| Literature DB >> 34743019 |
Obdulia Covarrubias-Zambrano1, Massoud Motamedi2, Bill T Ameredes3, Bing Tian3, William J Calhoun3, Yingxin Zhao3, Allan R Brasier4, Madumali Kalubowilage1, Aruni P Malalasekera5, Asanka S Yapa1, Hongwang Wang1, Christopher T Culbertson1, Deryl L Troyer6, Stefan H Bossmann7.
Abstract
We report the design and adaptation of iron/iron oxide nanoparticle-based optical nanobiosensors for enzymes or cytokine/chemokines that are established biomarkers of lung diseases. These biomarkers comprise ADAM33, granzyme B, MMP-8, neutrophil elastase, arginase, chemokine (C-C motif) ligand 20 and interleukin-6. The synthesis of nanobiosensors for these seven biomarkers, their calibration with commercially available enzymes and cytokines/chemokines, as well as their validation using bronchoalveolar lavage (BAL) obtained from a mouse model of TLR3-mediated inflammation are discussed here. Exhaled Breath Condensate (EBC) is a minimally invasive approach for sampling airway fluid in the diagnosis and management of various lung diseases in humans (e.g., asthma, COPD and viral infections). We report the proof-of-concept of using human EBC in conjunction with nanobiosensors for diagnosis/monitoring airway inflammation. These findings suggest that, with nanosensor technology, human EBC can be utilized as a liquid biopsy to monitor inflammation/remodeling in lung disease.Entities:
Keywords: Iron/iron oxide core/shell nanoparticle; Lung inflammation; Nanodiagnostics; Nanomedicine; Optical biosensor
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Year: 2021 PMID: 34743019 PMCID: PMC9127977 DOI: 10.1016/j.nano.2021.102476
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 6.096