Developing a label-free full-range highly selective pH nanobiosensor using a novel high quantum yield pH-responsive activated-protein-protected gold nanocluster prepared by a novel ultrasonication-protein-assisted procedure.

A novel, label-free, ultra-selective, reproducible, and reversible pH nanobiosensor was developed for analyzing biofluids, food samples, and real water media utilizing a novel activated-protein-protected gold nanocluster with an ultra-narrow emission band, termed as ABSA-AuNCs. The ABSA-AuNCs were synthesized via a novel ultrasonication-protein-assisted procedure, for the first time, using activated bovine serum albumin as both capping and reducing agents. The ABSA-AuNCs revealed a highly narrow symmetric emission spectrum (λmax = 330.0 nm upon excitation at 312-317 nm), and a highly narrow size distribution of 2.9-3.7 nm along with an enhanced quantum yield of 28.3 %. At present, with a full width at half maximum (FWHM) of 14.0 nm, ABSA-AuNCs have the narrowest bandwidth of fluorescent nanomaterials reported to date. The ABSA-AuNCs were characterized for their stability, size, morphology, crystallinity, structural, and optical properties. The ABSA-AuNCs were found to be appropriate for constructing a label-free ultraselective pH nanobiosensor. A linear range over 2.0-11.0, fast response time of less than 5 s, and long-term stability of 99.7 % after 500 min were achieved. The %RSD for repeatability, intra-day reproducibility, and inter-day reproducibility was found to be 1.4 %, 1.7 %, and 2.3 %, in order, to reveal high repeatable and reproducible results. The selectivity of the pH biosensor was evaluated upon the addition of different interferents, indicating an excellent pH selectivity for the ABSA-AuNCs. Real sample analysis proved the feasibility of the ABSA-AuNCs for accurate, precise, and reliable pH sensing in biofluids (undiluted blood and urine), a variety of food samples, and several real water samples.

A novel selective and sensitive multinanozyme colorimetric method for glutathione detection by using an indamine polymer.

A sensitive and selective novel multinanozyme colorimetric method for glutathione (GSH) detection was developed. MnO2-nanozymes can catalyze the oxidation reaction of 3, 3՛-diaminobenzidine (DAB) and produce a brown indamine polymer. In the presence of GSH, this reaction slowly proceeds. When Au-nanozymes was used as peroxidase mimic along with MnO2-nanozymes, the analytical signal and selectivity (particularly, over Cys and AA) were significantly improved for GSH detection. Therefore, this novel multinanozyme system was further developed through optimization for the colorimetric detection of GSH. The calibration curve presented two wide linear range from 0.05 to 0.19 and 0.19-11.35 mg L̶ 1 with a very low detection limit of 0.02 mg L̶ 1 (5 nM) for GSH. The developed method was employed for human serum analysis without any dilution and any deproteinization.

A field-applicable colorimetric assay for notorious explosive triacetone triperoxide through nanozyme-catalyzed irreversible oxidation of 3, 3'-diaminobenzidine.

A field-applicable colorimetric assay for fast detection of notorious explosive triacetone triperoxide (TATP) has been developed through the selective irreversible oxidation of 3, 3'-diaminobenzidine by hydrogen peroxide (HP) liberated during the acidic hydrolysis/degradation of TATP in the presence of MnO2 nanozymes. The generated HP was detected by probing the absorbance of the product (indamine polymer) of the 3, 3'-diaminobenzidine (DAB) oxidation reaction at 460.0 nm. The UV-Vis measurements provided a linear range from 1.57 to 10.50 mg L-1 TATP with a detection limit of 0.34 mg L-1. The oxidation of DAB cannot proceed by molecular oxygen, thus it is selectively oxidized by H2O2; this prevents false-positive results from laundry detergents (containing O2-releasing substances). Moreover, a naked-eye field test was developed, and a fast spot test analyzing time of 5 s was achieved. The selectivity of the assay was checked by analyzing some synthetic samples prepared with a laundry detergent as camouflage. The results of the developed assay revealed quantitative recoveries for TATP whereas the standard nanozyme-based method showed significant false-positive results. Graphical abstract.