壳聚糖包覆隐形眼镜治疗棘阿米巴角膜炎的眼科给药系统:初步假设

M. Sadeghi, P. Tajzadeh, S. Zarei‐Ghanavati, M. Arefnezhad
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引用次数: 1

摘要

背景:棘阿米巴可引起毁灭性的与隐形眼镜(CL)相关的微生物角膜炎。它的培养不太敏感,而且几乎没有证据表明药物的安全性或有效性。因此,早期诊断和最佳治疗仍然很困难。本研究的目的是提出一种新型壳聚糖包被cl基眼科给药系统对棘阿米巴角膜炎具有治疗和预防作用的假设。假设:基于cl的给药是一种流行的缓释给药方式,延长了药物释放时间,从而提高了药物的生物利用度和治疗效果。壳聚糖是几丁质的衍生物,对真菌、酵母和细菌具有抗氧化和广谱抗菌特性。它对微生物细胞起作用;然而,其作用机制是抑菌还是杀菌仍不清楚。它具有伤口愈合和成膜特性。壳聚糖复合薄膜允许可见光的高透射率,使其透明,因此是开发CLs的理想选择。壳聚糖/Ag/ZnO共混膜具有抗菌活性。此外,壳聚糖、透明质酸钠、氢溴酸聚赖氨酸和海藻酸钠包覆的软CLs显示出药物传递特性,并减少了细菌的生长。近年来,研究人员报道了壳聚糖和纳米壳聚糖对棘阿米巴滋养体和囊状棘阿米巴的抗阿米巴活性。基于现有证据,我们假设壳聚糖包被的cl基眼科给药系统可能对棘阿米巴角膜炎或随后的眼内炎具有治疗和预防作用。结论:壳聚糖纳米涂层的CLs或眼内植入物单独或联合常规治疗可预防或治疗棘阿米巴角膜炎或眼内炎。需要进行实验研究和进一步的临床试验来探索其有效性和安全性。此外,在健康眼睛(软性或硬质CLs或角膜塑形镜)中进行的随机对照试验可能会揭示这种新型药物输送系统的预防作用。使用壳聚糖基纳米涂层的其他形式的眼科药物输送系统应该进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chitosan-coated contact lens-based ophthalmic drug delivery system to manage Acanthamoeba keratitis: a preliminary hypothesis
Background: Acanthamoeba species can cause devastating contact lens (CL)-related microbial keratitis. Its culture is less sensitive, and little evidence is available for the safety or efficacy profile of medications. Therefore, early diagnosis and optimal treatment remain difficult. The aim of this study was to present the hypothesis that a novel chitosan-coated CL-based ophthalmic drug delivery system has therapeutic and prophylactic effects on acanthamoeba keratitis. Hypothesis: CL-based drug delivery is a popular sustained-release drug delivery that extends the drug release time, thus increasing its bioavailability and treatment efficacy. Chitosan, a derivative of chitin, has antioxidant and broad-spectrum antimicrobial properties against fungi, yeasts, and bacteria. It acts against microbial cells; however, whether its mechanism of action is microbiostatic or microbicidal remains unknown. It exhibits wound healing and film-forming properties. Chitosan composite films permit high transmittance of visible light, making it transparent and therefore desirable for the development of CLs. Chitosan/Ag/ZnO blend films exhibit antimicrobial activities. Further, soft CLs coated with chitosan, sodium hyaluronate, polylysine hydrobromide, and sodium alginate show drug delivery properties and reduced bacterial growth. Recently, concentration-dependent anti-amoebic activities of chitosan and nano-chitosan against the trophozoite and cystic forms of Acanthamoeba have been reported. Based on the existing evidence, we hypothesized that a chitosan-coated CL-based ophthalmic drug delivery system could have therapeutic and prophylactic effects on acanthamoeba keratitis or subsequent endophthalmitis. Conclusions:  CLs or intraocular implants with chitosan-based nanocoatings alone or in combination with routine treatment may be preventive or therapeutic for acanthamoeba keratitis or endophthalmitis. Experimental studies and further clinical trials are required to explore the efficacy and safety profile. Moreover, randomized controlled trials in healthy eyes with soft or hard CLs or orthokeratology lenses for refractive error correction may shed light on the prophylactic effect of this novel drug delivery system. Other forms of ophthalmic drug delivery systems using chitosan-based nanocoatings should be studied additionally.
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