Identification of Gliadin Presence in Pharmaceutical Products
Summary Celiac disease is characterized by hypersensitivity to the alcohol‐soluble wheat proteins called gliadins. Total avoidance of gliadin is the lifelong treatment for such patients. However, wheat gliadins are often present as impurities in industrial starch commonly used in the preparation of...
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Veröffentlicht in: | Journal of pediatric gastroenterology and nutrition 1994-07, Vol.19 (1), p.27-33 |
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creator | Miletic, Ivanka Dj Miletic, Vojislav D. Sattely‐Miller, Elizabeth A. Schiffman, Susan S. |
description | Summary
Celiac disease is characterized by hypersensitivity to the alcohol‐soluble wheat proteins called gliadins. Total avoidance of gliadin is the lifelong treatment for such patients. However, wheat gliadins are often present as impurities in industrial starch commonly used in the preparation of different pharmaceutical products. Therefore, some drugs might contain gliadin, which can be dangerous for sensitive patients if taken in large amounts or used permanently. The purpose of this study was to develop a sensitive, reliable assay that is specific for the detection of gliadins in pharmaceutical products. Gliadins were extracted here using sodium dodecyl sulfate rather than 70% ethyl alcohol, which has been the traditional solvent. This gliadin extract was utilized in a dot‐blot assay that incorporated an antigliadin antibody developed in rabbit and labeled with peroxidase. 4‐Chloro‐1‐naphthol was used as a peroxidase‐specific substrate. Isolated wheat gliadin was used as the positive control. Dilution experiments showed that the lower level of sensitivity for the assay was in the range of 0.0045 mg/ml of gliadin, which is a concentration level lower than that suggested for a gluten‐free diet. The assay developed here revealed that 71.2% of 59 prescription and nonprescription drugs tested contained gliadin in the amount detected by our dot‐blot assay. The prescription drugs tested were among the top 50 most frequently dispensed in U.S. community pharmacies. The nonprescription drugs were among those that constitute the largest sales in the United States. The results showed that the simple dot‐blot assay developed here can be used for pharmaceutical testing performed either by hospital laboratories or by patients themselves. |
doi_str_mv | 10.1002/j.1536-4801.1994.tb11237.x |
format | Article |
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Celiac disease is characterized by hypersensitivity to the alcohol‐soluble wheat proteins called gliadins. Total avoidance of gliadin is the lifelong treatment for such patients. However, wheat gliadins are often present as impurities in industrial starch commonly used in the preparation of different pharmaceutical products. Therefore, some drugs might contain gliadin, which can be dangerous for sensitive patients if taken in large amounts or used permanently. The purpose of this study was to develop a sensitive, reliable assay that is specific for the detection of gliadins in pharmaceutical products. Gliadins were extracted here using sodium dodecyl sulfate rather than 70% ethyl alcohol, which has been the traditional solvent. This gliadin extract was utilized in a dot‐blot assay that incorporated an antigliadin antibody developed in rabbit and labeled with peroxidase. 4‐Chloro‐1‐naphthol was used as a peroxidase‐specific substrate. Isolated wheat gliadin was used as the positive control. Dilution experiments showed that the lower level of sensitivity for the assay was in the range of 0.0045 mg/ml of gliadin, which is a concentration level lower than that suggested for a gluten‐free diet. The assay developed here revealed that 71.2% of 59 prescription and nonprescription drugs tested contained gliadin in the amount detected by our dot‐blot assay. The prescription drugs tested were among the top 50 most frequently dispensed in U.S. community pharmacies. The nonprescription drugs were among those that constitute the largest sales in the United States. The results showed that the simple dot‐blot assay developed here can be used for pharmaceutical testing performed either by hospital laboratories or by patients themselves.</description><identifier>ISSN: 0277-2116</identifier><identifier>EISSN: 1536-4801</identifier><identifier>DOI: 10.1002/j.1536-4801.1994.tb11237.x</identifier><identifier>PMID: 7965473</identifier><identifier>CODEN: JPGND6</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott-Raven Publishers</publisher><subject>Biological and medical sciences ; Blotting, Western ; Celiac disease ; Dot‐blot assay ; Drug Contamination ; Drugs ; Electrophoresis, Polyacrylamide Gel ; Enzyme-Linked Immunosorbent Assay ; Ethanol ; Gastroenterology. Liver. Pancreas. Abdomen ; Gliadin ; Gliadin - analysis ; Medical sciences ; Other diseases. Semiology ; Pharmaceutical Preparations - chemistry ; Sodium Dodecyl Sulfate ; Solvents ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><ispartof>Journal of pediatric gastroenterology and nutrition, 1994-07, Vol.19 (1), p.27-33</ispartof><rights>1994 by European Society for European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition</rights><rights>Lippincott-Raven Publishers.</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2935-6c4231deb89d55309734c9da8b0af9a626a24bf60526c3fc6dd45cabf8e16c9d3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4222121$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7965473$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Miletic, Ivanka Dj</creatorcontrib><creatorcontrib>Miletic, Vojislav D.</creatorcontrib><creatorcontrib>Sattely‐Miller, Elizabeth A.</creatorcontrib><creatorcontrib>Schiffman, Susan S.</creatorcontrib><title>Identification of Gliadin Presence in Pharmaceutical Products</title><title>Journal of pediatric gastroenterology and nutrition</title><addtitle>J Pediatr Gastroenterol Nutr</addtitle><description>Summary
Celiac disease is characterized by hypersensitivity to the alcohol‐soluble wheat proteins called gliadins. Total avoidance of gliadin is the lifelong treatment for such patients. However, wheat gliadins are often present as impurities in industrial starch commonly used in the preparation of different pharmaceutical products. Therefore, some drugs might contain gliadin, which can be dangerous for sensitive patients if taken in large amounts or used permanently. The purpose of this study was to develop a sensitive, reliable assay that is specific for the detection of gliadins in pharmaceutical products. Gliadins were extracted here using sodium dodecyl sulfate rather than 70% ethyl alcohol, which has been the traditional solvent. This gliadin extract was utilized in a dot‐blot assay that incorporated an antigliadin antibody developed in rabbit and labeled with peroxidase. 4‐Chloro‐1‐naphthol was used as a peroxidase‐specific substrate. Isolated wheat gliadin was used as the positive control. Dilution experiments showed that the lower level of sensitivity for the assay was in the range of 0.0045 mg/ml of gliadin, which is a concentration level lower than that suggested for a gluten‐free diet. The assay developed here revealed that 71.2% of 59 prescription and nonprescription drugs tested contained gliadin in the amount detected by our dot‐blot assay. The prescription drugs tested were among the top 50 most frequently dispensed in U.S. community pharmacies. The nonprescription drugs were among those that constitute the largest sales in the United States. The results showed that the simple dot‐blot assay developed here can be used for pharmaceutical testing performed either by hospital laboratories or by patients themselves.</description><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Celiac disease</subject><subject>Dot‐blot assay</subject><subject>Drug Contamination</subject><subject>Drugs</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Ethanol</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Gliadin</subject><subject>Gliadin - analysis</subject><subject>Medical sciences</subject><subject>Other diseases. Semiology</subject><subject>Pharmaceutical Preparations - chemistry</subject><subject>Sodium Dodecyl Sulfate</subject><subject>Solvents</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><issn>0277-2116</issn><issn>1536-4801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkc1u1DAURi1U1A6FR0Aaoaq7BP87QWIxqkopqqALWFuOfa3x1JMUO1Hbt8fpRLNn5Wt_5_paxwh9IrgmGNPPu5oIJiveYFKTtuX12BFCmaqf36DVMTpBK0yVqigh8gy9y3mHMVZc4FN0qlopuGIr9PXWQT8GH6wZw9CvB7--icG40K_vE2ToLaznemvS3liYxgLGEg1usmN-j956EzN8WNZz9Ofb9e-r79Xdr5vbq81dZWnLRCUtp4w46JrWCcFwqxi3rTNNh41vjaTSUN55iQWVlnkrnePCms43QGQB2Tm6PNz7mIa_E-RR70O2EKPpYZiyVrKhmBBWwC8H0KYh5wReP6awN-lFE6xnd3qnZ0F6FqRnd3pxp59L88dlytTtwR1bF1klv1hyk4sFn0xvQz5inFJKKCkYP2BPQxwh5Yc4PUHSWzBx3OryB1gQJat5OFZlV70elbbN0hYivPzHu_WP-5_stWb_AMMwm2g</recordid><startdate>199407</startdate><enddate>199407</enddate><creator>Miletic, Ivanka Dj</creator><creator>Miletic, Vojislav D.</creator><creator>Sattely‐Miller, Elizabeth A.</creator><creator>Schiffman, Susan S.</creator><general>Lippincott-Raven Publishers</general><general>Lippincott</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199407</creationdate><title>Identification of Gliadin Presence in Pharmaceutical Products</title><author>Miletic, Ivanka Dj ; Miletic, Vojislav D. ; Sattely‐Miller, Elizabeth A. ; Schiffman, Susan S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2935-6c4231deb89d55309734c9da8b0af9a626a24bf60526c3fc6dd45cabf8e16c9d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Celiac disease</topic><topic>Dot‐blot assay</topic><topic>Drug Contamination</topic><topic>Drugs</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Ethanol</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Gliadin</topic><topic>Gliadin - analysis</topic><topic>Medical sciences</topic><topic>Other diseases. Semiology</topic><topic>Pharmaceutical Preparations - chemistry</topic><topic>Sodium Dodecyl Sulfate</topic><topic>Solvents</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miletic, Ivanka Dj</creatorcontrib><creatorcontrib>Miletic, Vojislav D.</creatorcontrib><creatorcontrib>Sattely‐Miller, Elizabeth A.</creatorcontrib><creatorcontrib>Schiffman, Susan S.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miletic, Ivanka Dj</au><au>Miletic, Vojislav D.</au><au>Sattely‐Miller, Elizabeth A.</au><au>Schiffman, Susan S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of Gliadin Presence in Pharmaceutical Products</atitle><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle><addtitle>J Pediatr Gastroenterol Nutr</addtitle><date>1994-07</date><risdate>1994</risdate><volume>19</volume><issue>1</issue><spage>27</spage><epage>33</epage><pages>27-33</pages><issn>0277-2116</issn><eissn>1536-4801</eissn><coden>JPGND6</coden><abstract>Summary
Celiac disease is characterized by hypersensitivity to the alcohol‐soluble wheat proteins called gliadins. Total avoidance of gliadin is the lifelong treatment for such patients. However, wheat gliadins are often present as impurities in industrial starch commonly used in the preparation of different pharmaceutical products. Therefore, some drugs might contain gliadin, which can be dangerous for sensitive patients if taken in large amounts or used permanently. The purpose of this study was to develop a sensitive, reliable assay that is specific for the detection of gliadins in pharmaceutical products. Gliadins were extracted here using sodium dodecyl sulfate rather than 70% ethyl alcohol, which has been the traditional solvent. This gliadin extract was utilized in a dot‐blot assay that incorporated an antigliadin antibody developed in rabbit and labeled with peroxidase. 4‐Chloro‐1‐naphthol was used as a peroxidase‐specific substrate. Isolated wheat gliadin was used as the positive control. Dilution experiments showed that the lower level of sensitivity for the assay was in the range of 0.0045 mg/ml of gliadin, which is a concentration level lower than that suggested for a gluten‐free diet. The assay developed here revealed that 71.2% of 59 prescription and nonprescription drugs tested contained gliadin in the amount detected by our dot‐blot assay. The prescription drugs tested were among the top 50 most frequently dispensed in U.S. community pharmacies. The nonprescription drugs were among those that constitute the largest sales in the United States. The results showed that the simple dot‐blot assay developed here can be used for pharmaceutical testing performed either by hospital laboratories or by patients themselves.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott-Raven Publishers</pub><pmid>7965473</pmid><doi>10.1002/j.1536-4801.1994.tb11237.x</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences Blotting, Western Celiac disease Dot‐blot assay Drug Contamination Drugs Electrophoresis, Polyacrylamide Gel Enzyme-Linked Immunosorbent Assay Ethanol Gastroenterology. Liver. Pancreas. Abdomen Gliadin Gliadin - analysis Medical sciences Other diseases. Semiology Pharmaceutical Preparations - chemistry Sodium Dodecyl Sulfate Solvents Stomach. Duodenum. Small intestine. Colon. Rectum. Anus |
title | Identification of Gliadin Presence in Pharmaceutical Products |
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