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High-Aperture Optical Microscopy Methods for Super-Resolution Deep Imaging and Quantitative Phase Imaging

High-Aperture Optical Microscopy Methods for Super-Resolution Deep Imaging and Quantitative Phase Imaging PDF Author: Jeongmin Kim
Publisher:
ISBN:
Category :
Languages : en
Pages : 111

Book Description
Optical microscopy, thanks to the noninvasive nature of its measurement, takes a crucial role across science and engineering, and is particularly important in biological and medical fields. To meet ever increasing needs on its capability for advanced scientific research, even more diverse microscopic imaging techniques and their upgraded versions have been intensively developed over the past two decades. However, advanced microscopy development faces major challenges including super-resolution (beating the diffraction limit), imaging penetration depth, imaging speed, and label-free imaging. This dissertation aims to study high numerical aperture (NA) imaging methods proposed to tackle these imaging challenges. The dissertation first details advanced optical imaging theory needed to analyze the proposed high NA imaging methods. Starting from the classical scalar theory of optical diffraction and (partially coherent) image formation, the rigorous vectorial theory that handles the vector nature of light, i.e., polarization, is introduced. New sign conventions for polarization ray tracing based on a generalized Jones matrix formalism are established to facilitate the vectorial light propagation with physically consistent outcomes. The first high NA microscopic imaging of interest is wide-field oblique plane microscopy (OPM) for high-speed deep imaging. It is a simple, real-time imaging technique recently developed to access any inclined cross-section of a thick sample. Despite its experimental demonstration implemented by tilted remote focusing, the optical resolution of the method has not been fully understood. The anisotropic resolving power in high NA OPM is rigorously investigated and interpreted by deriving the vectorial point spread function (PSF) and vectorial optical transfer function (OTF). Next, OPM is combined with stochastic optical reconstruction microscopy (STORM) to achieve super-resolution deep imaging. The proposed method, termed obliqueSTORM, together with oblique lightsheet illumination paves the way for deeper penetration readily available in localization-based super-resolution microscopy. The key performance metrics of obliqueSTORM, quantitative super-resolution andaxial depth of field, are studied. obliqueSTORM could achieve sub-50-nm resolution with a penetration depth of tens of microns for biological samples. The last part of the thesis covers the development of nonparaxial imaging theory of high NA differential phase contrast (DPC) microscopy for high resolution quantitative phase imaging. The phase retrieval in conventional optical DPC microscopy relies on the paraxial transmission cross-coefficient (TCC) model. However, this paraxial model becomes invalid in high NA DPC imaging. Formulated here is a more advanced nonparaxial TCC model that considers the nonparaxial nature of light propagation, apodization in high NA imaging systems, and illumination source properties. The derived nonparaxial TCC is numerically compared with the paraxial TCC to demonstrate its added features. The practical forms of the TCC for high resolution phase reconstruction are discussed for two special types of objects, weak objects and slowly varying phase objects. The theoretical studies conducted here can help to bring such high NA microscopy techniques into the real world to solve imaging challenges.

High-Aperture Optical Microscopy Methods for Super-Resolution Deep Imaging and Quantitative Phase Imaging

High-Aperture Optical Microscopy Methods for Super-Resolution Deep Imaging and Quantitative Phase Imaging PDF Author: Jeongmin Kim
Publisher:
ISBN:
Category :
Languages : en
Pages : 111

Book Description
Optical microscopy, thanks to the noninvasive nature of its measurement, takes a crucial role across science and engineering, and is particularly important in biological and medical fields. To meet ever increasing needs on its capability for advanced scientific research, even more diverse microscopic imaging techniques and their upgraded versions have been intensively developed over the past two decades. However, advanced microscopy development faces major challenges including super-resolution (beating the diffraction limit), imaging penetration depth, imaging speed, and label-free imaging. This dissertation aims to study high numerical aperture (NA) imaging methods proposed to tackle these imaging challenges. The dissertation first details advanced optical imaging theory needed to analyze the proposed high NA imaging methods. Starting from the classical scalar theory of optical diffraction and (partially coherent) image formation, the rigorous vectorial theory that handles the vector nature of light, i.e., polarization, is introduced. New sign conventions for polarization ray tracing based on a generalized Jones matrix formalism are established to facilitate the vectorial light propagation with physically consistent outcomes. The first high NA microscopic imaging of interest is wide-field oblique plane microscopy (OPM) for high-speed deep imaging. It is a simple, real-time imaging technique recently developed to access any inclined cross-section of a thick sample. Despite its experimental demonstration implemented by tilted remote focusing, the optical resolution of the method has not been fully understood. The anisotropic resolving power in high NA OPM is rigorously investigated and interpreted by deriving the vectorial point spread function (PSF) and vectorial optical transfer function (OTF). Next, OPM is combined with stochastic optical reconstruction microscopy (STORM) to achieve super-resolution deep imaging. The proposed method, termed obliqueSTORM, together with oblique lightsheet illumination paves the way for deeper penetration readily available in localization-based super-resolution microscopy. The key performance metrics of obliqueSTORM, quantitative super-resolution andaxial depth of field, are studied. obliqueSTORM could achieve sub-50-nm resolution with a penetration depth of tens of microns for biological samples. The last part of the thesis covers the development of nonparaxial imaging theory of high NA differential phase contrast (DPC) microscopy for high resolution quantitative phase imaging. The phase retrieval in conventional optical DPC microscopy relies on the paraxial transmission cross-coefficient (TCC) model. However, this paraxial model becomes invalid in high NA DPC imaging. Formulated here is a more advanced nonparaxial TCC model that considers the nonparaxial nature of light propagation, apodization in high NA imaging systems, and illumination source properties. The derived nonparaxial TCC is numerically compared with the paraxial TCC to demonstrate its added features. The practical forms of the TCC for high resolution phase reconstruction are discussed for two special types of objects, weak objects and slowly varying phase objects. The theoretical studies conducted here can help to bring such high NA microscopy techniques into the real world to solve imaging challenges.

Coherent Light Microscopy

Coherent Light Microscopy PDF Author: Pietro Ferraro
Publisher: Springer Science & Business Media
ISBN: 3642158137
Category : Science
Languages : en
Pages : 378

Book Description
This book deals with the latest achievements in the field of optical coherent microscopy. While many other books exist on microscopy and imaging, this book provides a unique resource dedicated solely to this subject. Similarly, many books describe applications of holography, interferometry and speckle to metrology but do not focus on their use for microscopy. The coherent light microscopy reference provided here does not focus on the experimental mechanics of such techniques but instead is meant to provide a users manual to illustrate the strengths and capabilities of developing techniques. The areas of application of this technique are in biomedicine, medicine, life sciences, nanotechnology and materials sciences.

Super Resolution Optical Imaging and Microscopy

Super Resolution Optical Imaging and Microscopy PDF Author: Junle Qu
Publisher: John Wiley & Sons
ISBN: 3527349863
Category : Science
Languages : en
Pages : 261

Book Description
Super Resolution Optical Imaging and Microscopy Extremely comprehensive resource containing cutting-edge and practical knowledge of super-resolution optical imaging This book covers both the basic principles and specific technical details of super-resolution microscopy techniques. It covers the criteria to choose different fluorophores for various SRM methods and critically assesses the nitty-gritty of associated problems that are often encountered in practical applications. A progressive guide to designing the next generation of advanced fluorophores to meet the goal of advanced SR imaging studies is also put forward. Written by two well-qualified authors, the book contains exclusive content to enhance readers’ understanding on innovation of newer SRM technologies. Sample topics covered in the book include: Optical techniques, fluorescent probe design, and algorithm development Recent highlight and breakthroughs in biology using SRM methods The overall success of SRM in biological inventions The future direction and scope of the field This book is an invaluable resource for chemists and researchers/scientists involved in designing newer fluorescent materials for SRM studies. It can also assist biologists engaged in advanced biological studies using SRM by guiding them through sample preparation, image processing, and precautions to be taken in practical imaging studies.

Superresolution Optical Microscopy

Superresolution Optical Microscopy PDF Author: Barry R. Masters
Publisher: Springer Nature
ISBN: 3030216918
Category : Science
Languages : en
Pages : 415

Book Description
This book presents a comprehensive and coherent summary of techniques for enhancing the resolution and image contrast provided by far-field optical microscopes. It takes a critical look at the body of knowledge that comprises optical microscopy, compares and contrasts the various instruments, provides a clear discussion of the physical principles that underpin these techniques, and describes advances in science and medicine for which superresolution microscopes are required and are making major contributions. The text fills significant gaps that exist in other works on superresolution imaging, firstly by placing a new emphasis on the specimen, a critical component of the microscope setup, giving equal importance to the enhancement of both resolution and contrast. Secondly, it covers several topics not typically discussed in depth, such as Bessel and Airy beams, the physics of the spiral phase plate, vortex beams and singular optics, photoactivated localization microscopy (PALM), stochastic optical reconstruction microscopy (STORM), structured illumination microscopy (SIM), and light-sheet fluorescence microscopy (LSFM). Several variants of these techniques are critically discussed. Noise, optical aberrations, specimen damage, and artifacts in microscopy are also covered. The importance of validation of superresolution images with electron microscopy is stressed. Additionally, the book includes translations and discussion of seminal papers by Abbe and Helmholtz that proved to be pedagogically relevant as well as historically significant. This book is written for students, researchers, and engineers in the life sciences, medicine, biological engineering, and materials science who plan to work with or already are working with superresolution light microscopes. The volume can serve as a reference for these areas while a selected set of individual chapters can be used as a textbook for a one-semester undergraduate or first-year graduate course on superresolution microscopy. Moreover, the text provides a captivating account of curiosity, skepticism, risk-taking, innovation, and creativity in science and technology. Good scientific practice is emphasized throughout, and the author’s lecture slides on responsible conduct of research are included as an online resource which will be of interest to students, course instructors, and scientists alike.

Optical Imaging and Microscopy

Optical Imaging and Microscopy PDF Author: Peter Török
Publisher: Springer
ISBN: 3540460225
Category : Science
Languages : en
Pages : 402

Book Description
This text draws together the fields of optical microscopy and optical data storage, in a unique compilation of valuable and novel scientific work that is scarcely to be found elsewhere. The contributing authors are unquestioned leaders of their respective fields.

Biomedical Optical Phase Microscopy and Nanoscopy

Biomedical Optical Phase Microscopy and Nanoscopy PDF Author: Natan T. Shaked
Publisher: Academic Press
ISBN: 0124158862
Category : Science
Languages : en
Pages : 428

Book Description
Written by leading optical phase microscopy experts, this book is a comprehensive reference to phase microscopy and nanoscopy techniques for biomedical applications, including differential interference contrast (DIC) microscopy, phase contrast microscopy, digital holographic microscopy, optical coherence tomography, tomographic phase microscopy, spectral-domain phase detection, and nanoparticle usage for phase nanoscopy The Editors show biomedical and optical engineers how to use phase microscopy for visualizing unstained specimens, and support the theoretical coverage with applied content and examples on designing systems and interpreting results in bio- and nanoscience applications. Provides a comprehensive overview of the principles and techniques of optical phase microscopy and nanoscopy with biomedical applications Tips/advice on building systems and working with advanced imaging biomedical techniques, including interpretation of phase images, and techniques for quantitative analysis based on phase microscopy Interdisciplinary approach that combines optical engineering, nanotechnology, biology and medical aspects of this topic. Each chapter includes practical implementations and worked examples

Confocal Scanning Optical Microscopy and Related Imaging Systems

Confocal Scanning Optical Microscopy and Related Imaging Systems PDF Author: Gordon S. Kino
Publisher: Academic Press
ISBN: 008052978X
Category : Science
Languages : en
Pages : 353

Book Description
This book provides a comprehensive introduction to the field of scanning optical microscopy for scientists and engineers. The book concentrates mainly on two instruments: the Confocal Scanning Optical Microscope (CSOM), and the Optical Interference Microscope (OIM). A comprehensive discussion of the theory and design of the Near-Field Scanning Optical Microscope (NSOM) is also given. The text discusses the practical aspects of building a confocal scanning optical microscope or optical interference microscope, and the applications of these microscopes to phase imaging, biological imaging, and semiconductor inspection and metrology.A comprehensive theoretical discussion of the depth and transverse resolution is given with emphasis placed on the practical results of the theoretical calculations and how these can be used to help understand the operation of these microscopes. Provides a comprehensive introduction to the field of scanning optical microscopy for scientists and engineers Explains many practical applications of scanning optical and interference microscopy in such diverse fields as biology and semiconductor metrology Discusses in theoretical terms the origin of the improved depth and transverse resolution of scanning optical and interference microscopes with emphasis on the practical results of the theoretical calculations Considers the practical aspects of building a confocal scanning or interference microscope and explores some of the design tradeoffs made for microscopes used in various applications Discusses the theory and design of near-field optical microscopes Explains phase imaging in the scanning optical and interference microscopes

Super-Resolution Microscopy

Super-Resolution Microscopy PDF Author: Udo J. Birk
Publisher: John Wiley & Sons
ISBN: 3527341331
Category : Science
Languages : en
Pages : 405

Book Description
This unique book on super-resolution microscopy techniques presents comparative, in-depth analyses of the strengths and weaknesses of the individual approaches. It was written for non-experts who need to understand the principles of super-resolution or who wish to use recently commercialized instruments as well as for professionals who plan to realize novel microscopic devices. Explaining the practical requirements in terms of hardware, software and sample preparation, the book offers a wealth of hands-on tips and practical tricks to get a setup running, provides invaluable help and support for successful data acquisition and specific advice in the context of data analysis and visualization. Furthermore, it addresses a wide array of transdisciplinary fields of applications. The author begins by outlining the joint efforts that have led to achieving super-resolution microscopy combining advances in single-molecule photo-physics, fluorophore design and fluorescent labeling, instrument design and software development. The following chapters depict and compare current main standard techniques such as structured illumination microscopy, single-molecule localization, stimulated emission depletion microscopy and multi-scale imaging including light-sheet and expansion microscopy. For each individual approach the experimental setups are introduced, the imaging protocols are provided and the various applications illustrated. The book concludes with a discussion of future challenges addressing issues of routine applications and further commercialization of the available methods. Guiding users in how to make choices for the design of their own experiments from scratch to promising application, this one-stop resource is intended for researchers in the applied sciences, from chemistry to biology and medicine to physics and engineering.

Fourier Ptychographic Imaging

Fourier Ptychographic Imaging PDF Author: Guoan Zheng
Publisher: Morgan & Claypool Publishers
ISBN: 1681742748
Category : Science
Languages : en
Pages : 126

Book Description
This book demonstrates the concept of Fourier ptychography, a new imaging technique that bypasses the resolution limit of the employed optics. In particular, it transforms the general challenge of high-throughput, high-resolution imaging from one that is coupled to the physical limitations of the optics to one that is solvable through computation. Demonstrated in a tutorial form and providing many MATLAB® simulation examples for the reader, it also discusses the experimental implementation and recent developments of Fourier ptychography. This book will be of interest to researchers and engineers learning simulation techniques for Fourier optics and the Fourier ptychography concept.

Deep Learning-based Microscopy

Deep Learning-based Microscopy PDF Author: Vahid Ebrahimi
Publisher:
ISBN:
Category :
Languages : en
Pages : 0

Book Description
Fluorescence microscopy has been a valuable tool in the field of biological science as it allows one to study the structure and interaction of protein complexes and organelles in living cells. However, conventional optical microscopy technique has been limited by a trade-off between spatiotemporal resolution, signal contrast, and photodamage to the biological samples. It means that an increase in spatial resolution or signal contrast comes at the cost of higher laser power, serial-scanning, or longer image acquisition time. Unfortunately, this leads to severe photobleaching and photodamage to the samples and/or limited throughput of imaging, which is highly challenging to be circumvented through only optical imaging technique. Therefore, one has turned to artificial intelligence (AI) in image processing, applying deep learning algorithms to different imaging modalities to overcome these traditional limitations in optical microscopy systems. Herein we present multiple strategies on how deep learning can be applied to solve challenging and fundamental problems in different fluorescence microscopy modalities. To do so, we present UNet-RCAN, a two-step deep learning network architecture based on a residual U-Net and residual channel attention network (RCAN) for image restoration. We demonstrate that UNet-RCAN achieves higher prediction accuracy compared to other state-of-the-art deep learning algorithms while maintaining the resolution of an output image compared to ground-truth data acquired with optical microscopes. We applied our method to three fluorescence imaging modalities. Firstly, we successfully demonstrate that UNet-RCAN can achieve up to two orders of magnitude acceleration in stimulated emission depletion (STED) imaging while maintaining super-resolution. This significant acceleration enables mitigation of photobleaching and photodamage by robust restoration of noisy 2D and 3D STED images from multiple targets as well as live-cell STED imaging of inner-mitochondrial dynamics with a ten-fold increase in the number of acquired frames compared to conventional STED microscopy. Secondly, we apply our approach in restoring high-resolution widefield deconvolution images of living cells with low light intensity and low photodamage. We show that the accuracy of deconvolution can significantly improve after image restoration with deep learning. Lastly, we show the application of UNet-RCAN in the resolution enhancement of single-shot volumetric imaging with a low numerical aperture objective lens.