Just taking a 500mg x 2 Vitamin C supplements should provide enough for skin repair.
Oral and transdermal (topical) application of Vitamin C (and other molecules in general) follow completely different routes with different absorption rates and accompanying nuances.
Oral intake. Absorption rate is dosage dependent:
– At moderate doses (≤ 250 mg/day): 70–90 per cent of ascorbate is absorbed into the bloodstream. Bloodstream means just that – Vitamin C will be distributed throughout the entire body, which includes tissues, internal organs and skin. Active absorption takes place in the small intestine predominantly by SVCT1 and SVCT2 sodium-ascorbate co-transporters.
– At high doses (≥ 1g a day): passive diffusion takes over and also takes place in the small intestine although now via GLUT transporters that become saturated and absorption efficiency drops to 50 per cent or lower.
The half-life of Vitamin C taken orally is approximately four hours anyway, after which any excess of it still circulating will be rapidly excreted via the renal route (kidneys). Studies report that significantly less than 0.1 per cent makes into the epidermal (skin) layer.Transdermal (topical) application. Depends on the concentration and several factors, but a 20% concentration serum (not a cream) can achieve a > 80% absorption rate through the skin into receptor fluid after 24 hours. Half-life of Vitamin C applied topically is approximately 4 days.
Recap: less than < 0.1 % / 4 hours half-life for the oral route vs more than 80 % / 4 days half-life for the transdermal route.
Otherwise, the absorption of high doses depends on stress level - when you are not healthy, your body will absorb A LOT more, as shown by vitamin C bowel tolerance method.
To be sure you have it where it counts, take all forms of C - liposomal, film, AA and topical
Topical application of ascorbyl palmitate/«liposomal C», on the other hand, has very poor uptake due to the molecule size being too big to penetrate the skin layer[0]:
L-ascorbic acid must be formulated at pH levels less than 3.5 to enter the skin. Maximal concentration for optimal percutaneous absorption was 20%. Tissue levels were saturated after three daily applications; the half-life of tissue disappearance was about 4 days. Derivatives of ascorbic acid including magnesium ascorbyl phosphate, ascorbyl-6-palmitate, and dehydroascorbic acid did not increase skin levels of L-ascorbic acid.
Key takeway: «Derivatives of ascorbic acid including magnesium ascorbyl phosphate, ascorbyl-6-palmitate (a.k.a «liposomal C», and dehydroascorbic acid did not increase skin levels of L-ascorbic acid».[0] Source: https://europepmc.org/article/MED/11207686
Taking any form of vitamin C orally still confers statistically insignificant benefits for the skin due to having to propagate and get distributed throughout the entire body.
The article in question discusses the benefits of the topical application of vitamin C, the benefits of which have been extensively studied. Vitamin C (especially in combination with ferulic acid) is amongst very few skincare products that actually work – it has been known for a long time.
Maybe not if you take it in multiple of grams, e.g. you brute force it to replace non-working GULO gene you have, that would do it in that range if not defective.
One of the common strategies to prolong the circulation of vitamin C is to recycle it by coupling it with, e.g. N-acetyl cysteine.
Yes when your body gets enough of it (its called Vitamin C Flush and its not harmful), which is dynamic. I take 10+ grams and do not have diarrhoea, I might get it on 20+ IF I am healthy. I don't get it with 100g when I have influenza which is the state of the system when body requires more and SVCT pumps are active like crazy. This is trivially easy to check out yourself, you don't need a study. I have never seen a better feedback system for any drug, really.
> Can you explain and cite a study reference?
There are no studies about it, you need to try it yourself. Vitamin C is non-toxic and doesn't produce kidney stones, contrary to popular belief.
There are medical hypothesis and Linus Pauling wrote a few books about it long time ago.
https://www.sciencedirect.com/science/article/abs/pii/030698...
Check out pharmacokinetics here:
https://www.tandfonline.com/doi/abs/10.1080/1359084080230542...
> One of the common strategies to prolong the circulation of vitamin C is to recycle it by coupling it with, e.g. N-acetyl cysteine.
Yes, I take NAC too, however, the worst offender is sugar, as GLUT2 transports both C and glucose, and since its passive transporter C gets outcompeted given the levels of both.
I can explain 2 decades of experience with it, if you need some info send me a note.