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Ranibizumab and bevacizumab for neovascular age-related macular degeneration.雷珠单抗和贝伐单抗治疗新生血管性年龄相关性黄斑变性。
N Engl J Med. 2011 May 19;364(20):1897-908. doi: 10.1056/NEJMoa1102673. Epub 2011 Apr 28.
2
Drug delivery to the posterior segment of the eye.药物递送至眼部后节。
Drug Discov Today. 2011 Mar;16(5-6):270-7. doi: 10.1016/j.drudis.2010.12.004. Epub 2010 Dec 15.
3
A prospective randomized trial of intravitreal bevacizumab or laser therapy in the management of diabetic macular edema (BOLT study) 12-month data: report 2.一项关于玻璃体内注射贝伐单抗或激光治疗糖尿病性黄斑水肿的前瞻性随机试验(BOLT 研究)12 个月数据:报告 2。
Ophthalmology. 2010 Jun;117(6):1078-1086.e2. doi: 10.1016/j.ophtha.2010.03.045. Epub 2010 Apr 22.
4
Infectious endophthalmitis after intravitreal injection of antiangiogenic agents.玻璃体内注射抗血管生成药物后发生的感染性眼内炎。
Retina. 2009 May;29(5):601-5. doi: 10.1097/IAE.0b013e31819d2591.
5
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6
Incidence of endophthalmitis related to intravitreal injection of bevacizumab and ranibizumab.与玻璃体内注射贝伐单抗和雷珠单抗相关的眼内炎发病率。
Retina. 2008 Nov-Dec;28(10):1395-9. doi: 10.1097/IAE.0b013e3181884fd2.
7
Efficient intraocular penetration of topical anti-TNF-alpha single-chain antibody (ESBA105) to anterior and posterior segment without penetration enhancer.局部抗TNF-α单链抗体(ESBA105)在无渗透促进剂的情况下对眼内前后节的高效穿透。
Invest Ophthalmol Vis Sci. 2009 Feb;50(2):779-86. doi: 10.1167/iovs.08-2372. Epub 2008 Aug 29.
8
Pharmacokinetics and posterior segment biodistribution of ESBA105, an anti-TNF-alpha single-chain antibody, upon topical administration to the rabbit eye.抗TNF-α单链抗体ESBA105经局部给药至兔眼后的药代动力学及眼后段生物分布
Invest Ophthalmol Vis Sci. 2009 Feb;50(2):771-8. doi: 10.1167/iovs.08-2370. Epub 2008 Aug 29.
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Comparison of bevacizumab, ranibizumab, and pegaptanib in vitro: efficiency and possible additional pathways.贝伐单抗、雷珠单抗和派加他尼的体外比较:疗效及可能的其他作用途径
Invest Ophthalmol Vis Sci. 2008 Oct;49(10):4523-7. doi: 10.1167/iovs.08-2055. Epub 2008 Apr 25.
10
Endophthalmitis associated with intravitreal anti-vascular endothelial growth factor therapy injections in an office setting.门诊环境中玻璃体内注射抗血管内皮生长因子治疗相关的眼内炎
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局部雷珠单抗(Lucentis)在兔眼的潜在穿透性。

Potential penetration of topical ranibizumab (Lucentis) in the rabbit eye.

机构信息

Department of Ophthalmology, University of Virginia, Charlottesville, VA, USA.

出版信息

Eye (Lond). 2011 Nov;25(11):1504-11. doi: 10.1038/eye.2011.225. Epub 2011 Sep 16.

DOI:10.1038/eye.2011.225
PMID:21921952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3213670/
Abstract

PURPOSE

To assess ranibizumab (Lucentis) penetration into the retina after topical administration in a rabbit model.

METHODS

Ranibizumab was topically applied to the right eye of rabbits according to three regimens: every 2 h (q2hr), four times daily (qid), and twice daily (bid). Intraocular penetration of ranibizumab was assessed at 3, 7, 14, 21, and 28 days following initiation of drops. At each time point, the anterior chambers, vitreous cavities, and blood of one of the rabbits from each subgroup were sampled for ranibizumab detection using enzyme-linked immunosorbent assay (ELISA), and both eyes were then enucleated for ranibizumab detection in the retina by confocal immunohistochemistry (CI). Another group of rabbits received intravitreal ranibizumab and was similarly sampled for comparison.

RESULTS

CI showed ranibizumab staining in the right retina after 7 and 14 days of q2hr topical administration in two out of four experiments. No ranibizumab was detected in the left retina at any of the sampling time points. ELISA was positive in the vitreous of the right eye at 14 and 21 days in the q2hr treated rabbits in one out of four experiments. No ranibizumab was detected in the qid and bid subgroups. CI and ELISA of the aqueous and vitreous were consistently positive in the intravitreal group. Mild ranibizumab levels were detected in the blood in both the topical and intravitreal groups.

CONCLUSIONS

Topically applied ranibizumab can be detected in the retina following high-frequency administration in a rabbit model. A trans-scleral route of penetration is suggested.

摘要

目的

评估雷珠单抗(Lucentis)经眼部给药后在兔模型中的视网膜穿透情况。

方法

根据三种方案将雷珠单抗局部应用于兔的右眼:每 2 小时(q2hr)一次、每日四次(qid)和每日两次(bid)。在开始滴眼后第 3、7、14、21 和 28 天,评估雷珠单抗的眼内穿透情况。在每个时间点,从每个亚组的一只兔子的前房、玻璃体腔和血液中取样,使用酶联免疫吸附测定法(ELISA)检测雷珠单抗,然后对双眼进行共聚焦免疫组织化学(CI)检测视网膜中的雷珠单抗。另一组兔接受玻璃体内雷珠单抗注射,并进行类似采样以作比较。

结果

CI 在四个实验中的两个实验中显示,q2hr 局部给药后 7 天和 14 天,右视网膜有雷珠单抗染色。在任何采样时间点,左眼均未检测到雷珠单抗。在一个实验中,q2hr 治疗的兔右眼玻璃体在第 14 和 21 天的 ELISA 为阳性。qid 和 bid 亚组均未检测到雷珠单抗。玻璃体内组的 CI 和 ELISA 均在房水和玻璃体中呈阳性。在局部和玻璃体内组均检测到轻度的雷珠单抗水平在血液中。

结论

在兔模型中,高频给药后可在视网膜中检测到局部应用的雷珠单抗。提示存在经巩膜渗透途径。