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New gel material releases drug under patient’s pressure

By Drug Discovery Trends Editor | March 14, 2013

Conceptual scheme of controlled release of ODN from a hydrogel composed of a CyD-containing molecular network by mechanical compression.A research team at the National Institute of Materials Science in Japan has recently developed a gel material which is capable of releasing drugs in response to pressure applied by the patient.

Drugs are generally taken by oral administration, injection, etc. However, the conventional methods may cause side effects and inconveniences. Although stimuli-responsive drug delivery systems are an effective technique which solves such problems, a special device is necessary in order to apply the stimulus.

The research group is headed by Dr. Katsuhiko Ariga, a MANA principal investigator, Dr. Kohsaku Kawakami, a MANA scientist, and Dr. Hironori Izawa, a MANA Post-Doctoral researcher (currently assistant professor at Tottori University) of the International Center for Materials Nanoarchitectonics (MANA), National Institute for Materials Science.

The MANA research group developed a gel material envisioning a new drug administration method in which the drug is released when the patient applies manual pressure to the gel. Using samples of the gel containing the anti-emetic drug ondansetron, the researchers confirmed that the drug was released when stimulus mimicking finger-pressure by the patient was applied, and found that this effect was maintained for at least 3 days. Although oral administration of drugs is difficult for patients experiencing nausea during cancer chemotherapy, if this material is introduced under the skin, it is expected to release the drug simply by pressing or rubbing it.

Because this material does not require special devices, electricity, etc., it can be used even when lifeline infrastructure has been interrupted by disasters, in developing countries where the lifeline is inherently inadequate, etc. It will also be possible for patients to administer drugs under any environment at their own intention. Many situations where patients wish to administer drugs quickly “on-demand” are also assumed, for example, for relief from cancer pain, hay fever, or asthma. Thus, this material offers an extremely convenient new dosing strategy.

The gel is produced by cross-linking calcium alginate, which is a naturally-derived component contained in algae, with cyclodextrin, which is a saccharide. Both substances are already used in pharmaceuticals. Cyclodextrin hosts a drug as a guest. This is the first report in which a host-guest interaction is controlled by mechanical stimulus.

These research results were obtained in the Research Theme “Dynamic Interfacial Nanotechnology for Integration between Nano and Macroscopic Worlds” (Principal Investigator: Katsuhiko Ariga) in the JST-CREST Research Area “Development of high performance nanostructures for process integration” (Research Supervisor: Masahiro Irie).

These results were published in the online bulletin of the English scientific journal Journal of Materials Chemistry B.

β-Cyclodextrin-crosslinked alginate gel for patient-controlled drug delivery systems: regulation of host–guest interactions with mechanical stimuli

Source: National Institute of Materials Science


Filed Under: Drug Discovery

 

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