A stepwise procedure for evaluating irritant materials in normal volunteer subjects

1 The cutaneous response to a known irritant has been assessed in human volunteer subjects using both clini cal scoring and two non-invasive instrumental meth ods ; erythema measurement using an erythema meter and capillary blood flow using a laser Doppler device. 2 Aqueous solutions (0.5% and 1%) o...

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Published inHuman & experimental toxicology Vol. 14; no. 2; pp. 204 - 211
Main Authors Dykes, P.J., Black, D.R., York, M., Dickens, A.D., Marks, R.
Format Journal Article
LanguageEnglish
Published Thousand Oaks, CA SAGE Publications 01.02.1995
Arnold
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ISSN0960-3271
1477-0903
DOI10.1177/096032719501400209

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Abstract 1 The cutaneous response to a known irritant has been assessed in human volunteer subjects using both clini cal scoring and two non-invasive instrumental meth ods ; erythema measurement using an erythema meter and capillary blood flow using a laser Doppler device. 2 Aqueous solutions (0.5% and 1%) of sodium hydroxide were applied to back skin for 3, 15 and 60 min with assessments immediately after removal and at 1, 24 and 48 hours. 3 Increased erythema was seen with increasing duration of exposure and an increase was also seen at 1 h, 24 h and 48 h after removal of the patch. The results obtained with the erythema meter paralleled the clini cal erythema scores. However, the laser Doppler device showed the greatest changes immediately after removal of the patch with subsequent readings show ing a gradual decrease. 4 Statistical analysis of the data has been carried out to determine the accuracy and precision of the assess ment procedures and to determine the minimum test panel size for detecting irritant reactions. 5 Comparison between back and forearm skin indicated a greater sensitivity to sodium hydroxide on the back. 6 The results of this study define an ethical approach to testing irritant materials in human subjects and pro vide the basis for the development of a classification system for cutaneous irritants.
AbstractList 1 The cutaneous response to a known irritant has been assessed in human volunteer subjects using both clini cal scoring and two non-invasive instrumental meth ods ; erythema measurement using an erythema meter and capillary blood flow using a laser Doppler device. 2 Aqueous solutions (0.5% and 1%) of sodium hydroxide were applied to back skin for 3, 15 and 60 min with assessments immediately after removal and at 1, 24 and 48 hours. 3 Increased erythema was seen with increasing duration of exposure and an increase was also seen at 1 h, 24 h and 48 h after removal of the patch. The results obtained with the erythema meter paralleled the clini cal erythema scores. However, the laser Doppler device showed the greatest changes immediately after removal of the patch with subsequent readings show ing a gradual decrease. 4 Statistical analysis of the data has been carried out to determine the accuracy and precision of the assess ment procedures and to determine the minimum test panel size for detecting irritant reactions. 5 Comparison between back and forearm skin indicated a greater sensitivity to sodium hydroxide on the back. 6 The results of this study define an ethical approach to testing irritant materials in human subjects and pro vide the basis for the development of a classification system for cutaneous irritants.
1 The cutaneous response to a known irritant has been assessed in human volunteer subjects using both clini cal scoring and two non-invasive instrumental meth ods ; erythema measurement using an erythema meter and capillary blood flow using a laser Doppler device.2 Aqueous solutions (0.5% and 1%) of sodium hydroxide were applied to back skin for 3, 15 and 60 min with assessments immediately after removal and at 1, 24 and 48 hours.3 Increased erythema was seen with increasing duration of exposure and an increase was also seen at 1 h, 24 h and 48 h after removal of the patch. The results obtained with the erythema meter paralleled the clini cal erythema scores. However, the laser Doppler device showed the greatest changes immediately after removal of the patch with subsequent readings show ing a gradual decrease.4 Statistical analysis of the data has been carried out to determine the accuracy and precision of the assess ment procedures and to determine the minimum test panel size for detecting irritant reactions.5 Comparison between back and forearm skin indicated a greater sensitivity to sodium hydroxide on the back.6 The results of this study define an ethical approach to testing irritant materials in human subjects and pro vide the basis for the development of a classification system for cutaneous irritants.
1. The cutaneous response to a known irritant has been assessed in human volunteer subjects using both clinical scoring and two non-invasive instrumental methods; erythema measurement using an erythema meter and capillary blood flow using a laser Doppler device. 2. Aqueous solutions (0.5% and 1%) of sodium hydroxide were applied to back skin for 3, 15 and 60 min with assessments immediately after removal and at 1, 24 and 48 hours. 3. Increased erythema was seen with increasing duration of exposure and an increase was also seen at 1 h, 24 h and 48 h after removal of the patch. The results obtained with the erythema meter paralleled the clinical erythema scores. However, the laser Doppler device showed the greatest changes immediately after removal of the patch with subsequent readings showing a gradual decrease. 4. Statistical analysis of the data has been carried out to determine the accuracy and precision of the assessment procedures and to determine the minimum test panel size for detecting irritant reactions. 5. Comparison between back and forearm skin indicated a greater sensitivity to sodium hydroxide on the back. 6. The results of this study define an ethical approach to testing irritant materials in human subjects and provide the basis for the development of a classification system for cutaneous irritants.1. The cutaneous response to a known irritant has been assessed in human volunteer subjects using both clinical scoring and two non-invasive instrumental methods; erythema measurement using an erythema meter and capillary blood flow using a laser Doppler device. 2. Aqueous solutions (0.5% and 1%) of sodium hydroxide were applied to back skin for 3, 15 and 60 min with assessments immediately after removal and at 1, 24 and 48 hours. 3. Increased erythema was seen with increasing duration of exposure and an increase was also seen at 1 h, 24 h and 48 h after removal of the patch. The results obtained with the erythema meter paralleled the clinical erythema scores. However, the laser Doppler device showed the greatest changes immediately after removal of the patch with subsequent readings showing a gradual decrease. 4. Statistical analysis of the data has been carried out to determine the accuracy and precision of the assessment procedures and to determine the minimum test panel size for detecting irritant reactions. 5. Comparison between back and forearm skin indicated a greater sensitivity to sodium hydroxide on the back. 6. The results of this study define an ethical approach to testing irritant materials in human subjects and provide the basis for the development of a classification system for cutaneous irritants.
1. The cutaneous response to a known irritant has been assessed in human volunteer subjects using both clinical scoring and two non-invasive instrumental methods; erythema measurement using an erythema meter and capillary blood flow using a laser Doppler device. 2. Aqueous solutions (0.5% and 1%) of sodium hydroxide were applied to back skin for 3, 15 and 60 min with assessments immediately after removal and at 1, 24 and 48 hours. 3. Increased erythema was seen with increasing duration of exposure and an increase was also seen at 1 h, 24 h and 48 h after removal of the patch. The results obtained with the erythema meter paralleled the clinical erythema scores. However, the laser Doppler device showed the greatest changes immediately after removal of the patch with subsequent readings showing a gradual decrease. 4. Statistical analysis of the data has been carried out to determine the accuracy and precision of the assessment procedures and to determine the minimum test panel size for detecting irritant reactions. 5. Comparison between back and forearm skin indicated a greater sensitivity to sodium hydroxide on the back. 6. The results of this study define an ethical approach to testing irritant materials in human subjects and provide the basis for the development of a classification system for cutaneous irritants.
Author York, M.
Dykes, P.J.
Dickens, A.D.
Marks, R.
Black, D.R.
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CitedBy_id crossref_primary_10_1016_S0378_4274_01_00290_9
crossref_primary_10_1016_S0278_6915_96_00115_9
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Issue 2
Keywords skin
classifica tion
irritancy
human
measurement
Human
Skin disease
Investigation method
Toxicity
Chemical compound
Volunteer
Classification
Prediction
Irritant compound
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Snippet 1 The cutaneous response to a known irritant has been assessed in human volunteer subjects using both clini cal scoring and two non-invasive instrumental meth...
1. The cutaneous response to a known irritant has been assessed in human volunteer subjects using both clinical scoring and two non-invasive instrumental...
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StartPage 204
SubjectTerms Adolescent
Adult
Back
Biological and medical sciences
Capillaries - physiology
Capillary Permeability
Dose-Response Relationship, Drug
Erythema - chemically induced
Erythema - metabolism
Female
Forearm
General aspects. Methods
Humans
Laser-Doppler Flowmetry
Male
Medical sciences
Middle Aged
Regional Blood Flow - drug effects
Skin - blood supply
Skin - drug effects
Skin Absorption - drug effects
Sodium Hydroxide - administration & dosage
Sodium Hydroxide - adverse effects
Toxicology
Title A stepwise procedure for evaluating irritant materials in normal volunteer subjects
URI https://journals.sagepub.com/doi/full/10.1177/096032719501400209
https://www.ncbi.nlm.nih.gov/pubmed/7779447
https://www.proquest.com/docview/21098277
https://www.proquest.com/docview/77326516
Volume 14
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