Showing posts with label New Drug Delivery Methods. Show all posts
Showing posts with label New Drug Delivery Methods. Show all posts

NuPathe ready with new drug application for migraine treatment

NuPathe Inc., the Conshohocken specialty pharmaceutical company that is getting ready to file a new drug application for its experimental migraine headache treatment, has expanded its partnership formed in 2007 to take on Parkinson’s disease.

Late Monday, NuPathe entered into a license agreement for drug-delivery technology with SurModics Inc., a publicly traded Minnesota life sciences company.

The companies began a collaboration in 2007 aimed a developing a biodegradable sustained-release formulation of an approved dopamine agonist.

The partnership has yielded NuPathe's NP201, which it described as “the first long-acting treatment available in broadly acceptable dose form that maintains the potential to provide sustained relief from Parkinson's disease without motor response complications.”

The experimental product combines NuPathe's long-acting delivery technology and SurModics' proprietary biodegradable polymer matrix implant technology.

Under the licensing agreement, NuPathe will lead and fund development and commercialization. SurModics will provide technical and manufacturing expertise and will be eligible to receive licensing fees and milestone payments related to development of products for the treatment of Parkinson's disease and other clinical indications. SurModics will also receive royalties on product sales.

Other financial details were not disclosed.

Parkinson's disease, a brain disorder, occurs when certain nerve cells in the substantia nigra portion of the brain die or become impaired. Normally, these cells produce a vital chemical known as dopamine. Dopamine allows smooth, coordinated function of the body's muscles and movement.

About 1.4 million people suffer from Parkinson's disease in the United States, Europe, and Japan. By 2050, this number is expected to double.




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Trinity Researchers Develop New Drug Delivery System for Retinal Disease

Researchers at the Smurfit Institute of Genetics’ Ocular Genetics Unit at Trinity College Dublin have reported the development of a new drug delivery system which has the potential to treat degenerative diseases of the retina, including retinitis pigmentosa, age-related macular degeneration and diabetic retinopathy, conditions which collectively represent the most prevalent causes of registered visual handicap in developed countries. The research was led by Dr Matthew Campbell and Professor Peter Humphries of TCD’s Smurfit Institute of Genetics and School of Genetics and Microbiology.

Currently an estimated 98% of clinically validated drugs, many of which would have utility in the treatment of these diseases, can not cross from the bloodstream into the retina because of the presence of the so-called inner blood-retina barrier, which, as its name implies, represents a tight seal between the blood-supply and retinal tissues. The researchers at Trinity have developed a method for periodically and reversibly opening the barrier in mice (mice have a similar barrier to humans) to very small molecules – just enough to allow therapeutic drugs into the eye, but small enough to keep harmful blood-born substances out.

The new process, the development of which has been supported by the Wellcome Trust, Science Foundation Ireland and Fighting Blindness Ireland, and which will shortly be reported in the international journal, Proceedings of the National Academy of Sciences (USA), has been used by the researchers to radically improve vision in mice modeling one form of the hereditary retinal disease, retinitis pigmentosa and it has also been used in the suppression of new retinal blood vessel growth in mice, a phenomenon called neovascularisation, which is the major sight-threatening symptom associated with age-related macular degeneration in humans. The researchers are optimistic that this novel method of drug delivery will be translatable into processes for human therapy targeting not only diseases of the retina but potentially also those causing degeneration of the brain for which there is a similar blood-brain barrier.

Commenting on the significance of the research Dr. Matthew Campbell stated: “Enhanced drug delivery to the retina has the potential to treat the hereditary retinal disorder retinitis pigmentosa as well as the common degenerative retinal condition age-related macular degeneration. There may also be applications for its use in glaucoma and diabetic retinopathy. In a broader sense however, aspects of this technology could be adapted for a range of neuro-degenerative conditions including Alzheimer's disease and multiple sclerosis, while also potentially allowing for enhanced drug delivery to un-treatable brain tumours.”




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New Cancer Drug Delivery System Is Effective and Reversible

The team of investigators, led by faculty members Li Yu, Ph.D., and Jianjun Cheng, Ph.D., M.S., who is also a member of the Siteman Center of Cancer Nanotechnology Excellence, began its work with the knowledge that small, membrane-bound compartments, called liposomes, are useful as drug-delivery vehicles. When linked to molecules that target receptors on cancer cells, liposomes can enter and dump their cancer-killing contents into those cells.

To target tumor cells, the investigators focused their efforts on a family of small molecules called aptamers. Aptamers are short strands of DNA or RNA; they are highly efficient at binding to biomolecules and are easy to make, label, and manipulate. Dr. Lu's laboratory specializes in isolating aptamers that bind to specific molecules and converting them into effective sensors and diagnostic agents. His team used an aptamer that binds to nucleolin receptors, which are found in abundance on certain breast cancer cells. The researchers then developed an effective method for attaching the aptamer to a liposome loaded with cisplatin, a drug that effectively kills cancer cells but has troublesome side effects when administered intravenously.

Tests in cells grown in the lab yielded promising results. Four days after the investigators exposed the cells to the new drug delivery system, 60% of the breast cancer cells had died, whereas less than 12% of breast cancer cells treated with cisplatin alone had died. "By labeling a liposome that contains cisplatin with a cancer cell-specific aptamer, we have shown delivery of the drugs to cancer cells without significant damage to regular cells," Dr. Lu said, "making it possible to maximize the drug potency while minimizing its side effects."

This approach "integrates the advantages of small molecules and antibodies," said Dr. Cheng, who helped pioneer the use of aptamers as targeting molecules for drug delivery. "This is the first study to integrate the aptamers and the liposome."

Another advantage of using aptamers as targeting agents is that they are easily disabled since they readily bind to complementary DNA (cDNA), which prevents them from interacting with cell receptors. In an additional set of experiments, the investigators showed that adding cDNA to cultured cells treated with the aptamer-targeted liposomes did in fact block all cell-killing activity of liposomal cisplatin.

"You can change aptamers to target a different type of cancer, you can change the therapeutic molecules to fight cancer or other diseases, and you can reverse the dose," Dr. Cheng said. "That's a lot of tools in the toolbox. It has great potential."

Source : www.nanotech-now.com


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Drug-releasing Contact Lenses

While there is no cure for glaucoma, medication can slow or prevent further vision loss. Glaucoma patients typically instill eyedrops on a daily basis to control the disease. However, only a minimal amount of the dose is actually absorbed by the eye. The rest either runs down the sides of the patient's face, is washed away by reflex tearing or dispersed by blinking.

Researchers are excited about new drug-releasing contact lenses that ensure glaucoma patients and others get correct and consistent dosages of medication. This could be a significant improvement on the traditional eyedrops that ophthalmologists prescribe for these patients, from which the eye absorbs as little as 1% of the dose. The contact lenses are capable of delivering the proper dosage and increasing the effectiveness of treatment.

What is Glucoma ?

Glaucoma refers to a group of diseases that affect the optic nerve and involves a loss of retinal ganglion cells in a characteristic pattern. It is a type of optic neuropathy. Raised intraocular pressure is a significant risk factor for developing glaucoma (above 22 mmHg or 2.9 kPa). One person may develop nerve damage at a relatively low pressure, while another person may have high eye pressure for years and yet never develop damage. Untreated glaucoma leads to permanent damage of the optic nerve and resultant visual field loss, which can progress to blindness.

Glaucoma can be divided roughly into two main categories, "open angle" and "closed angle" glaucoma. Angle closure can appear suddenly and is often painful. Visual loss can progress quickly but the discomfort often leads patients to seek medical attention before permanent damage occurs. Open angle, chronic glaucoma tends to progress more slowly and the patient may not notice that they have lost vision until the disease has progressed significantly.

Glaucoma has been nicknamed the "sneak thief of sight" because the loss of vision normally occurs gradually over a long period of time and is often only recognized when the disease is quite advanced. Once lost, this damaged visual field can never be recovered. Worldwide, it is the second leading cause of blindness. Glaucoma affects one in two hundred people aged fifty and younger, and one in ten over the age of eighty. If the condition is detected early enough it is possible to arrest the development or slow the progression with medical and surgical means.

Source : vision.about.com


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New Drug Delivery Methods in Spotlight




Early-phase treatment modalities -- ranging from a stem cell attack on metastatic cancer to what may be a true silver bullet against pulmonary infection -- were highlighted at the annual meeting of the American Thoracic Society.

The studies are all in the preclinical stages but could represent "exciting" new approaches to a range of illnesses, according to Beth Laube, Ph.D., of Johns Hopkins University School of Medicine, who moderated a press conference at which the studies were discussed.

The stem cell study combines two separate areas of research, according to Michael Loebinger, M.D., of University College London.

On one hand, he said, it has been known for some time that mesenchymal stem cells in bone marrow have the ability to home in on and bind to tumor cells.

On the other, he said, researchers have known that the molecule dubbed TNF-related apoptosis-inducing ligand -- or TRAIL -- kills cancer cells but not normal cells.

Combining the two using genetic engineering, Dr. Loebinger told reporters, the new cells induced programmed cell death in vitro in a variety of cancer cells, including lung, squamous cell, breast, and cervical cancer cells, while leaving normal cells intact.

In mice, Dr, Loebinger said, injections of the cells reduced tumor growth significantly (at P<0.001 p="0.03)">

"The two different aspects of this therapy have been used in humans," he said, but not together. TRAIL, for instance, has been used in phase I and II trials and appears to be safe.

The combination," he said, "is quite promising" and would be applicable to a wide range of cancers. Dr. Laube said the experiments are "very, very exciting," not least because of the ability of the cells to seek out and destroy tumor cells wherever they are in the body. "That's got to be helpful to patients," she said. Another new treatment modality targeted cystic fibrosis. In CF, the ion channel defects reduce airway surface liquid, which results in reduced mucociliary clearance and recurrent infections, said Andrew Hirsh, Ph.D., of Parion Sciences in Durham, N.C. One treatment that is sometimes used is the sodium channel blocker amiloride (Midamor), but it has several disadvantages, Dr. Hirsh said, including a relatively short effective span that requires frequent use.

Dr. Hirsh was reporting preclinical data on a new sodium channel blocker, dubbed GS-9411, that he said was 100 times more potent than amiloride (in terms of the 50% inhibition concentration). The drug also was able to maintain 85% of sodium channel blockage after multiple washes, compared with less than 10% for amiloride, which should translate to longer effective time in the body, he said.

The drug, delivered as an aerosol, is now in phase I clinical trials with healthy volunteers, Dr. Hirsh said. Meanwhile, researchers led by Carolyn Cannon, M.D., Ph.D., of Washington University School of Medicine in St. Louis, are studying how to deliver tiny nanoparticles containing silver compounds to lung infections. So-called silver carbene complexes have been shown to have antibiotic activity and one developed by Dr. Cannon and colleagues -- SCC1 -- is now the subject of an investigational new drug application, she said.

For technical reasons, that compound can't be put in nanoparticles, which she and colleagues thought would allow them to reduce the dose and number of doses needed to achieve a clinical effect. So they synthesized another molecule -- dubbed SCC22 -- which could be loaded into nanoparticles of L-tyrosine polyphosphate and delivered using a nebulizer.

In mice infected with Pseudomonas aeruginosa, Dr. Cannon said, 100% survived if they were treated intranasally with the SCC-loaded particles, while all of the untreated mice died.

The survival advantage left the researchers "surprised and thrilled," Dr. Cannon said. With the nano approach, she said, the mice could be given a smaller dose of the compound and be treated only once a day, compared with twice a day for the drug alone. Although the drug was tested in vivo against P. aeruginosa, Dr. Cannon said, it has been shown in vitro to be "effective against every bacterial species tested to date." It has not escaped her notice, she said, that -- if the animal studies are replicated in humans -- the compounds will be a true silver bullet against bacteria.

Source : www.medpagetoday.com


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