Safe-by-Design Strategies for Intranasal Drug Delivery Systems: Machine and Deep Learning Solutions to Differentiate Epithelial Tissues via Attenuated Total Reflection Fourier Transform Infrared Spectroscopy

IF 4.9 Q1 CHEMISTRY, MEDICINAL
Romain Topalian, Leo Kavallaris, Frank Rosenau and Chrystelle Mavoungou*, 
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Abstract

The development of nasal drug delivery systems requires advanced analytical techniques and tools that allow for distinguishing between the nose-to-brain epithelial tissues with better precision, where traditional bioanalytical methods frequently fail. In this study, attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy is coupled to machine learning (ML) and deep learning (DL) techniques to discriminate effectively between epithelial tissues. The primary goal of this work was to develop Safe-by-Design models for intranasal drug delivery using ex vivo pig tissues experiment, which were analyzed by way of ML modeling. We compiled an ATR-FTIR spectral data set from olfactory epithelium (OE), respiratory epithelium (RE), and tracheal tissues. The data set was used to train and test different ML algorithms. Accuracy, sensitivity, specificity, and F1 score metrics were used to evaluate optimized model performance and their abilities to identify specific spectral signatures relevant to each tissue type. The used feedforward neural network (FNN) has shown 0.99 accuracy, indicating that it had performed a discrimination with a high level of trueness estimates, without overfitting, unlike the built support vector machine (SVM) model. Important spectral features detailing the assignment and site of two-dimensional (2D) protein structures per tissue type were determined by the SHapley Additive exPlanations (SHAP) value analysis of the FNN model. Furthermore, a denoising autoencoder was built to improve spectral quality by reducing noise, as confirmed by higher Pearson correlation coefficients for denoised spectra. The combination of spectroscopic analysis with ML modeling offers a promising strategy called, Safe-by-Design, as a monitoring strategy for intranasal drug delivery systems, also for designing the analysis of tissue for diagnosis purposes.

鼻内给药系统的安全设计策略:通过衰减全反射傅立叶变换红外光谱区分上皮组织的机器和深度学习解决方案
鼻腔给药系统的开发需要先进的分析技术和工具,以便更好地区分鼻到脑上皮组织,而传统的生物分析方法往往无法做到这一点。在本研究中,衰减全反射傅里叶变换红外(ATR-FTIR)光谱与机器学习(ML)和深度学习(DL)技术相结合,有效区分上皮组织。本研究的主要目的是利用离体猪组织实验建立鼻内给药安全设计模型,并通过ML建模对模型进行分析。我们收集了嗅上皮(OE)、呼吸上皮(RE)和气管组织的ATR-FTIR光谱数据集。该数据集用于训练和测试不同的ML算法。准确性、灵敏度、特异性和F1评分指标用于评估优化模型的性能及其识别与每种组织类型相关的特定光谱特征的能力。所使用的前馈神经网络(FNN)显示出0.99的准确率,表明它与所构建的支持向量机(SVM)模型不同,它已经进行了高水平的真实度估计的区分,没有过拟合。通过FNN模型的SHapley加性解释(SHAP)值分析确定了详细描述每种组织类型二维(2D)蛋白质结构分配和位置的重要光谱特征。此外,建立了一个去噪自编码器,通过降低噪声来改善光谱质量,这证实了去噪后的光谱具有较高的Pearson相关系数。光谱分析与ML建模的结合提供了一种被称为“设计安全”的有前途的策略,作为鼻内给药系统的监测策略,也用于设计用于诊断目的的组织分析。
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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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