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  4. Pathology in a tube step 2: Simple rapid fabrication of curved circular cross section millifluidic channels for biopsy preparation/3D imaging towards pancreatic cancer detection and diagnosis
 
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Pathology in a tube step 2: Simple rapid fabrication of curved circular cross section millifluidic channels for biopsy preparation/3D imaging towards pancreatic cancer detection and diagnosis

Source
Progress in Biomedical Optics and Imaging Proceedings of SPIE
ISSN
16057422
Date Issued
2018-01-01
Author(s)
Das, Ronnie
Burfeind, Chris W.
Lim, Saniel D.
Patle, Shubham
Seibel, Eric J.
DOI
10.1117/12.2291018
Volume
10491
Abstract
3D pathology is intrinsically dependent on 3D microscopy, or the whole tissue imaging of patient tissue biopsies (TBs). Consequently, unsectioned needle specimens must be processed whole: A procedure which cannot necessarily be accomplished through manual methods, or by retasking automated pathology machines. Thus millifluidic devices (for millimeter-scale biopsies) are an ideal solution for tissue handling/preparation. TBs are large, messy and a solid-liquid mixture; they vary in material, geometry and structure based on the organ biopsied, the clinician skill and the needle type used. As a result, traditional microfluidic devices are insufficient to handle such mm-sized samples and their associated fabrication techniques are impractical and costly with respect to time/efficiency. Our research group has devised a simple, rapid fabrication process for millifluidic devices using jointed skeletal molds composed of machined, reusable metal rods, segmented rods and stranded wire as structural cores; these cores are surrounded by Teflon outer housing. We can therefore produce curving, circular-cross-section (CCCS) millifluidic channels in rapid fashion that cannot normally be achieved by microfabrication, micro-/CNC-machining, or 3D printing. The approach has several advantages. CLINICAL: round channels interface coring needles. PROCESSING: CCCS channels permit multi-layer device designs for additional (processing, monitoring, testing) stages. REUSABILITY: for a biopsy/needle diameter, molding (interchangeable) components may be produced one-Time then reused for other designs. RAPID: structural cores can be quickly removed due to Teflon®'s ultra-low friction; housing may be released with ethanol; PDMS volumes cure faster since metal skeleton molds conduct additional heat from within the curing elastomer.
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URI
https://d8.irins.org/handle/IITG2025/22983
Subjects
3D optical imaging and reconstruction | Cancer detection and diagnosis | Histopathology | Microfabrication | Millifluidics/microfluidics | Needle biopsy transport | Pathology lab-on-A-chip | Tissue sample preparation
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