The result of a three-year, Innovate UK collaborative project with Anglia Ruskin University.
By implementing our innovative SAIFx® technology, we have successfully achieved scaling up of the world's first true dry liposomes for nutraceutical application.
Third party validated, our dry liposomal powders have been scrutinised under Transmission Electron Microscopy which determines the size, shape and distribution of nanoparticles.
Date of Analysis 19th June 2024
Microscope JEM1400
Magnification 30kx
Enhanced stability
Ease of storage and transportation
Improved formulation flexibility
Enhanced bioavailability
Palatability
Convenience
The development of dry liposome powder represents a significant innovation in the field of drug delivery and nutritional supplements. This technology offers numerous potential uses and advantages over traditional liquid liposomal formulations, enhancing the efficacy, stability, and convenience of liposomal products.
Pharmaceutical Applications:
Nutritional Supplements:
Cosmetic and Skincare Products:
Veterinary Medicine:
Enhanced Stability:
Improved Bioavailability:
Ease of Storage and Transportation:
Controlled Release:
Versatility in Formulation:
Reduction of Side Effects:
Enhanced Solubility of Hydrophobic Compounds:
Protection from Degradation:
Dry liposome powder technology offers numerous advantages over traditional formulations, including enhanced stability, improved bioavailability, and ease of storage and transportation. These benefits make it a versatile and powerful tool for delivering pharmaceuticals, nutritional supplements, and cosmetic ingredients more effectively.
As GMPriority Pharma continues to innovate and expand the applications of this technology, the potential for improving health outcomes and product performance grows exponentially.
Spray drying is a common manufacturing method for producing dry powder liposomes. Spray drying is a simple, robust, continuous process.
In this process, a liquid liposomal suspension is atomised into fine droplets, which are then rapidly dried using hot air or inert gases. The resulting powder consists of individual or aggregated liposomes, encapsulating the active ingredient.
Freeze drying, also known as lyophilisation, is the process of freezing a liquid liposomal suspension followed by sublimation of ice under vacuum conditions.
Essentially, freeze drying is a dehydration technique. What differentiates the freeze drying process from other dehydration techniques, is that dehydration takes place whilst the product is in a frozen state and in a vacuum.
This gentle drying process preserves the integrity of the liposomal structure and prevents aggregation, resulting in a dry powder with high encapsulation efficiency and stability.
Both spray drying and freeze drying techniques offer advantages and are suitable for different applications and formulations. The choice of manufacturing method depends on factors such as the properties of the active ingredient, desired particle size distribution, and scalability of production.
Vitamin C samples physicochemical properties comparison processed using freeze and spray drying
Physical Properties | Freeze Drying | Spray Drying |
Particle size after processing | 236nm | 451nm |
Moisture content | 2.36% | 5.8% |
Angle of repose | Excellent | Excellent |
Compressibility index | Excellent | Excellent |