We demonstrate a multimodal superresolution microscopy technique based on a phase masked excitation beam in combination with spatially filtered detection. The theoretical foundation for calculating the focus from a non-paraxial beam with an arbitrary azimuthally symmetric phase mask is presented for linear and two-photon excitation processes as well as the theoretical resolution limitations. Experimentally this technique is demonstrated using two-photon luminescence from 80 nm gold particle as well as two-photon fluorescence lifetime imaging of fluorescent polystyrene beads. Finally to illustrate the versatility of this technique we acquire two-photon fluorescence lifetime, two-photon luminescence, and second harmonic images of a mixture of fluorescent molecules and 80 nm gold particles with > 120 nm resolution (λ/7). Since this approach exclusively relies on engineering the excitation and collection volumes, it is suitable for a wide range of scanning-based microscopies.
Keyphrases
- living cells
- single molecule
- energy transfer
- quantum dots
- high resolution
- monte carlo
- label free
- fluorescent probe
- photodynamic therapy
- pain management
- deep learning
- light emitting
- electron microscopy
- high throughput
- high speed
- magnetic resonance imaging
- mass spectrometry
- computed tomography
- silver nanoparticles
- fluorescence imaging
- obstructive sleep apnea
- single cell