School of Pharmacy, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.
Department of Molecular Medicine and Pathology, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.
Drug Dev Ind Pharm. 2021 Oct;47(10):1680-1692. doi: 10.1080/03639045.2022.2048666. Epub 2022 Mar 15.
Thymopentin (TP5) is a synthetic pentapeptide with immunomodulatory properties. Given the previously described poor absorption of TP5, preformulation data is required to support effective formulation development. In this manuscript, an analytical method of TP5 was developed and validated to determine the aqueous solubility, stability, and Log P of TP5. Thermal properties were investigated, and chemical, physical and enzymatic degradation were evaluated. TP5 was informed to load in a microemulsion (ME) system according to the preformulation parameters and characterized for rheological behavior, droplet size, morphology and drug release. TP5 displayed high aqueous solubility (294.3 mg/mL), low Log P (-4.2) and 2% water content with a melting temperature of 193 °C. TP5 degraded rapidly in alkaline conditions, at elevated temperature, in oxidizing agents, and with UV exposure, however TP5 had a longer half-life in acidic conditions. The fastest enzymatic degradation was with Trypsin (half-life 6.3 h) compared with other digestive enzymes. The different degradation pathways followed first-order kinetics, and half-lives were obtained from the kinetic studies. The TP5 loaded ME exhibited a droplet size of 143 ± 35 nm with a Higuchi-model fitted sustained release profile for 24 h. These data justify and support the design of formulations to stabilize and enhance the absorption of TP5, with a ME formulation demonstrated.
胸腺五肽(TP5)是一种具有免疫调节特性的合成五肽。鉴于之前描述的 TP5 吸收不良,需要进行预配方研究以支持有效的配方开发。在本文中,开发并验证了一种用于测定 TP5 的水溶解度、稳定性和 Log P 的分析方法。研究了热特性,并评估了化学、物理和酶降解。根据预配方参数,TP5 被指示载入微乳液(ME)系统,并对其流变行为、粒径、形态和药物释放进行了表征。TP5 表现出高水溶性(294.3mg/mL)、低 Log P(-4.2)和 2%含水量,熔点为 193°C。TP5 在碱性条件下、高温下、在氧化剂存在下以及在紫外线照射下迅速降解,但在酸性条件下具有更长的半衰期。与其他消化酶相比,胰蛋白酶(半衰期 6.3h)对 TP5 的降解最快。不同的降解途径遵循一级动力学,半衰期通过动力学研究获得。负载 TP5 的 ME 表现出 143±35nm 的粒径,并具有符合 Higuchi 模型的 24h 持续释放特征。这些数据证明并支持了设计制剂以稳定和增强 TP5 吸收的合理性,其中展示了 ME 制剂的效果。