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10.1089/dia.2016.0407

http://scihub22266oqcxt.onion/10.1089/dia.2016.0407
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C5399735!5399735!28221814
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suck abstract from ncbi


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pmid28221814      Diabetes+Technol+Ther 2017 ; 19 (4): 226-36
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  • An Amperometric Glucose Sensor Integrated into an Insulin Delivery Cannula: In Vitro and In Vivo Evaluation #MMPMID28221814
  • Ward WK; Heinrich G; Breen M; Benware S; Vollum N; Morris K; Knutsen C; Kowalski JD; Campbell S; Biehler J; Vreeke MS; Vanderwerf SM; Castle JR; Cargill RS
  • Diabetes Technol Ther 2017[Apr]; 19 (4): 226-36 PMID28221814show ga
  • Background: Labeling prohibits delivery of insulin at the site of subcutaneous continuous glucose monitoring (CGM). Integration of the sensing and insulin delivery functions into a single device would likely increase the usage of CGM in persons with type 1 diabetes.Methods: To understand the nature of such interference, we measured glucose at the site of bolus insulin delivery in swine using a flexible electrode strip that was laminated to the outer wall of an insulin delivery cannula. In terms of sensing design, we compared H2O2-measuring sensors biased at 600?mV with redox mediator-type sensors biased at 175?mV.Results: In H2O2-measuring sensors, but not in sensors with redox-mediated chemistry, a spurious rise in current was seen after insulin lis-pro boluses. This prolonged artifact was accompanied by electrode poisoning. In redox-mediated sensors, the patterns of sensor signals acquired during delivery of saline and without any liquid delivery were similar to those acquired during insulin delivery.Conclusion: Considering in vitro and in vivo findings together, it became clear that the mechanism of interference is the oxidation, at high bias potentials, of phenolic preservatives present in insulin formulations. This effect can be avoided by the use of redox mediator chemistry using a low bias potential.
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