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左甲状腺素缓释微球的研制及其在甲状腺功能减退症治疗中的体内评价。

Development and In Vivo Evaluation of Sustained Release Microparticles Loaded with Levothyroxine for Hypothyroidism Treatment.

机构信息

School of Medicine, The University of Jordan, Amman 11942, Jordan.

School of Pharmacy, The University of Jordan, Amman 11942, Jordan.

出版信息

J Pharm Sci. 2024 Jun;113(6):1566-1571. doi: 10.1016/j.xphs.2024.01.004. Epub 2024 Jan 15.

DOI:10.1016/j.xphs.2024.01.004
PMID:38232803
Abstract

Hypothyroidism is a chronic condition combated by a daily oral supplementation of levothyroxine. In addition to the need for frequent dosing, oral administration may result in variable absorption of the drug leading to a failure in achieving normal thyroid function. Therefore, the development of a long-acting injectable system capable of delivering the drug is necessary. This work was aimed at developing sustained release microparticles loaded with levothyroxine. The microparticles were produced through the emulsification-solvent evaporation method using 2 grades of biocompatible and biodegradable polyesters: poly(ᴅ,ʟ-lactide-co-glycolide) (PLGA) and poly(ᴅ,ʟ-lactide) (PLA). Both polymers produced microparticles with very similar sizes (1.9 µm) and zeta potential values (around -22.0 mV). However, PLA microparticles had a significantly higher drug loading (6.1% vs. 4.4%, respectively) and encapsulation efficiency (36.8%, vs. 26.1%, respectively) when compared to PLGA counterparts. While both types of microparticles displayed a biphasic release pattern in vitro, a slower rate of release was observed with PLA microparticles. Moreover, a similar biphasic release pattern was found in vivo, with an initial phase of rapid release followed by a slower phase in the subsequent 10 days. These results indicate the possibility of developing levothyroxine loaded polyester microparticles as a potential long-acting thyroid hormone replacement therapy.

摘要

甲状腺功能减退症是一种慢性疾病,需要每天口服左甲状腺素进行治疗。除了需要频繁给药外,口服给药可能导致药物吸收不稳定,从而导致甲状腺功能无法恢复正常。因此,有必要开发一种能够提供长效药物的可注射系统。本工作旨在开发载有左甲状腺素的缓释微球。通过乳化-溶剂蒸发法使用两种生物相容性和可生物降解的聚酯:聚(D,L-丙交酯-共-乙交酯)(PLGA)和聚(D,L-丙交酯)(PLA)来制备微球。这两种聚合物所产生的微球粒径(1.9μm)和zeta 电位值(约-22.0 mV)非常相似。然而,与 PLGA 微球相比,PLA 微球的载药量(6.1%比 4.4%)和包封效率(36.8%比 26.1%)明显更高。虽然两种类型的微球在体外均显示出双相释放模式,但 PLA 微球的释放速度较慢。此外,体内也发现了类似的双相释放模式,初始阶段快速释放,随后在接下来的 10 天内缓慢释放。这些结果表明,开发载有左甲状腺素的聚酯微球作为潜在的长效甲状腺激素替代疗法是可行的。

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