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English: Schematic sketch showing the transpor...

English: Schematic sketch showing the transport types at the blood-brain barrier. Deutsch: Schematische Darstellung der Transportmechanismen an der Blut-Hirn-Schranke. Français : Schéma des types de transport à travers la barrière hémato-encéphalique (Photo credit: Wikipedia)

Larry H Bernstein, MD
Reporter

Provided without comment.  Quite interesting.

novel protease resistant peptide shuttles able to cross the blood-brain barrier (BBB) by binding to a specific brain receptor

Description

A Catalan Research Institute based in Barcelona (Spain) has identified novel protease resistant peptide shuttles able to cross the blood-brain barrier (BBB) by binding to a specific brain receptor. These shuttles are a powerful alternative to carry a wide variety of small and large molecules as cargos. This represents a novel opportunity to develop new delivery carriers able to cross actively a range of biological barriers.

New and innovative aspects

These compounds are novel drug delivery carriers that provide a non-invasive, non-antigenic, stable and receptor-specific way to transport drugs across the Blood-Brain Barrier and into the Central Nervous System.

These compounds show high permeability, biocompatibility, good solubility in water and resistance to proteases.

Specifications

The treatment of most neurological disorders has not been fully addressed mainly because of the neuroprotective role of the blood-brain barrier (BBB) that hinders the delivery of many diagnostic and therapeutic agents into the brain. Consequently, therapeutic molecules and genes that might otherwise be effective in diagnosis and therapy do not cross the BBB in adequate amounts: 98% of compounds smaller than 400Da and 100% of larger ones do not reach further drug development stages.

Most central nervous system (CNS) diseases, however, are complex disorders with difficult molecular targets that require larger, safer and more selective drugs. As a result, brain tumors, neurodegenerative diseases such as Parkinson’s and Alzheimer’s, and central nervous system (CNS) diseases such as schizophrenia are not successfully treated. Therefore, finding an efficient CNS delivery system is one of the major challenges in neurological treatment and one our technology can potentially overcome.

One of the best approaches for drug delivery to the brain is the use of endogenous transport mechanisms, such as receptor-mediated transcystosis. Peptides are biocompatible molecules able to transport cargos (i.e. therapeutic compounds) to specific tissues such as the brain. However, one of the main limitations of peptides as therapeutic agents is their low stability in plasma.

The use of non-natural amino acids in peptidic sequences can circumvent this problem because they are resistant to human serum proteases. Using this approach, we obtained several modified peptides. Two of them were selected based on their protease resistance and transport capacity across the blood-brain barrier, using a specific endogenous receptor. Both peptides showed enhanced membrane permeability in vitro in comparison to standard peptides and even greater stability in plasma (over 24h).

Main advantages of its use

Novel delivery technology that provides a non-invasive, non-antigenic, permeable, stable, soluble and receptor-specific way to transport drugs across the BBB and into the CNS.

This technology may ultimately allow the delivery of therapeutic agents, even large ones, across the BBB and other biological barriers, thus increasing the effectiveness of existing or new drugs.

Potential of application in a wide number of fields and in transport through various biological barriers.

Applications

Biotechnological and Pharmaceutical companies specialized in drug discovery, drug delivery, neurological disorders, tools to cross the Blood-brain barrier. The final aim is to increase the efficiency of existing molecules for the treatment of neurological disorders.

Molecule and treatment design, drug manufacture, treatment of neurological disorders, drug delivery across the blood-brain barrier (BBB).

Intellectual property status

This invention is protected by a priority application in Spain and we plan to apply for a PCT in due time.

 

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Reported by: Dr. Venkat S. Karra, Ph.D.

Clinical trials get efficiency boost from virtual reality

Clinical trials can be time-consuming, expensive and intrusive, but they are also necessary.

Researchers at the University of Tennessee Space Institute in Tullahoma have developed an invention that makes clinical trials more efficient by moving them into the virtual world.

Called “digital Eye Bank,” the computer software eye modeling program includes data from people’s eyes for researchers to use when testing their inventions. Developed by Ying-Ling Chen, research assistant professor of physics and Jim Lewis, professor emeritus in physics, Eye Bank can take data from eyes of patients’ and build it into models from the commercial optics program to be used for researchers’ virtual clinical trials.

“The idea of Eye Bank is to use existing clinical data and build in realistic and personalized eye models stored in a ready-to-use tool kit like a group of volunteers,” said Chen. “Then we can call on any specific eye to test a newly designed optical instrument on the computer and see what kind of performance the design gets. This testing can be done repeatedly without hurting real human subjects.”

Read more at:

http://www.rdmag.com/News/2012/08/Life-Science-Medical-Technology-Computing-Clinical-trials-get-efficiency-boost-from-virtual-reality/?et_cid=2825670&et_rid=54746652&linkid=http%3a%2f%2fwww.rdmag.com%2fNews%2f2012%2f08%2fLife-Science-Medical-Technology-Computing-Clinical-trials-get-efficiency-boost-from-virtual-reality%2f

 

 

 

 

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A collaborative effort in reaching the set targets in a stipulated time frame is inevitable in every walk of life and the pharmaceutical industry seems to be in no exception. New products identification and their evaluation in terms of their safety and efficacy towards the targeted disease condition and finally bringing them to the needy as quickly as possible is a continuous and tedious process.

In order to minimize the time lines across the drug development process thru the market one may (have to) seek for external collaboration while safely and strategically harnessing the in-house resources to break new grounds in the field.

External collaboration will bring-in new talent into the existing system of Science and Business of the firm, whether small, mid-sized, or big company, that could lead to great innovations and investments on a win-win basis.

It is anticipated that Oncology therapeutic area will reach approximately $75 billion in global spending by 2015. OncoProducts continue to dominate the global therapeutics market and it is the leading research therapeutic, with 672 oncology drugs in development.

Conducting clincal trails is very challenging because:

  • clinical trials can vary in size from a single center in one country to multicenter trials in multiple countries.
  • Cost incur in a full series of clinical trials is enormous.
  • of the burden of paying for all the necessary people and services is usually borne by the sponsor.

Clinical trails can take place only after satisfactory information has been gathered on the quality of the nonclinical safety, and health authority/ethics committee approval is granted in the country where the trial is taking place.

Depending on the type of product and the stage of its development, investigators enroll healthy volunteers and/or patients into small pilot studies initially, followed by larger scale studies as and when positive safety and efficacy data are gathered.

Such a rigorous evaluation in clinical trials that assess effcacy and safety in appropriate patient populations are critical to the continued development of the highly sensitive targeted therapies. The challenges to such studies, especially in phase I, are particularly great in oncology and cannot be met solely by most small- to mid-size oncology companies’.

Thus, though many companies have a range of talent and tools to apply to trials, often a clinical trial is managed by an outsourced partner, such as a Contract Research Organization or a Clinical Trials Unit. Moreover partnering with external organizations can bolster expertise and experience to ensure successful trial outcomes in terms of quality, data and time.

One such organization to partner with to successfully conduct and complete especially optimizing early phase, which is most challenging, oncology clinical trails is “NOVELLA Clinical”.

Novella is a specialty clinical research organization (CRO), that offers a range of services ranging from protocol development thru data analysis, that can be tailored to and mesh seamlessly with a sponsor’s specific needs.

When selecting a sponsor one must consider the following:

  • Expert scientific staff availability
  • Synergistic clinical trail models (e.g., PM/CTM clubbing or effective coordination where possible)
  • Clinical site selection expertise
  • Clinical trail efficiency through Operation Excellence that uses eClinical technologies (e.g., EDC, CTM)
  • Effective Cohort Management
  • Quality Data Documentation, and last but not least
  • ‘Trust’.

Therefore selecting a specialty oncology CRO especially for early stage oncology trials is important and moreover partners bring sponsors ‘results that lay the foundation’ for advanced efficacy trials in the most appropriate oncology patients, particularly when acquired in a time- and cost-effective manner.

Sponsors interested, especially the small- to mid-size pharmaceutical and biotechnology companies who may be planning early stage oncology clinical trials, in taking advantages offered by “NOVELLA Clinical” can visit the source for further details.

 For further reading:

Website: “NOVELLA Clinical”

Reference:

Optimizing-Early-Phase-Oncology-Clinical-Trials-Novella-Clinical

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Reporter: Aviva Lev-Ari, PhD, RN

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