Perfluorocarbons Therapeutics in Modern Cancer Nanotechnology for Hypoxiainduced Anti-tumor Therapy

Saurabh Satija, Prabal Sharma, Harpreet Kaur, Daljeet S Dhanjal, Reena S Chopra, Navneet Khurana, Manish Vyas, Neha Sharma, Murtaza M Tambuwala, Hamid A Bakshi, Nitin B Charbe, Flavia C Zacconi, Dinesh K Chellappan, Kamal Dua, Meenu Mehta

Research output: Contribution to journalReview articlepeer-review

1 Scopus citations


With an estimated failure rate of about 90%, immunotherapies that are intended for the treatment of solid tumors have caused an anomalous rise in the mortality rate over the past decades. It is apparent that resistance towards such therapies primarily occurs due to elevated levels of HIF-1 (Hypoxia-induced factor) in tumor cells, which are caused by disrupted microcirculation and diffusion mechanisms. With the advent of nanotechnology, several innovative advances were brought to the fore; and, one such promising direction is the use of perfluorocarbon nanoparticles in the management of solid tumors. Perfluorocarbon nanoparticles enhance the response of hypoxia-based agents (HBAs) within the tumor cells and have been found to augment the entry of HBAs into the tumor micro-environment. The heightened penetration of HBAs causes chronic hypoxia, thus aiding in the process of cell quiescence. In addition, this technology has also been applied in photodynamic therapy, where oxygen self-enriched photosensitizers loaded perfluorocarbon nanoparticles are employed. The resulting processes initiate a cascade, depleting tumour oxygen and turning it into a reactive oxygen species eventually to destroy the tumour cell. This review elaborates on the multiple applications of nanotechnology based perfluorocarbon formulations that are being currently employed in the treatment of tumour hypoxia.

Original languageEnglish (US)
Pages (from-to)4376-4387
Number of pages12
JournalCurrent pharmaceutical design
Issue number43
StatePublished - 2021
Externally publishedYes

Bibliographical note

Copyright© Bentham Science Publishers; For any queries, please email at [email protected].


  • Cell Line, Tumor
  • Fluorocarbons/pharmacology
  • Humans
  • Nanoparticles
  • Nanotechnology
  • Neoplasms/pathology
  • Photochemotherapy/methods
  • Photosensitizing Agents/pharmacology
  • Tumor Microenvironment

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't
  • Review


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