The
effective loading or encapsulation of multimodal theranostic
agents within a nanocarrier system plays an important role in the
clinical development of cancer therapy. In recent years, the silk
fibroin protein-based delivery system has been drawing significant
attention to be used in nanomedicines due to its biocompatible and
biodegradable nature. In this study, silk fibroin nanoparticles (SNPs)
have been synthesized by a novel and cost-effective ultrasonic atomizer-based
technique for the first time. The fabricated SNPs were coencapsulated
by the FDA-approved indocyanine green (ICG) dye and the chemotherapeutic
drug doxorubicin (DOX). The synthesized SNPs are spherical, with an
average diameter of ∼37 ± 4 nm, and the ICG-DOX-coencapsulated
SNPs (ID-SNPs) have a diameter size of ∼47 ± 6 nm. For
the first time, here we demonstrate that DOX helps in the higher loading
of ICG within the ID-SNPs, which enhances the encapsulation efficiency
of ICG by ∼99%. This could be attributed to the interaction
of ICG and DOX molecules with the silk fibroin protein, which helps
ICG to get loaded more efficiently within these nanoparticles. The
overall finding of this study suggests that the ID-SNPs could be utilized
for enhanced ICG-complemented multimodal deep-tissue bioimaging and
synergistic chemo-photothermal therapy.