The surface decoration of nanoparticles with cell-penetrating peptides (CPPs) represents a common technique for intracellular delivery of nanotherapeutics. Conjugate formation can be performed via covalent or non-covalent strategies. Here, we describe on the synthesis of silica nanoparticles, a well-known inorganic drug delivery vehicle type, and their surface modification with cell-penetrating peptides using sC18 and derivatives thereof. Moreover, physicochemical as well as biological characterization methods, including cellular uptake measurements, of particle-peptide conjugates are described.
Keywords: Cell-penetrating peptides; Cellular uptake; Internalization; Nanoparticles; Particle-peptide conjugate; Surface modification.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.