Next Article in Journal
Fruit Quality Characters of Myrtle (Myrtus communis L.) Selections: Review of a Domestication Process
Previous Article in Journal
Analyses Implementation Realities of Legal Frameworks for Sustainable Management of Tanguar Haor Fisheries Resources in Bangladesh
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Quantitative Estimation of the Hydroquinone, Mercury and Total Plate Count in Skin-Lightening Creams

1
College of Earth and Environmental Sciences, University of the Punjab, Lahore 54000, Pakistan
2
Pakistan Council of Scientific & Industrial Research (PCSIR) Laboratories, Lahore 54000, Pakistan
3
Department of Environmental Sciences and Engineering, Government College University, Faisalabad 38000, Pakistan
4
Department of Biological Sciences and Technology, China Medical University, Taichung 40402, Taiwan
5
Adjunct Faculty Military College of Engineering, Risalpur 23200, Pakistan
6
Department of Agronomy, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL 32611, USA
7
Department of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia
*
Authors to whom correspondence should be addressed.
Sustainability 2021, 13(16), 8786; https://doi.org/10.3390/su13168786
Submission received: 29 January 2021 / Revised: 24 March 2021 / Accepted: 25 March 2021 / Published: 6 August 2021

Abstract

:
Generally white color of the skin is regarded as a feature of superiority and prettiness around the world. Both the males and females in Pakistan apply skin-lightening creams (SLC) but they do not know about the side-effects of their constituents. Skin-lightening products include SLC and related ointments. The SLC are made by mixing fates and water in standard procedure. Here, 20 SLC specimens were obtained and subjected to mercury, hydroquinone and the total plate count (TPC). The hydroquinone in SLC was determined using HPLC, mercury level was assessed by ICP OES and finally TPC were computing by utilizing nutrient media (Agar). The hydroquinone in SLC ranged from 0 to 7.14 ± 0.18% with a median value of 0.33%. In 25% of the studied samples, hydroquinone was not detected, 70% of the samples showed values within the limit and 5% of the samples (1 sample) had a hydroquinone concentration above the permissible limit defined by Pakistan (5%). The mercury ranged 0-7.7 ppm, with a median value of 2.5 ppm. Mercury was detected in 95% of the samples; thus, only 5% of the samples had no mercury. In turn, 20% had mercury within the limit value while 75% of the samples had concentration above the Pakistan standard limit (1 ppm). Moreover, TPC obtained in this study was less than the allowable value set according to European Union (EU). Hence, the SLC samples showed high concentration of toxic constituents which could cause deleterious skin diseases. Government must monitor such kind of cosmetic products regularly in order to reduce the danger.

1. Introduction

Currently, the skin-lightener or skin-whitener market is flourishing worldwide. The white color of individuals is regarded as a feature of social status and grace around the world [1]. Skin-lightening products include skin-whitening creams and ointments. Skin-lightening creams (SLC) are cosmetic products which are the mixture of fats and water and used on face in order to treat dermal issues such as dark and/or aging spots, hyperpigmentation and discoloration. Pigmentation in humans is owing to the presence of a pigment (melanin) in skin. If the melanin level increases in human body, this can lead to serious skin diseases for example hyperpigmentation, melisma and dark complexion. Individuals dislike dark color of skin and wish to possess white complexion, which makes them happy. Due to this perception, both women and men are intensively using different skin-whitening creams without any awareness about their toxic ingredients [2]. Ingredients used in skin-whitening creams are mercury, arbutin, hydroquinone, kojic acid, paraben, azelaic acid, vitamin C, niacinamide and glutathione which are dangerous to health [3].
Hydroquinone has been largely included previously as one of the major constituent in many SLC products. It inhibits the synthesis of melanin and restricts the production of skin-color-changing substances. The permissible limit for hydroquinone is 2% according to US FDA and WHO. Pakistan has also set a standard (PS3228/2006) for hydroquinone, which is 5%. Hydroquinone is considered to cause respiratory disorders and skin irritation as well as carcinogenic effects and is banned in many countries, such as Australia and in Europe, Asia and Africa [4]. Mercury is ranked among the top ten chemicals or group of chemicals which are considered serious health concerns to the people according to the World Health Organization (WHO) [5]. Mercury occurs in an elemental (or metallic) form as well as organic and inorganic forms [6,7]. It is a neurotoxicant that is strictly banned in various European and African countries [8]. The SLC containing toxic mercury has been applied widely by the dark-skinned individuals in various countries of Asia and Africa [9,10,11]. Mercury is added in skin-lightning creams as a skin-bleaching agent since it reduces the production of melanin. It is also used as a strong preservative in body- or hand-care creams/lotions and others cosmetic products, despite not justifying its use in these products [12]. The maximum permissible limit of mercury in cosmetics is 1 μg g−1, established in 1992 by the US FDA and WHO. Mercury has been reported to induce lethal effects on human skin such as rashes, scarring and discoloration [4,6]. Al-Saleh et al. [13] found mercury in skin-lightening creams and examined the chronic effects of mercury on mice. They observed maximum mercury accumulation in the ovaries of mice based on the frequency of mercury-containing creams application. It was also concluded that mercury accumulation could disrupt reproductive behavior, leading to ovarian failures. Hence, mercury exposure via creams causes a serious danger to the public health.
The bacterial growth occurring in skin whitening creams could deteriorate the quality of creams and this could happen due to various reasons. The components of creams are the major reason behind the occurrence of bacterial growth [14,15,16]. Among them, water is the main component of skin-whitening creams and inclusion of contaminated water results in the bacterial growth as it provides medium for the growth of bacteria in creams. Use of contaminated creams on the skin results in various kinds of skin diseases [15]. Thus, it is imperative to determine the microbial count of skin-whitening creams.
According to Asian culture, white color of the skin shows richness while and a dark/black skin color is linked to poorness. Furthermore the people are motivated to have white color because in many movies the hero or heroine is sleeted on the basis of white color showing positivity while villains are casted with dark skin color representing negativity. A large number of SLC and bleaching products are found in local markets of Asia. Moreover, many skin whitening treatments and procedures are also offered by the dermatologists as well as beauticians in beauty salons in Asian countries. Pakistani people are also greatly impressed with the SLC creams as white color of the skin adds value is marriage market [17,18,19]. People in Pakistan are also completely unaware of the toxic effects caused by constitutes in skin-whitening creams and using these creams extensively.
Despite many studies conducted worldwide on the determination of the mercury, hydroquinone and total plate count in SLC and cosmetics, to our knowledge, no data are available in the literature on the quantification of the abovementioned parameters in Pakistani local brands of skin-lightening creams. Thus, being first of its kind, the objectives of the current study are to (1) determine the concentration of hydroquinone and mercury in different skin-lightening creams of local brands available in Pakistan; (2) compare the hydroquinone and mercury concentrations in skin-whitening creams with the Pakistan standard limits; and (3) determine the risk posed to the Pakistani population. Moreover, the bacterial growth (TPC) was also examined in the present study.

2. Materials and Methods

The samples (Twenty) of SLC were obtained from local market in Lahore, Pakistan. These SLC were selected as they were inexpensive, famous and bought abundantly (Figure S1; Supplementary Materials). The date of production was demonstrated clearly and SLCs had no ointment in them. The major analyses were done in the labs of Pakistan Council of Scientific and Industrial Research (PCSIR) while TPC was examined at the lab of CEES, University of the Punjab, Lahore, Pakistan (Table 1).

2.1. Estimation of pH

The pH of the samples was measured by using a pH meter (HANNA Instrument, HI 2211, pH/ORP Meter, Woonsocket, RI, USA). An appropriate quantity of the sample solution was taken in a 100 mL beaker to immerse the tips of the electrodes. The electrodes of the pH meter were rinsed with distilled water and then with the sample solution. The temperature and pH of the samples were recorded.

2.2. HPLC Analysis

2.2.1. Preparation of Cream Sample

Samples of cream (2 g each) was added in a beakeralong with mobile phase (25 mL) (water:methanol, 40:60) [20,21]. The solution was thoroughly mixed using the water bath (model: HWS 26, Shanghai, China) for 45 min at optimum temperature of 60 °C. Afterwards cooling was done by putting the mixture in refrigerator which resulted in separation of waxes and fates. The solution was carefully filtered and stored in Teflon vials.

2.2.2. Preparation of the Reference Solution

A total of 0.1 g of hydroquinone was added into a 100 mL flask and mobile phase (very little amount) was added to make it soluble. Finally the remaining volume was filled with deionized water (DW). After that, about 5 mL was taken from this standard stock, and the volume was filled up to 50 mL using the mobile phase.

2.2.3. Prepartion of Mobile Phase

A mixture (methanol:water mixture 40:60) was prepared by the addition of about 100 mL methanol solution in about 150 mL of DW following heating and then for 20 min, the solution was sonicated using the ultrasonic bath (Elma, Wetzikon, Switzerland, model: JP-04OST) to degas the mobile phase.

2.2.4. Procedure for HPLC

Almost 20 μL of each sample was injected in the HPLC (Shemadzu, model: LC-9, Kyoto, Japan) and the chromatograms were recorded (Figure 1). The presence of hydroquinone was indicated by analytical determination. The area of the peak obtained for each cream sample was analyzed and then it was compared carefully with standard reference solution. The retention time determined for the hydroquinone standard reference solution against the cream sample solution was employed to confirm the presence of hydroquinone. The percentage of hydroquinone was computed using the following Equation 1 [20]:
%age of hydroquinone = bi/pi × wref/wspl × d × 100
where, bi and pi are the peak areas of hydroquinone in sample solution and standard solution, receptively while Wspl and Wref show the weight of sample solution and standard solution, respectively; d is dilution factor which is 0.1.

2.2.5. HPLC Conditions

Isocratic HPLC system;
Temperature: 30 °C;
Wavelength: 295 nm;
Column: 250 mmL, 4.6 mm ID, C-18, (Octadecyl-silica) ODS, reverse phase;
Flow rate: 1 mL/minute;
Mobile phase: methanol:water mixture (40:60);
Detector: UV (ultraviolet)—Vis (visible), with range 190–700 nm;
Extraction: Liquid/liquid extraction;
Pump: Reciprocating pump.

2.3. ICP OES Analysis

2.3.1. Preparation of Sample

A cream sample (1 g) was weighed in 100 mL of beaker and then 25 mL of nitric acid solution (10%) was put in all the prepared samples (each). The solution was subjected to heating at 120 120 °C using hotplate (A&E Lab, model: 106 MA, London, UK) to for digestion of cream samples and after that the mixture became clear. The solution was filtered (Whatman filter paper 41) and stored in a refrigerator.

2.3.2. Preparation of the Reference Solution

To analyze mercury in collected creams, a mercury reference standard solution of 1000 mg L−1 was employed and analyses were done by using the Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES) (Optima DV 5300 by Perkin Elmer, Waltham, MA, USA) technique. The standard solution of mercury was diluted up to make 1 mg L−1 of substock solution using the following Equation:
M1V1 = M2V2
where, M1 and M2 are stock solution and diluted solution concentrations (moles/L) while V1 and V2 are volume of stock and diluted solutions.

2.3.3. Procedure for ICP-OES

All skin-whitening cream samples were estimated by using ICP-OES containing an auto sampler along with a quartz nebulizer. A cinnabar spray chamber (25 mL) was used to reduce the memory effect. A mercury sampler and skimmer cones were also attached with ICP-OES. An auto sampler was used for the injection of samples while suction was done using quartz nebulizer.

2.3.4. ICP OES Operating Conditions

RF power: 1300 W;
RF generator: 40 MHz;
Air flow rate: 18 L/min;
Argon flow: 0.6 L/min;
Sample flow rate: 1.5 mL/min;
View: Dual view;
Nebulizer: 0.8 L/min;
Pump: Peristaltic pump;
Detector: Segmented-array Charge Coupled Device (SCD).

2.4. TPC Analysis

2.4.1. Media Preparation and Sterilization

Media was prepared by adding 28 g of nutrient agar (beef extracts + yeast extracts + peptone + sodium chloride) in 1 L of deionized water and it was heated/boiled to dissolve thoroughly. The nutrient media and other apparatus were carefully sterilized using autoclave (Biobas, model: LE-75D, Shandong, China) at 121 °C and 15 psi for 15 min.

2.4.2. Procedure for TPC

The air blower and UV lamp attached to laminar flow (Esko Company, model: LC-2A, Shanghai, China) were warmed up approximately 30 min before experiments. About 25 mL of agar media was added into each of the petri dish. The samples of the creams were thoroughly spreadin the petri dishes containing nutrient agar. The petri dishes were agitated manually clockwise for 4–5 times. The Petri dishes were placed in an incubator (Memmert, model: In-50, Büchenbach, Germany) at for 72 h time at 37 °C temperature and finally colonies of microorganisms were detected and they were counted by using a colony counter.

2.5. Statistical Tools

The microsft word® software was sed for basic statistical analyses. The skewness in the obtained data was computed using statistical software SPSS 16.0 to observe whether data is skewed or normal [22].

3. Results and Discussion

The pH was observed to be acidic, slightly acidic, neutral and slightly basic in 10, 20, 6 and 5% of the samples, respectively (Table 2). The HPLC analysis confirmed the existence of hydroquinone in the sampled skin-whitening creams at different concentrations (Table 3). The hydroquinone concentration ranged 0 to 7.1404 ± 0.1823% in creams samples. The skewness value was noted as 4.086 (Table 4) for the hydroquinone, that is above standard value (+1 to −1) [11], showing a normal distribution of the data. Moreover, hydroquinone was not detected in 25% of the samples, including SLC5, SLC8, SLC12, SLC16 and SLC17. Only one sample (SLC11, 7.1404 ± 0.1823%) showed a hydroquinone concentration above the permissible limit of Pakistan. This sample cream was manufactured in Pakistan and it was very economical. The hydroquinone level was within the permissible limit in 95% of the samples, ranging from 0.04 to 1.26.
The analyses of hydroquinone in different SLC have been reported previously n the United Kingdom [23]. It was reported that about 10 creams showed having hydroquinone, which were subjected to a chromatographic test in the Plateau state, Nigeria [24]. The researchers demonstrated positive results regarding hydroquinone; however, hydroquinone concentration was less than the allowable limit, i.e., 2% in seven cream samples, 2 to 5% for two samples and 5% for one cream sample [24]. In another study, the hydroquinone level ranged from 0.0002 to 0.0350%, showing low values reported in our study [25]. Long-term application of SLC with hydroquinone may lead to exogenous ochronosis, which is an uneven hyper pigmentation showing brown and yellow pigment deposition on skin. The long-term impacts of hydroquinone also include cancer in humans [26].
Table 3. Hydroquinone content of the skin-lightening cream samples available in Pakistan.
Table 3. Hydroquinone content of the skin-lightening cream samples available in Pakistan.
Serial #Name Hydroquinone (%)Peak Area (PA) § Retention Time (RT)
ISLC1 0.06 ± 0.02 92914.75
IISLC20.24 ± 0.09231354.74
IIISLC30.65 ± 0.061089334.73
IVSLC41.26 ± 0.032762844.74
VSLC50 ± 000
VISLC60.93 ± 0.00032214214.74
VIISLC70.04 ± 0.0290214.74
VIIISLC80 ± 000
IXSLC90.33 ± 0.08484514.73
XSLC100.98 ± 0.072056114.45
XISLC117.14 ± 0.0815091634.73
XIISLC120 ± 000
XIIISLC130.22 ± 0.02472414.74
XIVSLC140.43 ± 0.08552004.74
XVSLC150.23 ± 0.06413194.73
XVISLC160 ± 000
XVIISLC170 ± 000
XVIIISLC180.33 ± 0.003493514.74
XIXSLC190.14 ± 0.02301624.75
XXSLC200.46 ± 0.01557614.73
Note: Pakistan standard limit = 5% [24]. SLC = skin-lightening cream. Abovementioned readings are mean ± SD data. § PA for quantification. RT is retention time of the standard solution = 4.74. Minimum value of hydroquinone = 0 ± 0. Maximum value off hydroquinone = 7.14 ± 0.08. Average value of hydroquinone = 0.07 ± 0.03.
Table 4. Skewness value for various ingredients.
Table 4. Skewness value for various ingredients.
Obs. No.Ingredients Skewness Values
1.Hydroquinone4.086
2.Mercury 0.996
3.Total plate count1.044
Similarly, the mercury concentration ranged between 0 and 7.7 ± 0.2 ppm, with a median value of 2.5 ppm (Table 5). The skewness calculated for mercury was 0.996 (Table 4), which was close to the range defined (+1 to −1) and showing a normal data distribution. Mercury was detected in 95% of the samples; thus, only 5% of the samples showed a zero mercury concentration (SLC8). Mercury was within the permissible limit in 20% of the samples, i.e., SLC1, SLC10, SLC14 and SLC19. However, 75% of the samples had a concentration above the standard limit (1 ppm). Moreover, the manufacturing country was not mentioned in most of these samples. The maximum concentration of mercury found in this study was 7.7 ± 0.2 ppm. The sample cream with the highest mercury concentration was manufactured in India and was the most popular skin-whitening cream among the population of Pakistan.
A higher concentration of mercury in SLC obtained from Middle East Asia and Saudi Arabia and was also reported in another study [15]. A high concentration (0.16 to 25.30 mg/kg) of mercury (>standard limit) was estimated in skin-lightening cream samples obtained from the Dar es Salaam market of Tanzania [27]. The cumulative impact of the continuous/repetitive use of even a low level of mercury-containing creams can lead to nephritic syndrome [28]. A study confirmed that application of of SLC containing inorganic mercury resulted in accumulation and absorption of mercury in the body [29].
Moreover, Table 6 shows that the microbial count ranged from 0 to 7.0 × 102 ± 1 CFU/g in this study. Samples SLC12 and SLC19 showed no colony count while the skewness value (1.044) for data was also close to the standard range (+1 to −1) (Table 6), which is set for a normal distribution. The results showed that all SLC samples contained relatively less microbial count as compared to US FDA and ASEAN limits. In a study conducted on microbial contamination in Europe, approximately 24 cosmetic samples were observed to contain higher number of different types of microbes [30]. In another experiment TPC ranged from 1.7 × 102 to 5.4 × 102 CFU/g [31].
The occurrence of bacterial contamination in skin-whitening creams is expected very often because bacteria can grow even at a neutral pH, which is the dominant pH range in most of the cosmetics. The occurrence various pathogenic bacteria in different cosmetic products has been observed [32]. In a study, TPC in 13 out of 15 skin creams was 0.24 × 103 to 0.56 × 103 CFU/g [33]. In this study, TPC was less in SLC samples as compared to the standard value hence there is a low risk of bacterial growth and resulting skin diseases. However, the possible skin diseases with the prolonged use of skin-lightening creams containing high bacterial contamination include erythema, edema, inflammation, sensitization, photosensitization and itching [14]. Microbial presence in skin beauty creams could cause deterioration and wastage of these creams, posing a serious risk to the health of consumers [34].
Mercury concentration found in the current study was compared with various studies conducted in different countries. The concentration of mercury in skin-lightening creams of different countries is described in Table 7. It can be seen that the concentration of mercury was less in the skin-lightening creams that originated from Armenia, Nepal and India compared to Pakistan. In contrast, the mercury level was higher in the skin-lightening creams produced in the Philippines, Mexico, China, Caribbean, Cambodia, Norway, Denmark, Austria, USA, Bangladesh and Saudi Arabia compared to Pakistan. Overall, the mercury level in the skin-lightening creams was above the permissible limit in most of the countries compared here. The maximum concentration of mercury was observed in the skin-lightening creams that originated from Mexico.

4. Conclusions

The current study confirmed that that concentration of hydroquinone and mercury in the samples investigated were more than the permissible limit defined by the US FDA and WHO. The total plate count (TPC) analyzed in the present study was found to be below the standard limit set. Various skin-lightening creams did not mention hydroquinone and mercury on their ingredients list but were found to contain high levels of these two. The high concentrations of mercury and hydroquinone in skin-lightening creams may lead to serious health impacts, such as erythema, edema, inflammation, sensitization, photosensitization and itching. Although the TPC in all cream samples was lower as compared to the permissible limits, repetitive application of hydroquinone/mercury-containing skin-whitening creams should be avoided. Moreover, in future research work, analyses of both pathogens and molds/yeasts should be done in skin-lightening creams for better understanding of the effects caused by their use. The labeling of the mercury and hydroquinone concentration/content in skin-lightening creams by production brands as well as strict monitoring and control by the Pakistani government are required to minimize/avoid their presence in skincare products. This will also reduce the health risk of mercury toxicity to people using skin-lightening creams.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/su13168786/s1, Figure S1: Photographs of the skin-whitening creams used in the current study.

Author Contributions

Conceptualization, Y.S.; methodology, M.A.; software, F.B. and M.B.S.; validation, M.N., F.B. and N.K.; formal analysis, M.B.S. and F.B.; investigation, M.A.; resources, Y.S. and S.R.A.; data curation, S.A. and Y.S.; writing—original draft preparation, M.A., Y.S. and M.B.S.; writing—review and editing, Y.S. and M.B.S.; visualization, S.R.A., I.A. and M.N.A.; supervision, Y.S.; project administration, M.N.A.; funding acquisition, Y.S., S.R.A., N.K, S.A. and M.N.A. All authors have read and agreed to the published version of the manuscript.

Funding

The funding for this research work was provided by Researchers Supporting Project number (RSP 2021/180), King Saud University, Riyadh, Saudi Arabia. We thank University of the Punjab, Lahore, Pakistan, Government College University, Faisalabad, Pakistan for their support.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We are grateful to the University of the Punjab, Lahore, Pakistan and Applied Chemistry Research Centre, Pakistan Council of Scientific and Industrial Research (PCSIR) for their support. The authors also acknowledge Researchers Supporting Project number (RSP 2021/180), King Saud University, Riyadh, Saudi Arabia.

Conflicts of Interest

The authors do not have any conflict of interest.

References

  1. Pramanik, S.; Kumar, M.; Qureshi, A. Mercury in skin-care products in India and consumer exposure risks. Regul. Toxicol. Pharmacol. 2021, 121, 104870. [Google Scholar] [CrossRef] [PubMed]
  2. Charitra, S.R. Poisonous Cosmetics: The problem of mercury in skin whitening creams in Nepal. Poisonous Cosmet. 2012, 10, 9–19. [Google Scholar]
  3. Onyambu, Z.M.; Nawiri, M.P.; Kareru, P.; Wanjau, R.N. Levels of Selected Heavy Metals in Aloe vera Branded herbal Soaps sold in the Kenya Market. J. Kenya Chem. Soc. 2014, 8, 98–107. [Google Scholar]
  4. Dlova, N.C.; Hamed, S.H.; Tsoka-Gwegweni, J.; Grobler, A. Skin lightening practices: An epidemiological study of South African women of African and Indian ancestries. Br. J. Dermatol. 2015, 173, 2–9. [Google Scholar] [CrossRef] [PubMed]
  5. Pamphlett, R.; Kum Jew, S. Age-related uptake of heavy metals in human spinal interneurons. PLoS ONE 2016, 11, e0162260. [Google Scholar] [CrossRef] [PubMed]
  6. Boyd, A.S.; Seger, D.; Vannucci, S.; Langley, M. Mercury exposure and cutaneous disease. J. Am. Acad. Dermatol. 2000, 43, 81–90. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Michalek, I.M.; Benn, E.K.; Dos Santos, F.L.C.; Gordon, S.; Wen, C.; Liu, B. A systematic review of global legal regulations on the permissible level of heavy metals in cosmetics with particular emphasis on skin lightening products. Environ. Res. 2019, 170, 187–193. [Google Scholar] [CrossRef] [PubMed]
  8. WHO. Preventing Disease through Healthy Environments: Mercury in Skin Lightening Products. 2011. Available online: http://www.who.int/ipcs/assessment/public_health/mercury_flyer.pdf (accessed on 23 March 2021).
  9. Al-Saleh, I.; Al-Doush, I. Mercury content in skin lightening creams and potential health hazards to the health of Saudi women. J. Toxicol. Environ. Health 1997, 51, 123–130. [Google Scholar] [CrossRef]
  10. Borowska, S.; Brzóska, M.M. Metals in cosmetics: Implications for human health. J. Appl. Toxicol. 2015, 35, 551–572. [Google Scholar] [CrossRef]
  11. Gbetoh, M.H.; Amyot, M. Mercury, hydroquinone and clobetasol propionate in skin lightening products in West Africa and Canada. Environ. Res. 2016, 150, 403–410. [Google Scholar] [CrossRef]
  12. eCFR Electronic Code of Federal Regulations. Electronic Code of Federal Regulations. §700.13 Use of Mercury Compounds in Cosmetics Including Use as Skinbleaching Agents in Cosmetic Preparations Also Regarded as Drugs [WWW Document]. 2020. Available online: https://www.ecfr.gov/ (accessed on 7 November 2020).
  13. Al-Saleh, I.; Shinwari, N.; Al-Amodi, M. Accumulation of mercury in ovaries of mice after the application of skin-lightening creams. Biol. Trace Elem. Res. 2009, 131, 43–54. [Google Scholar] [CrossRef] [PubMed]
  14. Muhammed, H.J. Bacterial and fungal contamination in three brands of cosmetic marketed in Iraq. Iraqi J. Pharm. Sci. 2017, 20, 38–42. [Google Scholar]
  15. Al-Saleh, I. Potential health consequences of applying mercury-containing skin-lightening creams during pregnancy and lactation periods. Int. J. Hyg. Environ. Health 2016, 219, 468–474. [Google Scholar] [CrossRef]
  16. Elmorsy, T.H.; Hafez, E.A. Microbial contamination of some cosmetic preparations in Egypt. Int. J. Agric. Technol. 2016, 12, 471–481. [Google Scholar]
  17. Blay, Y.A. Struck by lightening: The transdiasporan phenomenon of skin bleaching. Jenda J. Cult. Afr. Women Stud. 2014, 14, 1–10. [Google Scholar]
  18. Mahé, A. The practice of skin-bleaching for a cosmetic purpose in immigrant communities. J. Travel Med. 2014, 21, 282–287. [Google Scholar] [CrossRef] [Green Version]
  19. Shankar, P.R.; Subish, P. Fair skin in South Asia: An obsession? J. Pak. Assoc. Dermatol. 2016, 17, 100–104. [Google Scholar]
  20. Siddique, S.; Parveen, Z.; Ali, Z.; Zaheer, M. Qualitative and quantitative estimation of hydroquinone in skin whitening cosmetics. J. Cosmet. Dermatol. Sci. Appl. 2012, 2, 224. [Google Scholar] [CrossRef] [Green Version]
  21. Gao, W.; Legido-Quigley, C. Fast and sensitive high performance liquid chromatography analysis of cosmetic creams for hydroquinone, phenol and six preservatives. J. Chromatogr. A 2011, 1218, 4307. [Google Scholar] [CrossRef]
  22. Cain, M.K.; Zhang, Z.; Yuan, K.H. Univariate and multivariate skewness and kurtosis for measuring nonnormality: Prevalence, influence and estimation. Behav. Res. Methods 2017, 49, 1716–1735. [Google Scholar] [CrossRef]
  23. Agorku, E.S.; Kwaansa-Ansah, E.E.; Voegborlo, R.B.; Amegbletor, P.; Opoku, F. Mercury and hydroquinone content of skin toning creams and cosmetic soaps, and the potential risks to the health of Ghanaian women. SpringerPlus 2016, 5, 319. [Google Scholar] [CrossRef] [Green Version]
  24. Odumosu, P.O.; Ekwe, T.O. Identification and spectrophometric determination of hydroquinone levels in some cosmetic creams. Afr. J. Pharm. Pharmacol. 2010, 4, 231–234. [Google Scholar]
  25. Terer, E.k.; Magut, H.; Mule, S. UV–Vis analysis and determination of hydroquinone in body lotions and creams sold in retail outlets in Baraton, Kenya. Baraton Interdispl. Res. J. 2013, 3, 23–28. [Google Scholar]
  26. Toxicology Data Network (TOXNET)—USA National Library of Medicine (NIH). Available online: https://toxnet.nlm.nih.gov/ (accessed on 7 March 2021).
  27. Mahugija, J.A. Levels of Heavy Metals in Drinking Water, Cosmetics and Fruit Juices from Selected Areas in Dar Es Salaam. Tanzan. J. Sci. 2018, 44, 1–11. [Google Scholar]
  28. Cappelletti, S.; Piacentino, D.; Fineschi, V.; Frati, P.; D’Errico, S.; Aromatario, M. Mercuric chloride poisoning: Symptoms, analysis, therapies, and autoptic findings. A review of the literature. Crit. Rev. Toxicol. 2019, 49, 329–341. [Google Scholar] [CrossRef]
  29. Truisi, G.L.; Maibach, H.I.; Hewitt, P.G. Systemic toxicity 6. In Dermatotoxicology; CRC Press: Boca Raton, FL, USA, 2012; pp. 55–69. [Google Scholar]
  30. Gopalkrishna, B.K.; Philip, A.S.; Shenoy, S. Bacteriological profile of skin-moisturizing creams and lotions during use. Indian J. Pathol. Microbiol. 2010, 53, 863. [Google Scholar] [CrossRef]
  31. Aminu, M.; Christopher, O. Antibiogram of bacterial isolates and fungi associated with some creams and lotions sold in Zaria, Nigeria. Afr. J. Microbiol. Res. 2016, 10, 231–237. [Google Scholar]
  32. Al-Mijalli, S.H. Isolation and characterization of plant and human pathogenic bacteria from green pepper (Capsicum annum L.) in Riyadh, Saudi Arabia. 3 Biotech 2010, 4, 337–344. [Google Scholar] [CrossRef] [Green Version]
  33. Oluremi, B.B.; Osungunna, M.O.; Idowu, O.A.; Adebolu, O.O. Evaluation of anticaries activity of selected mouthwash marketed in Nigeria. Trop. J. Pharm. Res. 2010, 9, 1–10. [Google Scholar] [CrossRef] [Green Version]
  34. Dadashi, L.; Dehghanzadeh, R. Investigating incidence of bacterial and fungal contamination in shared cosmetic kits available in the women beauty salons. Health Promot. Perspect. 2016, 6, 159. [Google Scholar] [CrossRef]
  35. Afzal, B.; Raza, S.; Ali, S.W.; Abbas, Z.; Khwaja, M.A. Mercury Poisoning Associated with International and Local Skin Whitening Creams in Pakistan. 2018. Available online: http://hdl.handle.net/11540/9423 (accessed on 24 March 2021).
  36. Peregrino, C.P.; Moreno, M.V.; Miranda, S.V.; Rubio, A.D.; Leal, L.O. Mercury levels in locally manufactured Mexican skin-lightening creams. Int. J. Environ. Res. Public Health 2011, 8, 2516–2523. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Hamann, C.R.; Boonchai, W.; Wen, L.; Sakanashi, E.N.; Chu, C.Y.; Hamann, K.; Hamann, D. Spectrometric analysis of mercury content in 549 skin-lightening products: Is mercury toxicity a hidden global health hazard? J. Am. Acad. Dermatol. 2014, 70, 281–287. [Google Scholar] [CrossRef]
  38. Mohammed, T.; Mohammed, E.; Bascombe, S. The evaluation of total mercury and arsenic in skin bleaching creams commonly used in Trinidad and Tobago and their potential risk to the people of the Caribbean. J. Public Health Res. 2017, 6, 1097. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  39. Murphy, T.; Kim, S.; Chanra, P.; Lim, S.; Wilson, K.; Irvine, K.N.; Allen, L. Mercury contamination of skin-whitening creams in Phnom Penh, Cambodia. J. Health Pollut. 2015, 5, 33–46. [Google Scholar] [CrossRef] [PubMed]
Figure 1. (a) Chromatogram of the standard solution of hydroquinone; (b) chromatogram of the sample solution (SLC2) of hydroquinone.
Figure 1. (a) Chromatogram of the standard solution of hydroquinone; (b) chromatogram of the sample solution (SLC2) of hydroquinone.
Sustainability 13 08786 g001
Table 1. Different brands of skin-lightening creams available in Pakistan.
Table 1. Different brands of skin-lightening creams available in Pakistan.
Obs. No. Brand NameManufacturing DateManufactured ByIngredients Mentioned
on Packaging
1.SLC14 January 2016NA Bee wax, essential oils, petrolatum, preservatives, herbal extract, fragrance.
2.SLC2February 2016Mashyam Enterprise International (Pvt) Ltd.Carnuba wax, bees wax, herbal extract, sun screen agents, emulsifiers, DM water, vitamin E, softener, preservatives and FD&C colors.
3.SLC3 December 2015NAPetrolatum, bees wax, blackberry extract, titanium dioxide, bismuth subnitrate, methyl paraben, Vitamin A, E, fragrance.
4.SLC4 March 2016NAPetrolatum, bees wax, titanium dioxide, bismuth subnitrate, methyl paraben, Vitamin A, E, fragrance.
5. SLC530 April 2015NANot mentioned
6.SLC6 22 October 2015Shaheen Cosmetics Pakistan, Lahore, PakistanAlfha arbutine, giga white, kojic acid, licorice extract, niacinamide, mulberry extract, lactic acid, emblica extract, vitamin K, ceramide, zinc oxide, mica powder, petrolatum and fragrance.
7.SLC7December 2015NAKojic acid dipalmitate, Carnauba wax, bees wax, sun screen chemcials, emulsifier, herbal extract, FD&C colors and preservatives
8.SLC8 15 October 2015NAtalcum, Petrolatum, bees wax, zinc oxide, zinc oxide, squalane, candelilla wax, stearic acid, titanium dioxide, paraffin, glyceryl monostearate, calcium carbonate, bismuth subnitrate, BHT, triclosan, methyl paraben, propyl paraben, ascorbic acid tocopheryl acetate (vitamin E), fragrance.
9.SLC9 13 March 2016Poonia Brother (Pak),
Gujranwala, Pakistan
Deionized water, vitamin A, cetyl alcohol, vitamin E, vitamin B, citric acid, vitamin B3, propyl paraben, methyle paraben, natural wax, zinc oxide, white oil, petroleum jelly, natural colors, kojic acid, fragrance.
10.SLC10 6 May 2014Unilever Pakistan Limited, Karachi, PakistanStearic acid, demineralized aqua, glycerin, perfume, butyl methoxy dibenzoyl, prophyl paraben, methylparaben, cetyl alcohol, titanium dioxide, hydrolyzed milk protein.
11.SLC11 November 2013The Stillman’s beauty Karachi, PakistanMineral oil, emollient petrolatum, C12-C18 wax, zincum, liquorice extract, retinyl palmitate, fragrance, methylparaben.
12.SLC12 February, 2016NAPetrolatum, mineral oil, propylene glycol, bee wax, candelilla wax, zinc oxide, talc, titanium dioxide, allantoin, salicylic acid, kojic acid, bismuth subnitrate, aloe vera extract, tocopheryl acetate, perfume
13.SLC13 12 March 2016NAArbutin beeswax, carnuba wax, titanium, herbal extract, sun screen agents, emulsifiers, preservatives and FD&C color.
14.SLC14 May 2016Kohinoor Chemical Co. (Pvt) Ltd.Water, palmitic acid, stearic acid, perfume, potassium stearate, cetyl alcohol, methyl paraben.
15.SLC15July 2015Thailand Petrolatum, mineral oil, bees wax, Euphorbia cerifera (candelilla) wax, bismuth subnitrate, paraffin, arbutin CAS No. 497-76-7, kojic acid, CAS No. 501-30-4, allantoin, zinc oxide, titanium dioxide, triclosan, BHT, tocopheryl acetate (vitamin E), propyl paraben, iron oxide red Cl No. 77491, iron oxide black Cl No. 77499, fragrance (rose).
16.SLC16 January 2015L.P. inter-cosmetics Co., Ltd., Bangkok, ThailandVitamin A, C, D, E, B2, B6, pyridoxine pipalmitate, biosol, allantion.
17.SLC17 April 2016NANot mentioned.
18.SLC18 April 2013H & Sons Enterprises Lahore, Punjab, PakistanBee wax, natural skin tonic.
19.SLC19 July 2015HCL London, London, UKTalcum, Petrolatum, bees wax, zinc oxide, squalene, titanium dioxide, kojic acid, stearic acid, panax ginseng extract, glyceryl monostearate, BHT, bismuth subnitrate, methyl paraben, triclosan, tocopheryl propyl paraben, vitamin E, FD&C color and fragrance.
20.SLC20 February 2015Enaura Cosmetics, New York City, USANot mentioned.
SLC = skin-lightening cream.
Table 2. The pH level in the skin-lightening creams available in Pakistan.
Table 2. The pH level in the skin-lightening creams available in Pakistan.
Obs. No.Product Name Temperature pH
1SLC1  28.37.00
2SLC2287.17
3SLC3287.09
4SLC427.76.26
5SLC528.27.10
6SLC628.67.04
7SLC7286.34
8SLC8288.00
9SLC9284.97
10SLC1028.26.90
11SLC1128.34.92
12SLC12287.00
13SLC13287.00
14SLC14307.05
15SLC15287.00
16SLC1628.36.56
17SLC1728.57.12
18SLC18287.01
19SLC1928.57.03
20SLC20 27.37.23
SLC = skin-lightening cream. Minimum value of pH = 4.92. Minimum value of temperature = 27.3. Maximum value of pH = 8.00. Maximum value of temperature = 28.6. Average value of pH = 6.43. Average value of temperature = 28.19.
Table 5. Mercury content of the cream samples available in Pakistan.
Table 5. Mercury content of the cream samples available in Pakistan.
Serial #NameConcentration (mg/kg)
ISLC1 0.8 ± 0.3
IISLC21.9 ± 0.2
IIISLC32.6 ± 0.3
IVSLC45.5 ± 0.5
VSLC52.6 ± 0.1
VISLC63.1 ± 0.1
VIISLC72.3 ± 0.1
VIIISLC80 ± 0
IXSLC97.7 ± 0.2
XSLC100.3 ± 0.05
XISLC113.5 ± 0.05
XIISLC122.5 ± 0.05
XIIISLC132.5 ± 0.1
XIVSLC140.1 ± 0.05
XVSLC153.5 ± 0.1
XVISLC162.4 ± 0.1
XVIISLC172.5 ± 0.2
XVIIISLC181.6 ± 0.05
XIXSLC190.4 ± 0.2
XXSLC205.5 ± 0.2
Note: Standard limit (Pakistan’s standard) = 1 mg/kg [25]. SLC = skin-lightening cream. Abovementioned readings are mean ± SD data. Minimum value of mercury = 0 ± 0. Maximum value of mercury = 7.7 ± 0.2. Average value of mercury = 2.56 ± 0.1.
Table 6. Total plate count of the SLC samples available in Pakistan.
Table 6. Total plate count of the SLC samples available in Pakistan.
Serial #NameColony-Forming Unit (CFU/g)
1SLC1 80 ± 1
2SLC22.8 × 102 ± 2
3SLC31.4 × 102 ± 1
4SLC41.2 × 102 ± 1
5SLC560 ± 2
6SLC640 ± 1
7SLC73.6 × 102 ± 2
8SLC82.6 × 102 ± 2
9SLC94.0 × 102 ± 1
10SLC101.0 × 102 ± 2
11SLC111.8 × 102 ± 2
12SLC120 ± 0
13SLC136.6 × 102 ± 3
14SLC141.4 × 102 ± 2
15SLC152.4 × 102 ± 2
16SLC162.2 × 102 ± 1
17SLC172.8 × 102 ± 2
18SLC187.0 × 102 ± 1
19SLC190 ± 0
20SLC205.8 × 102 ± 2
Note: US DA, ASEAN and EU limit = 1000 CFU/g [26]. SLC = skin-lightening cream. Abovementioned readings are mean ± SD data. Minimum value of TPC = 0 ± 0. Maximum TPC value = 7.0 × 102 ± 1. Average value of TPC = 2.42 × 102 ± 1.5.
Table 7. Comparison of the mercury levels of the skin-lightening creams in Pakistan with various countries.
Table 7. Comparison of the mercury levels of the skin-lightening creams in Pakistan with various countries.
Sr. No.Source of ProductConcentration of Mercury (ppm)
1.Philippines62,200 [35]
2.Mexico210,000 [36]
3.China42,875 [37]
4.Caribbean490.75 [38]
5.Cambodia12,590 [39]
6.Norway24,000 [35]
7.Denmark40,000 [35]
8.Austria38,800 [35]
9.USA41,600 [35]
10.Armenia0.08860 [35]
11.Bangladesh4643 [35]
12.Saudi Arabia5650 [35]
13.Nepal0.52 [35]
14.India0.009 [35]
15.Pakistan (This study) 7.7
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Arshad, M.; Sadef, Y.; Shakoor, M.B.; Naeem, M.; Bashir, F.; Ahmad, S.R.; Ali, S.; Abid, I.; Khan, N.; Alyemeni, M.N. Quantitative Estimation of the Hydroquinone, Mercury and Total Plate Count in Skin-Lightening Creams. Sustainability 2021, 13, 8786. https://doi.org/10.3390/su13168786

AMA Style

Arshad M, Sadef Y, Shakoor MB, Naeem M, Bashir F, Ahmad SR, Ali S, Abid I, Khan N, Alyemeni MN. Quantitative Estimation of the Hydroquinone, Mercury and Total Plate Count in Skin-Lightening Creams. Sustainability. 2021; 13(16):8786. https://doi.org/10.3390/su13168786

Chicago/Turabian Style

Arshad, Mehreen, Yumna Sadef, Muhammad Bilal Shakoor, Muhammad Naeem, Farzana Bashir, Sajid Rashid Ahmad, Shafaqat Ali, Irfan Abid, Naeem Khan, and Mohammed Nasser Alyemeni. 2021. "Quantitative Estimation of the Hydroquinone, Mercury and Total Plate Count in Skin-Lightening Creams" Sustainability 13, no. 16: 8786. https://doi.org/10.3390/su13168786

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop