Department of Life Science Engineering, Faculty of New Sciences and Technologies, University of Tehran, Tehran, Iran.
School of Biomedical Engineering, University Technology of Sydney, Sydney, New South Wales, 2007, Australia.
Drug Deliv Transl Res. 2019 Jun;9(3):707-720. doi: 10.1007/s13346-019-00636-z.
Dexamethasone is a widely used drug in medical and biological applications. Since the systematic and controllable release of this drug is of significant importance, encapsulation of this anti-inflammatory drug in poly(lactic-co-glycolic acid) (PLGA) nanoparticles can minimize uncontrolled issues. As dexamethasone-encapsulated PLGA nanoparticles are synthesized in the presence of organic solvents, poly(dimethylsiloxane) (PDMS)-based microchannels collapse due to the swelling problem. In present study, PTFE nanoparticles were used for the surface modification of the microchannels to prevent absorption and adhesion of solvents into the microchannels' wall. The contact angle analysis of microchips after coating showed that the surface of microchannels bear the superhydrophobicity feature (140.30°) and SEM images revealed that PTFE covered the surface of PDMS, favorably. Then, the prepared microchip was tested for the synthesis of dexamethasone-loaded nanoparticles. SEM and atomic force microscopy (AFM) images of the synthesized nanoparticles represented that there was not any evidence of adhesion or absorption of nanoparticles. Furthermore, the monodispersity of nanoparticles was discernible. As AFM results revealed, the average diameters of 47, 63, and 82 nm were achieved for flow ratios of 0.01, 0.05, and 0.1, respectively. To evaluate the drug efficiency, cumulative release and encapsulation efficiency were analyzed which showed much more efficiency than the synthesized nanoparticles in the bulk mode. In addition, MTT test revealed that nanoparticles could be considered as a non-toxic material. Since the synthesis of drug-loaded nanoparticles is ubiquitous in laboratory experiments, the approach presented in this study can render more versatility in this regard.
地塞米松在医学和生物应用中是一种广泛使用的药物。由于这种药物的系统和可控释放非常重要,因此将这种抗炎药物封装在聚(乳酸-共-乙醇酸)(PLGA)纳米粒子中可以最小化不可控问题。由于地塞米松包封的 PLGA 纳米粒子是在有机溶剂的存在下合成的,因此聚二甲基硅氧烷(PDMS)基微通道会因溶胀问题而坍塌。在本研究中,使用聚四氟乙烯(PTFE)纳米颗粒对微通道进行表面改性,以防止溶剂吸收和粘附到微通道壁上。涂层后的微芯片接触角分析表明,微通道的表面具有超疏水性特征(140.30°),SEM 图像显示 PTFE 很好地覆盖了 PDMS 的表面。然后,对制备的微芯片进行了负载地塞米松纳米粒子的合成测试。合成纳米粒子的 SEM 和原子力显微镜(AFM)图像表明,没有纳米粒子粘附或吸收的证据。此外,还可以明显看出纳米粒子的单分散性。如 AFM 结果所示,当流量比分别为 0.01、0.05 和 0.1 时,分别获得了 47、63 和 82nm 的平均粒径。为了评估药物效率,分析了累积释放和包封效率,结果表明,与批量合成的纳米粒子相比,其效率更高。此外,MTT 测试表明,纳米粒子可以被认为是一种无毒材料。由于载药纳米粒子的合成在实验室实验中非常普遍,因此本研究中提出的方法在这方面具有更大的通用性。