Thesis

Design and development of an electrochemical and infrared spectroscopic medical device for serum-based cancer diagnostics

Creator
Rights statement
Awarding institution
  • University of Strathclyde
Date of award
  • 2020
Thesis identifier
  • T15633
Person Identifier (Local)
  • 201559983
Qualification Level
Qualification Name
Department, School or Faculty
Abstract
  • Development of an integrated electrochemical and spectroscopic serum diagnostic device would have significant potential as a triage tool for brain cancer and Hodgkin’s lymphoma in primary care settings to better inform clinical decisions and facilitate prompt referral to secondary care, whilst reducing financial and practical constraints placed on current diagnostic modalities. Additionally, the ability to detect IDH1 molecular status from serum samples would have significant clinical value to patients and clinicians alike, ultimately allowing earlier diagnosis and improved planning of surgery and treatment therapeutics. To this extent, the medical device has demonstrated the ability to electrochemically detect the biomarker CCL17/TARC at 387-50,000pg/ml concentrations with R2 = 0.979 and limit of detection of 387pg/ml in spiked buffer samples. Thereafter, the medical device demonstrated successful diagnosis of Hodgkin’s lymphoma in all 11 tested clinical patient samples. Additionally, ATR-FTIR discriminated between Hodgkin’s lymphoma and healthy controls in 200 patient samples with sensitivity of 83.2 ± 6.6% and specificity of 85.3 ± 8.1% with Random Forest classification, highlighting differences in protein secondary structures within clinical serum samples. The integrated diagnostic platform further demonstrated the ability to electrochemically detect IDH1-R132H proteins in spiked buffer samples at 0.05-10,000ng/ml concentrations with R2 = 0.958. However, it was not subsequently possible to detect IDH1 mutant proteins in clinical serum samples. Nevertheless, ATR-FTIR demonstrated the ability to discriminate between IDH1 molecular status in 104 glioma patients through consideration of the global molecular signatures ofserum samples with sensitivity of 89.0 ± 11.3% and specificity of 88.2 ± 10.1% with PLS classification.
Advisor / supervisor
  • Baker, Matthew
  • Dennany, Lynn
Resource Type
Note
  • Previously held under moratorium from 17 June 2020 until 22 June 2022
DOI
Date Created
  • 2020
Former identifier
  • 9912892791402996

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