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磷酸铁在大鼠体内的急性和亚急性口服毒性评估。

Acute and Sub-acute Oral Toxicity Assessment of Ferrum phosphoricum in Rats.

机构信息

Department of Pharmacology, Drug Standardisation, Dr D P Rastogi Central Research Institute (H), Noida, Uttar Pradesh, India.

Department of Biochemistry, Dr D P Rastogi Central Research Institute (H), Noida, Uttar Pradesh, India.

出版信息

Homeopathy. 2024 May;113(2):86-97. doi: 10.1055/s-0043-1770338. Epub 2023 Aug 21.

Abstract

BACKGROUND

(FP) has been used by traditional medicine practitioners for various ailments since ancient times. However, scientific evidence on the safety of FP is still unavailable. Thus, the current study aimed to investigate the acute and sub-acute oral toxicity of homeopathic FP in experimental rats.

METHODS

In an acute toxicity investigation, a single dose of 2,000 µL/kg of FP 6c, 30c and 200c was administered to female Wistar rats, which were monitored for up to 14 days according to the Organization for Economic Cooperation and Development (OECD) guideline 423. For a sub-acute toxicity study, FP 6c, 30c and 200c (200 µL/kg) were administered to male and female rats for 28 days as per the OECD guideline 407. All the animals were observed for mortality, clinical signs and body weight during the study. At the end of the experiment, hematological, biochemical and histopathological assessments were performed.

RESULTS

During the acute toxicity study, no mortality was observed in rats administered with FP, and thus the median lethal dose (LD) was identified as >2,000 µL/kg. In the sub-acute study, no mortality or adverse clinical signs were noticed with FP treatment. Moreover, weekly body weight gain was normal. Hematological and biochemical investigations revealed no abnormalities. Furthermore, histological analysis of FP-treated rats' vital organs revealed no pathological changes.

CONCLUSION

Overall, our findings imply that FP 6c, 30c and 200c potencies are safe and do not cause toxicity when given orally to Wistar albino rats for an extended period at a dose of 200 µL/kg.

摘要

背景

(FP)自古以来一直被传统医学从业者用于各种疾病。然而,FP 的安全性的科学证据仍然缺乏。因此,目前的研究旨在调查实验大鼠中顺势疗法 FP 的急性和亚急性口服毒性。

方法

在急性毒性研究中,给雌性 Wistar 大鼠单次口服 2000µL/kg 的 FP 6c、30c 和 200c,根据经济合作与发展组织(OECD)指南 423 监测至 14 天。对于亚急性毒性研究,根据 OECD 指南 407,雄性和雌性大鼠每天口服 FP 6c、30c 和 200c(200µL/kg)28 天。在研究过程中,所有动物均观察死亡率、临床症状和体重。实验结束时,进行血液学、生化学和组织病理学评估。

结果

在急性毒性研究中,给予 FP 的大鼠未观察到死亡,因此确定中位致死剂量(LD)为>2000µL/kg。在亚急性研究中,FP 治疗组未观察到死亡或不良临床症状。此外,每周体重增加正常。血液学和生化学研究未发现异常。此外,FP 处理大鼠重要器官的组织学分析未显示出病理变化。

结论

总体而言,我们的研究结果表明,FP 6c、30c 和 200c 剂量在给 Wistar 白化大鼠口服延长时间时,剂量为 200µL/kg 是安全的,不会引起毒性。

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