An Oxygen-Enriched Photodynamic Nanospray for Postsurgical Tumor Regression.

ACS Biomater Sci Eng

Department of Medical imaging, Zhuhai People's Hospital, Zhuhai Hospital affiliated with Jinan University, Zhuhai 519000, P.R. China.

Published: November 2020

AI Article Synopsis

  • Postoperative recurrence and metastasis are major challenges in cancer treatment, but photodynamic therapy (PDT) shows promise due to its targeted and non-invasive nature.
  • Conventional PDT often struggles with low oxygen levels, limiting its effectiveness, which prompted the development of a new oxygen-enriched nanospray using liposomes combined with indocyanine green (ICG) and perfluorooctyl bromide (PFOB).
  • This new treatment, Lip-PFOB-ICG, enhances the PDT effect under near-infrared light by improving oxygen absorption, leading to significant inhibition of local tumor recurrence and potentially offering a better postoperative therapy option.

Article Abstract

Postoperative local recurrence and metastasis are non-negligible challenges in clinical cancer treatment. Photodynamic therapy (PDT) has presented a great potential in preventing cancer recurrence owing to its noninvasiveness and high specificity for local irradiation of tumor sites. However, the application of conventional PDT is often limited by insufficient oxygen supply, making it difficult to achieve high PDT efficacy. Herein, we combined liposomes with photosensitizer indocyanine green (ICG) and perfluorooctyl bromide (PFOB) to develop a new oxygen-enriched photodynamic nanospray (Lip-PFOB-ICG) for cancer postoperative treatment. The Lip-PFOB-ICG not only has good biocompatibility but also enhanced the PDT effect under near-infrared light. More importantly, PFOB can continuously absorb oxygen, thus improving the collision energy transfer between the ICG photosensitizer and oxygen, and significantly inhibit local tumor recurrence in the subcutaneous tumor recurrence model. This oxygen-enriched photodynamic nanospray strategy may open up new avenues for effective postoperative cancer therapy in the clinic.

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Source
http://dx.doi.org/10.1021/acsbiomaterials.0c01099DOI Listing

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