Dear Editor-in-Chief
Worldwide, the most important factor of various qualifications of skin care experts is hygiene conception to maintain cleanliness. Among the many cleansing tools are cleansing cream or oil, massage cream, face pack, and sponge. Sponge is the most frequently used in washing and has the advantage of effectively removing dust, residue, and oil, without skin stimulation during skin care management. In particular, from a health perspective, it reduces skin temperature (1).
Sponge is classified into natural and synthetic resins. A natural sponge is harvested from oceanic organisms. Germ multiplication in natural sponges is low because they absorb and dries water rapidly. However, they are expensive and vulnerable to sunlight and soap. By contrast, synthetic sponges are relatively cheaper and less sensitive to sunlight. Hence, most Korean skin-care shops use synthetic sponges. However, the use of synthetic sponges has various adverse effects due to wrong reuse of sponges (2). Of these adverse effects are various types of microbism that causes skin infection. The representative pathogens that cause skin infections are Staphylococcus aureus, gram-positive bacteria, gram-negative bacteria, and eumycetes. These pathogens and eumycetes cause various skin problems such as folliculitis, boil, cellulites, and impetigo (3).
The number of times disinfection, drying, and rinsing are performed before reuse of sponges greatly differ between Korean skin-care shops. Regarding sponge drying, 62.6% of Korean skin-care shops dries sponges at closing (2). Of these shops, 60.0% use incompletely dried sponges (2).
To leave sponges at room temperature without completely drying them causes the germs from dead skin cells and cosmetics from the preceding customer to multiply in the sponges. Germ multiplication is largely affected by temperature and humidity and is activated as the temperature and humidity increase (4). Moreover, dead skin cells, sebum, and cosmetic oil in a used sponge induce germ multiplication. Meanwhile, a sponge that has a low water-absorbing ability suppresses germ multiplication but is fragile and has a rapidly decreasing density, which results in shortening of sponge life. With respect to health and hygiene, comparing two conditions, namely keeping in room or cold temperature, may be useful to resolve the aforementioned issues. Thus, this study aimed to determine the proper method of sponge storage, to inspire the conception of hygiene among beauticians, and to provide a hygiene plan by comparing germ pollution levels between room and cold temperatures.
The instruments used in this study were 150 sponges from Daejeon Metropolitan City, Republic of Korea. The sponges were assigned into room-temperature storage (n = 75) and cold storage (n = 75), and the germ distribution status in bacillus cultures was compared. This study used the chi-square test, and statistical significance was set at P < 0.05 by using SPSS Window version 18.0 (Chicago, IL, USA). In sponges with multiplicated germ clusters, Corynebacterium, Bacillus, Acinetobacter, and Micrococcus species were colonized in this order (2). By using the decuple method, the number of germs was counted from the spread plates with the diluted samples. The cultures were classified into 4 groups, namely the “no colony,” “less than 103 colonies,” “more than 103–105 colonies,” and “more than 105 colonies” groups. Our results indicate no statistically significant differences in the number of Corynebacterium, Bacillus, Acinetobacter, and Micrococcus species the two storage methods (P > 0.05) (Table 1).
Table 1:
Comparison of bacterial pollution level according to sponge storage method
| Species | Temperature | Colony count/sponge number | X2 | P | ||||
|---|---|---|---|---|---|---|---|---|
| Total | No colony | <103 CFU/mL | 103–105 CFU/mL | >105 CFU/mL | ||||
| Corynebacterium | Room | 75 | 19 | 12 | 16 | 28 | 2.462 | 0.482 |
| Cold | 75 | 27 | 13 | 13 | 22 | |||
| Bacillus | Room | 75 | 39 | 14 | 15 | 7 | 6.289 | 0.098 |
| Cold | 75 | 52 | 12 | 9 | 2 | |||
| Acinetobacter | Room | 75 | 60 | 4 | 5 | 6 | 2.351 | 0.503 |
| Cold | 75 | 64 | 5 | 4 | 2 | |||
| Micrococcus | Room | 75 | 62 | 5 | 6 | 2 | 0.804 | 0.848 |
| Cold | 75 | 65 | 5 | 4 | 1 | |||
The P values were obtained by using the chi-square test.
Room temperature, 23–25°C; cold temperature, 2–3°C
Acknowledgments
The authors declare that there is no conflict of interests.
References
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