Engineered insulin could offer better diabetes control


 

mit_logoFor 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.

Massachusetts Institute of Technology (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 hrs, 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 Dept. 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 the Proceedings of the National Academy of Sciences. The paper’s lead authors are Hung-Chieh (Danny) Chou, former postdoctoral researcher Matthew Webber, and postdoctoral researcher 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 hrs, to ensure there is always some present when needed. Other patients calculate how much they should inject based on how many calories they consume or how much sugar is present in their blood.

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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 hrs. 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.

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.

Source: Massachusetts Institute of Technology

Nano-particles Release Insulin into Diabetics’ Bloodstream


QDOTS imagesCAKXSY1K 8Diabetics could cut their need for injections to less than once a week thanks  to new insulin-releasing “smart” particles.

Researchers in the US have developed a type of nanoparticle that  automatically releases insulin into the blood when glucose levels get too high,  and have demonstrated that its effects last for 10 days in mice.

Regular injections of the particles could mean type 1 diabetics  wouldn’t have to check their blood sugar levels several times a day, or inject  the exact right amount of insulin when needed, which can result in too high or  low doses being administered, with further health problems following.

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‘We’ve created a ‘smart’ system that is injected into the body and  responds to changes in blood sugar by releasing insulin, effectively controlling  blood-sugar levels,’ said Dr Zhen Gu, an assistant professor in the joint  biomedical engineering program at North Carolina State University and the  University of North Carolina.

‘This technology effectively creates a ‘closed-loop’ system that mimics  the activity of the pancreas in a healthy person, releasing insulin in response  to glucose level changes. This has the potential to improve the health and  quality of life of diabetes patients.’

The nanoparticles have a solid core of insulin surrounded by a layer of  a modified glucose-based material known as dextran and another of glucose  oxidase enzymes.

When the enzymes are exposed to high glucose levels they effectively  convert the sugar into gluconic acid, which breaks down the modified dextran and  releases the insulin.

The insulin then brings the glucose levels under control. The gluconic  acid and dextran are biocompatible and dissolve in the body.

The nanoparticle cores are given a biocompatible coating that makes  them positively or negatively charged, causing them to form a network that  prevents them from dispersing throughout the body.

The positively charged coatings are made of chitosan (a material  normally found in shrimp shells), abnd the negatively charged coatings are made  of alginate (a material normally found in seaweed).

When the solution of coated nanoparticles is mixed together, the  positively and negatively charged coatings are attracted to each other to form a “nano-network.”

Once injected into the subcutaneous layer of the skin, the nano-network  holds the nanoparticles together. Both the nano-network and the coatings are  porous, allowing blood – and blood sugar – to reach the nanoparticle cores.

Gu’s research team is now in discussions to move the technology into  clinical trials for use in humans.

A paper on the research has been published in the scientific journal  ACS Nano.

Read more:  http://www.theengineer.co.uk/medical-and-healthcare/news/smart-particles-release-insulin-into-diabetics-bloodstream/1016213.article#ixzz2ScNHSXmx