (NIR) illumination. The system demonstrates efficient inhibition of human hepatoma (HepG2) cancer cells through a combination of NIR‐triggered photodynamic therapy (PDT) and enhanced photothermal therapy (PTT). Initially, upconversion nanoparticles (UCNP) are synthesized using a simple thermal decomposition method. To improve their biocompatibility and aqueous dispersibility, polydopamine (PDA) is introduced to the UCNP via a ligand exchange technique. Indocyanine green (ICG) molecules are electrostatically attached to the surface of the UCNP‐polydopamine (UCNP@PDAs) complex to enhance the PDT and PTT effects. Moreover, polyethylene glycol (PEG)‐modified folic acid (FA) is incorporated into the UCNP‐polydopamine‐indocyanine‐green (UCNP@PDA‐ICGs) nanoparticles to enhance their targeting capability against cancer cells. The excellent UCL properties of these UCNP enable the final UCNP@PDA‐ICG‐PEG‐FA nanoparticles (referred to as UPIPF) to serve as a potential candidate for efficient anticancer drug delivery, real‐time imaging, and early diagnosis of cancer cells. Furthermore, the UPIPF system exhibits PDT‐assisted PTT effects, providing a convenient approach for efficient cancer cell inhibition (more than 99% of cells are killed). The prepared UPIPF system shows promise for early diagnosis and simultaneous treatment of malignant cancers.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Materials Chemistry,Polymers and Plastics,Organic Chemistry

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