Liposome Formulation for Tumor-Targeted Drug Delivery Using Radiation Therapy
Amanda J Stolarz1,2, Bijay P Chhetri2, Michael J Borrelli3
1Department of Pharmaceutical Sciences, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
International Journal of Molecular Sciences
|October 14, 2022
Summary
Radiation-triggered liposomes (RTLs) release therapeutic payloads upon X-ray exposure. These novel liposomes enhance chemotherapy and radiation efficacy, improving tumor cell killing and growth delay.
Area of Science:
- Nanomedicine
- Drug Delivery Systems
- Radiation Oncology
Background:
- Targeted drug delivery using triggered release from liposomes is established.
- Few studies utilize therapeutic X-rays as a trigger for liposomal drug release.
Purpose of the Study:
- To synthesize and characterize liposomes triggered by ionizing radiation (RTLs) for controlled therapeutic payload release.
- To evaluate the efficacy of RTLs loaded with SN-38 chemotherapy and near-infrared fluorescent dyes in vitro and in vivo.
Main Methods:
- Liposomes composed of PE, DSPC, cholesterol, and DSPE-PEG-2000 were synthesized.
- Nanoparticle tracking analysis (NTA) determined RTL size (114-133 nm).
- Chloral hydrate within RTLs generates protons under ionizing radiation, causing pH drop and payload release.
Main Results:
- RTLs demonstrated radiation-induced release of fluorescent tracers.
- Biodistribution imaging showed preferential uptake and release at tumor irradiation sites.
- RTLs loaded with SN-38 enhanced tumor cell killing with radiation in vitro and improved tumor growth delay in vivo.
Conclusions:
- Radiation-triggered liposomes (RTLs) offer a novel approach for targeted drug delivery.
- RTLs combined with chemotherapy and radiation show enhanced anti-tumor effects.
- This technology holds promise for improving cancer treatment outcomes.
Related Concept Videos
Targeted Cancer Therapies
The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against specific...
There are several types of targeted therapies against specific...
Tumor Immunotherapy
Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
Modified-Release Drug Delivery Systems: Site-Targeted
Site-targeted drug delivery systems enhance therapeutic efficacy while minimizing systemic toxicity and treatment costs. Unlike conventional methods, these systems ensure precise drug delivery, improving bioavailability and reducing side effects. Targeted drug delivery is classified into three levels. First-order targeting directs drugs to the capillary beds of specific organs or tissues. Second-order targets specific cell types, such as tumor cells, using receptor-mediated interactions.
Site-Targeted Drug Delivery Systems: Polymeric Carriers
Polymeric carriers enhance targeted drug delivery by increasing efficacy while minimizing off-target effects. These carriers comprise a biodegradable polymeric backbone integrated with functional elements that enable targeting, improve physicochemical properties, and regulate drug release.Targeting MechanismsThe targeting ability of polymeric carriers is mediated by a homing device, which is a molecular recognition component designed to selectively bind to specific tissues or cells. Monoclonal...


