Review of Microdevices for Hemozoin-Based Malaria Detection
- PMID: 35200370
- PMCID: PMC8870200
- DOI: 10.3390/bios12020110
Review of Microdevices for Hemozoin-Based Malaria Detection
Abstract
Despite being preventable and treatable, malaria still puts almost half of the world's population at risk. Thus, prompt, accurate and sensitive malaria diagnosis is crucial for disease control and elimination. Optical microscopy and immuno-rapid tests are the standard malaria diagnostic methods in the field. However, these are time-consuming and fail to detect low-level parasitemia. Biosensors and lab-on-a-chip devices, as reported to different applications, usually offer high sensitivity, specificity, and ease of use at the point of care. Thus, these can be explored as an alternative for malaria diagnosis. Alongside malaria infection inside the human red blood cells, parasites consume host hemoglobin generating the hemozoin crystal as a by-product. Hemozoin is produced in all parasite species either in symptomatic and asymptomatic individuals. Furthermore, hemozoin crystals are produced as the parasites invade the red blood cells and their content relates to disease progression. Hemozoin is, therefore, a unique indicator of infection, being used as a malaria biomarker. Herein, the so-far developed biosensors and lab-on-a-chip devices aiming for malaria detection by targeting hemozoin as a biomarker are reviewed and discussed to fulfil all the medical demands for malaria management towards elimination.
Keywords: biosensor; diagnosis; hemozoin; lab-on-a-chip; malaria; microdevices.
Conflict of interest statement
The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results. Table 1. Features of developed biosensors lab-on-a-chip and microdevices for malaria diagnosis based on the detection of hemozoin and its variants. Equivalent parasite/µL of blood was calculated using previous works [29,30,72]. PBS: Phosphate-based saline; RBCs: red blood cells; FRET: Fluorescence Resonance Energy Transfer; MRR: Magnetic Resonance Relaxation; PDMS: Polydimethylsiloxane; SERS: Surface-Enhanced Raman Spectroscopy; SERRS: Surface-Enhanced Resonance Raman Spectroscopy; SPR: Surface Plasma Resonance.
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