A high potential for drug delivery has been attributed to particulate drug carriers, especially
small particles such as microparticles and colloidal systems in the nanometer range …

Solid lipid nanoparticles (SLN) introduced in 1991 represent an alternative carrier system to
traditional colloidal carriers, such as emulsions, liposomes and polymeric micro-and …

Solid lipid nanoparticle (SLN) dispersions have been proposed as a new type of colloidal
drug carrier system suitable for intravenous administration. The system consists of spherical …

SLNs are colloidal carriers as an alternative system to the existing traditional carriers
emulsions, liposomes and polymeric nanoparticles had emerged. They are a new …

The introduction of solid Lipid Nanoparticles (SLN) for the first time in late 1991 to be a
substitute transporter system to what known old colloidal carriers, like emulsions, liposomes …

Solid lipid nanoparticles (SLN) are aqueous colloidal dispersions, the matrix of which
comprises of solid biodegradable lipids. They are introduced in 1990 as an alternative …

Solid lipid nanoparticles (SLN) introduced in 1991 represent an alternative carrier system to
traditional colloidal carriers, such as emulsions, liposomes and polymeric micro-and …

Development of colloidal delivery systems has opened new avenues/frontiers for improving
drug delivery. Solid lipid nanoparticles have come up as the latest development in the arena …

The chapter on solid lipid nanoparticles introduces colloidal suspensions of crystalline lipids
as carrier systems for poorly water‐soluble drugs. It describes and compares the various …

This review describes the use of nanoparticles based on solid lipids for the parenteral
application of drugs. Firstly, different types of nanoparticles based on solid lipids such as …