Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
Scanning 1988 memoir
attached. Does not explicitly state that he used the term in
1957
Searching PubMed for "confocal" turned up an irrelevant 1969
reference (something to do with prolate spheroids) and several early 1980's
papers (but is clearly missing stuff in the 1970's). Some of the 1980's papers
have full text online. The Valkenburg
JA 1985
http://jb.asm.org/cgi/reprint/161/2/478?view=long&pmid=3918013 paper had
references to three Brackenhoff 1979 papers, including two in J
Microscopy:
Brakenhoff, G. J. 1979. Imaging modes in confocal
scanning
light microscopy (CSLM). J. Microsc. 117:233-242.
Brakenhoff,
G. J., P. Blom, and P. J. Barends. 1979. Confocal
scanning light microscopy
with high aperture lenses. J. Microsc.
117:219-232.
I note the above
articles do not mention laser.
Brad Amos (2003) wrote in Biology of the
Cell 95: 335-342 (history of his and John White's MRC series of confocal scopes
... available online):
"White decided to investigate the confocal
microscope, which had been invented by Minsky in 1955 (see Minsky, 1988). The
word ’confocal’ seems to have been first used by Brakenhoff and others in 1979
to mean a microscope in which the illumination is confined to a
diffraction-limited spot in the specimen and the detection is similarly confined
by placing an aperture in front of the detector in a position optically
conjugate to the focussed spot. The result of this arrangement is that the
response of the instrument to a fluorescent point object falls off approximately
according to an inverse fourth-power rule with distance from the plane of focus.
This produces an ’optical sectioning’ effect, in which the glare from
out-of-focus regions is almost completely eliminated. Brakenhoff et al. (1979 )
had demonstrated this experimentally with microscope objectives of the highest
available numerical aperture, of the type used in cell biology, and also
verified the prediction that the resolution (as measured by the full-width at
half maximum intensity of the point spread function) is improved relative to the
nonconfocal microscope by a factor of the square root of 2 (1.414). (In
practical microscopes, it is the optical sectioning effect that is more
important than the resolution improvement.) The underlying physics was
understood (Wilson and Sheppard, 1984): why, then, had the method not been
applied earlier to biological fluorescence?
Egger and Petran
published their first reflected light tandem scanning scope in 1967 (Science,
online). They do not cite Minsky (not surprising - independent invention).
"Light reflected from above or below the plane of the object was largely
intercepted by the opaque portions of the disc; thus the reflected light image
could not be degraded by scattered light reflecting into the
microscope."
Clearly a confocal scope, though the word confocal was not used
in the paper.
Minsky published as a US patent only. M. Minsky
(1957) U.S. patent #3013467, Microscopy Apparatus.
US Patent Office
link:
3,013,467
356/432 250/215 348/79
359/389 issued December 19, 1961
best wishes with
your search,
George
At 11:53 AM 8/22/2007, you
wrote:
Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
Hello.
Does anyone know who (or when/where) the term "confocal"
was actually coined? I presume it refers to "conjugate focal
planes". Possibly this is mentioned in Pawley's book, but I alas
do not have a copy. I also don't know if it was mentioned in Minsky's
original patent or not; it seems that at this time Minsky referred
to the method as "double-focusing" rather than confocal, but I
do not have a copy of the full patent.
thanks for any information,
Don
Donald M. O'Malley
Dept. Biology
Northeastern University
George McNamara, Ph.D.
University of Miami,
Miller School of Medicine
Image Core
Miami, FL
33010
[hidden email]
[hidden email]
305-243-8436
office
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