Abstract

Multicolor fluorescence microscopy is a powerful technique to fully visualize many biological phenomena by acquiring images from different spectrum channels. This study expands the scope of multicolor fluorescence microscopy by serial imaging of polystyrene micro-beads as surrogates for drug carriers, cancer spheroids formed using HeLa cells, and microfluidic channels. Three fluorophores with different spectral characteristics are utilized to perform multicolor microscopy. According to the spectrum analysis of the fluorophores, a multicolor widefield fluorescence microscope is developed. Spectral crosstalk is corrected by exciting the fluorophores in a round-robin manner and synchronous emitted light collection. To report the performance of the multicolor microscopy, a simplified 3D tumor model is created by placing beads and spheroids inside a channel filled with the cell culture medium is imaged at varying exposure times. As a representative case and a method for bio-hybrid drug carrier fabrication, a spheroid surface is coated with beads in a channel utilizing electrostatic forces under the guidance of multicolor microscopy. Our experiments show that multicolor fluorescence microscopy enables crosstalk-free and spectrally-different individual image acquisition of beads, spheroids, and channels with the minimum exposure time of 5.5 ms. The imaging technique has the potential to monitor drug carrier transportation to cancer cells in real-time.

Highlights

  • The functionalization of tetherless manipulatable micro-agents as drug carriers offers a remedy for required dose delivery to cancer cells

  • We report the performance of the multicolor fluorescence microscope by imaging microbeads and HeLa cell spheroids placed inside a microfluidic channel

  • To acquire 8-bit individual grayscale images of beads, spheroids, and channel with the minimum noise level, emitted light from the fluorophores is collected with 0 dB gain and 66 ms exposure time in the wavelength ranges of 500–540 nm, 592.5–667.5 nm, and 817.5–875.5 nm, respectively

Read more

Summary

Introduction

The functionalization of tetherless manipulatable micro-agents as drug carriers offers a remedy for required dose delivery to cancer cells. Microfluidic channels have been used as a controlled experimental environment to validate the effectiveness of such micro-agents [1, 2]. Since the channels are fabricated using optically transparent materials, microscopy is the most widely used method for imaging [3]. Fluorescence microscopy is the most effective way to visualize a specific target structure with a relatively high contrast-to-noise ratio by eliminating the background.

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call