Otuya David O, Farrokhi Hamid, Verma Yogesh, Dong Jing, Choy Peter, Kumar Aditya, Shore Rachel E, Zemlok Sarah K, Sevieri Evan, Schellenberg Mason, Spicer Graham, Lopez Dan Rolando, Osman Hany A, Gardecki Joseph A, Kyrollos Kelada Alfred A F, Gao Anna H, Chung Anita, Grant Catriona N, Bhat Nitasha G M, Rosenberg Mireille, Jacobson Brian C, Nishioka Norman S, Colson Yolonda, Tearney Guillermo J
Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, MA 02114, USA.
Harvard Medical School, Boston, MA 02115, USA.
Sci Transl Med. 2025 Apr 30;17(796):eado9609. doi: 10.1126/scitranslmed.ado9609.
Luminal organ biopsies are critical for disease diagnosis and are obtained using single-bite forceps inserted through the working channel of large endoscopes. Procedures using these endoscopes frequently require patient sedation or anesthesia and may not be feasible for use in pediatric patients. Additionally, forceps-derived biopsies can suffer from difficulty maintaining tissue orientation, crush artifacts, and lack of precise control of biopsy depth. The high cost and risks of anesthesia and sedation have driven the development of smaller endoscopes for unsedated procedures. However, reduced endoscope size limits working-channel dimensions, restricting biopsy forceps to sizes that may yield insufficient or nondiagnostic samples. To address these limitations, we developed an image-guided, depth-controlled, ultrasmall-diameter (1.2-millimeters) cryobiopsy device (μCryoProbe). We optimized the coolant flow profile into the device to enhance tissue freezing, optimizing device-tissue contact time and freezing depth. We tested the device for gastrointestinal biopsy collection in ex vivo preclinical tissues, in an in vivo porcine model, and in sedated human participants. Dimensions and quality of mucosal cryobiopsies from esophagus, stomach, and duodenum were compared with those of forceps-derived biopsies, and it was found that the μCryoProbe device consistently produced high-quality biopsies with optimal tissue orientation and no evidence of crush artifacts. We also demonstrated the ability to capture gastrointestinal biopsies from sedated human participants. By capturing large, well-oriented samples using a small-diameter biopsy tool, this technology has the potential to shift procedures from large to small endoscopes, reducing the need for sedation and improving patient diagnosis through the acquisition of tissue samples with better quality.
