Archive for the ‘NanoTechnology’ Category

Ensysce says carbon nanotubes delivered cancer drug

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Posted 29 Feb 2012 — by James Street
Category NanoTechnology, nanotubes, RNAi
By mhollmer
Created 02/14/2012 – 12:07

Ensysce Biosciences says early in vivo experiments using single-walled carbon nanotubes to deliver siRNA drugs to cancer tumors have been so promising, the company will proceed to human clinical trials within the next year or so.

The Houston startup is touting data published recently in the open-access online journal Materials, showing the single-walled, fullerene carbon nanotube tech protects the siRNA drug while carrying it through the blood. Once the treatment reached the tumor target, the company claims that it successfully penetrated the tumor and slammed into the target protein, releasing a drug payload that properly displayed anti-tumor activity. What’s more, the delivery system also appeared to generate very little toxicity to other cells.

Based on that data, Ensysce says it will launch human trials within 12 to 18 months, tweaking its drug delivery formulation in the interim, company CEO Lynn Kirkpatrick said in a statement. To get there, Ensysce will be armed, in part, with up to $1.5 million in funding from Texas’ Emerging Technology Fund and ongoing collaborations with researchers at M.D. Anderson Cancer Center and Rice University.

We’ll see. RNAi drugs hold enormous promise in their potential to turn off bad genes that cause disease, but scientists have struggled to find a competent way to deliver the drugs so they reach their target and do their job. Human trials will be interesting to follow because many of the delivery advances so far have taken place in the preclinical stage. One exception: Alnylam ($ALNY [1]) and Tekmira ($TKMR [2]), which have jointly pursued lipid nanoparticles as a tool to deliver RNAi drugs and produced some promising results in early human trials. The two have also fought bitterly over patent and license issues, highlighting what’s at stake with finding a successful RNAi delivery mechanism.

Medtronic ($MDT [3]) also has made some progress, working again with Alnylam. But rather than use nanotech, they’ve generated encouraging results in preclinical testing using a small implantable infusion system and convection-enhanced delivery to break the blood-brain barrier, and deliver an RNAi-based Huntington’s disease treatment to the brain.

- here’s the release [4]
- access the published study [5]

Nanotech Fuels A Cancer Research Gold Rush

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Posted 25 Feb 2012 — by James Street
Category NanoTechnology, Physics and Engineering, polymers

by Gwyneth K. Shaw | Feb 23, 2012 11:51 am

(3) Comments | Post a Comment | E-mail the Author

Posted to: Nanotech, Science/ Medical

 

Gwyneth K. Shaw PhotoGwyneth K. Shaw Photo

Salzman in his Yale lab.

W. Mark Saltzmanhas been trying to cure brain tumors for decades. Time after time, he hit a common roadblock: A delivery device that works is too toxic, but a good treatment doesn’t work if it’s not in the right place.

It’s a kind of Holy Grail for the people who have made fighting cancer their life’s work—getting potentially life-saving treatment to the part of the brain where it’s most likely to save a patient.

Now, Saltzman (pictured), a Yale professor, and his colleagues may have found a way to hit the sweet spot, using an ultra-tiny tool as their chief weapon: a new nanoparticle that could have benefits for treating a variety of diseases.

Potentially, Saltzman said, therapeutic nanoparticles—a nanometer is a billionth of an inch—could be injected directly into the brain through catheters, then steered to just the right place using varying pressure. That means hurdling the barrier between the bloodstream and the brain, an impediment to many treatments for brain cancer. Once delivered, the drug would continue to release the drug to do its cancer-killing work.

“We’re optimistic that this is going to be a much better approach,” said Saltzman, the Goizueta Foundation professor of biomedical engineering and chemical and environmental engineering at Yale’s School of Engineering & Applied Science. He’s also the chair of the biomedical engineering department

Saltzman and his colleagues published a paper outlining the new nanoparticle formula late last year; he said recently that additional work looking at its effectiveness on brain cancer is ongoing.

The Gold Rush

Nano-enabled applications are exploding in the medical world, perhaps nowhere more than in the fight against cancer.

It’s not just ultra-effective, targeted treatments, but a whole range of innovations that could usher in the long-promised era of dominance over a host of debilitating, or lethal, diseases. Super fast diagnostic tests, now in development, could tell you what strain of cancer you have, or tell the difference between a benign and malignant tumor, without surgery or an invasive test.

Researchers like Saltzman see nanotechnology as a way to give patients a better prognosis while minimizing the well-known toxic side effects associated with more established chemotherapy and radiation treatments.

Potential breakthroughs like this one were inconceivable 30 years ago, before scientists began unlocking the potential of therapies using individual genes to concoct cures—and started looking to the promise of nanotechnology for better ways to zap cancer cells.

The list of treatments in development is long. Researchers are heating nano-gold shells to target, and torch, tumors. They’re using super-small iron oxide and titanium dioxide to override ovarian cancer cells’ resistance to chemotherapy.

Tiny silica particles that light up, known as “Cornell dots” for the university where they were developed, are shaping up as crack cancer detectors—and have moved into the clinical-trial phase.

Only a few nano-type drugs are on the market; a larger set are in the testing stage. But inside laboratories at universities and pharmaceutical companies, the science of the very small is a big deal when it comes to stopping cancer.

As with all efforts that tap into nanotechnology, however, there are potential drawbacks. The interesting properties of these super-small materials sometimes raise other questions. Among them are whether some materials, such as nano-sized gold, can be eliminated from the body without doing any damage.

“My understanding is that the biggest hurdle is actually the clearance of these particles,” said Ming Su, a professor at the University of Central Florida, who’s associated with the school’s NanoScience Technology Center. Su has been working on using nanomaterials for cancer detection, as well as on the toxicity of a number of ultra-tiny substances.

“It’s really hard to estimate the long-term effect of particles in your body,” he said. “People have only been doing this for a few years.”

FDA & Nano

Nanomaterials are increasingly common in both research laboratories and everyday products, turning up in everything from sunscreens to stain-repellent pants. In many of these workaday applications, nano-enabled products face little, if any, scrutiny from the federal government, although there are signs that may be changing.

In medical treatments, however, nanotechnology is as carefully controlled as any drug. The U.S. Food and Drug Administration has a lengthy process just for allowing new therapies to be tested on people, let alone approved for widespread use.

The FDA has said it considers any drug or treatment that uses nanotechnology to be a new drug, which subjects a therapy to the tightest controls. Regardless of the ongoing argument over whether the FDA’s process is the most efficient way to bring new drugs to the market, there’s no question that nano-enabled therapies will be vetted before they hit your doctor’s prescription pad—something that can’t be said about a number of other products that use nanomaterials.

Given that anticipated scrutiny, toxic consequences are on the mind of nanomedical researchers. Part of that is built into their everyday mindset; after all, drugs and treatments that hurt people generally aren’t approved, and if they are, subsequent problems are literally fatal.

The possibility of side effects or long-term fallout has particular resonance for cancer research, because the existing treatments take such a toll on patients. Researchers see themselves as having a dual role: To find treatments that are not just better, but less debilitating.

Gene Therapy: Promise, With A Price

Another project that Saltzman and his colleagues are working on aims squarely at that goal. It involves making gene therapy—a hot topic in biomedicine, with potential to help curtail a number of diseases—easier to use. Gene therapy revolves around DNA, using the very strands of life to improve treatments, often by correcting the mutations that make people sick, or by killing a cell that’s causing problems like cancer.

“There are lots of ways to try to deliver genes to cells. Almost all of them are toxic,” Saltzman said. “The challenge is to deliver with the least amount of toxicity.”

That has been a key challenge of gene therapy: Making polymers to deliver the DNA without making it dangerous. That means resolving imbalances in electrical charge; DNA carries a negative charge, while most polymers are positively charged. Too much positive charge, and the treatment is poisonous.

Salzman and his colleagues tried to design polymers that strike a better balance, making their polymer more water-repellent and creating a more balanced—and less toxic—substance. A better delivery, he said, may open doors treating a variety of diseases, from cancer to cystic fibrosis.

 

Yale University ImageYale University Image

The team uses polyester-based polymers, which dissolve fairly easily.

“Because of water, they slowly degrade, which the body can clear,” Salzman said. “We intentionally design our polymers so that they disappear.”

And, in the process, solves the toxicity problems on both ends.

Special Delivery

At this point, Saltzman said, the race to build a better delivery system is on par with the effort to find better treatments.

“I think it’s both,” he said. “Certainly, our focus has been if you can’t get the agent to the cells you can’t do anything. At the same time, we’re trying to identify the best kind of agents.”

That’s where the interdisciplinary nature of the nanomedical field is most useful, at Yale and around the world. Uniting medical researchers and engineers allows cross-pollination of ideas, so that a novel drug and a new way to get it into the body can be developed in concert.

Meanwhile, nanotechnology researchers are also chasing better diagnostic tools and medical devices that leverage tiny materials for big gains.

 

NanoDiscovery Inc. PhotoNanoDiscovery Inc. Photo

Qun Huo,pictured, a professor with UCF’s nano center, is zeroing in on gold nanoparticles to spot cancer cells and do other analysis. The technique she’s developing basically monitors the changes in size, or an increase in clustering, of the nanoparticles as they’re exposed to the cells being tested.

Nanomedicine is still in its infancy, she said, but has great potential to transform the diagnostic field.

Instead of waiting days or weeks for a test result, nano-enabled sensors or diagnostic tools might give you an answer in minutes. Some use magnetic nanoparticles to improve existing imaging tools, perhaps finding smaller tumors much sooner. Others use sensors to detect cancer, like a nano-based “nose” that can detect lung cancer in a patients breath.

These types of developments are not only faster, but they could also enable patients to skip biopsies or surgeries just to find out what’s going on inside their bodies.

“It allows them to see what they could not see before and do what they could not do before,” Huo said. “When it comes to cancer diagnosis, it may not be me, but I do actually believe with the technology we have that we can really bring breakthroughs.”

Development: Risk Vs. Reward

Of course, all the potential in the world won’t help bring these treatments, tests and devices to the marketplace. The crucial first step in developing a new treatment is money.

Many of these new ideas are coming from pharmaceutical companies. Others are germinating within the academic community, sometimes with federal funding, sometimes with money from drug companies. At the university level, however, there’s tension between teaching, research and the long and sometimes arduous path to commercializing a laboratory discovery.

The federal government is funding lots of research. For example, the National Cancer Institute, part of the National Institutes of Health, has its own Alliance for Nanotechnology in Cancer, which aims to push innovation as well as keep an eye on questions about impacts on health and the environment.

The NCI has established Centers of Cancer Nanotechnology Excellence to foster research, and also funds the Nanotechnology Characterization Laboratory, which supports researchers with critical work on safety.

Most big research universities, including Yale, have divisions that handle finding investors and selling off patents and ideas. Huo took another route, starting her own spinoff company, Nano Discovery Inc., and has hired staff to deal with the tasks she doesn’t have time for.

But while academics are rewarded for home-run research, actually bringing a therapy to market doesn’t have much currency inside a university setting.

“If the university wants faculty to succeed in commerce, then you do have to concede that faculty have to spend time doing this,” Huo said.

The Evolution Of A Cancer Fighter

Saltzman is familiar with the difficulties of navigating the science, the testing and the successes and failures of new treatments. He started working in Gliadel, a chemo-coated wafer that’s implanted directly into the brain of a cancer patient, in 1988, while at Johns Hopkins University. FDA approval came in 1996—a relatively fast track to the market.

But Gliadel, while helpful to many, wasn’t the magic bullet. More than 20 years later, Saltzman is still trying to find the panacea. His optimism is stronger than ever, he said, because of the way scientists are able to manipulate cells, genes and particles—pushing the envelope in new ways almost every day.

“I’m very confident that once we work out the delivery system … I think we’ll quickly get to things that are better,” he said. “These kinds of tools have really changed what we can think about doing.”

A New Way to Treat Cancer

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Posted 09 Feb 2012 — by James Street
Category Drug Delivery, NanoTechnology, nanotechnology, Physics and Engineering
By Bill Weir, C. Michael Kim & David Miller | This Could Be Big – Thu, Nov 17, 2011

What if we could find out if a cancer drug is working or not almost instantly? Cancer patients could avoid the frustration of suffering through painful side effects and lost time only to learn that the treatment wasn’t effective.

Professor Michael Cima and his team at the Koch Institute for Integrative Cancer Research at MIT may have come up with the answer. They’re building on what is already the best practice for detecting cancer, which is the biopsy. Unfortunately, the information that is retrieved from a biopsy only tells the doctor what’s happening with the tumor in the very moment that it’s taken, like a photograph, and tumors are constantly changing and diversifying, especially during treatment.

In order to monitor the progress of a tumor doctors need a better tool – one that can monitor a tumor continuously. If a biopsy is equal to a photograph, Professor Cima is working on building a video camera.

His video camera comes in the form of a tiny implant that is so small it fits inside a biopsy needle. It is implanted in the tumor during a routine biopsy, which means it requires no extra procedure or treatment. Even though the implant is small enough to fit into a needle, there are thousands of tiny iron nanoparticles trapped inside like leaves in a tea bag. Its porous outer layer allows fluids to move in and out of the implant, and when cancer related molecules flow in, the iron nanoparticles cluster around it. The resulting clumps can be detected with a non invasive magnetic scan allowing doctors to monitor the tumor over time, letting them know the progress of a patient’s treatment and providing doctors with a real-time snapshot of the tumor itself.

Coating Improves Cancer Detection Efficiency of Iron Oxide Nanoparticle-Based Contrast Agent

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Posted 27 Dec 2011 — by James Street
Category Imaging, MRI, NanoTechnology
Published on December 26, 2011 at 6:31 AM

By Cameron Chai

A research team at the University of Pennsylvania has developed a safer, efficient and economical method to coat contrast agents made of nanoparticles comprising iron oxide in order to make them interfere only with the tumor’s acidic environment, paving the way for eliminating the potential health risks and limitations of heavy or radiation metals that are commonly used as contrast agents in cancer imaging technologies.

To improve the image quality of magnetic resonance imaging (MRI), physicians are nowadays using the iron oxide nanoparticles as contrast agents, which are coated with dextran whose outer layer avoids the absorption or bonding of these nanoparticles by the body, thus avoiding potential risks to the patients. This inert coating makes the nanoparticles to be removed safely subsequent to the completion of the imaging. However, this technique also prevents the target-specific treatment of diseased tissues by these nanoparticles. Receptor-based methods also have their own limitations.

The Penn research team used the behavior of tumor metabolism dubbed as the Warburg effect to overcome these limitations. The team took advantage of the pH conditions of the cancer tissues that are lower than that of healthy tissues. It used a sugar-based polymer known as glycol chitosan that interacts with acids as the coating material for the transfer of nanocarriers, which stays neutral when they are close to the healthy tissues but getting ionized in the acidic conditions of the tumors. The charge change that happens in the region of the tumor sites attracts and retains the nanocarriers at these sites.

The acidity of a tumor site varies with the intensity of the malignancy of a tumor. Thus, glycol chitosan coating can effectively detect the intensity of the malignancy of a tumor, paving the way for more treatment options of cancer. According to Andrew Tsourkas, one of the researchers, glycol chitosan finds use in applications other than imaging, as it can be used to coat any kind of nanoparticle. It can be used to supply drugs to the cancer sites, he added.

Due to their capability to precisely identify malignancy sites, glycol-chitosan-coated iron oxide nanoparticles can immediately be used in place of current contrast agents in certain breast cancer MRI scans. The research team believes that the glycol-chitosan-coated nanoparticles are able to enhance the diagnostic screening’s specificity within the next 7-10 years.

Source: http://www.upenn.edu

Inhaled nanoparticles deliver potent anticancer cocktail to lung tumors and block resistance

(Nanowerk News) An ideal treatment for lung cancer would be one that could be inhaled deep into lung tissue where it would deliver tumor-killing agents that would then largely stay in the lungs, avoiding the toxicities that limit the effectiveness of today’s lung cancer therapies. Now, researchers at Rutgers, The State University of New Jersey, have developed an inhalable porous silica nanoparticle that not only delivers potent anticancer drugs only to non-small cell lung tumors, but also delivers agents that prevent the development of drug resistance.
Reporting its work in the Journal of Drug Targeting (“Innovative strategy for treatment of lung cancer: targeted nanotechnology-based inhalation co-delivery of anticancer drugs and siRNA”), a research team headed by Tamara Minko showed that a targeted silica nanoparticle was effective at getting a cocktail of drugs into lung tumors in animals and triggering cancer cell death. The inhaled nanoparticles largely remaining in the lungs, with a small amount accumulating in the liver and kidneys, the organs that are typically involved in excreting nanoparticles and other administered compounds.
Minko and her colleagues began this project by first developing mesoporous silica nanoparticles that could effectively deliver a mixture of traditional anticancer drugs and siRNA molecules specifically to lung cancer cells. The investigators chose mesoporous silica nanoparticles for two reasons – their pore size makes them ideal for delivering large loads of different types of molecules and they are biocompatible.
The researchers chose the anticancer agents doxorubicin and cisplatin, used today to treat lung cancer, as the primary tumor killing agents. They then designed two siRNA molecules to stop the development of drug resistance that develops during conventional anticancer treatment. One siRNA molecule would block tumor cell production of a drug pump that they use to expel anticancer agents, while the other siRNA would limit production of a protein that tumor cells use to prevent the programmed cell death, or apoptosis, that doxorubicin and cisplatin normally triggers.
To target the nanoparticles to lung tumors, the researchers added a molecule known as LHRH to the surface of the nanoparticle. LHRH binds to a receptor that is produced at high levels by many types of cancers, including lung cancers.
Tests with non-small cell lung tumor cells demonstrated that this complex formulation was highly effective at killing the cells and preventing the expression of the two types of drug resistance responses normally seen. Tests in animals showed that nearly three quarters of the inhaled nanoparticles remained in the lungs and were taken up by tumor cells. In this study, the researchers did not measure efficacy in killing tumors in the animals.

Source: National Cancer Institute

High tech detection of breast cancer using nanoprobes and SQUID

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Posted 28 Oct 2011 — by James Street
Category Breast Cancer, Diagnostic, HER2/neu, NanoTechnology, Physics and Engineering

Contact: Dr Hilary Glover
hilary.glover@biomedcentral.com
44-020-319-22370
BioMed Central

Mammography saves lives by detecting very small tumors. However, it fails to find 10-25% of tumors and is unable to distinguish between benign and malignant disease. New research published in BioMed Central’s open access journal Breast Cancer Research provides a new and potentially more sensitive method using tumor–targeted magnetic nanoprobes and superconducting quantum interference device (SQUID) sensors.

A team of researchers from University of New Mexico School of Medicine and Cancer Research and Treatment Center, Senior Scientific, LLC, and the Center for Integrated Nanotechnologies facility at Sandia National Laboratories created nanoprobes by attaching iron-oxide magnetic particles to antibodies against HER-2, a protein overexpressed in 30% of breast cancer cases. Using these tiny protein-iron particles the team was able to distinguish between cells with HER-2 and those without, and were able to find HER-2 cancer cells in biopsies from mice. In their final test the team used a synthetic breast to determine the potential sensitivity of their system.

Dr Helen Hathaway explained, “We were able to accurately pinpoint 1 million cells at a depth of 4.5 cm. This is about 1000x fewer cells than the size at which a tumor can be felt in the breast and 100x more sensitive than mammographic x-ray imaging. While we do not expect the same level of nanoparticle uptake in the clinic, our system has an advantage in that dense breast tissue, which can mask traditional mammography results, is transparent to the low-frequency magnetic fields detected by the SQUID sensors.”

Future refining of the system could allow not only tumor to be found but to be classified according to protein expression (rather than waiting for biopsy results). This in turn could be used to predict disease progression and refine treatment plans and so improve patient survival.

Attacking cancer cells with nanoparticles

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Posted 26 Oct 2011 — by James Street
Category Drug Delivery, Drugs, gold nanoparticles, gold nanorod antennas, NanoTechnology, nanotechnology

October 25, 2011 By Judy Holmes

(PhysOrg.com) — About every three days, Colleen Alexander, a chemistry graduate student, feeds cells that cause a deadly type of brain cancer. It’s a ritual that involves assessing the health of the cells under a microscope, washing away dead cells with a special solution and instilling clean medium that will nurture the living cells and generate new ones. At some point, these cells will be subjected to chemotherapy agents attached to nanoparticles made of gold.

It’s a revolutionary idea for a molecular system developed by two chemists in Syracuse University’s College of Arts and Sciences who have combined their very different areas of expertise. Their work was recently featured in the Journal of the National Cancer Institute (NCI) in a news article that highlights the NCI’s increasing focus on using nanotechnology to diagnose and treat cancer. It’s an area of research in which the NCI is investing $30 million per year, nationally, over the next five years.

The idea for attaching chemotherapy to nanoparticles made of gold developed from a series of hallway conversations and “what ifs” between James Dabrowiak and Mathew Maye. Both are members of the college’s Department of Chemistry and of the Syracuse Biomaterials Institute, which provides highly specialized laboratory facilities for their work.

Dabrowiak has devoted the better part of his career to cancer drug research and is Alexander’s Ph.D. faculty adviser. Maye’s expertise lies in nanotechnology. He uses biomimetic methods to assemble nanomaterials. Biomimetic means using DNA to make nanoparticles mimic nature.

“You can put an enormous amount of small drug molecules onto a single nanoparticle,” Dabrowiak says. “That results in very high concentrations of the drug getting into cancer , making the drug a more effective killing agent with fewer side effects.”

The trick is in finding the most effective way to build the drug-laden nanoparticles. That’s where Maye’s expertise comes in. His lab has developed a way to attach DNA to gold nanoparticles. The drug molecules stick to the DNA-coated nanoparticles, coded to attract specific types of drugs. Once the drug is attached, the surface of the nanoparticle is coated with inert materials to prevent the immune system from attacking the nanoparticle as a foreign invader before it makes its way to the tumor.

“Ours is a completely different way of designing a molecular drug delivery system,” Maye says. “The method we use to attach drug molecules to the DNA is a unique part of the system. It’s an area of research that no one is exploring.”

In addition to delivering a higher concentration of drugs to individual , the scientists say nanoparticles could potentially be more efficient at getting inside tumors than current drug delivery systems. Because of their rapid growth, tumors are less densely packed and more porous than healthy tissues. Drug molecules are small and tend to leak out of the pores, reducing the drug’s effect on the tumor. In contrast, the larger nanoparticles tend to get stuck inside the pores, allowing the drug more time to penetrate the tumor.

“The nanoparticles are more easily caught by tumors than by normal tissue,” Dabrowiak says. “More drug gets inside tumors and less gets inside healthy tissue, which leads to fewer side effects for patients.”

The scientists’ ultimate goal is to develop “smart nanoparticles” that would only seek out cancer cells, leaving healthy cells and tissue untouched. “We can attach several kinds of molecules to a single nanoparticle, including particles that recognize specific features of cancer cells,” Maye says. “Our goal is to develop smart nanoparticle delivery systems for existing chemotherapy drugs.”

Provided by Syracuse University

Targeting tumors with nanotechnology

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Posted 03 Oct 2011 — by James Street
Category experimental treatments, Hypoxia, NanoTechnology, Personalized, Physics and Engineering

October 3, 2011

Mansoor Amiji, Distinguished Professor and Chair of the Department of Pharmaceutical Sciences at Northeastern University, has designed a nano-cocktail that targets multi-drug resistant tumors with remarkable accuracy and makes chemotherapy more efficient.

The findings, which were reported in the online-only scientific journal PLoS ONE, may lead to an increase in cancer patient survival by decreasing their exposure to large doses of chemotherapeutic agents.

The study, which dovetails with Northeastern’s focus on use-inspired research that solves global challenges in health, security and sustainability, was supported by a five-year, $2.32 million Cancer Nanotechnology Platform Partnership grant from the National Cancer Institute’s Alliance for Nanotechnology in Cancer program.

Lara Milane, a Ph.D. graduate in pharmaceutical science, and Zhenfeng Duan, an assistant professor of medicine with joint appointment at Massachusetts General Hospital and Harvard Medical School, also contributed to the report.

The Northeastern research team operated under the condition that tumor cells that grow in low-oxygen environments convert glucose into lactic acid, which makes cancer cells more drug resistant and harder to treat with chemotherapy.

They found that treating breast cancer cells with a glucose metabolism inhibitor, called lonidamine, made tumors more susceptible to the chemotherapeutic agent paclitaxel.

When coupled with lonidamine, only one-third of the typical dose of paclitaxel should be needed to kill as many cancer cells as a full dosage without the glucose metabolism inhibitor, Amiji said.

Administering smaller doses of anticancer drugs bodes well for patient health, he noted. “When you give patients more and more drugs, their bodies suffer from side effects and they may die from drug toxicity,” Amiji said. “The dilemma is to figure out a way to kill the drug-resistant tumor cells without exposing patients to too many drugs.”

In testing, lonidamine and paclitaxel were loaded into a tumor-targeted nanoparticle, which could not be seen without a high-resolution electron microscope, and then delivered through the bloodstream to the tumor’s exact location.

The smart-luggage system, as Amiji called it, is similar to that of a stamp-addressed envelope that could only be delivered to one particular mailbox. As he put it, “The nanoparticle only carries these two drugs to the tumor cells and does not expose the other parts of the body. At the tumor site, the drugs stay there longer so a patient won’t need as frequent dosing.”

The cocktail is at least five years away from being used in clinical practice, Amiji said. First, the drug’s safety and efficacy must be vetted in clinical trials, which are two or three years away.

“The FDA requires rigorous analysis of safety, especially when creating nanoparticles,” Amiji said.

View selected publications of Mansoor Amiji in IRis, Northeastern’s digital archive.

For more information, please contact Jason Kornwitz at 617-373-5729 or at j.kornwitz@neu.edu.

The Smallest Revolution: 5 Recent Breakthroughs in Nanomedicine

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Posted 01 Oct 2011 — by James Street
Category gold nanoparticles, MicroRNA, NanoTechnology, Physics and Engineering
Guest Blog

Guest Blog


By Julian Taub | September 30, 2011

Nanotechnology is a cutting-edge advancement within science and engineering. It is not a single field but an intense collaboration between disciplines to manipulate materials on the atomic and molecular level. When this technology is applied to medicine, the results are especially exciting, and can better our lives in drastic new ways. Its inventive and interdisciplinary nature constantly surprises me, as do the men and women behind these projects. Each breakthrough in nanotechology solves a problem that many thought could not be overcome. Here are five innovations in nanomedicine in the past year and the faces behind them:

Lung Cancer Early Screening:

We constantly come across depictions of lung cancer in anti-smoking ads. In addition to the gruesome nature of these images, there’s another reason to be afraid: until now, lung cancer has been almost impossible to detect in its early stages. Thousands of people go about their daily lives unaware that tumors are forming inside of them.

The lung cancer screening test, designed by pathologist Dr. Michael Wang and biomedical engineer Dr. Li-Qun Gu at the University of Missouri, relies on a simple yet efficient design. The principle behind it is that when cancer starts forming in the lungs, it distorts the sequence on a molecule called microRNA. If the scientist can find the irregularities in the microRNA, he can discover if the patient has cancer. To do this, he takes a sample of microRNA (which is easily extracted from a sample of blood plasma), and runs it through a nanopore, a hole in a protein-based membrane that is so small it lets only one molecule pass through at a time. Running a current through the pore, a machine picks up on the signals given off by the base pairs of the RNA as each one interacts chemically with the protein hole and can detect any abnormalities in the sequence. The test is so straightforward to perform that patients can be diagnosed and begin therapy during their first visit.

Dr. Wang is a professor at the University of Missouri in clinical molecular genetic pathology. He also works at the Ellis Cancer Center in Columbus MO. Dr. Gu works in biomedical engineering at Dalton Cardiovascular Center. He was inspired by the way ions move across cell membranes and has worked to make similar structures that perform important tasks.

Gold Nanoparticle Flu Test:

Most flu tests today are either time-consuming or incredibly inaccurate. The most accurate technique is called PCR, where a sample is taken, stored for a few days, its RNA is replicated, and then two weeks later, the results arrive. At that point it could be too late to halt an epidemic.

However, with the gold nanoparticle test, the results can be found out immediately, and the patient can be treated right away without spreading it to more people. Created by a team at the University of Georgia headed by Ralph A. Tripp, the test takes advantage of gold nanoparticle’s ability to scatter light in drastically different ways, depending on its geometry. The scientists attached the nanoparticles to antibodies that bind specifically to the flu virus. When the particles surround the virus, their geometry changes and they disperse light differently, making it clear that the virus is present. All the doctor has to do is take a fluid sample and mix it with a gold nanoparticle filled solution. If the virus is present, the solution will scatter light in a measureable pattern. Not only is the test quick, it’s inexpensive as well. The gold used is in such a minute amount that it costs 100th of a cent to take the test.

Besides for determining influenza, the test works for a whole host of other diseases as well. Scientists can attach any antibody necessary to the nanoparticles. Each type of antibody has special receptors that bind only to a certain type of virus. The test can even tell if there is salmonella in your chicken.

Dr. Tripp, the research group leader behind this breakthrough, is a Georgia Alliance Eminent Scholar. He has worked with state-of-the-art solutions to infectious diseases, such as RNA silencing and trying to create a vaccine for the avian flu. He strives to understand how cells respond to infection to learn how to better fight disease.

Sandia Cancer Hunters:

All over the world people suffer from tumors. Sometimes they can be removed surgically, but many times the affected cell is in an inaccessible area. Chemotherapy is another option, but radiation isn’t picky about what it kills. Oncology needs a version of “going for the jugular” in their arsenal.

That weapon might just have been invented. The protocell, engineered by Jeff Brinker and his team at Sandia National Labs in New Mexico, is a contraption to carry nanoparticles filled with toxins and RNA silencers to a cancer cell. It’s a capsule of porous silicon dioxide (think: quartz) encased in a double layer of lipids. Once it approaches the cancer cell, the protocell’s proteins latch onto the tumor’s receptors, allowing the cell to engulf it. It lets it enter and float around in a bubble of the tumor’s own cell barrier, called an endosome. To release the death blow, the fusogenic peptides, a type of protein attached to the protocell’s outer coating, create holes in the endosome that bring hydrogen ions into the bubble. The pH of the bubble increases, releasing the cell toxins and breaking the endosome. The toxins now go about poisoning the tumor and halting protein production. Some toxins have nucleotides attached to them, allowing them to be picked up by transport RNA and brought to the nucleus, where they can destroy the tumor’s DNA.

Protocells target cancerous cells; they have at least a 99% affinity to bond with the overgrowth of receptors that occur on the cell membrane of tumors. It is highly specialized and economical as well; only one protocell is necessary to silence a tumor. They are remarkably stable in body fluid, won’t leak nanoparticles onto healthy tissue, and are simple to prepare. Scientists only need to soak the protocell in a solution containing whatever nanoparticles and other toxins that they want to use.

This remarkable invention has an equally remarkable man behind it. Dr. Brinker is one of those scientists who you think only exists in sci-fi movies. Neither of his parents went to college, and his chemistry set inspired him to pursue a science career. As a novice working at Sandia, he solved a scientific problem concerning aerosol-gels, was elevated to the expert of his field, and then wrote the textbook on the subject. He was at the forefront of molecular self-assembly, creating a new technique that made porous nanostructures, like the one used in the protocell. He also created biosensors made out of cells imbedded into nanostructures that change colors when exposed to toxic material.

Cell Feedback:

To put a new drug on the market pharmaceutical companies usually spend about twelve years and over $300 million in the process. They go through various stages of testing, from cell cultures, to animal testing and eventually human trials. However, there has been one crucial step of testing that they have not been able to perform: testing the cell’s response to the drug from the inside.

Professor  Karen Martinez, with her team at the University of Copenhagen, has made a breakthrough in biosensors. They inserted semiconductor nanowires into a cell without interfering with its internal processes or killing it. Human liver cells and rat neurons were placed on a bed of indium-arsenide nanowires, and were still able to function, living for several days. The researchers then measured processes inside the cell in real-time, including internal response to stimuli and cell membrane potential. They could also transport drugs along the wire into the cell and test the reaction from the inside.

The ability to enter electronics into a cell without disturbing its behavior opens up a new field of drug testing. Now researchers can test drugs on an individual neuron and receive feedback on the interaction. This technique can be used with any new drug and can help explain its side effects. It can also help improve existing drugs by obtaining detailed feedback on its effects inside the cell. This breakthrough has put Copenhagen on the map in the nanotechnology world.

Martinez came to the University of Copenhagen after conducting research in Switzerland, where she studied protein receptors to make more affective drugs. Along with teaching courses in bionanotechnology, she sits on the board of directors for a company called inXell, a company that she founded with two other collaborators on the cell-nanowire project. inXell will become the business end of this breakthrough, working to create microchips that possess the feedback nanotechnology to test new drugs on cells.

Spinal Cord Repair:

Accidents occur every year that leave individuals paralyzed and wheelchair-bound for life. When a spine is injured, a cyst can form, blocking the nervous tissue from regenerating. The nerves below the break are then cut off from the rest of the nervous system and atrophy. One of the most famous examples is the late actor Christopher Reeve. Many see stem cells as the solution to spine rehabilitation, but two researchers in Milan have utilized another approach.

Fabrizio Gelain and Angelo Vescovi constructed nanotubes filled with self-assembling peptides to act as support for the damaged area and mimic the structure of the spine. They tested the procedure on rats and inserted the nanotubes into their broken spines where cysts where forming. After six months, they observed that the cysts were replaced by newly formed cells that included neurons, blood vessels, and bone cells. There were also neurons inside the nanotubes where the peptides originally were. Once the area recovered, the tubes would biodegrade and be eaten by microorganisms.

Tests on the rats’ motor skills showed that their legs and back motor movements improved and they didn’t have to drag their back legs around anymore. They also responded better to electrophysical stimuli than a control group of rats that were not given nanotubes.

Gelain is the vice-director of the Center of Nanoscience and Tissue Engineering in Milan. His work centers on developing nanomaterials to repair nerve tissue in victims of spinal cord injuries and strokes. He was a visiting professor at MIT and is an editor at the journals PLoS One and Frontiers in nanotechnology.

Vescovi, on the other hand, is one of the leading stem cell researchers in Italy and is interested in the regulation of cell growth. His focus is on neural stem cells in the brain and how to use them to treat disorders. He is the director of the Italian Consortium of Stem Cell Research and worked as the stem cell consultant for the Pontifical Academy of Life at the Vatican.

These innovations I’ve mentioned are just the beginning of how nanotechnology can change our quality of life. Its combined fields are so vast that different disciplines are intertwining and making unpredictable discoveries all the time. Searching nanotechnology online, more often than not I learn about a new breakthrough each day. The question then becomes: What does this all mean? Where is nanotechnology taking us? I don’t think anyone knows at this point, but I’m sure looking forward to the journey.

References

Wang, Y., et al. (2011) “Nanopore-based detection of circulating microRNAs in lung cancer patients.” Nature Nanotechnology [doi:10.1038/nnano.2011.147]

Driskell, J.D., et al. (2011) “One-step assay for detecting influenza virus using dynamic light scattering and gold nanoparticles.” Analyst (136): 3083-3090 [doi:10.1039/C1AN15303J]

Ashley, C.E., et al. (2011) “The targeted delivery of multicomponent cargos to cancer cells by nanoporous particle-supported lipid bilayers.” Nature Matter 10(5):389-97

Berthing, T., et al. (2011) “Intact Mammalian Cell Function on Semiconductor Nanowire Arrays: New Perspectives for Cell-Based Biosensing.” Small (7): 640-647 [doi: 10.1002/smll.201001642]

Gelain, F., et al. (2011) “Transplantation of nanostructured composite scaffolds results in the regeneration of chronically injured spinal cords.” ACS Nano 5(1): 227-236

Julian TaubAbout the Author: Julian Taub studied Interdisciplinary Science and Writing at Eugene Lang College at the New School. He is a freelance science writer and performance poet in the East Village of NYC. He writes a nanotechnology blog called Julian’s TechSplurge, and runs Late Nite Labs’ science blog. You can follow him on Twitter: @JulianTaub, or visit his website. Follow on Twitter  @JulianTaub.

A Radio-Frequency Coupling Network for Heating of Citrate-Coated Gold Nanoparticles for Cancer Therapy: Design and Analysis

Dustin E. Kruse*, Douglas N. Stephens, Member, IEEE, Heather A. Lindfors, Elizabeth S. Ingham, Eric E. Paoli,
and Katherine W. Ferrara, Fellow, IEEE

Abstract—Gold nanoparticles (GNPs) are nontoxic, can be functionalized
with ligands, and preferentially accumulate in tumors.
We have developed a 13.56-MHz RF-electromagnetic field (RFEM)
delivery system capable of generating high E-field strengths
required for noninvasive, noncontact heating of GNPs. The bulk
heating and specific heating rates were measured as a function
of NP size and concentration. It was found that heating is both
size and concentration dependent, with 5 nm particles producing
a 50.6 ± 0.2 ◦C temperature rise in 30 s for 25 μg/mL gold
(125 W input). The specific heating rate was also size and concentration
dependent, with 5 nm particles producing a specific
heating rate of 356 ± 78 kW/g gold at 16 μg/mL (125 W input).
Furthermore, we demonstrate that cancer cells incubated
with GNPs are killed when exposed to 13.56 MHz RF-EM fields.
Compared to cells that were not incubated with GNPs, three out
of four RF-treated groups showed a significant enhancement of
cell death with GNPs (p < 0.05). GNP-enhanced cell killing appears
to require temperatures above 50 ◦C for the experimental
parameters used in this study. Transmission electron micrographs
showextensive vacuolizationwith the combination of GNPs andRF
treatment.
Index Terms—Cancer therapy, gold nanoparticles (GNPs), nanotechnology,
RF hyperthermia, resonant circuits.
Link to DF file