Design and Optimization of Ganciclovir Nanosuspension Loaded In Situ Gelling Mucoadhesive Eye Drops for Herpetic Keratitis

Phuvamin Suriyaamporn, Boonnada Pamornpathomkul, Theerasak Rojanarata, Prasopchai Patrojanasophon, Praneet Opanasopit, Tanasait Ngawhirunpat
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Abstract

Ganciclovir (GCR), an antiviral drug used to treat herpetic keratitis, is less effective because of its poor bioavailability (BCS III). Nanosuspension (NS) is a promising technique for improving solubility and the dissolution of poorly soluble drugs by size reduction. Topical solution or conventional eye drop represents the easiest route to deliver drugs to the anterior eye segment; however, low precorneal retention, high nasolacrimal drainage, and metabolic degradation lead to low bioavailability. To overcome these limitations, incorporating GCR-NS into mucoadhesive in situ gel-forming (ISG) could enhance its ocular permeability and drug bioavailability. Therefore, this study aimed to design and optimize GCR-NS-loaded in situ gelling mucoadhesive eye drops (GCR-NS-loaded mucoadhesive ISG) for improving ophthalmic delivery. Pluronic® F127 (P127), an ophthalmic gel forming, was selected as a polymer due to self-gelling formation by temperature-triggered in situ gelling at ocular temperature. Moreover, hyaluronic acid-modified catechol (HA-cat), a novel mucoadhesive polymer, was combined to achieve the desired ocular mucoadhesion and facilitate ophthalmic delivery. Optimized GCR-NS formulation prepared using the nanoprecipitation technique was selected based on the central composite design (CCD) model by evaluating their particle size, polydispersity index (PDI), and zeta potential, before being loaded into mucoadhesive ISG. The optimal GCR-NS-loaded mucoadhesive ISG (F7) revealed the desired physicochemical properties with better viscosity, mucoadhesion, and gelling capacity at physiological conditions, high ocular permeation with a sustained manner over 24 h compared to eye drop suspension. Accordingly, GCR-NS-loaded mucoadhesive ISG could be a promising ocular delivery system for the effective local delivery of GCR for herpetic keratitis. Keywords: Ganciclovir, Nanosuspension, Mucoadhesive eye drop, Ophthalmic delivery, In situ gelling
更昔洛韦纳米混悬液原位胶凝黏液滴眼液的设计与优化
更昔洛韦(GCR)是一种用于治疗疱疹性角膜炎的抗病毒药物,由于其生物利用度差(BCS III),效果较差。纳米混悬液(NS)是一种很有前途的技术,可以通过减小粒径来改善难溶性药物的溶解性和溶解性。局部滴眼液或常规滴眼液是最容易将药物输送到前眼段的途径;然而,低角膜前潴留,高鼻泪引流和代谢降解导致低生物利用度。为了克服这些局限性,将GCR-NS加入黏液原位凝胶形成(ISG)中可以提高其眼通透性和药物生物利用度。因此,本研究旨在设计和优化加载gcr - ns的原位胶凝黏液滴眼液(gcr - ns加载黏液ISG),以改善眼部给药。Pluronic®F127 (P127)是一种眼科凝胶形成剂,由于其在眼温下通过温度触发原位凝胶形成自凝胶,因此被选为聚合物。此外,结合透明质酸修饰的儿茶酚(HA-cat),一种新型的黏附聚合物,可以达到理想的眼部黏附,方便眼内输送。基于中心复合设计(CCD)模型,通过评价纳米沉淀法制备的GCR-NS的粒径、多分散性指数(PDI)和zeta电位,选择最佳的GCR-NS配方,然后将其加载到黏胶ISG中。与滴眼液相比,最佳的gcr - ns负载黏液ISG (F7)在生理条件下具有更好的黏度、黏附性和胶凝能力,并具有高的持续24小时的眼透性。因此,负载GCR- ns的黏附ISG可能是一种有前景的用于疱疹性角膜炎的GCR局部有效递送的眼部递送系统。关键词:更昔洛韦,纳米悬浮液,黏液滴眼液,眼内给药,原位胶凝
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