Camlik Gamze, Bilakaya Besa, Küpeli Akkol Esra, Velaro Adrian Joshua, Wasnik Siddhanshu, Muhar Adi Muradi, Degim Ismail Tuncer, Sobarzo-Sánchez Eduardo
Department of Pharmaceutical Technology, Faculty of Pharmacy, Biruni University, Istanbul 34015, Türkiye.
Biruni University Research Center (B@MER), Biruni University, Istanbul 34015, Türkiye.
Pharmaceuticals (Basel). 2024 Oct 19;17(10):1395. doi: 10.3390/ph17101395.
BACKGROUND/OBJECTIVES: Metformin (Met), an oral drug used to treat type II diabetes, is known to control blood glucose levels. Metformin carbon quantum dots (MetCQDs) were prepared to enhance the bioavailability and effectiveness of metformin. Several studies have shown that carbon quantum dots (CQDs) have attractive properties like small particle size, high penetrability, low cytotoxicity, and ease of synthesis. CQDs are made from a carbon source, namely, citric acid, and a heteroatom, such as nitrogen. The active molecule can be a carbon source or a heteroatom, as reported here.
This study aims to produce MetCQDs from an active molecule. MetCQDs were successfully produced by microwave-based production methods and characterized. The effect of the MetCQDs was tested in Wistar albino rats following a Streptozocin-induced diabetic model.
The results show that the products have a particle size of 9.02 ± 0.04 nm, a zeta potential of -10.4 ± 0.214 mV, and a quantum yield of 15.1 ± 0.045%. Stability studies and spectrophotometric analyses were carried out and the effectiveness of MetCQDs evaluated in diabetic rats. The results show a significant reduction in blood sugar levels (34.1-51.1%) compared to the group receiving only metformin (37.1-55.3%) over a period of 30 to 360 min. Histopathological examinations of the liver tissue indicate improvement in the liver health indicators of the group treated with MetCQDs.
Based on these results, the products have potential therapeutic advantages in diabetes management through their increased efficacy and may have reduced side effects compared to the control group.
背景/目的:二甲双胍(Met)是一种用于治疗II型糖尿病的口服药物,已知其可控制血糖水平。制备了二甲双胍碳量子点(MetCQDs)以提高二甲双胍的生物利用度和有效性。多项研究表明,碳量子点(CQDs)具有诸如粒径小、高穿透性、低细胞毒性和易于合成等吸引人的特性。CQDs由碳源(即柠檬酸)和杂原子(如氮)制成。如本文所报道,活性分子可以是碳源或杂原子。
本研究旨在从活性分子制备MetCQDs。通过基于微波的生产方法成功制备了MetCQDs并进行了表征。在链脲佐菌素诱导的糖尿病模型的Wistar白化大鼠中测试了MetCQDs的效果。
结果表明,产物的粒径为9.02±0.04nm,zeta电位为-10.4±0.214mV,量子产率为15.1±0.045%。进行了稳定性研究和分光光度分析,并在糖尿病大鼠中评估了MetCQDs的有效性。结果显示,在30至360分钟的时间段内,与仅接受二甲双胍的组(37.1 - 55.3%)相比,血糖水平显著降低(34.1 - 51.1%)。肝组织的组织病理学检查表明,用MetCQDs治疗的组的肝脏健康指标有所改善。
基于这些结果,该产物通过提高疗效在糖尿病管理中具有潜在的治疗优势,并且与对照组相比可能具有降低的副作用。