Aline Broch’s scientific contributions

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Publications (2)


Optical layout and implementation of the proposed system using a surgical microscope. a. Photo of the system implementation. b. Optical design. BS1, BS2, BS3: virtual beam-splitters; E1&2: eye pieces; L1: plano-concave lens; LF: laser line filter; LP&BP: long-pass filter and band-pass filter; LP1&2: linear polarizers; OA: observation arm; Obj.: main objective lens.
The overall processing framework of image analysis based on a graphics processing unit. CPU: central Processing Unit; CUDA: parallel computing platform; GPU: graphics processing unit; NIR: near-infrared.
Graphical user interface (imaging mode options: color, LSCI, polarization, and fluorescence; image field of view; camera selection and control; multimodal image alignment using the openGL function). LSCI: laser-speckle-contrast-imaging
Polarimetric imaging for subsurface pattern extraction. (a) Color photo taken with the color camera. (b) Representative Retaradance map from birefringence imaging; pelvic nerve branches, with individual fascicles, are highlighted by the intrinsic zig-zag spiral patterns of ‘Bands-of-Fontana’. Please note that sub-surface fascicles within pelvic nerve are identified and differentiated. White bars: 1 cm.
Imaging of sciatic nerve in rats. (a) Color image of sciatic nerve in a rat. The spiral pattern is barely seen. (b) BMB injected fluorescence image. (c) Polarimetric kernel processed image highlighting ‘Bands-of-Fontana’. (d) Overlay image. White bars: 5 mm.

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Real-time, label-free, intraoperative visualization of peripheral nerves and micro-vasculatures using multimodal optical imaging techniques
  • Article
  • Full-text available

February 2018

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1,207 Reads

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31 Citations

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Aline Broch

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Peter Kim

Accurate, real-time identification and display of critical anatomic structures, such as the nerve and vasculature structures, are critical for reducing complications and improving surgical outcomes. Human vision is frequently limited in clearly distinguishing and contrasting these structures. We present a novel imaging system, which enables noninvasive visualization of critical anatomic structures during surgical dissection. Peripheral nerves are visualized by a snapshot polarimetry that calculates the anisotropic optical properties. Vascular structures, both venous and arterial, are identified and monitored in real-time using a near-infrared laser-speckle-contrast imaging. We evaluate the system by performing in vivo animal studies with qualitative comparison by contrast-agent-aided fluorescence imaging.

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Fig 1. Key prior cyanines, IRDye-800CW and FNIR-774, and the compound reported here, UL 
Fig 3. NIR fluorescence-guided intraoperative identification of the ureter. Shown are the color video (left column), NIR fluorescence (middle column), and a pseudo-colored (Cyan) merged image of the 2 (right column). Exposure time was 33 ms for all NIR fluorescence images. Li:liver, Du:Duodenum, Ki:kidney, Ur: ureter, Ut: uterine, Bl: Bladder. 
A Chemically Stable Fluorescent Marker of the Ureter

February 2018

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196 Reads

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50 Citations

Bioorganic & Medicinal Chemistry Letters

Surgical methods guided by exogenous fluorescent markers have the potential to define tissue types in real time. Small molecule dyes with efficient and selective renal clearance could enable visualization of the ureter during surgical procedures involving the abdomen and pelvis. These studies report the design and synthesis of a water soluble, net neutral C4'-O-alkyl heptamethine cyanine, Ureter-Label (UL)-766, with excellent properties for ureter visualization. This compound is accessed through a concise synthetic sequence involving an N- to O-transposition reaction that provides other inaccessible C4'-O-alkyl heptamethine cyanines. Unlike molecules containing a C4'-O-aryl substituent, which have also been used for ureter visualization, UL-766 is not reactive towards glutathione and the cellular proteome. In addition, rat models of abdominal surgery reveal that UL-766 undergoes efficient and nearly exclusive renal clearance in vivo. In total, this molecule represents a promising candidate for visualizing the ureter during a variety of surgical interventions.

Citations (2)


... Significant efforts have been made toward urological disease monitoring, including intraoperative ureteral identification using near-infrared fluorescence (NIRF, 700-900 nm) [12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28], Significant efforts have been made toward urological disease monitoring, including intraoperative ureteral identification using near-infrared fluorescence (NIRF, 700-900 nm) [12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28], which demonstrates deep tissue penetration, low autofluorescence in tissue, and low tissue scattering [29]. Near-infrared fluorescent CW800 CA and UreterGlow together facilitate intraoperative ureteral identification in rats and pigs [17][18][19][20][21]. ...

Reference:

Evaluation of the Utilization of Near-Infrared Fluorescent Contrast Agent ASP5354 for In Vivo Ureteral Identification in Renal Diseases Using Rat Models of Gentamicin-Induced Acute Kidney Injury
A Chemically Stable Fluorescent Marker of the Ureter

Bioorganic & Medicinal Chemistry Letters

... Moreover, existing endeavors within the surgical robotics domain underscore the necessity of dynamic tracking. This imperative arises from the surgical operations' millimeter-scale precision [38][39][40]. ...

Real-time, label-free, intraoperative visualization of peripheral nerves and micro-vasculatures using multimodal optical imaging techniques