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Durlip™ Liposomal NAD+
Disclaimer: These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.
Form and Application
Product Dosage Form
Powder
Scope of Application
Tablets | Hard Capsules | Solid Beverages |
Core Selling Points
Spherical Liposome Structure Confirmed by Optical, SEM and TEM
Uniform Particle Size
Fast Water Dispersion
High Bioavailability
Detailed Introduction
Advantage Description
●Spherical Liposome Structure Confirmed by Optical, SEM and TEM
Uniform spherical structure under microscope, significantly better than fragmentary morphology of competitors.
●Uniform Particle Size
Durlip™ liposomal NAD+ shows unimodal distribution after rehydration, with uniform particle size for better application and absorption.
●Fast Water Dispersion
Rapid dispersing for easy downstream processing and application.
●High Bioavailability
Animal tests show Durlip™ liposomal NAD+ improves NAD+ level by 4.1 times over the raw material group.
Additional Data
●Physicochemical parameters: Dynamic light scattering (DLS) measured an average reconstituted particle size of 206.4 nm, with a unimodal distribution indicating uniform particle size.
●Microstructural characterization: Multi-dimensional characterization via optical microscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM) shows that Durlip™ Liposomal NAD+ exhibits a complete spherical liposome structure with no distinct crystalline structure of the raw material.
●X-ray diffraction (XRD): Raw β-NAD+ material shows distinct crystalline absorption peaks at diffraction angles of 26.65°, 29.7°, and 37.75°. In Durlip™ Liposomal NAD+, these crystalline absorption peaks are either absent or significantly attenuated, indicating that the crystalline structure of NAD+ has been transformed and the active ingredient is well encapsulated within the liposomes.
●Bioavailability (SD rat model):
Experimental design: Healthy rats were selected and administered treatments. NAD+ concentrations in plasma were measured for raw NAD+ material, Durlip™ Liposomal NAD+, and other branded liposomal NAD+ products.
Conclusion: The relative NAD+ increase brought by Durlip™ NAD+ was 4.1× higher than that of the raw material group. Liposomal encapsulation significantly improves the oral bioavailability of NAD+, transforming it from nearly non-absorbable to effectively utilizable.
Reference
Liposomal solution manufacturer
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