“…[182][183][184] As an alternative to Ln 3+chelates, the advantages of Ln 3+ -doped luminescent nanoprobes in bioassays have been utilized. [185][186][187] In the past years, many novel luminescent bioassay methods such as heterogeneous sandwich assay, competitive assay, DNA microarrays, magnetic separation-assisted assay and homogeneous FRET assay, have been established based on Ln 3+ -doped DSL nanoprobes, for the detection of pathogenic microorganisms, 188,189 nucleic acids, [190][191][192] drugs of abuse, 193,194 antibodies, [195][196][197] glucose, 198,199 and reactive oxygen species, 200 to name a few. However, these bioassays were performed under steady-state PL detection, and were somewhat limited by either the poor dispersibility or broad size distribution of the nanoprobes.…”