纳米乳化大车前子提取物对wistar大鼠口腔伤口的愈合作用。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Fatemeh Jahanimoghadam, Amirhossein Javidan, Mehdi Ranjbar, Molook Torabi, Sina Kakooei, Fariba Sharififar
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引用次数: 0

摘要

简介口腔病变是由各种病因引起的常见临床症状,会影响患者的生活质量。然而,由于口腔环境的不断变化,目前尚无确切的治疗方法。近年来,草药治疗因其易得、安全、经济实惠和抗菌特性而受到患者和医生的青睐。本研究旨在利用组织形态学和立体学参数,研究主车前子标准化提取物纳米乳液(PMSE)对 Wistar 大鼠口腔溃疡的治疗效果:研究涉及 72 只 Wistar 大鼠,随机分为 24 组,每组 3 只:A1至A4组接受一剂至四剂5% PMSE纳米乳液,B1至B4组接受一剂至四剂10% PMSE纳米乳液,C1至C4组接受一剂至四剂20% PMSE纳米乳液,D1至D4组接受一剂至四剂不含PMSE的纳米乳液,E1至E4组接受一剂至四剂PMSE,F组为对照组。用活检打孔器在动物的硬腭上切开一个直径为 2 毫米的切口。用含有必要材料的棉签在伤口处口服药物。在第 2、4、6 和 8 天收集组织学样本并送至病理实验室进行检查。使用 SPSS 26 进行数据分析,以 p 为统计显著性:与其他组相比,A 组伤口完全正常再上皮率高达 66.7%。D 组的再上皮率为 50%,C、E 和 F 组为 7.41%,B 组为 7.16%。在炎症消退方面,A 组有 23.88%的人没有炎症,与其他组相比比例较高。B 组和 D 组无炎症的比例为 3.33%,低于其他组别。研究评估了不同组别在四次用药后第 2、4、6 和 8 天的再上皮化频率和炎症水平,各组之间没有发现显著差异:结论:纳米乳剂和 PMSE 都不能提高口腔溃疡的愈合率。结论:纳米乳剂和 PMSE 均不能提高口腔溃疡的愈合率,但 5% PMSE 纳米乳剂可增加病灶的再上皮化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The healing effect of nano emulsified Plantago major L extract on oral wounds in a wistar rat model.

Introduction: Oral lesions are a common clinical symptom arising from various etiologies and disrupt the patient's quality of life. However, no definite treatment is not yet possible, due to the constantly changing environment of the mouth. In recent years, herbal treatments have gained popularity among patients and physicians due to their availability, safety, affordability, and antimicrobial properties. This research aims to investigate the therapeutic effects of a nano-emulsion of Plantago major standardized extract (PMSE) on oral ulcers in a Wistar rat model using histomorphometry and stereological parameters.

Materials and methods: The study involved 72 Wistar rats divided randomly into 24 groups of 3 each: groups A1 to A4 received one dose to 4 doses of 5% PMSE nano emulsion, groups B1 to B4 received one dose to 4 doses of 10% PMSE nano emulsion, and groups C1 to C4 received one dose to 4 doses of 20% PMSE nano emulsion, groups D1 to D4 received one dose to 4 doses of nano-emulsion without PMSE, groups E1 to E4 received one dose to 4 doses of PMSE, and group F served as the control group. An incision measuring 2 mm in diameter was made in the animals' hard palate using a biopsy punch. A swab containing the necessary material was used to administer the medication orally to the wound. Histological samples were collected on days 2, 4, 6, and 8 and sent to the pathology laboratory for examination. Data analysis was performed using SPSS 26 and setting statistical significance at p < 0.05.

Results: Group A showed a high rate of complete and normal re-epithelialization of the wound at 66.7%, compared to the other groups. Group D had a re-epithelialization rate of 50%, while groups C, E, and F had rates of 7.41% and group B had 7.16%. In terms of inflammation reduction, 23.88% of group A had no inflammation, a higher percentage compared to the other groups. Group B and D had no inflammation in 3.33% of cases, lower than the other groups. The study evaluated frequency of re-epithelialization and inflammation levels in different groups on days 2, 4, 6, and 8 after four doses of the drug with no significant differences found among the groups.

Conclusion: None of the nano emulsions or PMSE enhanced the healing rate of oral ulcers. However, a 5% PMSE nano emulsion displayed an increase in lesion re-epithelialization.

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