Abstract

Malaria diagnosis relies on optical microscopy and/or rapid diagnostic tests based on detecting specific malaria antigens. The clinical sensitivity of these methods is highly dependent on parasite density, with low levels of detection at low parasite density, challenging the worldwide malaria elimination efforts. Therefore, there is a need for diagnostic methods with higher sensitivity, demanding innovative diagnostics devices able to detect malaria at low parasite density and at early stages of the disease. We propose an innovative optical device for malaria diagnosis, based on optical reflectance spectrophotometry, for the detection of parasites through the quantification of haemozoin. For this purpose, a set of eight thin-film optical filters, based on multilayer stacks of MgO/TiO2 and SiO2/TiO2 thin-films, with high transmittance and low full width at half maximum (FWHM) at specific wavelengths, was designed and fully characterized (both numerically and experimentally). A preliminary assessment of its potential to reconstruct the original spectra of red blood cells was performed, both in uninfected and Plasmodium falciparum-infected samples. The obtained results show that, although the experimental filters have a non-ideal performance characteristic, they allow us to distinguish, based on only 8 discrete points in the optical spectrum, between healthy and malaria infected samples, up to a detection limit of 12 parasites/μL of red blood cells. Those results enhance the potential of using such a device for malaria diagnostics, aiming for non-invasiveness.

Highlights

  • The main methods for field malaria diagnosis are based on the detection of the etiological agent, Plasmodium spp., in the patients0 blood through optical microscopy [4] and/or through rapid diagnostic tests (RDT) based on detecting specific malaria antigens [5]

  • Molecular diagnosis by polymerase chain reaction (PCR) [4,6], it allows the detection of low parasitaemia

  • The results show of that, with the numerically optical filters, is low possible sitaemia the variation of the slopes between the uninfected and infected samples may be correctly extract the original reflectance spectra (Figure 1), based on only eight spectral difficult to detect, it is clearly higher as the parasitaemia increases

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Summary

Introduction

The main methods for field malaria diagnosis are based on the detection of the etiological agent, Plasmodium spp., in the patients0 blood through optical microscopy [4] and/or through rapid diagnostic tests (RDT) based on detecting specific malaria antigens [5]. These methods are low cost and relatively easy to implement, they face several challenges in many malaria-endemic regions, including the requirement for expert microscopists, inadequate quality control and the possibility of falsenegative results due to low parasitaemia (

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