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Noninvasive assessment of tissue‐engineered graft viability by oxygen‐17 magnetic resonance spectroscopy
Author(s) -
Einstein Samuel A.,
Weegman Bradley P.,
Kitzmann Jennifer P.,
Papas Klearchos K.,
Garwood Michael
Publication year - 2017
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.26227
Subject(s) - viability assay , transplantation , biomedical engineering , oxygen , in vivo , materials science , biophysics , nuclear magnetic resonance , nanotechnology , chemistry , in vitro , surgery , medicine , biochemistry , biology , microbiology and biotechnology , physics , organic chemistry
Transplantation of macroencapsulated tissue‐engineered grafts (TEGs) is being investigated as a treatment for type 1 diabetes, but there is a critical need to measure TEG viability both in vitro and in vivo. Oxygen deficiency is the most critical issue preventing widespread implementation of TEG transplantation and delivery of supplemental oxygen (DSO) has been shown to enhance TEG survival and function in vivo. In this study, we demonstrate the first use of oxygen‐17 magnetic resonance spectroscopy ( 17 O‐MRS) to measure the oxygen consumption rate (OCR) of TEGs and show that in addition to providing therapeutic benefits to TEGs, DSO with 17 O 2 can also enable measurements of TEG viability. Macroencapsulated TEGs containing βTC3 murine insulinoma cells were prepared with three fractional viabilities and provided with 17 O 2 . Cellular metabolism of 17 O 2 into nascent mitochondrial water (H 2 17 O) was monitored by 17 O‐MRS and, from the measured data, OCR was calculated. For comparison, OCR was simultaneously measured on a separate, but equivalent sample of cells with a well‐established stirred microchamber technique. OCR measured by 17 O‐MRS agreed well with measurements made in the stirred microchamber device. These studies confirm that 17 O‐MRS can quantify TEG viability noninvasively. Biotechnol. Bioeng. 2017;114: 1118–1121. © 2016 Wiley Periodicals, Inc.