Benefits
Astaxanthin made by yeast fermentation instead of algae
AstaFerm is astaxanthin produced by the yeast Phaffia rhodozyma, which the maker says it grows in closed fermentation tanks. The maker describes it as free, non-esterified astaxanthin that is neutral in taste and odor, supplied as oils for softgels and powders for gummies and drinks. No published human trial has tested it for any health outcome.
Absorption of a single 50 mg dose: registered, results not posted
The maker registered an open-label study in which 12 healthy men took one 50 mg dose of AstaFerm with breakfast, with blood levels tracked for 7 days and side effects recorded. The registry lists it as completed, but no results have been posted and no published paper was found, so its absorption and tolerance are not known.
Mirror-image form compared with algae astaxanthin
Phaffia yeast makes mainly 3R,3'R astaxanthin, while algae astaxanthin contains the 3S,3'S form. Human data on how each form is absorbed disagree: in 3 men given a blend of forms, 3R,3'R rose more in blood than its share of the dose, while in men eating salmon for 4 weeks the 3R,3'R share in blood ended slightly lower than in the fish.
Antioxidant enzyme and safety findings in rats
In rats, a Phaffia astaxanthin extract from another maker showed no toxic effects at up to 1,000 mg/kg a day for 4 weeks, and it did not damage genes in bacterial and mouse tests. In a 90-day rat study, whole Phaffia yeast powder showed no regular toxic effects and raised the antioxidant enzyme glutathione peroxidase. Neither study tested AstaFerm or people.
Blood fats in a registered trial of another Phaffia product
A separate company registered a 12-week placebo-controlled trial of a Phaffia astaxanthin supplement (6 mg capsules, two a day) in 68 adults with raised blood triglycerides. It is listed as completed, but no results have been posted and it did not use AstaFerm, so it adds no evidence on outcomes.
Evidence from algae astaxanthin applies to a different material
Many human astaxanthin trials, summarized on the Astaxanthin page, used Haematococcus algae astaxanthin, which contains the 3S,3'S form as esters, where the clearest results are for skin moisture and elasticity. Those results come from another source, form and stereoisomer and have not been shown for AstaFerm.
Mechanism of action
Same molecule, different mirror-image form
Astaxanthin has two chiral centers. In lab analyses, Phaffia yeast produced astaxanthin mainly in the 3R,3'R configuration, and a recent chiral test found no 3S,3'S astaxanthin in Phaffia yeast powder while detecting it in Haematococcus algae powder. Whether this difference changes effects in people has not been tested.
Free astaxanthin versus esters
NextFerm describes AstaFerm as free, non-esterified astaxanthin and says this boosts uptake, while algae extracts carry astaxanthin as fatty acid esters. In a small human study, esters were not found in blood after a meal, meaning they are split during absorption; no study has compared free and esterified forms for AstaFerm.
Gut transporter preference (lab and animal work)
In cell experiments and an animal intestine model, the uptake protein CD36 took up 3S,3'S astaxanthin more readily than 3R,3'R, and blocking CD36 cut absorption of the 3S,3'S form more. These lab findings suggest the two forms may be absorbed differently, but they have not been confirmed in people.
Clinical trials
Single-center, open-label, non-randomized, single-dose study registered as NCT03807050; one 50 mg dose of astaxanthin from Phaffia rhodozyma in capsules after a fat-balanced breakfast, with blood sampling up to 168 hours; sponsored by the maker (NextFerm Technologies LTD 2019, ClinicalTrials.gov)
12 healthy non-smoking men aged 18 to 45.
The registry lists the study as completed in February 2019, with peak blood level, exposure over time and adverse events as outcomes. No results have been posted on the registry and no published paper was found, so nothing is known about how well AstaFerm was absorbed or tolerated.
Randomized, quadruple-blind, placebo-controlled, parallel trial registered as NCT02343497; astaxanthin from Phaffia rhodozyma, 6 mg capsules, two a day for 12 weeks; primary outcome fasting plasma triglycerides; not AstaFerm (Ajinomoto Foods Europe SAS 2018, ClinicalTrials.gov)
68 adults aged 18 to 60 with fasting triglycerides of 1.2 to under 4 g/L.
The registry lists the trial as completed in November 2015. No results have been posted and no published paper was found, so it provides no evidence on blood fats or safety for Phaffia astaxanthin.
Small human pharmacokinetic study; single meals with 10 mg and, 4 weeks later, 100 mg of astaxanthin as fatty acid diesters, made up of 3R,3'R, meso and 3S,3'S forms in a 31:49:20 ratio; plasma followed for 76 hours; not AstaFerm (Coral-Hinostroza et al. 2004, Comp Biochem Physiol C Toxicol Pharmacol)
3 healthy middle-aged men aged 41 to 50.
The 3R,3'R form made up 54% of astaxanthin in blood but only 31% of the dose, so it accumulated selectively. No esters were found in plasma. Peak blood level after 100 mg was 0.28 mg/L at about 11.5 hours, and the response to dose was not linear. With only 3 people, this is a pharmacokinetic signal, not proof of a benefit.
Randomized, double-blind study; 250 g of wild or farmed salmon daily for 4 weeks, providing 5 micrograms of astaxanthin per gram of fish; plasma astaxanthin and its isomers measured by chiral HPLC; not AstaFerm (Rüfer et al. 2008, Br J Nutr)
28 healthy men.
Plasma astaxanthin plateaued after 6 days (39 nmol/L with wild and 52 nmol/L with farmed salmon), and the isomer pattern in blood resembled the fish eaten. After 28 days, the 3S,3'S share in blood was slightly higher and the 3R,3'R share slightly lower than in the fish, which the authors suggest reflects selective absorption.