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在啮齿动物模型中,从单一水凝胶药物递送系统中双释放阿柏西普和地塞米松的治疗效果。

Treatment Efficacy of a Dual Release of Aflibercept and Dexamethasone From a Single Hydrogel Drug Delivery System in a Rodent Model.

作者信息

Rudeen Kayla M, Maloney Chryssa M, Lydon Katherine L, Teixeria Leandro B C, Mieler William F, Kang-Mieler Jennifer J

机构信息

Department of Biomedical Engineering, Illinois Institute of Technology, Chicago, IL, USA.

Local Delivery Translational Sciences, AbbVie, North Chicago, IL, USA.

出版信息

Transl Vis Sci Technol. 2025 Jun 2;14(6):31. doi: 10.1167/tvst.14.6.31.

Abstract

PURPOSE

Age-related macular degeneration (AMD) is the leading cause of vision loss for the elderly population. Wet AMD, which accounts for approximately 15% of AMD cases, is characterized by abnormal blood vessel growth from the choroid into the subretinal space. Although intravitreal anti-vascular endothelial growth factor (VEGF) agents have become the standard of care for wet AMD, there is a growing subset of patients who do not fully respond to monotherapy anti-VEGF treatment. In previously published reports, corticosteroids have shown improvements in treatment efficacy when administered with anti-VEGF in a subset of non-responders to anti-VEGF monotherapy.

METHODS

A combination dexamethasone and aflibercept drug delivery system (Combo-DDS) was evaluated in a laser-induced rodent model of choroidal neovascularization (CNV). Longitudinal monitoring was done through week 22 using fluorescein angiography (FA) and spectral domain optical coherence tomography (SD-OCT). Multi-Otsu thresholding was used to quantify the lesion area based on late-phase FA images. In addition, preliminary safety and biocompatibility of the Combo-DDS were evaluated by intraocular pressure (IOP) measurements, electroretinogram (ERG), and histology (n = 6 eyes/group).

RESULTS

In the laser-induced CNV model, CNV lesions (n = 28-36 lesions/group) were monitored longitudinally. Combo-DDS showed a regression in lesion size starting at week 2 that continued through the end of study. IOP, ERG, and histology showed preliminary safety and biocompatibility of the Combo-DDS.

CONCLUSIONS

This study demonstrated that Combo-DDS maintained treatment efficacy in a laser-induced CNV rodent model for 6 months.

TRANSLATIONAL RELEVANCE

The Combo-DDS shows the potential to eliminate the need for separate dosing regiments of anti-VEGF and corticosteroids for non-responders to anti-VEGF monotherapy.

摘要

目的

年龄相关性黄斑变性(AMD)是老年人群视力丧失的主要原因。湿性AMD约占AMD病例的15%,其特征是脉络膜血管异常生长至视网膜下间隙。尽管玻璃体内抗血管内皮生长因子(VEGF)药物已成为湿性AMD的标准治疗方法,但越来越多的患者对抗VEGF单药治疗没有完全反应。在先前发表的报告中,对于一部分抗VEGF单药治疗无反应的患者,皮质类固醇与抗VEGF联合使用时显示出治疗效果的改善。

方法

在激光诱导的脉络膜新生血管(CNV)啮齿动物模型中评估地塞米松和阿柏西普联合药物递送系统(Combo-DDS)。使用荧光素血管造影(FA)和光谱域光学相干断层扫描(SD-OCT)对第22周进行纵向监测。基于晚期FA图像,采用多阈值分割法量化病变面积。此外,通过眼压(IOP)测量、视网膜电图(ERG)和组织学(每组6只眼)评估Combo-DDS的初步安全性和生物相容性。

结果

在激光诱导的CNV模型中,对CNV病变(每组28 - 36个病变)进行纵向监测。Combo-DDS在第2周开始显示病变大小缩小,并持续到研究结束。IOP、ERG和组织学显示了Combo-DDS的初步安全性和生物相容性。

结论

本研究表明,Combo-DDS在激光诱导的CNV啮齿动物模型中维持了6个月的治疗效果。

转化相关性

对于抗VEGF单药治疗无反应的患者,Combo-DDS显示出有可能无需分别使用抗VEGF和皮质类固醇给药方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e91/12212448/4c6152f61e5e/tvst-14-6-31-f001.jpg

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