Sphingosomes are considered to be the most effective new vesicular drug delivery system due to their high drug loading capacity, stability, targeting, release, host cell compatibility, safety, etc. CD Formulation's professional team provides sphingosomes vesicular drug delivery system development services, which can be performed by improving drug loading, carrier stability, etc. carried out.
Fig. 1 Cross section view of sphingosomes. (Chaudhari et al., 2020)
Sphingosomes are important lipid vesicle drug delivery systems. They are vesicles composed of a membranous bilayer that encloses an aqueous space in which the drug can be encapsulated. The membranous bilayer consists of natural or synthetic sphingolipids. Sphingosomes are mainly composed of cholesterol and sphingolipids and have higher acid hydrolysis stability and better drug retention properties compared to other liposomes. Sphingosomes are administered by various routes, such as trans-intestinal, inhalation, oral, transdermal, etc.
The classification of sphingosomes is based on the number of lipid bilayers formed and the size of the vesicles. Sphingosomes can be monolayered or multilayered.
The typical average diameter of sphingosomes is 0.05-0.45 microns. The most desirable diameter range is 0.05-0.2 microns.
Small unilamellar vesicles (SUV)
Large unilamellar vesicles (LUV)
Multilamellar vesicles (MLV)
Oligomeric vesicles (OLV)
Multi-vesicular vesicles (MVV)
Vesicles larger than 1 micron in diameter are called giant vesicles (GV).
Sphingosomes are considered to be the most effective new vesicular drug delivery system due to their improved properties as well as compatibility and safety to the host cells. Sphingosomes have been used for diagnostic purposes, clinical delivery of chemotherapeutic compounds, treatment of fungal infections, and ocular delivery. CD Formulation can provide comprehensive sphingosomes system development services, from sphingosomes-based drug delivery characterization and delivery system construction services to in vitro efficacy validation, we can provide you with the most comprehensive services and professional solutions for your project.
Vesicle characterization, including particle size, shape and zeta potential.
Differential scanning calorimetry is used to assess the transition temperature of bilayer vesicles.
The primary method for penetration studies is confocal laser scanning microscopy (CLSM).
Vesicle stability depends on parameters such as structure and shape. Changes in shape and structure can be observed by transmission electron microscopy (TEM).
Ultracentrifugation technique can be used to measure the trapping efficiency.
Differential scanning calorimetry is used to analyze sphingolipid-cholesterol interactions.
Permeability studies are performed by binding sphingosomes to gels. Franz diffusion cell can be used for diffusion studies.
Drug content analysis is performed using UV spectrophotometry and high performance liquid chromatography.
CD Formulation provides integrated and innovative solutions from strategy to implementation to help you increase your opportunities and address your challenges. Through our in-depth experience in many different industries, including consumer and technology, we bring innovative solutions and cross-industry best practices to drug development. If you have any requests for our services, please contact us by phone or email and one of our colleagues will get back to you within three business days.
Reference
Easy access to products and services you need from our library via powerful searching tools.