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BEGIN:VEVENT
SUMMARY:Preparation of laser-proton cell irradiation experiments at L2A2
DTSTART;VALUE=DATE-TIME:20201215T114500Z
DTEND;VALUE=DATE-TIME:20201215T120000Z
DTSTAMP;VALUE=DATE-TIME:20260811T021432Z
UID:indico-contribution-1950-13915@indico.ific.uv.es
DESCRIPTION:Speakers: Alberto Torralba Torregrosa ()\nUltra-short and ultr
 a-intense pulsed lasers allow for accelerating short bunches of protons an
 d ions to MeV-range energies. Our aim is to design and build an experiment
 al setup for the L2A2 laboratory\, at the University of Santiago de Compos
 tela\, for the study of radiobiological effects caused by laser-accelerate
 d protons on human cancer cell cultures. The Ti:Sapphire laser at L2A2 del
 ivers 1.2 J pulses at a rate of 10 Hz and peak power of 50 TW. The corresp
 onding focused intensity is sufficient for accelerating protons to 5-10 Me
 V through the Target Normal Sheath Acceleration mechanism (TNSA).\nThe bea
 m of accelerated protons/ions passes through a pinhole collimator followed
  by a sequence of permanent magnets that generate a configuration of antip
 arallel magnetic fields with the purpose of bending the trajectories of th
 e protons and separating them from electrons and photons originating from 
 the laser-plasma interaction. In addition\, the magnetic fields act as an 
 energy separator with a resulting\, lateral displacement of the protons de
 pending on their momentum. This allows for selecting a narrow range of ene
 rgies with approximately uniform dose deposition within the irradiated are
 a. This entire setup is located inside a vacuum chamber. The particles lea
 ve the chamber through a thin foil of kapton (polyimide) and finally impin
 ge on the cell culture outside the vacuum system. Cell cultures are prepar
 ed and analysed at the Fundación Pública Galega Medicina Xenómica and I
 DIS. The first trials will be centred around the quantification of DNA dou
 ble-strand breaks as a function of radiation dose.\nA major challenge of t
 his project is the precise measurement of the dose deposited by the laser-
 driven beams. For significant doses (up to 5 Gy)\, several shots have to b
 e accumulated. Shot-to-shot fluctuations of the proton flux impose the nec
 essity for online monitoring which is demanding in our range of energies. 
 Furthermore\, the response of electronic detectors to ultra-high instantan
 eous rates will be studied in careful cross-calibration measurements with 
 passive materials. The experiment is under construction and it is planned 
 to be running in 2021.\n\nhttps://indico.ific.uv.es/event/5983/contributio
 ns/13915/
LOCATION:Virtuales
URL:https://indico.ific.uv.es/event/5983/contributions/13915/
END:VEVENT
BEGIN:VEVENT
SUMMARY:TERMOGRAFÍA INFRARROJA: TÉCNICA DE IMAGEN ÚTIL EN PEDIATRÍA
DTSTART;VALUE=DATE-TIME:20201215T121500Z
DTEND;VALUE=DATE-TIME:20201215T123000Z
DTSTAMP;VALUE=DATE-TIME:20260811T021432Z
UID:indico-contribution-1950-13914@indico.ific.uv.es
DESCRIPTION:Speakers: Olga Benavent Casanova (Departamento de Salud de la 
 Ribera)\n**Introducción y objetivo**\nLa Termografía Infrarroja\, permit
 e registrar el mapa de temperaturas de la piel\, de manera inocua\, rápid
 a y sin contacto con el paciente. Detecta las asimetrías que se producen 
 en la microcirculación cutánea cuando existen procesos inflamatorios\, i
 nfecciosos\, vasculares...que alteran su distribución. Por estas razones\
 , su uso resultaría especialmente útil en población pediátrica\, y en 
 patologías que alteran la vascularización periférica. El objetivo de es
 te trabajo es realizar una correlación descriptiva entre las imágenes ob
 tenidas mediante técnicas convencionales y mediante Termografía Infrarro
 ja en diferentes patologías pediátricas.\n\n**Material y métodos**\nSe 
 realizó un estudio prospectivo descriptivo en 6 niños (2 anomalías vasc
 ulares\, 2 complicaciones de catéteres y 2 óseas) atendidos en el Hospit
 al Clínico Universitario de Valencia. Se realizaron los controles rutinar
 ios y las técnicas de imagen convencionales cuando estaban indicadas\, y 
 además se complementó la valoración con imágenes termográficas. El re
 gistro de las imágenes termográficas se realizó con cámara Flir E60\, 
 siguiendo el protocolo estándar\, adaptado a población pediátrica. Los 
 parámetros termográficos fueron: emisividad: 0\,98\, distancia: 1 metro\
 , temperatura ambiente: 24°C y humedad ambiente: 50%. El análisis de las
  imágenes se realizó con el programa ThermaCAMResearcher Pro 2.10\, dete
 rminando temperatura media (TM)\, máxima (Tmáx) y mínima (Tmín) de las
  regiones de interés (ROIs): zona afecta\, sana y referencia (frente). Se
  realizó valoración cualitativa de las imágenes termográficas y cuanti
 tativa\, mediante el cálculo de un Índice Térmico ((IT= (TM ROIafecta 
 – TM ROIsana/TM frente) x 100)\n\n**Resultados**\nEn las imágenes termo
 gráficas se apreció cualitativamente y cuantitativamente (IT) asimetría
  térmica entre la zona patológica y la contralateral sana\, mayor al dia
 gnóstico que tras la administración de tratamiento\, cuando la evolució
 n fue favorable. Las imágenes termográficas se correlacionaron con las p
 ruebas complementarias rutinarias y con la evolución clínica del pacient
 e. Ejemplos de hemangioma infantil en Figura 1 y de celulitis de catéter 
 de derivación ventrículo-peritoneal en Figura 2.\n\n**Conclusiones**\nLa
  Termografía Infrarroja aporta información relevante para el diagnóstic
 o y seguimiento de pacientes pediátricos con patologías que alteran la v
 ascularización periférica\, ya que es capaz de identificar incluso halla
 zgos que pasan inadvertidos en la exploración clínica\, y detectar cambi
 os en la microcirculación cutánea no detectables mediante pruebas conven
 cionales.\n\nhttps://indico.ific.uv.es/event/5983/contributions/13914/
LOCATION:Virtuales
URL:https://indico.ific.uv.es/event/5983/contributions/13914/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Complete characterization of the energy spectra of laser-accelerat
 ed protons for the production of radioisotopes used in medical imaging.
DTSTART;VALUE=DATE-TIME:20201215T120000Z
DTEND;VALUE=DATE-TIME:20201215T121500Z
DTSTAMP;VALUE=DATE-TIME:20260811T021432Z
UID:indico-contribution-1950-13906@indico.ific.uv.es
DESCRIPTION:Speakers: Juan Peñas Nadales (Universidade de Santiago de Com
 postela)\nLaser-driven ion accelerators may represent a competitive techno
 logy for the future production of medical radioisotopes. First experiments
  on laser-driven proton acceleration in the Target Normal Sheath Accelerat
 ion (TNSA) regime were performed at the Laser Laboratory for Acceleration 
 and Applications (L2A2) by focusing a 45 TW\, 10 Hz repetition rate femtos
 econd laser on Al foils of a few micrometer thickness. Typical exponential
  maxwellian-like proton spectra with a cut-off energy up to 1.65 MeV were 
 measured with a time-of-flight (ToF) detector system. Results have been co
 mpared to recently published data\, regarding maximum energy\, particle nu
 mber\, and distribution temperature in order to infer correlations between
  these parameters and the laser pulses characteristics. These correlations
  were used to extrapolate our results to obtain estimations on production 
 activities for various proton- and deuteron-induced nuclear reactions\, fo
 r optimized experimental parameters. Activity levels of ~32.1 MBq for 11C 
 via 11B(p\;n)11C reaction are estimated for one hour of irradiation at a l
 aser repetition rate of 10 Hz\, which are in the range of doses required f
 or preclinical Positron Emission Tomography (PET) imaging. Other radioisot
 ope production reactions are also considered and studied.\n\nhttps://indic
 o.ific.uv.es/event/5983/contributions/13906/
LOCATION:Virtuales
URL:https://indico.ific.uv.es/event/5983/contributions/13906/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Simultaneous imaging of hard and soft biological tissues in a low-
 field MRI scanner
DTSTART;VALUE=DATE-TIME:20201215T113000Z
DTEND;VALUE=DATE-TIME:20201215T114500Z
DTSTAMP;VALUE=DATE-TIME:20260811T021432Z
UID:indico-contribution-1950-13904@indico.ific.uv.es
DESCRIPTION:Speakers: José Miguel Algarín (MRILab\, I3M\, CSIC and Unive
 rsitat Politècnica de València Valencia)\n**INTRODUCTION**\nHere we pres
 ent “DentMRI – Gen I” (Fig. 1(a))\, a home-made special-purpose MRI 
 scanner designed with the goal of demonstrating dental imaging at low fiel
 d (260 mT). We use two variations of zero echo time (ZTE) pulse sequences 
 (Fig. 1(b)): standard PETRA [1\,2]\, and Double Radial Non Stop Spin Echo 
 (DRaNSSE)\, which we have devised to address limitations we encounter with
  PETRA. We perform image reconstruction by Algebraic Reconstruction Techni
 ques (ART\, [3]).\n\n**METHODS**\n“DentMRI – Gen I” operates with a 
 “C”-shaped permanent NdFeB magnet that provides 260 mT over a spherica
 l region of 150 mm in diameter. The system is equipped with a gradient sys
 tem capable of reaching strengths > 0.4 T/m along any spatial direction an
 d a TxRx RF solenoid coil able to induce a flip angle of 90 degrees in a f
 ew microseconds.\n\n**RESULTS**\nFigure 2(c) contains selected slices from
  the full 3D ART reconstruction of a rabbit head employing a PETRA sequenc
 e with 0.5 mm isotropic resolution. We acquired two images: one with a sho
 rt (90 µs) dead time (Fig. 3(c) top) with a scan time of 61 minutes\; and
  one with a long (1 ms) dead time (Fig. 2(c) middle) with a scan time of 3
 1 minutes. The bottom image in Fig. 3(c) shows difference between both ima
 ges to highlight hard tissues.\nFigure 3 shows ART reconstructions slices 
 from DRaNSSE (top) and PETRA (bottom) acquisitions. Images were acquired w
 ith 1 mm isotropic resolution with a total scan time of 30 (15) minutes fo
 r DRaNSSE (PETRA). Due to the long echo time for the second echo (10 ms)\,
  tissue contrast is higher with DRaNSSE.\n\n**DISCUSSION/CONCLUSION**\nIn 
 the present work we have demonstrated the capability of our new low-cost 
 “DentMRI – Gen I” scanner to simultaneously image hard and soft biol
 ogical tissues\; we have devised a new pulse sequence (DRaNSSE) that\, com
 pared to standard sequences such as PETRA\, yields higher SNR images and e
 nhanced tissue contrast.\n\n**ACKNOWLEDGMENT**\nThis work was supported by
  the European Commission under Grants 737180 (FET-OPEN: HISTO-MRI) and 481
  (ATTRACT: DentMRI). S. Aja-Fernández acknowledges Ministerio de Ciencia 
 e Innovación of Spain for Research grant RTI2018-094569-B-I00\n\n**REFERE
 NCES**\n[1] M. Weiger\, K. P. Pruessmann\, A.-K. Bracher\, S. Köhler\, V.
  Lehmann\, U. Wolfram\, F. Hennel\, and V. Rasche\, “High-resolution ZTE
  imaging of human teeth\,” NMR in Biomedicine\, vol. 25\, no. 10\, pp. 1
 144–1151\, oct 2012. [Online]. Available: http://doi.wiley.com/10.1002/n
 bm.2783\n\n[2] D. M. Grodzki\, P. M. Jakob\, and B. Heismann\, “Ultrasho
 rt echo time imaging using pointwise encoding time reduction with radial a
 cquisition (PETRA)\,” Magnetic Resonance in Medicine\, vol. 67\, no. 2\,
  pp. 510–518\, feb 2012.\n\n[3] R. M. Gower and P. Richtarik\, “Random
 ized iterative methods for linear systems\,” SIAM Journal on Matrix Anal
 ysis and Applications\, vol. 36\, no. 4\, pp. 1660–1690\, 2015.\n\nhttps
 ://indico.ific.uv.es/event/5983/contributions/13904/
LOCATION:Virtuales
URL:https://indico.ific.uv.es/event/5983/contributions/13904/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Hologramas acústicos bilaterales para terapia transcraneal
DTSTART;VALUE=DATE-TIME:20201215T111500Z
DTEND;VALUE=DATE-TIME:20201215T113000Z
DTSTAMP;VALUE=DATE-TIME:20260811T021432Z
UID:indico-contribution-1950-13903@indico.ific.uv.es
DESCRIPTION:Speakers: Diana Andrés Bautista (Universitat Politècnica de 
 València)\nEn los últimos años se ha demostrado la utilidad de la aplic
 ación de los ultrasonidos focalizados en el interior del cerebro con fina
 lidades terapéuticas. Mediante la ablación térmica se han desarrollado 
 tratamientos para el temblor esencial y el Parkinson\, mientras que a inte
 nsidades moderadas se emplean para neuromodulación y apertura de la barre
 ra hematoencefálica\, permitiendo administrar fármacos de una forma no i
 nvasiva\, localizada y reversible. No obstante\, el haz de ultrasonidos su
 fre aberraciones en su camino hacia el sistema nervioso central (SNC) debi
 do a la atenuación y dispersión que introduce el cráneo. Además\, las 
 estructuras cerebrales presentan una forma y distribución compleja a la q
 ue se debe adaptar el haz ultrasónico.\n\nHemos diseñado hologramas acú
 sticos impresos en 3D para compensar las aberraciones introducidas por el 
 cráneo y dirigir el haz ultrasónico hacia dianas terapéuticas bilateral
 es en el SNC\, concretamente hacia el putamen\, núcleo caudado e hipocamp
 o\, cuya forma y tamaño se ha obtenido con imágenes MRI. Hemos empleado 
 un cráneo exvivo (varón\, 73 años) del cual sabemos sus propiedades med
 iante una imagen TAC. Los hologramas se diseñan haciendo uso de la simetr
 ía de inversión temporal de las ecuaciones que dominan la propagación d
 e ondas acústicas y empleando fuentes virtuales que siguen la forma de es
 tructuras a tratar\, utilizando métodos numéricos pseudoespectrales. La 
 información holográfica se registra en la ubicación del transductor y s
 e diseñan lentes de solo fase basadas en resonadores Fabry-Perot\, utiliz
 ando métodos de conjugación de fase. Las mismas se imprimen en 3D median
 te estereolitografía de fotopolímeros.\n\nLos experimentos se han realiz
 ado en un tanque de agua\, con un transductor ultrasónico focalizado de 1
 00 mm de apertura y 140 mm de focal\, con una frecuencia central de 500 kH
 z. Para posicionar la lente holográfica respecto del cráneo de forma que
  la localización coincida con la de las simulaciones y además asegurar q
 ue la posición del cráneo permanezca constante a lo largo de las medidas
 \, se ha diseñado e impreso un soporte. Las medidas se han realizado con 
 un hidrófono de aguja con una sensibilidad de -228 dB ref. 1V/µPa.\n\nSe
  ha simulado el campo acústico generado por las lentes diseñadas para la
 s tres estructuras bilaterales en el interior del cerebro. De media\, el v
 olumen tratado ha sido de un 24 % del volumen total\, mientras que con el 
 foco natural del transductor solo trataríamos un 5%. Las ganancias han si
 do de 3.5 p/p0\, donde p0 es la presión en la superficie del transductor\
 , mientras que sin usar lente es de 6.8 p/p0. Los experimentos ex vivo con
  las lentes impresas 3D han demostrado un completo acuerdo con los valores
  obtenidos mediante simulaciones numéricas.\n\nEn conclusión\, los holog
 ramas pueden usarse para diseñar sistemas robustos y económicos para foc
 alizar los ultrasonidos en estructuras complejas en el interior del cerebr
 o para neuromodulación y la apertura de la barrera hematoencefálica.\n\n
 https://indico.ific.uv.es/event/5983/contributions/13903/
LOCATION:Virtuales
URL:https://indico.ific.uv.es/event/5983/contributions/13903/
END:VEVENT
BEGIN:VEVENT
SUMMARY:Organ-dedicated high-performance PET developments at i3M
DTSTART;VALUE=DATE-TIME:20201215T110000Z
DTEND;VALUE=DATE-TIME:20201215T111500Z
DTSTAMP;VALUE=DATE-TIME:20260811T021432Z
UID:indico-contribution-1950-13902@indico.ific.uv.es
DESCRIPTION:Speakers: Antonio J. Gonzalez (i3M (CSIC-UPV))\nPositron Emiss
 ion Tomography (PET) systems have significantly evolved in the last decade
  with the access to new photosensor technology such as Silicon Photomultip
 liers (SiPM) and novel readout electronics enabling the possibility to acc
 urately determine the Coincidence Timing Resolution (CTR) of the two annih
 ilation photons. \n\nThere has been a large effort into the so-called Tota
 l-Body PET (TB-PET) imaging for humans. That means\, PET systems with a ve
 ry large axial coverage\, in one case up to 2 meters long. This developmen
 t makes it possible to increase the system sensitivity a factor 40 compare
 d to 20-25 cm axial length of conventional whole-body PET systems. TB-PET 
 also allows clinicians to perform multi-organ imaging. The non-negligible 
 drawback of such TB-PET endeavors is their huge cost.\n\nAn alternative to
  increase the effective sensitivity is to improve the timing capabilities.
  For instance\, a CTR of 100 ps FWHM will boost this sensitivity by a fact
 or of 16. Moreover\, organ-dedicated systems exhibit higher overall perfor
 mance than WB or TB-PET due to their smaller geometries. I3M has developed
  several organ-dedicated PET systems\, recently including the capabilities
  to reach 240 ps CTR. In most of the systems monolithic crystal technology
  is used\, offering determination of the depth of interaction of the annih
 ilation event and\, thus\, allowing one to correct for the parallax error.
 \n\nIn this contribution we describe systems such as the breast dedicated 
 MAMMI reaching 1.4 mm spatial resolution with few thousands of patients al
 ready scanned. Two new designs are ongoing\, one based on two-panels PET a
 nd another on an edgeless crystal geometry. We will also describe the brai
 n dedicated PET so-called MINDView that is also an insert\, that means MR 
 compatible. This system uses the largest volume of monolithic crystals in 
 a clinical PET scanner. A circular prostate-dedicated PET system was devel
 oped few years ago\, after the attempt of using novel geometries\, and tes
 ted at the neighboring largest hospital in our region. Our last developmen
 t is a heart PET system\, based on crystal arrays but reaching timing reso
 lutions below 240 ps CTR. Other novel designs will also be discussed.\n\nh
 ttps://indico.ific.uv.es/event/5983/contributions/13902/
LOCATION:Virtuales
URL:https://indico.ific.uv.es/event/5983/contributions/13902/
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