Visible light pulses knock out viruses in blood
Viruses lurking in biological samples could be killed off with an intense pulse of visible light, new research shows.
Scientists in the US say the technique seems to have significant advantages over alternative methods, including use of UV irradiation or microwaves, as it kills viruses more effectively and safely.
The technique destroys a virus with a pulse of light from a low-power laser. The pulse produces mechanical vibrations in the virus shell, or capsid, irreversibly damaging and disintegrating it, and so "deactivating" the virus for good. The technique might be used to kill HIV, as well as hepatitis C, say the researchers involved.
Traditional methods of destroying viruses, such as UV irradiation, can cause mutations, which eventually make the micro-organisms resistant. UV light can also damage the DNA of surrounding healthy cells.
Scientists have also tried using microwaves to kill viruses but this is even less promising since the water in and around a micro-organism strongly absorbs this frequency of light. Most of the energy from the microwave radiation is absorbed by the water and does not even reach the virus itself.
Human cells undamaged
Kong-Thon Tsen of Arizona State University, and colleagues at Johns Hopkins School of Medicine, and the Uniformed Services University of The Health Sciences, all in the US, found that visible light can overcome this problem.
The researchers applied pulses of purple-coloured light lasting just 100 femtoseconds (10-15 seconds) to viruses called M13 bacteriophages. It takes just a single pulse to destroy the viruses completely, say the researchers.
The "power density" of the laser is just 5 microjoules per square centimetre, which is low enough to leave surrounding human cells and tissue undamaged, but high enough to produce large-amplitude vibrations in a virus's capsid. It is also too low to cause genetic mutations, meaning the virus will not build up resistant to the treatment over time.
Disinfecting blood
Tsen told New Scientist that the technique could be used to disinfect blood or other biological samples in hospitals.
"In addition, we believe that the method may be especially important in designing novel treatments for blood-borne viral diseases," he said. "For example blood dialysis allows us to irradiate a patient's blood outside the body and potentially cleanse it of infectious virus particles before reintroducing it into the patient. In this way, we could reduce mortality associated with diseases like hepatitis C and AIDS."
The team now plans to test the efficacy of its technique in killing a wide range of deadly viruses, including HIV and hepatitis C. "We also plan to conduct further tests on the effects of the low-power visible laser on mammalian cells to determine any potential side effects and confirm that it selectively kills viruses," said Tsen.
Journal reference: Journal of Physics: Condensed Matter (19 322102)
Viruses Killed by Light Pulses
The wavelength (which is related to frequency and energy) of the light determines the perceived color. The ranges of these different colors are listed in the table below. Some sources vary these ranges pretty drastically, and the boundaries of them are somewhat approximate as they blend into each other. The edges of the visible light spectrum blend into the ultraviolet and infrared levels of radiation.
Most light that we interact with is in the form of white light, which contains many or all of these wavelength ranges within them.
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The Visible Light Spectrum
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This is what causes a rainbow, with airborn water particles acting as the refractive medium. The order of wavelengths (as shown to the right) is in order of wavelength, which can be remembered by the mneumonic "Roy G. Biv" for Red, Orange, Yellow, Green, Blue, Indigo (the blue/violet border), and Violet. You'll notice that in the image and table Cyan is also appears fairly distinctly, between green & blue.
By using special sources, refractors, and filters, you can get a narrow band of about 10 nm in wavelength that is considered monochromatic light. Lasers are special because they are the most consistent source of narrowly monochromatic light that we can achieve.
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The Visible Light Spectrum |
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| Color | Wavelength (nm) | |
| Red | 625 - 740 | |
| Orange | 590 - 625 | |
| Yellow | 565 - 590 | |
| Green | 520 - 565 | |
| Cyan | 500 - 520 | |
| Blue | 435 - 500 | |
| Violet | 380 - 435 | |
More on Electromagnetic Radiation
Electromagnetic SpectrumWhat is a Photon?
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Inactivation of viruses with a very low power visible femtosecond laser
2007 J. Phys.: Condens. Matter 19 322102 (9pp) doi:10.1088/0953-8984/19/32/322102
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1 Department of Physics, Arizona State University, Tempe, AZ 85287, USA
2 Department of Pathology, Johns Hopkins School of Medicine, Baltimore, MD 21231, USA
3 Department of Oncology, Johns Hopkins School of Medicine, Baltimore, MD 21231, USA
4 Department of Obstetrics and Gynecology, Johns Hopkins School of Medicine, Baltimore, MD 21231, USA
5 Department of Molecular Microbiology and Immunology, Johns Hopkins School of Medicine, Baltimore, MD 21231, USA
6 Scientific Research Department, Armed Forces Radiobiology Research Institute, Uniformed Services University of The Health Sciences, Bethesda, MD 20889-5603, USA
7 Department of Medicine, Uniformed Services University of The Health Sciences, Bethesda, MD 20889-5603, USA
8 Department of Pharmacology, Uniformed Services University of The Health Sciences, Bethesda, MD 20889-5603, USA
Abstract. We demonstrate for the first time that, by using a visible femtosecond laser, it is effective to inactivate viruses such as bacteriophage M13 through impulsive stimulated Raman scattering. By using a very low power visible femtosecond laser having a wavelength of 425 nm and a pulse width of 100 fs, we show that M13 phages were inactivated when the laser power density was greater than or equal to 50 MW cm-2. The inactivation of M13 phages was determined by plaque counts and depended on the pulse width as well as power density of the excitation laser.
Print publication: Issue 32 (15 August 2007)
Received 22 May 2007, in final form 21 June 2007
Published 13 July 2007
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