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评价甘草酸载药聚合物纳米粒通过抑制炎症介质和氧化应激对 5-氟尿嘧啶诱导的小鼠肠道黏膜炎的黏膜保护作用。

Evaluating the mucoprotective effects of glycyrrhizic acid-loaded polymeric nanoparticles in a murine model of 5-fluorouracil-induced intestinal mucositis via suppression of inflammatory mediators and oxidative stress.

机构信息

Department of Pharmacy, Quaid-I-Azam University, Islamabad, 45320, Pakistan.

出版信息

Inflammopharmacology. 2021 Oct;29(5):1539-1553. doi: 10.1007/s10787-021-00866-z. Epub 2021 Aug 22.

Abstract

OBJECTIVES

5-Fluorouracil (5-FU), a chemotherapeutic drug, has severe deteriorating effects on the intestine, leading to mucositis. Glycyrrhizic acid is a compound derived from a common herbal plant Glycyrrhiza glabra, with mucoprotective, antioxidant and anti-inflammatory actions, however, associated with poor pharmacokinetics. Owing to the remarkable therapeutic action of glycyrrhizic acid-loaded polymeric nanocarriers in inflammatory bowel disease, we explored their activity against 5-FU-induced intestinal mucositis in mice. Polymeric nanocarriers have proven to be efficient drug delivery vehicles for the long-term treatment of inflammatory diseases, but have not yet been explored for 5-FU-induced mucositis. Therefore, this study aimed to produce glycyrrhizic acid-loaded polylactic-co-glycolic acid (GA-PLGA) nanoparticles to evaluate their protective and therapeutic effects in a 5-FU-induced mucositis model.

METHODS

GA-PLGA nanoparticles were prepared using a modified double emulsion method, physicochemically characterized, and tested for in vitro drug release. Thereafter, mucositis was induced by 5-FU (50 mg/kg; IP) administration to the mice for the first 3 days (day 0, 1, 2), and mice were treated orally with GA-PLGA nanoparticles for 7 days (day 0-6).

RESULTS

GA-PLGA nanoparticles significantly reduced mucositis severity measured by body weight, diarrhea score, distress, and anorexia. Further, 5-FU induced intestinal histopathological damage, altered villi-crypt length, reduced goblet cell count, elevated pro-inflammatory mediators, and suppressed antioxidant enzymes, all of which were reversed by GA-PLGA nanoparticles.

CONCLUSION

Morphological, behavioral, histological, and biochemical results suggested that GA-PLGA nanoparticles were efficient, biocompatible, targeted, and sustained release drug delivery nano-vehicle for enhanced mucoprotective, anti-inflammatory, and antioxidant effects in 5-FU-induced intestinal mucositis.

摘要

目的

5-氟尿嘧啶(5-FU)是一种化疗药物,对肠道有严重的恶化作用,导致黏膜炎。甘草酸是一种从甘草属植物甘草中提取的化合物,具有黏膜保护、抗氧化和抗炎作用,但药代动力学较差。由于甘草酸载药聚合物纳米载体在炎症性肠病中的显著治疗作用,我们探索了其在小鼠 5-FU 诱导的肠道黏膜炎中的活性。聚合物纳米载体已被证明是治疗炎症性疾病的有效药物递送载体,但尚未用于 5-FU 诱导的黏膜炎。因此,本研究旨在制备甘草酸载药聚乳酸-羟基乙酸共聚物(GA-PLGA)纳米粒,评估其在 5-FU 诱导的黏膜炎模型中的保护和治疗作用。

方法

采用改良的双乳液法制备 GA-PLGA 纳米粒,对其进行理化性质表征,并进行体外药物释放试验。然后,用 5-FU(50mg/kg;IP)对小鼠进行 3 天(第 0、1、2 天)的首次给药诱导黏膜炎,并用 GA-PLGA 纳米粒对小鼠进行 7 天(第 0-6 天)的口服治疗。

结果

GA-PLGA 纳米粒显著减轻了 5-FU 诱导的黏膜炎严重程度,体质量、腹泻评分、痛苦和厌食情况均得到改善。此外,5-FU 诱导的肠道组织病理学损伤、绒毛-隐窝长度缩短、杯状细胞计数减少、促炎介质升高和抗氧化酶活性降低,均被 GA-PLGA 纳米粒逆转。

结论

形态学、行为学、组织学和生物化学结果表明,GA-PLGA 纳米粒是一种高效、生物相容、靶向、缓释的药物递送纳米载体,可增强 5-FU 诱导的肠道黏膜炎的黏膜保护、抗炎和抗氧化作用。

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