Optimizing riboflavin delivery with co-crystal and in situ hydrogel formulations for management of keratoconus: A comprehensive investigation with in vitro, ex vivo and in vivo studies

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY International Journal of Pharmaceutics Pub Date : 2025-03-07 DOI:10.1016/j.ijpharm.2025.125435
Eren Aytekin , Melih Zeki Kaya , Göksu Eylül İlkar , Heybet Kerem Polat , Naile Öztürk , İmran Vural , Hasan Basri Çakmak , Mustafa Çelebier , Erhan Palaska , Sema Çalış , Sibel Bozdağ Pehlivan
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Abstract

Keratoconus is a progressive disease characterized by corneal thinning and conical deformation. Corneal cross-linking, a common treatment, strengthens collagen fibers using vitamin B2 (riboflavin) and UVA light. However, the surgical removal of the corneal epithelium (Epi-Off) required for riboflavin penetration causes complications and may affect treatment success. To address this, research has focused on delivering riboflavin without removing the epithelium (Epi-On). In this study, riboflavin-based hydrogel and co-crystal formulations were developed and evaluated through in vitro, ex vivo, and in vivo studies.
Co-crystals were prepared using trehalose, dextrose, mannitol, and nicotinamide as agents, employing solvent evaporation and co-mixing methods. These formulations were characterized using DSC (Differential Scanning Calorimetry), XRD (X-Ray Diffraction), and FTIR (Fourier Transform Infrared Spectroscopy), identifying 1R1N (1 unit mol riboflavin and 1 unit mol nicotinamide co-crystals) and 1R1M (1 unit mol riboflavin and 1 unit mol mannitol co-crystals) groups as promising candidates. Thermosensitive hydrophilic gels containing riboflavin or riboflavin-5-phosphate sodium and Transcutol P (a permeation enhancer) were also developed, using Pluronic F-127 as the polymer. The 18 % Pluronic F-127 gel formed at 31.4 ± 0.2 °C. Drug release studies showed faster release from riboflavin-5-phosphate sodium formulations, while ex vivo retention studies revealed higher corneal retention for co-crystals. In vivo studies on rat corneas demonstrated superior drug concentrations for riboflavin formulations compared to riboflavin-5-phosphate sodium, with hydrophilic gels showing prolonged corneal contact time.
The THJ-TP formulation (Riboflavin-5-phosphate sodium and permeation enhancer (Transcutol P) containing hydrophilic gel formulations), containing riboflavin-5-phosphate sodium and Transcutol P, emerged as the most promising candidate. This research represents a significant advancement towards a non-invasive riboflavin-based treatment for keratoconus.

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优化核黄素递送的共晶和原位水凝胶配方管理圆锥角膜:一个全面的调查与体外,离体和体内研究。
圆锥角膜是一种以角膜变薄和锥形变形为特征的进行性疾病。角膜交联是一种常用的治疗方法,利用维生素B2(核黄素)和UVA光增强胶原纤维。然而,手术切除核黄素渗透所需的角膜上皮(Epi-Off)会引起并发症,并可能影响治疗成功。为了解决这个问题,研究重点是在不去除上皮的情况下递送核黄素(Epi-On)。在这项研究中,基于核黄素的水凝胶和共晶配方被开发出来,并通过体外、离体和体内研究进行了评估。以海藻糖、葡萄糖、甘露醇和烟酰胺为原料,采用溶剂蒸发和共混法制备共晶。利用DSC(差示扫描量热法)、XRD (x射线衍射)和FTIR(傅里叶变换红外光谱)对这些配方进行了表征,确定了1R1N(1单位mol核黄素和1单位mol烟酰胺共晶)和1R1M(1单位mol核黄素和1单位mol甘露醇共晶)基团是有希望的候选基团。以Pluronic F-127为聚合物,制备了含有核黄素或5-磷酸核黄素钠和Transcutol P(一种渗透增强剂)的热敏亲水性凝胶。18 % Pluronic F-127凝胶形成于31.4 ± 0.2 °C。药物释放研究表明,核黄素-5-磷酸钠制剂的释放速度更快,而体外保留研究显示,共晶体的角膜保留率更高。对大鼠角膜的体内研究表明,与5-磷酸核黄素钠相比,核黄素制剂的药物浓度更高,亲水性凝胶的角膜接触时间更长。含有5-磷酸核黄素钠和trans - cutol P的THJ-TP制剂(含亲水性凝胶制剂)是最有希望的候选制剂。本研究在以核黄素为基础的非侵入性圆锥角膜治疗方面取得了重大进展。
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来源期刊
CiteScore
10.70
自引率
8.60%
发文量
951
审稿时长
72 days
期刊介绍: The International Journal of Pharmaceutics is the third most cited journal in the "Pharmacy & Pharmacology" category out of 366 journals, being the true home for pharmaceutical scientists concerned with the physical, chemical and biological properties of devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture and evaluation. This includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials. The journal has special sections on pharmaceutical nanotechnology and personalized medicines, and publishes research papers, reviews, commentaries and letters to the editor as well as special issues.
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