Bhandare Saurabh Dilip
Foxabell-Laboratorium Investigativum, "Laboratorium Scientiae et Studiorum Investigativorum", Nashik 422101, Maharashtra, India.
Toxicol Res (Camb). 2025 May 4;14(3):tfaf065. doi: 10.1093/toxres/tfaf065. eCollection 2025 Jun.
This investigative study examines the transfer of maternal medications into breast milk and their potential impact on breastfeeding infants. Significant factors influencing drug transfer, including physiochemical properties and milk composition, are analysed to corroborate judicious drug administration in nursing mothers. The study investigates, evaluates, and interprets drugs such as: H|chlorpromazine (New England Nuclear [NEN]), diazepam Roche, C|diclofenac (Ciba-Geigy, 6.6 mCi/mmol, K-277), diclofenac (Ciba-Geigy, 0.1317), digoxin (Wellcome, 11725), fluphenazine (Squibb 12240), phenytoin (NEN, 46 Ci/mmol, 2315-061), phenytoin (Parke-Davis 5419972), pirenzepine (Boehringer-Ingelheim-660206), H|prednisolone (Amersham, 67.4 Ci/mmol, 88), warfarin (Amersham, 46 mCi/mmol, 30), outlining and assessing their transferability and perils notably presented. Ferguson's principle was leveraged to predict drug toxicity, specifically for central nervous system depressants, elucidating drug lethality and safety evaluation. On top of that, advancements in toxicological risk assessment were evaluated, articulated as focusing on naloxone programs, predictive modelling, quantitative structure-activity relationship (QSAR) applications, toxicogenomics, and ordinary differential equation (ODE) models. The comparison between risk assessments and biological monitoring highlights the prominence of evaluating internal dosages. Progress in 3D-QSAR modelling augmented its role in forecasting chemical toxicity, while advancements in toxicogenomics and the application of ODE models have contributed to toxicological research. Hence, the shift toward alternate toxicity assessment methodologies was driven by ethical concerns, budgetary limits, and the demand for more human-relevant data without sacrificing an animal life, which was a concern of the present scientific investigation; fixed by machine algorithms, e.g. random forest, Support Vector Machine (SVM), Ferguson's principle, etc.; an omics data set for correlation through tactile programmed computational heuristics for decision science.
这项调查研究探讨了母体药物向母乳中的转移及其对母乳喂养婴儿的潜在影响。分析了影响药物转移的重要因素,包括物理化学性质和乳汁成分,以证实哺乳期母亲合理用药。该研究调查、评估并解释了以下药物:氯丙嗪(新英格兰核公司[NEN])、地西泮(罗氏公司)、双氯芬酸(汽巴-嘉基公司,6.6毫居里/毫摩尔,K-277)、双氯芬酸(汽巴-嘉基公司,0.1317)、地高辛(威康公司,11725)、氟奋乃静(施贵宝公司12240)、苯妥英(NEN公司,46居里/毫摩尔,2315-061)、苯妥英(帕克-戴维斯公司5419972)、哌仑西平(勃林格殷格翰公司-660206)、氢化泼尼松(阿默沙姆公司,67.4居里/毫摩尔,88)、华法林(阿默沙姆公司,46毫居里/毫摩尔,30),概述并评估了它们的可转移性和特别呈现的风险。利用弗格森原理预测药物毒性,特别是针对中枢神经系统抑制剂,阐明药物致死率和安全性评估。除此之外,还评估了毒理学风险评估的进展,阐述为侧重于纳洛酮项目、预测建模、定量构效关系(QSAR)应用、毒理基因组学和常微分方程(ODE)模型。风险评估与生物监测之间的比较突出了评估内部剂量的重要性。三维定量构效关系建模的进展增强了其在预测化学毒性方面的作用,而毒理基因组学的进展和常微分方程模型的应用推动了毒理学研究。因此,向替代毒性评估方法的转变是由伦理问题、预算限制以及在不牺牲动物生命的情况下对更多与人类相关数据的需求驱动的,这是当前科学研究关注的问题;由机器算法固定,例如随机森林、支持向量机(SVM)、弗格森原理等;通过触觉编程计算启发式方法用于决策科学的组学数据集进行相关性分析。