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Ingredient collection

Microencapsulated Ingredients

Food-grade encapsulation for oxidation, light, heat and moisture protection, taste and odour masking, oil-to-powder conversion and improved dispersibility. This range is immediate / non-modified release — we do not describe encapsulation as controlled release.

Microencapsulated Ingredients — 12 ingredients

Showing 1–12 of 12 ingredients

Formulator’s buyer guide

Choosing microencapsulated nutraceutical ingredients

Microencapsulation is most useful when it solves a defined formulation problem and the relevant performance is supported by appropriate evidence. This guide explains how to compare immediate-release microencapsulated ingredients without assuming that every coating provides the same protection or handling benefit.

What are the benefits of microencapsulation in nutraceuticals?

Microencapsulation can protect sensitive ingredients from oxygen, light, heat or moisture; reduce unwanted taste and odour; convert oils into manageable powders; reduce direct contact between reactive ingredients; and improve dispersibility or powder handling. The relevant benefit depends on the active, the wall matrix and the finished formulation.

Microencapsulation alone does not demonstrate sustained, delayed or enteric release. The NexaGens range on this page is immediate / non-modified release.

How should formulators choose a microencapsulated ingredient?

Begin with the formulation problem rather than the technology label. For oxidation or light sensitivity, review the protection mechanism and stability evidence. For taste or odour masking, assess performance in the intended dosage form. For oil-to-powder conversion, examine oil loading, surface oil, dispersibility and oxidation controls.

Use our guides to stability protection, taste and odour masking, oil-to-powder conversion and ingredient interaction protection to narrow the requirement.

What evidence should buyers request?

Request the current product-specific document set. Depending on the ingredient, qualification status, manufacturer and batch, this may include a technical data sheet, approved specification, batch Certificate of Analysis, composition information, stability information, microbiological and contaminant specifications, allergen and GMO statements, storage guidance and product-specific performance data.

NexaGens confirms the current documents for each enquiry. Confirm that public claims match the controlled evidence and are relevant to the intended application. Finished-product suitability, dose, labelling and market compliance remain the customer’s responsibility.

Discuss your formulation requirement

Tell us the active, dosage form, target market, processing conditions and expected volume. We can help identify suitable evaluation materials and confirm which technical documents are available.