Synthetic "smart gel" provides glucose-responsive insulin delivery in diabetic mice.
Akira MatsumotoMiyako TanakaHiroko MatsumotoKozue OchiYuki Moro-OkaHirohito KuwataHironori YamadaIbuki ShirakawaTaiki MiyazawaHitoshi IshiiKazunori KataokaYoshihiro OgawaYuji MiyaharaTakayoshi SuganamiPublished in: Science advances (2017)
Although previous studies have attempted to create "electronics-free" insulin delivery systems using glucose oxidase and sugar-binding lectins as a glucose-sensing mechanism, no successful clinical translation has hitherto been made. These protein-based materials are intolerant of long-term use and storage because of their denaturing and/or cytotoxic properties. We provide a solution by designing a protein-free and totally synthetic material-based approach. Capitalizing on the sugar-responsive properties of boronic acid, we have established a synthetic polymer gel-based insulin delivery device confined within a single catheter, which exhibits an artificial pancreas-like function in vivo. Subcutaneous implantation of the device in healthy and diabetic mice establishes a closed-loop system composed of "continuous glucose sensing" and "skin layer"-regulated insulin release. As a result, glucose metabolism was controlled in response to interstitial glucose fluctuation under both insulin-deficient and insulin-resistant conditions with at least 3-week durability. Our "smart gel" technology could offer a user-friendly and remarkably economic (disposable) alternative to the current state of the art, thereby facilitating availability of effective insulin treatment not only to diabetic patients in developing countries but also to those patients who otherwise may not be strongly motivated, such as the elderly, infants, and patients in need of nursing care.
Keyphrases
- type diabetes
- glycemic control
- blood glucose
- end stage renal disease
- chronic kidney disease
- transcription factor
- ejection fraction
- drug delivery
- wound healing
- cancer therapy
- randomized controlled trial
- clinical trial
- binding protein
- skeletal muscle
- metabolic syndrome
- peritoneal dialysis
- case control
- amino acid
- study protocol
- combination therapy
- wild type