Random access stimulated emission depletion (STED) microscopy

Patent metadata

Field	Value
Publication number	US-9810966-B2
Application number	US-201414778217-A
Country	US
Kind code	B2
Filing date	Mar 21, 2014
Priority date	Mar 22, 2013
Publication date	Nov 7, 2017
Grant date	Nov 7, 2017

Abstract

Optical scanning system, comprising an optical system for guiding a first and a second light beam, and deflector devices for deflecting first and second light beams in a directionally variable manner. The deflector devices comprise at least one acousto-optic deflector, and the optical system is arranged in such a way that the first and second light beams are counter-propagating through the acousto-optic deflector, which is controllable for deflecting the first and second light beams simultaneously or in pulse sequence. STED microscopy apparatus comprising an optical scanning system based on acousto-optic deflectors.

First claim

The invention claimed is:

1. Apparatus for irradiating a target material in order to excite elements of an excitable chemical species contained within said target material to an excited state, comprising
an optical scanning system comprising:
an optical system for guiding a first and a second light beam, and
a deflecting device for deflecting said first and second light beams in a directionally variable manner,
wherein said deflecting device comprises at least one acousto-optic deflector, and said optical system is arranged in such a way that said first and second light beams are counter-propagating through said at least one acousto-optic deflector, said at least one acousto-optic deflector being controllable for deflecting, simultaneously or in pulse sequence, said first and second light beams,
wherein said first light beam is constituted by a short-pulsed excitation beam and is adapted to excite said elements of an excitable chemical species to said excited state, and said second light beam is constituted by a long-pulsed depletion beam and is adapted to reduce the number of excited elements in said excited state, and
a directing system for directing said first and second light beams onto said target material in such a way that said first and second light beams form respective movable, partially overlapped, irradiation areas on said target material,
wherein the pulse length of the excitation beam is less than 1 ps, and wherein the pulse length of the depletion beam is longer than 50 ps.

2. Apparatus according to claim 1 , wherein the wavelength of the excitation beam is within a spectral window where spontaneous fluorescence emission of the excitable chemical species is possible, and the multi-photon excitation fluorescence cross-section is not zero.

3. Apparatus according to claim 1 , wherein the pulse length of the excitation beam is 150 fs at the focal point, and wherein the pulse length of the depletion beam is in the range between 200 ps and 2 ns.

4. Apparatus according to claim 1 , wherein both the excitation beam and the depletion beam are linearly polarized upon entry into said optical scanning system.

5. Apparatus according to claim 1 , comprising a beam-shaping device for shaping the depletion beam, arranged preferably in a conjugated plane after the optical scanning system and before a point where said first and second light beams are combined.

6. Apparatus according to claim 2 , wherein the pulse length of the excitation beam is 150 fs at the focal point, and wherein the pulse length of the depletion beam is in the range between 200 ps and 2 ns.

7. Apparatus according to claim 3 , wherein both the excitation beam and the depletion beam are linearly polarized upon entry into said optical scanning system.

8. Apparatus according to claim 4 , comprising a beam-shaping device for shaping the depletion beam, arranged preferably in a conjugated plane after the optical scanning system and before a point where said first and second light beams are combined.

Assignees

• Fond St Italiano Tecnologia
• Baylor College Medicine

Inventors

• Bianchini Paolo
• Saggau Peter
• Diaspro Alberto

Classifications

• G02B27/58

  Optics for apodization or superresolution; Optical synthetic aperture systems · CPC title

• G02B21/16

  adapted for ultraviolet illumination {; Fluorescence microscopes (G02B21/0076 takes precedence)} · CPC title

• G02B21/002

  Scanning microscopes (scanning near field optical microscopes G01Q60/18) · CPC title

• G01N21/6456

  Spatial resolved fluorescence measurements; Imaging · CPC title

• G02F1/33 Primary

  Acousto-optical deflection devices {(circuit or control arrangements therefor G02F1/113)} · CPC title