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Soluplus 接枝共聚物:用于伤口治疗的纤维状药物输送系统电纺中的潜在新型载体聚合物。

Soluplus graft copolymer: potential novel carrier polymer in electrospinning of nanofibrous drug delivery systems for wound therapy.

机构信息

Department of Pharmacy, Faculty of Medicine, University of Tartu, Nooruse 1, 50411 Tartu, Estonia.

Department of Pharmacy, Faculty of Medicine, University of Tartu, Nooruse 1, 50411 Tartu, Estonia ; Immunology Group, Institute of Biomedicine and Translational Medicine, Faculty of Medicine, University of Tartu, Ravila 19, 50411 Tartu, Estonia.

出版信息

Biomed Res Int. 2014;2014:789765. doi: 10.1155/2014/789765. Epub 2014 Jan 20.

Abstract

Electrospinning is an effective method in preparing polymeric nanofibrous drug delivery systems (DDSs) for topical wound healing and skin burn therapy applications. The aim of the present study was to investigate a new synthetic graft copolymer (Soluplus) as a hydrophilic carrier polymer in electrospinning of nanofibrous DDSs. Soluplus (polyvinyl caprolactam-polyvinyl acetate-polyethylene glycol graft copolymer (PCL-PVAc-PEG)) was applied in the nonwoven nanomats loaded with piroxicam (PRX) as a poorly water-soluble drug. Raman spectroscopy, X-ray powder diffraction, differential scanning calorimetry, and scanning electron microscopy (SEM) were used in the physical characterization of nanofibrous DDSs. According to the SEM results, the drug-loaded PCL-PVAc-PEG nanofibers were circular in cross-section with an average diameter ranging from 500 nm up to 2  µm. Electrospinning stabilized the amorphous state of PRX. In addition, consistent and sustained-release profile was achieved with the present nanofibrous DDSs at the physiologically relevant temperature and pH applicable in wound healing therapy. In conclusion, electrospinning can be used to prepare nanofibrous DDSs of PCL-PVAc-PEG graft copolymer (Soluplus) and to stabilize the amorphous state of a poorly water-soluble PRX. The use of this synthetic graft copolymer can open new options to formulate nanofibrous DDSs for wound healing.

摘要

静电纺丝是一种将聚合物纳米纤维药物输送系统(DDS)用于局部伤口愈合和皮肤烧伤治疗的有效方法。本研究的目的是研究一种新的合成接枝共聚物(Soluplus)作为电纺纳米纤维 DDS 的亲水性载体聚合物。Soluplus(聚己内酯-醋酸乙烯酯-聚乙二醇接枝共聚物(PCL-PVAc-PEG))被应用于载有吡罗昔康(PRX)的无纺纳米垫中,PRX 是一种水溶性差的药物。拉曼光谱、X 射线粉末衍射、差示扫描量热法和扫描电子显微镜(SEM)用于纳米纤维 DDS 的物理特性研究。根据 SEM 结果,载药的 PCL-PVAc-PEG 纳米纤维呈圆形横截面,平均直径从 500nm 到 2μm 不等。静电纺丝稳定了 PRX 的无定形状态。此外,本研究中的纳米纤维 DDS 在生理相关温度和 pH 值下实现了一致且持续的释放,适用于伤口愈合治疗。总之,静电纺丝可用于制备 PCL-PVAc-PEG 接枝共聚物(Soluplus)的纳米纤维 DDS,并稳定水溶性差的 PRX 的无定形状态。这种合成接枝共聚物的使用可以为伤口愈合配方提供新的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2d6/3918357/8f16b3b9d0d6/BMRI2014-789765.001.jpg

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