二甲双胍
表面张力
微流控
材料科学
纳米颗粒
分散性
纳米技术
2型糖尿病
纳米粒子跟踪分析
药物输送
医学
化学工程
生物医学工程
微气泡
化学
聚合物
糖尿病
复合材料
高分子化学
微泡
生物化学
量子力学
小RNA
超声波
内分泌学
工程类
放射科
物理
基因
作者
Sumeyye Cesur,Muhammet Emin Çam,Fatih Serdar Sayın,Sena Su,A. H. Harker,Mohan Edirisinghe,Oğuzhan Gündüz
出处
期刊:Langmuir
[American Chemical Society]
日期:2021-06-06
卷期号:38 (17): 5040-5051
被引量:48
标识
DOI:10.1021/acs.langmuir.1c00587
摘要
Type 2 diabetes mellitus (T2DM) is a chronic metabolic disease that is increasingly common all over the world with a high risk of progressive hyperglycemia and high microvascular and macrovascular complications. The currently used drugs in the treatment of T2DM have insufficient glucose control and can carry detrimental side effects. Several drug delivery systems have been investigated to decrease the side effects and frequency of dosage, and also to increase the effect of oral antidiabetic drugs. In recent years, the use of microbubbles in biomedical applications has greatly increased, and research into microactive carrier bubbles continues to generate more and more clinical interest. In this study, various monodisperse polymer nanoparticles at different concentrations were produced by bursting microbubbles generated using a T-junction microfluidic device. Morphological analysis by scanning electron microscopy, molecular interactions between the components by FTIR, drug release by UV spectroscopy, and physical analysis such as surface tension and viscosity measurement were carried out for the particles generated and solutions used. The microbubbles and nanoparticles had a smooth outer surface. When the microbubbles/nanoparticles were compared, it was observed that they were optimized with 0.3 wt % poly(vinyl alcohol) (PVA) solution, 40 kPa pressure, and a 110 μL/min flow rate, thus the diameters of the bubbles and particles were 100 ± 10 μm and 70 ± 5 nm, respectively. Metformin was successfully loaded into the nanoparticles in these optimized concentrations and characteristics, and no drug crystals and clusters were seen on the surface. Metformin was released in a controlled manner at pH 1.2 for 60 min and at pH 7.4 for 240 min. The process and structures generated offer great potential for the treatment of T2DM.
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