Pastório Nayla Francine Garcia, Vecchi Camila Felix, Said Dos Santos Rafaela, Bruschi Marcos Luciano
Laboratory of Research and Development of Drug Delivery Systems, Postgraduate Program in Pharmaceutical Sciences, Department of Pharmacy, State University of Maringa, Maringa 87020-900, PR, Brazil.
Pharmaceutics. 2021 Jul 31;13(8):1187. doi: 10.3390/pharmaceutics13081187.
Tramadol hydrochloride is a synthetic analogue of codeine and shows activity on the central nervous system as an opioid agonist and inhibitor of serotonin and norepinephrine reuptake. It has been used for controlling moderate to severe pain. Mucoadhesive fast-dissolving films can present greater drug availability and patient acceptance when compared to the systems of peroral administration. The films were prepared using the solvent casting method with ethylcellulose, polyvinylpyrrolidone and poly(vinyl alcohol). The effect of each polymer concentration was investigated using a 2³ factorial design with repetition at the central point. The formulations were subjected to physicochemical, mechanical, ex vivo mucoadhesive and in vitro drug release profile analysis. These properties were dependent on the polymeric composition (independent factors) of each system. The optimized formulations showed good macroscopic characteristics, improved resistance to bending, rigidity, rapid swelling up to 60 s, improved mechanical and mucoadhesive characteristics, and also fast dissolving and tramadol release. The optimized formulations constitute platforms and strategies to improve the therapy of tramadol with regard to availability at the site of application, considering the necessity of rapid pain relief, and show potential for in vivo evaluation.
盐酸曲马多是可待因的合成类似物,作为阿片类激动剂以及5-羟色胺和去甲肾上腺素再摄取抑制剂,对中枢神经系统有活性。它一直用于控制中度至重度疼痛。与口服给药系统相比,粘膜粘附速溶膜可呈现更高的药物利用率和患者接受度。这些膜采用溶剂浇铸法,使用乙基纤维素、聚乙烯吡咯烷酮和聚乙烯醇制备。使用2³析因设计并在中心点重复研究了每种聚合物浓度的影响。对制剂进行了物理化学、机械、体外粘膜粘附和体外药物释放曲线分析。这些特性取决于每个系统的聚合物组成(独立因素)。优化后的制剂显示出良好的宏观特性、改善的抗弯曲性、刚性、在60秒内快速溶胀、改善的机械和粘膜粘附特性,以及快速溶解和曲马多释放。考虑到快速缓解疼痛的必要性,优化后的制剂构成了在应用部位提高曲马多治疗可用性的平台和策略,并显示出体内评估的潜力。