Theranostic nanoparticles
have incredible potential for biomedical
applications by enabling visual confirmation of therapeutic efficacy.
Numerous issues challenge their clinical translation and are primarily
related to the complex chemistry and scalability of synthesizing Nanoparticles.
We report a 2-step chemical strategy for high-throughput intracellular
delivery of organic and inorganic solid nanoparticles. This process
takes an additional step beyond hydrophobic surface modification facilitated
by inverted micelle transfer, toward the packing of multiple solid
nanoparticles into a soft-shelled lipid capsule, termed the Nano-multicapsule
(NMC). This technique is high yielding and does not require the complex
purification steps in anaerobic/hydrophobic reactions for hydrophobic
modification. To demonstrate the efficacy across different material
compositions, we separately entrapped ∼10 nm gold and carbon
nanoparticles (AuNP and CNP) within inverted micelles, and subsequently
NMCs, then quantified their internalization in a human breast cancer
cell line. For encapsulated AuNPs (NMC-AuNP), we confirmed greater
cellular internalization of gold through ICP-OES and TEM analyses.
Raman spectroscopic analysis of cells treated with encapsulated CNPs
(NMC-CNP) also exhibited high degrees of uptake with apparent intracellular
localization as opposed to free CNP treatment.