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近红外光热激活载药微胶囊用于体外靶向递送和释放:糖尿病视网膜病变的一种替代治疗方法。

NIR photothermal-activable drug-conjugated microcapsules for in vitro targeted delivery and release: An alternative treatment of diabetic retinopathy.

机构信息

Nanobiophotonics and Laser Microspectroscopy Centre, Interdisciplinary Research Institute in Bio-Nano-Sciences, Babes-Bolyai University, 42 Treboniu Laurian Street, 400271 Cluj-Napoca, Romania.

Faculty of Veterinary Medicine, University of Agricultural Sciences and Veterinary Medicine, 3-5 Mănăştur Street, 400372 Cluj-Napoca, Romania.

出版信息

Int J Pharm. 2023 Mar 25;635:122700. doi: 10.1016/j.ijpharm.2023.122700. Epub 2023 Feb 9.

Abstract

Diabetic retinopathy (DR) is one of the most serious complications of diabetes, which leads to blindness. By addressing the traditional treatment limitations, we developed a novel light-responsive targeted polymeric microcapsule able to encapsulate a near infrared (NIR) photoactive fluorophore - Indocyanine Green, owing to its photothermal properties. Moreover, for an efficient in vitro targeted drug delivery, the fluorescent microsystem was conjugated with a therapeutic agent, i.e., Avastin drug - a Food and Drug Administration approved therapeutic antibody. The microcapsules were fabricated and evaluated in terms of morphology, encapsulation and drug conjugation efficiency and its release capacity. Avastin-conjugated microcapsules with an average dimension of 4.5 ± 0.35 μm were obtained, according to Scanning Electron Microscopy and Re-Scanning Confocal Microscopy (RCM) investigations. The capacity of the microcapsules to operate as effective phototherapeutic agents by generating heat under NIR laser irradiation was evaluated, followed by the investigation of the microcapsule's shell rupture and NIR laser-induced release of Avastin. The biocompatibility of the Avastin-conjugated microcapsules was proven by WST-1 assay. In vitro cellular internalization and localization of the Avastin microcarriers were determined through Conventional fluorescence microscopy, RCM and Transmission Electron Microscopy imaging techniques. Finally, the Avastin-conjugated microcapsules were validated for in vitro targeted drug delivery and release directly under simulated DR conditions, which could certainly become a successful strategy in DR fighting.

摘要

糖尿病性视网膜病变(DR)是糖尿病最严重的并发症之一,可导致失明。通过解决传统治疗的局限性,我们开发了一种新型的光响应靶向聚合物微胶囊,能够封装近红外(NIR)光活性荧光染料-吲哚菁绿,由于其光热性质。此外,为了实现高效的体外靶向药物递送,荧光微系统与治疗剂(即阿瓦斯汀药物-一种获得美国食品和药物管理局批准的治疗性抗体)缀合。根据扫描电子显微镜和再扫描共聚焦显微镜(RCM)研究,对微胶囊进行了形态、包封和药物缀合效率及其释放能力的评估。根据扫描电子显微镜和再扫描共聚焦显微镜(RCM)研究,获得了平均尺寸为 4.5±0.35μm 的阿瓦斯汀缀合微胶囊。评估了微胶囊在 NIR 激光照射下产生热量作为有效光疗剂的能力,随后研究了微胶囊壳的破裂和 NIR 激光诱导的阿瓦斯汀释放。通过 WST-1 测定法证明了阿瓦斯汀缀合微胶囊的生物相容性。通过常规荧光显微镜、RCM 和透射电子显微镜成像技术确定了阿瓦斯汀微载体的体外细胞内化和定位。最后,对阿瓦斯汀缀合微胶囊在模拟 DR 条件下的体外靶向药物递送和释放进行了验证,这无疑将成为对抗 DR 的一种成功策略。

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