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Print version ISSN 0365-0596
An. Bras. Dermatol. vol.86 no.3 Rio de Janeiro May/June 2011
Sun protection factor: meaning and controversies*
Sergio SchalkaI; Vitor Manoel Silva dos ReisII
IM.Sc. in Dermatology - Associate Professor of Dermatology - University of Santo Amaro (UNISA) - São Paulo (SP), Brazil
IIPh.D. in Dermatology - Professor of Dermatology, School of Medicine, University of São Paulo (FMUSP) - São Paulo (SP), Brazil
The Sun Protection Factor (SPF) is the most important data to quantify the effectiveness of a sunscreen, being universally accepted. The method is based on determining the minimum erythematous dose (MED), defined as the smallest amount of energy required for triggering the erythema, in areas of protected and unprotected skin. The SPF value is then calculated as the ratio between the MED of protected and unprotected skin. The first publication of a method for determining the SPF was presented in 1978 by the U.S. FDA agency, followed by other publications of FDA and other international regulatory agencies. Although considered the reference method for quantification of sunscreen efficacy of topical products, there are controversies in literature about the method for determining the SPF and the implications of the real conditions of use in the protection achieved in practice by users.
Keywords: Dermatology; Solar radiation; Sunscreening agents
It has always been part of human nature to protect the skin against sunburn through the use of clothes and accessories or simply by avoiding sun exposure. The first scientific reports on the attempted use of photoprotective agents emerged in the late XIX century, with substances of very limited effect.1
In 1891, Friedrich Hammer1 published the first monograph on photobiology, in which he discussed the use of different products in the prevention of sunburn (1891 apud Roelandts,1 2007, p.5).
In 1928, the first sunscreen becomes commercially available in the United States of America -an emulsion containing benzyl salicylate and benzyl cinnamate. 2 In subsequent years, however, little attention was given to photoprotective agents, and their use was very limited.
During World War II, due to the need for adequate photoprotection of American soldiers in battle fronts in the tropics, red petrolatum was used as a standard protective substance. 1
In 1943, para-aminobenzoic acid (PABA) was patented as the first sunscreen established, indicating a new stage of photoprotection. 2
However, it was only during the 1970s that the popularity of sunscreens increased with the incorporation of different UVB filters in creams and lotions. 3
The use of UVA filters effectively began in 1979, but only the introduction of inorganic particles of titanium dioxide in 1989 and of zinc oxide in 1992 led to more effective protection in the UVA range 2.
The classic definition of a sunscreen, according to Pathak4, is a product designed to block the sun and protect or shelter viable skin cells against the potentially harmful effects of ultraviolet radiation such as sunburn and skin cancer.
According to current concepts, topical photoprotectors or sunblocks (or sunscreens), are substances applied to the skin in different presentations which contain in their formulation ingredients capable of interfering with sun radiation, reducing its harmful effects. 5
Ultraviolet (UV) filters are the ingredients present in sunscreens that have the ability to interact with incident radiation through three (3) basic mechanisms: reflection, dispersion and absorption, as shown in Figure 1. 6
UV filters can be divided into inorganic (physical) or organic (chemical) filters, depending on their physico-chemical properties. 7
Inorganic filters are metal oxide particles capable of reflecting or dispersing incident radiation through an optical mechanism. Its main representatives are zinc oxide (ZnO) and titanium dioxide (TiO2), usually used in combination with organic filters. The main characteristics of inorganic filters are their low skin permeability and their high photostability, that is, their ability to maintain photoprotection even after long periods of sunlight. 7
Organic filters are molecules that interfere with incident radiation through the mechanism of absorption, when the filter acts as an exogenous chromophore by absorbing a photon of energy and evolving to the excited state of the molecule. Upon returning to the stable state (unexcited), the release of energy occurs at a longer wavelength, either in the range of visible light (as fluorescence) or in the range of infrared radiation (as heat). The process can be repeated numerous times by a mechanism called resonance. Depending on their capacity to absorb shorter or longer wavelengths, organic filters can be subclassified into UVA filters, UVB filters and filters for broad-spectrum protection (UVA and UVB). 9
The U.S. legislation (FDA 99) 10 classifies sunscreens as nonprescription medication and lists sixteen (16) substances approved as UV filters, allowed for use in photoprotectors.
In Brazil, the National Health Surveillance Agency (ANVISA) 11 defines sunscreens as cosmetic products and presents a list of permitted ultraviolet filters, containing thirty-eight (38) active ingredients.
The development and use of topical photoprotectors have always been related to the prevention of the acute effects of sun radiation, especially sunburn. 4
It was not until after the 1980s, with studies demonstrating the role of UV rays in the development of skin cancer, that the sunscreen came to be understood not only as an agent against sunburn, but also as an important element in preventing chronic actinic damage, particularly in relation to the development of skin cancer. 4
Different studies have shown that the sunscreen has a protective effect against chronic actinic damage.
Regular use of sunscreens can reduce the number of actinic keratoses. 12.13
According to Green, 14 only squamous cell carcinoma, and not basal cell carcinoma, can be prevented by the regular use of sunscreens.
Vainio, 15 in a recent publication, concluded that the daily use of photoprotectors reduces the risk of squamous cell carcinoma development.
Fourtanier 16 presented a work conducted with rats in which he demonstrated the superiority of broad-spectrum sunscreens in comparison to others that are not broad spectrum, in the protection against DNA damage and in the prevention of photocarcinogenesis, delaying tumor development.
The use of sunscreens has been reported as capable of preventing the development of skin cancer triggered by UV by decreasing the formation of cyclobutane-pyrimidine dimers, as well as preventing other immunological effects induced by UV rays, such as the suppression of contact hypersensitivity 7.
A study conducted by Hayag, 17 in 1997 concluded that the application of a sunscreen with SPF 30 before sun exposure can prevent the decrease of Langerhans cells in the irradiated site and reduce UV-induced suppression in contact hypersensitivity to dinitrochlorobenzene (DNCB).
With regard to the use of sunscreens and the risk of developing melanoma, the literature still shows some controversy.
Huncharek and Kupelnick 18 published a metaanalysis of eleven studies showing that the use of photoprotectors has only a small advantage in decreasing the risk of developing melanoma.
Rigel, 19 however, in a review of only the most recently published articles in which only sunscreens with a high SPF were used, concluded that that the use of these products seems to offer a clear protective effect against the risk of melanoma.
In 2005 Diffey 20 presented a review of the subject, in which the author concluded that recent improvements in the effectiveness of modern sunscreens will offer additional protection against melanoma. But this result will not be seen in the coming decades .
In view of all this, and also with the perception of the deleterious effect of UVA radiation on different photodermatoses, on the development of skin cancers, and on photoaging and photoimmunosuppression, new UV filters have been developed, with greater photoprotective capacity in the UVB band and broader absorption spectrum in UVA and UVB. This leads to a leap in photoprotective efficacy, particularly in the Sun Protection Factor (SPF) value 20.
The average SPF value of products used in Europe in 1984 was from four (4) to six (6), progressing to 6 to 10 in 1987 and to about 15 in 1997, showing the recent evolution of photoprotectors. 20
According to the International Agency for Research on Cancer (IARC), 21 despite insufficient evidence that sunscreens have a protective effect against BCC and melanoma, and only limited evidence that they prevent SCC, the use of the sunscreen should be considered as part of a complete photoprotection regimen.
For better photoprotective efficiency, the sunscreen should present in its composition ultraviolet filters with an absorption spectrum in the range of UVA and UVB rays and be photostable. Moreover, for an ideal protective effect, the product should form a homogeneous film, capable of delivering its ingredients on a regular basis throughout the skin surface. 9
SUN PROTECTION FACTOR - HISTORICAL ASPECTS
The first report on the evaluation of the protective efficacy of sunscreens was done by Friedrich Ellinger in 1934 22 in which the author determined the minimal erythemal dose (MED) for protected and unprotected skin, using both forearms and a mercury lamp. He proposed a coefficient of protection that decreased in value to the extent that protection increased.
In 1956, Rudolf Schulze 23 evaluated commercially available sunscreens by calculating a protection factor, later called "Schulze Factor". The author divided the exposure time required for the induction of erythema on sunscreen-protected skin by the time required for the production of erythema on unprotected skin, using incremental doses of radiation emitted by lamps with a radiation spectrum closer to sunlight. The Schulze method has been used for decades in European countries, as a reference in the evaluation of sunscreens.
It was only in 1974 that the term Sun Protection Factor (SPF) was introduced by Greiter 24, being only a new name for the already known "Schulze method."
The Sun Protection Factor, proposed by Greiter, quickly became popular and used worldwide. However, due to the lack of standardization of the method, the numerical values found and used in sunscreens varied considerably, not rendering it reliable. 25
In 1978, the North-American regulatory agency (FDA) proposed the first normatization to determine the Sun Protection Factor (SPF) 26.
SUN PROTECTION FACTOR - CONCEPT AND INTERNATIONAL METHODS
The Sun Protection Factor can be defined, as proposed by the FDA in 1978, 26 as the numerical ratio between the minimal erythemal dose (MED) of sunscreen-protected skin, applied in the amount of 2 mg / cm2 and the Minimal Erythemal dose of unprotected skin, a mathematical relation that can be represented by the following equation:
FPS = MED (protected skin) / MED (unprotected skin)
To determine the FPS value, a group of 10 to 20 volunteers (according to the reference method), with skin phototypes I-III (Fitzpatrick classification)27, is selected and subjected to increasing doses of ultraviolet radiation emitted by an artificial light source called solar simulator, in areas of unprotected and sunscreen-protected skin in the amount of 2 mg/cm2. After about 16 to 24 hours of exposure, the reading of the MED in both areas is done and their ratio is calculated (Fig. 2). The mean values found for the group of volunteers is the SPF of the product.
After the publication of the method by the FDA in 1978, new methods were proposed by international regulatory agencies.
The German agency Deutches Institut für Normung (DIN) presented a new version of the method in 1984, called DIN 67501, at that time used throughout Europe. 25 Methodological differences between them were large and mainly referred to the emitting source of ultraviolet (Xenon Arc lamp for the FDA Methodology and natural light or Mercury lamp for DIN) and the amount of sunscreen applied (2.0 mg / cm 2 for the FDA methodology and 1.5 mg / cm 2 for DIN). 25
All the following publications maintained the methodological concepts described in the monograph presented by the FDA in 1978, that is, xenon arc lamp as the emitting source and the amount of 2.0 mg / cm 2 as the standard amount of sunscreen to be applied.
After the first publication in 1978, 26 the FDA produced its proposal of a final monograph in 1993 28 and, finally, the final monograph in 1999. 10 Currently a new methodological revision proposed by the FDA at the end of 2007 is under discussion. 29
In addition to the FDA action, other institutions and international regulatory agencies have produced technical monographs describing the procedures necessary for conducting a clinical trial to assess sunscreen efficacy by determining the Sun Protection Factor 25.
The European community, through the European Cosmetic, Toiletry and Fragrance Association (Comité de Liason des Associations et Européenes de lndustrie et de la Parfumerie -COLIPA) developed its first version of a monograph in 1994. 30
In 2003 the method called International Sun Protection Factor Test Method (ISPF) was presented jointly by the European (COLIPA), Japanese (JCIA) and South African (CTFA-SA) associations, 31 followed by a subsequent revision in 2006, with the introduction of Cosmetic, Toiletry and Fragrance Association of the United States (CTFA-USA). 32
The North American (FDA) and European (COLIPA or international) methodologies have become a reference for determining the Sun Protection Factor (SPF) in different countries, among them Brazil, which through Resolution RDC 237 issued by the National Health Surveillance Agency (ANVISA) in 2002 11 determines that any product denominated sunscreen should present studies showing its photoprotective effectiveness (SPF determination test) through one of two international methodologies: FDA 1993 Methodology 28 or COLIPA 1994 30 or even through one of their updates.
Table 1 shows all the publications about methods for determining the FPS that have been presented by authorities since 1978. 25
Because these are the most currently employed methods in Brazil and other countries in the world, Table 2 shows the main methodological characteristics and the main differences of the methods for determining the FPS published by the FDA 1999 (standard method in North America) and the International Sun Protection Factor Method (ISPF) 2006 32 (standard method in the EU and Japan).
Despite the methodological differences shown in Table 2, studies on FPS conducted by the two different methods mentioned (FDA method and International method) yield similar results. In practice, we understand that the two methods produce equivalent SPF values.
FPS - Controversies
The Sun Protection Factor quantifies the protection that a product is able to offer in terms of exposure time in relation to sunburn when compared to unprotected exposure. 10 Therefore, if a particular sunscreen has SPF 30, this means in practice that a sun exposure 30 times greater is necessary to produce erythema, compared to the situation in which this user would not be photoprotected.
For us to calculate the length of protection with the use of sunscreen, we would need to know the time of exposure needed for the production of erythema without such protection for that individual. This time, however, suffers a strong influence of personal and environmental factors such as individual erythematogenic response (for which the phototype is an attempt at classification), the ultraviolet index (UVI) of that particular day (remembering that the UVI is an estimate for the solar noon), time of day, the index of exposure of that region of the body (eg, the face has an index of 0.3, ie, it receives only about 30% of the total radiation) and soil type (considering that the reflection index varies from soil to soil and is not estimated by UVI). For these reasons, the tendency is not to use the FPS value to determine time of sun exposure, but instead the level of protection.
Developed over thirty years, the Sun Protection Factor (SPF) is the most accepted method for evaluating the photoprotective efficacy of sunscreens, being universally considered as the main information in the labeling of sunscreens. Still, there are controversies regarding the method and its applicability in real conditions of use.
Because it uses a biological marker with individual variable response, such as erythema, the SPF is a method that can vary in its results.
According to Sayre, 33 the critical points for the SPF method to be reproducible, essential to the reliability of results, are the artificial source of ultraviolet radiation (currently standardized by the use of xenon-arc lamp) and the amount of product applied to the back of the volunteer.
In 1992 COLIPA put together a task force composed of scientists in the field of photoprotection and organized an inter-laboratory validation for the evaluation of Sun Protection Factor. 30 The evaluation was conducted at different stages: at first, six (6) European laboratories received four different sunscreens to determine their FPS. S The results showed a variation in the SPF value from 18.2% to 37%, the latter referring to a sunscreen made only with inorganic filters. We identified the following critical points of the method:
Amount and manner of application of the sunscreen
Spectrum and UV radiation flux of the emitting source
Reading of the minimal erythemal dose.
Two other inter-laboratory evaluations were subsequently conducted 30 in order to produce greater control of the parameters described above. In the end, based on a conclusion of the study, the key parameters of the method, which should be ideally controlled, are the amount and form of application of the product.
The definition of the amount of 2 mg/cm 2 of product application, presented by the FDA in 1978 and later maintained by revisions of the FDA, COLIPA, and the International Method, is based on the observation that lower amounts reduce the homogeneity of the protective film on the skin as a result of irregularities of the skin surface. 34
The skin surface is uneven, consisting of ridges and bumps that may have greater or lesser amplitude depending on the region of the body. 35
Figure 3 schematically shows the skin surface. 36
According to Brown and Diffey 34, although there is wide variation among individuals, the average volume for a given product to cover all the "ridges" present on the skin surface, corresponding to one (1) cm2 , would be between 1 to 2 µl . In this case, any topical product, assuming a density of 1 g/cm3 , would not cover the "top" of the epidermal ridges to the minimum of 1 mg/cm2. Thus, according to the authors, the amount of 2 mg/cm 2 would be necessary for the sunscreen to offer a minimum of 1 mm of coverage of the tops of the epidermal ridges (Figure 4).6
However, although recommended, sunscreen users do not apply the amount of 2 mg/cm 2 when exposed to the sun for leisure or work activities.
Several studies published in the literature 36-41 show that the amount of sunscreen applied by users varies from 0.39 to 1.3 mg/cm 2 , much less than the amount applied in the laboratory test to determine the SPF, as recommended by internationally accepted methods . 10,.32
The interference of the applied amount in the level of protection offered by sunscreens was evaluated by different authors. 36,38,42,43 The findings of these studies, particularly with regard to the evaluation of the interference pattern of the amount applied in determining the SPF value, are contradictory.
A recent study published by Schalka S, Reis VMS and Cuce LC 44 evaluated the interference of the applied amount of two photoprotectors (SPF values 15 and 30, respectively) in determining the SPF value, according to the methodology proposed by the FDA in 1999 10 and concluded that there is an exponential relationship between the amount applied and the change in value of the SPF.
The authors were able to develop a mathematical equation capable of estimating the protection achieved in practice by the volunteer, based on labeling data of SPF and the amount applied.
The main controversy, however, refers to the value of SPF being limited at 30, as suggested by the FDA in 1993. 28
This proposal was based on a previously published study by Groves, 45 in which the authors showed through mathematical analysis and spectrophotometry that the absorbance value of a given sunscreen may be related to the inverse of the SPF value, as expressed by the following equation:
A = 1 - 1/FPS
Where A = Absorbance of the product
When this equation is applied, we can develop a relationship curve between absorbance and SPF, as shown in Graph 1.
As we can see, the proportional gain of absorbance compared to an increase in the SPF value is reduced dramatically when the SPF value is above 30.
This rationale led the FDA to publish in its proposed final monograph in 1993 28 a decision to limit SPF values at 30, a concept that has been widely circulated.
However, the issue is still controversial.
Osterwalder and Herzog, 46 in a recent article published, show that the proposed mathematical reasoning could be done in reverse, by analyzing how much energy passes through the sunscreen (transmittance) instead of how much energy is absorbed by it (absorbance) where:
T = 1 -A
By applying this reasoning, we find that the amount of energy that passes through the sunscreen with SPF 60 (and therefore, affects the skin) would be half of that transmitted by a sunscreen with SPF 30. Thus, the protection offered by the product with SPF 60 would be double that offered by the product with SPF 30, as seen in graph 2.
Another point to consider is associated with the biological marker related to the protective effect. We know that the SPF measures the protection against sunburn, so the protection effect (in terms of percentage of absorption or transmission), as described above, refers exclusively to protect against the production of erythema. We cannot state, by this reasoning, what the percentage of protection against the development of skin cancer is or even discuss the effects of UVA radiation.
Finally, we must consider the relationship between the applied amount of sunscreen and SPF. As discussed above, the amount of the product applied is the main factor of interference in the SPF of a given sunscreen. 44 Therefore, if the amount of the sunscreen applied is inadequate, as in most cases, the protection achieved by the user is lower than that shown in the product label, and the relationship between absorbance and FPS, as proposed by Groves, 45 is no longer valid.
All these factors were considered by the FDA in its proposal to amend the final monograph on photoprotectors, presented in 2007 29 and not yet completed to date. In this document, the U.S. regulatory agency recommends raising the threshold value for SPF to 50 +, reconsidering the observations made in 1993.
Questions regarding proper use of sunscreens, as an essential factor in the effectiveness of the product, have been highlighted in the international literature. Recent publications. 46.47 reinforce the need for greater attention to compliance with the most appropriate use of the photoprotector, including the application of the correct amount and periodic reapplication.
As Osterwalder and Herzog 46 comment in their review article on the subject: "The best photoprotector may offer insufficient protection only if it is not applied uniformly, if it is applied in insufficient amount or if it is simply not applied."
Thus, as stated earlier, the SPF value should no longer be considered in absolute terms, such as additional exposure time before the formation of erythema.
The most up-to-date concept in terms of photoprotection is to consider the SPF value in a range of protection, as proposed by the FDA in 2007 29 and presented in Table 3.
A more appropriate interpretation is that the SPF value, in numerical terms, should be relative, as a result of the actual circumstances of product use. Therefore, in practice, the use of a sunscreen with SPF 30 or 35 makes no difference if, for example, it is not applied properly.
The Sun Protection Factor is still the main information about the photoprotective efficacy of a sunscreen, but its interpretation should not be based solely on its numeric value, but must also consider the proper way to use the product in terms of applied amount and regularity of reapplication.
Finally, in choosing a photoprotective agent, in addition to the SPF, data on the substantivity (water resistance), UVA protection and photostability should be considered for adequate protection.
1. Roelandts R. History of human photobiology In: Lim HW, Hönigsmann H, Hawk JLM. Photodermatology. New York: Informa Healthcare USA; 2007. p 1-13. [ Links ]
2. Giacomoni PU. Sunprotection: Historical perspective In: Shaath NA. Sunscreens: Regulation and commercial development. 3rd ed. Boca Raton: T&F Informa; 2005. p 71-85. [ Links ]
3. Urbach F, Forbes PD, Davies RE, Berger D. Cutaneous photobiology: past, present, and future. J Invest Dermatol. 1976;67:209-24. [ Links ]
4. Pathak MA. Photoprotection against harmful effects of Solar UVB and UVA radiation: An Update. In: Lowe NJ, Shaath NA, Pathak MA. Sunscreens: Development, evaluation, and regulatory aspects, 2nd ed. New York: Marcel Dekker; 1997. p 59-79. [ Links ]
5. Osterwalder U, Lim HW. Novel developments in photoprotection: Part I. In: Lim HW, Hönigsmann H, Hawk JLM. Photodermatology. New York: Informa Healthcare USA; 2007. p 279-95. [ Links ]
6. Schalka S. Influência da quantidade aplicada de protetores solares no fator de proteção solar (FPS): avaliação de dois protetores solares com os mesmos ingredientes em diferentes concentrações [Dissertação]. São Paulo (SP): Universidade de São Paulo; 2009. 152 p. [ Links ]
7. Kullavanijaya P, Lim HW. Photoprotection. J Am Acad Dermatol. 2005;52:937-58. [ Links ]
8. Tuchinda C, Lim HW, Osterwalder U, Rougier A. Novel emerging sunscreen technologies. Dermatol Clin. 2006;24:105-17. [ Links ]
9. Forestier S. Rationale for sunscreen development. J Am Acad Dermatol. 2008;58:S133-8. [ Links ]
10. Food and Drug Administration [Internet]. Department of Health and Human Services. FDA, USA. Sunscreen Drug Product for Over-The-Counter Human Use, Final Monograph. Federal Register. 1999;64(98):27689-93. [cited 2011 Apr 28]. Avaiable from: www.fda.gov/downloads/Drugs/DevelopmentApprovalProcess/DevelopmentResources/Over-the-CounterOTCDrugs/StatusofOTCRulemakings/ucm090244.pdf [ Links ]
11. Agência Nacional de Vigilância Sanitária (ANVISA) [Internet]. 2002. Regulamento Técnico Sobre Protetores Solares em Cosméticos, Resolução RDC 237. [acesso 28 Mar 2011]. Disponível em: http://e-legis.anvisa.gov.br/leisref/public/showAct.php?id=18298&word= [ Links ]
12. Naylor MF, Boyd A, Smith DW, Cameron GS, Hubbard D, Neldner KH. High sun protection factor sunscreens in the suppression of actinic neoplasia. Arch Dermatol. 1995;131:170-5. [ Links ]
13. Thompson SC, Jolley D, Marks R. Reduction of solar keratoses by regular sunscreen use. N Engl J Med. 1993;329:1147-51. [ Links ]
14. Green A, Williams G, Neale R, Hart V, Leslie D, Parsons P, et al. Daily sunscreen application and betacarotene supplementation in prevention of basal-cell and squamous-cell carcinomas of the skin: a randomized controlled trial. Lancet. 1999;354:723-9. [ Links ]
15. Vainio H, Miller AB, Bianchini F. An international evaluation of the cancer-preventive potential of sunscreens. Int J Cancer. 2000;88:838-42. [ Links ]
16. Fourtanier A. Mexoryl SX protects against solar-simulated UVR-induced photocarcinogenesis in mice. Photochem Photobiol. 1996;64:688-93. [ Links ]
17. Hayag MV, Chartier T, DeVoursney J, Tie C, Machler B, Taylor JR. A high SPF sunscreen's effects on UVB-induced immunosuppression of DNCB contact hypersensitivity. J Dermatol Sci. 1997;16:31-7. [ Links ]
18. Huncharek M, Kupelnick B. Use of topical sunscreens and the risk of malignant melanoma: a meta-analysis of 9067 patients from 11 case-control studies. Am J Public Health. 2002;92:1173-7. [ Links ]
19. Rigel DS. The effect of sunscreen on melanoma risk. Dermatol Clin. 2002;20:601-6. [ Links ]
20. Diffey BL. Sunscreen and melanoma: The future looks bright. Br J Dermatol. 2005;153:378-81. [ Links ]
21. IARC Handbooks of Cancer Prevention. World Health Organization. Lyon, France: International Agency for Research on Cancer; 2001. p. 62. (Sunscreens; vol. 5). [ Links ]
22. Henne W. In vivo determination of the sunscreen factor of cosmetic preparations, history and the present state of art. Parf Kosm. 1983;64:415-423. [ Links ]
23. Schulze R, Einige Versuche und Bemerkungen zum Problem der handelsüblichen Lichtschutzmittel. Praf u Kosm. 1956;37: 310-5. [ Links ]
24. Greiter F. Sun protection factor-development methods. Parf Kosm. 1974;55:70-75. [ Links ]
25. Brown M. SPF testing in Europe: The International SPF Test Method. In: Shaath NA. Sunscreens: Regulation and Commercial Development. 3rd ed. Boca Raton: T&F Informa; 2005. p 779-806. [ Links ]
26. Food and Drug Administration (FDA). Department of Health, Education and Welfare. USA: Sunscreen drug products for over-the-counter drugs: proposed safety, effective and labeling conditions. Federal register. 43/166. 1978;38206-69. [ Links ]
27. Fitzpatrick TB. The validity and practicability of sun-reactive skin types I through VI. Arch Dermatol. 1988;124:869-71. [ Links ]
28. Food and Drug Administration, Department of Health and Human Services, FDA. USA: Sunscreen Drug Product for Over-The-Counter Human Use, Tentative Final Monograph. Federal Register. 1993;58(90):27693-28194. [ Links ]
29. Food and Drug Administration (FDA). Department of Health and Human Services. USA: Sunscreen Drug Product for Over-The-Counter Human Use, Proposed Amendment of Final Monograph, Propose Rule, Federal Register. 2007:72(165):49070-122. [ Links ]
30. COLIPA. Sun protection factor test method. COLIPA Publication. Ref 94/289. October 1994. [ Links ]
31. COLIPA [Internet]. International Sun Protection Factor Test Method, February 2003. [cited 2011 May 05]. Avaiable from: http://www.ncv-cosmetica.nl/upload/File/20030201_Colipa_SPF_methode.pdf [ Links ]
32. COLIPA [Internet].Guidelines. The European Cosmetics Association. International Sun Protector Factor Test Method, May 2006. [cited 2011 Apr 29]. Avaiable from: http://www.colipa.eu/publications-colipa-the-european-cosmetic-cosmeticsassociation/guidelines.html?view=item&id=21 [ Links ]
33. Sayre RM, Agin PP, LeVee GJ, Marlowe E. A comparison of In Vivo and in Vitro testing of sunscreening formulas. Photochem photobiol. 1979; 29:559-66. [ Links ]
34. Brown S, Diffey BL. The effect of applied thichness on sunscreen protection: In vivo and in vitro studies. Photochem Photobiol. 1986;44:509-13. [ Links ]
35. Freeberg IM, Eisen AZ, Wolff K, Auster KF, Goldsmith LA, Katz SI. Fitzpatrick's Dermatology in General Medicine. 6th ed. New York: Mc Graw-Hill; 2003. p.58-88. [ Links ]
36. Stenberg C, Larko O. Sunscreen application and its importance for the sun protection factor. Arch Dermatol. 1985;121:1400-2. [ Links ]
37. Bech-Thomsen N, Wulf HC. Sunbather's application of sunscreen is probably inadequate to obtain the sun protection factor assigned to the preparation. Photodermatol Photoimmunol Photomed. 1992;9:242-4. [ Links ]
38. Gottieb A, Bourget TD, Lowe NJ. Effects of amounts of application of sun protection factor. In: Lowe NJ, Shaath NA, Pathak MA. Sunscreens: Development, evaluation, and regulatory aspects. 2nd ed. New York: Marcel Dekker; 1997. p 583-9. [ Links ]
39. Azurdia RM, Pagliaro JA, Diffey BL, Rhodes LE. Sunscreen application by photosensitive patients is inadequate for protection. Br J Dermatol. 1999;140:255-8. [ Links ]
40. Autier P, Boniol M, Severi G, Dore JF. European Organization for Research and Treatment of Cancer Melanoma Co-operative Group. Quantity of sunscreen used by European students. Br J Dermatol. 2001;144:288-91. [ Links ]
41. Neale R, Williams G, Green A. Application patterns among participants randomized to daily sunscreen use in a skin cancer prevention trial. Arch Dermatol. 2002;138:1319-25. [ Links ]
42. Faurschou A, Wulf HC. The relation between sun protection factor and amount applied in vivo. Br J Dermatol. 2007;156: 716-9. [ Links ]
43. Bimczok R, Gers-Barlag H, Mundt C, Klette E, Bielfeldt S, Rudolph T, et al. Influence of applied quantity of sunscreen products on Sun Protection Factor - A multicenter study organized by the DGK Task force Sun Protection. Skin Pharmacol Physiol. 2007;20:57-64. [ Links ]
44. Schalka S, dos Reis VM, Cucé LC. The influence of the amount of sunscreen applied and its sun protection factor (SPF): Evaluation of two sunscreens including the same ingredients at different concentrations. Photodermatol Photoimmunol Photomed. 2009;25:175-80. [ Links ]
45. Groves GA, Agin PP, Sayre PM. In vitro and In vivo methods to define sunscreen protection. Australas J Dermatol. 1979;20:112-9. [ Links ]
46. Osterwalder U, Herzog B. SPF: World Wide Confusion. Br J Dermatol. 2009;161(Suppl. 3):13-24. [ Links ]
47. Diffey B. Sunscreens: Expectation and Realizations. Photodermatol Photoimmunol Photomed. 2009;25:233-6. [ Links ]
Mailing address: Approved by the Editorial Board and accepted for publication on 12.05.2010. * Work conducted at a private clinic - São Paulo (SP), Brazil.
Av. Dr. Carlos de M. Barros, 304
06023 000 Osasco (SP) - Brasil
Conflict of interest: None
Financial funding: None
Approved by the Editorial Board and accepted for publication on 12.05.2010.
* Work conducted at a private clinic - São Paulo (SP), Brazil.