酮咯酸、褪黑素和拉坦前列素三负载PLGA微球对青光眼的神经保护作用。

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Drug Delivery Pub Date : 2025-12-01 Epub Date: 2025-04-11 DOI:10.1080/10717544.2025.2484277
Miriam Ana González-Cela-Casamayor, María J Rodrigo, Marco Brugnera, Inés Munuera, Teresa Martínez-Rincón, Catalina Prats-Lluís, Pilar Villacampa, Julián García-Feijoo, Luis E Pablo, Irene Bravo-Osuna, Elena Garcia-Martin, Rocío Herrero-Vanrell
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引用次数: 0

摘要

青光眼是一种影响视网膜和视神经的多因素神经退行性疾病。这项工作的目的是通过将三种具有降压(拉坦前列素)、抗氧化(褪黑素)和抗炎(酮酸)活性的神经保护物质共包埋在可生物降解的聚乳酸-羟基乙酸(PLGA)微球(MSs)中,达到不同的治疗目标,这些微球在玻璃体内注射后能够释放药物数月,避免重复给药。采用水包油乳化溶剂萃取蒸发技术制备了多负载PLGA质谱,并对其进行了理化表征。PLGA 85:15为所选配方选择的聚合物比例。添加维生素E的三负载MSs在暴露24 h后对视网膜色素上皮细胞表现出良好的耐受性(细胞存活率为90%)。最终制剂(KMLVE)的粒径为33.58±5.44µm,药物含量(µg/mg ms)分别为39.70±5.89、67.28±4.17和7.51±0.58。KMLVE能够在70天内持续释放三种药物。分别于Long-Evans大鼠(n = 20)慢性青光眼诱导后2周和12周注射KMLVE。进行眼科检查,并与未治疗的青光眼动物(n = 45)和健康动物(n = 17)进行比较。经治疗的青光眼大鼠眼压达到最低,双极和视网膜神经节细胞的功能增强,光学相干断层扫描显示神经视网膜厚度增加(p
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ketorolac, melatonin and latanoprost tri-loaded PLGA microspheres for neuroprotection in glaucoma.

Glaucoma is a multifactorial neurodegenerative disease that affects the retina and optic nerve. The aim of this work was to reach different therapeutics targets by co-encapsulating three neuroprotective substances with hypotensive (latanoprost), antioxidant (melatonin) and anti-inflammatory (ketorolac) activity in biodegradable poly (lactic-co-glycolic acid) (PLGA) microspheres (MSs) capable of releasing the drugs for months after intravitreal injection, avoiding the need for repeated administrations. Multi-loaded PLGA MSs were prepared using the oil-in-water emulsion solvent extraction-evaporation technique and physicochemically characterized. PLGA 85:15 was the polymer ratio selected for the selected formulation. Tri-loaded MSs including vitamin E as additive showed good tolerance in retinal pigment epithelium cells after 24 h exposure (>90% cell viability). The final formulation (KMLVE) resulted in 33.58 ± 5.44 µm particle size and drug content (µg/mg MSs) of 39.70 ± 5.89, 67.28 ± 4.17 and 7.51 ± 0.58 for melatonin, ketorolac and latanoprost respectively. KMLVE were able to release in a sustained manner the three drugs over 70 days. KMLVE were injected at 2 and 12 weeks in Long-Evans rats (n = 20) after the induction of chronic glaucoma. Ophthalmological tests were performed and compared to not treated glaucomatous (n = 45) and healthy (n = 17) animals. Treated glaucomatous rats reached the lowest intraocular pressure, enhanced functionality of bipolar and retinal ganglion cells and showed greater neuroretinal thickness by optical coherence tomography (p < 0.05) compared to not treated glaucomatous rats at 24 weeks follow-up. According to the results, the tri-loaded microspheres can be considered as promising controlled-release system for the treatment of glaucoma.

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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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