Oxidative stress biomarker triggered multiplexed tool for auxiliary diagnosis of atherosclerosis

Author:

Ma Yuan1ORCID,Sun Wei23ORCID,Ye Zhifei4ORCID,Liu Liuhui1,Li Menghuan2,Shang Jinhui1,Xu Xinyu1ORCID,Cao Hui1,Xu Li1,Liu Yongchao1,Kong Xiangqing5,Song Guosheng1ORCID,Zhang Xiao-Bing1ORCID

Affiliation:

1. State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China.

2. Department of Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.

3. Key Laboratory of Targeted Intervention of Cardiovascular Disease, Collaborative Innovation Center for Cardiovascular Disease Translational Medicine, Nanjing Medical University, Nanjing 210029, China.

4. Department of Chemistry, Case Western Reserve University, Cleveland, OH 44106, USA.

5. The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Gusu School, Nanjing Medical University, Suzhou 215002, China.

Abstract

Oxidative stress is integral in the development of atherosclerosis, but knowledge of how oxidative stress affects atherosclerosis remains insufficient. Here, we design a multiplexed diagnostic tool that includes two functions (photoacoustic imaging and urinalysis), for assessing intraplaque and urinary malondialdehyde (MDA), a well-recognized end-product of oxidative stress. Molecular design is conducted to develop the first near-infrared MDA-responsive molecule (MRM). Acid-unlocked ratiometric photoacoustic nanoprobe is designed to report intraplaque MDA, enabling it to reflect plaque burden. Furthermore, MRM is tailored for urinary MDA detection with excellent specificity in a blind study. Moreover, we found a significant difference in urinary MDA between healthy adults and atherosclerotic patients (more than 600 participants). Combining these two functions, such a multiplexed diagnostic tool can dynamically report intraplaque and systemic oxidative stress levels during atherosclerosis progression, pneumonia infection, and drug treatment in atherosclerotic mice, which is promising for the auxiliary diagnosis of atherosclerosis.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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