Since
insulin's crucial discovery nearly a century ago, diabetes patients have had to
inject themselves with the life-saving medicine. Now scientists are reporting a
new development toward a long-sought insulin pill that could save millions the
pain of daily shots. Published in the ACS journal Biomacromolecules, the
advance could someday not only eliminate the "ouch" factor, but also
get needle-wary - and weary - patients to take their medicine when they should.
Sanyog Jain and
colleagues explain that patients with diabetes sometimes skip doses or stop
taking their insulin because the injections can be painful. But doing so puts
their health in danger. An estimated 347 million people globally (about 26
million in the U.S.) are living with diabetes. In the U.S., more than a quarter
of these patients are taking some kind of insulin therapy. For years,
researchers have sought a way to transform delivery of this therapy from a shot
to a pill, but it has been a challenge. The body's digestive enzymes that are
so good at breaking down food also break down insulin before it can get to
work. In addition, insulin doesn't get easily absorbed through the gut into the
bloodstream. To overcome these hurdles, Jain's team combined two approaches to
shield insulin from the digestive enzymes and then get it into the blood.
They packaged insulin in
tiny sacs made of lipids, or fats, called liposomes, which are already used in
some treatments. Then, they wrapped the liposomes in layers of protective
molecules called polyelectrolytes. To help these "layersomes" get
absorbed into the bloodstream, they attached folic acid, a kind of vitamin B
that has been shown to help transport liposomes across the intestinal wall into
the blood. In rats, the delivery system lowered blood glucose levels almost as
much as injected insulin, though the effects of the layersomes lasted longer
than that of injected insulin.
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