数量结构-活动关系
细胞毒性
纳米颗粒
纳米-
化学
纳米技术
材料科学
工程类
立体化学
化学工程
生物化学
体外
作者
Jaehyeon Park,Suraya Abdul Rashid,Helena Copsey,Lang Tran,Alex Zabeo,Danail Hristozov,Georgios P. Gakis,Costas A. Charitidis,Seokjoo Yoon,Hyun Kil Shin
标识
DOI:10.1021/acsnanoscienceau.5c00035
摘要
Nanotechnological advances have led to the development of nanoparticles with complex structures. In this context, nano-QSAR models have been developed to assess toxicity; however, the applicability domain (AD) of such models is significantly restricted to specific types of nanoparticles (i.e., bare metal oxides, coated metals, or carbon-based nanomaterials) and target cell lines. Accordingly, NanoToxRadar, a web-based platform for predicting the toxicity of multicomponent nanoparticles (MC-NPs) toward various cell lines, was developed to extend the AD of the nano-QSAR model. The size-dependent electron-configuration fingerprint was used to represent the molecular structures of MC-NPs, and one-hot encoded cell types were used to predict toxicities toward 110 cell lines. The CatBoost regression model achieved good performance (R2 Test = 0.877) and was deployed online (https://www.kitox.re.kr/nanotoxradar). The Web site takes the nanoparticle composition of the core as well as the shell, dopant, coating material, and diameter as inputs and predicts pIC50 values for 110 cell lines.
科研通智能强力驱动
Strongly Powered by AbleSci AI