Serrano Dolores R, Fernandez-Garcia Raquel, Mele Marta, Healy Anne Marie, Lalatsa Aikaterini
Department of Pharmaceutics and Food Technology, School of Pharmacy, Universidad Complutense de Madrid, Plaza Ramon y Cajal s/n, 28040 Madrid, Spain.
Instituto Universitario de Farmacia Industrial (IUFI), School of Pharmacy, Universidad Complutense de Madrid, Avenida Complutense, 28040 Madrid, Spain.
Pharmaceutics. 2019 Aug 1;11(8):369. doi: 10.3390/pharmaceutics11080369.
Amphotericin B possesses high activity against spp. with low risk of resistance. However, Amphotericin B's high molecular weight compared to other antifungal drugs, such as miconazole and clotrimazole, and poor water solubility hampers its efficacy at the physiological conditions of the oropharyngeal cavity (saliva pH, limited volume for dissolution) and thereby limits its clinical use in oropharyngeal candidiasis. We have prepared fast-dissolving orodispersible films with high loading (1% ) using solvent casting that enables amphotericin B to remain solubilised in saliva in equilibrium between the monomeric and dimeric states, and able to produce a local antifungal effect. Optimisation of the amphotericin B-loaded orodispersible films was achieved by quality by design studies combining dextran and/or maltodextrin as dextrose-derived-polymer film formers with cellulose-derived film formers (hydroxypropylmethyl/hydroxypropyl cellulose in a 1:4 weight ratio), sorbitol for taste masking, microcrystalline cellulose (Avicel 200) or microcrystalline cellulose-carboxymethylcellulose sodium (Avicel CL-611) for enhancing the mechanical strength of the film, and polyethylene glycol 400 and glycerol (1:1 ) as plasticizers. The optimised amphotericin B orodispersible films (containing 1% AmB, 25% dextran, 25% maltodextrin, 5% sorbitol, 10% Avicel 200, 10% polyethylene glycol 400, 10% glycerol, 3% hydroxypropylmethyl cellulose acetate succinate, 12% hydroxypropyl cellulose) possessed a fast disintegration time (60 ± 3 s), quick release in artificial saliva (>80% in 10 min), high burst strength (2190 mN mm) and high efficacy against several spp. (, and ) (>15 mm inhibition halo). Amphotericin B orodispersible films are stable for two weeks at room temperature (25 °C) and up to 1 year in the fridge. Although further toxicological and in vivo efficacy studies are required, this novel Amphotericin B orodispersible films is a promising, physicochemically stable formulation with potential wide application in clinical practice, especially for immunocompromised patients suffering from oropharyngeal candidiasis.
两性霉素B对某些菌种具有高活性,产生耐药性的风险较低。然而,与其他抗真菌药物(如咪康唑和克霉唑)相比,两性霉素B分子量高,且水溶性差,这限制了其在口腔咽腔生理条件下(唾液pH值、溶解体积有限)的疗效,从而限制了其在口腔念珠菌病中的临床应用。我们采用溶剂浇铸法制备了高载药量(1%)的速溶口腔崩解膜,使两性霉素B在唾液中以单体和二聚体状态平衡保持溶解状态,并能够产生局部抗真菌作用。通过设计质量研究实现了对载两性霉素B口腔崩解膜的优化,该研究将葡聚糖和/或麦芽糊精作为葡萄糖衍生聚合物成膜剂与纤维素衍生成膜剂(羟丙基甲基纤维素/羟丙基纤维素,重量比为1:4)、用于掩味的山梨醇、用于增强膜机械强度的微晶纤维素(微晶纤维素200)或微晶纤维素 - 羧甲基纤维素钠(微晶纤维素CL - 611)以及作为增塑剂的聚乙二醇400和甘油(1:1)相结合。优化后的载两性霉素B口腔崩解膜(含有1%两性霉素B、25%葡聚糖、25%麦芽糊精、5%山梨醇、10%微晶纤维素200、10%聚乙二醇400、10%甘油、3%醋酸琥珀酸羟丙基甲基纤维素、12%羟丙基纤维素)具有快速崩解时间(60±3秒)、在人工唾液中快速释放(10分钟内>80%)、高破裂强度(2190 mN·mm)以及对几种菌种(白色念珠菌、热带念珠菌和近平滑念珠菌)具有高效性(抑菌圈>15毫米)。载两性霉素B口腔崩解膜在室温(25℃)下可稳定保存两周,在冰箱中可保存长达1年。尽管还需要进一步的毒理学和体内疗效研究,但这种新型的载两性霉素B口腔崩解膜是一种有前景的、物理化学性质稳定的制剂,在临床实践中具有潜在的广泛应用,特别是对于患有口腔念珠菌病的免疫功能低下患者。