Biomedical subjects

Agata Scordino

Publications and source records attributed to Agata Scordino.

4 recordsLinked to original sources

PubMed2005

Spectral analysis of laser-induced ultraweak delayed luminescence in cultured normal and tumor human cells: temperature dependence.

The emission spectrum of ultraviolet A laser induced ultraweak delayed luminescence in cell cultures of mammalian cells depended on the temperature during irradiation and photonic measurements. A new method using a sophisticated photomultiplier system was developed in order to find differences between normal and tumor cells. The maximal peak of the emitted light for cultures measured at low temperature of 10 degrees C was near 510 nm in the green visible region while following irradiation at 32 degrees C this maximum was shifted to yellow-orange at 570 nm both in normal and melanoma cells. Overall, this ultraweak photonic model of cultured cells provides to be a new and powerful non-invasive tool for developing new strategies in skin cancer detection.

Adult↗

PubMed2003

Nonlinear dependence of the delayed luminescence yield on the intensity of irradiation in the framework of a correlated soliton model.

We generalize the correlated soliton model in order to describe the delayed luminescence arising from biological systems after their exposition to the irradiation by relatively high dose (high intensity and/or long duration of irradiation). The quantum yield of the delayed luminescence is calculated as a function of the irradiation and is shown to depend nonlinearly on the intensity and dose of the irradiation. At relatively low intensity, the yield of luminescence increases with increasing dose, and monotonously reaches saturation. At high intensity of the irradiation, the yield of the photosystem under study is restricted from above by the concentration of photosystem units. As a result, the total yield of the delayed luminescence first increases with the dose till the maximum value that, in the general case, is less than the maximum number of available photosystem units. With further increase of the dose, the yield gradually decreases, reaching the saturation value at large dose of illumination. These results are obtained within the steady state approximation in the description of the luminescence kinetics. To check the applicability of this approximation at high levels and large time of illumination, the corrections to the steady state solution have been calculated, and shown to decrease exponentially with increase in time till the small finite constant value. The results of the theoretical model are shown to describe well the experimental data on the dose dependence of the quantum yield of the luminescence of algae Acetabularia acetabulum, for which the correlated soliton model describes well the kinetics of the delayed luminescence at low levels of irradiation.

Journal Article↗

PubMed2003

Solid state approach in biophoton research.

Main characteristics of the delayed luminescence (DL) emitted in the seconds range from biological systems is analyzed. The correlation between change in DL and cell's organization, and similarity with some characteristics of DL from solid state system suggest to connect DL in biological system to decay of collective electron states, formed during energy and charge transport along the macromolecular ordered structures which form the cell. Results of a proposed soliton model are discussed, together with some phenomenological evidence which emphasize the possibility of using DL measurements as an intrinsic probe in biophysical investigations.

Luminescent Measurements↗

PubMedDate not supplied

Laser-ultraviolet-A-induced ultraweak photon emission in mammalian cells.

Photobiological research in the last 30 yr has shown the existence of ultraweak photon emission in biological tissue, which can be detected with sophisticated photomultiplier systems. Although the emission of this ultraweak radiation, often termed biophotons, is extremely low in mammalian cells, it can be efficiently increased by ultraviolet light. Most recently it was shown that UV-A (330 to 380 nm) releases such very weak cell radiation in differentiated human skin fibroblasts. Based on these findings, a new and powerful tool in the form of UV-A-laser-induced biophotonic emission of cultured cells was developed with the intention to detect biophysical changes between carcinogenic and normal cells. With suspension densities ranging from 1 to 8 x 10(6) cells/mL, it was evident that an increase of the UV-A-laser-light induced photon emission intensity could be observed in normal as well as melanoma cells. Using this new detection procedure of ultraweak light emission, photons in cell suspensions as low as 100 microL could be determined, which is a factor of 100 lower compared to previous procedures. Moreover, the detection procedure has been further refined by turning off the photomultiplier system electronically during irradiation leading to the first measurements of induced light emission in the cells after less than 10 micros instead of 150 ms, as reported in previous procedures. This improvement leads to measurements of light bursts up 10(7) photons/s instead of several hundred as found with classical designs. Overall, we find decreasing induction ratings between normal and melanoma cells as well as cancer-prone and melanoma cells. Therefore, it turns out that this highly sensitive and noninvasive device enables us to detect high levels of ultraweak photon emission following UV-A-laser-induced light stimulation within the cells, which enables future development of new biophysical strategies in cell research.

Adolescent↗