Harmony in nature's elixir: a comprehensive exploration of ethanol and nano-formulated extracts from Passiflora incarnata leaves: unveiling in vitro cytotoxicity, acute and sub-acute toxicity profiles in Swiss albino mice

IF 2.9 4区 生物学 Q3 CELL BIOLOGY Journal of Molecular Histology Pub Date : 2024-08-19 DOI:10.1007/s10735-024-10245-x
Balasubramanian Deepika, Pemula Gowtham, Vijayashree Raghavan, Jane Betsy Isaac, Sobita Devi, Venkatakrishnan Kiran, Devadass Jessy Mercy, P. S. Sharon Sofini, A. Harini, Agnishwar Girigoswami, Koyeli Girigoswami
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Abstract

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.

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自然灵药的和谐:西番莲叶乙醇和纳米配方提取物的综合探索:揭示瑞士白化小鼠体外细胞毒性、急性和亚急性毒性概况。
我们在体外和体内模型(斑马鱼胚胎和瑞士白化小鼠)中分析了西番莲乙醇提取物(EEP)及其纳米制剂(N-EEP)的毒性作用。通过植物化学和气相色谱-质谱分析验证了 EEP 的成分。利用紫外可见光谱和扫描电子显微镜对合成的 N-EEP 进行了表征。体外实验结果表明,EEP 和 N-EEP 对 L132 细胞(正常胚胎肺细胞)具有剂量依赖性作用。在斑马鱼胚胎中,当 EEP 和 N-EEP 的浓度为 200 微克/毫升时,均未观察到发育变化。通过对瑞士白化小鼠进行口服,确定了 EEP 和 N-EEP 的急性和亚急性毒性。在急性毒性研究中,小鼠单日口服不同浓度的环氧乙烷和壬基酚,72 小时后体重、进食量、饮水量、体温、呼吸频率、皮肤颜色和眼睛颜色均发生变化。在亚急性毒性研究中,口服不同浓度的 EEP 和 N-EEP 28 天。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,低于 600 毫克/千克的 EEP 和 N-EEP 可以安全地用于各种疾病的治疗。
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来源期刊
Journal of Molecular Histology
Journal of Molecular Histology 生物-细胞生物学
CiteScore
5.90
自引率
0.00%
发文量
68
审稿时长
1 months
期刊介绍: The Journal of Molecular Histology publishes results of original research on the localization and expression of molecules in animal cells, tissues and organs. Coverage includes studies describing novel cellular or ultrastructural distributions of molecules which provide insight into biochemical or physiological function, development, histologic structure and disease processes. Major research themes of particular interest include: - Cell-Cell and Cell-Matrix Interactions; - Connective Tissues; - Development and Disease; - Neuroscience. Please note that the Journal of Molecular Histology does not consider manuscripts dealing with the application of immunological or other probes on non-standard laboratory animal models unless the results are clearly of significant and general biological importance. The Journal of Molecular Histology publishes full-length original research papers, review articles, short communications and letters to the editors. All manuscripts are typically reviewed by two independent referees. The Journal of Molecular Histology is a continuation of The Histochemical Journal.
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Editorial: New perspectives from the new Editor-in-Chief of Journal of Molecular Histology. Correction: Dendrobine alleviates oleic acid-induced lipid accumulation by inhibiting FOS/METTL14 pathway. Correction: Zinc-alkaline phosphatase at sites of aortic calcification. PODXL promotes malignant progression of hepatocellular carcinoma by activating PI3K/AKT pathway. Biotoxicity of paraquat to lung cells mediated by endoplasmic reticulum-mitochondria interaction.
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