Tailored Sticky Solutions: 3D-Printed Miconazole Buccal Films for Pediatric Oral Candidiasis.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Konstantina Chachlioutaki, Anastasia Iordanopoulou, Orestis L Katsamenis, Anestis Tsitsos, Savvas Koltsakidis, Pinelopi Anastasiadou, Dimitrios Andreadis, Vangelis Economou, Christos Ritzoulis, Dimitrios Tzetzis, Nikolaos Bouropoulos, Iakovos Xenikakis, Dimitrios Fatouros
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Abstract

In this research, 3D-printed antifungal buccal films (BFs) were manufactured as a potential alternative to commercially available antifungal oral gels addressing key considerations such as ease of manufacturing, convenience of administration, enhanced drug efficacy and suitability of paediatric patients. The fabrication process involved the use of a semi-solid extrusion method to create BFs from zein-Poly-Vinyl-Pyrrolidone (zein-PVP) polymer blend, which served as a carrier for drug (miconazole) and taste enhancers. After manufacturing, it was determined that the disintegration time for all films was less than 10 min. However, these films are designed to adhere to buccal tissue, ensuring sustained drug release. Approximately 80% of the miconazole was released gradually over 2 h from the zein/PVP matrix of the 3D printed films. Moreover, a detailed physicochemical characterization including spectroscopic and thermal methods was conducted to assess solid state and thermal stability of film constituents. Mucoadhesive properties and mechanical evaluation were also studied, while permeability studies revealed the extent to which film-loaded miconazole permeates through buccal tissue compared to commercially available oral gel formulation. Histological evaluation of the treated tissues was followed. Furthermore, in vitro antifungal activity was assessed for the developed films and the commercial oral gel. Finally, films underwent a two-month drug stability test to ascertain the suitability of the BFs for clinical application. The results demonstrate that 3D-printed films are a promising alternative for local administration of miconazole in the oral cavity.

Abstract Image

量身定制的粘性解决方案:用于治疗小儿口腔念珠菌病的三维打印咪康唑颊黏膜。
本研究制造了三维打印抗真菌口腔薄膜(BFs),作为市售抗真菌口腔凝胶的潜在替代品,主要考虑因素包括易于制造、给药方便、增强药效和适合儿科患者。制造过程包括使用半固态挤压法,将玉米蛋白-聚乙烯吡咯烷酮(玉米蛋白-PVP)聚合物混合物制成 BF,作为药物(咪康唑)和增味剂的载体。生产后发现,所有薄膜的崩解时间均小于 10 分钟。不过,这些薄膜的设计目的是粘附在口腔组织上,确保药物的持续释放。大约 80% 的咪康唑在 2 小时内从 3D 打印薄膜的沸石/PVP 基质中逐渐释放出来。此外,还进行了详细的物理化学表征,包括光谱和热学方法,以评估薄膜成分的固态和热稳定性。此外,还研究了黏附性能和机械评估,而渗透性研究则揭示了与市售口服凝胶制剂相比,薄膜装载的咪康唑通过口腔组织的渗透程度。随后还对处理过的组织进行了组织学评估。此外,还对开发的薄膜和商用口服凝胶进行了体外抗真菌活性评估。最后,对薄膜进行了为期两个月的药物稳定性测试,以确定 BFs 是否适合临床应用。研究结果表明,三维打印薄膜是口腔局部给药咪康唑的理想选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
7.20
自引率
4.30%
发文量
567
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