Hollow Mesoporous Carbon Nanospheres/Ni Hybrids Aid in Metabolic Encoding for COVID-19 Recovery Assessment in Mothers and Fetuses

Metabolite analysis of body fluids is an advanced method for disease diagnosis and status assessment. Laser desorption/ionization-mass spectrometry (LDI-MS) has been widely employed for metabolic analysis due to the fast detection speed and simple sample pretreatment. Here, we designed and synthesized hollow mesoporous carbon nanospheres anchored with Ni (HMCSs/Ni) to simultaneously enhance the ionization and thermal desorption processes of the LDI process owing to their hollow and mesoporous structure, large surface area, and abundant Ni-N bonds. Based on HMCSs/Ni, we built an LDI-MS platform that can be used for metabolic information extraction and achieved the rapid detection (about seconds per sample) of metabolic fingerprints in trace serum samples (∼0.1 μL) without complicated preprocessing procedures. Then, we conducted serum metabolic screening in a cohort of COVID-19-recovered pregnant women. The optimized machine learning model could distinguish recovered pregnant women from uninfected pregnant women based on metabolic features with an AUC value of 0.901. In addition, the model indicates that maternal COVID-19 infection does not significantly affect the metabolic fingerprints of the fetuses. Overall, our work shows the prospect of HMCSs/Ni-assisted LDI-MS in disease recovery assessment and metabolite analysis.

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Publication Details

Journal
Analytical Chemistry
Published
2025-03-11
DOI
https://doi.org/10.1021/acs.analchem.4c06790
Citations
3
Primary Topic
Neonatal and fetal brain pathology
Type
article
Field-Weighted Citation Impact
10.48

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article

Hollow Mesoporous Carbon Nanospheres/Ni Hybrids Aid in Metabolic Encoding for COVID-19 Recovery Assessment in Mothers and Fetuses

Wen J. Di, Weikang Shu, Jingjing Wan, Rongxin Li et al.
3 citations
Analytical Chemistry
Neonatal and fetal brain pathology
10.48
article

Hollow Mesoporous Carbon Nanospheres/Ni Hybrids Aid in Metabolic Encoding for COVID-19 Recovery Assessment in Mothers and Fetuses

Wen J. Di, Weikang Shu, Jingjing Wan, Rongxin Li, Quan Hu, You Wang, Yinbing Zhao, Weihua Lou, Yu Zeng, Weixiu Zhao, Shuhuan Feng
article en
3 citations

Abstract

Metabolite analysis of body fluids is an advanced method for disease diagnosis and status assessment. Laser desorption/ionization-mass spectrometry (LDI-MS) has been widely employed for metabolic analysis due to the fast detection speed and simple sample pretreatment. Here, we designed and synthesized hollow mesoporous carbon nanospheres anchored with Ni (HMCSs/Ni) to simultaneously enhance the ionization and thermal desorption processes of the LDI process owing to their hollow and mesoporous structure, large surface area, and abundant Ni-N bonds. Based on HMCSs/Ni, we built an LDI-MS platform that can be used for metabolic information extraction and achieved the rapid detection (about seconds per sample) of metabolic fingerprints in trace serum samples (∼0.1 μL) without complicated preprocessing procedures. Then, we conducted serum metabolic screening in a cohort of COVID-19-recovered pregnant women. The optimized machine learning model could distinguish recovered pregnant women from uninfected pregnant women based on metabolic features with an AUC value of 0.901. In addition, the model indicates that maternal COVID-19 infection does not significantly affect the metabolic fingerprints of the fetuses. Overall, our work shows the prospect of HMCSs/Ni-assisted LDI-MS in disease recovery assessment and metabolite analysis.

Analytical ChemistryVol. 97(11)
Shanghai Jiao Tong University (CN), Renji Hospital (CN), East China Normal University (CN)
Shanghai Municipal Health Commission, National Natural Science Foundation of China, China Postdoctoral Science Foundation, Science and Technology Commission of Shanghai Municipality, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Zero hunger
Openalex Percentile: Top 3%
Neonatal and fetal brain pathology
10.48
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