A Review on Solid-lipid Nanoparticle

Abstract

Abstract: Hydrophilic and hydrophobic medicines can both be carried by solid lipid nanoparticles (SLNs), which are solid core lipid nanocarriers. They are one of the favoured options for medication delivery since they may be constructed of components that are biocompatible. Surface alterations of SLNs may also provide them distinctive qualities like mucoadhesiveness or targeting capacity. A wide range of drug delivery technologies are being developed at an astounding rate. The two main compounds that are widely delivered to target areas are various manufactured nanoparticles and medications with poor pharmacokinetic and solubility characteristics. The features of biodegradability and nontoxicity make nanolipid dispersions (liposomes, deformable liposomes, virosomes, ethosomes, and solid lipid nanoparticles) the best colloidal carriers for administration. Solid lipid nanoparticles (SLNs), which may be manipulated to demonstrate a variety of benefits over liposomes and polymeric nanoparticles, are the most prevalent among them.