Stolarz, A.J.; Chhetri, B.P.; Borrelli, M.J.; Jenkins, S.V.; Jamshidi-Parsian, A.; Phillips, J.H.; Fologea, D.; Gandy, J.; Griffin, R.J. Liposome Formulation for Tumor-Targeted Drug Delivery Using Radiation Therapy. Int. J. Mol. Sci.2022, 23, 11662.
Stolarz, A.J.; Chhetri, B.P.; Borrelli, M.J.; Jenkins, S.V.; Jamshidi-Parsian, A.; Phillips, J.H.; Fologea, D.; Gandy, J.; Griffin, R.J. Liposome Formulation for Tumor-Targeted Drug Delivery Using Radiation Therapy. Int. J. Mol. Sci. 2022, 23, 11662.
Stolarz, A.J.; Chhetri, B.P.; Borrelli, M.J.; Jenkins, S.V.; Jamshidi-Parsian, A.; Phillips, J.H.; Fologea, D.; Gandy, J.; Griffin, R.J. Liposome Formulation for Tumor-Targeted Drug Delivery Using Radiation Therapy. Int. J. Mol. Sci.2022, 23, 11662.
Stolarz, A.J.; Chhetri, B.P.; Borrelli, M.J.; Jenkins, S.V.; Jamshidi-Parsian, A.; Phillips, J.H.; Fologea, D.; Gandy, J.; Griffin, R.J. Liposome Formulation for Tumor-Targeted Drug Delivery Using Radiation Therapy. Int. J. Mol. Sci. 2022, 23, 11662.
Abstract
Targeted delivery of drugs or other therapeutic agents through internal or external triggers has been used to control and accelerate the release from liposomal carriers in a number of studies, but relatively few utilize energy of therapeutic X-rays as a trigger. We have synthesized liposomes that are triggered by ionizing radiation (RTLs) to release their therapeutic payload. These liposomes are composed of natural egg PE, DSPC, cholesterol, and DSPE-PEG-2000, and the mean size of the RTL was in the range of 114 to 133 nm, as measured by NTA. The trigger mechanism is the organic halogen, chloral hydrate, which is known to generate free protons upon exposure to ionizing radiation. Once protons are liberated, a drop in internal pH of the liposome promotes destabilization of the lipid bilayer and escape of the liposomal contents. In proof of principle studies, we assessed RTL radiation-release of fluorescent tracers upon exposure to a low pH extracellular environment or exposure to X-ray irradiation. Biodistribution imaging before and after irradiation demonstrated a preferential uptake and release of the liposomes and their cargo at the site of local tumor irradiation. Finally, a potent metabolite of the commonly used chemotherapy irinotecan, SN-38, was loaded into RTL along with near infrared (NIR) fluorescent dyes for imaging studies and measuring tumor cell cytotoxicity alone or combined with radiation exposure, in vitro and in vivo. Fully loaded RTLs were found to increase tumor cell killing with radiation in vitro and enhance tumor growth delay in vivo after three i.v. injections combined with three, 5 Gy local tumor radiation exposures compared to either treatment modality alone.
Keywords
liposome; tumor-targeted; radiation; tumor; drug delivery; chemotherapy
Subject
Medicine and Pharmacology, Oncology and Oncogenics
Copyright:
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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