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Multicell tumor spheroids in photodynamic therapy
Steen J Madsen1, Chung-Ho Sun, Bruce J Tromberg
1Department of Health Physics, University of Nevada, Las Vegas, Nevada 89154-3037, USA.
Lasers in Surgery and Medicine
|June 22, 2006
Summary
Multicell spheroids (MCSs) are valuable in vitro models for studying photodynamic therapy (PDT) effects. Recent advancements include developing in vivo brain tumor models and using computer simulations to predict PDT treatment outcomes.
Area of Science:
- Oncology
- Biomedical Engineering
- Photomedicine
Background:
- Multicell spheroids (MCSs) offer a simplified in vitro system for evaluating investigational treatments.
- MCSs have been instrumental in understanding photodynamic therapy (PDT) parameters, including sensitizer photobleaching.
- MCSs facilitate the study of complex PDT regimens, such as multiple treatments and combined therapies with radiation or hyperthermia.
Purpose of the Study:
- To review the current literature on MCS applications in PDT.
- To present novel MCS models for investigating tumor cell invasion and angiogenesis in high-grade gliomas.
- To explore the utility of in silico models for predicting PDT treatment responses.
Main Methods:
- Literature review of MCS studies in PDT.
- Development of in vivo brain tumor models using human tumor spheroids in immunodeficient rats.
- Utilizing computer simulations (in silico models) to describe MCS growth and predict therapeutic effects.
Main Results:
- Elucidation of PDT sensitizer photobleaching mechanisms through MCS studies.
- Progress in developing an in vivo brain tumor model with biopsy-derived human tumor spheroids.
- In silico models have generated verifiable predictions for MCS growth and PDT responses.
Conclusions:
- MCSs are versatile tools for PDT research, aiding in understanding mechanisms and treatment strategies.
- Advanced in vivo and in silico models are emerging for more accurate brain tumor and PDT investigations.
- Computer simulations show promise in guiding the development of improved PDT therapeutics.