For patients with diabetes, insulin is critical to maintaining good health and normal blood-sugar levels. However, it’s not an ideal solution because it can be difficult for patients to determine exactly how much insulin they need to prevent their blood sugar from swinging too high or too low.

MIT engineers hope to improve treatment for diabetes patients with a new type of engineered insulin. In tests in mice, the researchers showed that their modified insulin can circulate in the bloodstream for at least 10 hours, and that it responds rapidly to changes in blood-sugar levels. This could eliminate the need for patients to repeatedly monitor their blood sugar levels and inject insulin throughout the day.

“The real challenge is getting the right amount of insulin available when you need it, because if you have too little insulin your blood sugar goes up, and if you have too much, it can go dangerously low,” says Daniel Anderson, the Samuel A. Goldblith Associate Professor in MIT’s Department of Chemical Engineering, and a member of MIT’s Koch Institute for Integrative Cancer Research and Institute for Medical Engineering and Science. “Currently available insulins act independent of the sugar levels in the patient.”

Anderson and Robert Langer, the David H. Koch Institute Professor at MIT, are the senior authors of a paper describing the engineered insulin in this week’s Proceedings of the National Academy of Sciences. The paper’s lead authors are Hung-Chieh (Danny) Chou, former postdoc Matthew Webber, and postdoc Benjamin Tang. Other authors are technical assistants Amy Lin and Lavanya Thapa, David Deng, Jonathan Truong, and Abel Cortinas.

Glucose-responsive insulin

Patients with Type I diabetes lack insulin, which is normally produced by the pancreas and regulates metabolism by stimulating muscle and fat tissue to absorb glucose from the bloodstream. Insulin injections, which form the backbone of treatment for diabetes patients, can be deployed in different ways. Some people take a modified form called long-acting insulin, which stays in the bloodstream for up to 24 hours, to ensure there is always some present when needed. Other patients calculate how much they should inject based on how many carbohydrates they consume or how much sugar is present in their blood.

The MIT team set out to create a new form of insulin that would not only circulate for a long time, but would be activated only when needed — that is, when blood-sugar levels are too high. This would prevent patients’ blood-sugar levels from becoming dangerously low, a condition known as hypoglycemia that can lead to shock and even death.

To create this glucose-responsive insulin, the researchers first added a hydrophobic molecule called an aliphatic domain, which is a long chain of fatty molecules dangling from the insulin molecule. This helps the insulin circulate in the bloodstream longer, although the researchers do not yet know exactly why that is. One theory is that the fatty tail may bind to albumin, a protein found in the bloodstream, sequestering the insulin and preventing it from latching onto sugar molecules.

The researchers also attached a chemical group called PBA, which can reversibly bind to glucose. When blood-glucose levels are high, the sugar binds to insulin and activates it, allowing the insulin to stimulate cells to absorb the excess sugar.

The research team created four variants of the engineered molecule, each of which contained a PBA molecule with a different chemical modification, such as an atom of fluorine and nitrogen. They then tested these variants, along with regular insulin and long-acting insulin, in mice engineered to have an insulin deficiency.

To compare each type of insulin, the researchers measured how the mice’s blood-sugar levels responded to surges of glucose every few hours for 10 hours. They found that the engineered insulin containing PBA with fluorine worked the best: Mice that received that form of insulin showed the fastest response to blood-glucose spikes.

“The modified insulin was able to give more appropriate control of blood sugar than the unmodified insulin or the long-acting insulin,” Anderson says.

The new molecule represents a significant conceptual advance that could help scientists realize the decades-old goal of better controlling diabetes with a glucose-responsive insulin, says Michael Weiss, a professor of biochemistry and medicine at Case Western Reserve University.

"It would be a breathtaking advance in diabetes treatment if the Anderson/Langer technology could accomplish the translation of this idea into a routine treatment of diabetes," says Weiss, who was not part of the research team.

New alternative

Giving this type of insulin once a day instead of long-acting insulin could offer patients a better alternative that reduces their blood-sugar swings, which can cause health problems when they continue for years and decades, Anderson says. The researchers now plan to test this type of insulin in other animal models and are also working on tweaking the chemical composition of the insulin to make it even more responsive to blood-glucose levels.

“We’re continuing to think about how we might further tune this to give improved performance so it’s even safer and more efficacious,” Anderson says.

The research was funded by the Leona M. and Harry B. Helmsley Charitable Trust, the Tayebati Family Foundation, the National Institutes of Health, and the Juvenile Diabetes Research Foundation.

iF YOU SHOULD NEED AN OLDER PATIENT FOR A CLINICAL TRIAL, I CAN AND WILL VOLUNTEER. I WAS DIAGNOSED WITH TYPE 1 AT 52 YEARS OF AGE. IT IS STILL NOT CONTROLLED AND I AM 55 YEARS OLD. MY A1C IS 7.4 DOWN FROM 10.8 AT FIRST DIAGNOSIS. I WAS TREATED FOR TYPE 2 FOR 5 MONTHS WITH METFORMIN. I LOSDT 30 POUNDS AND I WASNT A BIG GIRL TO START WITH. THIS IS PROMISING AND HOPEFUL.

Another amazing Mit's brainchild !

Great idea, has this been published yet and where can I read the paper?

How can people get in contact with researchers to apply for the human trials? My husband is very interested.

I am also interested in applying for the trials. Please contact me. I am 64 and was diagnosed when I was 56.

I also would be interested. Was diagnosed in my mid 30's and am now 63.

I'm excited. I hope new advances happen very soon! My son would be a great candidate when this gets to human trials.

For those looking for the research publication, here is a link: http://www.pnas.org/content/ea...

I would be glad to try it I am 63 and was diagnosed at 30 have an insulin pump now but still have a1c of 7.4 last check , my sister was diagnosed at 5she is61 and had implants of islet of langrahand 10 years ago and still uses almost no insulin

I would be extremely interested in participating in clinical trials. I am 55 and was diagnosed almost 10yrs ago. I have been on multiple medications and inject Humulin R three times a day as well as a combination of Humulin R and N at night- and my readings can be low in the evening(so I cut back on my nighttime dose), and over 250-300 in the morning. And I don't sleepwalk and snack in my sleep! My last A1c was 7.0, up from 6.4, so my MD wants me to get a pump. I'm ok with that, but insulin 1-2 times a day that prevents these spikes and crashes would be awesome- and it would prevent future medical complications. I'm in!!

I would be very interested in participating in your trials. I am 67 years old on an insulin pump presently as a type 2 turned into a type 1. I constantly forget to enter the carbs I have calculated and am anxiously awaiting a product upgrade such as yours. I missed a low and fell down a flight of stairs recently & need help.

I have two children with T1D and we are always looking at new research. This really would be a breakthrough. I have watched both of them, one since age 9 and the other since age 11 deal with daily blood sugars and insulin shots. You sometimes feel helpless as a parent when your child is suffering. They are both teenagers now and for the biggest part have learned to accept their Diabetes, but how wonderful could this be if it works in human trials.

Possible solution by out of box approach would be to administer insulin through anima process in the large intestine to get the insulin absorbed directly without any interaction without manipulated by gastric or pancreatic juices, direct into the blood stream. If you have not already tried this technique then do try it and save patients the painful process of puncturing their bodies many times a day.

Reprinted with permission of MIT News