Nanozyme Database

	ref	title	DOI	material type	comment
3557	364	A ratiometric fluorescence and colorimetric dual-mode assay for H2O2 and xanthine based on Fe, N co-doped carbon dots	https://doi.org/10.1016/j.dyepig.2020.108486	Carbon	Fe, N-CDs

	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
7604	364	Fe, N-CDs	4–6		nm	TEM

	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
6243	364	Fe, N-CDs	POD	TMB			0.434			mM	1		-7	M/s					364
6242	364	Fe, N-CDs	POD	H2O2			0.207			mM	7.487		-7	M/s					364			364

	ref	material	application	target	method	linear range	linear ran unit	LOD	lod unit	comment
5270	364	Fe, N-CDs	the H2O2 and xanthine determination in human serum and the urine	H2O2	Color	0–100	μM	0.047	μM	The detection limits of H2O2 and xanthine were 0.047 μM and 0.02 μM for ratiometric fluorometric and 0.05 μM and 0.023 μM for colorimetric, respectively.
5269	364	Fe, N-CDs	the H2O2 and xanthine determination in human serum and the urine	H2O2	Color	0–100	μM	0.047	μM
5268	364	Fe, N-CDs	the H2O3 and xanthine determination in human serum and the urine	xanthine	Color	0-70	μM	0.02	μM
5267	364	Fe, N-CDs	the H2O3 and xanthine determination in human serum and the urine	xanthine	Color	0-70	μM	0.02	μM	The detection limits of H2O2 and xanthine were 0.047 μM and 0.02 μM for ratiometric fluorometric and 0.05 μM and 0.024 μM for colorimetric, respectively.