The University of Auckland

Project #82: Improved filtering for Non-Invasive Blood-Glucose detection

Back

Description:

The primary objective of this project is to improve the accuracy of results when testing using non­invasive methods to calculate glucose levels. The project aims to design and implement a signal processing and filtering system for an existing non-invasive blood glucose sensor. 

Around 415 million individuals today are afflicted with diabetes. These individuals need to monitor their insulin levels, necessitating self-testing through the use of existing medical devices that involve pricking, which can be a painful and tiring process. While some non-invasive blood-glucose detection devices are available in the market, they lack the accuracy of traditional devices. In recent years, there has been extensive research on non-invasive blood-glucose detection using techniques such as NIR light, with universities around New Zealand such as the University of Canterbury exploring such methods in this field . 

Many previous studies have highlighted similar challenges, such as the difficulty in accurately detecting, filtering and clearing the photo-diode signals to get an accurate result of glucose levels. 

The aim of this project is to design a filter for the existing blood-glucose sensor with the purpose of enhancing the identification and effective filtration of the blood-glucose signal; aiming to increase accuracy of non-invasive methods when compared to invasive methods currently publicly available. In developing this design, we will explore options such as FIR filter, IIR filter, and look through parameters such as filter output stability, among others to identify relationships between the signals detected and glucose levels. The outcomes will be communicated through a dedicated application, providing users with a user-friendly tool for monitoring their blood-glucose levels. 

Type:

Undergraduate

Outcome:

1. Are we able to identify and document a correlation between a detected signal and the glucose levels in that sample? If so, what is the most effective way of filtering out the required signal from the range of signals?

2. Are we able to get similar test results when comparing non-invasive methods to traditional invasive methods?

Prerequisites

None

Specialisations

Categories

Supervisor

Co-supervisor

Team

Lab

No lab has been assigned to this project