Optical imaging probes
The present invention relates to methods of visualizing cells especially although not exclusively in vivo using a dye, such as a dendrimer-dye molecule or polybranched-dye molecule which is internalized by the cells and thus permits subsequent visualization by confocal fluorescence endomicroscopy or other optical detectors. There is also provided internally quenched probes for use in visualizing cells especially although not exclusively in vivo by confocal fluorescence endomicroscopy and the use of internally quenched probes in combination with confocal fluorescence endomicroscopy, for visualizing cells by virtue of internalization and dequenching of a probe by the cells. In a particular embodiment the cells are activated neutrophils, such as within the lung of a subject.
1. A method of visualising a cell or cells within a mixture of cells in vivo using confocal fluorescence endomicroscopy, comprising the step of administering a dye construct to cells of a subject; and observing a cell or cells which have internalised the dye construct, by observing an increase in fluorescence by a factor of 1.2 or more from said cell or cells using a confocal endomicroscope; wherein
(a) the dye construct is a poly-branched molecule having any of the following generalized structures:
wherein R is selected from the group consisting of NH 2 , CONH 2 , an amino acid, OH, amino acid —CONH 2 , CONH 2 — amino acid, alkylamino, alkoxyamino, urea, thiol, carboxylic acid, or a fluorophore moiety which is the same or different from the fluorescent moieties of the poly-branched molecule of structure (i)-(iv) above, and wherein the R group is directly attached to the branch point, or is separated from the branch point by a spacer selected from the group consisting of a PEG group, or an alkyl or alkenyl chain; or
(b) the dye construct is a poly-branched molecule selected from one of the following structures:
wherein (AA)n is absent or is present and wherein AA is any amino acid and n is a positive integer from 1 to 30; and wherein Q* is a dark quencher moiety and *F is a fluorescent moiety and wherein the dark quencher moiety Q* is independently selected from DABCYL, Methyl Red, BHQ1, BHQ2 and BHQ3.
2. The method according to claim 1 wherein the construct is to be administered locally and fluorescence is to be carried out in the gut; arteries and veins; the respiratory system, the brain; or the reproductive system.
3. The method according to claim 2 , wherein the method is carried out in the lung.
4. The method according to claim 3 in order to detect activated neutrophils.
5. The method according to claim 1 , wherein the fluorescent moiety *F is independently selected from FAM, rhodamine, a cyanine dye or a BODIPY dye.
6. The method according to claim 1 wherein the dye construct is locally administered to an area of tissue to be imaged.
7. The method according to claim 6 wherein detection of the cells which have internalized the dye construct is carried out within 1-30 min of the dye construct being administered to a subject.
8. The method according to claim 1 wherein the cell or cells to be detected are activated neutrophils.
9. The method according to claim 1 wherein the amount of the construct to be administered to a subject is less than 100 μg.
10. The method according to claim 1 , wherein the dye construct is administered to the subject by a catheter inserted into the confocal endomicroscope.
11. A method of visualizing a cell or cells within a mixture of cells in vivo using confocal fluorescence endomicroscopy, comprising the step of administering a dye construct to cells of a subject, and observing fluorescence from said cell or cells using a confocal endomicroscope, wherein the dye construct is a poly-branched molecule selected from one of the following structures:
where (AA)n is optional and wherein when present AA is any amino acid and n is a positive integer from 1 to 30, and *F is independently selected from FAM, rhodamine, a cyanine dye or a BODIPY dye, and Q* is independently selected from DABCYL, Methyl Red, BHQ1, BHQ2 and BHQ3.
12. The method according to claim 11 wherein detection of the cells which have internalized the dye construct is carried out within 1-30 min of the dye construct being administered to a subject.
13. The method according to claim 11 wherein the cell or cells to be detected are activated neutrophils.