1. Introduction
Most women of reproductive age use sanitary pads during their menstrual periods for an average of 1800 days in their lifetime [1]. Similarly, the diaper is a hygiene product that is in direct contact with the external genitalia of infants and toddlers for several months to years [2]. In recent years, synthetic plastic materials have been used as liquid absorbents to improve the functionality and softness of sanitary pads and diapers [3]. However, some of these plastic materials release volatile organic compounds (VOCs) and endocrine-disrupting chemicals [4–6], potentially posing risks to women and children who use them [7–9]. In particular, since VOCs and phthalates are absorbed through the skin [2, 10–13], it is necessary to understand whether household products such as sanitary pads and diapers that contact the skin contain these chemicals. As a result, the safety of sanitary pads or diapers is becoming a world-wide public health concern with growing suspicions that some substances in those products may adversely influence the health of women and children.
In the summer of 2017, South Korean media outlets reported a few newly marketed brands of commercial sanitary pads containing VOCs [14, 15] with a high degree of suspicion that these chemicals might be the causes of menstrual irregularities as some of the consumers experienced after using the particular branded pads [16]. Soon, the issue became a societal concern after the public became aware that sanitary pads in direct contact with the skin around the external genitalia were likely causing menstrual irregularities. The skin of this area tends to be thinner and more absorbent than those of others such as the hands [17]. In response to these concerns and confusions, we decided to undertake an independent small-scale measurement of VOCs and phthalates in commercially available sanitary pads and diapers sampled from South Korea and other countries. To estimate the risk of the VOCs contained in sanitary pads and diapers, the measured contents from these hygienic products were compared with publicly available measurement data from other consumer products such as beverages, foods, and plastic wares and also with the regulatory guidelines for such products.
We measured VOCs contents primarily because they were reportedly detected in the sanitary diapers and suspected to be the causes of menstrual irregularities. VOCs are released from a variety of anthropogenic sources such as cleaning products, paints, solvents, personal care products, and tobacco smoke [18]. Previous studies assessed the exposure level to VOCs by measuring their contents in the air, urine, and water [19, 20]. VOCs increase the risk for neurocognitive impairment, asthma, congenital disability, and cancer [21]. Notably, exposure to methylene chloride, toluene, and xylene are known to negatively affect the development and function of reproductive system [22–25]. However, to date, no study has measured VOC contents in the sanitary pads and diapers or reported their impact on female reproductive function and child health.
We included phthalates in our measurement because studies in animal models indicated that phthalates might disrupt menstrual cycles [26, 27] and that a particular subsets of phthalates such as di(2-ethylhexyl) phthalate (DEHP), diethyl phthalate (DEP), di-n-butyl phthalate (DBP), and benzyl butyl phthalate (BBP) are routinely detected in women [28–30]. Phthalates are widely used plasticizers found in common consumer products such as medical devices, feminine hygiene products, cosmetics, toys and childcare articles [31–33]. They are non-covalently bound to plastics and are easily released from them and absorbed into the body by inhalation, ingestion, and dermal absorption, thus resulting in systemic contact [34]. Exposure to phthalates is known to affect the development and functions of the cardiovascular, reproductive and endocrine systems [27, 35–38].
2. Methods
2.1. Sample preparation
Sanitary pads and diapers were collected from markets in Korea, Japan, Finland, France, Greece, and the United States (Supplementary Table 1). To measure VOC contents, air (750 μL) was taken from the center of each pack of sanitary pads or diapers using a sample lock syringe (gas-tight) and then injected directly into a gas chromatograph. The procedure was carried out at the University of Illinois Metabolomics Center (http://biotech.illinois.edu/metabolomics).
To measure phthalate contents, a single pad or diaper from each pack was weighed before sample collection. Samples of one square centimeter (1 cm2) were collected using clean scissors from four different locations of each pad or diaper (Figure 1). They were weighed together and placed in a 20 mL glass vial. Then, 6 mL of 80% methanol (v/v) was added to the vial and kept on a rocker for 15 minutes for extraction. Next, 1 mL was transferred from the vial to a new 2 mL glass vial. The samples were analyzed by LC/MS/MS at the University of Illinois Metabolomics Center.
2.2. Measurement of VOCs by GC/MS
The VOC contents were measured by using a GC/MS system (Agilent Inc., CA, USA) consisting of an Agilent 7890B gas chromatograph and an Agilent 5977A MSD. Separation was performed on a ZB-624 (30 m × 0.32 mm I.D. and 1.4 μm film thickness) capillary column (Phenomenex, CA, USA). The inlet, MSD interface, and ion source temperatures for the GC/MS system were adjusted to the following, respectively: 1800°C, −230°C, and 230°C. An aliquot of 750 μL air/gas was injected with a gastight syringe (Hamilton, HV, USA) in a split-less mode (9mL/min @ 2min). The helium carrier gas was kept at a constant flow rate of 1.1 mL/min. The temperature was programmed to 5 min isothermal heating at 40°C followed by a temperature increase of 20°C/min until it reached 200°C. The mass spectrometer was operated in positive electron impact mode (EI) at 69.9 eV ionization energy at m/z 33–300 scan range. Mass spectra were recorded in a combined scan/SIM mode. For a SIM mode, m/z fragments were tracked: 84 (methylene chloride), 92 (toluene) and 106 (xylenes). Target peaks were evaluated using the Mass Hunter Quantitative Analysis B.08.00 (Agilent Inc., CA, USA) software. Target peaks indicate the chemical-specific peaks in presented histogram (Figure 2).
2.3. Measurement of phthalates by LC/MS/MS
Samples were analyzed with the 5500 QTRAP LC/MS/MS system (Sciex, Framingham, MA), and Software Analyst 1.6.2 was used for data acquisition and analysis. The 1200 series HPLC system (Agilent Technologies, Santa Clara, CA) includes a degasser, an auto-sampler, and a binary pump. The LC separation was performed on a C6-phenyl Phenomenex column (2 × 100mm, 3μm) with mobile phase A (0.1% formic acid in water) and mobile phase B (0.1% formic acid in acetonitrile). The flow rate was 0.25 mL/min. The linear gradient was: 0–1min, 90%A; 10–16min, 0%A; 17–21min, 90%A. The auto-sampler was set at 10°C, and the injection volume was 10μL. Mass spectra were acquired under both positive (ion spray voltage was +5500 V) and negative (ion spray voltage was −4500 V) electrospray ionization (ESI). The source temperature was 450°C. The curtain gas, ion source gas 1, and ion source gas 2 were 32, 65, and 55, respectively. Multiple reaction monitoring (MRM) was used for quantitation: in the positive ESI, DBP m/z 279.2 --> m/z 149.0; DEP m/z 223.1 --> m/z 149.0; DEHP m/z 391.4 --> m/z 149.0, and BBP m/z 313.1 --> m/z 149.0 (Figure 2).
2.4. Quantitation of measurements
For quantification of VOC contents, 1 mL of each standard was placed into a sealed glass vial and vaporized under room temperature with the following dilutions using a gas tight syringe: an aliquot of 25 μL was taken with gas-tight syringe from the stock vapor and transferred into another sealed vial. The glass vial volume was measured before dilution, and concentrations in each vial were measured in parts per billion (ppb). Sample concentrations were calculated based on a calibration curve obtained from standard dilutions (concentration/peak area). Methylene chloride, toluene, and xylenes were confirmed by certified standards (Fisher Scientific International, Inc., NH, USA) and quantified using 518 ppb, 6.7 ppb, 0.09 ppb, 0.0011 ppb standard mixture dilutions. In the quantitative analysis, the limit of quantitation is 0.001 ppb for each VOC. The actual VOC concentration in samples were presented as respective calculated value/volume of collected air samples. The data were expressed by average ± SEM (standard error mean, pbb, n=3–5, numbers of packs per brand). The concentrations of phthalates were calculated using the LC/MS/MS data and were expressed by average ± SEM (standard error mean, ppb, n=3–5, numbers of packs per brand). The quantitation limit is 0.1 ppb (0.1 ng/mL) for DBP/DEHP/DEP and 0.05 ppb (0.05 ng/mL) for BBP. Certified Standards for each phthalate were purchased from Sigma-Aldrich (St. Louis, MO). The actual phthalate concentration in samples were presented as respective calculated value/weight of excised samples. The concentrations were used to calculate the total content per pad or diaper.
2.5. Statistical analysis
The data were analyzed using the statistical software package SPSS. Average concentrations of each VOC and phthalates were calculated from all sanitary pad or diaper products. To determine if the average VOC or phthalates content of each product was significantly higher than the product average, Student’s t-tests were performed between the overall average of each VOC or phthalates and average VOC or phthalate content of each product. Statistical significance was assigned as p ≤ 0.05 and marked as (*). The data are expressed as mean ± SEM.
3. Results
3.1. VOC contents in sanitary pads
The levels of methylene chloride, toluene, and xylene were measured in the air of the sanitary pad and diaper packages (Table 1). The GC/MS analysis detected methylene chloride in two sanitary pad packages: Brand-2 (0.028 ppb) and -6 (0.008 ppb). The package of Brand-2 contained significantly higher (p<0.01) methylene chloride than the average of all products tested. Toluene was detected in packages from nine brands, except Brand-10 and -11. The packages of Brand-3 (5.230 ppb) and -4 (5.471 ppb) contained significantly higher concentration of toluene (p<0.01) than the average of all products. Xylene was detected in all of the sanitary pad packages. In Brand-11, m-xylene and o-xylene were not detected. The highest concentrations of m-xylene (0.192 ppb) and p-xylene (0.278 ppb) were found in Brand-2. Brand-2 (0.263 ppb), Brand-3 (0.276 ppb), and Brand-4 (0.287 ppb) contained the highest concentration of o-xylene among the sanitary pad packages. The Brand-2 package contained significantly higher (p<0.01) m-xylene and p-xylene than the average of all products.
Table 1.
Brands | n | Methylene Chloride | Toluene | o-Xylene | m-Xylene | p-Xylene |
---|---|---|---|---|---|---|
1 | 5 | BD | 0.235 ± 0.059 | 0.017 ± 0.005 | 0.012 ± 0.004 | 0.015 ± 0.005 |
2 | 5 | 0.028 ± 0.012* | 0.836 ± 0.351 | 0.263 ± 0.066 | 0.192 ± 0.047* | 0.278 ± 0.077* |
3 | 5 | BD | 5.23 ± 0.914* | 0.276 ± 0.071 | 0.086 ± 0.025 | 0.084 ± 0.025 |
4 | 5 | BD | 5.471 ± 2.438* | 0.287 ± 0.101 | 0.095 ± 0.029 | 0.103 ± 0.038 |
5 | 5 | BD | 0.427 ± 0.225 | 0.048 ± 0.019 | 0.027 ± 0.009 | 0.034 ± 0.011 |
6 | 4 | 0.008 ± 0.008 | 0.205 ± 0.069 | 0.127 ± 0.049 | 0.09 ± 0.033 | 0.132 ± 0.048 |
7 | 3 | BD | 0.107 ± 0.014 | 0.008 ± 0.004 | 0.002 ± 0.002 | 0.004 ± 0.002 |
8 | 4 | BD | 0.005 ± 0.003 | 0.003 ± 0.001 | 0.001 ± 0.001 | 0.002 ± 0.001 |
9 | 4 | BD | 0.635 ± 0.365 | 0.277 ± 0.195 | 0.136 ± 0.09 | 0.12 ± 0.081 |
10 | 4 | BD | BD | 0.008 ± 0.003 | 0.003 ± 0.002 | 0.003 ± 0.002 |
11 | 4 | BD | BD | BD | BD | 0.001 ± 0.001 |
significantly different from the average concentration of all sanitary pads
BD, below detection limit (detection limit, 0.001 ppb for each VOCs)
3.2. VOC contents in commercial diapers
In the diaper packages, methylene chloride was not detected by GC/MS analysis, but all contained toluene and xylene as determined by the GC/MS measurement (Table 2). Brand-A (0.397 ppb) had the highest concentration of toluene. The highest concentrations of xylene, including m-, p-, and o-xylene, were measured in Brand-C (0.013, 0.014, and 0.021 ppb, respectively).
Table 2.
Brands | n | Methylene Chloride | Toluene | o-Xylene | m-Xylene | p-Xylene |
---|---|---|---|---|---|---|
A | 3 | BD | 0.397 ± 0.187 | 0.005 ± 0.002 | 0.003 ± 0.001 | 0.004 ± 0.001 |
B | 3 | BD | 0.102 ± 0.023 | 0.008 ± 0.003 | 0.002 ± 0.001 | 0.003 ± 0.001 |
C | 3 | BD | 0.36 ± 0.112 | 0.021 ± 0.009 | 0.013 ± 0.005 | 0.014 ± 0.005 |
D | 3 | BD | 0.192 ± 0.048 | 0.02 ± 0.002 | 0.009 ± 0.001 | 0.01 ± 0.001 |
BD, below detection limit (detection limit, 0.001 ppb for each VOCs)
3.3. Phthalate content in commercial sanitary pads
Phthalate (DBP, DEHP, DEP, and BBP) concentrations were measured in 11 different brands of sanitary pads (Table 3). BBP was not detected in any of sanitary pads tested. However, every sanitary pad contained DBP (52.1–7,820.4 ppb) and DEHP (5.5–197.4 ppb). The highest concentration of DBP was measured in Brand-1 (7,820.4 ppb) (p<0.01). While DEHP concentration was lower than DBP concentration in each sample measured, Brand-1 (134.5 ppb) and Brand-4 (197.4 ppb) contained significantly higher concentration than the average of all sanitary pads examined (p<0.05, p<0.01; respectively). The highest concentration of DEP was found in Brand-6 (134.3 ppb), which was significantly higher than average of all sanitary pads examined (p<0.03). DEP was not detected in Brand-2, -5, -10, and -11. Brand-10 and Brand-11 had the lowest total phthalate concentrations.
Table 3.
Brands | n | DBP | DEHP | DEP | BBP |
---|---|---|---|---|---|
1 | 5 | 7820.4 ± 2734.6* | 134.5 ± 37.7* | 60.0 ± 12.8 | BD |
2 | 5 | 144.9 ± 40.3 | 51.2 ± 10.0 | BD | BD |
3 | 5 | 1127.8 ± 492.3 | 34.1 ± 4.4 | 11.2 ± 6.2 | BD |
4 | 5 | 782.0 ± 149.0 | 197.4 ± 17.6* | 58.9 ± 47.6 | BD |
5 | 5 | 848.6 ± 364.8 | 47.8 ± 12.8 | BD | BD |
6 | 4 | 1995.3 ± 1630.3 | 37.7 ± 11.1 | 134.3 ± 101.6* | BD |
7 | 3 | 2478.6 ± 2216.0 | 46.9 ± 16.2 | 8.4 ± 8.4 | BD |
8 | 4 | 629.1 ± 466.2 | 37.3 ± 9.6 | 8.1 ± 8.1 | BD |
9 | 4 | 486.0 ± 411.3 | 11.3 ± 6.9 | 109.1 ± 42.2 | BD |
10 | 4 | 150.8 ± 66.9 | 5.5 ± 2.6 | BD | BD |
11 | 4 | 52.1 ± 10.8 | 9.8 ± 6.4 | BD | BD |
significantly different from the average concentration of all sanitary pads
BD, below detection limit (detection limit, 0.1 ppb for DBP, DEHP, and DEP; 0.05 ppb for BBP)
3.4. Phthalate contents in commercial diapers
Phthalate (DBP, DEHP, DEP, and BBP) concentrations were measured in four different diaper brands (Table 4). BBP was not detected in any diapers. However, every diaper contained DBP (13.4–1,609.7 ppb) and DEHP (12.6–62.8 ppb). Brand C had the highest concentration of DBP (1,609.7 ppb) while Brand-D had the highest concentration of DEHP (62.8 ppb). DEP was found only in Brand-C (0.8 ppb) and Brand-D (2.9 ppb).
Table 4.
Number | n | DBP | DEHP | DEP | BBP |
---|---|---|---|---|---|
A | 3 | 13.4 ± 5.4 | 12.6 ± 2.1 | BD | BD |
B | 3 | 984.5 ± 422.8 | 30.1 ± 3.3 | BD | BD |
C | 3 | 1609.7 ± 1516.9 | 42.2 ± 3.3 | 0.8 ± 0.8 | BD |
D | 3 | 1005.8 ± 403.1 | 62.8 ± 6.7 | 2.9 ± 0.8 | BD |
BD, below detection limit (detection limit, 0.1 ppb for DBP, DEHP, and DEP; 0.05 ppb for BBP)
4. Discussion
This study found that a majority of sanitary pads or diapers surveyed in this study contained both VOCs and phthalates with varying amounts measured among them. The packages of Brand-3 and -4 sanitary pads contained the highest total VOC concentration (5.676 ppb and 5.956 ppb, respectively) (Table 1), and Brand-1 sanitary pads contained the highest total phthalate concentration (8,014.9 ppb) (Table 3). In the following, the amount of VOCs and phthalates measured in the sanitary pads and diapers are compared with previously reported contents of VOCs (Table 5) and phthalates (Table 6) in other consumer products and their potential impact on health discussed.
Table 5.
Category | Samples | Sample number (n) | Methylene chloride | Toluene | o-xylene | m-xylene | p-xylene | Method | Ref. |
---|---|---|---|---|---|---|---|---|---|
Indoor air | Residence indoor air | 284 | NA | 5.33–7.08 | 0.58–0.76 | 1.52–2.10 | GC/MS | [43] | |
Newly built house indoor air (< 1yr) | 4 | NA | 0.80–23.35 | 3.22–66.55 | TD-GC/FID | [73] | |||
Elementary school indoor air | 1 | NA | 0.6–2.2 | 1.1–2.2 | GC/MS | [74] | |||
Scented candles (before lighting) | 6 | NA | 0.01–10.3 | 0.01–0.01 | 0.01–0.32 | 0.01–0.01 | TD–GC/MS | [75] | |
Scented candles (after lighting) | 6 | NA | 0.01–1.58 | 0.01–0.01 | 0.01–0.04 | 0.01–0.01 | TD–GC/MS | [75] | |
New cars (leather trim, <4 month) | 3 | NA | 0.08–0.09 | ND | ND | GC/MS | [44] | ||
New cars (fabric trim, <4 month) | 3 | NA | 0.48–0.69 | 0.88–1.20 | 1.75–2.53 | GC/MS | [44] | ||
Drinks | Household drinking water (Taiwan) | 131 | ND-21.08 ppm | ND-16.77 ppm | NA | NA | NA | GC/MS | [76] |
Household drinking water (Kuwait) | 624 | NA | ND-490.91 | ND-133.58 | GC/MS | [77] | |||
Bottled water (various countries) | 71 | NA | ND-313.12 | ND-117.34 | GC/MS | [77] | |||
Sports beverages (PET bottled) | 6 | NA | 0.27–25.9 ppt | 0.11–0.61 ppt | NA | NA | HS/SPME-GC/MS | [78] | |
Foods | American cheese (USA market) | 3–11 | NA | 17–255 | 3–4 | 4–112 | GC/MS | [79] | |
Cheddar cheese (USA market) | 7–13 | NA | 7–1300 | ND | 5–43 | GC/MS | [79] | ||
Pork bacon (USA market) | 1–14 | NA | 12–230 | 2 | 5–25 | GC/MS | [79] | ||
Olive/safflower oil (USA market) | 3–7 | NA | 6–32 | 6–23 | 2–110 | GC/MS | [79] | ||
Scrambled eggs (USA market) | 2–8 | NA | 4–100 | ND | 2–4 | GC/MS | [79] | ||
Fruit-flavored cereal (USA market) | 3–6 | NA | 3–140 | ND | 4–7 | GC/MS | [79] | ||
Cereal products (Belgian market) | NA | NA | ND-71.8 | ND-3.5 | NA | NA | HS-GC/MS | [80] | |
Plastic | Wrapping Films (PVC polymer) | 3 | NA | 3.70–3.77 ppm | 12.90–13.50 ppm | 23.51–24.59 ppm | 2.16–2.26 ppm | HS/SPME-GC/MS | [81] |
Data were adopted from previous studies.
FID, flame ionization detection; GC, gas chromatography; HS, headspace analysis; MS, mass spectrometry; NA, not available; ND, not detected; SPME, solid phase micro extraction; TD, thermal desorption
Table 6.
Category | Samples | Sample number (n) | DBP (Dibutyl phthalate) | DEHP (Di-ethylhexy phthalate) | DEP (diethyl phthalate) | BBP (Benzyl-butyl phthalate) | Method | Ref. |
---|---|---|---|---|---|---|---|---|
Consumer products | Baby diapers top sheet | 50 | 0.2 ppm | 0.6 ppm | NA | 0.1 ppm | GC/MS | [2] |
Adult-use cosmetic products | 60 | 123–62607 ppm | ND | 80–36006 ppm | ND | HPLC | [82] | |
Baby-care products contained | 24 | ND | ND | 10–274 ppm | ND | HPLC | [82] | |
Paper cup | 19 | 12.87–31.48 | 13.94–15.23 | NA | NA | HPLC | [57] | |
Drinks | Bottled water (Hungary) | 3 | 0.8– 6.6 | 1.7–16.0 | NA | 0.1– 6.0 | GC/MS | [83] |
Bottled water (Jordan) | 14 | 1.17–13.9 | 1.15–4.86 | NA | NA | HPLC | [84] | |
Bottled water (Ireland) | 3 | 0.062–0.068 | 1.19–1.68 | ND | ND | GC/MS | [85] | |
plastic water bottle (Ireland) | 3 | 20.92–71.68 ppm | 0.39–1.49 ppm | ND | ND | GC/MS | [85] | |
Foods | Cereals (Chinese market) | 44 | 12.1–279 | 62.9–1380 | 1.40–20.8 | 0.45–62.9 | GC/MS | [58] |
Snacks (Chinese market) | 17 | 3.81–181 | 63.8–933 | 1.33–8.50 | 0.63–59.0 | GC/MS | [58] | |
Beverages (Chinese market) | 3 | 32.8–52.9 | 72.3–160 | 6.96–13.9 | 0.03–0.36 | GC/MS | [58] | |
Condiments (Chinese market) | 7 | 9.42–101 | 61.5– 400 | 0.77–90.1 | 0.30–8.68 | GC/MS | [58] | |
Seafood (Chinese market) | 3 | 85.8–116 | 523–1110 | 2.34–5.13 | 1.61–8.67 | GC/MS | [58] | |
Meat products (Chinese market) | 4 | 23.7–6.8 | 103–400 | 2.61–22.8 | 0.52–1.83 | GC/MS | [58] | |
Plastic (ppm) | Reusable plastic cup | 5 | 9.84 | 119.35 | ND | 0.44 | GC/MS | [56] |
Milk package bag | 5 | 9.84 | 42.5 | ND | 0.07 | GC/MS | [56] | |
Microwavable box | 5 | 1.44 | 8.72 | ND | 0.1 | GC/MS | [56] | |
Package film | 5 | 1.88 | 27.58 | ND | 0.09 | GC/MS | [56] | |
Disposable cup | 5 | 1.12 | 2.88 | ND | ND | GC/MS | [56] | |
Storage box | 5 | 1.18 | 3.94 | ND | ND | GC/MS | [56] |
Data were adopted from previous studies.
GC, gas chromatography; MS, mass spectrometry; NA, not available; ND, not detected
Methylene chloride is a VOC that dissolves in a wide range of organic compounds, which makes it a useful solvent. This chemical compound is used in a variety of industrial applications such as adhesives, paints and coating products, pharmaceuticals, and aerosols [39]. A study showed that animals exposed to methylene chloride experienced behavioral alterations and also induced developmental abnormalities in their offspring. This is supported by another finding that methylene chloride can cross the placenta [40]. Studies found methylene chloride in human breast milk, indicating potential postnatal exposure via breast feeding [41]. A recent study showed that prolonged contact with methylene chloride caused chemical burns in the skin [31]. Our measurement revealed that neither sanitary pads nor diapers contained methylene chloride at the level of concern (Tables 1 and 2).
Toluene is a volatile aromatic hydrocarbon that is used mainly in blending motor gasoline but also as a solvent for paints, thinners, adhesives, inks, fabric dyes, and cosmetics [42]. In air samples from packages of sanitary pads, the highest concentration measured was 5.471 ppb (Table 1). This concentration is similar to reported toluene levels in residential indoor air [43] but higher than those measured in the airs of new cars [44] (Table 6). Toluene crosses the placenta and has been detected in amniotic fluid and breast milk [45]. Previous animal studies showed that toluene administered to pregnant females increased fetal mortality, caused developmental defects, and induced neurobehavioral toxicity [42, 46]. In humans, toluene vapor is rapidly absorbed from the respiratory tract through inhalation and is absorbed via skin [47]. The skin absorption rate of toluene is higher than those of benzene and tetrachloroethylene (perclene) [9]. The absorption rate of toluene in mouse skin was 16.38 mg/cm2/h when they were exposed to 1,000 ppm solvent vapor. The rate of toluene absorption is proportional to its concentration. If human skin is exposed to the measured 5.471 ppb of toluene, the absorption rate will be 0.09 μg/cm2/h (5.471 ppb/1000 ppm x 16.38 mg/cm2/h x 24 h/day = 2.15 μg/cm2/day). Assuming a contact area of skin by a sanitary pad of 250 cm2 (25 cm x 10 cm), the skin making a contact with a sanitary pad may absorb as much as 537.7 μg/day (2.15 μg/cm2/day x 250 cm2). The Reference Dose (RfD) for toluene is 20 μg/kg/day [48]. Therefore, if a woman who weighs 70 kg were exposed to such amount, the absorption rate would be 7.7 μg/kg/day (537.7 μg/day/70 kg, predicted daily absorption rate). Hence, based upon this calculation, she may absorb 38.4% of RfD (predicted daily absorption rate / RfD x 100) (See supplementary Table 2).
Xylene is an aromatic hydrocarbon widely used in manufacturing a variety commercial products including medical devices as a solvent [49]. In air samples from packages of sanitary pads, the highest xylene concentration measured was 0.757 ppb (Table 1), which was much lower than in residential indoor air [43] or new cars [44] (Table 5). In a whole-body inhalation exposure experiment conducted on pregnant Sprague Dawley rats (gestation day 6–20 inclusive, 6 h/day), the no observed/lowest observed adverse effect level (NOAEL and LOAEL) for developmental toxicity was 100 ppm and 500 ppm (o-xylene), respectively [50]. The study also found that VOCs adversely affect the systemic and neuronal development as well. A study with a human cohort showed that in utero exposure to o-xylenes (OR=1.42 [1.19–1.70]) or m/p-xylene (OR=1.51 [1.26–1.82]) increased the risk of developing childhood autism [51]. Exposure to xylene occurs via inhalation, ingestion, or eye or skin contact. The main consequences of inhaling xylene vapor are neuropsychological and neurophysiological dysfunction accompanied by as headache, dizziness, nausea, and vomiting [52]. Moreover, frequent or prolonged skin contact with xylene causes irritation, dermatitis, dryness, and skin cracking [53]. In humans, the absorption rate of the liquid form of xylene through the skin is from 4.5 to 9.6 mg/cm2/h, which is about 3 times lower than that of toluene (14–23 mg/cm2/h) [11]. If human skin is exposed to 0.757 ppb of xylene, the absorption rate will be 0.004 μg/cm2/h (0.757 ppb / 1000 ppm x 16.38 mg/cm2/h / 3, = 0.10 μg/cm2/day) based on reported studies on xylene absorption rate. Assuming a contact area of skin by a sanitary pad of 250 cm2, skin making a contact with a sanitary pad may absorb as much as 24.8 μg of xylene per day (0.10 μg/cm2/day x 250 cm2). The RfD for xylene is 2 mg/kg/day [54]. If a woman who weighs 70 kg is exposed to such amount, the predicted daily absorption rate will be 0.35 μg/kg/day (24.8 μg/day / 70 kg). Hence, based upon this calculation, she may absorb 0.02% of RfD (predicted daily absorption rate / RfD x 100) (See supplementary Table 2).
The Guideline on Establishment of Test Item in Preparation of Standards and Analytical Methods of Quasi-Drugs of South Korea’s Ministry of Food and Drug Safety (MFDS) (2016; http://www.mfds.go.kr/eng/eng/download.do?boardCode=17840&boardSeq=71866&fileSeq=1) has only four criteria (pigments, acid and alkali, fluorescent whitening agent, and formaldehyde) to determine the safety of sanitary pads. All that is needed to market a diaper is to submit a “conformity” confirmation from the third inspection agency in Korea. This suggests the possibility of human exposure to other hazardous chemicals contained in sanitary pads and diapers. In August 2017, a company that produced some of the products tested in this study officially announced that their products meet the Oeko-Tex Standard 100, class 1 of Europe (toluene <30 ppb for fabric, xylene <10 ppm for accessories, methylene chloride <1 ppm for accessories) and the VOC content standards for drinking water (toluene <1 ppm, xylene <10 ppm, methylene chloride <5 ppb; National Primary Drinking Water Regulations, EPA) [55]. The VOC concentrations in the sanitary pad and diaper packages (Tables 1 and 2) measured in this study met the above criteria. However, we found that there was a difference in concentration depending on the brands. Of note, Brand-4 sanitary pad package contained a 5,900-fold higher total VOC contents than Brand-11 (Table 1). In diapers, 3- to 63-fold differences of VOC (Table 2) concentrations were seen among the brands. These results show that there is a considerable difference in the concentration of VOCs among the sanitary pad and the diaper products.
Phthalate contents were also vastly different among the brands surveyed (Table 3 and 4). All of the sanitary pads and diapers examined contained DBP (52.1–7,820.4 ppb in sanitary pads, 13.4–1,609.7 ppb in diapers) and DEHP (5.5–197.4 ppb in sanitary pads, 12.6–62.8 ppb in diapers). Sanitary pads from seven brands and diapers from two brands contained DEP (8.1–134.3 ppb in sanitary pads, 0.8–2.9 ppb in diapers). Of note, Brand-1 sanitary pads contained 130-fold higher total phthalate content than Brand-11 (Table 3). The highest concentration of DBP detected in sanitary pads (Table 3) and diapers (Table 4) were 7,820.4 ppb and 1,609.7 ppb, respectively. These concentrations are considerably higher than concentrations detected in package film [56], paper cups [57], and even cereals [58] (Table 6). The highest DEHP concentrations detected in sanitary pads (Table 3) and diapers (Table 4) were 197.4 ppb and 62.8 ppb, respectively; these are higher than the DEHP concentrations in paper cups [57], package film [56], and microwavable boxes [56] (Table 6). Moreover, the highest concentration of DEP measured in a sanitary pad was 134.3 ppb, which is higher than DEP concentrations in condiments [58], plastic cups [56], cereals [58] and many plastic products [56] (Table 6).
Among the phthalates, oral exposure to DBP was reported to decrease maternal weight gain, fetal weight gain, food consumption, and increase miscarriages in rats [59, 60]. Furthermore, prenatal DEHP exposure (20 and 200 µg/kg/day and 500 and 750 mg/kg/day) from gestation day 10.5 until birth increased uterine weight, decreased anogenital distance, disrupted estrous cyclicity, and reduced fertility, which likely resulted from the anti-androgenic effect of DEHP [61, 62]. Exposure to DEHP during fetal development altered follicular recruitment and development, eventually causing premature ovarian failure [34]. In a recent Japanese diaper study, DEHP and DBP were detected in the top sheets and determined to be 600 ppb and 200 ppb, respectively [2]. When taken with our work, which detected DEHP and DBP with a concentration of 12.6–62.8 ppb and 13.4–1,609.7 ppb from an entire layer including top sheet to back sheet, the Japanese study indicates that DEHP is likely concentrated in the top sheet of the diaper, while DBP present in all layers. Low-molecular-weight phthalates such as DBP, DEP, and DEHP readily dissolve into lipids in the epidermis of the skin and are taken up by systemic circulation [10]. The testicular development during infancy influence the pubertal onset and normal adult fertility [63]. Because the top sheet of the diaper is in direct contact with the external genitalia of the newborn, phthalates in the top sheet can be absorbed into the skin and adversely impact the development and function of the reproductive and urinary systems. Compared to other parts of human body, scrotum showed the highest dermal absorption rate for parathion (4 ppm in acetone) with a 5.5-fold and 9.1-fold increased absorption rates when compared to abdominal skin and palm, respectively [64]. Vulvar tissue is more permeable to most of chemicals than other skins due to it is hydrated, thin and extensively vascularized [17]. Due to the high absorbency for chemicals, vaginal tissue is often used as a drug delivery route [65]. Thus, repeated wearing of sanitary pads and diapers makes the tissue vulnerable to toxicants released from the sanitary pads or diapers.
Due to their reproductive toxicity, some of phthalates are classified as Category 1B by European authorities. Particularly, DEHP, DBP, DiBP and BBP are banned from using them in producing toys, baby care products, cosmetics, and medical devices [66, 67]. According to the renewed Directive (EU) 2015/863, contents of four phthalates, DBP, DEHP, BBP, and DIBP, will be restricted to < 0.1% in all electrical and electronic equipment (from 22 July 2019) and medical devices (from 22 July 2021) after the grace periods end [68]. The use of DEHP, BBP, and DBP in toys is already subject to REACH Regulation (EC) No 1907/2006. This regulation limits the total DEHP+DBP+BBP content to be lower than 0.1% (1,000 ppm) and total DINP + DIDP + DNOP content lower than 0.1% in toys and child care products [69]. Obviously, the concentrations of phthalates contained in the sanitary pads and diapers measured in this study were below the European guidelines. However, recent reports showed that environmentally relevant exposure to phthalate (20–200 μg/kg/day) induced severer reproductive toxicity and behavioral disorders than exposure to a considerably higher dose (500–750 mg/kg/day) in rodents [70, 71], raising a question if exposure to a low dose is always safer. In our result, sanitary pads containing maximum 7,820.4 ppb (7.82 mg/kg), and each pad of Brand-1 (6.8 g) containing 0.05 mg of DBP. In a previous study using hairless guinea pig, in vivo absorption of DBP after dermal application was 62% [12]. According to this, if a woman wore the sanitary pad (Brand-1), daily absorption of DBP will be 0.03 mg (0.05 mg/day x 62%). If a woman who weighs 70 kg is exposed to such amount, the absorption rate will be 0.47 μg/kg/day (0.03 mg/day / 70 kg, predicted daily absorption rate). The RfD for DBP is 0.1 mg/kg/day [72]. Hence, based upon this calculation, she may absorb 0.47% of RfD (predicted daily absorption rate / RfD x 100) from sanitary pad (See supplementary Table 2).
5. Conclusions
This study found that most of sanitary pads or diapers surveyed contained both VOCs and phthalates. The amounts measured were different among the brands and was below the RfD. However, daily absorption of toluene from sanitary pad reached to the maximum of 38.4% RfD. Given the fact that women are exposed to various chemicals through various routes, consideration should be given to the risks of chemicals that are additionally absorbed from the sanitary pad. This finding raises a concern for the safety of using some of the products and a need for efforts to reduce VOC and phthalate contents. Most of all, the physical location of the exposure site, the high absorption rate of the genitalia for chemicals, and the long-term exposure period demand a thorough investigation on the potential impact of the exposure to VOCs and phthalates. This manuscript is a report of a preliminary investigation, which calls for future studies into the potential health risk of using sanitary pads and diapers with high VOC or phthalate contents.
Supplementary Material
Acknowledgements
Funding
This work was supported by the National Institute of Environmental Health Sciences grant (P01-ES022848 to C.K and J.A.F); Environmental Protection Agency grant (RD-83459301 to C.K and J.A.F.); and Egyptian Mission Sector (JS-3041) Higher Ministry of Education to R.B.
Abbreviations
- BBP
Benzyl butyl phthalate
- DBP
Di-n-butyl phthalate
- DEHP
Di-2-ethylhexyl phthalate
- DEP
Diethyl phthalate
- EPA
Environmental Protection Agency
- EU
European Union
- GC/MS
Gas chromatography–mass spectrometry
- LC/MS/MS
Liquid chromatography-tandem mass spectrometry
- REACH
Registration, Evaluation, Authorization and Restriction of Chemicals
- RfD
Reference Dose
- VOCs
Volatile organic compounds
Footnotes
Conflicts of interest
The authors declare that there are no conflicts of interest.
References
- [1].Anand E, Singh J, Unisa S, Menstrual hygiene practices and its association with reproductive tract infections and abnormal vaginal discharge among women in India, Sexual & reproductive healthcare : official journal of the Swedish Association of Midwives 6(4) (2015) 249–54. [DOI] [PubMed] [Google Scholar]
- [2].Ishii S, Katagiri R, Minobe Y, Kuribara I, Wada T, Wada M, Imai S, Investigation of the amount of transdermal exposure of newborn babies to phthalates in paper diapers and certification of the safety of paper diapers, Regulatory toxicology and pharmacology : RTP 73(1) (2015) 85–92. [DOI] [PubMed] [Google Scholar]
- [3].Woeller KE, Hochwalt AE, Safety assessment of sanitary pads with a polymeric foam absorbent core, Regulatory toxicology and pharmacology : RTP 73(1) (2015) 419–24. [DOI] [PubMed] [Google Scholar]
- [4].Bolden AL, Rochester JR, Schultz K, Kwiatkowski CF, Polycyclic aromatic hydrocarbons and female reproductive health: A scoping review, Reproductive toxicology 73 (2017) 61–74. [DOI] [PubMed] [Google Scholar]
- [5].Benjamin S, Masai E, Kamimura N, Takahashi K, Anderson RC, Faisal PA, Phthalates impact human health: Epidemiological evidences and plausible mechanism of action, Journal of hazardous materials 340 (2017) 360–383. [DOI] [PubMed] [Google Scholar]
- [6].Santangeli S, Maradonna F, Olivotto I, Piccinetti CC, Gioacchini G, Carnevali O, Effects of BPA on female reproductive function: The involvement of epigenetic mechanism, General and comparative endocrinology 245 (2017) 122–126. [DOI] [PubMed] [Google Scholar]
- [7].Kounang N, What’s in your pad or tampon?, CNN Health, CNN Center, Atlanta, GA, 2015. [Google Scholar]
- [8].Ishii S, Katagiri R, Kataoka T, Wada M, Imai S, Yamasaki K, Risk assessment study of dioxins in sanitary napkins produced in Japan, Regulatory toxicology and pharmacology : RTP 70(1) (2014) 357–62. [DOI] [PubMed] [Google Scholar]
- [9].Tsuruta H, Skin absorption of organic solvent vapors in nude mice in vivo, Industrial health 27(2) (1989) 37–47. [DOI] [PubMed] [Google Scholar]
- [10].Howard J, Page N, Perkins M, Toxicology Tutor II: Toxicokinetics, Absorption: Dermal Route. Bethesda, MD: Division of Specialized Information Services, National Library of Medicine, National Institutes of Health, 2001. [Google Scholar]
- [11].Dutkiewicz T, Tyras H, Skin absorption of toluene, styrene, and xylene by man, British journal of industrial medicine 25(3) (1968) 243. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [12].Doan K, Bronaugh RL, Yourick JJ, In vivo and in vitro skin absorption of lipophilic compounds, dibutyl phthalate, farnesol and geraniol in the hairless guinea pig, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 48(1) (2010) 18–23. [DOI] [PubMed] [Google Scholar]
- [13].Pan TL, Wang PW, Aljuffali IA, Hung YY, Lin CF, Fang JY, Dermal toxicity elicited by phthalates: evaluation of skin absorption, immunohistology, and functional proteomics, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 65 (2014) 105–14. [DOI] [PubMed] [Google Scholar]
- [14].Choi K, Chemical exposure in living environment - Health issues and policy suggestions, Korean Journal of Public Health 54(2) (2017) 35–41. [Google Scholar]
- [15].Kim S, Reviewing the Korean episodes of environmental chemicals in summer 2017, Korean Journal of Public Health 54(2) (2017) 3–12. [Google Scholar]
- [16].Ock H.-j., Fears mount over ‘toxic’ sanitary pads, 2017. http://www.koreaherald.com/view.php?ud=20170824000747. (Accessed Oct 07 2018).
- [17].Farage M, Maibach HI, The vulvar epithelium differs from the skin: implications for cutaneous testing to address topical vulvar exposures, Contact dermatitis 51(4) (2004) 201–9. [DOI] [PubMed] [Google Scholar]
- [18].Jain RB, Distributions of selected urinary metabolites of volatile organic compounds by age, gender, race/ethnicity, and smoking status in a representative sample of U.S. adults, Environmental toxicology and pharmacology 40(2) (2015) 471–9. [DOI] [PubMed] [Google Scholar]
- [19].Dahl AR, Dose concepts for inhaled vapors and gases, Toxicology and applied pharmacology 103(2) (1990) 185–97. [DOI] [PubMed] [Google Scholar]
- [20].Boyle EB, Deziel NC, Specker BL, Collingwood S, Weisel CP, Wright DJ, Dellarco M, Feasibility and informative value of environmental sample collection in the National Children’s Vanguard Study, Environmental research 140 (2015) 345–53. [DOI] [PubMed] [Google Scholar]
- [21].Boyle EB, Viet SM, Wright DJ, Merrill LS, Alwis KU, Blount BC, Mortensen ME, Moye J Jr., Dellarco M, Assessment of Exposure to VOCs among Pregnant Women in the National Children’s Study, International journal of environmental research and public health 13(4) (2016) 376. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [22].Nakai N, Murata M, Nagahama M, Hirase T, Tanaka M, Fujikawa T, Nakao N, Nakashima K, Kawanishi S, Oxidative DNA damage induced by toluene is involved in its male reproductive toxicity, Free radical research 37(1) (2003) 69–76. [DOI] [PubMed] [Google Scholar]
- [23].Sirotkin AV, Harrath AH, Influence of oil-related environmental pollutants on female reproduction, Reproductive toxicology 71 (2017) 142–145. [DOI] [PubMed] [Google Scholar]
- [24].Hannigan JH, Bowen SE, Reproductive toxicology and teratology of abused toluene, Systems biology in reproductive medicine 56(2) (2010) 184–200. [DOI] [PubMed] [Google Scholar]
- [25].Brown-Woodman PD, Hayes LC, Huq F, Herlihy C, Picker K, Webster WS, In vitro assessment of the effect of halogenated hydrocarbons: chloroform, dichloromethane, and dibromoethane on embryonic development of the rat, Teratology 57(6) (1998) 321–33. [DOI] [PubMed] [Google Scholar]
- [26].Ma M, Kondo T, Ban S, Umemura T, Kurahashi N, Takeda M, Kishi R, Exposure of prepubertal female rats to inhaled di(2-ethylhexyl)phthalate affects the onset of puberty and postpubertal reproductive functions, Toxicological sciences : an official journal of the Society of Toxicology 93(1) (2006) 164–71. [DOI] [PubMed] [Google Scholar]
- [27].Hannon PR, Flaws JA, The effects of phthalates on the ovary, Frontiers in endocrinology 6 (2015) 8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [28].Adibi JJ, Perera FP, Jedrychowski W, Camann DE, Barr D, Jacek R, Whyatt RM, Prenatal exposures to phthalates among women in New York City and Krakow, Poland, Environmental health perspectives 111(14) (2003) 1719–22. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [29].Adibi JJ, Whyatt RM, Williams PL, Calafat AM, Camann D, Herrick R, Nelson H, Bhat HK, Perera FP, Silva MJ, Hauser R, Characterization of phthalate exposure among pregnant women assessed by repeat air and urine samples, Environmental health perspectives 116(4) (2008) 467–73. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [30].Koo HJ, Lee BM, Human monitoring of phthalates and risk assessment, Journal of toxicology and environmental health Part A 68(16) (2005) 1379–92. [DOI] [PubMed] [Google Scholar]
- [31].ATSDR, Toxicological profile for diethyl phthalate, Agency for Toxic Substances and Disease, Atlanta, GA, 1995. [PubMed] [Google Scholar]
- [32].ATSDR, Toxicological profile for di-n-butyl phthalate, Agency for Toxic Substances and Disease, Atlanta, GA, 2001. [PubMed] [Google Scholar]
- [33].ATSDR, Toxicological Profile for Di (2-ethylhexyl) phthalate (DEHP), Agency for Toxic Substances and Disease, Atlanta, GA, 2002. [PubMed] [Google Scholar]
- [34].Niermann S, Rattan S, Brehm E, Flaws JA, Prenatal exposure to di-(2-ethylhexyl) phthalate (DEHP) affects reproductive outcomes in female mice, Reproductive toxicology 53 (2015) 23–32. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [35].Mariana M, Feiteiro J, Verde I, Cairrao E, The effects of phthalates in the cardiovascular and reproductive systems: A review, Environment international 94 (2016) 758–776. [DOI] [PubMed] [Google Scholar]
- [36].Ejaredar M, Nyanza EC, Ten Eycke K, Dewey D, Phthalate exposure and childrens neurodevelopment: A systematic review, Environmental research 142 (2015) 51–60. [DOI] [PubMed] [Google Scholar]
- [37].Caldwell JC, DEHP: genotoxicity and potential carcinogenic mechanisms-a review, Mutation research 751(2) (2012) 82–157. [DOI] [PubMed] [Google Scholar]
- [38].Rusyn I, Corton JC, Mechanistic considerations for human relevance of cancer hazard of di(2-ethylhexyl) phthalate, Mutation research 750(2) (2012) 141–58. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [39].Schlosser PM, Bale AS, Gibbons CF, Wilkins A, Cooper GS, Human health effects of dichloromethane: key findings and scientific issues, Environmental health perspectives 123(2) (2015) 114–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [40].Mulware SJ, The mammary gland carcinogens: the role of metal compounds and organic solvents, International journal of breast cancer 2013 (2013) 640851. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [41].Fisher J, Mahle D, Bankston L, Greene R, Gearhart J, Lactational transfer of volatile chemicals in breast milk, American Industrial Hygiene Association journal 58(6) (1997) 425–31. [DOI] [PubMed] [Google Scholar]
- [42].Roberts LG, Nicolich MJ, Schreiner CA, Developmental and reproductive toxicity evaluation of toluene vapor in the rat II. Developmental toxicity, Reproductive toxicology 23(4) (2007) 521–31. [DOI] [PubMed] [Google Scholar]
- [43].Adgate JL, Eberly LE, Stroebel C, Pellizzari ED, Sexton K, Personal, indoor, and outdoor VOC exposures in a probability sample of children, Journal of exposure analysis and environmental epidemiology 14 Suppl 1 (2004) S4–S13. [DOI] [PubMed] [Google Scholar]
- [44].Chien YC, Variations in amounts and potential sources of volatile organic chemicals in new cars, The Science of the total environment 382(2–3) (2007) 228–39. [DOI] [PubMed] [Google Scholar]
- [45].Fabietti F, Ambruzzi A, Delise M, Sprechini MR, Monitoring of the benzene and toluene contents in human milk, Environment international 30(3) (2004) 397–401. [DOI] [PubMed] [Google Scholar]
- [46].Bowen SE, Batis JC, Mohammadi MH, Hannigan JH, Abuse pattern of gestational toluene exposure and early postnatal development in rats, Neurotoxicology and teratology 27(1) (2005) 105–16. [DOI] [PubMed] [Google Scholar]
- [47].Win-Shwe TT, Fujimaki H, Neurotoxicity of toluene, Toxicology letters 198(2) (2010) 93–9. [DOI] [PubMed] [Google Scholar]
- [48].U.S. EPA, Integrated Risk Information System (IRIS) on Toluene, National Center for Environmental Assessment, Office of Research and Development, Washington, DC, 2005. [Google Scholar]
- [49].Kandyala R, Raghavendra SP, Rajasekharan ST, Xylene: An overview of its health hazards and preventive measures, Journal of oral and maxillofacial pathology : JOMFP 14(1) (2010) 1–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [50].Saillenfait AM, Gallissot F, Morel G, Bonnet P, Developmental toxicities of ethylbenzene, ortho-, meta-, para-xylene and technical xylene in rats following inhalation exposure, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 41(3) (2003) 415–29. [DOI] [PubMed] [Google Scholar]
- [51].von Ehrenstein OS, Aralis H, Cockburn M, Ritz B, In utero exposure to toxic air pollutants and risk of childhood autism, Epidemiology 25(6) (2014) 851–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [52].Jacobson GA, McLean S, Biological monitoring of low level occupational xylene exposure and the role of recent exposure, The Annals of occupational hygiene 47(4) (2003) 331–6. [DOI] [PubMed] [Google Scholar]
- [53].Buesa RJ, Peshkov MV, Histology without xylene, Annals of diagnostic pathology 13(4) (2009) 246–56. [DOI] [PubMed] [Google Scholar]
- [54].U.S. EPA, Integrated Risk Information System (IRIS) on Xylenes, National Center for Environmental Assessment, Office of Research and Development, Washington, DC, 1999. [Google Scholar]
- [55].Usepa M, National primary drinking water regulations, EPA-816-F-09–004 Search PubMed, 2009.
- [56].Shen H-Y, Simultaneous screening and determination eight phthalates in plastic products for food use by sonication-assisted extraction/GC–MS methods, Talanta 66(3) (2005) 734–739. [DOI] [PubMed] [Google Scholar]
- [57].Park YN, Choi MS, Rehman SU, Gye MC, Yoo HH, Simultaneous GC-MS determination of seven phthalates in total and migrated portions of paper cups, Environmental Science and Pollution Research 23(10) (2016) 10270–10275. [DOI] [PubMed] [Google Scholar]
- [58].He M, Yang C, Geng R, Zhao X, Hong L, Piao X, Chen T, Quinto M, Li D, Monitoring of phthalates in foodstuffs using gas purge microsyringe extraction coupled with GC–MS, Analytica chimica acta 879 (2015) 63–68. [DOI] [PubMed] [Google Scholar]
- [59].Kay VR, Chambers C, Foster WG, Reproductive and developmental effects of phthalate diesters in females, Critical reviews in toxicology 43(3) (2013) 200–19. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [60].Lee KY, Shibutani M, Takagi H, Kato N, Takigami S, Uneyama C, Hirose M, Diverse developmental toxicity of di-n-butyl phthalate in both sexes of rat offspring after maternal exposure during the period from late gestation through lactation, Toxicology 203(1–3) (2004) 221–38. [DOI] [PubMed] [Google Scholar]
- [61].Zhou C, Gao L, Flaws JA, Prenatal exposure to an environmentally relevant phthalate mixture disrupts reproduction in F1 female mice, Toxicology and applied pharmacology 318 (2017) 49–57. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [62].Swan SH, Environmental phthalate exposure in relation to reproductive outcomes and other health endpoints in humans, Environmental research 108(2) (2008) 177–84. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [63].Chemes HE, Infancy is not a quiescent period of testicular development, International journal of andrology 24(1) (2001) 2–7. [DOI] [PubMed] [Google Scholar]
- [64].So J, Ahn J, Lee TH, Park KH, Paik MK, Jeong M, Cho MH, Jeong SH, Comparison of international guidelines of dermal absorption tests used in pesticides exposure assessment for operators, Toxicological research 30(4) (2014) 251–60. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [65].Hussain A, Ahsan F, The vagina as a route for systemic drug delivery, Journal of controlled release : official journal of the Controlled Release Society 103(2) (2005) 301–13. [DOI] [PubMed] [Google Scholar]
- [66].Ventrice P, Ventrice D, Russo E, De Sarro G, Phthalates: European regulation, chemistry, pharmacokinetic and related toxicity, Environmental toxicology and pharmacology 36(1) (2013) 88–96. [DOI] [PubMed] [Google Scholar]
- [67].Kim JH, Yun J, Sohng JK, Cha JM, Choi BC, Jeon HJ, Kim SH, Choi CH, Di(2-ethylhexyl)phthalate leached from medical PVC devices serves as a substrate and inhibitor for the P-glycoprotein, Environmental toxicology and pharmacology 23(3) (2007) 272–8. [DOI] [PubMed] [Google Scholar]
- [68].Han A, Han E, Han Hv E, DIRECTIVE 2011/65/EU OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 8 June 2011 on the restriction of the use of certain hazardous substances in electrical and electronic equipment (RoHS II), (2011).
- [69].Merenyi S, REACH: Regulation (EC) No 1907/2006, (2014).
- [70].Barakat R, Lin PP, Rattan S, Brehm E, Canisso IF, Abosalum ME, Flaws JA, Hess R, Ko C, Prenatal Exposure to DEHP Induces Premature Reproductive Senescence in Male Mice, Toxicological sciences : an official journal of the Society of Toxicology 156(1) (2017) 96–108. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [71].Barakat R, Lin PC, Park CJ, Best-Popescu C, Bakery HH, Abosalum ME, Abdelaleem NM, Flaws JA, Ko C, Prenatal Exposure to DEHP Induces Neuronal Degeneration and Neurobehavioral Abnormalities in Adult Male Mice, Toxicological sciences : an official journal of the Society of Toxicology (2018). [DOI] [PMC free article] [PubMed]
- [72].U.S. EPA, Integrated Risk Information System (IRIS) on DBP, National Center for Environmental Assessment, Office of Research and Development, Washington, DC, 1987. [Google Scholar]
- [73].Crump DR, Squire RW, Yu CW, Sources and concentrations of formaldehyde and other volatile organic compounds in the indoor air of four newly built unoccupied test houses, Indoor and Built Environment 6(1) (1997) 45–55. [Google Scholar]
- [74].Jian RS, Sung LY, Lu CJ, Measuring real-time concentration trends of individual VOC in an elementary school using a sub-ppb detection muGC and a single GC-MS analysis, Chemosphere 99 (2014) 261–6. [DOI] [PubMed] [Google Scholar]
- [75].Ahn J-H, Kim K-H, Kim Y-H, Kim B-W, Characterization of hazardous and odorous volatiles emitted from scented candles before lighting and when lit, Journal of hazardous materials 286 (2015) 242–251. [DOI] [PubMed] [Google Scholar]
- [76].Kuo HW, Chiang TF, Lo II, Lai JS, Chan CC, Wang JD, VOC concentration in Taiwan’s household drinking water, The Science of the total environment 208(1–2) (1997) 41–7. [DOI] [PubMed] [Google Scholar]
- [77].Al-Mudhaf HF, Alsharifi FA, Abu-Shady AS, A survey of organic contaminants in household and bottled drinking waters in Kuwait, The Science of the total environment 407(5) (2009) 1658–68. [DOI] [PubMed] [Google Scholar]
- [78].Pandey SK, Kim K-H, An evaluation of volatile compounds released from containers commonly used in circulation of sports beverages, Ecotoxicology and environmental safety 74(3) (2011) 527–532. [DOI] [PubMed] [Google Scholar]
- [79].Fleming-Jones ME, Smith RE, Volatile organic compounds in foods: a five year study, Journal of agricultural and food chemistry 51(27) (2003) 8120–8127. [DOI] [PubMed] [Google Scholar]
- [80].Vinci RM, Jacxsens L, De Meulenaer B, Deconink E, Matsiko E, Lachat C, de Schaetzen T, Canfyn M, Van Overmeire I, Kolsteren P, Occurrence of volatile organic compounds in foods from the Belgian market and dietary exposure assessment, Food Control 52 (2015) 1–8. [Google Scholar]
- [81].Panseri S, Chiesa LM, Zecconi A, Soncini G, De Noni I, Determination of volatile organic compounds (VOCs) from wrapping films and wrapped PDO Italian cheeses by using HS-SPME and GC/MS, Molecules 19(7) (2014) 8707–8724. [DOI] [PMC free article] [PubMed] [Google Scholar]
- [82].Hubinger JC, A survey of phthalate esters in consumer cosmetic products, Journal of cosmetic science 61(6) (2010) 457–465. [PubMed] [Google Scholar]
- [83].Keresztes S, Tatár E, Czégény Z, Záray G, Mihucz VG, Study on the leaching of phthalates from polyethylene terephthalate bottles into mineral water, Science of the Total Environment 458 (2013) 451–458. [DOI] [PubMed] [Google Scholar]
- [84].Zaater MF, Tahboub YR, Al Sayyed AN, Determination of phthalates in jordanian bottled water using GC–MS and HPLC–UV: environmental study, Journal of chromatographic science 52(5) (2013) 447–452. [DOI] [PubMed] [Google Scholar]
- [85].Otero P, Saha SK, Moane S, Barron J, Clancy G, Murray P, Improved method for rapid detection of phthalates in bottled water by gas chromatography–mass spectrometry, Journal of Chromatography B 997 (2015) 229–235. [DOI] [PubMed] [Google Scholar]
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