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应用共聚焦显微镜对商业性软性接触镜中全长重组人蛋白聚糖-4 的定位研究。

Localization of full-length recombinant human proteoglycan-4 in commercial contact lenses using confocal microscopy.

机构信息

Centre for Ocular Research & Education (CORE), School of Optometry and Vision Science, University of Waterloo, Waterloo, Ontario, Canada.

Department of Emergency Medicine, Alpert Medical School & School of Engineering, Brown University, Providence, Rhode Island, USA.

出版信息

J Biomater Sci Polym Ed. 2020 Jan;31(1):110-122. doi: 10.1080/09205063.2019.1678454. Epub 2019 Oct 21.

Abstract

The aim of this study was to determine the sorption location of full-length recombinant human proteoglycan 4 (rhPRG4) tagged with fluorescein isothiocyanate (FITC) to four silicone hydrogel contact lenses [balafilcon A (PureVision, Bausch + Lomb), senofilcon A (Acuvue Oasys, Johnson & Johnson), comfilcon A (Biofinity, CooperVision), lotrafilcon B (Air Optix, Alcon)] and one conventional hydrogel lens [etafilcon A (Acuvue 2, Johnson & Johnson)], using confocal laser scanning microscopy (CLSM). Lenses ( = 3 each) were incubated under two conditions: (1) FITC-rhPRG4 solution at 300 μg/mL and (2) phosphate-buffered saline, for 1 h at 37 °C in darkness with gentle shaking. The central 4 mm of each lens was removed and viewed with the Zeiss 510 CLSM using an argon laser at 488 nm (FITC excitation 495 nm, emission 521 nm). Depth scans were taken at 1 μm intervals to a maximum depth of 100 μm. All lens materials demonstrated sorption of rhPRG4. Both senofilcon A and balafilcon A revealed FITC-rhPRG4 penetration into the bulk of the lens, generally favoring the surface. rhPRG4 was observed exclusively on the surface of lotrafilcon B, with no presence within the bulk of the lens. rhPRG4 was evenly distributed throughout the bulk of the lens, as well as on the surface, for comfilcon A and etafilcon A. The sorption profile of FITC-rhPRG4 was successfully visualized using CLSM in various contact lens materials. The polymer composition, surface treatment and pore size of the material can influence the sorption of rhPRG4.

摘要

本研究旨在通过共焦激光扫描显微镜(CLSM)确定全人源蛋白聚糖 4(rhPRG4)与荧光素异硫氰酸酯(FITC)缀合后的吸附位置,该蛋白被标记的 rhPRG4 用于四种硅水凝胶接触镜[巴非康 A(PureVision,Bausch + Lomb)、新氧康 A(Acuvue Oasys,强生)、康菲康 A(Biofinity,库博)、露得清 B(Air Optix,爱尔康)]和一种常规水凝胶镜片[埃夫康 A(Acuvue 2,强生)]。镜片(各 3 个)在两种条件下孵育:(1)300μg/mL 的 FITC-rhPRG4 溶液;(2)磷酸盐缓冲盐水,在 37°C 黑暗中以轻微摇动的方式孵育 1 小时。每个镜片的中央 4mm 被切除,并使用 Zeiss 510 CLSM 进行观察,氩激光 488nm(FITC 激发 495nm,发射 521nm)。每隔 1μm 进行深度扫描,最大深度为 100μm。所有镜片材料均显示出 rhPRG4 的吸附。新氧康 A 和巴非康 A 均显示出 FITC-rhPRG4 渗透到镜片的大部分,通常偏向于表面。仅在露得清 B 的表面观察到 rhPRG4,而在镜片的大部分中没有存在。rhPRG4 在康菲康 A 和埃夫康 A 的镜片大部分中均匀分布,以及在表面上。在各种接触镜材料中,使用 CLSM 成功地可视化了 FITC-rhPRG4 的吸附模式。材料的聚合物组成、表面处理和孔径大小会影响 rhPRG4 的吸附。

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