Showing posts with label gold nanoparticles. Show all posts
Showing posts with label gold nanoparticles. Show all posts

Tuesday, March 16, 2010

Double action cancer therapy | NNVC.OB Message Board Posts

From IV

[SNIP]

[While not directly related to NNVC it is of important interest in that it uses a polymer nanoparticle - PLGA - to carry the ingredients to the source - in this case a cancer whereas NNVC targets viruses using a polymer nanoparticle.]

16 March 2010

Scientists in Taiwan have demonstrated a more effective approach to treat cancer using multifunctional nanoparticle. The particles simultaneously attack tumours with chemotherapy and photothermal therapy as well as allowing their position and size to be ascertained.

While metal nanoparticles have been shown to kill tumour cells when irradiated with light from a laser, the limited size of the laser beam spot can mean that some cancerous cells are missed. Combining chemotherapy with phototherapy could be a promising approach to overcome this disadvantage. Now, Chen-Sheng Yeh at the National Cheng Kung University, Tainan, and colleagues have made nanoparticles that deliver the anticancer drug Taxol and also contain gold for phototherapy.

Thursday, February 18, 2010

Using Gold Nanoparticles to Hit Cancer Where It Hurts

ScienceDaily (Feb. 18, 2010) — Taking gold nanoparticles to the cancer cell and hitting them with a laser has been shown to be a promising tool in fighting cancer, but what about cancers that occur in places where a laser light can't reach? Scientists at the Georgia Institute of Technology have shown that by directing gold nanoparticles into the nuclei of cancer cells, they can not only prevent them from multiplying, but can kill them where they lurk.

Abstract
Abstract Image

By properly conjugating gold nanoparticles with specific peptides, we were successful in selectively transporting them to the nuclei of cancer cells. Confocal microscopy images of DNA double-strand breaks showed that localization of gold nanoparticles at the nucleus of a cancer cell damages the DNA. Gold nanoparticle dark-field imaging of live cells in real time revealed that the nuclear targeting of gold nanoparticles specifically induces cytokinesis arrest in cancer cells, where binucleate cell formation occurs after mitosis takes place. Flow cytometry results indicated that the failure to complete cell division led to programmed cell death (apoptosis) in cancer cells. These results show that gold nanoparticles localized at the nuclei of cancer cells have important implications in understanding the interaction between nanomaterials and living systems.

The research appeared as a communication in the February 10 edition of the Journal of the American Chemical Society.

"We've developed a system that can kill cancer cells by shining light on gold nanoparticles, but what if the cancer is in a place where we can't shine light on it? To fix that problem, we've decorated the gold with a chemical that brings it inside the nucleus of the cancer cell and stops it from dividing," said Mostafa El-Sayed, Regents professor and director of the Laser Dynamics Laboratory at Georgia Tech.

Once the cell stops dividing, apoptosis sets in and kills the cell.

"In cancer, the nucleus divides much faster than that of a normal cell, so if we can stop it from dividing, we can stop the cancer," said El-Sayed.

The team tested their hypothesis on cells harvested from cancer of the ear, nose and throat. They decorated the cells with an argininge-glycine-aspartic acide petipde (RGD) to bring the gold nano-particles into the cytoplasm of a cancer cell but not the healthy cells and a nuclear localization signal peptide (NLS) to bring it into the nucleus.

In previous work they showed that just bringing the gold into the cytoplasm does nothing. In this current study, they found that implanting the gold into the nucleus effectively kills the cell.

"The cell starts dividing and then it collapses," said El-Sayed. "Once you have a cell with two nuclei, it dies." The gold works by interfering with the cells' DNA, he added. How that works exactly is the subject of a follow-up study.

"Previously, we've shown that we can bring gold nanoparticles into cancer cells and by shining a light on them, can kill the cells. Now we've shown that if we direct those gold nanoparticles into the nucleus, we can kill the cancer cells that are in spots we can't hit with the light," said El-Sayed.

Next the team will test how the treatment works in vivo.

Story Source:Adapted from materials provided by Georgia Institute of Technology.Original article written by David Terraso.

Journal Reference:

  1. Bin Kang, Megan A. Mackey and Mostafa A. El-Sayed. Nuclear Targeting of Gold Nanoparticles in Cancer Cells Induces DNA Damage, Causing Cytokinesis Arrest and Apoptosis. Journal of the American Chemical Society, 2010; 132 (5): 1517 DOI: 10.1021/ja9102698

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Monday, August 17, 2009

Nanoparticles could treat cardiovascular disease by mimicking “good cholesterol”

Northwestern University

C. Shad Thaxton, 33

To combat cardiovascular disease, Shad Thaxton, an assistant professor of urology, designed a nanoparticle that may be able to carry cholesterol right out of the body.

Several drugs treat cardiovascular disease by lowering levels of the lipoprotein complex LDL, commonly called "bad cholesterol" because it deposits the cholesterol in blood-vessel walls. But no existing therapies can directly increase HDL, or "good cholesterol," which carries the sticky molecule through the bloodstream and to the liver for excretion. Thaxton's nanoparticles mimic HDL. At their heart are gold spheres five nanometers in diameter; these are coated with fat and protein molecules that enable them to bind tightly to cholesterol. The work is in its early stages, but ­Thaxton envisions synthetic-HDL nanoparticles that will transport cholesterol from blood-vessel plaques to the liver to prevent and treat cardiovascular disease. If proved safe and effective, he says, synthetic HDL could be used to prevent heart attacks and strokes within 10 years. --Katherine Bourzac


Good as gold: The bloodstream carries synthetic HDL to arterial plaques. Lipids and proteins on the gold particle's surface help it interact with cells in the plaque to extract cholesterol; the particle with the cholesterol is then excreted.
Credit: Bryan Christie Design

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Tuesday, March 3, 2009

Preying On a Tumor's Weakness With Nanotechnology to Fight Cancer

Winner of this year's $30,000 Lemelson-MIT Student Prize uses gold nanoparticles to kill malignancies but spare healthy tissue

By Larry Greenemeier

cancer, nanotechnology

GEOFFREY VON MALTZAHN: The 28-year-old Ph.D. candidate has won this year's $30,000 Lemelson-MIT Student Prize for his work developing ways to use nanotechnology to fight cancer.
COURTESY OF HARVARD-MIT DIVISION OF HEALTH SCIENCES AND TECHNOLOGY

The Harvard-MIT Division of Health Sciences and Technology (HST) today named Geoffrey von Maltzahn this year's recipient of the $30,000 Lemelson-MIT Student Prize for developing a technique that utilizes nano-sized gold particles to target malignant tumors and kill cancer cells while leaving healthy tissue unscathed. Established in 1994, the award is given out annually to an MIT senior or graduate student who has contributed significantly to the fields of science or technology.

The approach capitalizes on "tumors behaving like tumors," says von Maltzahn, a 28-year-old Ph.D. candidate, and so, triggering the growth of as many new blood vessels as quickly as possible to nourish and help them thrive. But instead of feeding these tumors, von Maltzahn relies on these ultra-porous nascent blood vessels to transport rod-shaped gold nanoparticles injected into cancer patients to the tumor, where they latch onto malignant tissue.

Although other researchers have tested the use of nanoparticles to fight cancer (read about another MIT/Harvard effort here), Von Maltzahn has developed two ways to attack tumors once the nanoparticles have set up shop there. The first is to shine a near-infrared laser on the patient's skin above the malignancies; the light heats the gold to high enough temps to interrupt and destroy cancer cells with minimal if any damage to surrounding healthy cells. In pre-clinical mouse trials a single nanoparticle injection (which includes trillions of nanoparticles) eradicated 100 percent of tumors when combined with near-infrared light. The problem with current radiation therapy is that in most cases it is not confined to malignant growths and healthy tissue gets caught in the crossfire, according to von Maltzahn.

His other award-winning technique involves two injections: the first batch are sent out as scouts to identify and attach to tumors, where they serve as markers for a second battalion of nanoparticles covered with cancer-fighting agents that home in on and destroy the tumors but ignore healthy tissue. In mouse trials, von Maltzahn and his colleagues found that this "scout-assassin" system successfully delivered doses of medicine in mice that were more than 40-times more potent and much more successful at killing tumors than were medicine-coated particles injected sans the ability to communicate with nanoparticle advance teams. The major benefit of von Maltzahn's methods is that the medication could be injected anywhere in the body but would only latch onto the cancerous tissue. "If we were injecting this directly into the tumor, it wouldn't be a transformative technology," he says. "It's essential to be able to inject it intravenously anywhere in the body and have it …. home in on the tumor." Once the medicine has been delivered, the nanoparticles would be stripped bare and could safely pass out of the body after being filtered from the blood by the spleen or liver, von Maltzahn says, noting that gold has a very low toxicity profile.

According Catherine Murphy, a chemistry professor at the University of South Carolina in Columbia, the shape of a metal determines how much light it absorbs. "If you want to shine near-infrared light, which is really good for tissue penetration, and burn something up," she says, "a rod shape works really well." Murphy developed the process for transforming spherical bits of gold into the nanorods that von Maltzahn used in his research.

Von Maltzahn, who has worked with his advisor Sangeeta Bhatia, a Harvard-MIT HST electrical engineering and computer science professor, on this research for the past five years, is co-founder of a pair of companies that he hopes will help commercialize his technique: In July 2007, he helped form Salt Lake City, Utah, -based Nanopartz Inc., a worldwide supplier of gold nanoparticles, and in September 2008, he helped create Boston-based Resonance Therapeutics, which will further develop his cancer-fighting techniques. Eugene Zubarev, an assistant chemistry professor at Rice University in Houston, developed the method for mass producing nanoparticles that Nanopartz relies on to make the nanoparticles it sells.

Von Maltzahn two years ago developed another nanotech-based approach to stopping cancer that relied on polymer-coated iron oxide nanoparticles held together by DNA tethers that together help create a visual image of a tumor through magnetic resonance imaging (MRI), as Scientific American.com reported in November, 2007. To test the particles, he and his team implanted mice with a tumor-like gel saturated with nanoparticles and placed those mice into the wells of cup-shaped electrical coils, which activated the nanoparticles via magnetic pulses.

Von Maltzahn says he's currently conducting clinical trials of his near-infrared laser technology (to ablate cancerous tumors), but it is still years away from becoming a routine treatment. The scout-assassin model is even farther from becoming a cancer-fighting staple, says Maltzahn, noting that it could take him and his colleagues another two decades to make it safe and effective enough to use in humans.

Von Maltzahn plans to keep close tabs on his companies but to continue to pursue an academic career as a professor of biomedical or chemical engineering. Neither the business nor the academic aspects of research can be overlooked if medicine is to make its way from the lab to the patient, he says. "One of the things that appeals to me," von Maltzahn says, "is developing therapeutics such as these in a way that they can be commercialized."

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