Potential of solid lipid nanoparticles in brain targeting.
By I. Kaur, R. Bhandari, S. Bhandari, Vandita Kakkar. Journal of Controlled Release, 2008
604 citations recorded by the source corpus.
Subfields: Molecular Biology, Pharmaceutical Science
View Paper: https://www.semanticscholar.org/paper/5e26fabb7216a6077c870af48c5544016aa00617
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Citations in the corpus
- SOLID LIPID NANOPARTICLES: A REVIEW (2017, methodology): “Thirty milliliter of 30% v/v PEG 400 in phosphate cushion (pH-6) arrangement was utilized as dialyzing medium [47].”
- Effect of Zeta Potential on the Properties of Nano-Drug Delivery Systems - A Review (Part 2) (2013, background): “The other example is the etoposide-loaded positively charged tripalmitin nanoparticles that achieve highest brain concentration when compared to negatively charged etoposide incorporated tripalmitin nanoparticles and etoposide solution [61].”
- Solid lipid nanoparticles and nanostructured lipid carriers as novel drug delivery systems: applications, advantages and disadvantages (2018, positive): “Lipid nanoparticles are suitable for incorporating both lipophilic and hydrophilic drugs which could be administered via different routes (120-129).”