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A flexible electronic strain sensor for the real-time monitoring of tumor regression.
Abramson, Alex; Chan, Carmel T; Khan, Yasser; Mermin-Bunnell, Alana; Matsuhisa, Naoji; Fong, Robyn; Shad, Rohan; Hiesinger, William; Mallick, Parag; Gambhir, Sanjiv Sam; Bao, Zhenan.
Affiliation
  • Abramson A; Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
  • Chan CT; Department of Radiology, Stanford University, Stanford, CA 94305, USA.
  • Khan Y; Molecular Imaging Program at Stanford (MIPS) and Bio-X Program, Stanford University, Stanford CA, 94305, USA.
  • Mermin-Bunnell A; Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
  • Matsuhisa N; Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
  • Fong R; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.
  • Shad R; Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.
  • Hiesinger W; Department of Cardiothoracic Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Mallick P; Department of Cardiothoracic Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Gambhir SS; Department of Cardiothoracic Surgery, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Bao Z; Department of Radiology, Stanford University, Stanford, CA 94305, USA.
Sci Adv ; 8(37): eabn6550, 2022 09 16.
Article in En | MEDLINE | ID: mdl-36112679
ABSTRACT
Assessing the efficacy of cancer therapeutics in mouse models is a critical step in treatment development. However, low-resolution measurement tools and small sample sizes make determining drug efficacy in vivo a difficult and time-intensive task. Here, we present a commercially scalable wearable electronic strain sensor that automates the in vivo testing of cancer therapeutics by continuously monitoring the micrometer-scale progression or regression of subcutaneously implanted tumors at the minute time scale. In two in vivo cancer mouse models, our sensor discerned differences in tumor volume dynamics between drug- and vehicle-treated tumors within 5 hours following therapy initiation. These short-term regression measurements were validated through histology, and caliper and bioluminescence measurements taken over weeklong treatment periods demonstrated the correlation with longer-term treatment response. We anticipate that real-time tumor regression datasets could help expedite and automate the process of screening cancer therapies in vivo.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cognition / Electronics Limits: Animals Language: En Journal: Sci Adv Year: 2022 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cognition / Electronics Limits: Animals Language: En Journal: Sci Adv Year: 2022 Type: Article Affiliation country: United States