When taken as oral supplements, NAD+ and its precursors are almost entirely degraded to Nicotinamide (NAM) in the stomach, intestines, and liver, greatly diminishing the effectiveness. (1,2,3,4)

Delivery methods that avoid digestion and deliver the product intact to cells throughout the body are needed to realize the potential of NAD+ Boosters.

When taken as oral supplements, NAD+ and its precursors are almost entirely degraded to Nicotinamide (NAM) in the stomach, intestines, and liver, greatly diminishing the effectiveness. (1,2,3,4)

Delivery methods that avoid digestion and deliver the product intact to cells throughout the body are needed to realize the potential of NAD+ Boosters.

“Oral NR dosing increased circulating NAM ~40-fold while NMN remained unchanged and NR was detected only at trace levels in the blood.”

“Thus, the majority of the orally administered NR that reaches the muscle appears to enter in the form of liberated NAM or as NMN.” (6)

Digested by bacteria in stomach – NAD+ and precursors are mostly digested in the stomach, with research pointing to bacteria as voracious consumers.

(The chart above shows huge increase in NMN after antibiotics.)

“Oral NR dosing increased circulating NAM ~40-fold while NMN remained unchanged and NR was detected only at trace levels in the blood.”

“Thus, the majority of the orally administered NR that reaches the muscle appears to enter in the form of liberated NAM or as NMN.” (6)

Digested by bacteria in stomach – NAD+ and precursors are mostly digested in the stomach, with research pointing to bacteria as voracious consumers. 

(The chart above shows huge increase in NMN after antibiotics.)

NR quickly degraded in bloodstream – NR has an even bigger bio-availabilty problem than NMN and NAD+.  It is very unstable in the bloodstream, so it is never found at more than trace levels.(7)  Even supplementation of 1,000 mg a day of NR in humans does not increase NR levels in the blood. (Learn More)

Digested by enzymes in intestines – “Dietary NAD was hydrolyzed primarily in the small intestine…to NMN… was rapidly hydrolized to NR… and NR more slowly to NAM.” (8)

Metabolized to NAM in Liver – Any that makes it past the gauntlet of the GI tract to the liver get mostly metabolized to the less effective Nicotinamide (NAM) before being excreted to the bloodstream. (9)

NR quickly degraded in bloodstream – NR has an even bigger bio-availabilty problem than NMN and NAD+.  It is very unstable in the bloodstream, so it is never found at more than trace levels.(7)  Even supplementation of 1,000 mg a day of NR in humans does not increase NR levels in the blood. (Learn More)

Digested by enzymes in intestines – “Dietary NAD was hydrolyzed primarily in the small intestine…to NMN… was rapidly hydrolized to NR… and NR more slowly to NAM.” (8)

Metabolized to NAM in Liver – Any that makes it past the gauntlet of the GI tract to the liver get mostly metabolized to the less effective Nicotinamide (NAM) before being excreted to the bloodstream. (9)

“Unlike in cell culture where NR and NMN are readily incorporated into NAD, oral administration fails to deliver NR or NMN to tissues.” (10)

“Interestingly, we found that neither compound was able to enter the circulation intact in substantial quantities when delivered orally.” (10)

“Orally delivered NR and NMN are converted into NAM before reaching the systemic circulation.” (10)

“Unlike in cell culture where NR and NMN are readily incorporated into NAD, oral administration fails to deliver NR or NMN to tissues.” (10)

“Interestingly, we found that neither compound was able to enter the circulation intact in substantial quantities when delivered orally.” (10)

“Orally delivered NR and NMN are converted into NAM before reaching the systemic circulation.” (10)

Delivery methods that bypass the gastrointestinal tract completely, or protect NAD+ metabolites are necessary.

Liposomal delivery offers targeted and complete absorption of active ingredients with a delayed‑release effect, unlike all other nutrient delivery methods.

This increased circulation time of key nutrients in the bloodstream significantly improves bioavailability. The higher the bioavailability of an active substance, the more effect it has on the body. (3) 

  • Protects against the harsh environment of the GI tract and increases  oral uptake and absorption.
  • Timing of the dose does not require accompaniment or exclusion of food as the absorption via the liposome avoids the digestive processes.
  • Provides a larger nutrient payload per particle.
  • Offers higher bioavailability and absorption compared to conventional capsules.

Learn More About Improved Bioavailability with Liposomes.

Delivery methods that bypass the gastrointestinal tract completely, or protect NAD+ metabolites are necessary.

Liposomal delivery offers targeted and complete absorption of active ingredients with a delayed‑release effect, unlike all other nutrient delivery methods.

This increased circulation time of key nutrients in the bloodstream significantly improves bioavailability. The higher the bioavailability of an active substance, the more effect it has on the body. (3) 

  • Protects against the harsh environment of the GI tract and increases  oral uptake and absorption.
  • Timing of the dose does not require accompaniment or exclusion of food as the absorption via the liposome avoids the digestive processes.
  • Provides a larger nutrient payload per particle.
  • Offers higher bioavailability and absorption compared to conventional capsules.

Learn More About Improved Bioavailability with Liposomes.