Novel Methods of Tissue Processing and Imaging
The present invention includes novel methods of processing a tissue sample. The present invention also includes novel methods of imaging a tissue sample. The present invention further includes a specimen holding device for performing the novel methods of processing a tissue sample and a microscope system for performing the novel methods of imaging a tissue sample.
1 . A method of processing a tissue sample, the method comprising the steps of:
obtaining a tissue sample; and
contacting the tissue sample with a fixative solution comprising at least one fixative and at least one fluorescent dye;
wherein the step of contacting the tissue sample with a fixative solution is performed over a period of less than 1 hour.
2 . The method of claim 1 , further comprising the step of contacting the tissue sample with a clearing solution.
3 . (canceled)
4 . The method of claim 1 , wherein the at least one fluorescent dye is selected from the group consisting of eosin, DAPI, SYTOX green, acridine orange, rhodamine B, propidium iodide, and a Hoechst dye.
5 . The method of claim 1 , wherein the at least one fixative is methacarn.
6 . The method of claim 1 , wherein the fixative solution further comprises a permeation enhancer.
7 . The method of claim 1 , wherein the step of contacting the tissue sample with a fixative solution is performed at about 45° C.
8 . The method of claim 1 , wherein the fixative solution further comprises a red blood cell lysing agent.
9 . (canceled)
10 . The method of claim 1 , wherein the step of contacting the tissue sample with a fixative solution is performed over a period of less than 15 minutes.
11 . The method of claim 2 , wherein the clearing solution comprises benzyl alcohol and benzyl benzoate.
12 . The method of claim 11 , wherein the ratio of benzyl alcohol to benzyl benzoate is about 1:2.
13 . The method of claim 2 , wherein the step of contacting the tissue sample with a clearing solution is performed over a period of time of less than 10 minutes.
14 . The method of claim 2 , wherein a partially fixed and a partially cleared tissue is placed in fixative after imaging.
15 . (canceled)
16 . The method of claim 1 , wherein the tissue sample is fixed prior to obtaining the tissue sample.
17 . A method of imaging a tissue sample, the method comprising the steps of:
obtaining a tissue sample;
contacting the tissue sample with a fixative solution comprising at least one fluorescent dye;
contacting the tissue sample with a clearing solution; and
producing a tissue sample image by measuring intensity values of the fluorescence of the tissue sample, and converting the intensity values to effective optical densities, such that the optical densities recreate the coloration of a stain in a produced image of the tissue sample.
18 . The method of claim 17 , wherein the tissue sample image is produced using an optical sectioning microscope.
19 . The method of claim 18 , wherein the optical sectioning microscope is selected from the group consisting of: a multiphoton microscope (MPM), a confocal microscope, a structured illumination microscope, a super-resolution microscope, a selective plane illumination microscope (SPIM), a side-plane illumination microscope, a spinning disk confocal microscope, and a deconvolution microscope.
20 . The method of claim 17 , wherein the step of producing a tissue sample image further comprises second harmonic generation (SHG).
21 . The method of claim 17 , wherein the sample image is a three dimensional (3-D) sample image.
22 . The method of claim 17 , wherein the sample image is obtained at a sample depth greater than 50 μm.
23 . The method of claim 17 , wherein the intensity values are converted to effective optical densities using an exponential pseudo-coloration process.
24 - 48 . (canceled)