ABSTRACT
PURPOSE: To determine the intrinsic energy dependence of LiF:Mg,Ti thermoluminescent dosimeters (TLD-100) for (125)I and (103)Pd brachytherapy sources relative to (60)Co. METHODS: LiF:Mg,Ti TLDs were irradiated with low-energy brachytherapy sources and with a (60)Co teletherapy source. The brachytherapy sources measured were the Best 2301 (125)I seed, the OncoSeed 6711 (125)I seed, and the Best 2335 (103)Pd seed. The TLD light output per measured air-kerma strength was determined for the brachytherapy source irradiations, and the TLD light output per air kerma was determined for the (60)Co irradiations. Monte Carlo (MC) simulations were used to calculate the dose-to-TLD rate per air-kerma strength for the brachytherapy source irradiations and the dose to TLD per air kerma for the (60)Co irradiations. The measured and MC-calculated results for all irradiations were used to determine the TLD intrinsic energy dependence for (125)I and (103)Pd relative to (60)Co. RESULTS: The relative TLD intrinsic energy dependences (relative to (60)Co) and associated uncertainties (k = 1) were determined to be 0.883 ± 1.3%, 0.870 ± 1.4%, and 0.871 ± 1.5% for the Best 2301 seed, OncoSeed 6711 seed, and Best 2335 seed, respectively. CONCLUSIONS: The intrinsic energy dependence of TLD-100 is dependent on photon energy, exhibiting changes of 13%-15% for (125)I and (103)Pd sources relative to (60)Co. TLD measurements of absolute dose around (125)I and (103)Pd brachytherapy sources should explicitly account for the relative TLD intrinsic energy dependence in order to improve dosimetric accuracy.
Subject(s)
Brachytherapy , Thermoluminescent Dosimetry/methods , Biophysical Phenomena , Cobalt Radioisotopes/therapeutic use , Computer Simulation , Fluorides , Humans , Iodine Radioisotopes/therapeutic use , Lithium Compounds , Magnesium , Monte Carlo Method , Palladium/therapeutic use , Radioisotopes/therapeutic use , Radiotherapy Dosage , Thermoluminescent Dosimetry/instrumentation , Thermoluminescent Dosimetry/statistics & numerical data , TitaniumABSTRACT
A computer model of ion transport across amphibian skin epithelium containing two types of cellular units, their relative number and sizes, and a paracellular pathway has been developed. The two cellular units are, a large Na+ transporting compartment representing the major epithelium from stratum granulosum to str. germinativum, and a small, Cl- transporting compartment representing the mitochondria rich cell. The cellular units both contain dissipative and active pathways according to the two-membrane model. The Na+ transporting unit includes a (Na+, K+, 2 Cl-) co-transport system in the inward facing membrane. The outward facing membrane of the Cl- transporting units contains a potential gated Cl- permeability. Effects of ion distributions and changes in gating variables on the time course of transepithelial voltage clamp currents and their steady states are analyzed. The model predicts communication between the two cellular units under open circuit conditions.
Subject(s)
Biological Transport, Active , Potassium/metabolism , Skin/metabolism , Sodium/metabolism , Amphibians , Animals , Cell Membrane/physiology , Cell Membrane Permeability , Chlorides/metabolism , Epithelium/metabolism , Epithelium/physiology , Kinetics , Mathematics , Membrane Potentials , Models, BiologicalABSTRACT
The Cl- -current through toad skin epithelium depends on the potential in a way consistent with a potential-controlled Cl- permeability. Computer analysis of the Koefoed-Johnsen Ussing two-membrane model provided with constant membrane permeabilities indicates that the voltage- and time-dependent currents are not caused by a trivial Goldmand-type rectification and ion redistributions following transepithelial potential pertubations. Extended with a dynamic Cl- permeability in the apical membrane according to a Hodgkin-Huxley kinetic scheme, the model predicts voltage clamp data which closely resemble experimental observations. This extension of the classic frog skin model implies that the Cl- permeability is activated by a voltage change caused by the inward Na+ current through the apical membrane.
Subject(s)
Chlorides/metabolism , Skin Physiological Phenomena , Animals , Biological Transport, Active , Bufo bufo , Cell Membrane/physiology , Computers , Epithelium/physiology , Kinetics , Membrane PotentialsABSTRACT
A study of the voltage and time dependence of a transepithelial Cl- current in toad skin (Bufo bufo) by the voltage-clamp method leads to the conclusion that potential has a dual role for Cl- transport. One is to control the permeability of an apical membrane Cl-pathway, the other is to drive Cl- ions through this pathway. Experimental analysis of the gating kinetics is rendered difficult owing to a contamination of the gated currents by cellular ion redistribution currents. To obtain insight into the effects of accumulation-depletion currents on voltage clamp currents of epithelial membranes, a mathematical model of the epithelium has been developed for computer analysis. By assuming that the apical membrane Cl- permeability is governed by a single gating variable (Hodgkin-Huxley kinetics), the model predicts fairly well steady-state current-voltage curves, the time course of current activations from a closed state, and the dependence of unidirectional fluxes on potential. Other predictions of the model do not agree with experimental findings, and it is suggested that the gating kinetics are governed by rate coefficients that also depend on the holding potential. Evidence is presented that Cl- transport through open channels does not obey the constant-field equation.
