Phytochemical and Toxicological Analyses of Herbal Mixtures Containing Hypericum perforatum and Melissa officinalis.

IF 1.8 Q3 PHARMACOLOGY & PHARMACY Turkish Journal of Pharmaceutical Sciences Pub Date : 2024-09-02 DOI:10.4274/tjps.galenos.2023.28092
Faezeh Fatemi, Mehran Zamany, Somayeh Farahmand, Salome Dini
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Abstract

Objectives: This study aimed to formulate a novel herbal mixture of Hypericum perforatum (H) and Melissa officinalis (M) and evaluate its toxicity, microbial load, and phytochemical content.

Materials and methods: Total flavonoids were measured using the AlCl3/NaNO2 complex formation method and colorimetric assay. The quercetin content of the herbal mixture was determined by reverse-phase high-performance liquid chromatography. The in vitro and in vivo safety of the herbal formulations were analyzed using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and acute oral toxicity analysis in the rat model, respectively.

Results: The formulated extract (HM), compared with the standard rutin extract, had a total flavonoid content of 15.29 ± 0.64 mg rutin per mL sample. Reverse-phase high-performance liquid chromatography revealed a quercetin content of 0.187 mg/mL. Microbial tests for Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Salmonella spp. were negative. Colony counts for total aerobic microbial and yeast and mold counts were 10 in each case. The MTT assay (with up to about 5% v/v HM extract) using the NIH/3T3 cell line revealed no cell toxicity in the range of concentrations tested. Acute oral toxicity was tested in the Wistar rat model, and the LD50 was 695.2 ± 7.5 mg/kg. The dry weight of the HM extract was 38.1 mg/mL.

Conclusion: Preliminary results proved the safety of the HM herbal mixture, with its toxicity and microbial load within the limits of accepted guidelines allowable for use in clinical trials.

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贯叶连翘与金缕梅混合药材的植物化学及毒理学分析
目的:制备贯叶金丝桃(H)和厚朴(M)的新草药混合物,并对其毒性、微生物负荷和植物化学成分进行评价。材料与方法:采用AlCl3/NaNO2复合物形成法和比色法测定总黄酮含量。采用反相高效液相色谱法测定了该草药混合物中槲皮素的含量。在大鼠模型中分别使用MTT法和急性口服毒性分析来分析该草药制剂的体外和体内安全性。结果:与作为标准品的芦丁相比,该制剂提取物的总黄酮含量为15.29±0.64mg芦丁/ml。反相HPLC显示槲皮素含量为0.187mg/ml。大肠杆菌、铜绿假单胞菌、金黄色葡萄球菌和沙门氏菌的微生物检测结果均为阴性。菌落计数的需氧微生物总数,以及酵母和霉菌总数在每种情况下都小于10。在NIH/3T3细胞系上的MTT测定(具有高达约5%v/vHM提取物)显示在所测试的浓度范围内没有细胞毒性。在Wistar大鼠模型中测试急性口服毒性,LD50为695.2±7.5mg/Kg。HM提取物的干重为38.1mg/ml。结论:初步结果证明了中药混合物HM的安全性,其毒性和微生物负荷均在临床试验允许使用的公认指南范围内。
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来源期刊
CiteScore
3.60
自引率
5.90%
发文量
79
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