Open Access Paper
24 May 2019 Front Matter: Volume 10873
Abstract
This PDF file contains the front matter associated with SPIE Proceedings Volume 10873 including the Title Page, Copyright information, Table of Contents, Introduction, and Conference Committee listing.

The papers in this volume were part of the technical conference cited on the cover and title page. Papers were selected and subject to review by the editors and conference program committee. Some conference presentations may not be available for publication. Additional papers and presentation recordings may be available online in the SPIE Digital Library at SPIEDigitalLibrary.org.

The papers reflect the work and thoughts of the authors and are published herein as submitted. The publisher is not responsible for the validity of the information or for any outcomes resulting from reliance thereon.

Please use the following format to cite material from these proceedings:

Author(s), “Title of Paper,” in Optical Biopsy XVII: Toward Real-Time Spectroscopic Imaging and Diagnosis, edited by Robert R. Alfano, Stavros G. Demos, Angela B. Seddon, Proceedings of SPIE Vol. 10873 (SPIE, Bellingham, WA, 2019) Seven-digit Article CID Number.

ISSN: 1605-7422

ISSN: 2410-9045 (electronic)

ISBN: 9781510623880

ISBN: 9781510623897 (electronic)

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Paper Numbering: Proceedings of SPIE follow an e-First publication model. A unique citation identifier (CID) number is assigned to each article at the time of publication. Utilization of CIDs allows articles to be fully citable as soon as they are published online, and connects the same identifier to all online and print versions of the publication. SPIE uses a seven-digit CID article numbering system structured as follows:

  • The first five digits correspond to the SPIE volume number.

  • The last two digits indicate publication order within the volume using a Base 36 numbering system employing both numerals and letters. These two-number sets start with 00, 01, 02, 03, 04, 05, 06, 07, 08, 09, 0A, 0B … 0Z, followed by 10-1Z, 20-2Z, etc. The CID Number appears on each page of the manuscript.

Authors

Numbers in the index correspond to the last two digits of the seven-digit citation identifier (CID) article numbering system used in Proceedings of SPIE. The first five digits reflect the volume number. Base 36 numbering is employed for the last two digits and indicates the order of articles within the volume. Numbers start with 00, 01, 02, 03, 04, 05, 06, 07, 08, 09, 0A, 0B … 0Z, followed by 10-1Z, 20-2Z, etc.

Alfano, Robert R., 0T, 1A, 1C

Arce-Diego, J. L., 0N

Balasundaram, Ghayathri, 0B

Bang, Ole, 0X

Barh, Ajanta, 0X

Bharathan, G., 11

Bi, Renzhe, 0B

Birkhoff, W., 0Q

Bjorgan, Asgeir, 0O

Burggraaf, J., 0Q

Campbell, Colin J., 0R

Chen, Hong, 1A

Chen, Shuo, 0W

Cheng, Gangge, 1A

Dehghani, Hamid, 0U

Delgado, Robert, 0V

Demos, S. G., 1D

Dijkstra, J., 0Q

Dinish, U.S., 0B

Dutta Gupta, Shourya, 0V

Eggermont, J., 0Q

Fang, Ruogu, 05

Fanjul-Vélez, F., 0N

Fernandez, Cristianne, 05

Finlayson, Neil, 0R

Fuerbach, A., 11

Gao, Xin, 1F

Gennet, Camille, 0J

Godavarty, Anuradha, 04, 05

Gregory, Christopher D., 0R

Hannesschläger, Günther, 0X

Henderson, Robert K., 0R

Howle, Christopher R., 0U

Huang, Steven H., 0V

Hudson, D. D., 11

Hume, Kelly, 0V

Icaza, Michael, 15

Imai, Toru, 0B

Israelsen, Niels M., 0X

Jackson, S. D., 11

Jain, Deepak, 0X

Jain, Manu, 15

Jensen, Mikkel, 0X

Jeon, Seungwan, 0B

Judd, Nicolas, 15

K., Chithra, 08

Kaile, Kacie, 04

Kelp, Glen, 0V

Khandavilli, Dinesh, 04

Kim, Chulhong, 0B

Kopp, K., 1D

Kosc, Tanya Z., 1D

Kwasinski, Rebecca, 05

Leiva, Kevin, 04, 05

Li, Shenglin, 1A

Liang, Qijun, 1A

Lindberg, Arvid, 0J

Liu, Cheng-hui, 1A

Liu, Xiaogang, 0W

Lozano, Priscilla, 04

Mahadevan, Jagadeesh, 04

Majewski, M. R., 11

McHugh, Thomas, 0W

Mellors, Ben O. L., 0U

Mieog, J. S. D., 0Q

Mukherjee, Sushmita, 15

Muthukrishnan, Varalakshmi, 04

Narayanan, Sivakumar, 04

Ng, Lai Guan, 0B

Olivo, Malini, 0B

Pedersen, Christian, 0X

Perez-Clavijo, Francisco, 05

Petersen, Christian R., 0X

Pierangelo, Angelo, 0J

Podoleanu, Adrian, 0X

Prakasarao, Aruna, 08

Pu, Yang, 0B

Randeberg, Lise L., 0O, 0Y

Rehbinder, Jean, 0J

Robinson, D. J., 0Q

Robledo, Edwin, 04, 05

S., Vijayaraghavan, 08

Schutzman, Richard, 04, 05

Seddon, Angela B., 12

Shi, Lingyan, 0T

Shvets, Gennady, 0V

Singaravelu, Ganesan, 08

Sordillo, Diana C., 0T

Sordillo, Laura A., 0T, 1C

Sordillo, Peter P., 0T, 1C

Spear, Abigail M., 0U

Tidemand-Lichtenberg, Peter, 0X

Usai, Andrea, 0R

Vahrmeijer, A. L., 0Q

Vanel, Jean-Charles, 0J

van Manen, L., 0Q

Viswanathan, Mohan, 04

Vizet, Jérémy, 0J

Wang, Lihong, 0B

Woodward, R. I., 11

Wu, Binlin, 15, 1A, 1F

Wu, Wensong, 04

Yu, Xinguang, 1A

Zhang, Chunyuan, 1A

Zhang, Lin, 1C

Zhang, Mingqian, 1A

Zhao, Mingyue, 1A

Zhou, Yan, 1A

Zhu, Ke, 1A

Zong, Rui, 1A

Conference Committee

Symposium Chairs

  • James G. Fujimoto, Massachusetts Institute of Technology (United States)

  • R. Rox Anderson, Wellman Center for Photomedicine, Massachusetts General Hospital (United States) and Harvard Medical School (United States)

Symposium Co-chairs

  • Jennifer K. Barton, The University of Arizona (United States)

  • Wolfgang Drexler, Medical University of Vienna (Austria)

Program Track Chairs

  • Tuan Vo-Dinh, Fitzpatrick Institute for Photonics, Duke University (United States)

  • Anita Mahadevan-Jansen, Vanderbilt University (United States)

Conference Chairs

  • Robert R. Alfano, The City College of New York (United States)

  • Stavros G. Demos, University of Rochester Laboratory for Laser Energetics (United States)

  • Angela B. Seddon, The University of Nottingham (United Kingdom)

Conference Program Committee

  • Nicole J. Crane, Naval Medical Research Center (United States)

  • Zhiwei Huang, National University of Singapore (Singapore)

  • Nicusor V. Iftimia, Physical Sciences Inc. (United States)

  • Amir Gandjbakhche, National Institutes of Health (United States)

  • Israel Gannot, Johns Hopkins University (United States) and Tel Aviv University (Israel)

  • Richard M. Levenson, University of California, Davis (United States)

  • Igor V. Meglinski, University of Oulu (Finland)

  • Lingyan Shi, Columbia University (United States)

  • Milind Rajadhyaksha, Memorial Sloan-Kettering Cancer Center (United States)

  • Kestutis Sutkus, The City College of New York (United States)

  • Siavash Yazdanfar, Corning Incorporated (United States)

  • Min Xu, Fairfield University (United States)

Session Chairs

  • 1 Optical Bioassay Platforms I

    Nicusor V. Iftimia, Physical Sciences Inc. (United States)

  • 2 Optical Bioassay Platforms II

    Lingyan Shi, Columbia University (United States)

  • 3 Optical Histology I

    J. Stewart Russell, The City College of New York (United States)

  • 4 Optical Histology II

    Stavros G. Demos, University of Rochester Laboratory for Laser Energetics (United States)

  • 5 Spectroscopic Methods I

    Yang Pu, MicroPhotoAcoustics, Inc. (United States)

    Min Xu, Fairfield University (United States)

  • 6 Spectroscopic Methods II

    Francesco Saverio Pavone, LENS - Laboratorio Europeo di Spettroscopie Non-Lineari (Italy)

  • 7 SWIR and IR Methods I

    J. Stewart Russell, The City College of New York (United States)

  • 8 SWIR and IR Methods II

    Angela B. Seddon, The University of Nottingham (United Kingdom)

Introduction

The SPIE Photonics West Conference, Optical Biopsy, was conceived 17 years ago by Professor Alfano, the founding Conference Chair. His simple aim was, and remains, for photonic engineering and scientific development to realise the optical biopsy for real-time information on cancer and disease detection for screening, early diagnosis, and intra-operative monitoring acquiring clinically relevant data without the need for excision biopsies. Thus, to give clinicians the means to have objective medical and biological data to hand at the point of need, the better to take effective and efficient clinical decisions for curative outcomes. The optical biopsy photonic systems aimed at, ideally, should be compact and provide high resolution tissue imaging within seconds, underpinned by machine learning for diagnostic capability based on morphology or molecular recognition and ideally both.

In our 2019 Optical Biopsy conference, we held two days of oral presentations and discussion. These included sessions on optical bioassay platforms, optical histology, spectroscopic methods, and SWIR (short wave infrared) and (mid-infrared) MIR methods, with lively poster sessions on both days. An average of around 70 attendees, throughout the two days, is indicative of vigorous interest from photonic engineers, scientists, and clinicians. Here follows a synopsis of key papers.

Optical Bioassay Platforms included an invited talk on chip-based Raman spectroscopy for microbial sensing from Jürgen Popp (10873-1, Liebniz Institute, Jena, Germany). The WHO (World Health Organization) has stated that in heading toward a post-antibiotic era, microbial resistance is a serious worldwide threat to public health. Raman bio-assay of body-fluid may give faster, reliable, specific diagnostics to inform therapeutic decision-making. Electrophoresis is used to concentrate pathogens in a capturing unit, on-chip. Lingyan Shi (10873-8, Colombia University, United States) presented her very high standard work on SRS (stimulated Raman), with ~ 108x sensitivity of spontaneous Raman, and outstanding label-free 3D imaging; the novelty was introducing D+ for H+ to give tissue signatures in the normally cell-silent vibrational region 4-5μm wavelength.

In the Optical Histology session, high standard work from Virginia University (United States) (paper 10873-10) was on multiparametric photoacoustic microscopy: PAM, which has a unique niche giving label-free imaging with hemoglobin contrast to similar depth as OCT. With a pulsed laser to excite tissue, the absorption gives transient heating and thermoelastic expansion with acoustic emission, for instance, to track brain vasculature (brain cells are invisible to PAM) after stroke.

Day two featured Spectroscopic Methods with innovative, high performance instrumentation for Mueller polarimetric imaging in vivo (10873-18, from Ecole Polytechnique and Strasburg University, France) across the visible with multispectral images, wide field, low error, fast acquisition 1-2 s and compact system. Impressive imaging in a hospital setting of cancer margins; collagen orientation is being detected using liquid crystal alignment. The SWIR and MIR Methods session began with Laura Sordillo (City College of New York, United States, paper 10873-28) who reviewed the state-of-the-art in SWIR, the 4 NIR windows: 650-950 nm, 1100-1350 nm, 1600-1870 nm (so-called: ‘Golden Window’) and 2100-2300 nm. Light scattering through these windows ranges from none (ballistic photons), to weak (snake-like quasi) to multiple scatter (diffuse scattering). The brain is lipid-rich and 1700 nm is the preferred imaging wavelength. InGaAs IR CCD array suits the third window, which fields the deepest penetration of radiation to see hard wire below chicken tissue. The use of supercontinuum laser for high power, broadband confocal microscopy was discussed. Next up was paper 10873-29 from Birmingham University (United Kingdom) presented by Chris R. Howle; the mod-infrared for wound healing from military injuries like a blast pressure wave, shrapnel, victim-hits-object and flash-burn. FT-(Fourier transform)-IR spectroscopy followed amide B at 3200 cm-1 arising from Fermi resonance of the first overtone of amide II and N-H stretching. Two computational methods applied and machine learning: principal components analysis on normalised spectra, taking first derivative, was found best. For the future, a field-compact technique is being developed based on negative contrast instead of FT-IR. Impressive work by Christian Petersen, a young scientist from Denmark Technical University, was on MIR OCT based on 1.5-2.7μm MOPA laser pumping of a fluoride glass optical fibre (transparent: 0.9-4.7μm for SC output of 40mW total over 3.6-4.6 μm. For the imaging, a neat solution was to upconvert the radiation to 820-865 nm for Si detection. Tissue was imaged to 8.6μm depth and 15μm spatial resolution—a proof of concept study (10873-51). The conference was brought to a close with exciting developments in the MIR spectral domain by two invited papers. First, Stuart D. Jackson, an acknowledged leader in MIR narrow-line fibre lasers reviewed the state of the art and how this can input molecular hyperspectral imaging (Macquarie University, Australia, paper 10873-36). Finally, paper 10873-37 (Nottingham University, United Kingdom) gave an update of MIR molecular imaging using fibre MIR-SC broadband sources showing the state of the art, but still on excised tissue rather than in vivo, the ultimate goal.

Robert R. Alfano

Stavros G. Demos

Angela B. Seddon

© (2019) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
"Front Matter: Volume 10873", Proc. SPIE 10873, Optical Biopsy XVII: Toward Real-Time Spectroscopic Imaging and Diagnosis, 1087301 (24 May 2019); https://doi.org/10.1117/12.2532072
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KEYWORDS
Biomedical optics

Tissue optics

Short wave infrared radiation

Raman spectroscopy

Spectroscopy

Biopsy

Imaging spectroscopy

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