- Parvaiz Ahmad Shiekh added an answer:7Do cells experience mechanical force if they are place in magnetic or electromagnetic field ?
Physical stimulation of cells damage them. Is it possible to use magnetic force which can create a mechanical force on cells to stimulate them. If possible, what will be its prerequisites?
thanks for answer. u can drop me the article ASAPFollowing
- Ghanshyam Dass Jindal added an answer:3How ICG signal is different from ECG signal while denoising of artefacts?
However there are many papers on denoising of ECG signal, and same thing can be applied for ICG signal.
Ensemble Averaging Method suggested by Dr DeMarzo is the best for getting rid of respiratory artifacts in ICG signal, which permits accurate analysis. Now a days, ICG is employed for Cardiac Output Monitoring in ICU/ICCU, there again one can employ the same method (ensemble averaging) in running mode. Meaning at any time one averages recent 8 cardiac cycles. When 9th comes in 1st cycle gets out of averaging. Similarly when 10th cycle comes in 2nd cycle gets out and so on.Following
- Reina Jimenez added an answer:3Has anyone experienced better dosimetric outcomes with symmetric planning in LDR prostate brachy?
Is there any literature evidence on symmetric planning and its advantages over asymmetric planning in ldr brachy. Thanks
After more than 600 patients implanted one thing is certain to me: Each prostate is unique, and despiting more of them are symetric in their external aspect, internal composition, drive by biopsy results, made us to plan almost symetric distributions of needles but asymetric distribution of dose. One of the wonders of brachytherapy is the power of intensity modulated therapy design for each prostate form and content.. We also use 0.496 U and D90 is ever greater than planned. More dose in Ca nodules, better local control. All of this happened inside the gland. D90 must ever respect margins 2-3 mm for rectal wall, up to 4 mm outside the capsule in the rest of the glandFollowing
- Michele Di Foggia added an answer:3Which laser should be used for composition analysis of bone in Raman Spectroscopy?
Using raman spectroscopy I want to find compositional constituents of bone sample.
FT-Raman spectroscopy using the 1064 nm Nd:YAG laser has been successfully used for the characterization of bone: in some cases fluorescence was almost absent.Following
- Mark Collins added an answer:4Are there any studies about the late effects of simultaneously integrated boost techniques?
I am working on SIB technique planning. I have done dosimetry on Phantom but I am curious about acute and late effects.
Take a look here http://www.icr.ac.uk/our-research/our-research-centres/clinical-trials-and-statistics-unit/clinical-trials/import_high this is a trial a lot of UK departments are recruiting for. Also, a number of UK department use SIB in prostate treatments, delivering a different dose to the seminal vesicle and the prostate.Following
- Prashant Shukla added an answer:1What differences can be seen in the degree of polarization (DOP) for forward and backscattered mode from a thin epithelial tissue section?
I want to understand, how differently polarized light influence on forward and back scattered mode. Some articles mentioned results are different from thin and thick tissue. What is the boundary decided for thick and thin tissue?
Pl. see this reference "A. D. Kim, M. Moscoso, Phys. Rev. E 64, 026612 (2001)."
if light is circularly polarized then in backscatteing mode because of helicity flip depolarization will be more.Following
- Hanno Krieger added an answer:10Reasons behind the different peak shapes in radiation spectrometry?
In case of alpha spectroscopy the peak shape is different from that observed in photo peak of photon spectroscopy. I have not observed one for mono-energetic electrons.
What are the reasons of different shape of these peaks?
A literature tip is ICRU report 49.Following
- Yuan jl added an answer:4How can I optimize this SOBP curve in MATLAB?
Could you give more detail about how to optimize the needed SOBP from many known different energies' bragg peaks?
happy new year,i"m looking forward to your reply about the optimized problemFollowing
- Abbas Haghparast added an answer:1What dimensionals and which materials does one use for miniphantom for SC using film dosimetry?
I want to built a miniphantom for SC measuring using EBT2 film for small field 6MV photon beam, 2 plexiglass cubes (density 1.19g/cm3) dimensions 3x3 with height of 5 cm for top and 10cm for bottom as a holder.
1- Which materials do you recomment for top for electron contamination in small field film dosimetry? Brass top or plexiglass
2- Is it necessary to calculate the equivalent thickness for top (plexi or brass)?
3- What dimensional did you consider for your phantom? lateral dimensions and top thickness?
It dependent to your protocol. For estro is 5 cm lateral and 10 cm depth of phantom. Brass used for 10 mv and higher. In iaea protocol use of build up phantom. You can use of fc65 instead of ebt2.Following
- Y.P.Y.P. Ariyasinghe added an answer:5How does to calculate treatment time of Cobalt-60 Teletherapy unit ?
How does to calculate treatment time of Cobalt-60 Teletherapy unit ?
There are two technique.
treatment time for Co60 = Prescribe daily dose/(PDD(x,y)% X BSF(x,y) X Machine Output rate(x,y) X (802/80.52))
treatment time for Co60 = Prescribe daily dose /(TAR(x,y) X machine Output rate(x,y) )
x- Field width
y- Field highFollowing
- Sajjad Ahmed Memon added an answer:5What is the differences of the monitor unit (MU) calculation method between the Report of the AAPM TG 71 and the old method?
"Monitor Unit Calculation for External photon and electron beams : Report of the AAPM Therapy Physics Committee Task Group No.71" --> published 26 february 2014.
Is it the newest method?
and then is it applicable for cobalt-60 (treatment time calculation) ?
For each formalism of MUs calc which uses isocentric or PDD formalism, what is the difference in monitor unit (MU) calculation method between Report of the AAPM TG 71 and the old method?
In last method,field size determinations for Sc,Sp&PDD in SSD technique are same value. But in aapm 71,there are different. How about it?
Please discuss it here! :))
AAPM TG 71 can be applicable for cobalt-60 for treatment time calculation but it wholly used for LINAC for MU calculations. in report MU can be replaced by Treatment Time in formalism.Following
- Yagoubi Wassima added an answer:3How can I deconvolute a reverse peak in origin 8.5 ?
I want to deconvolute a reverse peak using origin 8.5 , plz give the steps.
I think, the version origin8.5 does not allow for the deconvolution but version 8.6 can do it with the peak analyzer. (see OriginLab tutorial)Following
- Nahid Chegeni added an answer:7Does any written program exist, for optical density measuring for EBT2 film by MATLAB?
I apply EBT2 Film for dosimetry. to measure collimator scatter factor (Sc), I want to use Matlab for reading the optical density of the films . How can I write a program for MATLAB to average the optical density for some points in a circle with radius of 0.5 cm?
Thanks for all your suggestions. I will consider all key points. I also want to thank to Mr. Leon Dunn for his program.Following
- Philip Von Voigts-Rhetz added an answer:1Can anyone share with me the egsinp (input file) of Beamnrc code for calculating the phase space file of a True BEAM LINAC (FFF)?
Monte Carlo simulation for FFF LINAC (TURE BEAM)
I am sorry, but no one can share you beaminputifles. For constructing a real model, a "non-disclosure agreement" is signed with the company's.
But you can find phsp files at the IAEA database.
- Matteo Levantino added an answer:5Can somebody suggest a source of tabulated spectral data of absorption coefficients for myoglobin and oxy-myoglobin?-Following
- Hakan Akyildirim added an answer:11Easy to use program for dosimetry simulation?
Hi. Currently, I'm working with the simulation of a device to measure density. The goal is to determine if the design will be compliant with the regulations of my country over devices using radioactive materials. So, I have to do a simulation of the device.
I'm already familiar with the GEANT 4 framework, but my supervisor told me to look at FLUKA/Flair. So, I was wondering if someone knows a better program to do this. I know there is a framework called GAMOS that works with GEANT 4 to do dosimetry, but I'm not sure if the purpose (more specifically the produced output) is what I need. So if anyone knows which of these software, or, even better, other software better for this, I'd be very happy to know. Thank you in advance.
I can suggest you to use FLUKA, if you have some time to learn the code. Using it with FLAIR interface, you can save time and calculate requested quantities easily.Following
- DEEPAK KUMAR AKAR added an answer:18Can any one explain the ICRP dose limits, radiation weighting factors and tissue weighting factors?
ICRP has revised its dose limits, radiation and tissue weighting factors a number of times in its reports.
Can any one explain the basis on which they were derived/ judged and what basis was they were revised?
Any discussions, references including review articles or presentations will be appreciated.
For some of the judgements e.g radiation weighting factor for proton it seems so but not sure?Following
- Lambert Zijp added an answer:1How to create a fluence map from dynalog files?
I extracted successfully actual leaf positions, control points and dose rate by using matlab. Now need help to build fluence map with dynalog file.
I have no experience with those Varian files, but you might try "Dynalog Analysis Package":
- Marios Bazis added an answer:5Does anyone know how to find the dose in multiple volumes on example B1 in GEANT4?
I am working with the easiest example B1 and I want to find the dose in multiple shapes (G4_Bone_compact_ICRU) and not only the general dose.
I have already made 3 ideal shapes with distance 2mm and I want to find the dose in each shape.
Thanks in advance.
At first step it cannot link and compile the whole file HandsOn_5 in order to use the G4SensitiveDetector . I am using Virtual studio express.Following
- Roberto Capote added an answer:4How can I read the file IAEA.phsp in the MCNPX code?Despite the IAEA document to recommend the disclosure of IAEA.phsp files and it is not clear how this is done in different codes for existing Monte Carlo, I am especially interested in the MCNPX code.
There is no official tool as we estimulate developers to implement the IAEA interfase into their codes. It is done for Penelope, EGSnrc and Geant-4. Not for the others.
To convert those files into ASCII will be very unefficient.
But there are available examples from the website that you can use to read the files and write them into whatever format is available.Following
- Dushyant Kumar added an answer:4How do I generate a slice profile of refocusing pulses in MRI?
I am wondering if someone can help me out with some slice profile simulation.
I am trying to simulate the slice profile of 180 degree refocusing pulse surrounded by “crusher pair”. I can simulate without crusher pair, but I am unable to incorporate the effect of crusher pair along X and Z direction.
Any help would be appreciated.
I am also attaching generating code, along with RF profile and the corresponding plot. Please see the attachment.
I simulated the slice profile of refocusing pulse using Fourier transform and Bloch equation. X-axis on plots 3rd and 4th rows are HZ; while, it's bin# for Fourier transform. I would convert Hz to corresponding slice thickness later.
Dear Dr. Schilling,
Thanks for responding.
I would double check my code.
Also I would go through the paper that you referred.
- Bagher Aslibeiki added an answer:6Which materials are the best candidates for magnetic hyperthermia cancer therapy?
For magnetic hypermedia therapy different materials have been studied in literature. The question is that, which nanoparticles are the most appropriate candidates for hypothermia therapy. May be the first answer is iron oxide(Fe3o4&gammaFe2O3) nanoparticles. but why? If the only reason for this answer is the nontoxic nature of these nanoparticles? Or there are other reasons?
Thanks for your good explanation and the references.Following
- Andrey Borodach added an answer:4Physicists, help calculate the nozzle effects in the biliary tree. Do they any matter for the bile hydrodynamics?
There are a system of the physiologic (normal) narrowings and distentions in the human biliary tree (see the pictures below):
1) a cone-shaped zone narrows the distal common bile duct when it opens into the intestine resembling a convergent nozzle;
2) a cone-shaped zone ('neck') narrows the gall bladder in place where it and the cystic duct join together resembling a convergent nozzle too (when bile flows into the gall bladder lumen from the common bile duct);
3) the same cone-shaped zone of the gall bladder may act as a divergent nozzle when the dense, viscous bile flows out from it into the bile duct.
Under pathological conditions, each of the cones' apertures (or all of them) may become increased markedly. I'd like to learn more about possible hydrodynamic effects of these conditions even in some first approximation.
Thank you again! Shall be reading at once!
Studies on the biliary ducts and the gallbladder biomechanics (or, at least, related to) are scarce indeed. What I know of is as follows:
1) Walsh T.H., Akoglu T. The muscle content and contractile capability of the common bile duct . Ann R Coll Surg Engl. 1979; 61(3):206-209;
2) Die Biokonstruktion der extrahepatische Gallenwege des Menschen / R.Henning, D.Steiner, W.Lierse, G.Weinland, P.Matthaes // Aktuel. Chir. – 1988. - Bd.23. – S.74-8
3) Gallensaure-unabhangige Wirkung von Hymecromon auf die Gallesekretion und die Motilität der Gallenwege / R.M.Hoffmann, G.Schwarz, C.Pohl, D.J.Ziegenhagen, W.Kruis // Dtsch. Med. Wochenschr. – 2005. – Bd.130, H.34-35. – S.1938-43Following
- Amin Asadi added an answer:2Can anybody tell me how to import CT-Numbers in dosxyz-nrc software?
Please show me the guideline of importing CT numbers in dosxyznrc software
Thanks Dear Sandro. I appreciate youFollowing
- Sergio Faermann added an answer:3LINACS?T lead.
I would like to warn about the use of Antimony
My concern about the use of Antimony have started when I took notice of the report of materials that appear on the restricted substances list, published by the European Union ( REACH)-"Regulation Concerning the Registration, Evaluation, Authorization and Restriction of Chemicals"-
(http://www.echa.europa.eu ) and (http://esis.jrc.ec.europa.eu/ index.php?PGM=pbt)- substances of very high concern.(Antimony is considered a carcinogenic material)
Antimony is an important material employed by many manufacturers and also electronic component manufacturers ,and I don't know if they are aware of these publication and may be other countries will adopt similar restrictions.Following
- Timo Eppig added an answer:2I want to connect anterior surface corneal Zernike (the Z[4,0], or Z8) with the asphericity Q value. Is there a formula that provides this connection?
Corneal Asphericity and Zernike coefficients
To my knowledge it 1st order spherical aberration (Z(4,0) / Z8) is not enough for representing aspherics which can be described by an aspheric coefficient (Q) or a conic constant. You need at least Z(2,0) or Z3 (defocus). Using Z(4,0) and Z(2,0) only you will get a rough approximation. You would need at least 2nd and 3rd order spherical aberration to calculate Q or accurately.
See also a publication from Tim Schwiegerling et al.:
"The effects of Radial Keratotomy on the Asphericity of the Cornea"
Please note that the conic constant k is equivalent to Q (refer also to publication from Antonio Calossi). There are several definitions of the conic constant which may be confusing. You wil havbe to check which one applies.Following
- Kevin Flintham added an answer:4What is the relationship between applied kVp of conventional x-ray and backscatter?I am carring out practical work to find a mathematical equation between kVP and the backscatter factor.
In order to carry out your work, as long as the other factors mentioned here remain constant then obtaining a mathematical relationship should be relatively straightforward. Remember to control for field size, mAs, incident material, secondary incident material (eg is there a wall just behind your target), filtering and HVL.
Once all other factors are controlled for then simply varying kVp will allow measurements of backscatter to be undertaken.
Bear in mind also that the location of the detector will affect how much backscatter is detected (angle from the incident beam).
Depending on your resources you could do multiple experiments to assess these relationships individually, but also be aware that for some of these factors there is an interlinking effect, eg increasing kVp will increase backscatter but it will also affect the scattering angles as well so there will be two factors changing from the one exposure change.