载万古霉素的纳米结构脂质载体热响应原位凝胶的配方开发和渗透研究:Box-Behnken设计实现眼内炎眼部给药的方法。

Amit Kumar Singh, Prabhat Kumar Upadhyay, Manish Kumar
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引用次数: 0

摘要

眼内炎是眼内腔的一种炎症性疾病,由于其快速进展和潜在的视力丧失,在眼科领域提出了重大挑战。传统的治疗方式,如全身抗生素或口服给药,在达到目标部位所需的治疗水平时往往面临局限性。因此,反复玻璃体内注射抗生素是目前治疗眼内炎的首选和推荐的治疗方法,这是一种侵入性技术,存在一定的缺点,眼压升高,眼内出血,视网膜脱离的可能性增加,视网膜毒性等。万古霉素是治疗眼内炎的首选药物,通过玻璃体内注射给药。目的:本研究旨在设计、开发和评估将万古霉素负载的NLCs整合到原位凝胶中,为眼内炎的治疗提供一种新的无创治疗选择。方法:采用Box - Behnken设计,采用双乳液/溶剂蒸发法制备万古霉素负载的无糖玉米片。通过改变Pluronic F127的浓度,将优化后的配方掺入原位凝胶体系中。通过物理外观、pH值、粘度、胶凝强度、胶凝温度、体外释放曲线和体外渗透研究等参数对配制的凝胶进行表征。结果:该制剂外观光滑,pH值为7 ~ 7.5,接近人眼生理pH值,含量为97.5±1.0% ~ 99.2±1.0%,凝胶温度接近体温。与对照凝胶相比,释放研究制剂(VISG2)的数据显示药物持续释放。体外渗透研究的数据显示,与对照凝胶相比,药物形式(VISG2)的渗透性增加了约3倍(p小于0.0001),与市售配方(p小于0.0001)相比,渗透性显著增加(2.02倍)。结论:负载万古霉素的NLCs结合原位凝胶可作为有创性玻璃体内注射治疗眼内炎的可行选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation Development and Permeation Studies of Vancomycin Hydrochloride-Loaded Nanostructured Lipid Carrier Incorporated Thermoresponsive In-Situ Gel: A Box-Behnken Design Implemented Approach for Ocular Delivery in Endophthalmitis.

Background: Endophthalmitis, an inflammatory condition of the intraocular cavity, poses a significant challenge in ophthalmology due to its rapid progression and potential for vision loss. Conventional treatment modalities, such as systemic antibiotics or oral administration, often face limitations in achieving the required therapeutic levels at the target site. Hence, repeated intravitreal injections of antibiotics are currently the most preferred and recommended therapy for the management of endophthalmitis, which is an invasive technique and has certain shortcomings, elevated intraocular pressure, bleeding inside the eye, heightened likelihood of retinal detachment, retinal toxicity, and many more. Vancomycin is the first choice drug for the management of endophthalmitis and is given through intravitreal injection.

Aim: The work aims to design, develop, and evaluate Vancomycin-loaded NLCs incorporated into an in-situ gel offering a new non-invasive therapeutic option for the management of Endophthalmitis.

Method: The Vancomycin-loaded NLCs were successfully produced through a double emulsion/ solvent evaporation method employing a Box Behnken design. The optimized formulations were incorporated into an in-situ gel system by varying the concentration of Pluronic F127. The formulated gels were characterized for several parameters such as physical appearance, pH, viscosity, gelling strength, gelation temperature, in vitro release profile, and ex-vivo permeation study.

Results: The result revealed that the formulation had a smooth appearance with a pH range from 7 to 7.5, was near the physiological pH of the eye, had content in the range of 97.5 ± 1.0 %to 99.2 ± 1.0 % and gelation temperature near body temperature. The data of release study formulation (VISG2) revealed sustained drug release compared to the control gel. The data ex vivo permeation study revealed that there was approximately a 3 folds increase in permeation of drug form (VISG2) compared to control gel (p˂0.0001) and significant (2.02folds) permeation compared to commercially available formulation (p˂0.0001).

Conclusion: In conclusion, the Vancomycin-loaded NLCs incorporated in-situ gel may serve as a feasible alternative to invasive intravitreal injection for the management of endophthalmitis.

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