ARTICLE pubs.acs.org/JPCC
Two-Photon Upconversion Laser (Scanning and Wide-Field) Microscopy Using Ln3+-Doped NaYF4 Upconverting Nanocrystals: A Critical Evaluation of their Performance and Potential in Bioimaging Jothirmayanantham Pichaandi,† John-Christopher Boyer,† Kerry R. Delaney,*,‡ and Frank C. J. M. van Veggel*,† † ‡
Department of Chemistry, University of Victoria, P.O. Box 3065,Victoria, British Columbia, Canada, V8W 3V6 Department of Biology, University of Victoria, P.O. Box 3020, Victoria, British Columbia, Canada, V8W 3N5
bS Supporting Information ABSTRACT: We report a simple, yet effective method to disperse NaYF4 nanocrystals (NCs) doped with luminescent Ln3+ ions in water and physiological buffers using an amphiphilic polymer poly(ethylene glycol) monooleate. These water-dispersible NCs were used for in vivo imaging by employing two-photon upconversion laser scanning microscopy (TPULSM) and two-photon upconversion wide field microscopy (TPUWFM) techniques. Using the 800 nm upconverted emission from Tm3+ ions, we show that (i) TPULSM imaging can be performed up to a depth of ∼600 μm inside an agar-milk gel tissue phantom and (ii) the edges of the object can still be identified. At depths beyond 600 μm, we observed a drastic decrease in the lateral resolution. Images of a mouse lung tissue obtained using this technique resulted in a lateral resolution with which we could observe the capillaries surrounding the alveoli air caps. The images lacked optical sectioning due to the high power density (∼2000 W/cm2) necessary to achieve an adequate signal-to-noise ratio. In addition, the time taken to obtain these images was prolonged because of the slow scanning speed necessitated by the long lifetimes and the poor quantum yield of the upconversion process. Conversely, in vivo TPUWFM imaging using the same 800 nm emission of brain blood vessels of a mouse after skull thinning gave excellent lateral resolution to differentiate blood vessels separated by a few micrometers. In addition to this, optical sectioning was observed over a depth of 100 μm, which is the first instance of optical sectioning shown in in vivo imaging employing Ln3+-doped NCs as imaging agents. Experiments with the aforementioned tissue phantom showed that imaging up to a depth of ∼400 μm could be obtained with the 800 nm emission from Tm3+/Yb3+ codoped NaYF4 NCs with a lateral resolution that allows us to distinguish micrometer-sized biological structures. In contrast, when employing the green upconverted emission from Er3+/Yb3+ codoped NaYF4 NCs, lateral resolution was completely lost at a depth of ∼300 μm.
’ INTRODUCTION In vivo imaging with fluorescent probes faces several challenges because of autofluorescence, absorption of light by cells and tissues, and scatter due to refractive mismatches primarily at the lipid water interfaces of cells. Traditional microscopy techniques (confocal and one-photon) give excellent lateral resolution, but photobleaching of the whole sample and poor depth penetration (
