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Researchers Develop Microneedle Patch for Flu Vaccination
A National Institutes of Health (NIH)-funded study led by a team at the Georgia Institute of Technology and Emory University has shown that an influenza vaccine can produce substantial immune responses and be administered safely with an experimental patch of dissolving microneedles. The new method is an alternative to needle-and-syringe immunization; with further development, it could eliminate the discomfort of an injection as well as the inconvenience and expense of visiting a flu clinic, according to the investigators.
“This bandage-strip sized patch of painless and dissolvable needles can transform how we get vaccinated,” said Roderic I. Pettigrew, PhD, MD, director of the National Institute of Biomedical Imaging and Bioengineering, which funded the study. “A particularly attractive feature is that this vaccination patch could be delivered in the mail and self-administered. In addition, this technology holds promise for delivering other vaccines in the future.”
The vaccine patch consists of 100 solid, water-soluble needles that are just long enough to penetrate the skin. “The skin is an immune surveillance organ,” said Mark R. Prausnitz, PhD, leader of the team that designed the patch. “It’s our interface with the outside world, so it’s very well equipped to detect a pathogen and mount an immune response against it.”
Adhesive helps the patch grip the skin during the administration of the vaccine, which is encapsulated in the needles and is released as the needle tips dissolve within minutes. The patch is peeled away and discarded like a used bandage strip.
In a study published online in The Lancet, 100 adults were randomly assigned to receive vaccination with a microneedle patch administered by a health care provider; vaccination with a microneedle patch self-administered by the study participant; vaccination with intramuscular injection administered by a health care provider; or a placebo microneedle patch administered by a health care provider. The researchers used an inactivated influenza vaccine formulated for the 2014–2015 flu season to inoculate participants other than those in the placebo group.
The investigators found that vaccination with the microneedle patches was safe, with no serious patch-related adverse events. Some participants developed local skin reactions to the patches, described as faint redness and mild itching, that lasted two to three days.
The results also showed that antibody responses generated by the vaccine, as measured through an analysis of blood samples, were similar in the groups vaccinated using patches and those receiving intramuscular injection, and these immune responses were still present after six months. More than 70% of patch recipients reported they would prefer patch vaccination to injection or intranasal vaccination for future vaccinations.
No significant difference was seen between the doses of vaccine delivered by health care workers and the volunteers who self-administered the patches, showing that participants were able to correctly self-administer the patch. After vaccination, imaging of the used patches found that the microneedles had dissolved in the skin, suggesting that the used patches could be safely discarded as non-sharps waste. The vaccines remained potent in the patches without refrigeration for at least one year.
The prospective vaccine technology could offer economic and manufacturing advantages, according to the researchers. The manufacturing cost for the patch is expected to be competitive with that of prefilled syringe costs. The patch, however, can dramatically reduce the cost of vaccination because self-administration can eliminate the need to have health workers oversee the process. A patch can be easily packaged for transportation, requires no refrigeration, and is stable.
The team plans to conduct further clinical trials to pursue the technology’s ultimate availability to patients. They also are working to develop microneedle patches for use with other vaccines, including measles, rubella, and polio.
Source: NIH; June 27, 2017.