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超分子共晶水凝胶作为一种新的口服儿科给药系统,可提高苯并硝唑的生物利用度。

Supramolecular eutectogel as new oral paediatric delivery system to enhance benznidazole bioavailability.

机构信息

Department of Pharmacy and Biotechnology, University of Bologna, Via San Donato 19/2, I-40127 Bologna, Italy.

Department of Pharmacy and Biotechnology, University of Bologna, Via San Donato 19/2, I-40127 Bologna, Italy.

出版信息

Int J Pharm. 2024 Aug 15;661:124417. doi: 10.1016/j.ijpharm.2024.124417. Epub 2024 Jul 2.

Abstract

Benznidazole (BNZ) serves as the primary drug for treating Chagas Disease and is listed in the WHO Model List of Essential Medicines for Children. Herein, a new child-friendly oral BNZ delivery platform is developed in the form of supramolecular eutectogels (EGs). EGs address BNZ's poor oral bioavailability and provide a flexible twice-daily dose in stick-pack format. This green and sustainable formulation strategy relies on the gelation of drug-loaded Natural Deep Eutectic Solvents (NaDES) with xanthan gum (XG) and water. Specifically, choline chloride-based NaDES form stable and biocompatible 5 mg/mL BNZ-loaded EGs. Rheological and Low-field NMR investigations indicate that EGs are viscoelastic materials comprised of two co-existing regions in the XG network generated by different crosslink distributions between the biopolymer, NaDES and water. Remarkably, the shear modulus and relaxation spectrum of EGs remain unaffected by temperature variations. Upon dilution with simulated gastrointestinal fluids, EGs results in BNZ supersaturation, serving as the primary driving force for its absorption. Interestingly, after oral administration of EGs to rats, drug bioavailability increases by 2.6-fold, with a similar increase detected in their cerebrospinal fluid. The noteworthy correlation between in vivo results and in vitro release profiles confirms the efficacy of EGs in enhancing both peripheral and central BNZ oral bioavailability.

摘要

苯硝唑(BNZ)是治疗恰加斯病的主要药物,被列入世界卫生组织儿童基本药物标准清单。在此,我们开发了一种新的儿童友好型 BNZ 口服递药超分子共晶胶(EGs)。EGs 解决了 BNZ 口服生物利用度差的问题,并提供了灵活的每日两次剂量棒状包装形式。这种绿色可持续的配方策略依赖于载药天然深共晶溶剂(NaDES)与黄原胶(XG)和水的胶凝作用。具体来说,基于氯化胆碱的 NaDES 可形成稳定且生物相容的 5mg/mL BNZ 载 EG。流变学和低场 NMR 研究表明,EGs 是粘弹性材料,由 XG 网络中两种共存区域组成,这两种区域由生物聚合物、NaDES 和水之间不同的交联分布产生。值得注意的是,EGs 的剪切模量和弛豫谱不受温度变化的影响。用模拟胃肠道液稀释后,EGs 导致 BNZ 过饱和,这是其吸收的主要驱动力。有趣的是,在大鼠口服 EGs 后,药物生物利用度增加了 2.6 倍,其脑脊液中也检测到类似的增加。体内结果与体外释放曲线的显著相关性证实了 EGs 能够提高外周和中枢 BNZ 口服生物利用度的功效。

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