Next Article in Journal / Special Issue
Hidden Formaldehyde Content in Cosmeceuticals Containing Preservatives that Release Formaldehyde and Their Compliance Behaviors: Bridging the Gap between Compliance and Local Regulation
Previous Article in Journal
Trending Anti-Aging Peptides
Previous Article in Special Issue
Insight of Malaysian Users of Cosmetic Regarding Cosmetovigilance
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

An Investigation into Incidences of Microbial Contamination in Cosmeceuticals in the UAE: Imbalances between Preservation and Microbial Contamination

by
Ammar Abdulrahman Jairoun
1,2,*,
Sabaa Saleh Al-Hemyari
1,3,
Moyad Shahwan
4,5 and
Sa’ed H. Zyoud
6,7
1
Discipline of Social and Administrative Pharmacy, School of Pharmaceutical Sciences, Universiti Sains Malaysia, Pulau Pinang 11500, Malaysia
2
Health and Safety Department, Dubai Municipality, Dubai 67, UAE
3
Pharmacy Department, Ministry of Health and Prevention, Dubai 1853, UAE
4
Department of Clinical Sciences, College of Pharmacy and Health Sciences, Ajman University, Ajman 346, UAE
5
Center of Medical and Bio-Allied Health Sciences Research, Ajman University, Ajman 346, UAE
6
Poison Control and Drug Information Center (PCDIC), College of Medicine and Health Sciences, An-Najah National University, Nablus 44839, Palestine
7
Clinical Research Centre, An-Najah National University Hospital, Nablus 44839, Palestine
*
Author to whom correspondence should be addressed.
Submission received: 18 October 2020 / Revised: 18 November 2020 / Accepted: 19 November 2020 / Published: 24 November 2020
(This article belongs to the Special Issue Cosmetovigilance: Public Health Perspective)

Abstract

:
In recent years, concern about certain personal care products and cosmetics suffering from microbial contamination has increased. In this research, we aimed to determine the types and incidence of the most common microorganisms found in unopened/unused personal care and cosmetic products in the United Arab Emirates (UAE) market. This research involved an analysis of 100 personal care products and cosmetics. For every product, microbial (Candida albicans, Staphylococcus aureus, aerobic mesophilic bacteria, Escherichia coli, yeast and mold, and Pseudomonas aeruginosa) contamination was assessed, and levels were compared with the guidelines used in Europe. Of the total samples, 15% (95% CI: 0.79–22.1) were contaminated by aerobic mesophilic bacteria compared to the maximum microbial limit of 1000 CFU/g. In addition, 13% (95% CI: 0.63–19.7) of the samples were contaminated with yeast and mold compared to the maximum microbial limit of 1000 CFU/g. Of all samples, nine (9%) were contaminated with both aerobic mesophilic bacteria and yeast and mold. However, none of the tested samples were contaminated with Escherichia coli, Staphylococcus aureus, Candida albicans, or Pseudomonas aeruginosa. Manufacturers of cosmetics and personal care products should be developing and implementing best practices regarding quality control/quality assurance in partnership with government regulators. Additionally, there should be greater control of the quality and safety of this type of product regarding good manufacturing practice (GMP), regulation, research, education, and the reporting of adverse events.

1. Introduction

Personal care products/cosmetics are popular across the globe and can be easily purchased, with no need for a prescription. This means that these products are not under the same strict regulations as those of prescription medicines. Cosmetics include any substance designed to be applied to the exterior of the human body with the intention of altering a person’s appearance, cleaning the body, perfuming the body, maintaining the skin, addressing any body odor, and/or offering skin protection [1]. Because the skin and its defenses are capable of protecting the body against external substances, there is usually no requirement for cosmetics to be aseptic [2].
Cosmeceuticals are functional cosmetic products that provide features that extend beyond the conventional purpose of enhancing or scenting skin. However, while they claim to deliver tangible benefits, they are not formally recognized from a regulatory perspective in the United States and are viewed in the same light as alternative cosmetics [3]. Many dermatologists hold the view that cosmeceuticals can improve the appearance of the skin beyond that possible using standard cosmetics because they incorporate biologically active ingredients that can penetrate below the skin barrier to improve the health of the skin [4]. Cosmeceuticals combine active ingredients with a topical mechanism that serves to preserve the integrity of the active ingredient while delivering it in a biologically viable manner, accessing the target location in an adequate way to achieve a given effect. The topical employed also needs to have the ability to allow the active ingredient to be released from the carrier vehicle. In light of the lack of the regulatory acceptance of cosmeceuticals, there is a need for an efficacy assessment to be performed to verify the effectiveness of cosmeceuticals.
Although most cosmetic/personal care products are not harmful, recently, numerous concerns have been voiced regarding product quality and the marketing of such products. The manufacturing and sale of cosmetic/personal care products should undergo strict monitoring and regulation, and data should be collected and evaluated in relation to any adverse effects caused by them to make them safer for use. A significant concern regarding the quality/safety of cosmetic products is that the product can become spoiled by contamination with microorganisms, which can pose significant health risks for users [5,6].
The skin barrier ceases to function with certain inflammatory dermatoses, such as atopic dermatitis; this is also the case where mechanical trauma or burns have been experienced. In these instances, the dangers of infection are significantly increased when the subject uses a cosmetic that has been microbially contaminated. Elderly people, children (below the age of three), and those whose immune systems are compromised are especially vulnerable to such contamination [7]. Because the skin in the periocular region is particularly delicate, products intended for application on or around the eyes are of particular concern [2].
Cosmetics can become microbially contaminated in two instances: (1) When manufactured or placed in a container and (2) when the consumer uses the product. In the first instance, the manufacturer must take steps to prevent microbial contamination so that the product is of the specified quality and consumer safety is protected. When the product is in use, consumers have a responsibility to keep it safe, e.g., by following the instructions for safe storage [2]. If cosmetic creams contain microorganisms, either from the manufacturing process or due to poor handling by users, this may cause a health hazard. Researchers have isolated a range of pathogenic microorganisms found in cosmetics [8].
One concerning issue is that cosmetics are not provided with production and/or expiration dates, which is surprising given that the preservatives used in cosmetics can degrade over time. In addition, cosmetics contain growth factors, organic and inorganic compounds, and essential minerals, and they are often stored under humid conditions, e.g., bathrooms, allowing microorganisms to flourish [9].
Cosmetic/personal care products sold in the United Arab Emirates (UAE) are generally tested as part of the consumer standards process, with regulators checking products for microbial contamination in the laboratory to make sure that there is no microbial growth in the product. Regulators also check that all products contain ingredients specified on their labels. One element of being approved for sale is that manufacturers provide a declaration that they have tested the product, that it does not have any microbial contamination, and that it is fully compliant with health and safety regulations. Guidelines specify that every new batch of products offered on the market should be routinely tested for microbial contamination. Such monitoring is essential as products are increasingly being recalled, and most recalls are due to contamination with potentially pathogenic microorganisms [8]. Further information about how these products become contaminated is required [10]. The objective of this study was to determine the type and incidence of predominant microorganisms and microbial contamination in unused cosmetic and personal care products (finished products) at the point of sale in the UAE.

2. Methodology/Materials

2.1. Collection of Samples (Sampling Methodology)

A search was performed on local business directories to find all retail outlets that offer cosmetic/personal care products. The business directories list all healthcare retailers, pharmacies, and parapharmacies in the UAE. In total, 2183 were listed, and a sampling framework was created using an Excel spreadsheet that contained all of the information required, e.g., the name of the business, address, telephone number, and email. The study sample was selected using standard random sampling methods employing the business ID numbers, which were categorized by location and type. For each location selected, a package of every cosmetic/personal care product being sold was randomly selected with no screening for the place of manufacturing. All items were given code reference numbers so that they could be tracked and to prevent duplication. The following details were recorded for each sample: The product name, brand name, type of item, country of origin/manufacturer, subcategory, dosage form, batch number, bar code, size/volume, recommended dosage, and location of the retail outlet supplying the particular product. If an identical product was stocked by multiple outlets (i.e., identical product name, manufacturer, formulation, barcode, and size/volume), the earliest selected product underwent testing, and duplicate products were returned. Products sharing the same name but had different manufacturers or more than one format (e.g., emulsion and cream) were classified as individual products, and both underwent testing. Each selected product underwent laboratory analysis on the same day it was chosen.

2.2. Standards and Guidelines Used for the Detection of Microorganisms

The BS EN ISO 21150:2015 standard was used to detect and identify the specified microorganisms. This procedure, which was applied to enumerate the microorganisms from cosmetic products, involves direct colony counts and enrichment culturing. In direct colony counts, we could count the total aerobic mesophilic bacteria (total aerobic microbial count and total yeast and mold count). In enrichment culturing, we could detect specified harmful pathogens and their presence, such as the detection of Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Candida albicans. All the chemicals used were of analytical grade and purchased from Sigma-Aldrich, USA.

2.3. Enumeration of Aerobic Mesophilic Bacteria

Based on the solubility of the product, enumeration was performed using the pour plate method or membrane filtration method. The pour plate method utilized 1 g/1 mL of the product transferred to 9 mL of diluent (MLB), which was mixed well until the sample dissolved. In the case of water-insoluble products, we transferred a 1 g/1 mL of sample to 9 mL of MLB containing 0.1% polysorbate 80 (neutralizer) and mixed it well. From this preparation, 1 mL of each sample was plated on a sterile 90 mm Petri dish in duplicate and pour plated with 20 mL of MLA for enumeration of the aerobic mesophilic bacteria. The MLA plates were incubated at 32.5 ± 2.5 °C for 3 to 5 days, and we calculated the number of CFUs per mL or per g of the product and reported the results.

2.4. Enumeration of Yeast and Mold

Based on the solubility of the product, enumeration was performed using the pour plate method or membrane filtration method. The pour plate method utilized 1 g/1 mL of the product transferred to 9 mL of diluent (MLB), which was mixed well until the sample dissolved. In the case of water-insoluble products, we transferred 1 g/1 mL of sample to 9 mL of MLB containing 0.1% polysorbate 80 (neutralizer) and mixed it well. From this preparation, 1 mL of each was plated on a sterile 90 mm Petri dish in duplicate, with 20 mL of SDCA for enumeration of the yeast and mold. For known or noncontaminated bacterial products, SDA medium was used. The media plates were incubated at 255 ± 2.5 °C for 3 to 5 days, and we calculated the number of CFUs per mL or per g of the product and reported the results.

2.5. Detection of Escherichia coli

First, 1 g/1 mL of the product was transferred to 9 mL of diluent (MLB) and incubated at 30–35 °C for 20–72 h. After completion of the enrichment broth, incubation of the subculture on a plate of Macconkey agar at 30–35 °C was performed for 18 to 72 h. The growth of brick red colonies with a surrounding zone of precipitated bile on the Macconkey agar indicated the presence of Escherichia coli. This was confirmed by an identification test using Indole and EMB agar. The confirmation test for Escherichia coli was the indole test. A loop full of culture was transferred to 5 mL of sterile tryptone broth and incubated at 42–44 °C for 24 h. After incubation, 0.5 mL of Kovac’s reagent was added to each tube, shaken well, and allowed to stand for 10 min. If any red color was observed in the reagent layer, indole was present, which confirmed the possible presence of Escherichia coli. From the Macconkey agar subculture, a loop full was placed on EMB agar and incubated for 18–24 h at 30–35 °C. E. coli colonies were dark, centered, and flat, with or without a metallic sheen. We performed Gram staining and found Gram-negative rods and motile and smooth colonies.

2.6. Detection of Staphylococcus aureus

First, 1 g/1 mL of the product was transferred to 9 mL of diluent (MLB) and incubated at 30–35 °C for 20–72 h. After completion of the enrichment broth, incubation of the subculture on a plate of Baired Parker agar was performed and incubated at 30–35 °C for 18 to 24 h. Black, shiny colonies surrounded by clear zones were observed. Further confirmation was performed using the catalase test, coagulase test, and Gram staining. Staphylococcus aureus is a Gram-positive coccus, catalase positive, and coagulase positive.

2.7. Detection of Pseudomonas aeruginosa

First, 1 g/1 mL of the product was transferred to 9 mL of diluent (MLB) and incubated at 30–35 °C for 20–72 h. After completion of the enrichment broth, incubation of the subculture on a plate of cetrimide agar was performed, and the plate was incubated at 30–35 °C for 18 to 24 h. Yellow to green colonies were fluorescent under UV. Further confirmation was performed by the oxidase test and Gram staining. Pseudomonas aeruginosa is a Gram-negative and oxidase-positive bacterium, allowing for the detection of pycocyanin in Pseudomonas agar.

2.8. Detection of Candida albicans

First, 1 g/1 mL of the product was transferred to 9 mL of diluent (MLB) and incubated at 30–35 °C for 20–72 h. After completion of the enrichment broth, incubation of the subculture on a plate of Sabouraud Chloramphenicol agar was performed, and the plate was incubated at 30–35 °C for 18 to 24 h. Candida albicans produces white to beige colonies on media. The presence of this fungus was also confirmed by a germ tube test using horse serum.

2.9. Reporting of Values

The total bacterial count and total fungal count are reported as CFU/g or mL, accounting for a dilution factor, and the detection parameter is reported as present or absent/g.

2.10. Quality Control and Assurance

All the media prepared were checked for sterility and contamination, and a quality control evaluation was performed with suitable positive and negative control strains of the respective media.

2.11. Ethical Considerations

The study was awarded approval from the Institutional Review Board of An-Najah National University (reference number Phd/3/20/3).

3. Statistical Analysis

The data were analyzed using SPSS version 24 (Chicago, IL, USA). Percentages and frequencies were used to summarize the qualitative variables. The concentrations of microbial contamination (mold and yeast, Staphylococcus aureus, Candida albicans, Pseudomonas aeruginosa, Escherichia coli, and aerobic mesophilic bacteria) were measured and checked against European guidelines (Table 1). The incidence of microbial contamination was classified as the proportion of the product that exceeded the maximum permitted microbiological level for any of the pathogens tested. Chi-square and Fisher exact tests were employed to study the prevalence of microbial contamination in accordance with the product characteristics. The statistically significant boundary was set at p < 0.05.

4. Results

4.1. Sample Description

A total of 100 cosmetics and personal care products were analyzed in this study. Of the 100 samples, 39 (39%) were body care preparations, 8 (8%) were eye care preparations, 21 (21%) were face and neck care preparations, 21 (21%) were hair and scalp care preparations, and 11 (11%) were oral hygiene products. Regarding the country of origin, 9 (9%) were manufactured in China, 15 (15%) in the EU, 14 (14%) in India, 8 (8%) in Korea, 10 (10%) in the Middle East, 32 (32%) in the United Arab Emirates, and 12 (12%) in the United States (Table 1).

4.2. Evaluation of the Incidence of Bacterial and Fungal Contamination in the Cosmetics and Personal Care Products

Table 2 summarizes the number of test results in which the measured colony-forming units were below the limit of detection (LOD). The incidence of microbial contamination is summarized in Table 3. These are the proportions of cosmetics and personal care products that were contaminated with microorganisms. Of all the samples, 15% (95% CI: 0.79–22.1) were contaminated by aerobic mesophilic bacteria compared to the maximum microbiological limit of 1000 CFU/g. Additionally, 13% (95% CI: 0.63–19.7) of the samples were contaminated with yeast and mold compared to the maximum microbiological limit of 1000 CFU/g. Of all samples, 9 (9%) were contaminated by both aerobic mesophilic and yeast and mold. However, none of the tested samples were contaminated with Escherichia coli, Staphylococcus aureus, Candida albicans, or Pseudomonas aeruginosa. The overall incidence of microbial contamination was 19% (95% CI: 11.2–26.8). The estimated microbial contamination for the 100 products is presented graphically in histograms (Figure 1 and Figure 2). The relevant microbiological maximum limits are displayed as vertical “cut-off” limits. The results of the microbial contamination categorized by sample characteristics for each sample are provided in Table 4.

4.3. Comparison of Microbial Contamination According to Sample Characteristics

Table 5 shows the distribution of microbial contamination according to the sample characteristics. The table also provides the estimates with the p-values. These p-values were obtained from the results of the chi-square and Fisher’s exact tests.
Comparisons of the groups did not reveal any significant differences in relation to microbial contamination.
Although not significant, the incidence of microbial contamination with aerobic mesophilic bacteria was higher for body care preparations (20.5%) and hair and scalp care (19%) than for the other categories of cosmetics. Moreover, the incidence of microbial contamination by yeast and mold was higher for oral hygiene products (18.2%) and body care preparations (15.4%) than for the other categories of cosmetics. Regarding the country of origin, products manufactured in the Middle East (30.0%), India (28.6%), and the USA (25.0%) were more susceptible to contamination with aerobic mesophilic bacteria than those manufactured in the other studied places. In addition, products manufactured in the USA (33.3%) and Middle East (20%) were more likely to be contaminated by yeast and mold than by the other contaminants.

5. Discussion

In recent years, concern has been increasing regarding the biological contamination of cosmetic/personal care products. As the consumption of such products has increased, considerable research has been undertaken to evaluate the microbial contamination in these products. The number of people buying these products has risen, and the size of the market has expanded more quickly than the population. This research looked at the levels of microbial contamination in cosmetic/personal care products offered to the market in the UAE and assessed the most important risk factors causing this type of contamination.
In this study, 19 of the 100 samples (19%) were shown to carry some level of microbiological risk. First, 15 samples (15%) displayed aerobic mesophilic bacteria contamination. The levels of contamination with colony-forming units of these microorganisms were between 200 and 8965 CFU/g for talcum powder, 7623 CFU/g for toothpaste, between 700 and 2345 CFU/g for hair gel, between 1120 and 5780 CFU/g for body care preparations, between 4200 and 6876 CFU/g for facial/neck care products, and between 500 and 57,000 CFU/g for henna products. Past research has revealed similar problems of microbial contamination with aerobic mesophilic bacteria in both new and partly used cosmetics [11,12].
Thirteen of the 100 samples under analysis in this study (13%) exhibited yeast and mold contamination. The levels of total colony-forming units were between 100 and 1872 CFU/g for talcum powder, between 1239 and 7623 CFU/g for oral hygiene products, 1287 CFU/g for eyebrow gel, between 700 and 2345 CFU/g for hair gel, between 300 and 2462 CFU/g for body care preparations, 2369 CFU/g for facial moisturizer, and between 100 and 7500 CFU/g for henna products. These findings agree with past research in which mold and yeast were found in certain tested cosmetic products [8,9,13]. However, other research found no mold or yeast in any of their product samples [14].
Microbiological contamination of cosmetic/personal care products can be caused by the conditions/environment employed for growing and harvesting raw materials, how these materials are stored and transported, and/or the manufacturing environment used for the final product. Therefore, high standards of manufacturing protocols must be adhered to, and all raw materials, especially those that originate naturally, should be analyzed for contamination beforehand and checked that they fall within acceptable parameters. Every area susceptible to contamination should be identified and suitable controls should be introduced. Interestingly, our findings showed that talcum powder was one of the most contaminated products, exhibiting yeast and mold and aerobic mesophilic bacterial contamination. Such products are frequently exposed to air. Additionally, the natural ingredients that comprise these products, including bentonite, Fuller’s earth, and talc, could increase the contamination levels [15]. Another significant concern surrounding this research was the high levels of contamination of yeast and mold and aerobic mesophilic bacteria in cosmetic creams. These levels are due to the fact that cosmetic creams have rich textures created using growth factors, essential minerals, and high moisture levels; with a wide spread of organic and inorganic compounds, this creates a good environment for microbes to grow [16,17,18]. Cosmetic products that have a high moisture content are those that are most likely to have microbial contamination; consideration should be given to changing the ingredients of these products, or they may threaten consumer health [19,20]. In terms of other forms of microbial contamination, this research found positive outcomes, with no samples displaying any contamination from Pseudomonas aeruginosa, Candida albicans, Staphylococcus aureus, or Escherichia coli. These findings do not match those of some European studies, which found that the majority of cosmetic contamination was caused by Gram-negative bacteria, chiefly Pseudomonas aeruginosa and Enterobacter gergoviae; Staphylococcus aureus was the most frequently identified of the Gram-positive bacteria. The same research found that Candida albicans was the most prevalent fungus [2]. The fact that products offered for sale in the UAE have such low levels of microbiological and other contamination may be attributed to the robust regulatory provisions in the UAE. All cosmetic/personal care products offered on the market are obliged by municipalities and health regulators to register so that they can be checked for safety, effectiveness, and quality. Furthermore, microbial contamination remains a central reason for the recall of products worldwide, especially in developing nations in the tropics [21]. The results of this study showed that products from India, the Middle East, and the USA had the highest levels of microbial contamination. In the European study previously mentioned, almost 50% of the products that were found to have microbiological risks were produced in one of the following five nations: Germany (18.27%), France (7.69%), the Czech Republic (6.73%), Greece (6.73%), and India (6.73%). Therefore, it is essential that preservative systems [20,21,22,23] are improved to prevent microorganism contaminants from growing or being manufactured, stored, and employed by consumers; the use of noninvasive packaging would also improve matters [24,25].

6. Conclusions

To date, no study has investigated the microbial contamination of cosmetic/personal care products offered for sale in the UAE. Furthermore, a quantitative analysis of international reports regarding this issue is lacking. This information could be useful for manufacturers, regulators, and health care providers, who may need to treat patients experiencing skin infections caused by organisms of unknown provenance. This study is a significant contribution to the knowledge regarding the distribution of microbiota within cosmetic products. Manufacturers should be prioritizing the ability to guarantee that their cosmetics contain appropriate preservatives. The findings of this study could be helpful for those producing novel challenge tests in experiments to develop guaranteed ways of preserving cosmetic products by identifying the most prevalent types of bacteria. These results have also indicated that it is vital that manufacturing facilities, equipment, tools, storage containers, etc., should all adhere to the highest standards of hygiene. To reduce contamination levels, manufacturers must adhere to all good manufacturing practice (GMP) protocols. All raw materials should meet an agreed standard and be properly tested for quality control. Further measures that manufacturers could take against contamination are taking control of validating processes, introducing training for workers, and revising and enhancing cleaning/sanitation procedures.
Cosmetic microbiology is a complicated field because there are numerous different formulations, manufacturing processes, and products that are used by a wide variety of consumers in many different environments. This study revealed two important elements: (1) Cosmetics are exposed to a wide range of possible contaminants in the manufacturing process, especially those carried by raw materials, and (2) moisture content (water) is the most frequently included ingredient that poses clear difficulties. However, even apparently benign substances, such as talc, may contain hazardous levels of pathogens. The manufacturers of cosmetic/personal care products must formulate and put into practice rigorous protocols for quality control and assurance, and these should be monitored by government regulation. Both the quality and safety of cosmetic/personal care products must be more strictly regulated concerning reporting mechanisms for issues of concern, research, education, regulatory procedures, and GMP.

Author Contributions

Conceptualization, A.A.J. and S.S.A.-H.; methodology, M.S.; software, A.A.J.; validation, S.H.Z. and M.S.; formal analysis, A.A.J.; investigation, S.S.A.-H.; resources, S.H.Z.; data curation, A.A.J.; writing—original draft preparation, S.S.A.-H.; writing—review and editing, M.S.; visualization, A.A.J.; supervision, S.H.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. European Parliament, Council of the European Union. Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009 on Cosmetic Products; European Parliament, Council of the European Union: Brussels, Belgium, 2009. [Google Scholar]
  2. Michalek, I.M.; John, S.M.; Caetano dos Santos, F.L. Microbiological contamination of cosmetic products–observations from Europe, 2005–2018. J. Eur. Acad. Dermatol. Venereol. 2019, 33, 2151–2157. [Google Scholar] [CrossRef] [PubMed]
  3. Kligman, A.M. Cosmeceuticals as a third category. Cosmet. Toilet 1998, 113, 33–41. [Google Scholar]
  4. Vermeer, B.J.; Gilchrest, B.A. Cosmeceuticals: A proposal for rational definition, evaluation and regulation. Arch. Dermatol. 1996, 132, 337–340. [Google Scholar] [CrossRef] [PubMed]
  5. Behravan, J.; Bazzaz, F.; Malaekeh, P. Survey of bacteriological contamination of cosmetic creams in Iran (2000). Int. J. Dermatol. 2005, 44, 482–485. [Google Scholar] [CrossRef] [PubMed]
  6. Becks, V.E.; Lorenzoni, N.M. Pseudomonas aeruginosa outbreak in a neonatal intensive care unit: A possible link to contaminated hand lotion. Am. J. Infect. Control 1995, 23, 396–398. [Google Scholar] [CrossRef] [PubMed]
  7. The Scientific Committee on Consumers Safety, Directorate-General for Health and Consumer Protection of the European Commission. The SSCS’s Notes of Guidance for the Testing of Cosmetic Ingredients and Their Safety Evaluation, 10th ed.; European Comission: Brussels, Belgium, 2018. [Google Scholar]
  8. Anelich, L.E.; Korsten, L. Survey of micro-organisms associated with spoilage of cosmetic creams manufactured in South Africa. Int. J. Cosmet. Sci. 1996, 18, 25–40. [Google Scholar] [CrossRef] [PubMed]
  9. 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, 159–163. [Google Scholar] [CrossRef] [PubMed]
  10. Lundov, M.D.; Zacharian, C. Recall of microbiologically contaminated cosmetics is Eu from 2005 to May 2008. Int. J. Cosmet. Sci. 2008, 30, 471–474. [Google Scholar] [CrossRef] [PubMed]
  11. Scientific Committee on Consumer Products. The SCCP’s Notes of Guidance for the Testing of Cosmetic Ingredients and Their Safety Evaluation. 2006. Available online: http://ec.europa.eu/health/scientific_committees/consumer_safety/docs/sccs_s_006.pdf (accessed on 13 June 2020).
  12. Nasser, L.A. Fungal profiles isolated from open and used cosmetic products collected from different localities in Saudi Arabia. Saudi J. Biol. Sci. 2008, 15, 121–128. [Google Scholar]
  13. Flores, M.; Morillo, M.; Crespo, M.L. Deterioration of raw materials and cosmetic products by preservative resistant microorganisms. Int. Biodeterior. Biodegrad. 1997, 40, 157–160. [Google Scholar] [CrossRef]
  14. Abaas, I.S.; Mohammed, H.R.; Majeed, A.H. The microbial contamination study of some herbal cosmatics products used in traditional medicine in Iraq. Karbala J. Pharm. Sci. 2013, 6, 132–140. [Google Scholar]
  15. Kulkarni, S.B.; Bajpai, N.D.; Meghre, V.S. Evaluation of dome marketed facepacks and cakes for microbial load. Asian J. Microbiol. Biotechnol. Environ. Sci. 2011, 13, 213–216. [Google Scholar]
  16. Kabara, J.J.; Orth, D.S. (Eds.) Preservative-free and self-preserving cosmetics and drugs. In Principles for Product Preservation; Marcel Dekker: New York, NY, USA, 1997; Volume 31, pp. 1–14. [Google Scholar]
  17. Wedderburn, D.L. Preservation of emulsions against microbial attack. In Advances in Pharmaceutical Sciences; Bean, A.H., Beckett, J.E., Carless, H.S., Eds.; Academic Press: London, UK, 1964; Volume 1, pp. 195–268. [Google Scholar]
  18. Elmorsy, T.H.; Hafez, E.A. Microbial contamination of some cosmetic preparations in Egypt. J. Agric. Technol. 2016, 12, 471–481. [Google Scholar]
  19. Steinberg, D.C. Preservatives for Cosmetics, 2nd ed.; Allured Publishing: Carol Stream, IL, USA, 2006; pp. 2–7. [Google Scholar]
  20. Lundov, M.D.; Moesby, L.; Zachariae, C.; Johansen, J.D. Contamination versus preservation of cosmetics: A review on legislation, usage, infections, and contact allergy. Contact Dermat. 2009, 60, 70–78. [Google Scholar] [CrossRef] [PubMed]
  21. Okeke, I.N.; Lamikanra, A. Bacteriological quality of skin-moisturizing creams and lotions distributed in a tropical developing country. J. Appl. Microbiol. 2001, 23, 922–928. [Google Scholar] [CrossRef] [PubMed]
  22. Farrington, J.K.; Martz, E.L.; Wells, S.J.; Ennis, C.C.; Holder, J.; Levchuk, J.W.; Avis, K.E.; Hoffman, P.S.; Hitchins, A.D.; Madden, J.M. Ability of laboratory methods to predict in-use efficacy of antimicrobial preservatives in an experimental cosmetic. Appl. Environ. Microbiol. 1994, 1, 4553–4558. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Lintner, K.; Genet, V. A physical method for preservation of cosmetic products. Int. J. Cosmet. Sci. 1998, 20, 103–115. [Google Scholar] [CrossRef] [PubMed]
  24. Brannan, D.K.; Dille, J.C. Type of closure prevents microbial contamination of cosmetics during consumer use. Appl. Environ. Microbiol. 1990, 1, 1476–1479. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Campana, R.; Scesa, C.; Patrone, V.; Vittoria, E.; Baffone, W. Microbiological study of cosmetic products during their use by consumers: Health risk and efficacy of preservative systems. Lett. Appl. Microbiol. 2006, 43, 301–306. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Histogram of the estimated aerobic mesophilic bacteria (CFU/g) for cosmetics and personal care products (n = 100). The vertical dashed line shows the microbiological maximum limits according to BS EN ISO 21150:2015.
Figure 1. Histogram of the estimated aerobic mesophilic bacteria (CFU/g) for cosmetics and personal care products (n = 100). The vertical dashed line shows the microbiological maximum limits according to BS EN ISO 21150:2015.
Cosmetics 07 00092 g001
Figure 2. Histogram of the estimated yeast and mold (CFU/g) for cosmetics and personal care products (n = 100). The vertical dashed line shows the microbiological maximum limits according to BS EN ISO 21150:2015.
Figure 2. Histogram of the estimated yeast and mold (CFU/g) for cosmetics and personal care products (n = 100). The vertical dashed line shows the microbiological maximum limits according to BS EN ISO 21150:2015.
Cosmetics 07 00092 g002
Table 1. Number and percentage of cosmetics and personal care product characteristics (n = 100).
Table 1. Number and percentage of cosmetics and personal care product characteristics (n = 100).
CharacteristicsGroupsFrequencyPercentage
CategoriesBody care3939%
Eye care88%
Face and neck care2121%
Hair and scalp care2121%
Oral hygiene products1111%
Country of originChina99%
EU1515%
India1414%
Korea88%
The Middle East1010%
UAE3232%
USA1212%
Table 2. Distribution of cosmetic products that contained the tested microorganisms below the limit of detection (n = 100).
Table 2. Distribution of cosmetic products that contained the tested microorganisms below the limit of detection (n = 100).
Microorganism TypeNumber of Cosmetics with Microorganisms under the LOD
FrequencyPercentage
Aerobic mesophilic bacteria8080%
Yeast and mold8282%
Escherichia coli100100%
Staphylococcus aureus100100%
Candida albicans100100%
Pseudomonas aeruginosa100100%
Table 3. Estimation of the microbial contamination rate in the sampled cosmetics and personal care products (n = 100).
Table 3. Estimation of the microbial contamination rate in the sampled cosmetics and personal care products (n = 100).
Microorganism TypeMicrobiological Maximum LimitsCosmetics Exceeding the Maximum Limit
N%95% CI
LowerUpper
Aerobic mesophilic bacteria1000 CFU/g1515%0.7922.1
Yeast and mold1000 CFU/g1313%0.6319.7
Escherichia coliAbsenceNDNDND
Staphylococcus aureusAbsenceNDNDND
Candida albicansAbsenceNDNDND
Pseudomonas aeruginosaAbsenceNDNDND
Maximum allowable limits according to BS EN ISO 21150:2015. ND, not deleted.
Table 4. List of tested cosmetics and personal care products according to microbial contamination and sample characteristics.
Table 4. List of tested cosmetics and personal care products according to microbial contamination and sample characteristics.
Name of the ProductMain CategoryCountry of OriginStaphylococcus aureus (per g)Yeast and Mold CFU/gCandida albicans (per g)Aerobic Mesophilic Bacteria CFU/gPseudomonas aeruginosa (per g)
Body lotionBody care preparationUAEND<10ND<10ND
Facial cleanserFace and neck careUAEND<10ND<10ND
Petroleum jellyBody care preparationUAEND<10ND<10ND
Petroleum jellyBody care preparationUAEND<10ND<10ND
HennaHair and scalp careIndiaND100ND500ND
HennaHair and scalp careIndiaND7500ND57,000ND
Herbal hennaHair and scalp careIndiaND3800ND13,800ND
ShampooHair and scalp careUAEND<10ND<10ND
Hair crèmeHair and scalp careUAEND<10ND<10ND
Hair styling gelHair and scalp careEUND<10ND<10ND
Shower gelBody care preparationEUND<10ND<10ND
Face moisturizing creamFace and neck careUAEND2369ND6876ND
Facial scrubFace and neck careUAEND<10ND<10ND
Body crème milkBody care preparationUSAND1500ND1235ND
Body washBody care preparationEUND<10ND<10ND
Hair styling gelHair and scalp careKoreaND<10ND<10ND
Hair oilHair and scalp careUAEND<10ND<10ND
EyelinerEye careUAEND<10ND50ND
Hair oilHair and scalp careEUND<10ND<10ND
Moisturizing body creamBody care preparationUAEND<10ND<10ND
Smooth hair creamHair and scalp careIndiaND<10ND<10ND
Vaseline body butterBody care preparationUAEND<10ND<10ND
EyelinerEye careUAEND<10ND<10ND
Moisturizing body emulsionBody care preparationChinaND<10ND<10ND
Facial nourishing cleanserFace and neck careChinaND<10ND<10ND
MouthwashOral hygiene productUSAND<10ND<10ND
Vaseline body creamBody care preparationChinaND<10ND<10ND
Face tonerFace and neck careChinaND<10ND<10ND
Petroleum jellyBody care preparationUAEND<10ND<10ND
Fair creamHair and scalp careIndiaND<10ND<10ND
Anti-stretch-mark moisturizing body creamBody care preparationKoreaND<10ND<10ND
Anticellulite stretch mark firming body creamBody care preparationUSAND2462ND1120ND
Cleansing facial soapFace and neck careKoreaND<10ND<10ND
Face cleansing and brighteningFace and neck careIndiaND<10ND<10ND
Hair loss shampooHair and scalp careUAEND<10ND<10ND
SunscreenBody care preparationUSAND<10ND<10ND
Mouth rinseOral hygiene productEUND<10ND<10ND
Face maskFace and neck careMiddle EastND<10ND<10ND
Hair styling gelHair and scalp careChinaND<10ND<10ND
Toothpaste and mouth rinseOral hygiene productUSAND<10ND<10ND
Facial cleanserFace and neck careIndiaND<10ND<10ND
Hair styling gelHair and scalp careMiddle EastND2345ND1700ND
SoapBody care preparationMiddle EastND<10ND<10ND
Facial scrubFace and neck careEUND<10ND<10ND
Facial scrubFace and neck careMiddle EastND<10ND4200ND
MouthwashOral hygiene productUAEND<10ND<10ND
Moisturizing body lotionBody care preparationEUND2000ND<10ND
Hair styling gelHair and scalp careUAEND<10ND<10ND
ToothpasteOral hygiene productUAEND<10ND<10ND
Face foundationFace and neck careUSAND<10ND<10ND
MouthwashOral hygiene productUSAND1239ND<10ND
Face cleaning waterFace and neck careKoreaND<10ND<10ND
Antistain body creamBody care preparationMiddle EastND1246ND5780ND
Firming and wrinkle removal body creamBody care preparationMiddle EastND<10ND<10ND
Body creamBody care preparationMiddle EastND<10ND<10ND
Body creamBody care preparationUSAND<10ND<10ND
Face wipe off fleckFace and neck careMiddle EastND<10ND<10ND
Whitening skin creamBody care preparationMiddle EastND<10ND<10ND
Extensions volume mascaraEye careChinaND<10ND<10ND
Fluoride toothpasteOral hygiene productEUND<10ND<10ND
ToothpasteOral hygiene productChinaND<10ND<10ND
ToothpasteOral hygiene productChinaND<10ND<10ND
Talc body powderBody care preparationUAEND<10ND200ND
Talc body powderBody care preparationUAEND1235ND8965ND
Talc body powderBody care preparationUAEND<10ND<10ND
Talc body powderBody care preparationUAEND<10ND400ND
Talc body powderBody care preparationUAEND<10ND600ND
Talc body powderBody care preparationUAEND1872ND<10ND
Talc body powderBody care preparationUAEND<10ND<10ND
Talc body powderBody care preparationUAEND100ND1200ND
Talc body powderBody care preparationUAEND100ND1500ND
Hair styling gelHair and scalp careIndiaND700ND21,000ND
HennaHair and scalp careIndiaND<10ND<10ND
Body oilBody care preparationEUND<10ND<10ND
Sun creamBody care preparationKoreaND<10ND<10ND
Body oilBody care preparationKoreaND<10ND<10ND
Face scrubFace and neck careIndiaND<10ND<10ND
Deodorant powderBody care preparationEUND<10ND1800ND
Face creamFace and neck careEUND<10ND<10ND
EyelinerEye careEUND<10ND<10ND
Milk body maskBody care preparationKoreaND<10ND<10ND
Fragrance talc body powderBody care preparationUSAND<10ND<10ND
MouthwashOral hygiene productKoreaND<10ND<10ND
Dead Sea concentrated waterBody care preparationMiddle East0<10ND<10ND
EyelinerEye careIndia0<10ND<10ND
Eyebrow powderEye careChina0<10ND<10ND
Eyes brow gelEye careEU01287ND<10ND
Facial balancing cleanserFace and neck careIndia0<10ND<10ND
Hair conditionerHair and scalp careUSA0<10ND<10ND
Face powderFace and neck careEU0<10ND<10ND
Facial argan oil scrubFace and neck careUAE0<10ND<10ND
Detoxifying scrubBody care preparationUAE0<10ND<10ND
Hair oilHair and scalp careIndia0<10ND<10ND
Heat powderBody care preparationIndia0300ND1900ND
Face cleansing gelFace and neck careUAE0<10ND<10ND
Under eye creamEye careUAE0<10ND<10ND
ShampooHair and scalp careEU0<10ND<10ND
ShampooHair and scalp careUSA0<10ND<10ND
ToothpasteOral hygiene productUSA07623ND1234ND
Facial scrubFace and neck careUAE0<10ND<10ND
Table 5. Incidence of microbial contamination according to sample characteristics.
Table 5. Incidence of microbial contamination according to sample characteristics.
Incidence of Microbial Contamination
Aerobic Mesophilic BacteriaYeast and MoldAll
Total15 (15%)13 (13%)19 (19%)
Categories
Body care preparations8 (20.5%)6 (15.4%)10 (25.6%)
Eye care01 (12.5%)1 (12.5%)
Face and neck care2 (9.5%)1 (4.8%)2 (9.5%)
Hair and scalp care4 (19.0%)3 (14.3%)4 (19%)
Oral hygiene products1 (9.1%)2 (18.2%)2 (18.2%)
p-Value0.4920.7820.633
Country of origin
China000
EU1 (6.7%)2 (13.3%)3 (20.0%)
India4 (28.6%)2 (14.3%)4 (28.6%)
Korea000
Middle East3 (30.0%)2 (20.0%)3 (30.0%)
UAE4 (12.5%)3 (9.4%)5 (15.6%)
USA3 (25.0%)4 (33.3%)4 (33.3%)
p-Value0.1910.2570.281
p < 0.05 was considered statistically significant.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Jairoun, A.A.; Al-Hemyari, S.S.; Shahwan, M.; Zyoud, S.H. An Investigation into Incidences of Microbial Contamination in Cosmeceuticals in the UAE: Imbalances between Preservation and Microbial Contamination. Cosmetics 2020, 7, 92. https://0-doi-org.brum.beds.ac.uk/10.3390/cosmetics7040092

AMA Style

Jairoun AA, Al-Hemyari SS, Shahwan M, Zyoud SH. An Investigation into Incidences of Microbial Contamination in Cosmeceuticals in the UAE: Imbalances between Preservation and Microbial Contamination. Cosmetics. 2020; 7(4):92. https://0-doi-org.brum.beds.ac.uk/10.3390/cosmetics7040092

Chicago/Turabian Style

Jairoun, Ammar Abdulrahman, Sabaa Saleh Al-Hemyari, Moyad Shahwan, and Sa’ed H. Zyoud. 2020. "An Investigation into Incidences of Microbial Contamination in Cosmeceuticals in the UAE: Imbalances between Preservation and Microbial Contamination" Cosmetics 7, no. 4: 92. https://0-doi-org.brum.beds.ac.uk/10.3390/cosmetics7040092

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