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基于熔融固化打印工艺(MESO-PP)的聚电解质复合物的 3D 打印苯并硝唑片剂:一种治疗恰加斯病的个体化治疗的创新策略。

3D printed benznidazole tablets based on an interpolyelectrolyte complex by melting solidification printing process (MESO-PP): An innovative strategy for personalized treatment of Chagas disease.

机构信息

Universidad Nacional de Córdoba, Facultad de Ciencias Químicas, Departamento de Ciencias Farmacéuticas, Córdoba, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas, CONICET, Unidad de Investigación y Desarrollo en Tecnología Farmacéutica, UNITEFA, Córdoba, Argentina.

Centro de Evaluación de Biodisponibilidad y Bioequivalencia de Medicamentos (CEBIOBE), Departamento de Ciencias Farmacéuticas, Facultad de Química, Universidad de la República, Montevideo, Uruguay.

出版信息

Int J Pharm. 2024 Sep 5;662:124476. doi: 10.1016/j.ijpharm.2024.124476. Epub 2024 Jul 18.

DOI:10.1016/j.ijpharm.2024.124476
PMID:39029635
Abstract

3D printing technology is revolutionizing pharmaceuticals, offering tailored solutions for solid dosage forms. This innovation is particularly significant for conditions like Chagas disease, which require weight-dependent treatments. In this work, a formulation of benznidazole (BNZ), the primary treatment for this infection, was developed to be utilized with the Melting Solidification Printing Process (MESO-PP) 3D printing technique. Considering the limited aqueous solubility of BNZ, an interpolyelectrolyte complex (IPEC), composed of chitosan and pectin, was integrated to improve its dissolution profile. The formulations, also called inks in this context, with and without IPEC were integrally characterized and compared. The printing process was studied, the release of BNZ from 3D-prints (3DP) was exhaustively analyzed and a physiologically based pharmacokinetic model (PKPB) was developed to forecast their pharmacokinetic performance. 3DP were successfully achieved loading 25, 50 and 100 mg of BNZ. The presence of the IPEC in the ink caused a decrease in the crystalline domain of BNZ and facilitated the printing process, reaching a print success rate of 83.3 %. Interestingly, 3DP-IPEC showed accelerated release dissolution profiles, releasing over 85 % of BNZ in 90 min, while 3DP took up to 48 h for doses above 25 mg. The PBPK model demonstrated that 3DP-IPEC tablets would present high bioavailability (0.92), higher than 3DP (0.36) and similar to the commercial product. This breakthrough holds immense potential for improving treatment outcomes for neglected diseases.

摘要

3D 打印技术正在彻底改变制药行业,为固体制剂提供定制化解决方案。对于恰加斯病等需要根据体重进行治疗的疾病,这项创新具有特别重要的意义。在这项工作中,开发了一种苯硝唑(BNZ)的制剂,用于利用熔融固化打印工艺(MESO-PP)3D 打印技术。考虑到 BNZ 的有限水溶性,加入了由壳聚糖和果胶组成的聚电解质复合物(IPEC),以改善其溶解特性。这些制剂,在这种情况下也称为墨水,进行了全面的特性描述和比较。研究了打印工艺,对 3D 打印(3DP)中 BNZ 的释放进行了详尽分析,并开发了基于生理的药代动力学模型(PKPB)来预测它们的药代动力学性能。成功实现了装载 25、50 和 100mg BNZ 的 3DP。墨水中 IPEC 的存在降低了 BNZ 的结晶域,促进了打印过程,打印成功率达到 83.3%。有趣的是,3DP-IPEC 显示出加速释放的溶解特性,在 90 分钟内释放超过 85%的 BNZ,而 3DP 则需要 48 小时以上才能释放 25mg 以上的剂量。PBPK 模型表明,3DP-IPEC 片剂将具有高生物利用度(0.92),高于 3DP(0.36),与商业产品相似。这一突破为改善被忽视疾病的治疗效果带来了巨大潜力。

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