UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London WC1N 1AX, UK.
Univ. Lille, Inserm, CHU Lille, U1008, F-59000 Lille, France.
J Control Release. 2024 Oct;374:103-111. doi: 10.1016/j.jconrel.2024.08.010. Epub 2024 Aug 12.
Colonic drug delivery offers numerous pharmaceutical opportunities, including direct access to local therapeutic targets and drug bioavailability benefits arising from the colonic epithelium's reduced abundance of cytochrome P450 enzymes and particular efflux transporters. Current workflows for developing colonic drug delivery systems involve time-consuming, low throughput in vitro and in vivo screening methods, which hinder the identification of suitable enabling materials. Polysaccharides are useful materials for colonic targeting, as they can be utilised as dosage form coatings that are selectively digested by the colonic microbiota. However, polysaccharides are a heterogeneous family of molecules with varying suitability for this purpose. To address the need for high-throughput material selection tools for colonic drug delivery, we leveraged machine learning (ML) and publicly accessible experimental data to predict the release of the drug 5-aminosalicylic acid from polysaccharide-based coatings in simulated human, rat, and dog colonic environments. For the first time, Raman spectra alone were used to characterise polysaccharides for input as ML features. Models were validated on 8 unseen drug release profiles from new polysaccharide coatings, demonstrating the generalisability and reliability of the method. Further, model analysis facilitated an understanding of the chemical features that influence a polysaccharide's suitability for colonic drug delivery. This work represents a major step in employing spectral data for forecasting drug release from pharmaceutical formulations and marks a significant advancement in the field of colonic drug delivery. It offers a powerful tool for the efficient, sustainable, and successful development and pre-ranking of colon-targeted formulation coatings, paving the way for future more effective and targeted drug delivery strategies.
结肠药物递送提供了许多药物方面的机会,包括直接接触局部治疗靶点以及由于结肠上皮细胞中细胞色素 P450 酶和特定外排转运蛋白的含量减少而带来的药物生物利用度的提高。开发结肠药物递送系统的当前工作流程涉及耗时且高通量的体外和体内筛选方法,这阻碍了合适的使能材料的识别。多糖是结肠靶向的有用材料,因为它们可以用作通过结肠微生物群选择性消化的剂型涂层。然而,多糖是具有不同用途的分子的异质家族。为了解决结肠药物递送中高通量材料选择工具的需求,我们利用机器学习 (ML) 和公开可用的实验数据来预测药物 5-氨基水杨酸从基于多糖的涂层在模拟的人类、大鼠和狗结肠环境中的释放。这是首次仅使用拉曼光谱来表征多糖,将其作为 ML 特征输入。该模型在 8 个新的多糖涂层的未见药物释放谱上进行了验证,证明了该方法的通用性和可靠性。此外,模型分析有助于理解影响多糖用于结肠药物递送的适用性的化学特征。这项工作代表了在使用光谱数据预测药物从药物制剂中的释放方面迈出了重要一步,标志着结肠药物递送领域的重大进展。它为高效、可持续和成功开发和预先排列结肠靶向制剂涂层提供了强大的工具,为未来更有效和有针对性的药物递送策略铺平了道路。