Antidiabetic Close Loop Based on Wearable DNA-Hydrogel Glucometer and Implantable Optogenetic Cells.
Tiantian ManGuiling YuFulin ZhuYaqi HuangYueyu WangYan SuSheng-Yuan DengHao PeiLi LiHaifeng YeYing WanPublished in: JACS Au (2024)
Diabetes mellitus and its associated secondary complications have become a pressing global healthcare issue. The current integrated theranostic plan involves a glucometer-tandem pump. However, external condition-responsive insulin delivery systems utilizing rigid glucose sensors pose challenges in on-demand, long-term insulin administration. To overcome these challenges, we present a novel model of antidiabetic management based on printable metallo-nucleotide hydrogels and optogenetic engineering. The conductive hydrogels were self-assembled by bioorthogonal chemistry using oligonucleotides, carbon nanotubes, and glucose oxidase, enabling continuous glucose monitoring in a broad range (0.5-40 mM). The optogenetically engineered cells were enabled glucose regulation in type I diabetic mice via a far-red light-induced transgenic expression of insulin with a month-long avidity. Combining with a microchip-integrated microneedle patch, a prototyped close-loop system was constructed. The glucose levels detected by the sensor were received and converted by a wireless controller to modulate far-infrared light, thereby achieving on-demand insulin expression for several weeks. This study sheds new light on developing next-generation diagnostic and therapy systems for personalized and digitalized precision medicine.
Keyphrases
- type diabetes
- glycemic control
- blood glucose
- induced apoptosis
- drug delivery
- healthcare
- carbon nanotubes
- poor prognosis
- cell cycle arrest
- tissue engineering
- hyaluronic acid
- wound healing
- stem cells
- wastewater treatment
- metabolic syndrome
- cell death
- extracellular matrix
- weight loss
- low cost
- drug release
- mass spectrometry
- insulin resistance
- adipose tissue
- oxidative stress
- multidrug resistant
- nucleic acid
- bone marrow
- health information
- cell proliferation
- reduced graphene oxide
- gestational age
- chemotherapy induced