Microencapsulation embeds or surrounds an active within a food-grade matrix or coating. The objective is protection and handling — not release modification.
The distinction that decides everything
Microencapsulation and modified release are different technologies with different evidence requirements, and conflating them is the single most common technical error in ingredient marketing. A matrix that protects an active from oxygen does not thereby delay its release. Describing it as “controlled release” asserts a functional property that has not been demonstrated and usually does not exist.
The entire NexaGens microencapsulated range is immediate / non-modified release. We state that on every product page and on the collection page, and we do not use the phrase “controlled release” anywhere except to explain why it is wrong.
What the matrix is asked to do
| Function |
Mechanism |
Typical actives |
| Oxidation protection |
Physical oxygen barrier, optionally with an antioxidant system in the matrix |
Carotenoids, CoQ10, marine and algal oils |
| Light protection |
Opaque or light-scattering matrix |
Astaxanthin, lycopene, lutein |
| Moisture protection |
Low-permeability matrix |
Hygroscopic salts |
| Taste and odour masking |
Barrier resistant in saliva, soluble in gastric fluid |
Caffeine, iron salts |
| Oil-to-powder conversion |
Emulsification followed by drying into a solid matrix |
Fish oil, algal DHA, essential oils |
| Interaction protection |
Physical separation of reactive species within a blend |
Iron |
| Dispersibility |
A carrier that wets and disperses more readily than the active |
CoQ10, carotenoids |
Quality control parameters
| Parameter |
Why it is specified |
| Active assay |
Label claim and dose calculation |
| Surface active or surface oil |
The most predictive parameter in the whole specification. Unprotected material on the particle surface oxidises first and dominates both sensory and early stability behaviour |
| Encapsulation efficiency |
Proportion of active genuinely held within the matrix |
| Particle size distribution |
Powder handling, blend uniformity, mouthfeel |
| Moisture and water activity |
Water activity, not total water, drives degradation |
| Dispersibility |
The functional outcome, measured rather than asserted |
| Peroxide, anisidine and TOTOX values |
For oil powders, measured over time rather than at release only |
| Payload leakage |
Whether the matrix holds under storage and compression |
Current maturity
All twelve products are at Qualified status: manufactured, released against a confirmed specification and held in stock. Each production batch is supplied with a batch-specific Certificate of Analysis. Documentation available per ingredient includes the TDS, product specification, COA, SDS, allergen, GMO, irradiation and BSE-TSE statements, stability documentation, composition, storage and handling, and the microbiological specification. Where a product page states a functional benefit, we will provide the supporting data on request; where it has not been generated, the page says so.
See the twelve products · Stability protection · Oil-to-powder conversion