化工儀器網(wǎng)
資料下載
Nanobrook Omni測(cè)量應(yīng)用案例-03
閱讀：224 發(fā)布時(shí)間：2018-6-19| 提 供 商 | 美國(guó)布魯克海文儀器公司 | 資料大小 | 2.8MB |
|---|---|---|---|
| 資料圖片 | 下載次數(shù) | 0次 | |
| 資料類(lèi)型 | PDF 文件 | 瀏覽次數(shù) | 224次 |
| 免費(fèi)下載 | 點(diǎn)擊下載 |
文獻(xiàn)名： Facile Preparation of Drug-Loaded Tristearin Encapsulated Superparamagnetic Iron Oxide Nanoparticles Using Coaxial Electrospray Processing
作者： Manoochehr Rasekh*†, Zeeshan Ahmad*‡, Richard Cross§, Javier Hernández-Gil†, James D. E. T. Wilton-Ely*† , and Philip W. Miller*†
† Department of Chemistry, Imperial College London, South Kensington, London SW7 2AZ, U.K.
‡ Leicester School of Pharmacy, De Montfort University, Leicester LE1 9BH, U.K.
§ Emerging Technologies Research Centre, De Montfort University, Leicester LE1 9BH, U.K.
摘要：Naturally occurring polymers are promising biocompatible materials that have many applications for emerging therapies, drug delivery systems, and diagnostic agents. The handling and processing of such materials still constitutes a major challenge, which can limit the full exploitation of their properties. This study explores an ambient environment processing technique: coaxial electrospray (CO-ES) to encapsulate genistein (an isoflavonoid and model drug), superparamagnetic iron oxide nanoparticles (SPIONs, 10–15 nm), and a fluorophore (BODIPY) into a layered (triglyceride tristearin shell) particulate system, with a view to constructing a theranostic agent. Mode mapping of CO-ES led to an optimized atomization engineering window for stable jetting, leading to encapsulation of SPIONs within particles of diameter 0.65–1.2 μm and drug encapsulation efficiencies of around 92%. Electron microscopy was used to image the encapsulated SPIONs and confirm core–shell triglyceride encapsulation in addition to further physicochemical characterization (AFM, FTIR, DSC, and TGA). Cell viability assays (MTT, HeLa cells) were used to determine optimal SPION loaded particles (∼1 mg/mL), while in vitro release profile experiments (PBS, pH = 7.4) demonstrate a triphasic release profile. Further cell studies confirmed cell uptake and internalization at selected time points (t = 1, 2, and 4 h). The results suggest potential for using the CO-ES technique as an efficient way to encapsulate SPIONs together with sensitive drugs for the development of multimodal particles that have potential application for combined imaging and therapy.