Faculty of Allied Health Sciences, Chettinad Hospital and Research Institute, Chettinad Academy of Research and Education, Chettinad Health City, Kelambakkam, Tamil Nadu, 603103, India.
Department of Pathology, Chettinad Hospital and Research Institute, Chettinad Academy of Research and Education, Chettinad Health City, Kelambakkam, 603103, India.
J Mol Histol. 2024 Oct;55(5):977-994. doi: 10.1007/s10735-024-10245-x. Epub 2024 Aug 19.
We analyzed the toxic effect of the ethanolic extract of Passiflora incarnata (EEP) and its nanoformulation (N-EEP) in the in vitro and in vivo models (zebrafish embryos and Swiss albino mice). The EEP composition was verified by phytochemical and GC-MS analysis. The synthesized N-EEP was characterized using UV-visible spectroscopy and scanning electron microscopy. In vitro results showed both EEP and N-EEP have a dose-dependent effect in L132 cells (normal embryonic lung cells). In zebrafish embryos, no developmental changes were observed for both EEP and N-EEP at 200 µg/ml. The acute and sub-acute toxicity of EEP and N-EEP was identified by oral administration in Swiss albino mice. A single-day oral dose of EEP and N-EEP at different concentrations was administered for acute toxicity, and changes in body weight, food, water intake, temperature, respiration rate, skin color changes, and eye color till 72 h was observed. In a sub-acute toxicity study, 28 days oral administration of different concentrations of EEP and N-EEP was done. Hematological analysis, serum hepatic biochemical parameter analysis, and histopathological analysis for the liver, kidney, spleen, intestine, and heart were performed. The results indicated that lower than 600 mg/kg of EEP and N-EEP can safely be used for the remediation of a spectrum of diseases.
我们分析了西番莲(Passiflora incarnata)乙醇提取物(EEP)及其纳米制剂(N-EEP)在体外和体内模型(斑马鱼胚胎和瑞士白化小鼠)中的毒性作用。EEP 的成分通过植物化学和 GC-MS 分析进行了验证。合成的 N-EEP 使用紫外可见光谱和扫描电子显微镜进行了表征。体外结果表明,EEP 和 N-EEP 在 L132 细胞(正常胚胎肺细胞)中均具有剂量依赖性效应。在斑马鱼胚胎中,EEP 和 N-EEP 在 200µg/ml 时均未观察到发育变化。通过口服给药在瑞士白化小鼠中确定了 EEP 和 N-EEP 的急性和亚急性毒性。对不同浓度的 EEP 和 N-EEP 进行了单次口服剂量的急性毒性试验,观察了体重、食物、水摄入、体温、呼吸频率、皮肤颜色变化和眼睛颜色的变化,直至 72 小时。在亚急性毒性研究中,对不同浓度的 EEP 和 N-EEP 进行了 28 天口服给药。进行了血液学分析、血清肝生化参数分析以及肝、肾、脾、肠和心脏的组织病理学分析。结果表明,EEP 和 N-EEP 的剂量低于 600mg/kg 时可安全用于治疗一系列疾病。