Nanozyme Database

	ref	title	DOI	material type	comment
3564	375	Zinc oxide particles catalytically generate nitric oxide from endogenous and exogenous prodrugs	https://doi.org/10.1002/smll.201906744	Metal oxide	Zinc oxide (ZnO) particles

	ref	material	size	size err	size unit	size type	size comment	BET	b _nanozyme	b 10ⁿ	b unit	specific act	sa 10ⁿ	sa unit	comment
7611	375	ZnO	10.1	1.8	μm	SEM	The average size of the bowtie was 10.1 ± 1.8 μm (length) and 2.6 ± 0.9 μm (width, defined as the distance of the two outmost branches at the edge) (Fig. 1ai and aii).

	ref	material	enzyme type	substrate	pH	T	k_m	k_m err	k_m 10ⁿ	k_m unit	v_max	v_max err	v_max 10ⁿ	v_max unit	k_cat	k_cat err	k_cat 10ⁿ	k_cat unit	k_cat/k_m	k_cat/k_m 10ⁿ	k_cat/k_m unit	comment

	ref	material	application	target	method	linear range	linear ran unit	LOD	lod unit	recovery	comment
5280	375	ZnO	NO-releasing biomaterials and devices	NO	E-chem			1 × 10−9	M
5279	375	ZnO	NO-releasing biomaterials and devices	NO	E-chem			1 × 10−9	M		In detail, the probe was suspended in a glass vial filled with 10 mL 0.1 M H2SO4/0.1 M KI solution. Incremental volumes of 25 × 10−6 m KNO2 solution were added to the glass vial after a stable current baseline was observed. NO concentration was determined based on the amount of KNO2 added as the conversion of KNO2 to NO was stoichiometrically 1:1. To assess the capability of ZnO particles to catalyze GSNO to generate NO, the NO probe was placed in a glass vial containing 3.95 mL ZnO particles (0.1–0.4 g L−1) in PBS. Fifty microliters of GSNO solutions (5× 10−6–100 × 10−6 m) was added to the glass vial when a stable baseline was reached. Changes in current response were recorded over time using LabScribe2 software. All NO measurements were carried out in dark at 37 °C on a hot plate with constant stirring.