Development of lipid nanoparticles with nystatin for an antifungal action

Cecília Nascimento, Filipa Sousa, S. Reis, P. Costa
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Abstract

Fungal diseases currently affect about a quarter of the population worldwide. Fungi infections caused by Candida albicans have been described as a significant concern to public health. The spectrum of clinical diseases caused by this fungi species range between vulvovaginal candidiasis, oral candidiasis, candidemia and mucositis. The emergence of resistance mechanisms towards antifungal therapy greatly hampers successful management of illness and patient outcome. Nystatin, an antifungal drug, is categorized as a class IV of Biopharmaceutical Classification System, presenting low aqueous solubility and low intestinal permeability. Nowadays, the emerging platform of nanotechnology and lipid nanoparticles, notably solid lipid nanoparticles (SLN), has been subject to growing attention over recent past, owing to the promising properties of vectorization among a substantial variety of pharmaceutical drugs. Due to its hydrophobic proprieties, nystatin was encapsulated in SLN. Thus aiming to understand the relationship between the use of nanosystems and the improvement of the therapeutic effect. The aim of this work was to formulate SLN with nystatin by different methods (high speed homogenization and ultrasonication) with optimization of several parameters and formulation of 2 gels (one of them containing nanoparticles). Initially, 3 lipids were used: Compritol®  888 ATO, cetyl palmitate and Precirol®  ATO 5 and, after the study of several parameters (size, encapsulation efficiency (EE) and polymorphic behaviour of the lipids), Precirol®  ATO 5 was chosen as the lipid with the most satisfactory results. The results of the present work showed that the assay method of nystatin was linear, specific and presented repeatability. The average diameter of empty nanoparticles (NPs) and with drug (Precirol-NYS NPs) was, respectively, 306 nm and 260 nm and an EE of 67.8%. Regarding stability, SLN with drug proved to be more stable than SLN without drug. The polymer used for formulation of gels was the polymer commonly known by the trade name Carbopol® 940. The yield of 0.5% Carbopol® gel preparations and 0.5% Carbopol® gel + 10% Precirol-NYS NPs were 87.2% and 91.39%, respectively.
具有制霉菌素抗真菌作用的脂质纳米颗粒的研制
真菌疾病目前影响着全世界约四分之一的人口。由白色念珠菌引起的真菌感染已被描述为对公共卫生的重大关切。由这种真菌引起的临床疾病范围包括外阴阴道念珠菌病、口腔念珠菌病、念珠菌病和粘膜炎。对抗真菌治疗的耐药机制的出现极大地阻碍了疾病的成功管理和患者的预后。制霉菌素是一种抗真菌药物,在生物制药分类系统中被列为IV类,具有低水溶性和低肠通透性。如今,纳米技术和脂质纳米颗粒的新兴平台,特别是固体脂质纳米颗粒(SLN),近年来受到越来越多的关注,这是由于矢量化在大量药物中的有前途的特性。由于制霉菌素的疏水性,制霉菌素被包裹在SLN中。因此,旨在了解纳米系统的使用与治疗效果的提高之间的关系。本研究的目的是通过不同的方法(高速均质和超声)来制备制霉菌素SLN,并优化了几个参数和两种凝胶(其中一种含有纳米颗粒)的配方。最初,我们使用了3种脂质:Compritol®888 ATO、棕榈酸cetyl和Precirol®ATO 5,在研究了几个参数(脂质的大小、包封效率(EE)和多态行为)后,我们选择了Precirol®ATO 5作为结果最满意的脂质。结果表明,制霉菌素的测定方法线性好,专属性好,重复性好。空纳米颗粒(NPs)和带药纳米颗粒(preciol - nys NPs)的平均直径分别为306 nm和260 nm, EE为67.8%。在稳定性方面,有药物的SLN比无药物的SLN更稳定。用于凝胶配方的聚合物是通常以商品名Carbopol®940著称的聚合物。0.5% Carbopol®凝胶制剂和0.5% Carbopol®凝胶+ 10% precirol - NPs的产率分别为87.2%和91.39%。
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