Abstract

HighlightsA novel all-in-one fluorescent nanomedicine platform based on silicon nanoparticles (SiNPs) was developed for imaging-guided co-delivery of short interfering RNA (siRNA) and doxorubicin (DOX).The intracellular time-dependent release behaviors of siRNA and DOX were visually monitored by tracking the strong and stable fluorescence of SiNPs.The SiNPs-based nanocarriers displayed pronounced therapeutic efficiency on drug-resistant breast cancer cells.

Highlights

  • Despite great progress in cancer treatment, multidrug resist‐ ance (MDR), which can lead to high recurrence rates and treatment failures, remains a tremendous challenge in cancer chemotherapy [1]

  • Transmission electronic microscopy (TEM) images revealed the spherical shape of the silicon nanoparti‐ cles (SiNPs)-DOX/small interfering RNA (siRNA) nanocomposites, with a diameter of ~ 6.3 nm (Fig. 1b, c)

  • We developed a novel fluorescent SiNPs-based nanomedi‐ cine platform, which is useful for imaging-guided co-deliv‐ ery of siRNA and doxorubicin, enabling the enhancement of therapeutic efficacy in drug-resistant cancer cells

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Summary

Introduction

Despite great progress in cancer treatment, multidrug resist‐ ance (MDR), which can lead to high recurrence rates and treatment failures, remains a tremendous challenge in cancer chemotherapy [1]. Novel, fluorescent, all-in-one nanocarriers with superior optical properties (e.g., high and stable fluorescence) and excellent biocompatibility are needed to facilitate the development of imaging-guided RNAi-based combination therapy in drug-resistant cancer cells. The prepared SiNPs-based nanocarri‐ ers with adjustable drug-loading capacity were very suit‐ able for optical imaging-guided cancer therapy because of their high fluorescence and robust photostability. It remains unknown whether these nanocarriers are available for imaging-guided co-delivery of siRNA and chemothera‐ peutic agents, facilitating the enhancement of the therapeutic efficacy in MDR cancer cells. Our results suggest that SiNPs-based fluorescent nanocomposites can be used as imaging-guided RNAi-based co-delivery nanoagents for the treatment of MDR cancer cells

Stability Evaluation
Dual‐Responsive Release Behavior
Intracellular Distribution
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Intracellular Release
In vitro Gene‐Silencing Efficiency
MTT Assay
Results and Discussion
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Dual‐Controlled Release of siRNA and DOX
Intracellular Trafficking
In Vitro Gene‐Silencing Efficiency
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Conclusions
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