Dosimetric investigations of laser-induced phase transition of MX1-cell membranes by use of quantum dots

Abstract

It is well known that laser scattered-light applicators when applied for laser-induced tumor therapy allow the precise thermal destruction of metastases. Using laser radiation in the NIR spectral range (usually, Nd:YAG laser systems λ = 1064 nm), a penetration depth of 5–10 cm (1/e is the decrease in radiation intensity) is achieved in biological tissues. The major tissue-optical parameters, i.e., absorption coefficient μa, scattering coefficient μs, and the anisotropy factor g, show biological tissues to be strongly scattering media which have a so-called optical window in the NIR. As a consequence, the therapeutic laser radiation is scattered and absorbed at a deeper level, leading to a virtual enlargement of the laser applicator. The thermal sclerotization and the thermal cell damage originate within the absorbing volume of the laser radiation and spread outward by thermal diffusion. There are three dosimetrically relevant zones of thermal and biological damage: (1) a zone of thermal coagulation; (2) a threshold of partial necrosis (destruction of all metabolic processes in the cell is the maintenance of essential parts of the cytoskeleton and the plasma membrane); this is characterized by a specific temperature range, the so-called phase transition, which refers to the transition from the gel phase of the biomembrane to the fluid phase; the determination of this temperature zone is an integral part of the following experimental investigations on MX1 cells; (3) an external zone of thermal effects made up of partial and multiple damage with a statistical chance of survival. This paper describes the investigations on heat stress in cancer cells to verify the maximum phase transition of the outer MX1 cell membranes and the related results. For this purpose, a novel method of quantum dot fluorescence dosimetry was developed. The evaluation of the measured laser-induced fluorescences yields a first approximation of the determination of the phase transition on MX1 cells.