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静电纺丝聚(丙烯酸)/葡聚糖纳米纤维缓释系统的制备及其在创伤敷料中的应用。

Fabrication of Sustained Release System of Electrospun Poly(acrylic acid)/Dextran Nanofibers Using Emulsion Electrospinning as Wound Dressing Applications.

机构信息

Department of Chemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.

PG and Research Department of Chemistry, Jamal Mohamed College (Affiliated to Bharathidasan University), Tiruchirappalli 620020, Tamilnadu, India.

出版信息

J Nanosci Nanotechnol. 2021 Mar 1;21(3):1613-1622. doi: 10.1166/jnn.2021.18987.

Abstract

The burst release of drug is a problem associated with the use of common blending electrospinning. This problem can be avoided via fabrication of core-shell nanofibers where drug can be coated with polymer nanofibers as a shell. Moreover, there is a need to provide wound dressing with prolonged system of sustained release to accelerate the recovery of the wound. Currently, electrospun ciprofloxacin loaded poly(acrylic acid)/Dextran (Cipro@PAA/Dex) core-shell nanofibers can be prepared in green method using emulsion electrospinning. For comparison study, blend electrospun nanofibers (Cipro/PAA/Dex) was also prepared. The entrapment of drug into the polymeric material and the interaction between polymer blends were confirmed by FT-IR. Moreover, DSC was used to identify the type of interaction between polymeric chains. Field emission scanning electron microscope (FE-SEM) was used to study the nanofiber morphology and transmission electron microscope (TEM) and confocal laser scanning microscope (CLSM) were used to confirm the formation of core-shell structure. drug release profile was monitored by UV-Vis spectrophotometer and the results showed that Cipro@PAA/Dex exhibited controlled release behavior whereas Cipro/PAA/Dex showed burst release behavior. Moreover, the release mechanism is kinetically followed diffusion.

摘要

药物的突释是与常见共混静电纺丝使用相关的问题。通过制备核壳纳米纤维可以避免这个问题,其中药物可以被聚合物纳米纤维作为壳包裹。此外,需要为伤口敷料提供延长的持续释放系统,以加速伤口的恢复。目前,可以使用乳液静电纺丝在绿色方法中制备载有环丙沙星的聚(丙烯酸)/葡聚糖(Cipro@PAA/Dex)核壳纳米纤维。为了进行比较研究,还制备了共混静电纺纳米纤维(Cipro/PAA/Dex)。通过傅里叶变换红外光谱(FT-IR)确认了药物被包埋在聚合物材料中和聚合物共混物之间的相互作用。此外,差示扫描量热法(DSC)用于鉴定聚合物链之间的相互作用类型。场发射扫描电子显微镜(FE-SEM)用于研究纳米纤维形态,透射电子显微镜(TEM)和共聚焦激光扫描显微镜(CLSM)用于确认核壳结构的形成。通过紫外可见分光光度计监测药物释放曲线,结果表明 Cipro@PAA/Dex 表现出控制释放行为,而 Cipro/PAA/Dex 表现出突释行为。此外,释放机制动力学上遵循扩散。

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