Solid lipid nanoparticle

TL;DR: Delivering RSV by SLN contributes to effectiveness of RSV on decreasing cell proliferation, with potential benefits for prevention of skin cancer.

TL;DR: In this article, particle internalization by granulocytes was followed using luminol enhanced chemiluminescence (CL) to assess their toxicological acceptance as intravenous formulation for magnetic resonance imaging and as potential carrier for drug targeting.

TL;DR: Results of stability evaluation showed a relatively long-term stability after storage at 4 degrees C for 6 months and SLNs with small particle size, excellent physical stability, high entrapment efficiency, good loading capacity for protein drug can be produced by this novel reverse micelle-double emulsion method.

TL;DR: Techniques to characterize drug loading to carrier systems and skin penetration profiles by using the lipophilic dye nile red as a model agent are described and drug targeting appears to be more strictly related to the mode of interaction of drug and particle than penetration enhancement.

TL;DR: Solid Lipid Nanoparticles (SLN) as discussed by the authors can be used as a drug reservoir providing controlled drug release by melting the lipid matrix material and dissolving the drug in the melted lipid.