Bacterial cellulose composite hydrogel for pre-concentration and mass spectrometric detection of thiol-containing biomarker.

Int J Biol Macromol

Department of Chemistry, Faculty of Science, Chulalongkorn University, Phayathai Road, Pathumwan, Bangkok 10330, Thailand; Center of Excellence in Materials and Biointerfaces, Chulalongkorn University, Phayathai Road, Pathumwan, Bangkok 10330, Thailand; Center of Excellence on Petrochemical and Materials Technology, Chulalongkorn University, Phyathai Road, Pathumwan, Bangkok 10330, Thailand. Electronic address:

Published: December 2023

Simple soaking of bacterial cellulose (BC) membrane in carboxymethyl cellulose (CMC) solution yielded BC/CMC hydrogel having re-swellable property. Then, gold nanoparticles (AuNPs) were embedded in the BC/CMC hydrogel via in situ chemical reduction to form BC/CMC/AuNPs composite hydrogel. It was found that the composite hydrogel exhibited physical/chemical characteristics similar to those of BC. The AuNPs with an average diameter of 13 nm distributed uniformly within the BC/CMC matrix as verified by transmission electron microscopy. The novelty of this work is the application of the BC/CMC/AuNPs composite hydrogel for selective adsorption of an important thiol-containing biomarker of Alzheimer's disease, glutathione (GSH), prior to direct laser desorption/ionization mass spectrometric (LDI-MS) detection. GSH adsorbed in the BC/CMC/AuNPs composite hydrogel showed the high ionization signal in LDI-MS providing a linear range of 50-10,000 nM with a limit of detection as low as 54.1 nM, which is a cut-off level for distinguishing between normal individuals and Alzheimer's patients. It should be emphasized that an additional matrix was not necessary as AuNPs can act as self-matrix for LDI-MS analysis. Furthermore, the BC/CMC/AuNPs composite hydrogel can effectively preconcentrate GSH approximately 10 times upon adsorption allowing for ultrasensitive detection of GSH required for disease diagnosis.

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Source
http://dx.doi.org/10.1016/j.ijbiomac.2023.126855DOI Listing

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