Stanford, CA (Scicasts) - Developing drugs to combat or cure human disease often involves a phase of testing with mice, so being able to peer clearly into a living mouse's innards has real value.
But with the fluorescent dyes currently used to image the interior of laboratory mice, the view becomes so murky several millimetres under the skin that researchers might have more success divining the future from the rodent's entrails than they do extracting usable data.
Researchers at Stanford University have now developed an improved imaging method using fluorescent carbon nanotubes that allows them to see centimetres deep into a mouse with far more clarity than conventional dyes provide, according to a report from the Institute. For a creature the size of a mouse, a few centimetres makes a great difference.
"We have already used similar carbon nanotubes to deliver drugs to treat cancer in laboratory testing in mice, but you would like to know where your delivery went, right?" said Hongjie Dai, a professor of chemistry. "With the fluorescent nanotubes, we can do drug delivery and imaging simultaneously – in real time – to evaluate the accuracy of a drug in hitting its target."
Researchers inject the single-walled carbon nanotubes into a mouse and can watch as the tubes are delivered to internal organs by the bloodstream.
The nanotubes fluoresce brightly in response to the light of a laser directed at the mouse, while a camera attuned to the nanotubes' near infrared wavelengths records the images.
By attaching the nanotubes to a medication, researchers can see how the drug is progressing through the mouse's body.
Dai is the one of the authors of a paper describing the research published online this month in Proceedings of the National Academy of Sciences.
The key to the nanotubes' usefulness is that they shine in a different portion of the near infrared spectrum than most dyes.
Biological tissues – whether mouse or human – naturally fluoresce at wavelengths below 900 nanometers, which is in the same range as the available biocompatible organic fluorescent dyes. That results in undesirable background fluorescence, which muddles the images when dyes are used. But the nanotubes used by Dai's group fluoresce at wavelengths between 1,000 and 1,400 nanometers. At those wavelengths there is barely any natural tissue fluorescence, so background "noise" is minimal.
The nanotubes usefulness is further boosted because tissue scatters less light in the longer wavelength region of the near-infrared, reducing image smearing as light moves or travels through the body, another advantage over fluorophores emitting below 900nm.
"The nanotubes fluoresce naturally, but they emit in a very oddball region," Dai said. "There are not many things – living or inert – that emit in this region, which is why it has not been explored very much for biological imaging."
By selecting single-walled carbon nanotubes (SWNTS) with different chiralities diameters and other properties, Dai and his team can fine-tune the wavelength at which the nanotubes fluoresce.
The nanotubes are imaged immediately upon injection into the bloodstream of mice.
Dai and graduate students Sarah Sherlock and Kevin Welsher, who are also coauthors of the PNAS paper, observed the fluorescent nanotubes passing through the lungs and kidneys within seconds after injection. The spleen and liver lit up a few seconds later.
The group also did some "post-production" work on digital video footage of the circulating nanotubes to further enhance the image quality using a process called "principal component analysis."
"In the raw imaging, the spleen, pancreas and kidney might appear as one generalized signal," Sherlock said. "But this process picks up the subtleties in signal variation and resolves what at first appears to be one signal into the distinct organs."
"You can really see things that are deep inside or blocked by other organs such as the pancreas," Dai said.
There are some other imaging methods that can produce deep tissue images, such as magnetic resonance imaging (MRI) and computer tomography (CT) scans. But fluorescence imaging is widely used in research and requires simpler machinery.
Dai said that the fluorescent nanotubes are not capable of reaching the depth of CT or MRI scans, but nanotubes are a step forward in broadening the potential uses of fluorescence as an imaging system beyond the surface and near-surface applications it has been restricted to up until now.
Since nanotube fluorescence was discovered about ten years ago, researchers have been trying to make the fluorescence brighter, Dai said. Still, he has been a little surprised at just how well they now work in animals.
"I did not imagine they could really be used in animals to get deep images like these," he said. "When you look at images like this, you get a sense that the body almost has some transparency to it."
But with the fluorescent dyes currently used to image the interior of laboratory mice, the view becomes so murky several millimetres under the skin that researchers might have more success divining the future from the rodent's entrails than they do extracting usable data.
Researchers at Stanford University have now developed an improved imaging method using fluorescent carbon nanotubes that allows them to see centimetres deep into a mouse with far more clarity than conventional dyes provide, according to a report from the Institute. For a creature the size of a mouse, a few centimetres makes a great difference.
 |
| An enhanced color image of fluorescence from single-walled carbon nanotubes (right) shows internal organs of a mouse next to a reference illustration (left). In the fluorescent image, on the left side of the mouse, the pancreas (thin green strip) is sandwiched between a kidney (yellow) and the spleen (pink). In the reference image, the kidneys are orange-brown, the spleen is pumpkin-colored and the pancreas is barely visible as a tiny red triangle between the other two organs. Image reproduced with permission from Proceedings of the National Academy of Sciences USA. |
"We have already used similar carbon nanotubes to deliver drugs to treat cancer in laboratory testing in mice, but you would like to know where your delivery went, right?" said Hongjie Dai, a professor of chemistry. "With the fluorescent nanotubes, we can do drug delivery and imaging simultaneously – in real time – to evaluate the accuracy of a drug in hitting its target."
Researchers inject the single-walled carbon nanotubes into a mouse and can watch as the tubes are delivered to internal organs by the bloodstream.
The nanotubes fluoresce brightly in response to the light of a laser directed at the mouse, while a camera attuned to the nanotubes' near infrared wavelengths records the images.
By attaching the nanotubes to a medication, researchers can see how the drug is progressing through the mouse's body.
Dai is the one of the authors of a paper describing the research published online this month in Proceedings of the National Academy of Sciences.
The key to the nanotubes' usefulness is that they shine in a different portion of the near infrared spectrum than most dyes.
Biological tissues – whether mouse or human – naturally fluoresce at wavelengths below 900 nanometers, which is in the same range as the available biocompatible organic fluorescent dyes. That results in undesirable background fluorescence, which muddles the images when dyes are used. But the nanotubes used by Dai's group fluoresce at wavelengths between 1,000 and 1,400 nanometers. At those wavelengths there is barely any natural tissue fluorescence, so background "noise" is minimal.
The nanotubes usefulness is further boosted because tissue scatters less light in the longer wavelength region of the near-infrared, reducing image smearing as light moves or travels through the body, another advantage over fluorophores emitting below 900nm.
"The nanotubes fluoresce naturally, but they emit in a very oddball region," Dai said. "There are not many things – living or inert – that emit in this region, which is why it has not been explored very much for biological imaging."
By selecting single-walled carbon nanotubes (SWNTS) with different chiralities diameters and other properties, Dai and his team can fine-tune the wavelength at which the nanotubes fluoresce.
The nanotubes are imaged immediately upon injection into the bloodstream of mice.
Dai and graduate students Sarah Sherlock and Kevin Welsher, who are also coauthors of the PNAS paper, observed the fluorescent nanotubes passing through the lungs and kidneys within seconds after injection. The spleen and liver lit up a few seconds later.
The group also did some "post-production" work on digital video footage of the circulating nanotubes to further enhance the image quality using a process called "principal component analysis."
"In the raw imaging, the spleen, pancreas and kidney might appear as one generalized signal," Sherlock said. "But this process picks up the subtleties in signal variation and resolves what at first appears to be one signal into the distinct organs."
"You can really see things that are deep inside or blocked by other organs such as the pancreas," Dai said.
There are some other imaging methods that can produce deep tissue images, such as magnetic resonance imaging (MRI) and computer tomography (CT) scans. But fluorescence imaging is widely used in research and requires simpler machinery.
Dai said that the fluorescent nanotubes are not capable of reaching the depth of CT or MRI scans, but nanotubes are a step forward in broadening the potential uses of fluorescence as an imaging system beyond the surface and near-surface applications it has been restricted to up until now.
Since nanotube fluorescence was discovered about ten years ago, researchers have been trying to make the fluorescence brighter, Dai said. Still, he has been a little surprised at just how well they now work in animals.
"I did not imagine they could really be used in animals to get deep images like these," he said. "When you look at images like this, you get a sense that the body almost has some transparency to it."
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