ArticlePDF Available

Abstract

Abstract BB creams appeared on the market quite recently. These creams, which give a perfect complexion by covering up the skin's blemishes, have a photoprotective effect in the majority of cases. An SPF value ranging from 10 to 45 concerning the products we tested is displayed on the packaging. The 21 commercially-available BB creams were tested to assess their efficacy (determination of the SPF) and their photostability (determination of their efficacy after UV irradiation). It was shown that 70% of the products tested have an SPF determined in vitro by us which matches the SPF displayed on the product. For the remaining 30%, it can be seen that products have SPF values of between 2 and 10 times lower than those indicated on the products. It can also be noted that there is a large disparity in terms of photostability since, under the same experimental conditions, however, some products only lose 5% of their photoprotective efficacy, whereas others lose 60%.
http://informahealthcare.com/phd
ISSN: 1083-7450 (print), 1097-9867 (electronic)
Pharm Dev Technol, Early Online: 1–4
!
2014 Informa Healthcare USA, Inc. DOI: 10.3109/10837450.2014.965322
RESEARCH ARTICLE
BB creams and their photoprotective effect
Ce
´
line Couteau, Eva Paparis, and Laurence J. M. Coiffard
Faculty of Pharmacy, Universite
´
de Nantes, Nantes Atlantique Universite
´
s, Faculty of Pharmacy, Nantes, France
Abstract
BB creams appeared on the market quite recently. These creams, which give a perfect
complexion by covering up the skin’s blemishes, have a photoprotective effect in the majority
of cases. An SPF value ranging from 10 to 45 concerning the products we tested is displayed on
the packaging. The 21 commercially-available BB creams were tested to assess their efficacy
(determination of the SPF) and their photostability (determination of their efficacy after UV
irradiation). It was shown that 70% of the products tested have an SPF determined in vitro by us
which matches the SPF displayed on the product. For the remaining 30%, it can be seen that
products have SPF values of between 2 and 10 times lower than those indicated on the
products. It can also be noted that there is a large disparity in terms of photostability since,
under the same experimental conditions, however, some products only lose 5% of their
photoprotective efficacy, whereas others lose 60%.
Keywords
BB cream, photostability, skin, SPF
History
Received 15 April 2014
Revised 4 September 2014
Accepted 6 September 2014
Published online 30 September 2014
Introduction
For a number of years, a fashion has been emerging for cosmetic
products other than sun products which have a Sun Protection
Factor (SPF) a universal indicator of a given product’s
photoprotective nature in the UVB field. Cosmetics companies
are now highlighting in their marketing argument the fact that
their products have properties which protect the user against
photo-aging
1
. We have chosen to study around twenty BB creams.
BB Cream, otherwise known as Blemish Baume/Blemish Balm is
a cosmetic cream which originated in Germany, and which was
first used by dermatologists for its calming properties and also for
hiding various problems after laser treatments such as peeling/
skin resurfacing. Since then, several Korean stars made the
product popular after revealing the secret of their perfect yet
natural-looking complexion. The trend then spread to Japan, the
whole of south-east Asia, the United States and now Europe
2
.
BB cream, which is an alternative to foundation, is a polyvalent
cosmetic product, presented as having several properties such as
moisturizing and soothing the skin, giving it an even tone,
working against wrinkles and dark patches, as well as giving
protection against UV rays. This is the aspect we wanted to study
by determining their photoprotective efficacy with an in vitro
method.
Materials and methods
The commercially-available products tested are presented in
Table 1. Thirty milligrams of product exactly weighed were
spread on PMMA plates over the whole surface (25 cm
2
) using a
finger cot. Polymethylmethacrylate (PMMA) plates (Roughness
Value Sa ¼ 5.5) were purchased from Europlast (Aubervilliers,
France). The final mass remaining on the plate after spreading
is 18 mg. The SPF of the creams was measured in vitro. Three
plates were prepared for each product to be tested and 9
measurements were performed on each plate
3
. Transmission
measurements between 290 and 400 nm were carried out using
two spectrophotometers equipped with an integrating sphere (UV
Transmittance Analyzer UV1000S, and UV 2000 - Labsphere,
North Sutton, Melbourne). The calculations for either term use
the same relationship:
SPF ¼
X
400
290
E
S
d
=
X
400
290
E
S
T
d
ð1Þ
where E
is CIE erythemal spectral effectiveness, S
is solar
spectral irradiance and T
is spectral transmittance of the sample
4
.
Studies of stability were led using a previously-established
protocol
5
. The PMMA plates coated with creams are placed for
2 h in a solar simulator (Suntest CPS + ) at 650 W/m
2
. The SPF is
determined at the beginning (SPF
0
) and after 2 h (SPF
2h
). The
ratio SPF
2h
-SPF
0
/SPF
0
100 enables us to classify the products
into two categories: photostable products which retain more than
90% of their efficacy and non-photostable products which do
not retain 90% of their efficacy under the conditions of our
experiment.
Filters in products tested for photostability were subjected to
dosing by High Performance Liquid Chromatography based on
the method of Rastogi and Jensen with some modifications.
Firstly, 0.1 g of each of the products which were to be analyzed
was weighed. Then tetrahydrofurane or potassium hydroxide was
added (0.1% w/w) in the case of phenylbenzimidazole sulfonic
acid, until a total mass of approximately 10 g was obtained. The
mixture was homogenized by putting it in a vortex for about 30 s
until the sample was well homogenized and then put in an
ultrasonic bath for 30 min. The solution was extracted using a
syringe, then filtered directly in an HPLC vial. All chemicals were
analytical grade and suitable for HPLC where appropriate.
Address for correspondence: L. J. M. Coiffard, Universite
´
de Nantes,
Nantes Atlantique Universite
´
s, LPiC, MMS, EA2160, Faculty of
Pharmacy, 9 rue Bias Nantes, F-44000 France. Tel +33 253 484317.
E-mail: laurence.coiffard@univ-nantes.fr
Pharmaceutical Development and Technology Downloaded from informahealthcare.com by Faculte De Chirurgie Dentaire on 09/30/14
For personal use only.
Separation was performed on a HPLC system (Shimadzu LC2010
CHT) equipped with quaternary pump, DAD (Photo Diode Array
Detector) detector, autosampler, thermostated column oven,
degasser and LC Solutions software. A X-bridge Shield RP18
column (150 4.6 mm; 3.5 mm) was used for separation.
Separation was performed by following a gradient time program.
The mobile phase consisted of solvent A (H
3
PO
4
0.1% w/w) and
solvent B (MeOH) with the elution profile as follows: 0–7 min,
80% B; 7–30 min, 100% B; 30–40 min, 80% B. Elution was
performed at a flow rate of 1.0 mL/min. The C
18
column was
maintained at 30
C throughout the analysis. The detection
wavelength was set at 300 nm. The injection volume was set at
10 mL. The run time was set at 40 min. The peaks were identified
by comparing the retention times of the reference standards with
the sample.
Results and discussion
The SPF values determined by using two spectrophotometers are
presented in Table 2. In 70% of cases, we observed that the values
found matched the values displayed on the packaging, no matter
which of the two machines was used. The percentage is equivalent
to that found during previous studies on other types of products
6
.
These products are formulated using a mixture of organic and/or
inorganic filters. However, for 6 products, the SPF value displayed
on the packaging was higher than the one we found. This was the
case particularly concerning products formulated with mineral
filters. During a previous study, we showed the lack of efficacy of
this type of filter
7
, which is again the case here with
commercially-available products. This is all the more true in the
present case, since the raw material is used in some cases here in
pigmentary form as we said before. Only the products whose
actual SPF values matched the values displayed on the packaging
were studied for their photostability. We defined previously that a
product was considered to be photostable if the SPF determined
after 2 h of irradiation in a Suntest was at least 90% of its initial
value
5
. By applying this criterion, we notice that almost all of the
products studied are photolabile. The results of the dosages
carried out show an large decrease in the concentration of certain
filters (Table 3). Product N
19 is the only photostable product
(Figure 1). This is due to the fact that it is formulated using
titanium dioxide which is a very photostable filter
8
. We can
consider that the products number 1 and number 16 are quite
photostable, insofar as the SPF loss does not exceed 15% after
irradiation in a Suntest. These two products contain octocrylene,
a filter which is known to improve the photostability of other
filters such as ethylhexylmethoxycinnamate, butyl methoxydi-
benzoylmethane and benzophenone-3
9
. All the other products
found to be photo-unstable are formulated with ethylhexyl-
methoxycinnamate, ethylhexylsalicylate and/or benzophenone-3.
Salicylates turn out to be particularly photo-unstable products
5
.
We should remind ourselves here that BB creams are cosmetic
products destined for facial make-up and that, therefore, they are
not designed to be reapplied throughout the course of the day.
Besides BB creams are not labeled as sunscreens, their marketing
argument presents them as being products which protect the user’s
skin from the harmful effects of UV rays.
After studying the formulation of the products tested, it can
be noticed that 25% contain benzophenone-3, also known as
oxybenzone. Benzophenones and particularly oxybenzone, are
Table 1. UV combinaison in commercial products tested.
Products tested
(SPF labeled) UV filters
1 (30) Octocrylene, Titanium dioxide, Bis-ethylhexyloxy-
phenol methoxyphenyl triazine, Methylene bis-
benzotriazolyl tetramethylbutylphenol
2 (20) Ethylhexylmethoxycinnamate
3 (30) Ethylhexylmethoxycinnamate, Ethylhexylsalicylate,
Benzophenone-3, Titanium dioxide
4 (30) Ethylhexylmethoxycinnamate (3,75%), Titanium
dioxide (3,55%), Benzophenone-3 (1,00%)
5 (30) Homosalate, Benzophenone-3, Ethylhexylsalicylate,
Octocrylene, Butylmethoxydibenzoylmethane,
Titanium dioxide
6 (25) Titanium dioxide, Ethylhexylmethoxycinnamate,
Zinc oxide (10)
7(35) Ethylhexylmethoxycinnamate, Ethylhexylsalicylate,
Benzophenone-3, Titanium dioxide
8 (15) Ethylhexylmethoxycinnamate, Bis-ethylhexyloxy-
phenol methoxyphenyl triazine, Diethylamino
hydroxybenzoyl hexyl benzoate
9 (20) Ethylhexylmethoxycinnamate
10 (15) Ethylhexylmethoxycinnamate
11 (20) Octocrylene, Butylmethoxydibenzoylmethane,
Terephtalydene dicamphor sulfonic acid,
Drometrizole trisiloxane
May contain: Titanium dioxide
12 (10) Zinc oxide
13 (20) Ethylhexylsalicylate, Octocrylene,
Butylmethoxydibenzoylmethane,
Phenylbenzimidazole sulfonic acid
14 May contain: Titanium dioxide
15 (30) May contain: Titanium dioxide
16 (10) Octocrylene, Butylmethoxydibenzoylmethane
17 (25) Ethylhexylsalicylate, Ethylhexylmethoxycinnamate,
Butylmethoxydibenzoylmethane, Octocrylene,
Titanium dioxide
18 (15) Ethylhexylmethoxycinnamate, Octocrylene,
Phenylbenzimidazole sulfonic acid
May contain: titanium dioxide
19 (20) Titanium dioxide, Ethylhexylmethoxycinnamate
20 (45) Titanium dioxide, Zinc oxide
21 (20) Ethylhexylmethoxycinnamate, Zinc oxide, Titanium
dioxide, Octocrylene, Benzophenone-3,
Butylmethoxydibenzoylmethane
Table 2. In vitro determination of SPF for 21 bb creams tested before and
after irradiation.
Products tested
(SPF labelled)
SPF ± DS
Labsphe
`
re 1000S Labsphe
`
re 2000
Before
irradiation
After
irradiation
Before
irradiation
After
irradiation
1 (30) 47 ± 6 42 ± 6 64 ± 2 57 ± 1
2 (20) 10 ± 2 9 ± 2 12 ± 2 10 ± 1
3 (30) 28 ± 3 18 ± 2 28 ± 1 18 ± 0
4 (30) 29 ± 4 25 ± 2 29 ± 0 28 ± 3
5 (30) 34 ± 3 14 ± 2 38 ± 3 14 ± 1
6 (25) 14 ± 1 11 ± 1 15 ± 1 14 ± 1
7 (35) 32 ± 4 21 ± 3 38 ± 4 24 ± 3
8 (15) 33 ± 4 23 ± 3 40 ± 3 28 ± 0
9 (20) 29 ± 4 22 ± 3 31 ± 1 24 ± 0
10 (15) 17 ± 2 10 ± 2 17 ± 1 11 ± 1
11 (20) 20 ± 3 16 ± 2 24 ± 2 16 ± 1
12 (10) 5 ± 0 5 ± 0 5 ± 1 5 ± 0
13 (20) 23 ± 2 12 ± 2 24 ± 2 14 ± 1
14 2±02±03±03±0
15 (30) 3 ± 0 3 ± 0 4 ± 0 3 ± 0
16 (10) 14 ± 2 13 ± 1 15 ± 2 13 ± 2
17 (25) 29 ± 4 13 ± 2 34 ± 2 16 ± 1
18 (15) 36 ± 4 29 ± 4 38 ± 4 29 ± 3
19 (20) 32 ± 2 31 ± 3 35 ± 3 36 ± 3
20 (45) 16 ± 3 16 ± 2 16 ± 2 19 ± 3
21 (20) 24 ± 4 17 ± 2 25 ± 1 18 ± 1
2 C. Couteau et al. Pharm Dev Technol, Early Online: 1–4
Pharmaceutical Development and Technology Downloaded from informahealthcare.com by Faculte De Chirurgie Dentaire on 09/30/14
For personal use only.
common causes of photoallergy and are increasingly used in
products other than sunscreens. Benzophenones may also produce
photoallergic contact urticaria, in addition to delayed contact
and photocontact dermatitis, which may complicate the clinical
presentation
10
.
Studying the list of ingredients allows us to state that 7 out of
the 21 products tested contain alcohol, which is not desirable as
this ingredient is a penetration enhancer. Very few products
are formulated with mineral filters only: titanium dioxide and/or
zinc oxide.
Few studies enable us to conclude that daily photoprotection is
beneficial
11
. We can even reasonably think that it is not necessary
for a person having no particular problems to use a photo-
protective product every day of the year and at all latitudes. If
we take Nantes as an example, low UV levels are seen even now,
in May.
The use of the BB creams is similar to a normal day
moisturizer or foundation cream. BB creams must not be
considered as sunscreen products. Considering the results of this
research, it is highlighted that most of these products have their
Table 3. UV filters concentration before and after irradiation.
Products tested
UV-filters (% w/w)
N
Before
irradiation
After
irradiation
1
Octocrylene 8.44 ± 0.42 7.07 ± 0.33
Bis-ethylhexyloxyphenol methoxyphenyl triazine 3.16 ± 0.08 1.72 ± 0.07
Methylene bis-benzotriazolyl tetramethylbutylphenol 1.33 ± 0.02 1.32 ± 0.03
3
Ethylhexylmethoxycinnamate 7.75 ± 0.27 3.25 ± 0.09
Ethylhexylsalicylate 4.09 ± 0.02 1.26 ± 0.04
Benzophenone-3 2.35 ± 0.29 2.33 ± 0.27
4
Ethylhexylmethoxycinnamate 3.80 ± 0.09 0.75 ± 0.09
Benzophenone-3 1.03 ± 0.04 1.00 ± 0.07
5
Homosalate 5.12 ± 0.04 3.33 ± 0.50
Benzophenone-3 3.98 ± 0.03 3.90 ± 0.02
Ethylhexylsalicylate 2.27 ± 0.01 0.85 ± 0.05
Octocrylene 2.09 ± 0.01 1.80 ± 0.06
Butylmethoxydibenzoylmethane 1.89 ± 0.01 0.66 ± 0.04
7
Ethylhexylmethoxycinnamate 7.41 ± 0.18 3.00 ± 0.02
Ethylhexylsalicylate 3.96 ± 0.05 1.12 ± 0.01
Benzophenone-3 2.25 ± 0.01 2.20 ± 0.05
8
Ethylhexylmethoxycinnamate 6.58 ± 0.57 3.00 ± 0.02
Bis-ethylhexyloxyphenol methoxyphenyl triazine 2.44 ± 0.07 0.85 ± 0.01
Diethylamino hydroxybenzoyl hexyl benzoate 2.31 ± 0.06 2.28 ± 0.06
9
Ethylhexylmethoxycinnamate 9.50 ± 0.56 4.41 ± 0.12
10
Ethylhexylmethoxycinnamate 4.35 ± 0.07 0.43 ± 0.01
13
Ethylhexylsalicylate 2.39 ± 0.01 0.84 ± 0.05
Octocrylene 2.22 ± 0.01 1.92 ± 0.01
Butylmethoxydibenzoylmethane 1.99 ± 0.01 0.71 ± 0.01
Phenylbenzimidazole sulfonic acid 1.60 ± 0.01 1.45 ± 0.01
16
Octocrylene 3.03 ± 0.02 2.85 ± 0.02
Butylmethoxydibenzoylmethane 0.43 ± 0.01 0.15 ± 0.01
17
Ethylhexylsalicylate 5.93 ± 0.04 1.54 ± 0.01
Ethylhexylmethoxycinnamate 3.72 ± 0.02 1.50 ± 0.01
Butylmethoxydibenzoylmethane 2.63 ± 0.02 0.94 ± 0.01
Octocrylene 2.60 ± 0.02 2.30 ± 0.02
18
Ethylhexylmethoxycinnamate 7.74 ± 0.05 3.80 ± 0.02
Octocrylene 2.99 ± 0.02 2.50 ± 0.05
Phenylbenzimidazole sulfonic acid 2.81 ± 0.02 2.56 ± 0.02
19
Ethylhexylmethoxycinnamate 9.95 ± 0.22 4.95 ± 0.13
21
Ethylhexylmethoxycinnamate 5.52 ± 0.25 2.33 ± 0.15
Octocrylene 1.93 ± 0.02 1.85 ± 0.01
Benzophenone-3 0.89 ± 0.01 0.86 ± 0.01
Butylmethoxydibenzoylmethane 1.21 ± 0.05 0.41 ± 0.01
DOI: 10.3109/10837450.2014.965322 BB creams and photoprotection 3
Pharmaceutical Development and Technology Downloaded from informahealthcare.com by Faculte De Chirurgie Dentaire on 09/30/14
For personal use only.
photo-protection efficacy reduced after irradiation. The consumer
must use correctly the product.
Declaration of interest
The authors report no declaration of interest.
References
1. Seite S, Fourtanier A, Rougier A. Photoprotection in moisturizers
and daily-care products. G Ital Dermatol Venereol 2010;145:
631–636.
2. Misery L. BB creams: a revolutionary product dating from 1860.
Ann Dermatol Venereol 2014;141:74–76.
3. Couteau C, Pommier M, Paparis E, Coiffard L. Study of the efficacy
of 18 sun filters authorized in the European Union tested in vitro.
Pharmazie 2007a;62:449–452.
4. Sayre MR, Agin PP, Le Vee GJ, Marlowe E. A comparison of in vivo
and in vitro testing of sunscreening formulas. Photochem Photobiol
1978;29:559–566.
5. Couteau C, Faure A, Fortin J, et al. Study of the photostability
of 18 sunscreens in creams by measuring the SPF in vitro. J Pharm
Biomed Anal 2007b;44:270–273.
6. Couteau C, Coiffard L. Les produits solaires: des proble
`
mes en
termes d’efficacite
´
. Act pharm 2013;523:35–40.
7. Couteau C, Alami S, Guitton M, et al. Interest of mineral filters in
sunscreen products comparison of the efficacy of zinc oxide and
titanium dioxide by in vitro method. harmazie 2008;63:58–60.
8. Hojerova
´
J, Medovcı
´
kova
´
A, Mikula M. Photoprotective efficacy
and photostability of fifteen sunscreen products having the
same label SPF subjected to natural sunlight. Int J Pharm 2011;
408:27–38.
9. Gaspar LR, Maia Campos PMBG. Photostability and efficacy
studies of topical formulations containing UV-filters combination
and vitamins A, C and E. Int J Pharm 2007;343:181–189.
10. Nedorost ST. Facial erythema as a result of benzophenone allergy.
J Am Acad Dermatol 2003;49:S259–S261.
11. Seite
´
S, Fourtanier AM. The benefit of daily photoprotection. J Am
Acad Dermatol 2008;58:S160–S166.
12. Rastogi SC, Jensen GH. Identification of UV filters in sunscreen
products by high-performance liquid chromatography–diode-array
detection. J Chrom A 1998;828:311–316.
0
10
20
30
40
50
60
70
19 16 1 4 11 18 9 8 21 3 7 10 13 17 5
Decrease of SPF (%)
Products tested
Figure 1. Photostability of products tested.
4 C. Couteau et al. Pharm Dev Technol, Early Online: 1–4
Pharmaceutical Development and Technology Downloaded from informahealthcare.com by Faculte De Chirurgie Dentaire on 09/30/14
For personal use only.
... Com isso, à frente da aplicação, a proporção de cores é primordial na otimização da cobertura sobre a acne e rosácea. Alguns estudos recomendam a cor verde para neutralizar as áreas eritematosas e os tons bege/amarelo para as áreas hiperpigmentadas (Goh et al., 2016;Padilla-Espanã et al., 2014;Couteau, Paparis & Coiffard, 2016 ...
... Fonte:(Antoniou & Stefanaki, 2006) Entretanto, alguns autores afirmam que esta contraposição de cores não combina na pele e que, para cobrir com eficiência a vermelhidão causada pelo eritema da acne, por exemplo, as melhores escolhas são os tons amarelados. Se o eritema não for tão pronunciado, uma cor equivalente ao tom de pele pode ser aplicada e, caso não seja obtida a cobertura suficente, um tom amarelado deve ser aplicado antes da cobertura na cor equivalente ao tom da pele(Iredale & Linder, 2009;Couteau et al., 2016).Uma camuflagem cosmética ideal para acne deve ter uma aparência natural, nao ser irritante, comedogênica ou acnegênica, além de possuir fácil aplicação. A escolha dependerá da preferência do paciente pela paleta de cores disponíveis, da presença de componentes específicos, como os beta-hidroxiácidos naturais presentes no extrato da casca de salgueiro ou óleos essenciais, como por exemplo a Matricaria recutita, que possui propriedades antiinflamatórias e antimicrobianas, ou vitaminas com propriedades antioxidantes, como a vitamina(Levy & Emer, 2012;Goh et al., 2016) .Em um estudo realizado por Matsuoka e colaboradores, foi avaliado se o uso da maquiagem e cuidados com a pele poderia influenciar a qualidade de vida dos pacientes afetados sem prejudicar os tratamentos convencionais da acne. ...
Article
Full-text available
Algumas dermatoses, por serem aparentes, podem estabelecer consequências na vida pessoal, social e profissional de seus portadores e, devido ao poder de criar impressões e sentimentos, a aparência pessoal pode influenciar na qualidade de vida destes. Em razão disso, pessoas acometidas por problemas dermatológicos como a acne e suas lesões possuem maior propensão em desenvolver problemas de autoestima e estresse psicológico. A acne é uma afecção caracterizada por lesões cutâneas que incluem comedões, pápulas eritematosas, pústulas, nódulos e cicatrizes, sendo a região facial a mais afetada. A camuflagem cosmética pode então, ter uma influência positiva na qualidade de vida dos pacientes com acne. Assim, o objetivo do estudo foi realizar uma pesquisa bibliográfica sobre o uso da camuflagem cosmética em pacientes acometidos pela acne e suas lesões. Foi conduzida uma busca nas bases de dados PubMed e Scopus nos últimos 10 anos, utilizando os termos (MeSH), “cosmetic camouflage”, “acne” e “make up”. Nos estudos encontrados, foi possível observar que a camuflagem cosmética é um método eficaz para a satisfação imediata dos pacientes, principalmente para aqueles acometidos pela acne, visto que o tratamento terapêutico pode demorar a apresentar os resultados visíveis, e assim, a camuflagem pode ser utilizada de forma complementar a esse tratamento. Alguns estudos mostraram ainda uma melhora na qualidade de vida após o uso da camuflagem para disfarçar as lesões. É necessário educar os pacientes em relação aos produtos mais adequados, escolhidos sob a orientação do profissional de saúde, levando em consideração a terapia farmacológica em andamento.
... Attempts to achieve consistent skin tone have led to breakthroughs in base makeup products that can mask skin imperfections and correct skin tone (Couteau et al. 2016). In the cosmetic industry, Korean products are currently leading the global market, with popular items ranging from blemish balm (BB) cream to the cushion compact (Park and Chin 2010;Baek 2015). ...
Article
Bare face L*a*b* values are needed to serve as a standard reference point for the development of base makeup products for Korean women. A total of 543 Korean women ranging in age from their 20s to 50s underwent spectrophotometer skin analysis under constant temperature (22 ± 2%) and humidity (50 ± 5%) conditions. Eight parts of each subject’s face (center of the forehead, right cheekbone, right cheek, under the chin, left cheek, left cheekbone, philtrum, and under the lips) were measured, and average values were calculated. Subjects were then asked to complete questionnaires regarding their use and preferences for base makeup products. Skin tone was classified into three categories (dark, normal, bright) based on L* values. Compared with the contrast value, the dark group L* was 60.66 and the normal group L* was 63.87 (with a difference of 3.21), and the bright group L* was 66.66 (with a difference of 2.79 from the normal group). According to the survey responses regarding preferences and use of base makeup products, the most common answer for all respondents regardless of age was that their skin tone was average or slightly darker than that of their peers. Preferred base makeup products usually were found to be of slightly brighter color than actual skin tone. As in previous studies, the most frequently used base makeup product regardless of age was BB cream. Given that the average L* standard deviation between groups was 3, a difference of one step in skin tone may be considered to be equivalent to this L* value difference. The survey results suggest that target colors for base makeup product development should be brighter than bare face tones.
... They can be used to contour and correct pigment abnormalities, control oil, moisturize, protect against UV light, increase absorption of acne treatment, improve the skin barrier, and improve personal well-being. [80,81] These products that come as cover creams, powders, or liquids can quickly conceal visible scars or active lesions. [82] An ideal acne camouflage should have a natural appearance, be nongreasy, noncomedogenic, and can be easily applied. ...
Article
Full-text available
Conventional acne treatment presents several challenges such as intolerable side effects and antibiotic resistance. Dermocosmetic products may be used to reduce these unwanted effects. Dermocosmetics include skin cleansers, topical sebum-controllers, skin antimicrobial/anti-inflammatory agents, moisturizers, sunscreens, and camouflage products. Appropriate use of these products may help augment the benefit of acne treatment, minimize side effects, and reduce the need for topical antibiotics. In Asia, there is currently limited scientific data on the application and recommendations for dermocosmetic use in acne vulgaris (AV). This article reviews the evidence on dermocosmetics for AV and provides practice recommendations as discussed during the 4(th) Asia-Pacific Acne Leaders' Summit held in Bangkok, Thailand, on 7 and 8 February 2015. Through a premeeting survey, a series of plenary lectures, a stepwise program of discussion sessions, and Medline article review, the Expert Panel set forth relevant recommendations on the role of dermocosmetics as adjunct for treating AV in Asian patients.
Article
Full-text available
Treating acne vulgaris remains a significant challenge for dermatologists. Dermocosmetics are becoming an essential component of acne management. The active ingredients in dermocosmetics help support dermatological treatments, while gentle formulations help maintain the skin's lipid barrier, reduce transepidermal water loss, and minimize the risk of irritation. Our objective was to review the active ingredients and various preparations used in dermocosmetics for acne, and to emphasize the clinical evidence supporting their effectiveness.
Article
Background: Cosmeceuticals are commonly used in skincare regimens to maintain healthy skin and improve visible signs of aging. In recent years, South Korean skincare has gained prominence in the global beauty industry by introducing innovative cosmeceutical products and aesthetic trends. Objectives: To describe the global impact of Korean skincare and to review the current research evidence for bioactive ingredients commonly found in Korean cosmeceuticals. Methods: A review of the biomedical literature was conducted using PubMed to identify laboratory, animal, and clinical studies that evaluated the biological properties and potential dermatologic uses of ingredients found in Korean cosmeceuticals. Results: Bioactive ingredients in Korean cosmeceutical products are increasingly undergoing scientific validation and are derived from various sources including animals (eg, bee venom and snail mucin), plants (eg, dragon's blood and tiger grass extract), and biotechnology (eg, synthetic snake venom). Their bioactive components and pharmacologic activities have been shown to provide dermatologic benefits with potential applications for skin rejuvenation, photoprotection, wound healing, and more. Conclusion: Further research studies are warranted to elucidate any biological or therapeutic mechanisms of action of these ingredients, which may translate into clinical practice. With the rising public awareness and interest in Korean cosmeceuticals, patients may seek advice from dermatologists about how to incorporate these bioactive ingredients into their skincare regimens to improve skin health and aesthetics.
Article
Full-text available
The target of this research was to evaluate the photostability of various sunscreen agents incorporated into an O/W emulsion. The concept of photostability is very important in the field of solar protection. The effectiveness of the anti-solar products is quantified using a universal indicator: the sun protection factor (SPF). This number which can be found on packaging can be given in two different ways: by methods in vivo (Colipa method) and in vitro. It is this last method which was adopted for this study. According to selected filter UVB (currently directive 76/768/EEC modified authorized 18 filters UVB), we can obtain more or less effective creams. We chose the irradiation of sun lotions formulated using the authorized filters, used with their maximum amount of employment, in a Suntest, with an irradiance of 650 W/m(2) throughout variable time. With interval of regular time, one carries out a measurement of SPF in order to establish for each filter the kinetics SPF=f(time). An indicator of stability (t(90)) is then given. In this way, we could classify the filters by order of increasing photostability.
Article
Benzophenones are common causes of photoallergy and are increasingly used in products other than traditional sunscreens. Patients may be unaware of any sunscreen exposure when using a product such as shampoo containing benzophenone. Benzophenones also may produce photoallergic contact urticaria, in addition to delayed contact and photocontact dermatitis, which may complicate the clinical presentation. Allergy to benzophenone should be considered in the diagnosis of patients with patchy erythema of the face and neck that is not typically eczematous and that may otherwise be attributed to a rosacea diathesis, lupus erythematosis, or simple flushing. Patch and photopatch testing are indicated to evaluate these patients for allergy to benzophenone.
Article
Tanning is still fashionable today. The link between sun exposure and skin cancer development has been clearly established. Accordingly, the use of a sunscreen seems essential. However, care should be taken in regard to products formulated exclusively with mineral filters. Out of 17 products of this type studied, the sun protection factor determined by the in vitro method was lower than that displayed on the packaging. For products containing mixtures of organic filters and/or minerals, the compliance rate is 71%, or 77% when only those sold in pharmacies are considered. A very specific warning should be given in relation to products marketed with no displayed SPF.
Article
A HPLC method for the identification of twenty UV filters has been developed in the present study. The method employs an analytical column with polymer packing, ion pairing and gradient elution followed by diode-array detection of UV filters. No problems were encountered for the analysis of UV filters in 24 sunscreen products by the present method.
Article
Benzophenones are common causes of photoallergy and are increasingly used in products other than traditional sunscreens. Patients may be unaware of any sunscreen exposure when using a product such as shampoo containing benzophenone. Benzophenones also may produce photoallergic contact urticaria, in addition to delayed contact and photocontact dermatitis, which may complicate the clinical presentation. Allergy to benzophenone should be considered in the diagnosis of patients with patchy erythema of the face and neck that is not typically eczematous and that may otherwise be attributed to a rosacea diathesis, lupus erythematosis, or simple flushing. Patch and photopatch testing are indicated to evaluate these patients for allergy to benzophenone.
Article
Abstract— Seven commercially available sunscreens were compared by three different methods. Absorbance spectra were measured for each product in isopropanol solution and also on hairless mouse epidermis. In vivo tests were performed on human volunteers using a Xe arc solar simulator. Sun Protection Factors (SPF) were calculated by each method for each product tested and the results compared. By all methods used, the combination of 7% octyl dimethyl para-aminobenzoic acid and 3% oxybenzone provided the most protection from U.V. light. While estimates of the effectiveness of all products were much too high when calculated by the isopropanol solution method, the hairless mouse epidermis technique seems to be an accurate tool for predicting product efficacy in vivo.
Article
The first objective of this study is to show how different can be photoprotection by sunscreens with an identical SPF given on the packaging, when subjected to sunlight radiation. The second objective is to highlight the need for global harmonization of photostability testing and UVA protection labelling. Fifteen products with various combinations of UV filters marketed in Europe were assessed based on transmission measurements of 0.75 mg cm⁻² layer covered onto polymethylmethacrylate plate roughness 2 μm. Two absolute UV spectroscopic indices (in vitro SPF, UVA-PF), four well-known relative UVA indices: the UVA-PF/SPF ratio and critical wavelength by European Commission (EC); UVA/UVB ratio by Boots Star Rating system; UVA1/UV ratio by FDA Proposed Ruling and one new relative indices the Spectral Uniformity Index (SUI) by Diffey, were compared before and after sunlight exposure with dose about 42 SEDs. The UVA-PF values before exposure proved a high degree of variation among samples. After exposure only five sunscreens observed UVA protection standard by EC and the same products showed compliance with the first UVA rating by Boots system (three stars). According to the UVA1/UV ratio, except for one product, all sunscreens manifested certain UVA protection level (low, medium or high). In compliance with criteria of new rating proposed by Diffey, exactly all fifteen sunscreens gave some UVA rating exhibited as SUI (low, medium or high). These results mean that the different UVA protection indices can exhibit various data and be confusing for consumer. Photostability of each product was assessed with three indices: the area under curve (Auc) Index for the total UV range, and UVB, UVA, UVA2, UVA1 range separately; the residual effectiveness of in vitro SPF and UVA-PF. All fifteen sunscreens were photostable in the UVB region. Seven products exhibited photoinstability in the total UV range (290-400 nm); all of them contained a combination of the ethylhexyl methoxycinnamate (EHMC) and butyl methoxydibenzoylmethane (BMBM) together with other UV filters. Eight products lacked their stability in the UVA1 range (340-400 nm) thus confirmed that photodegradation of some current sunscreens is primarily problem of this region. The most photoinstability showed sunscreens S1 (EHMC, BMBM and phenylbenzimidazole sulphonic acid) and S6 (EHMC, BMBM, phenylbenzimidazole sulphonic acid and ethylhexyl triazone); Auc-UVA1 Index was 0.15 only. Excellent UVA1 photostability showed sunscreen S8 (EHMC, EHT and methylene bis-benzotriazolyl tetramethylbutylphenol); Auc-UVA1 Index was of 1.00. Three sunscreens showed very good UVA1 photostability (Auc-UVA1 Index ranged from 0.98 to 0.93). The fact that these products applied only in the layer of 0.75 mg cm⁻² were photostable under the sunlight dose, which corresponds to layer of 2 mg cm⁻², is proof of their quality. Comparison of the residual effectiveness of in vitro SPF and UVA-PF values with the Auc-Index showed that methods give a similar ranking of the sunscreens' photostability.
Article
During usual daily activities, an appropriate protection against solar UV exposure should prevent clinical, cellular and molecular changes potentially leading to photoaging. In skin areas regularly exposed to sun, UV-damage is superimposed to tissue degeneration resulting from chronological aging. It is, therefore, important to know if moisturizers and daily-care products containing UVA absorbers combined with UVB ones are able to prevent these skin damages. This review will summarize clinical studies evaluating this topic. These studies demonstrate that broad-spectrum protection in moisturizers or daily-care products can prevent the "silent" sub-erythemal cumulative effects of UVR from inadvertent sun exposure.