Department of Pharmacy Division of Pharmaceutical Technology, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Center for Interdisciplinary Research and Innovation (CIRI-AUTH), Thessaloniki, Greece.
AAPS PharmSciTech. 2024 Aug 20;25(7):190. doi: 10.1208/s12249-024-02908-5.
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.
在这项研究中,制造了 3D 打印抗真菌颊膜(BFs),作为替代市售抗真菌口腔凝胶的潜在选择,以解决关键问题,如易于制造、给药方便、增强药物疗效和适合儿科患者。制造过程涉及使用半固态挤压法从玉米醇溶蛋白-聚乙烯吡咯烷酮(zein-PVP)聚合物共混物中制造 BFs,该聚合物共混物作为药物(咪康唑)和味觉增强剂的载体。制造后,确定所有薄膜的崩解时间都小于 10 分钟。然而,这些薄膜旨在粘附在颊组织上,以确保药物持续释放。大约 80%的咪康唑在 2 小时内从 3D 打印薄膜的 zein/PVP 基质中逐渐释放。此外,还进行了详细的物理化学特性研究,包括光谱和热法,以评估薄膜成分的固态和热稳定性。还研究了粘膜粘附性能和机械评估,同时进行了渗透研究,以了解载有咪康唑的薄膜与市售口腔凝胶制剂相比渗透颊组织的程度。对处理后的组织进行了组织学评估。此外,还评估了开发的薄膜和市售口腔凝胶的体外抗真菌活性。最后,薄膜进行了两个月的药物稳定性测试,以确定 BFs 是否适合临床应用。结果表明,3D 打印薄膜是口腔局部给予咪康唑的一种有前途的替代方法。