Every childhood vaccine may go into a single jab

Authored by bbc.com and submitted by mvea

A technology that could eventually see every childhood vaccine delivered in a single injection has been developed by US researchers.

Their one-shot solution stores the vaccine in microscopic capsules that release the initial dose and then boosters at specific times.

The approach has been shown to work in mouse studies, described in the journal Science.

The researchers say the technology could help patients around the world.

Childhood immunisations come with tears and screams. And there are a lot of them.

Diphtheria, tetanus, whooping cough, polio, Hib and hepatitis B at eight, 12 and 16 weeks.

Pneumococcal jab at eight weeks, 16 weeks and one year

Men B vaccine at eight weeks, 16 weeks and one year

Measles, mumps and rubella at one year and three years and four months

A team at Massachusetts Institute of Technology has designed a new type of micro-particle that could combine everything into a single jab.

The particles look like miniature coffee cups that are filled with vaccine and then sealed with a lid.

Crucially, the design of the cups can be altered so they break down and spill their contents at just the right time.

One set of tests showed the contents could be released at exactly nine, 20 and 41 days after they were injected into mice.

Other particles that last for hundreds of days have also been developed, the researchers say.

The approach has not yet been tested on patients.

Prof Robert Langer, from MIT, said: "We are very excited about this work.

"For the first time, we can create a library of tiny, encased vaccine particles, each programmed to release at a precise, predictable time, so that people could potentially receive a single injection that, in effect, would have multiple boosters already built into it.

"This could have a significant impact on patients everywhere, especially in the developing world."

The work differs from previous attempts, which slowly released medicines over a long period of time.

The idea is the short, sharp bursts of vaccine more closely mimic routine immunisation programmes.

Fellow researcher Dr Kevin McHugh said: "In the developing world, that might be the difference between not getting vaccinated and receiving all of your vaccines in one shot."

Z_as_in_Zebra on September 15th, 2017 at 15:30 UTC »

I heard a BBC report on this. The focus for this project is to make vaccines easier for people to access in developing worlds, where it's difficult to get to a doctor for boosters. Seems like a great idea.

whats-ittoya on September 15th, 2017 at 14:23 UTC »

What does this mean to someone who may be allergic to just 1 of these vaccines?

mvea on September 15th, 2017 at 12:37 UTC »

Journal reference:

Fabrication of fillable microparticles and other complex 3D microstructures

Kevin J. McHugh, Thanh D. Nguyen,†, Allison R. Linehan, David Yang, Adam M. Behrens, Sviatlana Rose, Zachary L. Tochka, Stephany Y. Tzeng, James J. Norman‡, Aaron C. Anselmo§, Xian Xu, Stephanie Tomasic, Matthew A. Taylor, Jennifer Lu, Rohiverth Guarecuco, Robert Langer||, Ana Jaklenec

Science 15 Sep 2017: Vol. 357, Issue 6356, pp. 1138-1142 DOI: 10.1126/science.aaf7447

Link: http://science.sciencemag.org/content/357/6356/1138

Putting the pieces together

One route to improving the delivery of existing drugs is by encapsulation inside a protective but slowly degrading shell. Such slow-release capsules improve drug availability in vivo, reduce side effects, and allow for more constant dose delivery. McHugh et al. leverage a number of existing fabrication techniques to make tiny (∼400-µm), hollow injectable microparticles that can be filled with fluid containing the therapeutic agent. By adjusting the degradation rate of the microparticle material (in this case, a lactic/glycolic copolymer), the cargo in the internal reservoir can be released at a desired time, ranging from a few days to 2 months.

Abstract

Three-dimensional (3D) microstructures created by microfabrication and additive manufacturing have demonstrated value across a number of fields, ranging from biomedicine to microelectronics. However, the techniques used to create these devices each have their own characteristic set of advantages and limitations with regards to resolution, material compatibility, and geometrical constraints that determine the types of microstructures that can be formed. We describe a microfabrication method, termed StampEd Assembly of polymer Layers (SEAL), and create injectable pulsatile drug-delivery microparticles, pH sensors, and 3D microfluidic devices that we could not produce using traditional 3D printing. SEAL allows us to generate microstructures with complex geometry at high resolution, produce fully enclosed internal cavities containing a solid or liquid, and use potentially any thermoplastic material without processing additives.