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Published on: August 9, 2019
Lysosome-Targeted Dual-Functional Probe Capable of Detecting Acute Kidney Injury via In Vivo Imaging and Urinary
Siyu Jiang1, Bo Dai1, Guoqiang Feng1
1Engineering Research Center of Photoenergy Utilization for Pollution Control and Carbon Reduction, Ministry of Education, College of Chemistry, Central China Normal University, 152 Luoyu Road, Wuhan 430079, China.
A new fluorescent probe, MDSM-L, enables real-time detection of drug-induced acute kidney injury (AKI) by monitoring albumin and viscosity changes in the kidneys. This dual-target probe offers a novel diagnostic tool for early AKI detection.
Area of Science:
- Biomedical Engineering
- Molecular Imaging
- Diagnostic Tools
Background:
- Drug-induced acute kidney injury (AKI) is a significant global health issue.
- Current detection methods lack sensitivity and real-time in vivo capabilities.
- Dual-target responsive fluorescent probes offer enhanced reliability for disease diagnosis.
Purpose of the Study:
- To develop a lysosome-targeted, dual-functional fluorescent probe (MDSM-L) for quantitative detection of albumin and real-time in vivo imaging of drug-induced AKI.
- To assess the probe's ability to detect changes in serum/urine albumin and kidney lysosomal viscosity during AKI.
- To evaluate MDSM-L as a novel diagnostic tool for drug-induced AKI.
Main Methods:
- Synthesis and characterization of the dual-functional fluorescent probe MDSM-L.
- In vitro studies using bovine serum albumin (BSA) and living cells to assess fluorescence activation by albumin and viscosity.
- In vivo studies using a mouse model of drug-induced AKI for kidney targeting, albumin quantification, and imaging.
- Analysis of serum/urine albumin levels and kidney lysosomal viscosity changes.
Main Results:
- MDSM-L demonstrated sensitive fluorescence activation in response to albumin and viscosity changes at specific wavelengths.
- The probe successfully detected albumin and lysosomal viscosity changes in living cells.
- MDSM-L specifically targeted the kidney and enabled quantitative analysis of albumin in serum and urine of AKI mice.
- AKI was associated with decreased serum albumin, increased urine albumin, and elevated lysosomal viscosity in kidney tissue.
Conclusions:
- MDSM-L serves as an effective lysosome-targeted, dual-responsive fluorescent probe for albumin and viscosity.
- The probe facilitates real-time in vivo imaging and quantitative analysis of drug-induced AKI.
- MDSM-L presents a promising novel diagnostic strategy for early detection and monitoring of AKI.
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