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PelleTune™ Functional Pellets

Functional pellets are small multiparticulate ingredient units whose core and coating are engineered for a defined release or protection profile. This is the most differentiated platform NexaGens operates, and the reason is architectural rather than chemical.

Modules, not fixed blends

Most sustained-release ingredients are supplied as a finished profile. You take the curve the manufacturer chose. If your product needs 40% immediate and 60% over eight hours rather than the ratio on offer, you cannot get there.

NexaGens supplies release profiles as independent modules. You choose the ratio. That only works if the populations are physically matched — which is why every pellet intended for blending is specified to a 500–850 µm size range with matched bulk density and shape.

Populations that differ in size, shape or density segregate during blending, transfer and capsule filling. The dose per capsule then drifts and the dissolution result stops matching the blend you designed. Physical matching is not a detail; it is the whole mechanism.

The five profiles

Type What the coating does Release profile
Immediate release (IR) Minimal coating; rapid disintegration NLT 80% at 30 min
Sustained release SR-4 Diffusion-controlling membrane 15–30% at 1 h; 40–65% at 2 h; NLT 85% at 4 h
Sustained release SR-8 Lower-permeability membrane 10–20% at 1 h; 20–40% at 2 h; 45–65% at 4 h; NLT 85% at 8 h
Taste- and odour-masked IR Saliva-resistant, gastric-soluble sensory barrier NMT 10% in simulated saliva at 2 min; NLT 80% gastric at 60 min
Enteric pH-responsive outer layer NMT 10% after 2 h gastric; NLT 80% within 60 min intestinal
Stability-protected IR Opaque or antioxidant barrier, no intentional delay Protection profile stated per product

Dissolution is by Ph. Eur. 2.9.3. Release and dissolution data is included in the product documentation where applicable.

Quality control parameters

Parameter Why it is specified
Active assay Label claim; also falls as coating weight rises, which is why SR-8 loads lower than IR
Particle size distribution Decides whether a blend survives handling. D10/D50/D90 by sieve or laser diffraction
Bulk and tapped density Segregation behaviour and capsule-fill weight
Coating weight gain The primary process variable controlling the release rate
Dissolution profile Multiple time points, with batch-to-batch variability at each
Dissolution after processing Capsule filling and tableting can damage a membrane. Pre-process data alone is not enough
Friability Mechanical robustness through downstream handling
Moisture Affects both coating performance and core stability

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, the microbiological specification, and release / dissolution data where applicable. Six further pellets — sodium butyrate, Lactobacillus acidophilus, protease, lipase, amylase and stability-protected algal DHA — are in development and not currently supplied. That means the enzyme and probiotic proposition, where activity-unit rather than weight-based specification is essential, is not yet available. We would rather state that than imply a broader range.

See the twelve products · Modified release · Enteric and intestinal delivery

Ingredient portfolio

Functional pellets on this platform

Compare available ingredients, then review the formulation objective and controlled documentation relevant to your intended application.

View all Functional Pellets