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Corneal changes after collagen crosslinking for keratoconus using dual scheimpflug imaging
摘要： Purpose: To evaluate corneal changes after collagen crosslinking (CXL) therapy for keratoconus (KCN) using the Galilei dual Scheimpflug analyzer. Methods: This prospective, nonrandomized clinical study included 35 eyes of 32 keratoconus patients who had undergone CXL. The eyes were saturated with riboflavin solution and were subjected for 30 minutes to ultraviolet-A (UV-A) light with irradiance of 3 mW/cm2. Effectiveness of the treatment was assessed by measuring uncorrected visual acuity (UCVA), best-corrected visual acuity (BCVA), manifest cylinder/sphere, keratometry, pachymetry, posterior and anterior elevations by the Galilei dual Scheimpflug analyzer. Prior to treatment and 8 months after therapy, Scheimpflug analysis was performed using the Galilei system. The four sets of data including keratometry values, pachymetry, elevation parameters and surface indices were statistically analyzed and compared. Results: Mean patient age was 22.3 ± 3.8 years and mean postoperative follow-up was 8.1 ± 3.2 months. There was a significant increase in UCVA (0.54 ± 0.35 Log MAR preoperatively to 0.49 ± 0.34 LogMAR postoperatively, P = 0.01) and BCVA (0.21 ± 0.19 Log MAR preoperatively to 0.16 ± 0.17 LogMAR postoperatively, P = 0.01). Mean cycloplegic spherical equivalent refractive error was ?4.13 ± 2.65 Diopter (D) preoperatively and ? 4.67 ± 2.96 D postoperatively (P < 0.001). During the follow-up period, no significant difference was observed in pachymetric and elevation data postoperatively. Conclusion: Corneal stabilization could be achieved by collagen crosslinking therapy for keratoconus in terms of corneal thickness, keratometry values, elevation parameters and surface indices.
关键词： Keratoconus,Galilei Dual Scheimpflug Analyzer,Collagen Crosslinking
更新于2025-09-04 15:30:14
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Synthesis and characterization of photo-crosslinkable coumarin-containing polymer dielectric for organic transistors
摘要： Herein, a photo-crosslinkable coumarin-containing polymer, poly(7-(4-vinyl-benzyloxyl)-4-methylcoumarin) or PVBMC, was prepared, and its physicochemical and electrical properties as a gate dielectric in organic electronic devices, such as organic thin-film transistor (OTFT) and inverter, was evaluated. The crosslinking of PVBMC by exposure to UV light (365 nm) over time was characterized using Fourier-transform IR and UV-visible spectroscopy. The measured capacitance of the cross-linked PVBMC thin film in a metal-insulator-metal-type capacitor was as high as 36.4 pF/mm2. Pentacene-based OTFT and load-type inverter with the cross-linked PVBMC gate dielectric were prepared, and their electrical responses were evaluated under ambient conditions. The OTFT showed dominant hole charge carrier transport behavior with a field-effect mobility of 1.52 · 10-1 cm2/Vs and negligible hysteresis. The load-type inverter based on the OTFT exhibited moderate static and dynamic switching responses to the applied electrical pulse. These results suggest the potential application of photo-crosslinked PVBMC as a gate dielectric in the fabrication of high-performance OTFT-based devices.
关键词： Gate dielectric,Polymer film,Organic thin-film transistor,Photo-crosslinking
更新于2025-09-04 15:30:14
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RNA-protein UV-crosslinking Assay
摘要： RNA-protein interactions play a crucial role in every aspect of RNA metabolism, and also plays a major role in post-transcriptional gene regulation. RNA-binding proteins have been implicated in viral gene expression (Ray and Das, 2002) and microRNA-mediated gene regulation (Poria et al., 2016). Here we have described the protocol which (1) covalently links transiently interacting RNA-protein complexes by UV crosslinking, (2) removes the unprotected RNA by RNase digestion and (3) detects the RNA-protein complexes by SDS-PAGE analysis. This protocol provides a rapid and reliable means to directly assay RNA-protein interactions and their kinetics using purified proteins and also help in identifying novel RNA-protein interactions
关键词： UV-crosslinking,RNA-protein interaction,RNA-binding proteins
更新于2025-09-04 15:30:14