Science

C-MATE
(Ascorbic acid 2-phosphate Magnesium Salt)

INTRODUCTION:

Vitamin C fatty acid esters and Vitamin C sulfonates have been used in cosmetics for the purpose of preventing pigmentation. These compounds, however, are unstable when formulated into water-miscible cosmetic creams and considerable discoloration of the products as well as decrease in the vitamin C content occurs with lapse of time.

C-MATE is a vitamin C derivative that is more stable in cosmetics.

Chemical Structure

CHARACTERISTICS:

  1. C-MATE is extremely stable in cosmetic bases compared with vitamin C.
  2. C-MATE is well absorbed through the skin.
  3. C-MATE is converted into vitamin C in the skin and exerts vitamin C activity.
  4. C-MATE is safe to use.

PHYSICAL AND CHEMICAL PROPERTIES:

  1. C-MATE is a white to yellowish-white powder.
  2. C-MATE is a soluble in water but insoluble in organic solvents.
  3. C-MATE has no reducing action so that is hardly oxidized.
  4. C-MATE is dephosphorylated into free vitamin C in an acidic solution or in the presence of phosphatase.

HIGH STABILITY

C-MATE is extremely stable in cosmetic bases compared with ordinary vitamin C.

1. CONTENT STABILITY

The stability of C-MATE was examined by mixing C-MATE at a rate of 3% with these two ointment bases.

METHOD:

Three- percent creams containing C-MATE, vitamin C stearate and vitamin C, respectively, were prepared. The samples were left standing on a glass pane at room temperature and the rate of breakdown was determined 10-30 days later.

RESULT:

C-MATE cream was extremely stable, while the vitamin C cream was unsuitable, as the major part of vitamin C had been decomposed in 10 days. Vitamin C stearate was found to rank between C-MATE and vitamin C.

2. COLOR STABILITY

Observation was also carried out on the appearance of cosmetics containing C-MATE. It was found that discoloration and foaming (due to carbon dioxide gas forming as a result of vitamin C breakdown) scarcely developed even when the sample was stored at room temperature for more than 1 year. Table 1 shows variations in the quality of creams (o/w type) containing 3% as vitamin C or C-MATE filled into tubes and stored at room temperature and 40 C. It is clear that C-MATE is extremely stable.

 


HIGH ABSORPTION THROUGH THE SKIN

C-MATE is well absorbed through the skin.

1. URINARY VC AFTER PERCUTANEOUS APPLICATION

Method:

Healthy human subjects were given a prescribed diet and prohibited from excessive vitamin C intake. The urinary output of vitamin C was determined every 2 hours thereafter.

Result:

Figure 2 shows that the urinary output of vitamin C in the C-MATE group was 2-3 times higher than that of the control.

The findings suggest that C-MATE is percutaneously absorbed by human skin and is converted into vitamin C in the skin tissue or other organs. As a result, the urinary output of vitamin C increases.

Graph: Urinary VC After Percutaneous Application of C-Mate Cream and Control


CONVERSION OF C-MATE INTO VITAMIN C IN THE SKIN

C-MATE is converted into vitamin C in the skin and exhibits vitamin C activity.

1.  CONVERSION OF C-MATE INTO VITAMIN C BY SKIN EXTRACT (IN VITRO)

Method:

A skin extract was used.  To 10 ml of the extract  was added 1 mg of C-MATE.  After incubation at 37 C, the vitamin C formed was quantitively assayed.

Result:

Figure 3 shows that 70-90% of C-MATE was converted into vitamin C under an optimal condition (pH 4 - 5).  The conversion of C-MATE into vitamin C decreases a pH above 7.0 and this dephosphorylation is due to acid phosphatase activity in the skin.

2. COMPARISON STUDY ON VITAMIN C FORMATION FROM VITAMIN C DERIVATIVES

A similar experiment was undertaken on C-MATE, comparing it against vitamin C dipalmitate.  Under acid conditions, the amount of vitamin C formed from C-MATE was 30 times more than that from vitamin C dipalmitate in the skin, 300 times more in the liver, and 15 times more in the intestine.  Under neutral conditions, it was 3 times, 40 times and 20 times more in the skin, liver and intestine, respectively.

Graph: Production of VC from C-Mate or VC-Dipalmaitate by Skin Extract and Liver and Intestinal Homogenates