Investigation of synthesis and processing of cellulose, cellulose acetate and poly(ethylene oxide) nanofibers incorporating anti-cancer/tumor drug cis-diammineplatinum (II) dichloride using electrospinning techniques

静电纺丝 纳米纤维 材料科学 醋酸纤维素 环氧乙烷 化学工程 扫描电子显微镜 纤维素 聚合物 药物输送 高分子化学 复合材料 纳米技术 共聚物 工程类
作者
Saheem Absar,Mujibur R. Khan,Kyle Edwards,Jeffrey Neumann
出处
期刊:Journal of Polymer Engineering [De Gruyter]
卷期号:35 (9): 867-878 被引量:29
标识
DOI:10.1515/polyeng-2015-0057
摘要

Abstract A model anti-cancer/tumor drug cis-diammineplatinum (II) dichloride (cisplatin) was loaded into micro- and nanofibers of cellulose, cellulose acetate (CA) and poly(ethylene oxide) (PEO), using various electrospinning techniques. Single-nozzle electrospinning was used to fabricate neat fibers of each category. Drug loading in cellulose fibers was performed using single-nozzle electrospinning. Encapsulation of cisplatin in CA and PEO-based fibers was performed using coaxial electrospinning. Morphological analysis of the fibers was performed using scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). The various categories of fibers exhibited diverse morphological features depending on the material compositions and applied process parameters. The drug-loaded cellulose nanofibers showed attached particles on the surface. These particles were composed of both the polymer and the drug. The CA-cisplatin fibers exhibited drug encapsulation within various diverse morphological conformations: hierarchical structures such as straw-sheaf-shaped particles, dendritic branched nanofibers and swollen fibers with large beads. However, in the case of PEO fibers, drug encapsulation was observed inside repeating dumbbell-shaped structures. Morphological development of the fibers and corresponding mode of drug encapsulation were correlated with process parameters such as applied voltage, concentrations and relative feed rates of the solutions and conductivities of the solvents.

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