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Towards the Oral Treatment of Ileo-Colonic Inflammatory Bowel Disease with Infliximab Tablets: Development and Validation of the Production Process

机译:英夫利昔单抗片口服治疗肠结肠炎性肠病:生产工艺的开发和验证

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摘要

Infliximab (IFX) is an intravenously administered monoclonal antibody antagonizing the effects of tumor necrosis factor-alpha (TNF) systemically and is efficacious in the treatment of inflammatory bowel disease (IBD). However, studies suggest that the anti-inflammatory effects result from local immunomodulation in the inflamed regions. Furthermore, topical inhibition of TNF in IBD ameliorates inflammation. We therefore hypothesized that orally administered IFX targeted to the ileo-colonic region in IBD may be an efficacious new treatment option. This study describes the development and validation of the production process of ileo-colonic-targeted 5 mg IFX tablets (ColoPulse-IFX) intended for the oral treatment of IBD by means of producing three consecutive validation batches (VAL1, VAL2, and VAL3, respectively). UV-VIS spectroscopy, HPLC-SEC analysis (content, fragments, aggregates), fluorescence spectroscopy (tertiary protein structure), and ELISA (potency) showed no noticeable deviations of IFX compounded to ColoPulse-IFX compared to fresh IFX stock. The average ± SD (n = 10) IFX content of VAL1, VAL2, and VAL3 was 96 ± 2%, 97 ± 3%, and 96 ± 2%, respectively, and complied with the European Pharmacopeia (Ph. Eur.) requirements for Content Uniformity. The average ± SD (n = 3) ColoPulse-IFX potency was 105 ± 4%, 96 ± 4%, and 97 ± 5%, respectively, compared to fresh IFX stock. The IFX release profile from the tablet core was complete (≥85%) after 10 min in simulated ileum medium. The in vitro coating performance of ColoPulse-IFX showed that the formulation was targeted to the simulated ileo-colonic region. Stability data showed that ColoPulse-IFX was stable for up to 6 months stored at 25 °C/60% RH. Based on these results, the production process can be considered validated and its application is discussed in light of the rationale and available evidence for the topical treatment of IBD with IFX.
机译:英夫利昔单抗(IFX)是静脉内施用的单克隆抗体,可全身性拮抗肿瘤坏死因子-α(TNF)的作用,在治疗炎症性肠病(IBD)方面有效。然而,研究表明抗炎作用是由发炎区域的局部免疫调节产生的。此外,在IBD中局部抑制TNF可改善炎症。因此,我们假设针对IBD的回肠结肠区域的口服IFX可能是一种有效的新治疗选择。这项研究描述了针对回肠结肠的5 mg IFX片剂(ColoPulse-IFX)的生产工艺的开发和验证,该片剂旨在通过分别生产三个连续的验证批次(VAL1,VAL2和VAL3)来对IBD进行口服治疗)。 UV-VIS光谱,HPLC-SEC分析(含量,片段,聚集物),荧光光谱(三级蛋白质结构)和ELISA(效价)显示,与新鲜IFX原料相比,与ColoPulse-IFX混合的IFX没有明显的偏差。 VAL1,VAL2和VAL3的平均±SD(n = 10)IFX含量分别为96±2%,97±3%和96±2%,并符合欧洲药典(Ph。Eur。)的要求内容统一性。与新鲜IFX股票相比,ColoPulse-IFX的平均±SD(n = 3)效力分别为105±4%,96±4%和97±5%。在模拟回肠培养基中放置10分钟后,片剂核心的IFX释放曲线完整(≥85%)。 ColoPulse-IFX的体外涂层性能表明,该制剂针对模拟的回肠结肠区域。稳定性数据表明,ColoPulse-IFX在25°C / 60%RH下储存长达6个月是稳定的。基于这些结果,可以考虑生产过程的有效性,并根据使用IFX局部治疗IBD的基本原理和可用证据讨论其应用。

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