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Featured researches published by P. Calzolari.


International Journal of Radiation Biology | 2000

Inactivation of human normal and tumour cells irradiated with low energy protons

M. Belli; D. Bettega; P. Calzolari; F. Cera; R. Cherubini; M. Dalla Vecchia; Marco Durante; S. Favaretto; G. Gialanella; G. F. Grossi

Purpose : To analyse the cell inactivation frequencies induced by low energy protons in human cells with different sensitivity to photon radiation. Materials and methods : Four human cell lines with various sensitivities to photon irradiation were used: the SCC25 and SQ20B derived from human epithelium tumours of the tongue and larynx, respectively, and the normal lines M/10, derived from human mammary epithelium, and HF19 derived from a lung fibroblast. The cells were irradiated with γ-rays and proton beams with linear energy transfer (LET) from 7 to 33keV/ μ m. Clonogenic survival was assessed. Results : Survival curves are reported for each cell line following irradiation with γ-rays and with various proton LETs. The surviving fraction after 2 Gy of γ-rays was 0.72 for SQ20B cells, and 0.28–0.35 for the other cell lines. The maximum LET proton effectiveness was generally greater than that of γ-rays. In particular there was a marked increase in beam effectiveness with increasing LET for the most resistant cells (SQ20B) whose 2 Gy-survival varied from 0.72 with γ-radiation down to 0.37 with 30keV/ μ m protons. The relative biological effectiveness (RBE(2Gy γ) ) with the 30 keV/ μ m beam, evaluated as the ratio of 2Gy to the proton dose producing the same inactivation level as that given by 2 Gy of γ-rays, was 3.2, 1.8, 1.3 and 0.8 for SQ20B, M/10, SCC25, and HF19, respectively. Conclusions : RBE for inactivation with high-LET protons increased with the cellular radioresistance to γ-rays. The cell line with the greatest resistance to γ-rays was the most responsive to the highest LET proton beam. A similar trend has also been found in studies reported in the literature with He, C, N ions with LET in the range 20–125keV/ μ m on human tumour cell lines.PURPOSE To analyse the cell inactivation frequencies induced by low energy protons in human cells with different sensitivity to photon radiation. MATERIALS AND METHODS Four human cell lines with various sensitivities to photon irradiation were used: the SCC25 and SQ20B derived from human epithelium tumours of the tongue and larynx, respectively, and the normal lines M/10, derived from human mammary epithelium, and HF19 derived from a lung fibroblast. The cells were irradiated with y-rays and proton beams with linear energy transfer (LET) from 7 to 33 keV/microm. Clonogenic survival was assessed. RESULTS Survival curves are reported for each cell line following irradiation with gamma-rays and with various proton LETs. The surviving fraction after 2 Gy of gamma-rays was 0.72 for SQ20B cells, and 0.28-0.35 for the other cell lines. The maximum LET proton effectiveness was generally greater than that of gamma-rays. In particular there was a marked increase in beam effectiveness with increasing LET for the most resistant cells (SQ20B) whose 2 Gy-survival varied from 0.72 with gamma-radiation down to 0.37 with 30 keV/microm protons. The relative biological effectiveness (RBE(2 Gy gamma)) with the 30 keV/microm beam, evaluated as the ratio of 2 Gy to the proton dose producing the same inactivation level as that given by 2 Gy of gamma-rays, was 3.2, 1.8, 1.3 and 0.8 for SQ20B, M/10, SCC25, and HF19, respectively. CONCLUSIONS RBE for inactivation with high-LET protons increased with the cellular radioresistance to gamma-rays. The cell line with the greatest resistance to gamma-rays was the most responsive to the highest LET proton beam. A similar trend has also been found in studies reported in the literature with He, C, N ions with LET in the range 20-125 keV/microm on human tumour cell lines.


Radiation Protection Dosimetry | 2016

Calculation of Nuclear Particles Production at High-Energy Photon Beams from a Linac Operating at 6, 10 and 15 MV

Renato Marchesini; D. Bettega; P. Calzolari; Emanuele Pignoli

Production of photonuclear particles in a tissue-equivalent medium has been calculated for linacs at 6, 10 and 15 MV from Varian TrueBeam. Based on the knowledge of bremsstrahlung fluence spectra and linac photon beam parameters, numerical integration was performed on the cross sections for photoparticle production of the constituent elements of tissue (2H,12C,13C,16O,17O,18O,14N,15N). At 15 MV, at the depth of photon maximum dose, the total absorbed dose due to neutrons, protons, alphas and residual nuclei from photon reactions in tissue (5.5E-05 Gy per Gy of photons) is comparable to that due to neutrons from accelerator head. Results reasonably agree with data reported in the literature using Monte Carlo models simulating linac head components. This work suggests a simple method to estimate the dose contributed by the photon-induced nuclear particles for high-energy photon beams produced by linacs in use, as it might be relevant for late stochastic effects.


Journal of Radiation Research | 2008

Effectiveness of monoenergetic and spread-out Bragg peak carbon ions for inactivation of various normal and tumour human cell lines

M. Belli; D. Bettega; P. Calzolari; Roberto Cherubini; G. Cuttone; Marco Durante; Giuseppe Esposito; Yoshiya Furusawa; S. Gerardi; G. Gialanella; G. F. Grossi; Lorenzo Manti; Renato Marchesini; M. Pugliese; P. Scampoli; G. Simone; E. Sorrentino; M. A. Tabocchini; L. Tallone


Advances in Space Research | 2005

Early and delayed reproductive death in human cells exposed to high energy iron ion beams.

D. Bettega; P. Calzolari; L. Doneda; Marco Durante; L. Tallone


Radiation Protection Dosimetry | 2002

Inactivation Cross Sections for Mammalian Cells Exposed to Charged Particles: A Phenomenological Approach

F. Belloni; D. Bettega; P. Calzolari; R. Cherubini; P. Massariello; L. Tallone


Journal of Radiation Research | 2001

Inactivation of human cells exposed to fractionated doses of low energy protons: relationship between cell sensitivity and recovery efficiency.

Francesca Antonelli; D. Bettega; P. Calzolari; R. Cherubini; Marta Dalla Vecchia; Marco Durante; S. Favaretto; G. F. Grossi; Renato Marchesini; M. Pugliese; P. Scampoli; G. Simone; E. Sorrentino; M. A. Tabocchini; L. Tallone; Paola Tiveron


Archive | 2001

Space radiation shielding: biological effects of accelerated iron ions and their modification by aluminum or lucite shields.

Marco Durante; Francesca Antonelli; F. Ballarini; M. Belli; D. Bettega; M. Biaggi; P. Calzolari; A. Ferrari; G. Gialanella; A. Giussani; G. F. Grossi; A. Massariello; A. Ottolenghi; M. Pugliese; P. Scampoli; G. Simone; E. Sorrentino; M. A. Tabocchini; L. Tallone


Archive | 2000

Inactivation of normal and tumour human cells irradiated with low energy protons.

M. Belli; D. Bettega; P. Calzolari; F. Cera; R. Cherubini; M. Dalla Vecchia; Marco Durante; S. Favaretto; G. Gialanella; G. F. Grossi; Renato Marchesini; G. Moschini; A. Piazzola; G. Poli; M. Pugliese; O. Sapora; P. Scampoli; G. Simone; E. Sorrentino; M. A. Tabocchini; L. Tallone Lombardi; P. Tiveron


Archive | 1996

RBE for inactivation of tumoural and normal cell lines of human origin irradiated with low-energy protons.

M. Belli; A. Ascatigno; D. Bettega; P. Calzolari; F. Cera; R. Cherubini; Marco Durante; S. Favaretto; G. Gialanella; G. F. Grossi; A. M. I. Haque; F. Ianzini; Renato Marchesini; G. Moschini; A. Piazzola; M. Pugliese; O. Sapora; P. Scampoli; G. Simone; E. Sorrentino; M. A. Tabocchini; L. Tallone; P. Tiveron


Biomedical Physics & Engineering Express | 2017

Combining proton or photon irradiation with epothilone B. An in vitro study of cytotoxicity in human cancer cells

D. Bettega; P. Calzolari; Mario Ciocca; Angelica Facoetti; Miriam Lafiandra; Renato Marchesini; S. Molinelli; Emanuele Pignoli; Barbara Vischioni

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G. F. Grossi

University of Naples Federico II

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G. Gialanella

University of Naples Federico II

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M. Pugliese

Istituto Nazionale di Fisica Nucleare

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E. Sorrentino

Istituto Superiore di Sanità

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G. Simone

Istituto Superiore di Sanità

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M. Belli

Istituto Superiore di Sanità

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R. Cherubini

Istituto Nazionale di Fisica Nucleare

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