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 in | Human & experimental toxicology Vol. 14; no. 2; pp. 204 - 211 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Thousand Oaks, CA
SAGE Publications
01.02.1995
Arnold |
Subjects | |
Online Access | Get full text |
ISSN | 0960-3271 1477-0903 |
DOI | 10.1177/096032719501400209 |
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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. |
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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. |
Author_xml | – sequence: 1 givenname: P.J. surname: Dykes fullname: Dykes, P.J. organization: Department of Dermatology, University of Wales College of Medicine, Heath Park, Cardiff, CF4 4XN – sequence: 2 givenname: D.R. surname: Black fullname: Black, D.R. organization: Department of Dermatology, University of Wales College of Medicine, Heath Park, Cardiff, CF4 4XN – sequence: 3 givenname: M. surname: York fullname: York, M. organization: Environmental Safety Laboratory, Unilever Research, Colworth House, sharnbrook, Bedford, MK44 1LQ, UK – sequence: 4 givenname: A.D. surname: Dickens fullname: Dickens, A.D. organization: Environmental Safety Laboratory, Unilever Research, Colworth House, sharnbrook, Bedford, MK44 1LQ, UK – sequence: 5 givenname: R. surname: Marks fullname: Marks, R. organization: Department of Dermatology, University of Wales College of Medicine, Heath Park, Cardiff, CF4 4XN |
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Cites_doi | 10.2340/00015555-70463467 10.1111/1523-1747.ep12319895 10.1007/BF00431067 10.1111/j.1600-0536.1989.tb03202.x 10.1016/0041-008X(75)90272-0 10.1111/j.1365-2133.1977.tb07148.x 10.1111/j.1365-2230.1992.tb02158.x 10.1111/j.1467-2494.1990.tb00521.x 10.1016/0041-008X(83)90005-4 10.1111/1523-1747.ep12504896 10.1016/0041-008X(72)90157-3 10.1016/0887-2333(91)90042-C 10.1111/j.1365-2133.1990.tb01477.x 10.1111/j.1365-2133.1991.tb14166.x 10.1017/CBO9780511759956.013 10.1016/0041-008X(71)90112-8 10.1016/S0022-3565(25)08751-8 10.1111/j.1365-2133.1984.tb14149.x 10.1111/j.1600-0536.1987.tb02701.x |
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Keywords | skin classifica tion irritancy human measurement Human Skin disease Investigation method Toxicity Chemical compound Volunteer Classification Prediction Irritant compound |
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References_xml | – volume: 31 start-page: 481 year: 1975 end-page: 90 article-title: Interspecies comparisons of skin irritancy. Toxicology publication-title: Applied Pharmacology – volume: 68 start-page: 206 year: 1983 end-page: 17 article-title: Quantitation of cutaneous toxicity: An in vitro approach using skin organ culture publication-title: Toxicology and Applied Pharmacology – volume: 19 start-page: 276 year: 1971 end-page: 300 article-title: Study of intra- and interlaboratory variability in the results of rabbit eye and skin irritation tests publication-title: Toxicology and Applied Pharmacology – volume: 70 start-page: 463 year: 1990 end-page: 7 article-title: Sodium hydroxide-induced subclinical irritation publication-title: Acta Dermatologica Venereologica – volume: 281 start-page: 293 year: 1989 end-page: 5 article-title: Quantification of sodium lauryl sulphate irritant dermatitis in man. Comparison of four techniques: skin colour reflectance, transepidermal water loss, laser Doppler flow measurement and visual scores publication-title: Archive for Dermatology Research – volume: 94 start-page: 42 year: 1979 end-page: 2 article-title: Comparative studies on the irritancy of oils and synthetic perfumes to the skin of rabbits, guinea pig, rat, miniature swine and man publication-title: Cosmetics and Toiletries – volume: 45 start-page: 257 year: 1965 end-page: 61 article-title: Patch test methods II: Regional variations of patch test responses. 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London: British Medical Association year: 1991 ident: atypb18 – ident: atypb3 doi: 10.1017/CBO9780511759956.013 – ident: atypb8 doi: 10.1016/0041-008X(71)90112-8 – volume: 82 start-page: 377 year: 1944 ident: atypb1 publication-title: Journal of Pharmacology and Experimental Therapeutics doi: 10.1016/S0022-3565(25)08751-8 – ident: atypb7 – volume-title: The design and analysis of industrial experiments year: 1956 ident: atypb16 – ident: atypb10 – ident: atypb13 doi: 10.1111/j.1365-2133.1984.tb14149.x – ident: atypb22 doi: 10.1111/j.1600-0536.1987.tb02701.x |
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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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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 |
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