This is the authors' abstract. We don't add key points for this paper.
Fluorescence lifetime imaging provides more possibility of in vivo multiplexing in second near infrared (NIR‐II) window. However, it still faces the obstacle that fluorescent probes with differentiable lifetime often exhibit quite different fluorescence intensity, especially the short lifetime usually accompanies with a weak fluorescence intensity, resulting in the difficulty for simultaneously decoding multiplexed lifetime information due to the interference of background noise. To facilitate high‐fidelity lifetime multiplexed imaging, we developed a series of Er 3+ doped double interface fluorescent nanoprobes (Er‐DINPs): α‐NaYF 4 @NaErF 4 : Ce@NaYbF 4 @NaErF 4 : Ce@NaYF 4 with strong fluorescence intensity and easily distinguishable fluorescence lifetime. Both in vitro and in vivo experimental results confirmed the advantage of these probes with comparable fluorescence intensity for high‐fidelity multiplexed lifetime bioimaging.
Answers are grounded in this paper and cite their sources.
No takes yet. Share an insight, caveat, or question.
Zhu et al. (2021) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: