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Novel drug delivery system releases drugs in response to compression by the patient's hand

Date:
March 17, 2013
Source:
National Institute for Materials Science
Summary:
Medical researchers have succeeded in developing a gel material which is capable of releasing drugs in response to pressure applied by the patient.

Conceptual scheme of controlled release of ODN from a hydrogel composed of a CyD-containing molecular network by mechanical compression.
Credit: Image courtesy of National Institute for Materials Science

A research group 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 of Tottori University) of the NIMS International Center for Materials Nanoarchitectonics (MANA) succeeded in developing 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 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 crosslinking 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 results were published in the online bulletin of the English scientific journal Journal of Materials Chemistry B.


Story Source:

The above story is based on materials provided by National Institute for Materials Science. Note: Materials may be edited for content and length.


Journal Reference:

  1. Hironori Izawa, Kohsaku Kawakami, Masato Sumita, Yoshitaka Tateyama, Jonathan P. Hill, Katsuhiko Ariga. β-Cyclodextrin-crosslinked alginate gel for patient-controlled drug delivery systems: regulation of host–guest interactions with mechanical stimuli. Journal of Materials Chemistry B, 2013; DOI: 10.1039/C3TB00503H

Cite This Page:

National Institute for Materials Science. "Novel drug delivery system releases drugs in response to compression by the patient's hand." ScienceDaily. ScienceDaily, 17 March 2013. <www.sciencedaily.com/releases/2013/03/130317154716.htm>.
National Institute for Materials Science. (2013, March 17). Novel drug delivery system releases drugs in response to compression by the patient's hand. ScienceDaily. Retrieved July 31, 2014 from www.sciencedaily.com/releases/2013/03/130317154716.htm
National Institute for Materials Science. "Novel drug delivery system releases drugs in response to compression by the patient's hand." ScienceDaily. www.sciencedaily.com/releases/2013/03/130317154716.htm (accessed July 31, 2014).

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