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尼罗红负载的纳米结构脂质载体(NLCs)经猪眼角膜的渗透。

Penetration of Nile red-loaded nanostructured lipid carriers (NLCs) across the porcine cornea.

机构信息

Faculty of Pharmaceutical Sciences, Naresuan University, Phitsanulok, Thailand.

School of Optometry, Indiana University, Bloomington, IN, United States.

出版信息

Colloids Surf B Biointerfaces. 2019 Apr 1;176:371-378. doi: 10.1016/j.colsurfb.2019.01.018. Epub 2019 Jan 9.

Abstract

Nile Red-loaded nanostructured lipid carriers (NR-NLCs), prepared by high-pressure homogenization technique, have been investigated for their transcorneal penetration using a confocal scanning microfluorometer (CSMF). Topical exposure of NR-NLCs led to their penetration into the epithelium and anterior stroma. The NR-NLC-40 (NR-NLCs of 40 nm) showed faster penetration compared to NR-NLC-150 (NR-NLCs of 150 nm). The surface modification of NR-NLC-40 with polyethylene glycol 400 (NR-NLC-PEG) and stearylamine (NR-NLC-SA), although did not cause any significant effect on size, resulted in an increased penetration into the epithelium concomitant with a reduced penetration into the stroma compared to the NR-NLC-40. Ex vivo mucoadhesion assay revealed that NR-NLC-PEG and NR-NLC-SA adhered more strongly to the porcine corneal surface compared to NR-NLC-40. Flow cytometry experiments with porcine corneal epithelial cells showed that NR-NLC-40 was internalized better than NR-NLC-PEG and NR-NLC-SA. These results, taken together, suggest that NLCs are potentially useful for lipophilic drug delivery to the corneal epithelium and anterior stroma without any surface modifications. However, surface modifications with polyethylene glycol 400 or stearylamine could be useful to treat ocular surface disorders.

摘要

尼罗红负载的纳米结构脂质载体(NR-NLCs),通过高压匀质技术制备,使用共聚焦扫描微荧光计(CSMF)研究了其穿透角膜的能力。NR-NLCs 的局部暴露导致其穿透上皮和前基质。与 NR-NLC-150(150nm 的 NR-NLCs)相比,NR-NLC-40(40nm 的 NR-NLCs)显示出更快的穿透速度。尽管 NR-NLC-40 的表面用聚乙二醇 400(NR-NLC-PEG)和硬脂胺(NR-NLC-SA)进行修饰并没有对粒径产生任何显著影响,但与 NR-NLC-40 相比,它增加了穿透上皮的能力,同时减少了穿透基质的能力。离体粘膜粘附试验表明,与 NR-NLC-40 相比,NR-NLC-PEG 和 NR-NLC-SA 更强烈地粘附在猪角膜表面。用猪角膜上皮细胞进行的流式细胞术实验表明,NR-NLC-40 的内化能力优于 NR-NLC-PEG 和 NR-NLC-SA。这些结果表明,NLC 可有效地将亲脂性药物递送至角膜上皮和前基质,而无需进行任何表面修饰。然而,用聚乙二醇 400 或硬脂胺进行表面修饰可能对治疗眼表面疾病有用。

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