Femtosecond Lasers for Nanosurgery
Roland Piquepaille writes "In "Lasers operate inside single cells," Nature writes that nanosurgery can be achieved by vaporizing some components of living cells without killing the cells themselves. "With pulses of intense laser light a millionth of a billionth of a second long, US researchers are vaporizing tiny structures inside living cells without killing them. The technique could help probe how cells work, and perform super-precise surgery." This was developed by Eric Mazur of Harvard University and his colleagues. This summary contains more details and references about the process and these microexplosions. Please note that it's a very different technique from the one described six months ago in a previous Slashdot reference, Surgery with Femtosecond Lasers."
In the future, when there are nanoprobes of all kinds, there will probably be lots of rogue nanoprobes infesting the cells. Maybe they can be zapped out with these lasers.
It has been said that evolution of cells must have been impossible, because each part of the cell is necessary for the cell to live, and thus they must have all evolved at the same time, which is highly unlikely. Perhaps this is a way to test that theory?
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Hmmmmm. These techniques, combined with multispectral analysis of tissues in real time could be just the ticket for surgical resection of certain cancers(meningiomas etc....). The multispectral analysis could be combined with a robotic laser that could automatically lase the "transformed" tissues, thus selectively killing cancerous cells. Cool.
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How often do you see something like "In "?
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If you can affect something inside a single cell accurately, couldn't this same technology be used to alter ink colors for super high-resolution laser printing? Like 10,000 DPI non-interpreted?
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I doubt they'll ever find weapons of micro destruction.
This was developed by Eric Mazur of Harvard University and his colleagues.
The MASER was the predecessor of the LASER. Though most don't know this, LASER is an acronym standing for "light amplification by stimulated emission of radiation." The difference is that MASERs amplify Microwaves instead of light.
Isn't it convenient that the lead scientist on this is named just happened to be named "Mazur?" . . . Waitaminut, where'd that black helicopter come from?
(You can get a little info about MASERs and LASERs here)
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Lay off the ketamine for a second and re-word that...
For the most part, magazines such as S.A., New Scientist, etc "paraphrase" the work presented in journals such as Nature or Science. While it may take a while for something to be peer-review and printed in a journal, it isn't really considered all that trustworthy until it is.
There are occasions where huge papers "debut" in a peer reviewed journal at the same time as a corresponding article in one of the mainstream science mags, but it was definitely the journal article which came "first."
Of course, that may have been exactly what you said...I just couldn't understand what you were saying.
millionth of a billionth of a second ??
That sounds, like, soooo way totally not a technical term
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Of course, this is wrong. Stupid me; multiplied where I should have divided.
The correct answer is 2.7432x10^-9 football fields, or two and three-quarters nanofootballfields.
Assuming, of course, that you meant American football.
Ce n'est pas un vrai mouvement de robot!
Aw, come on. I need more than that. Strapped which way? Vertically? Laterally? Longitudinally? How many coats of Purple are there? How fast are they going? (Relativity, don'cha know?)
This is science. We must maintain precision if our results are to mean anything.
Ce n'est pas un vrai mouvement de robot!
--Chag
I work with femto-second lasers. I have used them in living cells for a variety of applications. Two of which involve destroying structures inside of living cells. Of course, these structures are placed into the cells by us (injection, knock-in, electroporation, etc). It's not an extremely new technique, it's just being used in a slightly new way. Some of the similar techniques are known as uncaging, FRAP, and more.
/., semiconductor nanocrystals are starting to pop up in similar research. They are quite useful, if still hard to work with (they don't behave like most biological molecules). I got interested in quantum dots about a year ago, and have done a bit of work with them, but would like to do some more (when I find the time).
Personally, I rarely find anything that groundbreakingly new in Nature. Well, that's not exactly true. There is plenty of new data, and new applications and/or refinements of old techniques. There generally aren't wholly original techniques or completely new instruments discussed in that journal. My personal preference for that sort of thing are some physics journals.
One other thing, that may be of interest to
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I used to work on a biomedical project at the Univ. of Michigan involving high-speed lasers (usually femtosecond duration) as a tool to replace the larger ablative lasers used in standard refractive surgery (LASIK). The femtosecond lasers could be focused intrastromally, such that the material ablated was directly inside the cornea. Due to the relaxation of some stromal pressure, the cornea itself would reshape to a softer lens, without the huge amount of ablation required by current lasers. http://www.intralase.com/home.html
Mitochondria are about 5 micrometers across and your various cytoskeletal filaments and tubules range between 3 - 25 nanometers in diameter.
Human chromosomes, on the other hand, are essentially 2 meters of DNA packed into a 5 micrometer-wide nucleus. Now that's 6 billion base pairs (A/T's and G/C's), which are wrapped up pretty tight.
If you stretched out the DNA to full length, that's 3.4 x 10e-10 meters per base pair. Taking a randomish gene that's 10,000 base pairs long, that would work out to 3.4 micrometers of DNA, which this laser could work on. But if you think refolding maps is hard, imagine trying to repack 2 meters of DNA back into a 5 micrometer nucleus.
During metaphase, when the cell has all its chromosomes lined up and ready for splitting, the average size of a chromosome is 2 micrometers from end to end. Basically, your 10k base pair gene is now just 1.7 nanometers long. All of this winding and compacting means that it's blessedly hard to hit a single gene and only that gene within the DNA contained in a living cell with a tool this blunt.
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What I want to know is, can I mount one of these on a sharks head?
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