Document yr4MzdoNXpgY0LR9G6d41nGzr

AfLua _ i J. 4-2- TRADE SECRET hi.ZS.G- s z y - z . DuPont-10249 Study Title H-25240: Corrositex In Vitro Test Laboratory Project ED: DuPont-10249 Author: Carol Finlay, B.A. Study Completed on: April 10,2002 Performing Laboratory: E.I. du Pont de Nemours and Company Haskell Laboratory for Health and Environmental Sciences Elkton Road, P.O. Box 50 Newark, Delaware 19714-0050 Work Request Nu viber J uml1Service Code Number: Compaq Sanitized Does not contain TSCA CBS Page 1 o f 9 H-25240: Corrositex In Vitro Test DuPont-10249 CERTIFICATION We, the undersigned, declare that this report provides an accurate evaluation of data obtained from this study. R ev iew ed f James C .^ iack ay II Associate Scientist /& Efate Issued by Study Director: f L A lt ______________ Carol Fwlay, B .A. (J Staff Scientist D&te COmpani' -2 - Does not contain TSCA CM H-25240: Corrositex In Vitro Test STUDY INFORMATION 9th Collective Nomenclature Svnonyms/Codes H-25240 Haskell Number: 25240 DuPont-10249 J Sponsor: E.I. du Pont de Nemours and Company Wilmington, Delaware 19898 U.S.A. Study Initiated/Completed: February 26, 2002 / (see report cover page) In-Life Initiated/Completed: April 5, 2002 / April 5, 2002 Company Sanitized. Does not contain TSCA C8I -3 - H-25240: Corrositex In Vitro Test STUDY PERSONNEL Study Director: Carol Finlay, B.A. Management: Scott E. Loveless, Ph.D. Primary Technician: James C. Mackay II Toxicology Report Preparation: Lisa G. Burchfield, A.A. Management: Nancy S. Selzer, M.S. DuPont-10249 Company Sanitized. Does not contain TSCA CBI -4- H-25240: Corrositex In Vitro Test DuPont-10249 SUMMARY H-25240 was evaluated for skin corrosion potential using the In Vitro International Corrositex assay. Corrositex is a standardized and quantitative in vitro corrosivity test. The model is based on the time required for the test substance to pass through a biobarrier membrane and produce a change in a chemical detection system. An aliquot o f 500 fih o f H-25240 was applied to each o f 4 membrane discs. The test substance did not pass through any of the membranes. Under the conditions of this test, H-25240 was not a corrosive substance. CoHfMny Sanitized. Does not contain TSCA Cfil -5 - H-25240: Corrositex In Vitro Test DuPont-10249 INTRODUCTION The purpose o f this study was to determine skin corrosion potential o f H-25240 using the In Vitro International Corrositex assay kit. MATERIALS AND METHODS A. Test Substance The test substance, H-25240, was supplied by the sponsor as The test substance appeared to be stable under the conditions instability, such as a change in color or physical state, was observed. B. Principles of the Method Corrositex is an in vitro assay used to determine the skin corrosion potential o f a test substance. The assay is based on the ability o f a corrosive test substance to pass through a biobarrier membrane and to cause a color change in the liquid Chemical Detection System (CDS). The proprietary biobarrier membrane consists o f a reconstituted collagen mixture. The CDS is composed o f water and pH indicator dyes. Corrositex is conducted in three steps: 1. Qualification Step The test substance is pre-qualified to establish compatibility with the assay. The test substance is placed directly into a vial containing the CDS. If a change in color or consistency occurs, the test substance can be tested by using this assay. 2. Categorization Step This step establishes the category o f the test substance for use in the classification step. The test substance is placed into Vial A (containing an acid buffer) and Vial B (containing a base buffer), and the vials are observed for a color change. A color change observed in either vial is matched to a color chart. The test substance is assigned to either Category 1 or Category 2 based on the color change in each vial. Category 1 and Category 2 are indicative o f the time scales used in the classification step. 3. Classification Step This step determines if the test substance is a skin corrosive according to UN and DOT regulations and classifications. The test substance is applied on top o f the proprietary biobarrier membrane. A color change or consistency change in the CDS beneath the membrane indicates that the test substance has passed through the membrane. The determination o f corrosive/non- 6- - Compoiw Sanitized. Does figt'c ontnin TSCft CBt H-25240: Corrositex In Vitro Test DuPont-10249 corrosive and the Packing Group assigned are based on the amount of time it takes the test substance to pass through the membrane. The time scales differ for Category 1 and 2. The category assigned and the mean value of the breakthrough time for all 4 sample replicate vials determine the packing group. The following table is used to assign the appropriate Packing Group by category and breakthrough time. PACKING GROUP DESIGNATION Corrositex Times Category 1 0 to 3 minutes > 3 to 60 minutes > 60 to 240 minutes > 240 minutes Category 2 0 to 3 minutes > 3 to 30 minutes > 30 to 60 minutes > 60 minutes Packing Group I Packing Group II Packing Group HI Non-Corrosive > = greater than C. Protocol The biobarrier membrane discs provided by the manufacturer were stored in a refrigerator (2-8C) until the biobarrier membranes were prepared. The biobarrier membranes were prepared the day prior to conducting the assay. A thermometer was inserted into a water bath container that was placed on a hot plate/magnetic stirrer. The water bath container was filled with approximately 1 inch o f water and heated to 68-70C. While the water bath was warming, the membrane discs were removed from the refrigerator. The tray lid was removed to prevent condensation. The entire contents of the biobarrier diluent were added to the vial of biobarrier matrix powder. The vial was then placed inside the water bath. The mixture was stirred at medium speed until the biobarrier matrix powder was completely dissolved (approximately 20 minutes). The stir knob and heat were turned off. The solution remained in the water bath for 5 minutes to allow any air bubbles to rise to the surface. Two hundred microliters was pipetted into each membrane disc, ensuring the entire membrane was covered and no air bubbles had formed. The filled tray containing the biobarriers was wrapped with plastic wrap and immediately stored in a refrigerator (2-8C). 1. Qualification The test substance was first tested to determine if the sample was compatible with the Corrositex system. A 150 /L aliquot o f the test substance was added to the Qualify test tube, shaken, and allowed to stand for 1 minute. A change in color or consistency was observed qualifying the test substance for use in the Corrositex system. not contain TSCA C8* Game*** Sanitized- Ooes -7 - H-25240: Corrositex In Vitro Test DuPont-10249 2. Categorization A 150 nL aliquot o f H-25240 was added to Vial A (containing an acid buffer) and Vial B (containing a base buffer). The vials were capped and shaken. No color change was observed. Two drops o f Confirm Reagent were added to Vial B. The vial was capped and shaken until mixed. The color was matched to the colors on the color charts. The color change placed the sample in Category 2. 3. Classification The filled tray containing the biobarriers was put onto crushed ice. A membrane disc containing the biobarrier matrix was placed into a chemical detection system (CDS) vial. The CDS vials were at room temperature (17-25C). Within 2 minutes, an aliquot o f 500 fiL o f H-25240 was evenly applied on top o f the disc and a timer was started. This procedure was followed for each o f the 4 test vials (vials 1-4). One vial was similarly treated with 500 fiL o f a positive control [(vial labeled "+") containing sulfuric acid] and another was similarly treated with 500 fiL o f a negative control [(vial labeled "-") containing citric acid]. A vial labeled C served as a CDS color control. The vials were then observed for a change in the CDS. The time it took for the positive control to break through the membrane was documented. Company Sanitized. Does not contain TSCA CQI -8 - H-25240: Corrositex In Vitro Test DuPont-10249 RESULTS Breakthrough of the biobarrier occurred as follows (hour:minute:second): Vial 1 (Test Substance) - No breakthrough Vial 2 (Test Substance) - No breakthrough Vial 3 (Test Substance) - No breakthrough Vial 4 (Test Substance) - No breakthrough Vial 5 (Positive Control) - 00:01:11 Vial 6 (Negative Control) - No breakthrough CONCLUSION Under the conditions o f this test, H-25240 was not a corrosive substance. RECORDS AND SAMPLE STORAGE Specimens (if applicable), raw data, and the final report will be retained at Haskell Laboratory, Newark, Delaware, or at Iron Mountain Records Management, Wilmington, Delaware. sad* OO0 -CSC*cv -9 -