Abstract

The large consumer market has made cellphone lens modules available at low-cost and in high-quality. In a conventional cellphone camera, the lens module is used to demagnify the scene onto the image plane of the camera, where image sensor is located. In this work, we report a 3D-printed high-resolution Fourier ptychographic microscope, termed FPscope, which uses a cellphone lens in a reverse manner. In our platform, we replace the image sensor with sample specimens, and use the cellphone lens to project the magnified image to the detector. To supersede the diffraction limit of the lens module, we use an LED array to illuminate the sample from different incident angles and synthesize the acquired images using the Fourier ptychographic algorithm. As a demonstration, we use the reported platform to acquire high-resolution images of resolution target and biological specimens, with a maximum synthetic numerical aperture (NA) of 0.5. We also show that, the depth-of-focus of the reported platform is about 0.1 mm, orders of magnitude longer than that of a conventional microscope objective with a similar NA. The reported platform may enable healthcare accesses in low-resource settings. It can also be used to demonstrate the concept of computational optics for educational purposes.

Highlights

  • Optical microscopy pervades almost all aspects of modern bioscience and clinical applications

  • In a conventional cellphone camera, the lens module is used to demagnify the scene onto the image plane of the camera, where image sensor is located

  • We report a 3D-printed high-resolution Fourier ptychographic microscope, termed FPscope, which uses a cellphone lens in a reverse manner

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Summary

Introduction

Optical microscopy pervades almost all aspects of modern bioscience and clinical applications. It has been shown that, sub-micron resolution can be achieved using various lensless imaging techniques, such as optofluidic microscopy [1, 3], digital in-line holography [2, 5], and contact imaging microscopy [4]. Applications of these techniques range from malaria parasite screening, single cell tracking, to real-time cell culture monitoring and etc. We will summarize the results and discuss the future directions

System design of the FPscope
Discussion and conclusion

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