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Preparation characterization and evaluation of amphotericin B-loaded MPEG-PCL-g-PEI micelles for local treatment of oral Candida albicans

机译:载有两性霉素B的MPEG-PCL-g-PEI胶束的制备表征和评估用于口服治疗白色念珠菌

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摘要

Fatal Candida albicans infections in the mucosal system can occur in association with immune-compromised diseases and dysbacteriosis. Currently, amphotericin B (AmB) is considered to be the most effective antibiotic in the treatment of C. albicans infections, but its clinical application is limited by side effects and poor bioavailability. In order to use AmB in the local treatment of oral C. albicans infections, AmB/MPEG-PCL-g-PEI (monomethoxy poly(ethylene glycol)-poly(epsilon-caprolactone)-graft-polyethylenimine, MPP) micelles were prepared. A series of characterizations were performed. The micelles allowed a sustained in vitro release in both normal oral conditions (pH 6.8) and C. albicans infection conditions (pH 5.8). Then, buccal tablets containing freeze-dried powder of AmB/MPP micelles were produced by direct compression process and evaluated as regards to weight variation, hardness, and friability. In vitro drug release of the buccal tablets was measured in both the United States Pharmacopeia dissolution apparatus and the dissolution rate test apparatus, which was previously designed for simulating in vivo conditions of the oral cavity. The buccal tablets could sustainably release within 8 h and meet the antifungal requirements. Regarding safety assessment of AmB/MPP micelles, in vivo histopathological data showed no irritation toward buccal mucosa of the rats in both optical microscopy and ultrastructure observation of the tissues. MTT experiment proved that AmB/MPP micelles reduced the cytotoxicity of AmB. The micelles delivered through the gastrointestinal route were also found to be non-systemic toxicity by liquid chromatography-mass spectrometry analysis. Furthermore, the antifungal action of AmB/MPP micelles was evaluated. Although AmB/MPP had no obvious improvement as compared to AmB alone in the antifungal effect on planktonic C. albicans, the micelles significantly enhanced the antifungal activity against the biofilm state of C. albicans. Thus, it was concluded that AmB/MPP micelles represent a promising novel drug delivery system for the local treatment of oral C. albicans infections.
机译:粘膜系统中致命的白色念珠菌感染可能与免疫功能低下的疾病和菌群失调相关。目前,两性霉素B(AmB)被认为是治疗白色念珠菌感染的最有效抗生素,但其临床应用受到副作用和生物利用度差的限制。为了在局部治疗口腔白色念珠菌感染中使用AmB,制备了AmB / MPEG-PCL-g-PEI(单甲氧基聚(乙二醇)-聚(ε-己内酯)-接枝-聚乙烯亚胺,MPP)胶束。进行了一系列表征。胶束允许在正常口服条件(pH 6.8)和白色念珠菌感染条件(pH 5.8)下持续释放。然后,通过直接压片法制备含有AmB / MPP胶束冻干粉的含服片剂,并评价其重量变化,硬度和脆性。在美国药典溶出度仪和溶出度测试仪中都测量了颊片的体外药物释放,该装置先前设计用于模拟口腔的体内状况。颊片可在8小时内持续释放并满足抗真菌要求。关于AmB / MPP胶束的安全性评估,体内组织病理学数据显示,在光学显微镜和组织超微结构观察中均未刺激大鼠颊粘膜。 MTT实验证明AmB / MPP胶束降低了AmB的细胞毒性。通过液相色谱-质谱分析还发现,通过胃肠道递送的胶束具有非全身毒性。此外,评估了AmB / MPP胶束的抗真菌作用。尽管与单独使用AmB相比,AmB / MPP对浮游白色念珠菌的抗真菌作用没有明显改善,但微团显着增强了对白色念珠菌生物膜状态的抗真菌活性。因此,可以得出结论,AmB / MPP胶束代表了一种有前途的新型药物递送系统,用于局部治疗口腔念珠菌感染。

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