Magnesium Ascorbyl Phosphate

One of the best-researched derivatives of vitamin C. It is more resistant to light and air and retains all the properties of ascorbic acid – antioxidant, collagen-boosting, and anti-pigmentation, but with less irritation.
Antioxidant
Other functions
Origin
Magnesium Ascorbyl Phosphate

Overview

Magnesium ascorbyl phosphate (MAP) is a derivative of vitamin C. It is one of the best-researched derivatives and has a multitude of benefits for the skin.

You can read more about regular ascorbic acid (AA) here - Ascorbic Acid - to learn about its mechanism of action. In short, it is a skin-natural antioxidant, collagen boosting, and anti-pigment ingredient that unfortunately has some major stability and skin penetration problems.

Ascorbic acid derivatives such as MAP were developed in an attempt to resolve these issues and develop a more potent and practical version of vitamin C for use in skincare products.

Magnesium ascorbyl phosphate, like ascorbic acid, is water-soluble, but dramatically different in its range of stability. MAP is most stable at neutral and basic pH levels and is more resistant towards light and oxygen, whereas AA is only stable at a very acidic pH level.

This is a benefit to people with more sensitive skin who cannot tolerate highly concentrated and acidic AA serums. MAP also has a longer shelf life.

Older studies demonstrate that MAP, as a water-soluble, negatively charged molecule, has only limited absorption through the skin. New methods have been developed to increase its absorption, including special microemulsions, gels, and ultrasound.

MAP is a very promising ingredient in skincare. There are several studies in test-tubes and on animals that confirm its antioxidant and collagen-boosting properties, although the results from human trials are more relevant.

The application of a 2% MAP emulsion was found to improve skin hydration in the deeper layers of the skin, suggesting that MAP was effectively absorbed and converted into AA.

The biggest field of clinical research is dedicated to the effects of MAP on pigmentation issues. The following clinical studies all reported good results: A 10% MAP cream on age-related dark spots, a 3% MAP moisturizer for sun-induced spots in Japanese women, a 5% MAP cream in combination with pulsed light for Asian volunteers with melasma, and a 5% MAP cream combined with chemical peeling.

A specially formulated MAP cream reported even better results than a trichloroacetic acid peeling for the treatment of melasma. None of these studies reported any kind of side effects.

Science

1
Stamford N. P. (2012). Stability, transdermal penetration, and cutaneous effects of ascorbic acid and its derivatives. Journal of cosmetic dermatology, 11(4), 310–317.
2
Segall, A. I., & Moyano, M. A. (2008). Stability of vitamin C derivatives in topical formulations containing lipoic acid, vitamins A and E. International journal of cosmetic science, 30(6), 453–458.
3
Pinnell, S. R., Yang, H., Omar, M., Monteiro-Riviere, N., DeBuys, H. V., Walker, L. C., Wang, Y., & Levine, M. (2001). Topical L-ascorbic acid: percutaneous absorption studies. Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.], 27(2), 137–142.
4
Wang, P. C., Huang, Y. L., Hou, S. S., Chou, C. H., & Tsai, J. C. (2013). Lauroyl/palmitoyl glycol chitosan gels enhance skin delivery of magnesium ascorbyl phosphate. Journal of cosmetic science, 64(4), 273–286.
5
Liao, A. H., Lu, Y. J., Hung, C. R., & Yang, M. Y. (2016). Efficacy of transdermal magnesium ascorbyl phosphate delivery after ultrasound treatment with microbubbles in gel-type surrounding medium in mice. Materials science & engineering. C, Materials for biological applications, 61, 591–598.
6
Hwang, T. L., Tsai, C. J., Chen, J. L., Changchien, T. T., Wang, C. C., & Wu, C. M. (2012). Magnesium ascorbyl phosphate and coenzyme Q10 protect keratinocytes against UVA irradiation by suppressing glutathione depletion. Molecular medicine reports, 6(2), 375–378.
7
Kobayashi, S., Takehana, M., Kanke, M., Itoh, S., & Ogata, E. (1998). Postadministration protective effect of magnesium-L-ascorbyl-phosphate on the development of UVB-induced cutaneous damage in mice. Photochemistry and photobiology, 67(6), 669–675.
8
Geesin, J. C., Gordon, J. S., & Berg, R. A. (1993). Regulation of collagen synthesis in human dermal fibroblasts by the sodium and magnesium salts of ascorbyl-2-phosphate. Skin pharmacology : the official journal of the Skin Pharmacology Society, 6(1), 65–71.
9
Lakra, R., Kiran, M. S., & Korrapati, P. S. (2021). Effect of magnesium ascorbyl phosphate on collagen stabilization for wound healing application. International journal of biological macromolecules, 166, 333–341.
10
Campos, P. M., Gonçalves, G. M., & Gaspar, L. R. (2008). In vitro antioxidant activity and in vivo efficacy of topical formulations containing vitamin C and its derivatives studied by non-invasive methods. Skin research and technology, 14(3), 376–380.
11
Kameyama, K., et al. (1996). Inhibitory effect of magnesium L-ascorbyl-2-phosphate (VC-PMG) on melanogenesis in vitro and in vivo. Journal of the American Academy of Dermatology, 34(1), 29–33.
12
Miyamoto, K., Takiwaki, H., Hillebrand, G. G., & Arase, S. (2002). Utilization of a high-resolution digital imaging system for the objective and quantitative assessment of hyperpigmented spots on the face. Skin research and technology, 8(2), 73–77.
13
Shaikh, Z. I., & Mashood, A. A. (2014). Treatment of refractory melasma with combination of topical 5% magnesium ascorbyl phosphate and fluorescent pulsed light in Asian patients. International journal of dermatology, 53(1), 93–99.
14
Murtaza, F., Bangash, A. R., Khushdil, A., & Noor, S. M. (2016). Efficacy of Trichloro-Acetic Acid Peel Alone Versus Combined Topical Magnesium Ascorbyl Phosphate for Epidermal Melasma. Journal of the College of Physicians and Surgeons--Pakistan : JCPSP, 26(7), 557–561.
15
Aboul-Einien, M. H., Kandil, S. M., Abdou, E. M., Diab, H. M., & Zaki, M. (2020). Ascorbic acid derivative-loaded modified aspasomes: formulation, in vitro, ex vivo and clinical evaluation for melasma treatment. Journal of liposome research, 30(1), 54–67.