Identifying factors controlling cellular uptake of gold nanoparticles by machine learning.

IF 4.3 4区 医学 Q1 PHARMACOLOGY & PHARMACY Journal of Drug Targeting Pub Date : 2024-12-01 Epub Date: 2024-01-12 DOI:10.1080/1061186X.2023.2288995
Eyup Bilgi, David A Winkler, Ceyda Oksel Karakus
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Abstract

There is strong interest to improve the therapeutic potential of gold nanoparticles (GNPs) while ensuring their safe development. The utility of GNPs in medicine requires a molecular-level understanding of how GNPs interact with biological systems. Despite considerable research efforts devoted to monitoring the internalisation of GNPs, there is still insufficient understanding of the factors responsible for the variability in GNP uptake in different cell types. Data-driven models are useful for identifying the sources of this variability. Here, we trained multiple machine learning models on 2077 data points for 193 individual nanoparticles from 59 independent studies to predict cellular uptake level of GNPs and compared different algorithms for their efficacies of prediction. The five ensemble learners (Xgboost, random forest, bootstrap aggregation, gradient boosting, light gradient boosting machine) made the best predictions of GNP uptake, accounting for 80-90% of the variance in the test data. The models identified particle size, zeta potential, GNP concentration and exposure duration as the most important drivers of cellular uptake. We expect this proof-of-concept study will foster the more effective use of accumulated cellular uptake data for GNPs and minimise any methodological bias in individual studies that may lead to under- or over-estimation of cellular internalisation rates.

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通过机器学习识别控制金纳米颗粒细胞摄取的因素。
在确保金纳米颗粒安全开发的同时,提高其治疗潜力是人们非常关注的问题。GNPs在医学中的应用需要在分子水平上理解GNPs如何与生物系统相互作用。尽管为监测国民生产总值的内在化作出了相当大的研究努力,但对造成不同细胞类型的国民生产总值吸收变化的因素仍然了解不足。数据驱动的模型对于识别这种可变性的来源非常有用。在这里,我们对来自59个独立研究的193个纳米粒子的2077个数据点训练了多个机器学习模型,以预测GNPs的细胞摄取水平,并比较了不同算法的预测效果。五个集成学习器(Xgboost、随机森林、自举聚合、梯度增强、轻梯度增强机)对GNP摄取的预测效果最好,占测试数据方差的80-90%。这些模型确定了颗粒大小、zeta电位、GNP浓度和暴露时间是细胞摄取的最重要驱动因素。我们期望这项概念验证研究将促进更有效地利用累积的细胞摄取数据来获得GNPs,并最大限度地减少个别研究中可能导致细胞内化率低估或高估的方法学偏差。
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来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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