结合局部和全局特征预测药物-药物相互作用的优化Mobilenet V2注意力并行网络。

IF 1.7 4区 医学 Q3 PHARMACOLOGY & PHARMACY
S. K. Mydhili, S. Nithyaselvakumari, K. Padmanaban, D. Karunkuzhali
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引用次数: 0

摘要

药物-药物相互作用(ddi)在临床实践和药物开发过程中是一个重要的问题,因为这些相互作用可能会对患者安全产生严重的不良影响。全面的DDI预测对于有效的用药管理和减少危险因素非常重要。本文提出了一种基于简单注意力网络的并行卷积神经网络和独角鲸优化器的MV2SAPCNNO: MobileNetV2新技术,以提高DDI预测的精度。该方法从数据预处理开始,包括归一化和降噪,以提高数据质量。然后,使用MobileNetV2与简单关注网络(MV2SAN)从数据集中提取局部和全局特征。这些特征使用并行卷积神经网络(PCNN)进行处理,并由独角鲸优化器(NO)进行优化,以改进参数调整,最大限度地减少误差并降低计算复杂度。模型的性能通过准确性、精密度、召回率和f分进行评估。实验结果证明,MV2SAPCN-NO在准确率和增强的分类指标方面都优于现有的DDI预测模型。独角鲸优化器提高了模型的收敛效率,减少了计算时间,具有良好的预测性能。提出了一种高效、准确的DDI预测模型MV2SAPCNNO。该模型实际上优于传统模型,并且这些发现被展示用于安全的药物管理,药物开发过程和临床实践中对患者的保护。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

An Optimised Mobilenet V2 Attention Parallel Network for Predicting Drug–Drug Interactions Through Combining Local and Global Features

An Optimised Mobilenet V2 Attention Parallel Network for Predicting Drug–Drug Interactions Through Combining Local and Global Features

Drug–drug interactions (DDIs) are an important concern in the clinical practice and drug development process as these may lead to serious adverse effects on patient safety. Thorough DDI prediction is important for effective medication management and reduced risk factors. This work presents a new technique, namely MV2SAPCNNO: MobileNetV2 with simplicial attention network-based parallel convolutional neural network and narwhal optimiser, for improving the precision of DDI prediction. The proposed method starts with data preprocessing, including normalisation and noise reduction, to enhance the quality of the data. Then, MobileNetV2 with simplicial attention network (MV2SAN) is used to extract both local and global features from the dataset. These features are processed using a parallel convolutional neural network (PCNN), optimised by the narwhal optimiser (NO) to improve parameter tuning, minimise error and reduce computational complexity. The performance of the model is evaluated using accuracy, precision, recall and F-score. Experimental results prove that MV2SAPCN-NO achieves better performance over the current models of DDI prediction in accuracy and enhanced classification metrics. The narwhal optimiser enhances the model's convergence efficiency and decreases computational time with an excellent predictive performance. An efficient and accurate DDI prediction model was proposed called MV2SAPCNNO. This model actually outperformed traditional models, and such findings were exhibited to contribute towards secure medication administration, drug development processes and protection of patients in clinical practice.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
35
审稿时长
6-12 weeks
期刊介绍: Biopharmaceutics & Drug Dispositionpublishes original review articles, short communications, and reports in biopharmaceutics, drug disposition, pharmacokinetics and pharmacodynamics, especially those that have a direct relation to the drug discovery/development and the therapeutic use of drugs. These includes: - animal and human pharmacological studies that focus on therapeutic response. pharmacodynamics, and toxicity related to plasma and tissue concentrations of drugs and their metabolites, - in vitro and in vivo drug absorption, distribution, metabolism, transport, and excretion studies that facilitate investigations related to the use of drugs in man - studies on membrane transport and enzymes, including their regulation and the impact of pharmacogenomics on drug absorption and disposition, - simulation and modeling in drug discovery and development - theoretical treatises - includes themed issues and reviews and exclude manuscripts on - bioavailability studies reporting only on simple PK parameters such as Cmax, tmax and t1/2 without mechanistic interpretation - analytical methods
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