Lab-on-a-chip device to quantify buffer capacity of blood

An accurate estimation of physiological buffer capacity and total titratable buffer concentration of blood can give a great deal of insight into the physiological stability of a patient and yet it remains an undervalued diagnostic marker. This thesis highlights the need for a lab-on-chip device to q...

Full description

Bibliographic Details
Main Author: Gandhi, Sahir
Other Authors: O'Hare, Danny, Boutelle, Martyn
Format: Doctoral or Postdoctoral Thesis
Language:unknown
Published: Imperial College London 2016
Subjects:
Online Access:http://hdl.handle.net/10044/1/34399
https://doi.org/10.25560/34399
id ftimperialcol:oai:spiral.imperial.ac.uk:10044/1/34399
record_format openpolar
spelling ftimperialcol:oai:spiral.imperial.ac.uk:10044/1/34399 2023-05-15T15:52:55+02:00 Lab-on-a-chip device to quantify buffer capacity of blood Gandhi, Sahir O'Hare, Danny Boutelle, Martyn 2016-01 http://hdl.handle.net/10044/1/34399 https://doi.org/10.25560/34399 unknown Imperial College London Bioengineering Thesis or dissertation Doctoral Doctor of Philosophy (PhD) 2016 ftimperialcol https://doi.org/10.25560/34399 2019-11-14T23:38:47Z An accurate estimation of physiological buffer capacity and total titratable buffer concentration of blood can give a great deal of insight into the physiological stability of a patient and yet it remains an undervalued diagnostic marker. This thesis highlights the need for a lab-on-chip device to quantify buffer capacity of whole blood samples by estimating the total titratable buffer concentration. Buffer capacity is quantified by titrating the buffer to its end point using monoprotic acids. More sophisticated ways include electrolytic titration, i.e. producing a proton flux using electrodes in a controlled environment. This thesis looks at a novel approach to electrolytic (coulometric) titration by inhibiting the production of OH ions during electrolysis and titrating the sample due to the proton flux from the anode. By definition, is the amount of acid or base added to change the pH of 1 litre of buffer by 1 pH unit. The carbonic acid bicarbonate buffer system is the most important buffer that maintains the body’s pH within a stable range. To quantify this buffer’s total buffering concentration, it is important to know and indicate its titration end point which signifies the total exhaustion of all buffering constituents. Colorimetric indicators have been used to indicate this end point which can be quantified through cameras or spectrophotometric techniques. Using this novel coulometric titrator and the colorimetric end point detector, this thesis presents a portable lab-on-chip prototype to spectrophotometrically quantify total titratable buffer concentration. Clinically, this device could benefit patients with sickle cell disease, nephritic disease and those admitted in accident and emergency wards. This research work is aimed at presenting a proof-of-concept for a device that can titrate nano-litre samples and be able to detect the end point of a titration in a controlled way. Open Access Doctoral or Postdoctoral Thesis Carbonic acid Imperial College London: Spiral Sickle ENVELOPE(-66.783,-66.783,-68.867,-68.867)
institution Open Polar
collection Imperial College London: Spiral
op_collection_id ftimperialcol
language unknown
description An accurate estimation of physiological buffer capacity and total titratable buffer concentration of blood can give a great deal of insight into the physiological stability of a patient and yet it remains an undervalued diagnostic marker. This thesis highlights the need for a lab-on-chip device to quantify buffer capacity of whole blood samples by estimating the total titratable buffer concentration. Buffer capacity is quantified by titrating the buffer to its end point using monoprotic acids. More sophisticated ways include electrolytic titration, i.e. producing a proton flux using electrodes in a controlled environment. This thesis looks at a novel approach to electrolytic (coulometric) titration by inhibiting the production of OH ions during electrolysis and titrating the sample due to the proton flux from the anode. By definition, is the amount of acid or base added to change the pH of 1 litre of buffer by 1 pH unit. The carbonic acid bicarbonate buffer system is the most important buffer that maintains the body’s pH within a stable range. To quantify this buffer’s total buffering concentration, it is important to know and indicate its titration end point which signifies the total exhaustion of all buffering constituents. Colorimetric indicators have been used to indicate this end point which can be quantified through cameras or spectrophotometric techniques. Using this novel coulometric titrator and the colorimetric end point detector, this thesis presents a portable lab-on-chip prototype to spectrophotometrically quantify total titratable buffer concentration. Clinically, this device could benefit patients with sickle cell disease, nephritic disease and those admitted in accident and emergency wards. This research work is aimed at presenting a proof-of-concept for a device that can titrate nano-litre samples and be able to detect the end point of a titration in a controlled way. Open Access
author2 O'Hare, Danny
Boutelle, Martyn
format Doctoral or Postdoctoral Thesis
author Gandhi, Sahir
spellingShingle Gandhi, Sahir
Lab-on-a-chip device to quantify buffer capacity of blood
author_facet Gandhi, Sahir
author_sort Gandhi, Sahir
title Lab-on-a-chip device to quantify buffer capacity of blood
title_short Lab-on-a-chip device to quantify buffer capacity of blood
title_full Lab-on-a-chip device to quantify buffer capacity of blood
title_fullStr Lab-on-a-chip device to quantify buffer capacity of blood
title_full_unstemmed Lab-on-a-chip device to quantify buffer capacity of blood
title_sort lab-on-a-chip device to quantify buffer capacity of blood
publisher Imperial College London
publishDate 2016
url http://hdl.handle.net/10044/1/34399
https://doi.org/10.25560/34399
long_lat ENVELOPE(-66.783,-66.783,-68.867,-68.867)
geographic Sickle
geographic_facet Sickle
genre Carbonic acid
genre_facet Carbonic acid
op_doi https://doi.org/10.25560/34399
_version_ 1766388017558192128