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蚕丝工业废弃物蛋白:电纺丝蛋白纳米纤维的分离、纯化与制备,作为一种可能的漂浮型药物递释纳米载体。

Silk industry waste protein: isolation, purification and fabrication of electrospun silk protein nanofibers as a possible nanocarrier for floating drug delivery.

机构信息

Department of Pharmaceutics, Bharati Vidyapeeth College of Pharmacy, Kolhapur, Maharashtra 416013, India.

Department of Pharmaceutical Chemistry, H. R. Patel Institute of Pharmaceutical Education and Research, Shirpur, Maharashtra 425405, India.

出版信息

Nanotechnology. 2021 Jan 15;32(3):035101. doi: 10.1088/1361-6528/abb8a9.

Abstract

Amongst assorted regio-selective and targeted oral drug delivery strategies accepted for the gastro-retentive drug delivery system (GRDDS), the floating drug delivery system (FDDS) holds a major share as clinically accepted formulations. The major objective of the present investigation was to explore the silk industry waste protein, silk fibroin (SF) as a possible electrospun nanocarrier for the FDDS. In a nutshell, electrospinning (ES) is one of the flexible and astonishing strategies for the fabrication of porous electrospun nanofibers (NFs), which offers the potential to amend the floating profile, dissolution rate, solubility, and release patterns of the drug, etc as per compendial requirements. Looking at the prospects of floating SF-NFs preparation, we have isolated and lyophilized the SF from industrial waste cocoons and prepared drug-loaded SF single polymer nanofibers (SPN). Lafutidine (LF) being a good candidate for GRDDS selected as a model drug, which is an excellent proton pump inhibitor, mainly used in the treatment of gastric ulcers. Finally, the obtained LF loaded SF-NFs (LF-SF-NFs) were successfully analyzed for physicochemical characteristics, porosity, swelling index, antioxidant activity, mucoadhesion strength, floating properties, enzymatic degradation, and accelerated stability study, etc. Further, these LF-SF-NFs were evaluated for percent drug content, weight variation, in-vitro dissolution in 0.1 N hydrochloric acid (HCl, pH:1.2) and fasted state simulated gastric fluid (FSSGF), and accelerated stability study. It has shown significant floating time >18 h, about 99% ± 0.58% floating buoyancy with sustained release up to 24 h. LF-SF-NFs showed good compatibility, entrapment efficiency, antioxidant activity, mucoadhesion strength, enzymatic degradation, and long term stability. Soon, the essential floating and drug release profiles can claim single polymer (SF) based electrospun protein NFs as a possible novel oral nanocarrier for FDDS.

摘要

在各种区域选择性和靶向口服药物传递策略中,被接受用于胃滞留药物传递系统(GRDDS)的漂浮药物传递系统(FDDS)占有重要份额,作为临床接受的制剂。本研究的主要目的是探索丝业废料蛋白质丝素(SF)作为 FDDS 可能的电纺纳米载体。简而言之,静电纺丝(ES)是制造多孔电纺纳米纤维(NFs)的灵活而惊人的策略之一,它有可能根据药典要求改善药物的漂浮特性、溶解速率、溶解度和释放模式等。鉴于漂浮 SF-NFs 制备的前景,我们从工业废料蚕茧中分离并冻干 SF,并制备了载药 SF 单聚合物纳米纤维(SPN)。拉呋替丁(LF)是 GRDDS 的良好候选药物,作为质子泵抑制剂,主要用于治疗胃溃疡。最后,成功地对载 LF 的 SF-NFs(LF-SF-NFs)进行了物理化学特性、孔隙率、溶胀指数、抗氧化活性、黏膜粘附强度、漂浮性能、酶降解和加速稳定性研究等分析。此外,还对这些 LF-SF-NFs 进行了含量测定、重量变化、在 0.1N 盐酸(HCl,pH:1.2)和空腹模拟胃液(FSSGF)中的体外溶出度以及加速稳定性研究。结果表明,具有显著的漂浮时间>18 小时,约 99%±0.58%的漂浮浮力,可持续释放长达 24 小时。LF-SF-NFs 显示出良好的相容性、包封效率、抗氧化活性、黏膜粘附强度、酶降解和长期稳定性。很快,基本的漂浮和药物释放特性可以声称基于单一聚合物(SF)的电纺蛋白 NFs 作为 FDDS 的一种新型口服纳米载体。

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