Zhen Zixuan, Sudarjat Hadi, Pierce Katherine, Hu Jonathan, Pan Yuying, Qin Chaolong, Ingabire Diane, Zhao Long, Pearcy Adam, Moeller F Gerard, O'Keeffe Charles, Halquist Matthew S, Xu Qingguo, Lu Xiuling
School of Pharmacy, Department of Pharmaceutical Sciences, University of Connecticut, 06269, USA.
School of Pharmacy, Department of Pharmaceutics, Virginia Commonwealth University, Richmond, VA 23298, USA.
Int J Pharm. 2025 Oct 15;683:126042. doi: 10.1016/j.ijpharm.2025.126042. Epub 2025 Aug 5.
Levo-alpha-acetylmethadol (LAAM) has a long duration of action offering numerous behavioral and clinical advantages for treating opioid use disorders. In this study, we aim to develop a novel oral immediate-release capsule of LAAM, as an alternative to methadone, the major medication that requires daily visits. LAAM solid dispersion-coated pellets were developed with VIVAPUR® MCC Spheres 700 as the core, and LAAM-carrier coating solution was sprayed onto the core pellets using a fluid bed coater. The coating solution formulation was optimized for reduced coating time and improved drug loading efficiency. Design of Experiments (DoE) studies were conducted, revealing the impact of critical process parameters-nozzle air pressure and airflow-on the critical quality attributes of the LAAM-coated pellets. Capsules with different dosage strengths were prepared. Capsule weight variation, content uniformity, and in vitro release tests were conducted based on USP guidelines for quality assessment. The LAAM capsules showed the immediate release profile. The storage stability of the LAAM capsules was evaluated under accelerated condition and room temperature for 6 months. The weight gain, drug content, and dissolution profile were evaluated. The results showed that drug contents and immediate-release properties remained after 6 months of storage. Pharmacokinetic (PK) study in rabbits showed that capsules have longer t as well as higher C of LAAM compared with oral solution. These capsules have a similar AUC of LAAM and its metabolites to the oral solution. It has been demonstrated that the developed LAAM capsules have the desired properties for subsequent clinical studies.
左-α-乙酰美沙多(LAAM)作用持续时间长,在治疗阿片类药物使用障碍方面具有诸多行为学和临床优势。在本研究中,我们旨在开发一种新型的LAAM口服速释胶囊,作为美沙酮的替代品,美沙酮是主要药物,需要每日就诊。以VIVAPUR® MCC Spheres 700为核心开发了LAAM固体分散体包衣微丸,并使用流化床包衣机将LAAM-载体包衣溶液喷涂到核心微丸上。对包衣溶液配方进行了优化,以减少包衣时间并提高药物负载效率。进行了实验设计(DoE)研究,揭示了关键工艺参数——喷嘴气压和气流——对LAAM包衣微丸关键质量属性的影响。制备了不同剂量强度的胶囊。根据美国药典质量评估指南进行了胶囊重量差异、含量均匀度和体外释放测试。LAAM胶囊呈现速释特征。在加速条件和室温下对LAAM胶囊的储存稳定性进行了6个月的评估。评估了重量增加、药物含量和溶出曲线。结果表明,储存6个月后药物含量和速释特性依然存在。在兔子身上进行的药代动力学(PK)研究表明,与口服溶液相比,胶囊具有更长的LAAM半衰期以及更高的血药浓度。这些胶囊的LAAM及其代谢物的曲线下面积(AUC)与口服溶液相似。已经证明,所开发的LAAM胶囊具有用于后续临床研究的理想特性。