Science Behind Our Products
LipoQuest™ Products
Vitamin C | Glutathione |
Vitamin B₁₂ | Pearl Tomato® |
Vitamin D₃ | Hyal-Flex™ Hyaluronic Acid |
CoQ10 |
Useful Terms That Help Understand
The Science Behind Our Products
Quantification of Loading
Active ingredients are encapsulated inside liposomal material. The loading amount plays a pivotal role in the bioavailability of the product. One way to quantify the amount of loading is by measuring the percent encapsulation of the active ingredient in the liposome. Higher loading is correlated with longer shelf-life and better stability of the nanocarrier.
Particle Stability
Zeta Potential measures surface charge and is an index of particle stability. The larger the Zeta Potential absolute value, the larger the amount of surface charge.
Liposome Confirmation
Characterization of liposomes is completed by Cryogenic Transmission Electron Microscopy (Cryo-TEM). Successful images will clearly show a uniform round particle size. Cryo-TEM is routinely used to visualize amphiphilic structures in aqueous solutions.
Particle Size
Dynamic Light Scattering (DLS) is a non-invasive spectroscopic method that can determine the distribution of particles, including liposomes, in solution or suspension. DLS can be used to verify a uniform size and size distribution lower than 1nm. Liposomes are typically around 100nm.
Morphology and Particle Size Determination
Transmission electron microscopy (TEM) can be used to establish the size and shape of liposomes. Particle size of powders can be studied by scanning electron microscopy (SEM). The size distribution and surface morphology can be observed.
Encapsulation Efficiency
The amount of active ingredient represented by the percentage of active ingredient inside the liposome when compared with the total amount of active ingredient present. It can be quantified by a variety of methods that include size exclusion chromatography, or by ultrafiltration-centrifugation techniques.
In the Ultrafiltration-centrifugation technique, the free active ingredient can be separated from liposomes by spinning a solution in an ultracentrifuge. After spinning the solution, the liposomes form a solid pellet and can be isolated from the filtrate that contains the unbound material. Using spectroscopic methods, like HPLC, LCMS and absorbance readers, the concentration of the unbound material can be quantitated.
Encapsulation efficiency (EE%) can be calculated by the difference between the total (Ctotal) and free active ingredient (Cf) concentrations.
EE%= [Ctotal-Cf)/Ctotal] x 100

Unpublished data
- LipoQuest™ CoQ10 has enhanced in vitro cell uptake. Studies using HEK 293 cells show a ~3X increase in cell permeability compared to CoQ10. In addition, these studies also documented a 6-fold increase in solubility in aqueous environments compared to CoQ10.This result has been shown for other lipophilic active ingredients.
- Similar experiments with LipoQuest™ Vitamin C are in progress.
- LipoQuest™ Vitamin C has been visualized using cryo EM imaging. Spherical liposomes have been documented with an average radius of ~30nm-50nm.
- Encapsulation Efficiencies are currently being assessed for LipoQuest™ Vitamin C using both ultracentrifuge method. Analysis by LCMS, and also by Zeta Potential.
Our Qualifications

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The certification process entails a constant evaluation and inspection of equipment, facilities and production procedures and their ability to meet the safety standards

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