Document QkV3mLBbYNnzKR8KJko9j1Q2E
FILE NAME: CTFA (CTFA) DATE: 1973 Dec 10 DOC#: CTFA019 DOCUMENT DESCRIPTION: Unpublished Report to FDA
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I December 10, 1973 TO: MEMBERS OF THE CTFA TALC SUBCOMMITTEE fit SCIENTIFIC ADVISORY COMMITTEE: i
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Attached herewith and submitted for your reading and comments ia a finalized submission of the report of the CTFA Talc Subcommittee which we wish to submit to the Food 6 Drug Administration.
Please read-at once and,'likewise, call me at once if you disagree with any of the content matter.
In view of the very short time left to process this submission, your immediate attention is of paramount importance.
Thank you,
Chairman CTFA Talc Subcommittee
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REPORT OF CTFA TALC SUBCOMMITTEE ON METHOD TO DETECT CHRYSOTILE AND TEEMOLITE IN TALC.
December 10, 1973
The Scientific Advisory Committee of the Cosmetic, Toiletry & Fragrance Association, 1625 Eye Street, N.W., Washington, D.C. 20006 at a meeting held on September 2, 1973, designated that a subcommittee be set up to study the optical microscopic method proposed by the Food and Drug Administration. This method was published in the Federal Register of September 28, 1973. The present membership of the CTFA Talc Subcommittee is shown on an attached sheet.
At the first meeting of the Subcommittee, it was agreed to submit several samples of talc to members who volunteered to apply the FDA proposed optical microscopic methodI The following talc samples were distributed without identification - except for randomly applied and non-duplicated code numbers:
Italian Talc Montana Talc Montana Talc Vermont Talc Alabama Talc No. Carolina
Grade #1615 Source P Source F Grade #66
Talc Grade 643
In addition, a sample of Italian Talc spiked w/w with 1% cbryaotile and 0.15% tremolite was sent to each participant. The participants were aware that the sample was spiked, but id not know the percentage of spiking.
The attached table summarizes all reports submitted:
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Sample
No. of Fibers With R.I. Greater
Than 1590
No. of Fibers With R.I. Less
Than 1574
Status With Regard to Pro posed FDA Method
Mrs, Lucy McCrone, McCrone Associates for Chesebrough
Spiked
320
Italian
120
Montana-Pfizer
I 0
Alabama
0
Vermont
0
N o .Carolina
0
Montana-Ferry
0
16
Parses
0
Passes
0
Passes
0
Passes
0
Passes
0
Pajsses.
0
Passes
Mr. Harold Stanley of Pfizer
Italian
/*- 100
Montana-Pfizer
100
Montana-Ferry *N*100
Alabama
owlOO
Vermont
^ 100
No. Carolina
^100
>100 >100 >100 >100 >100 >100
Fails Chrysotile Passes tremolite Fails Chrysotile Passes tremolite Fails Chrysotile Passes tremolite Fails Chrysotile Passes tremolite Fails Chrysotile Passes tremolite Fails Chrysotile Passes tremolite
Mr. David Hamer of Johnson & Johnson
Italian
0
0
Montana-Pfize r
1
0
Montana-Ferry
25
0
Alabama
0
0
Vermont
0
0
No. Carolina
0
0
Passes Passes Passes Passes Passes Passes
Spiked Italian
Dr. John A. Reffner (U. of Conn.) for Avon
632
12,930
Fails Chrysotile
Passes Tremolite
220
1,114-
'Fails Chrysotile
Passes Tremolite
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Sample ,
N o . of Fibers With R.I. Greater
Than 1590
No. of Fibers With R.I, Less
Than 1574
Status With Regard to Pro posed FDA Method
Dr. John A. Refiner (U. of Conn.) for Avon Cont'd
Montana-Pfizer
Montana-Ferry I
Alabama '
Vermont
No. Carolina
0
13 I
26 1
41
14-
5,844
9,281
,
15,125
165
11,852
Fails chrysotile Passes tremolite Fails chrysotile Passes tremolite Fails chrysotile Passes tremolite Falls chrysotile Passes tremolite Fails chrysotile Passes tremolite
Dr. Tryggye Baak of United Sierra
Spiked Italian Montana-Pfizer Montana-Ferry Alabama Vermont No. Carolina
3,000 li 000
0 0 0 0 500
2,000 0 0 0 0 0 0
Fails Passes Passes Passee . Passes Passes Passes
Richard E. Stevens of Ernest F. Fullam, Inc. for Whittaker.C&D
Italian Montana-Pfizer Mont ana-Ferry Alabama Vermont No. Carolina
8,250 18,000 29,250 21,825
3,225 20,850
1,350 450
5,200 6,075-
675 6,000
Fails chrysotile & tremolite Fails chrysotile & tremolite Fails chrysotile & tremolite Fails chrysotile & tremolite Fails chrysotile & tremolite Fails chrysotile & tremolite
Spiked sample was not run.
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Sample
No, of-Fibers With R.. Greater
Than 1590
No, of Fibers With R.I. Less
Than 1574
Status With. Regard to Proposed FDA Method
Mrs, Lucy McCrone of McCrone Associates for Kolmar
Italian Montana-Pflzer Montana-Ferry Alabama Vermont1 *No. Carolina Spiked Sample
53 0 0i 0 0I 0
488
0
i
0
,
0
1
0
1
0
!
0
16
Passes Passes Passes Passes Passes Passes Passes
*Sample noted to contain some fiber bundles which are rolled up some non-fibrous tremolite
The following participants examined their samples hut were unable conscientously to count particles with'confidence, therefore, did not report numbers:
Miss Marie Jones for Dr. G . .Cohen - Bristol-Myers Products Research Labs. Mr. Salvatore DIBianca - The Mennen Company Liberty Mutual Insurance Co., Research Center - for Kolmar Laboratories Mr. John Facq - The Colgate Palmolive Company, Research Center
The table reveals strong inconsistency- between results obtained by the different scientists applying the method to the same group of coded talc samples. This inconsistency is the result of problems encountered in the methodology.
1. The alpha refractive index of talc - one of the two indices exhibited by talc plates standing on edge - varies in value between 1.539 and 1.550l. This in combination with item 2, below, may easily result in the mis-ciassifIcation of such plates as "fibrous, less than 1.574"`end therefore chrysotile.
Dr. Refiner of the University of to Avon, admits that this factor chrysotile are high since (talc) for fibrous particles".
Connecticut, in his report is pi.ramount - "counts for edges, will often be mistaken
2. The immersion method for the determination of relative refractive index becomes unreliable when applied to extremely small (ca. 1 pm) par t i d e s , This is due in part to the fact that partides around 1 J W in'width approach the limi t of resolution of the human eye- when both size and contrast are considered, especially when applying the Becke line technique- prescribed. This will
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2. cuse eye fatigue'and resulting errors, Thus, a fine talc shard or plate on edge may he easily mistaken for an asbestos fiber. This applies to both the chrysotile and amphibole portions of the test.
3. It is quite likely that chlorite - a mineral of varied compo
sition commonly found in pharmaceutical grade talc1- would
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be Incorrectly identified as tremoline. Refractive indices
for chlorite vary in the range 11.57-1.66^.
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4. The examination of a sample of one milligram dispersed on a
single microscope slide presents the investigator with a
preparation which is too dense r a petrographic study.
5. The method is laborious and time consuming. Dr. Ref fixer quotes an analysis time of about five hours per sample and at JOHNSON & JOHNSON the investigator (D. H. Hamer) estimated at least two or three hours.
6. Dr. Walter C. McCrone in an earlier letter to the FDA suggested that there were relatively few scientists in- the country who could use the method effectively.' Scientists at Bristol-Myers, The Mennen Company, Liberty Mutual and Colgate-Palmolive had great difficulty in following the method to conclusion,
7. The proposed PDA method Implies that all fibrous particles in talc, having optical properties similar to those of asbestos minerals are in fact asbestos. This is probably an unwarranted assumption.
REFERENCES :
1. Deer, W.A., Howie, R.A., and Zussman, J., ^ock-Formine Minerals, Voi. 3, p. 121 (1962).
2. ibid, p. 131.
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We have concluded that the method publishe 1 in the Federal Register does not provide a truly reliable means for the detection of. asbestos in talc. It results in both false-positive and fa..se-negative findings. It is also tedious and may consume as much as one half day per sample.
The subcommittee urges that the Food and Drug Administration defer finalizing the proposed optical microscopic method and proceed into a Phase II program which would combine FDA and Industry in a strong effort to develop a truly reliable method for measuring chrysotile content in talc. We are confident that the detection and estimation of fibrous tremolite can also be done, if necessary, as a Cringe benefit, at the same time.
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We estimate that a 'satisfactory method will taka at least six 'months to a year, to develop. We suggest a close liaison between FDA and industry in this all-out effort with updating reviews to take place as frequently as necessary.
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Review of Alternate Methods
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The CTFA Talc Subcommittee has reviewed several methods to jdetect
chrysotile and treniolite |in talc, including modifications of thej optical
microscopic method. These are listed with comments.
1. Optical Microscopic Method - mgy be used.with some modification. Possibly better selection of R.I. liquids and reduction of sample size per slide.
2. X-ray Step Scanning - A good method for detecting tremolite if we could accept about 0,2% as the threshhold of detection. It does not distinguish fibrous from non-fihrous tremolite. The simultaneous detection of chlorite makes method impractical for chrysotile.
3. X-Ray Step Scanning + Optical I-ficroscopy - Acceptable as in if2 above but the optical method continues to prsent the dilemma in reliable identification of chrysotile. However, this does not rule out a major revision of the optical method to do the chrysotile identification and counting.
4. X-Ray Scanning - The problem of chlorite interference in the detection of chrysotile is present iii all x-ray procedures thus far available. It is reliable for the detection.of 1% tremolite (both fibrous and non-fibrous),
5. Differential Thermal Analysis - This procedure is capable of detecting chrysotile at the 1% level, however, it will not detect tremolite.
6. Scanning Election Microscopy - This procedure is not capable of identi fying asbestos. Even with energy dispersive analysis, completely satisfactory identification is not possible.
7. Transmission Electron Microscopy 4- Electron Diffraction - This appears to offer the best, moat reliable method and is probably capable of detecting chrysotile and tremolite (fibrous), both at a level of 0.1%, It is estimated that an installation would cost about $130M +, and is obviously prohibitive for the small manufacturer who uses talc. The amount of talc sample examined by this procedure is miniscule.
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Summary
.'The CTFA Tale Subcommittee has completed its review of the Optical Microscopic Method for the Estimation of Chrysotile and Fibrous Tremolite in Talc, which appeared in the Federal Register, vol. 38 (No. 188), (p. 27076, September28, 1973). It recommends postponement of the finalization of the proposed regulation on talc. In addition, a coildborative effort i between FDA & industry to resolve a satisfactory method of estimating chrysotile andj tremolite in talc, jis recommended, with periodic liaison I reviews to monitor the project status. A task force of industry experts j has been designated to pursue alternate methods. We invite FDA to participate in collaboration with the task force.
y .J ..
/Cy V i--' L y
George W. Smidland-
Chairman CTFA Talc Subcommittee
GWS;dd
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MEMBERSHIP LIST - CTFA TALC SUBCOMMITTEE
G. W, Sandland, Chairman Bris tol-Myers Products
(SAC)
Dr. DeWitt Petterson Johnson & Johnson Research Center
Dr. Murray Berdick
(SAC)
Dr. Robert Rolle
Chesebrough-Ponds, Ine.
Johnson & Johnson Research Center
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Dr. george Cohen
i
Mr. Fred Roesch
Brlsjtol-Myers Products |
Whittaker, Clark and Daniels
Dr. Christopher Costello Colgate-Palmolive Company
Dr. Charles Rowland Avon Products, Inc.
(SAC)
Mr. Salvatore DiBianca The Mennen Company
Dr. Harold Schwartz The Mennen Company
(SAC)
Mr. John Facq Colgate-Palmolive Company
Dr. Joseph Sirnko Colgate-Palmolive Company
Mr. David Hamer Johnson & Johnson Research Center
Mr. Harold D. Stanley, Jr. Pfizer
Mr. Alan M. Harvey R. T. Vanderbilt, Inc.
Mr.. Wallace Steinberg Johnson & Johnson
(SAC)
Mr. Ray R. Krammec Whittaker, Clark and Daniels
Dr. John Travers Avon Products, Inc.
Mr. Adolph Maruszewski (SAC) Kolmar Laboratories, Inc.
Dr. C. `S. Thompson R. T. Vaiderhiit, Inc.
Mr. Louis D, Murir.o United Sierra
Mr. Ronald Yakupcin Kolmar Laboratories
December 11, 1973
* Goodhue WCD 000131