1. Academic Validation
  2. Oxygen tank for synergistic hypoxia relief to enhance mitochondria-targeted photodynamic therapy

Oxygen tank for synergistic hypoxia relief to enhance mitochondria-targeted photodynamic therapy

  • Biomater Res. 2022 Sep 22;26(1):47. doi: 10.1186/s40824-022-00296-0.
Xianghui Li  # 1 2 Haoran Wang  # 2 3 Zhiyan Li  # 1 2 Dandan Li 2 Xiaofeng Lu 1 Shichao Ai 1 Yuxiang Dong 4 Song Liu 5 Jinhui Wu 6 7 8 Wenxian Guan 9
Affiliations

Affiliations

  • 1 Department of Gastrointestinal Surgery, Affiliated Nanjing Drum Tower Hospital, Nanjing University Medical School, Nanjing, 210008, China.
  • 2 State Key Laboratory of Pharmaceutical Biotechnology, Medical School and School of Life Science, Nanjing University, Nanjing, 210093, China.
  • 3 Department of Pharmacology, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210023, China.
  • 4 First Clinical Medical College of Nanjing Medical University, Nanjing, 210029, China.
  • 5 Department of Gastrointestinal Surgery, Affiliated Nanjing Drum Tower Hospital, Nanjing University Medical School, Nanjing, 210008, China. [email protected].
  • 6 State Key Laboratory of Pharmaceutical Biotechnology, Medical School and School of Life Science, Nanjing University, Nanjing, 210093, China. [email protected].
  • 7 Chemistry and Biomedicine Innovation Center, Nanjing University, Nanjing, 210023, China. [email protected].
  • 8 Jiangsu Key Laboratory for Nano Technology, Nanjing University, Nanjing, 210093, China. [email protected].
  • 9 Department of Gastrointestinal Surgery, Affiliated Nanjing Drum Tower Hospital, Nanjing University Medical School, Nanjing, 210008, China. [email protected].
  • # Contributed equally.
Abstract

Background: Mitochondria play an essential role in cellular redox homeostasis maintenance and meanwhile serve as an important target for organelle targeted therapy. Photodynamic therapy (PDT) is a promising strategy for organelle targeted therapy with noninvasive nature and highly spatiotemporal selectivity. However, the efficacy of PDT is not fully achieved due to tumor hypoxia. Moreover, aerobic respiration constantly consumes oxygen and leads to a lower oxygen concentration in mitochondria, which continuously limited the therapeutic effects of PDT. The lack of organelle specific oxygen delivery method remains a main challenge.

Methods: Herein, an Oxygen Tank is developed to achieve the organelle targeted synergistic hypoxia reversal strategy, which not only act as an oxygen storage tank to open sources and reduce expenditure, but also coated with red blood cell membrane like the tank with stealth coating. Within the oxygen tank, a mitochondrion targeted photosensitizer (IR780) and a mitochondria respiration inhibitor (atovaquone, ATO) are co-loaded in the RBC membrane (RBCm) coated perfluorocarbon (PFC) Liposome core.

Results: Inside these bio-mimic nanoparticles, ATO effectively inhibits mitochondrial respiration and economized endogenous oxygen consumption, while PFC supplied high-capacity exogenous oxygen. These Oxygen modulators reverse the hypoxia status in vitro and in vivo, and exhibited a superior anti-tumor activity by mitochondria targeted PDT via IR780. Ultimately, the anti-tumor effects towards gastric Cancer and colon Cancer are elicited in vivo.

Conclusions: This oxygen tank both increases exogeneous oxygen supply and decreases endogenous oxygen consumption, may offer a novel solution for organelle targeted therapies.

Keywords

Artificial red blood cells; Mitochondrial respiratory inhibition; Organelle targeted therapy; PDT; Synergistic oxygen modulation; Tumor hypoxia.

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