Carbon Nanoparticles Inhibit Α-Glucosidase Activity and Induce a Hypoglycemic Effect in Diabetic Mice
Autor: | Honggang Xu, Li Ping, Taili Shao, Kaoshan Chen, Lei Zhu, Xichen Li, Pingchuan Yuan, Guodong Wang, Shu-guang He |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
Blood Glucose
Chemical structure Pharmaceutical Science 02 engineering and technology Pharmacology 010402 general chemistry Polysaccharide 01 natural sciences Analytical Chemistry Diabetes Mellitus Experimental lcsh:QD241-441 Mice lcsh:Organic chemistry In vivo Mice Inbred NOD Diabetes mellitus Drug Discovery Spectroscopy Fourier Transform Infrared medicine Animals Humans Glycoside Hydrolase Inhibitors Physical and Theoretical Chemistry IC50 Acarbose chemistry.chemical_classification Arctium lappa L. root Chemistry Communication Organic Chemistry carbon nanoparticles alpha-Glucosidases 021001 nanoscience & nanotechnology medicine.disease In vitro Carbon Hypoglycemia 0104 chemical sciences Streptozocin Disease Models Animal Chemistry (miscellaneous) polysaccharide diabetes mellitus Molecular Medicine Carbohydrate Metabolism Nanoparticles 0210 nano-technology medicine.drug |
Zdroj: | Molecules Molecules, Vol 24, Iss 18, p 3257 (2019) |
ISSN: | 1420-3049 |
Popis: | New, improved therapies to reduce blood glucose are required for treating diabetes mellitus (DM). Here, we investigated the use of a new nanomaterial candidate for DM treatment, carbon nanoparticles (CNPs). CNPs were prepared by carbonization using a polysaccharide from Arctium lappa L. root as the carbon source. The chemical structure and morphology of the CNPs were characterized using Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, elemental analysis, and transmission electron microscopy. CNPs were spherical, 10-20 nm in size, consisting of C, H, O, and N, and featuring various functional groups, including C=O, C=C, C−O, and C−N. In vitro, the as-prepared CNPs could inhibit α-glucosidase with an IC50 value of 0.5677 mg/mL, which is close to that of the reference drug acarbose. Moreover, in vivo hypoglycemic assays revealed that the CNPs significantly reduced fasting blood-glucose levels in mice with diabetes induced by high-fat diet and streptozocin, lowering blood glucose after intragastric administration for 42 days. To the best of our knowledge, this is the first report of CNPs exhibiting α-glucosidase inhibition and a hypoglycemic effect in diabetic mice. These findings suggest the therapeutic potential of CNPs for diabetes. |
Databáze: | OpenAIRE |
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