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Related Concept Videos

Dose-Response Relationship: Overview01:03

Dose-Response Relationship: Overview

Agonists can bind with and activate receptors, resulting in the formation of drug-receptor complexes. Once formed, these complexes catalyze many biochemical processes at the cellular level and subsequently induce a pharmacologic response. The degree of response is directly proportional to the fraction of activated receptors, which in turn, depends on the concentration of the drug at the receptor site as well as the sensitivity of the receptor. An increase in the administered dose contributes to...
Dose Response Curve: Conventional Versus Nonmonotonic01:21

Dose Response Curve: Conventional Versus Nonmonotonic

The correlation between a drug's dosage and its impact on a biological system is a cornerstone of pharmacology and toxicology. Conventional dose–response curves, which include graded and quantal relationships, are key to this understanding. Graded dose–response curves depict the spectrum of a biological reaction to different doses within an individual, indicating that as the drug dosage increases, so does the intensity of the response. On the other hand, quantal dose–response relationships...
Dose Size and Dosing Frequency: Determination Methods01:21

Dose Size and Dosing Frequency: Determination Methods

Determining the optimal dose size and dosing frequency in pharmacotherapy is crucial for achieving therapeutic effectiveness while minimizing adverse effects. This article explores the methodologies employed in determining these parameters, focusing on their significance and interplay to tailor dosing regimens.Dose Size: Dose size refers to the amount of a drug administered in a single dose. It is determined based on the drug's pharmacodynamics and pharmacokinetics properties and...
Dose-Response Relationship: Selectivity and Specificity01:25

Dose-Response Relationship: Selectivity and Specificity

Drugs exert their therapeutic effects by interacting with receptors, enzymes, or ion channels that are present throughout the human body. The strength and duration of the interaction between a drug and its target receptor are characterized by the selectivity and specificity of the drug. Selectivity refers to a drug's strong preference for its intended target over other targets. For instance, isoprenaline, a non-selective β-adrenergic agonist, interacts with both β1- and β2-adrenergic receptors...
Dose-Response Relationship: Potency and Efficacy01:22

Dose-Response Relationship: Potency and Efficacy

The potency of a drug is the measure of its ability to produce a biological response and can be compared by looking at the half-maximum effective concentration or EC50 values of different drugs. A lower EC50 value indicates higher potency of the drug. In the dose–response curve of two antihypertensive drugs, candesartan and irbesartan, a significant difference is observed in their EC50 values. A lower EC50 value for candesartan indicates that it is more potent than irbesartan, as it produces...
Pharmacokinetic–Pharmacodynamic Relationship: Dose to Pharmacological Effect01:28

Pharmacokinetic–Pharmacodynamic Relationship: Dose to Pharmacological Effect

A drug’s dosage and pharmacokinetic properties determine how quickly it acts, how intense its effects are, and how long it lasts. Higher doses increase drug concentration at receptor sites, producing a hyperbolic curve when pharmacologic response is plotted against drug dose. Converting this scale to a log-linear format results in a sigmoidal curve, better representing dose–response relationships.For drugs following a one-compartment model, the pharmacologic response is directly proportional to...

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Updated: Jun 13, 2026

Positron Emission Tomography-based Dose Painting Radiation Therapy in a Glioblastoma Rat Model using the Small Animal Radiation Research Platform
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Positron Emission Tomography-based Dose Painting Radiation Therapy in a Glioblastoma Rat Model using the Small Animal Radiation Research Platform

Published on: March 24, 2022

Dose convolution filter: incorporating spatial dose information into tissue response modeling.

Yimei Huang1, Michael Joiner, Bo Zhao

  • 1Karmanos Cancer Center, Wayne State University, Detroit, Michigan 48202, USA. yhuang2@hfhs.org

Medical Physics
|April 14, 2010
PubMed
Summary
This summary is machine-generated.

A new dose convolution filter (DCF) model integrates biological factors into radiotherapy dose distributions. This model improves normal tissue complication probability (NTCP) predictions, especially for complex dose patterns, enhancing treatment planning.

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Irradiator Commissioning and Dosimetry for Assessment of LQ &alpha; and &beta; Parameters, Radiation Dosing Schema, and in vivo Dose Deposition
06:20

Irradiator Commissioning and Dosimetry for Assessment of LQ α and β Parameters, Radiation Dosing Schema, and in vivo Dose Deposition

Published on: March 11, 2021

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Expedited Radiation Biodosimetry by Automated Dicentric Chromosome Identification (ADCI) and Dose Estimation
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Irradiator Commissioning and Dosimetry for Assessment of LQ &alpha; and &beta; Parameters, Radiation Dosing Schema, and in vivo Dose Deposition
06:20

Irradiator Commissioning and Dosimetry for Assessment of LQ α and β Parameters, Radiation Dosing Schema, and in vivo Dose Deposition

Published on: March 11, 2021

Area of Science:

  • Radiation Oncology
  • Medical Physics
  • Radiobiology

Background:

  • Current radiotherapy planning relies on physical dose distributions, often neglecting biological factors.
  • Accurate prediction of normal tissue complication probability (NTCP) is crucial for optimizing treatment outcomes.
  • Spatial variations in dose distributions can significantly impact tissue response.

Purpose of the Study:

  • To introduce a novel model integrating biological factors like cell migration and bystander effects into physical dose distributions.
  • To incorporate spatial dose information into radiotherapy plan analysis and optimization.
  • To improve the accuracy of NTCP modeling in radiotherapy.

Main Methods:

  • A dose convolution filter (DCF) model with a single parameter, sigma, was developed.
  • Tissue response was calculated using an existing NTCP model with DCF-applied dose distributions.
  • Sigma for rat spinal cord was determined from published data, and the GRID technique was simulated.

Main Results:

  • The DCF model successfully fitted rat spinal cord data with a predicted sigma of 2.6 ± 0.5 mm, correlating with cell migration distances.
  • The model accurately predicted high relative seriality for spinal cord.
  • Normal tissue sparing was predicted with the GRID technique when beam sizes approached sigma.

Conclusions:

  • The DCF model enhances NTCP estimation by incorporating spatial dose information into complex radiotherapy dose distributions.
  • It improves predictions for small or nonuniform dose fields, leading to increased tissue tolerance.
  • The model does not alter predictions for large, homogenous fields but refines them for heterogeneous ones.