Advanced Clinical Diagnosis of Malaria Using a Simple Red-Emissive Smart Fluorescent Probe

Malaria, a potentially life-threatening disease caused by the mosquito-borne parasitic infection of human red blood cells, still accounts for over half a million deaths worldwide every year. Accurate early-stage diagnosis of malaria is indispensable for quick medical intervention and the avoidance of any potential complications leading to fatality. In this regard, DNA-specific fluorescent probes coupled with flow cytometry techniques emerged as a promising cost-effective diagnostic platform for highly sensitive rapid detection of malaria. However, ideal DNA-specific fluorescent probes that can be efficiently employed for both fluorescence microscopic studies as well as flow cytometric analysis to enable precise, high-quality clinical diagnosis of malaria are inadequate. In this context, we have reported a rationally designed hemicyanine dye <b>MR-1</b> with blue absorption and red emission that can exhibit a turn-on fluorescence response upon effective binding with the AT-rich segments of dsDNA. The rationale behind designing the fluorescent probe <b>MR-1</b> was well explained with the help of control compounds <b>MR-2</b> and <b>MR-3</b>. The DNA-specific fluorescent probe <b>MR-1</b> revealed excellent cell permeability and localized in the cellular nucleus of both live and fixed cells. A marked enhancement in fluorescence intensity was observed when malaria parasite-infected red blood cells were incubated with <b>MR-1</b>, and the detection limit was found to be ∼20/μL. Further, the flow cytometric analysis of clinical malaria parasite-infected red blood cells incubated with <b>MR-1</b> not only demonstrated precise detection and classification of various malaria parasites but also smartly enabled the differentiation of malaria from Babesia-parasite infection with similar clinical symptoms.

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Publication Details

Journal
Analytical Chemistry
Published
2025-10-17
DOI
https://doi.org/10.1021/acs.analchem.5c04953
Primary Topic
Malaria Research and Control
Type
article
Field-Weighted Citation Impact
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article

Advanced Clinical Diagnosis of Malaria Using a Simple Red-Emissive Smart Fluorescent Probe

Gengwen Chen, Zhigang Yang, Soham Samanta, Xiaoyuan Shawn Chen et al.
Analytical Chemistry
Malaria Research and Control
article

Advanced Clinical Diagnosis of Malaria Using a Simple Red-Emissive Smart Fluorescent Probe

Gengwen Chen, Zhigang Yang, Soham Samanta, Xiaoyuan Shawn Chen, Ziyan Zhang, Keqian Xu, Jiarong Lian, Yi Ye, Zongjun Liu, Shiqing Zhang, Ruijian Luo, Zhaoqing Yang, Xuqian Zhao
article en

Abstract

Malaria, a potentially life-threatening disease caused by the mosquito-borne parasitic infection of human red blood cells, still accounts for over half a million deaths worldwide every year. Accurate early-stage diagnosis of malaria is indispensable for quick medical intervention and the avoidance of any potential complications leading to fatality. In this regard, DNA-specific fluorescent probes coupled with flow cytometry techniques emerged as a promising cost-effective diagnostic platform for highly sensitive rapid detection of malaria. However, ideal DNA-specific fluorescent probes that can be efficiently employed for both fluorescence microscopic studies as well as flow cytometric analysis to enable precise, high-quality clinical diagnosis of malaria are inadequate. In this context, we have reported a rationally designed hemicyanine dye <b>MR-1</b> with blue absorption and red emission that can exhibit a turn-on fluorescence response upon effective binding with the AT-rich segments of dsDNA. The rationale behind designing the fluorescent probe <b>MR-1</b> was well explained with the help of control compounds <b>MR-2</b> and <b>MR-3</b>. The DNA-specific fluorescent probe <b>MR-1</b> revealed excellent cell permeability and localized in the cellular nucleus of both live and fixed cells. A marked enhancement in fluorescence intensity was observed when malaria parasite-infected red blood cells were incubated with <b>MR-1</b>, and the detection limit was found to be ∼20/μL. Further, the flow cytometric analysis of clinical malaria parasite-infected red blood cells incubated with <b>MR-1</b> not only demonstrated precise detection and classification of various malaria parasites but also smartly enabled the differentiation of malaria from Babesia-parasite infection with similar clinical symptoms.

Analytical ChemistryVol. 97(42)
University of Engineering & Management (IN), Central South University (CN), Shenzhen University (CN), Kunming Medical University (CN), Institute of Physiology and Basic Medicine (RU), Integrated Optoelectronics (Norway) (NO), Pharmaceutical Product Development (India) (IN), Third Xiangya Hospital (CN), Mindray (China) (CN), Xiangtan University (CN)
Openalex Percentile: Top 61%
Malaria Research and Control
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