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Development, optimization and evaluation of tinidazole functionalized electrospun poly-(epsilon-caprolactone) nanofiber membranes for the treatment of periodontitis

机译:锡西唑官能化电纺 - (ε-己内酮)纳米纤维膜治疗牙周炎的开发,优化和评价

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摘要

The aim of this study was to alleviate shortcomings in the treatment of periodontitis by electrospinning of a novel biodegradable poly(epsilon-caprolactone) (PCL) based nanofiber membrane functionalized with tinidazole (TNZ). Box-Behnken design was employed for evaluating influence of formulation and processing variables on entrapment efficiency (EE) and diameter of nanofiber. The optimum batch selected by desirability approach was subjected to physicochemical characterization such as FTIR, DSC and PXRD which revealed entrapment of drug in a molecular dispersion devoid of any chemical interaction with the excipients. Electron microscopy showed smooth structure in nanometre range, without any visible sign of fiber break-up or disruption within the nanofiber membrane. Optimized TNZ-PCL nanofiber membrane exhibited a diameter of 147.6 +/- 7.6 nm and EE 84.36 +/- 1.5%. In vitro release study and antibacterial study demonstrated sustained drug release for up to 20 days, depending upon the drug to polymer ratio and solvent composition. Further, reduction of contact angle (from 123.6 +/- 2.8 to 57.2 +/- 1.9) revealed that incorporation of TNZ enhanced the hydrophilicity of the nanofiber membrane which would facilitate its adhesion to the site of action and instigate proliferation of cells. MTT assay and CLSM study suggested that nanofiber membrane showed no cytotoxicity on mouse fibroblasts (L-929 cell lines). Moreover, in vivo study by ligature-induced periodontitis in rats confirmed that TNZ loaded nanofiber membrane can significantly (p < 0.05) improve continuity of epithelium and transseptal fiber of interdental papilla in comparison to tinidazole gel.
机译:本研究的目的是缓解用酮氮唑(TNZ)官能化的新型可生物降解的聚(ε-己内酯)(PCL)基型纳米纤维膜治疗牙周炎的缺点。 Box-Behnken设计用于评估配方和加工变量对纳米纤维血管效率(EE)和直径的影响。通过期望方法选择的最佳批次进行物理化学表征,例如FTIR,DSC和PXRD,其揭示了含有与赋形剂的任何化学相互作用的分子分散体中的药物。电子显微镜显示纳米范围的光滑结构,没有任何可见的纤维分解或纳米纤维膜中断的迹象。优化的TNZ-PCL纳米纤维膜的直径显示为147.6 +/- 7.6nm,EE 84.36 +/- 1.5%。体外释放研究和抗菌研究证明了持续的药物释放,最多20天,取决于药物与聚合物比和溶剂组合物。此外,减少接触角(从123.6 +/- 2.8至57.2 +/-1.9)显示,掺入TNZ增强了纳米纤维膜的亲水性,这将促进其对动作部位的粘附并施加细胞的增殖。 MTT测定和CLSM研究表明,纳米纤维膜在小鼠成纤维细胞(L-929细胞系)上没有表现出细胞毒性。此外,在大鼠的结扎诱导的牙周炎的体内研究证实,TNZ负载的纳米纤维膜可以显着(P <0.05),与锡咪唑凝胶相比,改善了胞间乳头的上皮和静物纤维的连续性。

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  • 来源
    《RSC Advances》 |2016年第102期|共16页
  • 作者单位

    Banaras Hindu Univ Indian Inst Technol Dept Pharmaceut Varanasi 221005 Uttar Pradesh India;

    Banaras Hindu Univ Indian Inst Technol Dept Pharmaceut Varanasi 221005 Uttar Pradesh India;

    Banaras Hindu Univ Indian Inst Technol Dept Pharmaceut Varanasi 221005 Uttar Pradesh India;

    Banaras Hindu Univ Indian Inst Technol Dept Pharmaceut Varanasi 221005 Uttar Pradesh India;

    Banaras Hindu Univ Indian Inst Technol Dept Pharmaceut Varanasi 221005 Uttar Pradesh India;

    Banaras Hindu Univ Indian Inst Technol Dept Pharmaceut Varanasi 221005 Uttar Pradesh India;

    Banaras Hindu Univ Indian Inst Technol Dept Chem Engn Varanasi 221005 Uttar Pradesh India;

    Banaras Hindu Univ Indian Inst Technol Dept Pharmaceut Varanasi 221005 Uttar Pradesh India;

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  • 正文语种 eng
  • 中图分类 化学;
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