Q-Vitalon — NMN Delivered by QuanticSphere™ PQNS Nanotechnology | Integria Care
QuanticSphere™ PQNS · NAD+ Delivery Platform

NMN your body actually turns into NAD⁺

NMN delivered through PQNS cationic-phospholipid nanotechnology, part of the QuanticSphere™ delivery platform, engineered so more of every dose converts to circulating NAD⁺.

Dark, glowing render of a mitochondrion inside a molecular network sphere with orange nodes, from the Q-Vitalon sales sheet, representing NAD+ metabolism
Plasma NAD+ Response · Single 500 mg Dose · n=8

6.8× the NAD+ exposure of raw NMN

Measured, not modeled.

Q-Vitalon™ (PQNS) conventional NMN
6.8×
AUC vs raw
6004002000
2.9× higher peak
Cmax 575 vs 196 ng/mL
still measurable
at 24 h
0123456⁄⁄824
Mean plasma Beta-NAD (ng/mL) vs time (h) · axis break after 6 h · Time (h)
2.9×
Peak plasma NAD+ (Cmax)
575 vs 196 ng/mL
0
Adverse events
n=8 human study
8.3h
Plasma half-life
+63.5% vs conventional NMN
NAD+ & Healthy Aging

What restoring NAD+ supports

Healthy NAD+ levels
Cellular energy & metabolism
Antioxidant / cellular maintenance
Healthy aging & vitality
The Problem

Conventional NMN is wasted before it's absorbed

01
Absorption

Water-soluble, negatively charged and fragile — degraded in the gut and poorly transported across the intestinal wall.

02
Variability

Inconsistent uptake leads to a weak, unpredictable effect — even at a high labeled dose.

03
Stability

NMN degrades in heat, humidity and acid — cutting shelf life and potency.

Cross-section render of a PQNS cationic phospholipid nanosphere with concentric orange, white and blue layers, from the Q-Vitalon sales sheet
PQNS — Phytosome Quantum Nano Sphere

How it works

(ζ) +40 mV
Zeta potential
198.6 nm
Vesicle size · DLS
The Fix — PQNS Grabs It

NMN is negatively charged; PQNS cationic vesicles bind it electrostatically, shield it through the gut, and carry it into circulation.

Conventional NMN vs. Q-Vitalon (PQNS)

Why formulators are switching

Conventional NMN
Q-Vitalon (PQNS)
Absorption
Water-soluble, negatively charged, fragile — degraded in the gut
PQNS cationic vesicles shield and transport it
Bioavailability
Cmax 196 ng/mL, AUC baseline
Cmax 575 ng/mL (2.9×), AUC 6.8× vs raw
Persistence
Rapidly cleared, near-undetectable by 6 h
Plasma half-life 8.3 h (+63.5%), still measurable at 24 h
Stability
Degrades in heat, humidity and acid
GRAS-compliant phospholipid carrier, ~95–100% batch-consistent dissolution
Spec & Quality

Built for formulators

ActiveNMN (β-nicotinamide mononucleotide) · CAS 1094-61-7
Dissolution~95–100% release, batch-consistent
RegulatoryGMP · 21 CFR 111 · US DSHEA compliance
DeliveryPQNS cationic phospholipid · +139 mV · 198.6 nm
CarrierGRAS-compliant phospholipid
IPQuanticSphere™ · PQNS Patent Pending 202521095813

Common questions about Q-Vitalon

Straight answers for formulators, distributors and brand buyers.

Q-Vitalon is NMN delivered through PQNS cationic-phospholipid nanotechnology, part of the QuanticSphere™ delivery platform, engineered so more of every dose converts to circulating NAD⁺.

Conventional NMN is water-soluble, negatively charged and fragile — it degrades in the gut and is poorly transported across the intestinal wall, giving a weak, unpredictable effect even at a high labeled dose. Q-Vitalon's PQNS cationic vesicles bind NMN electrostatically, shield it through the gut, and carry it into circulation, for measured (not modeled) results: 6.8× the NAD+ exposure of raw NMN.

PQNS (Phytosome Quantum Nano Sphere) is a cationic phospholipid delivery system (+139 mV zeta potential, 198.6 nm vesicle size by DLS). Because NMN is negatively charged, PQNS's cationic vesicles bind it electrostatically, shield it through the gut, and carry it into circulation. This delivery system has a patent pending (No. 202521095813).

In a single 500 mg dose, human pharmacokinetic study (n=8), Q-Vitalon (PQNS) delivered 6.8× the NAD+ exposure (AUC) of raw NMN, measured not modeled. Peak plasma NAD+ (Cmax) reached 575 ng/mL vs 196 ng/mL for conventional NMN (2.9× higher), with a plasma half-life of 8.3 hours (+63.5% vs conventional NMN) — still measurable at 24 hours. There were 0 adverse events in the study.

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