Lipoza-Fe – Elevating Iron Supplementation with Liposomal Technology
Iron is an essential mineral required for the formation of hemoglobin, which plays a key role in oxygen transport throughout the body. It is also involved in energy metabolism, cognitive function, and overall physiological performance. However, conventional iron forms often show poor absorption and may cause gastrointestinal discomfort.
Lipoza-Fe is developed using advanced liposomal technology, which encapsulates iron (e.g., ferric pyrophosphate) within a phospholipid matrix to enhance its stability and bioavailability. This delivery system helps protect iron from interactions in the gastrointestinal tract and improves its absorption efficiency.
Liposomal Iron offers a more effective and well-tolerated solution for nutraceutical formulations, supporting improved iron delivery and better overall outcomes.
Experience the advantages of advanced liposomal curcumin technology designed to support better absorption, stability, and overall formulation performance.
Suitable for a wide range of nutraceutical and functional health formulations across multiple dosage formats.
Ideal for convenient daily nutraceutical supplementation.
Suitable for stable and easy-to-consume health formulations.
Designed for quick-mix and on-the-go nutritional applications.
Perfect for enjoyable and consumer-friendly wellness products.
Suitable for liquid formulations with enhanced ingredient delivery.
Ideal for precise and convenient liquid nutraceutical delivery.
Suitable for stable liquid formulations with easy administration.
Designed for versatile blending and convenient nutritional use.
Provides fast-dissolving delivery for enhanced consumer convenience.
Offers quick and convenient oral delivery of active ingredients.
Designed to dissolve rapidly in the mouth for easy consumption.
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Dynamic Light Scattering (DLS) is employed to evaluate the particle size distribution and polydispersity of liposomal formulations, providing essential information on colloidal stability, dispersion uniformity, and potential bioavailability.
For example – Lipoza®-Curcumin
Caco-2 studies utilize human intestinal epithelial cell monolayers to evaluate the permeability and predicted absorption of test substances across the gut barrier.
For example – Lipoza-Glutathione
Demonstrated superior permeability, showing 0.95% transport compared to 0.29% for Reduced L-Glutathione—an approximate 3.28-fold increase. This enhanced permeability, despite lower glutathione content, indicates improved intestinal absorption and supports its potential as a more bioavailable form of glutathione supplementation.
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