Document mbJRB8a96NgY8rdpnjB8Y269k
FILE NAME Talc TALC
DATE 2014
DOC TALC130 DOCUMENT DESCRIPTION Journal Article - Asbestos in Commercial Cosmetic Talcum Powder as a Cause of Mesothelioma in Women
Asbestos in commercial cosmetic talcum
powder as a cause of mesothelioma in women
Ronald E. GordonSean FitzgeraldJames Millette
Department of Pathology Icahn School of Medicine at Mount Sinai New York USA SAI Laboratory Greensboro NC USA MVAInc. Duluth GA USA
Background Cosmetic talcum powder products have been used for decades The inhalation of talc may cause lung fibrosis in the form of granulomatose nodules called talcosis Exposure to talc has also been suggested as a causative factor in the development of ovarian carcinomas gynecological tumors and
mesothelioma
Purpose To investigate one historic brand of cosmetic talcum powder associated with mesothelioma in
women
Methods Transmission electron microscope TEM formvar grids were prepared with concentrations of one brand of talcum powder directly on filters from air collections on filters in glovebox and simulated bathroom exposures and human fiber burden analyses The grids were analyzed on an analytic TEM using dispersive spectrometer EDS and selected electron diffraction SAED to determine asbestos fiber number and type Results This brand of talcum powder contained asbestos and the application of talcum powder released inhalable asbestos fibers Lung and lymph node tissues removed at autopsy revealed pleural
mesothelioma Digestions of the tissues were found to contain anthophyllite and tremolite asbestos Discussion Through many applications of this particular brand of talcum powder the deceased inhaled asbestos fibers which then accumulated in her lungs and likely caused or contributed to her mesothelioma
as well as other women with the same scenario
Keywords Asbestos Talcum powder Chamber test TEM SEM EDS SAED Mesothelioma
Introduction
Malignant mesothelioma occurs in both the peritoneum and in the lung pleura Mesothelioma cases have been attributed to direct occupational exposure
indirect exposure and secondary exposure A higher rate of idiopathic mesothelioma has been reported
in women as no link between asbestos exposure and
patients has been identified. Previous research suggests that ovarian cancer and peritoneal mesothelioma may be directly attributed to the use of talcum powder contaminated with asbestos or from exposure
7
to partners occupationally exposed to asbestos. Using talcum powder in closed spaces may increase the likelihood of inhaling the powder laced with asbestos Repeated applications increase the oppor-
tunities for inhalation and the asbestos could become
concentrated in the peripheral airways and alveoli of the lungs of the talcum powder users This has been supported by the presence of granulomas in the lungs of some talcum powder users
Corespondec Gordn Department Levy ofCorrespondMeonucnet GustGausvtavee
USA Email Ronald.Gordon@mountsinai.org Ronald.Gordon@mountsinai.org
Place New Icahn School
In 1976 Rohl and Langer tested 20 consumer products labeled as tale or talcum powder including body powders baby powders facial talcums and a
pharmaceuticalpharmaceutical tale Of the 20 products tested 10 were were found to contain tremolite and anthophyllite _ principally asbestiform The product with the highest
_asbestos content was the same product tested in this
study Both asbestiform anthophyllite and asbesti-
_form tremolite were found in the Rohl and Langer
tests Given that asbestos has been determined as the
primary cause of mesothelioma it is important to
note that cosmetic talc contained asbestos in the
past The contamination results from the mining
process since ore specimens taken directly from the mines have repeatedly been tested and shown to contain asbestos most often anthophyllite and tremolite but also serpentine chrysotile asbestos
In part from the review of corporate documents and the sworn testimony of those responsible for the sourcing of talc used in the products studied here it
was determined that three mines provided the raw material for use as talcum powder The tale used by
this cosmetic company that manufactured and
W S. Maney & Son Ltd 2014 DOI 2049396714Y 0000000081
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distributed the talcum powder was from three distinct
regions the Willow Creek mine in Southwest
Montana the Regal mine near Murphy North
Carolina and imported talc from the
1116
region of the Italian Piedmont
Val Chisone
The specific
geology of tale is an important indicator of whether
a talc source may be contaminated with asbestos
These three mines all contained asbestos fibers
anthophyllite and tremolite The Val Chisone
talc from Italy was studied by Pooley in 1972. Mine
sample had intergrowths with serpentine chry-
sotile asbestos along with tremolite and anthophyllite
asbestos The tale from Italy was named American
21
Ground Italian and designated as AGI 1615.19
This talc was diluted with a talc from another source
to make it acceptable based on ray diffraction XRD protocols However it contained asbestiform
tremolite and anthophyllite.22
In this study three laboratories analyzed a specific
brand of talc from more than 50 containers of this
cosmetic talcum powder product of different sizes
and colors produced over a year time span to
determine conducted
the presence of asbestos The independent product testing in
authors
unasso-
ciated laboratories in North Carolina Georgia and New York A fourth laboratory which also tested
this product will herein be referred to as Laboratory
D. The lung and lymph node tissues from a woman
who died from mesothelioma and testified to only
using this specific brand of talcum powder were
analyzed for the presence of asbestos and tale This is
the first report that explores the hypothesis that a
specific brand of talcum powder coming from
asbestos contaminated mines can find its way into
the finished product that can be inhaled during use
and cause or contribute to the development of
mesothelioma
Materials and Methods
Laboratory A product testing In Laboratory A over 50 containers of this particular brand of talcum powder were acquired from a variety
of sources for bulk testing Some of the containers were purchased online while others were provided directly from the manufacturer All of the containers
were verified to be the correct brand and product Laboratory A tested talcum powder from each of
the 50 samples using transmission electron microscope TEM methods The procedure for testing by
Lab A was as follows 0.01 g of talcum powder was removed from its vial and suspended in 1 ml of distilled water with one to two drops of ethanol by brief sonication From this suspension 10 laliquots were removed and placed on a series of five formvarcoated nickel grids 100 grid openings each In some
cases it was necessary to prepare additional sets of
five grids from the same 0.01 g sample of powder The drops were allowed to dry in a covered Petri dish The grids were then examined and analyzed with a Hitachi 7000 STEM equipped with an Evex dispersive spectrometer EDS for elemental composition and relative amounts of elements The microscope was equipped with a tilt stage and a rotary specimen holder which was employed with selected electron diffraction SAED analyses as described below Structures seen as fibers measuring at least five micrometers in length with aspect ratios of 5 or greater were analyzed to determine if they were regulated asbestos mineral fibers We used EDS to chemically establish the presence of asbestos fibers and the crystalline structure was assessed using SAED All 100 grid openings were observed and analyzed on each of the five grids for each product sample at least 500 grid openings per sample analyzed
Analyses were performed using a modification of the techniques described by Yamate et al and similarly adopted techniques used by the Environmental Protection Agency EPA American Society for Testing and Materials ASTM and International Organization for Standardization All techniques required the use of a TEM equipped with an EDS system Only in Yamate level III is the tilt and rotary stage optional to perform advanced SAED zone axis analysis Yamate et al stated that zone axis diffraction analysis is useful in differentiating between otherwise unidentifiable fibers In the Laboratory A analysis zone axis analyses were not necessary as the identified amphiboles clearly demonstrated that they were asbestiform tremolite and anthophyllite confirmed by morphology EDS chemistry and characteristic 5.3 ^ inter repeats on diffraction without tilting Both asbestiform and nonasbestiform particles and fibers were present
However in most cases this manuscript will refer to asbestiform fibers and state when they are tremolite anthophylite or chrysotile type asbestos A nonasbestos tremolite anthophylite will not be referred to as asbestos
To calculate the fiber concentrations per gram of talcum powder we first determined the number of
asbestos fibers on average per grid opening This number was multiplied by 552. The product of that equation was multiplied by 100 and then divided by 0.01 to yield the fibers talcum powder value The constant 552 is the number of grid opening areas on the entire grid One hundred is the number of 10 ...l drops in 1 ml that the talcum powder was dispersed and the 0.01 was the weight of the talcum powder dispersed Quality control procedures which included testing of blanks from water working in a clean hood environment and working with only one
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Figure 1 Pouring of powder into hands in glovebox
sample at a time ensured that no laboratory contamination of samples
Laboratory B asbestos releasability testing To determine if the user could inhale asbestos during a talcum powder application Laboratory B assessed asbestos releasability by air sample Air samples were generated during simulation in a glove box consis-
tent with normal product use in a controlled environment These three samples included the same samples tested by Laboratory A. Environmental and personal air samples were collected using standard airborne asbestos techniques using volume air pumps for environmental stationary samples inside and outside of the controlled area and volume air pumps for personal samples taken at a distance comparable to the breathing zone of the person simulating application Standard TEM 385 mm effective filter area 25 mm cassettes with 0.45 m MCE filters were used on the calibrated high 712 min and low volume 1-4 min air pumps Figs 1 and 2
The resulting air samples were analyzed for airborne asbestos following the analytical procedures
described in the U.S. Environmental Protection
Agency Code of Federal Regulations 40 CFR part 763 subpart E Appendix A - AHERA for direct
preparation of MCE filters All final analyses by Laboratory B were conducted on a JEOL 2000FX TEM equipped with an dispersive ray analyzer detector and SAED at magnifications up to ^ 50 000 using the fiber counting criteria specified
by Yamate et al.'s protocols
Laboratory C product bulk testing and bathroom chamber releasability
Bulk methods
Laboratory C examined nine samples under an Olympus SZ stereomicroscope at magnifications from x7 to x 40. Portions of the particulate found in the sample were mounted in Cargille refractive index liquids for analysis by polarized light microscopy PLM using an Olympus BH PLM with a magnification range from 100 to ^ 1000. The PLM analysis followed the procedures for bulk analysis of building materials described by the US EPA in 1993.24 Characterization of the fibers was
performed using a Philips EM420 100 TEM equipped with an Oxford INCA EDS ray analysis system and capable of SAED work involving tilting of amphibole fibers Zone axis determinations were
also conducted We used TEM asbestos fiber count-
ing criteria of fibers greater than 0.5 ...min length
with at least a 5 aspect ratio as described in
Asbestos
Hazard
Emergency
Response
Act
AHERA and ASTM methods D6281 D5755
Figure 2 TEM cassettes in simulation area in glovebox
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Gordon et al Asbestos in commercial cosmetic talcum powder
D5756 and D648.24 28 Data were recorded using the ASTM D6281 format XRD analysis was performed by an outside laboratory DCM Science Laboratory Inc. Wheat Ridge CO USA scanning over a range of 3 45 20 using 40 kV 25 mA Cu K radiation Mineral phases were identified with the aid of computer programs accessing a ROM powder diffraction database
Air testing
Tests to determine airborne levels of asbestos fibers
resulting from application of this brand of talcum powder were performed in a testing chamber The
chamber was built to match the bathroom of the patient that used this brand of cosmetic talc Her
bathroom was measured at 7 feet 9 inches high by 5 feet by 4 feet 1 inch All talc products used in these chamber tests had previously been tested in Laboratories A B. or both
Air test shaker container
Using Personal Protective Equipment a volunteer applied one of the bulk tested cosmetic talcum powders to his body using a shaker container This particular talcum powder contained approximately 01 by weight and approximately 18 million anthophyllite asbestos fibers per gram The container was weighed before and after the testing to determine the approximate weight of material applied The talcum user wore a respirator and a bathing suit The volunteer twisted the top of the container and shook material onto his hand He applied the tale under his
arm and around the shoulder and upper arm area He
then shook the talcum powder onto his other hand and applied it to the other underarm shoulder and
upper arm area He shook out additional material
and applied it to his neck and upper torso He shook out and applied material two more times for a total of five applications The total talcum application time was approximately 1 min and amounted to 0.37 g of the talcum powder Two air samples were collected in the applier's breathing zone at 0.5 1 per minute lpm and two additional air samples were collected in the breathing zone at 1.0 Ipm with commercial open air cassettes The minute sampling time included the application time and a waiting period The bystander in the test chamber had two air cassettes in his breathing zone for the minute period including application and the additional waiting time The bystander wore a respirator and full protective clothing These air samples were collected at rates of one and 2 1pm No activities were conducted during the waiting period other than checking the pumps
and cassettes The air filters and two additional blank
filters were analyzed by phase contrast microscopy PCM using National Institute for Occupational Safety and Health NIOSH Method 7400.9 Two air
samples
NIOSH
and two blanks were also analyzed by
Method 7402 via transmission electron
microscopy to determine the percentage of asbestos fibers among the fibers counted by PCM An air sample collected from within the test chamber before
the study was analyzed by a more sensitive TEM procedure following the EPA AHERA method.2
Air testing puff applicator In this test a volunteer applied a different cosmetic
talcum powder sample using a puff applicator This particular talcum powder contained approximately 0.05 anthophyllite asbestos approximately 70 mil-
lion asbestos fibers per gram The container was weighed before and after the testing to determine the approximate weight of material applied The talcum user wore a respirator and a bathing suit The talc user opened the puff container and applied the talcum powder as described above only this time with a powder puff He then repeated the process for a total of six applications The talcum application time was approximately 1 minute Two air samples were collected in the applier's breathing zone at 0.5 1pm for a sampling period of 4 minutes One air sample was collected for a shorter period 3.3 minutes that included the application period Another air sample was to be collected after the application period but this sample was voided because the
volunteer hit the air cassette and the cassette fell off
the vacuum hose The bystander in this test followed the same protocol as described above Both air samples were collected at a rate of 0.5 1pm No activities were conducted during the waiting period other than checking the pumps and cassettes The air filters and two additional blank filters were analyzed by PCM using NIOSH Method 7400 as described above One air sample and two blanks were also analyzed by NIOSH Method 7402 via TEM to determine the percentage of asbestos among the fibers counted by PCM An air sample collected from within was tested as described above by EPA AHERA method
Human Tissue Analysis
TEM
Tissue samples from a woman with no other known
exposure to asbestos other than her use of the product tested was supplied to Laboratory A. Human tissue analysis was performed according to
the techniques described in Wu et 29 Lung and lymph node tissue was received fixed in formalin Half of the tissue was removed from the lung and the lymph node tissue Two grams of lung tissue were divided twice The two halves of the lymph node weighed 0.16 g together The two specimen types were separated throughout the study The tissue from
each was first digested in a % solution of potassium
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hydroxide KOH for approximately hour at 60 The dissolved lung and lymph node material was then centrifuged in a speed centrifuge to separate the inorganic material from the dissolved organic tissue The solute material containing the dissolved organic
material and KOH was removed and distilled water
was added The inorganic material was suspended in the water by brief sonication The material was recentrifuged and the process of washing the inorganic material was performed five times After the fifth wash the distilled water was removed and replaced with 10 ml of fresh distilled water and the inorganic material was suspended by brief sonication Ten microliter samples were removed from the suspension and placed on formvar nickel grids on a metal mesh in a covered glass Petri dish to dry Five grids were initially prepared and an additional set of five grids was prepared for each tissue type for a second
analysis The dried grids were observed with a transmission electron microscope Four hundred grid
openings on at least four grids were analyzed and a fifth grid was used if grid openings were broken in the initial four examined grids The fiber concentrations per gram wet weight lung or lymph node tissues were
calculated from the number of fibers observed the
area analyzed the aliquot ratio and the total weight of the tissue sample digested
Light microscopy
Tissue sections
Small lung tissue samples were put into 10
phosphate formalin and processed for
embedding in paraffin Five micrometer paraffin
sections were cut mounted on glass slides and
stained with hemotoxylin eosin and an iron
stain The tissue was evaluated for the presence of
altered morphology and ferruginous bodies two
characteristics often seen in lung tissues that are
a byproduct iron protein deposits on asbestos
fibers
resulting
from
macrophage
frustrated
phagocytosis
.
Digested lung and lymph node tissue Two hundred and fifty microliters of digested lung and lymph node material suspension used for TEM analyses was placed in a cytocentrifuge and the slides were cover slipped and observed by phase contrast light microscopy The entire area was counted for ferruginous bodies and calculated back to the weight
of the tissue to determine the concentration of bodies
per gram of wet weight tissue
Scanning electron microscopy SEM SEM samples were prepared by taking 250 ...l of the suspended inorganic material used for the TEM and light microscopy analyses and placed on a 0.1 m pore size Nucleopore filter mounted on a carbon planchette on an aluminum SEM stub The material
was allowed to dry in a covered Petri dish The stub was then coated with vaporized carbon and observed with a Hitachi 4300 field emission scanning electron microscope equipped with an Evex EDS system The entire filter sample surface was scanned for fibers and
asbestos bodies
Results
All three laboratories confirmed in multiple tests the
presence of asbestiform anthophyllite and asbesti-
form tremolite in the talcum powder products just as
had been found and described by Rohl and Langer
over three decades ago
Initial bulk analyses of 50 samples of this product
in Laboratory A showed that all of the samples
contained asbestos fibers Eighty percent contained
only anthophyllite asbestos % only tremolite
asbestos % anthophyllite and tremolite asbestos
and % anthophyllite tremolite and chrysotile
asbestos The range in asbestos concentrations of
fibers > ...min length were calculated to be at a
minimum between 1840 and 1 104 000 fibers per
gram of talcum powder More than 80 of the tested
cans and plastic containers contained asbestos fibers of talcum powder
over 10 000 Four of the
containers had less than 5000 fibers per gram and six
containers had more than 250 000 fibers per gram
However it should be noted that there were many
asbestos fibers that also had aspect ratios less than
8 These fibers were generally found to be shorter
than 5 ...mand were noted but not counted in the
original product testing or in the lung and lymph
node tissue testing by Laboratory A. There were also
a number of fibrous talc particles that were easily
distinguishable from asbestos by morphology If
there was a question regarding their identity both
EDS and SAED were employed to recognize such
fibers as talc All the fibers that were actually counted
in bulk and tissue preparations were 5 ...mor greater
in length with aspect ratios for the most part greater
than 10 The majority of asbestos structures
counted demonstrated aspects ratios 15 with
many 20 A minimum of four fibers was identified in each sample making the concentration
determinations of asbestos statistically significant and
reproducible Laboratory C using PLM TEM and XRD tested
nine samples of the specific brand of talcum powder described above Generally the PLM analysis showed that the samples contained both platy and fibrous tale less than % by volume of the PLM visible amphibole fibers and some quartz The majority of the PLM amphibole particles had low aspect ratios length to width but some were 10 1 By XRD one of the talcum powder samples was found to contain % anthophyllite No amphibole
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Figure 3 Application of powder from shaker in bathroom-
sized chamber
minerals were detected in the other eight samples by XRD The XRD detection limit was approximately % by weight In TEM analysis all nine samples were positive for amphibole asbestos primarily anthophyllite and were confirmed with zone electron diffraction measurements At least five asbestos fibers per sample were recorded in each sample with concentrations ranging from 0.004 to 0.9 by weight and from 3 to 200 million asbestos fibers per gram of fibers greater than 0.5 ...min length with at least a 5 aspect ratio
Air monitoring Releasability of asbestos into the air from the products was assessed by glove box simulation testing by Laboratory B and by full chamber testing by Laboratory C. In a manner consistent with methods used by the EPA NIOSH or ASTM study product body powders and dusting powders were applied
hand to hand and hand to arm Consistent with bulk
testing results anthophyllite and tremolite asbestos was repeatedly found in the air tests resulting from these simulations Figs 6-8
Shaker container test The shaker application test used 0.37 g of talcum powder Fig 3 For the talc user the average PCM fiber concentration in his breathing zone during application was 4.8 cc 3.1 7.3 3.9 and 4.9 cc The asbestos to total fiber percentage as determined by TEM was 40 Therefore the asbestos concentration in the breathing zone of the talc user during application was 1.9 cc For the bystander the PCM fiber concentration was 1.35 cc 0.9 and 1.8 cc and the TEM derived percentage of asbestos was 35 which results in a bystander asbestos concentration of 0.5F No asbestos fibers were found in the sample collected in the chamber before the testing
or in the blank filters
Puff application The puff application test used 6.25 g of talcum powder Figs 4 and 5 For the talc user the average
Figure 4 Application with powder puff in bathroom
chamber
PCM fiber concentration in his breathing zone during the minute sampling period was 20 cc 23.6 and 16.5 cc The asbestos to total fiber percentage as determined by TEM was 21 Therefore the asbestos concentrations in the breathing zone of the talcum powder user were 5 and 3.5 cc The short term sample in the breathing zone of the applier had a PCM value of 60 cc Using the derived percentage of asbestos of % result for the shortterm sample was an asbestos concentration of 13 F cc For the bystander the PCM fiber concentration was 11.7 cc 13.7 and 9.7 cc Using the minimum derived percentage of asbestos of 36 results in a bystander asbestos concentration of 49
and 3.5 cc No asbestos fibers were found in the
sample collected in the chamber before the testing or in the blank filters
The tests performed independently by Laboratory C using a bathroom room confirmed the findings for asbestos fiber release found by Laboratory B's glovebox testing Samples showed that significant concentrations of anthophyllite tremolite and occasionally chrysotile asbestos were released in the simulated application of several iterations of the products This confirmed not only
Figure 5 Application with a powder puff in bathroom chamber
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HT 100KV TEM Magnification Magnification : 500
1300866 Tremolite
1300888 Tramalte SAED 0 angle new IA
Figure 6 Tremolite asbestos from TEM analysis of releasability air testing of product images EDS and SAED
the presence of asbestos in the talcum powders but also that the asbestos contained in the friable
powders was easily aerosolized in a manner consistent with the products intended use confirming the hypothesis that the cosmetic powders are capable agents of exposure to asbestos
Human tissue analysis Electron microscopic analysis of the lung tissue revealed amphibole type asbestos fibers in a calcu-
lated concentration of 1380 and fibers per gram
wet weight respectively with a limit of detection of 690 fibers per gram wet weight All fibers counted
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val SEP ge a, MEd bg cot ** ***
1300863 Anthophyllite
***** ***** ***** 3x34
1300861-2 Anthophyllite
30006.1.1 Anthophyllde SAED
1300881-1 Anthophyllite near ZA 6 degrees
cow
PE
em
eg
Senge
Se oe
ah
Figure 7 Anthophyllite asbestos from TEM analysis of releasability air testing of product images EDS and SAED
were 5 mor greater in length and had aspect ratios of 20 1 or greater The amphiboles were identified by EDS and SAED analysis as anthophyllite Fig 9 and tremolite Fig 10 asbestos The asbestos fibers were seen in a ratio of : and 2 respectively anthophyllite There were many anthophyllite and tremolite asbestos fibers less than 5 um in length that were not counted The majority of these smaller asbestos fibers were of the anthophyllite type Light microscopic analysis of the cytocentrifuge preparation revealed a calculated concentration of 140 asbestos bodies per gram wet weight of lung
tissue by phase contrast light microscopy in both samples
Electron microscopic analysis of the lymph node tissue revealed amphibole asbestos fibers in a
calculated concentration of 12 738 fibers per gram
wet weight with a limit of detection of 2123 fibers per gram wet weight All counted fibers were at least 5 min length with aspect ratios of 10 or greater The amphiboles were identified by EDS and SAED analysis as anthophyllite and tremolite and they were seen in a ratio of 5 anthophyllite There were many anthophyllite and tremolite fibers less
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>
Wee
met
vogla
1300886 Chrysotile
Figure 8 Chrysotile asbestos from TEM analysis of releasability air testing of product image and SAED
than 5 ...min length that were not counted We also
observed but did not count tremolite cleavage
fragments Light microscopic analysis of the cytocen-
trifuge preparation revealed a calculated concentra-
tion of 92 asbestos bodies per gram wet weight of
lymph node tissue by phase contrast light microscopy
Fig 11
Histological sections of the tissue showed focal
areas of mild parenchymal fibrosis and a more
generalized pleural fibrosis Although many ferrugi-
nous bodies were identified in the cytocentrifuge
preparation most were relatively small and not seen
in the stained paraffin sections These macro-
phages were clustered and contained a combination of fibrous and platy tale and small asbestos bodies
In addition to the fibrous and platy tale described
above
other
inorganic
materials
were
seen
Aluminum silicates and magnesium aluminum sili-
cates in both fibrous and platy form were identified
We elected not to count these fragments Their
presence supports the hypothesis that the lung and
lymph node samples match findings from the tested
talcum powder
The two analyses performed on the lung tissue
were from two separate tissue digestions The second
was prepared with tissue not previously analyzed but
Gordon et al Asbestos in commercial cosmetic talcum powder
saved from the original half of the tissue retained by Laboratory A. The results proved to be completely reproducible with no finding of any additional fiber types other than those reported above
Confirmation of interlaboratory analyses After several years of independent testing in separate
laboratories the authors became aware of one another's work through litigation The finding that this historic brand of cosmetic talcum powder contained asbestos fibers with generally the same morphological and chemical assemblage was confirmed A fourth laboratory Laboratory D tested many of the same samples but did not report asbestos findings Owing to the inconsistency with the other laboratories examination of results from Laboratory D was warranted
Two of the three authors of this study went to the Laboratory D and were supplied with the prepared filters on TEM grids or SEM stubs previously analyzed by Laboratory D. They were also supplied with both TEM and SEM microscopes to analyze the specimens along with data and locator sheets allowing for the same grid openings and areas to be observed as in the initial analyses
Reanalysis of subject product samples One author analyzed the TEM preparations of 20 study products of talcum powder prepared by Laboratory D. Asbestos structures were found in the analysis some of which were named in the original analysis as cleavage fragments intergrowths or fibrous talc rather than as asbestos Although the author reviewer agreed with many of the nonasbestos fibers identified he concluded the original analyses were incomplete Additional by the reviewers showed some of the incompletely analyzed fibers to be asbestos In other cases asbestos found on analysis was located on areas of the filter where no fibers were recorded in the original bench sheets or reports In some instances the overall distribution of particulates on the preparations was inhomogeneous in contrast with the method of choosing grid openings for the original analysis by skipping every other opening in a checkerboard
fashion Furthermore the methods named on the analytical count sheets were not the same as the methods cited in the reports from Laboratory D.
Laboratory D reported no asbestos fibers in the 20 samples analyzed In contrast asbestos fibers were identified in all 20 of the same products in Laboratory A and in 16.of 20 products tested by Laboratory B. In the analysis of those same 20 samples originally analyzed by Laboratory D via TEM eight were found to contain asbestiform anthophyllite six asbestiform tremolite and two were found to contain chrysotile fibers These findings were significant because analysis was not a
.
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Count
0.000
kev
10.230
3:39:12 PM 2014
75KV 40 Degree
Figure 9 This asbestos fiber is a representative sample removed from the lung tissue of the patient exposed to cosmetic talcum powder Anthophyllite asbestos fiber is observed and its SAED pattern is demonstrated beside it with the EDS spectra
complete replication of the original analysis due to time constraints damage or unsuitable preparations It was apparent that the technicians in Laboratory D missed
fibers and misidentified asbestos fibers as asbestos
analysis of human tissue Laboratory D also performed fiber burden analysis on human tissue with differing results than the study
of the authors Similar to the evaluation of bulk
analyses two reviewers analyzed the human tissue sample preparations of Laboratory D together and found significant differences in their analyses compared to the technicians who originally analyzed
the grids and stubs We determined that the technicians misidentified anthophyllite asbestos fibers that had been coated with iron and protein anthophyllite asbestos bodies as either cleavage fragments or as amosite fibers Fig 12 Furthermore it is the authors consensus that there are no generally accepted criteria to classify individual fibers as cleavage fragments by TEM when the sample
contains attributes of an asbestos fiber or countable
structure When Laboratory D technicians initially
looked for asbestos bodies to determine the fiber
core they concluded that most were amosite However when the two reviewers examined
10
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FA13-27LAZ FA13-27LAZ
3
Count
Gordon et al Asbestos in commercial cosmetic talcum powder
0.000 328 PM 2014
kev 75WV 40 Degree
230
Figure 10 This asbestos fiber is a representative sample removed from the lung tissue of the patient exposed to cosmetic talcum powder Tremolite asbestos fiber with its corresponding EDS spectra
the same structures it was clear that the cores were
either anthophyllite or could not be determined because there was exposed fiber core In previous studies of human tissue having anthophyllite and anthophyllite bodies Fig 11 it was common to find that the entire anthophyllite core even if quite long was completely coated
Zone axis confirmation in bulk tissue and air Laboratories A B and C confirmed original amphibole asbestos structures by zone axis diffraction Labora-
tories A B C and D analyzed archived preparations
with the intent of confirming amphiboles by zone axis diffraction In all four sets of analyzed preparations anthophyllite and tremolite asbestos were consistently
MAQ 96
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Figure 11 These are asbestos bodies from the patients lung tissue taken by SEM It is possible to see in the one to the left that
the fiber is almost completely covered by the iron protein coating This is compared to the one at the right which appears to have much more fiber exposed However upon EDS testing it was determined that in both cases these were anthophyllite
fibers and they were both entirely coated although much thicker is some areas as opposed to others
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Gordon et Asbestos in commercial cosmetic talcum powder
Figure 12 Tremolite and anthophyllite asbestos from analyses of Lab D preparations images EDS SAED
confirmed by zone axis diffraction pattern measure-
ments This included confirmation of asbestiform am-
phiboles including anthophyllite and tremolite asbestos
from the original product testing from the releasability air tests and from TEM preparations of lung and lymph node tissues
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Discussion
Historically many mesotheliomas
abdominal mesotheliomas in women
particularly
have been
labeled idiopathic due to a lack of an identifiable source for asbestos exposure Further there has been
an increase in the number of idiopathic pleural and abdominal mesotheliomas in women using this specific brand of talcum powder There have been a few studies that have examined talcum powder and its potential to cause ovarian tumors.5 The studies were inconclusive but suggested that talc asbestos or both may cause these cancers through vaginal exposure These studies attributed asbestos found
within the women's lesions to result from contact
with their partners There was no consideration for the potential of the asbestos being a contaminant in
the women's talcum powder However it has been
reported that cosmetic talcum was contaminated with asbestos and that asbestos was found in the mines
from which the talc originated Our findings
indicate that historic talcum powder exposure is a causative factor in the development of mesotheliomas and possibly lung cancers in women
Talc has been identified as a causative for
mesotheliomas in New York talc miners In recent
years more than 10 women developed mesothelioma and their only source of asbestos exposure was the use of one brand of talcum powder This study demonstrates that the brand of talcum powder tested contained asbestos Furthermore we have traced the
asbestos in the talc to the mines from which it
originated into the milled grades into the product and finally into the lung and lymph nodes of the users of those products including one woman who developed mesothelioma
Based on the testing and testing conducted by the authors it is evident that this product line has been consistently contaminated with asbestos tainted
tale derivatives The amount of asbestos was variable
based on the time of manufacture and the tale source
There have been numerous publications that have
indicated that the talc in many tale deposits had
asbestos contamination
The most common
types of asbestos were tremolite and anthophyllite
These are the same asbestos fiber types found in the
autopsied lungs and lymph nodes tested here for
asbestos presence In a few containers tested in this
study chrysotile was also found consistent with the
source ore geology Most if not all
testing
of cosmetic
talc
was
performed using techniques designed for light micro-
scopy PLM or by TEM criteria designed to test air
and water samples Testing determined if asbestos
levels were above the EPA standards under AHERA or
the Occupational Safety and Health Agency standards These protocols are based on the parameters described
Gordon al Asbestos in commercial cosmetic talcum powder
in the Yamate method There are significant limitations to these methods PLM analysis misses small fine
asbestos fibers or fibrils because the limits of the
resolution are approximately 0.2-0.5 ...mfor different forms of light microscopy Based on our findings approximately 90 of the fibers identified fall into this category Determining the number of TEM grid openings to be counted during the analysis requires stopping factors or limits on the quantity of analysis to be performed The Draft Yamate method 1984 gives the guidelines of 100 fibers or 10 grid openings whichever is first This counting rule was instituted
for cost limitation purposes The Draft Yamate method describes that while this guideline of using 10
grid openings represents a judicious compromise
between a reasonable experimental effort and a fairly
low value of the detection limit the analysis of additional TEM grid openings reduces the detection limit and improves the precision of the estimates In the tale study described here a very low level of detection was desired and therefore in some cases as many as 500 plus grid openings were analyzed to reduce the detection limit and improve sensitivity of the test TEM testing has been adequate for evaluating building material asbestos abatement projects local air sampling and potential water contammation with asbestos However these criteria are not acceptable for assessing asbestos fiber burden analyses in human tissues and for low asbestos content products that are used intermittently in small quantities over long periods of time such as cosmetic talcum powder Talc related asbestos exposures can be heavy at times
above 4000 cc The inhaled asbestos fibers are
extremely variable in the causation of asbestos related tumors and fiber burdens found in the deceased woman were within the reported ranges for amphiboles to be causative factors in the development of such a tumor
Therefore it is imperative to analyze products such as talcum powder for small amounts of asbestos fibers This requires that the limits of detection be lower than levels required in a typical Yamate analysis The author reviewers observed that the Laboratory D analyses were done using Yamate methodology and no more than 10-25 grid openings on bulk TEM grid preparations were observed
Based on Laboratory D's protocols for testing
millions of fibers of talc would have to present
in order to find fibers Lower concentrations in the
ranges found by Laboratories A B and C demonstrated that fibers were detectable and present at levels sufficient to cause mesotheliomas
Although long narrow asbestos fibers are highly carcinogenic shorter narrow fibers are also
dangerous36-38 It is now more common to find
shorter narrow fibers in human tissue digestions than
long narrow fibers especially for chrysotile This
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Gordon et al Asbestos in commercial cosmetic talcum powder
study provides evidence that low concentrations of asbestos in raw materials do not necessarily correlate to low health 38,39 Examples of recent studies of low asbestos content producing significant airborne concentrations in simulated activity include activitybased monitoring of asbestos as it naturally occurs in several sites as conducted by the EPA and Agency for Toxic Substances and Disease Registry and containing attic insulation studies.40 These studies have repeatedly shown that substantial
airborne concentrations could be derived from
materials with only a fraction of a percent asbestos content This has been especially true when a product was in a friable state or where the obvious
use of material intimates aerosolization of fibers
Significant airborne concentration can be easily generated from such conditions when asbestos is a constituent.40 43
.
The talc application studies were simulations of exposures to tale used by a deceased woman who had mesothelioma The air volume in the testing space
was 158 cubic feet This is in the range of the chamber
sizes used by talcum powder manufacturers in the 1970s in their studies of the quantity of talcum powder used in normal application The space used by Russell was 171 cubic feet and the space used by Aylott was between 152 and 163 cubic feet The
amount of material used in the shaker test was 0.37 g The amount used for the puff applicator test was
6.25 g The shaker test was a light application
and the puff heavy application However the heavy application was within the ranges published by Russell of 8.32 g and Aylott of 12.5 g The talcing times or the duration of talcum powder application were approximately 55 seconds for the shaker test and approximately 57 seconds for the puff applicator 44.45 These were within the ranges published by Russell of +33 seconds and
Aylott of 28-78 seconds for adult dusting
Laboratories A and B determined that the contami-
nated talcum powder released inhalable asbestos into
the air .
Another issue in this study was the documentation and identification of cleavage fragments The scientific community has not generally adopted cleavage fragment differentiation criteria It is unclear how to identify a cleavage fragment once the stone or material has been finely ground Two criteria for distinguishing cleavage fragments from asbestos fibers have been proposed The first is that the ends of cleavage fragments have oblique angles and second is that the aspect ratios are all less than 20 The ends criterion has not been validated with known
cleavage fragment standards and while an aspect ratio of 20 1 suggests that a fiber is likely to be an asbestos fiber some fibers with aspect ratios below
20 are also asbestos As the fiber aspect ratio increases the percentage of asbestos fibers versus cleavage fragments also increases However this
criteria falls short when the fiber is extremely thin and
is the smallest unit of diameter of a fiber When these
small fibers are removed and analyzed from human tissue these criteria have to be discarded because
enzymes with basic and acidic molecules within cells
can leach elements from the surface causing a breakdown of the fibers especially when thin in diameter van Orden et al propose criteria to identify cleavage fragments by SEM The criteria are based on surface contours which identify a cleavage
fragment However this method has not been
verified and is not generally accepted There were no photographs of TEM or resolution highmagnification SEM provided by Laboratory D which classified potential asbestos fibers as cleavage fragments
In conclusion we found that a specific brand of talcum powder contained identifiable asbestos fibers with the potential to be released into the air and inhaled during normal personal talcum powder application We also found that asbestos fibers consistent with those found in the same cosmetic tale product were present in the lungs and lymph node
tissues of a woman who used this brand of talc
powder and developed and died from mesothelioma
Disclaimer Statements
Contributors All authors did studies relevant to the manuscript and all contributed and accepted all the writing
Funding The work done was paid for by attorneys for litigation purposes No funds were for writing of this manuscript
Conflicts of interest Funding for all Labs was provided as part of litigation No funds were for writing this article Laboratories are available for defense or plaintiff litigation
Ethics approval Ethical consent was not needed
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