利鲁唑口服混悬液治疗肌萎缩性侧索硬化症:质地及与食品增稠剂的相容性评价

J Pub Date : 2020-08-19 DOI:10.3390/j3030021
G. Colombo, R. Artico, D. Barbareschi
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引用次数: 1

摘要

利鲁唑5mg /mL口服混悬液是唯一获批用于口服治疗肌萎缩性侧索硬化症(ALS)的液体药物。由于超过80%的ALS患者出现吞咽困难,口服液体制剂提供了一个重要的治疗选择。利鲁唑5mg /mL口服混悬液通过药包内的分级口服给药注射器给药。其浓度(5mg /mL)与小而易于测量的体积(10ml)一致,每天两次提供规定的50mg剂量。这项工作有双重目的。首先是根据国际吞咽困难饮食标准化倡议(IDDSI)流量测试评估利鲁唑5mg /mL口服混悬液的质地。本实验结果表明,利鲁唑5mg /mL口服混悬液基本属于“轻度粘稠”的IDDSI描述。这是一个重要的特征,因为粘稠的液体有助于吞咽困难患者更安全的吞咽。作为第二个目标,我们为科学目的评估利鲁唑5mg /mL口服混悬液与市场上一些最常见的食品增稠剂的相容性。利鲁唑5mg /mL口服混悬液与增稠剂的亲密混合物在制备后立即和室温下放置2小时后进行外观、pH、利鲁唑测定和利鲁唑相关物质的评价。利鲁唑5mg /mL口服混悬液与市售增稠剂的相容性良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Riluzole Oral Suspension for the Treatment of Amyotrophic Lateral Sclerosis: Texture and Compatibility with Food Thickeners Evaluation
Riluzole 5 mg/mL oral suspension is the only licensed liquid medicine to treat Amyotrophic Lateral Sclerosis (ALS) orally. As more than 80% of ALS patients develop dysphagia, an oral liquid formulation provides an important therapeutic option. The Riluzole 5 mg/mL oral suspension is administered by means of the graduated oral dosing syringe included in the medicine package. Its concentration (5 mg/mL) is consistent with a small and easy to measure volume (10 mL) to deliver the prescribed 50-mg dose twice daily. This work had a dual objective. The first was to evaluate the texture of the Riluzole 5 mg/mL oral suspension according to the International Dysphagia Diet Standardisation Initiative (IDDSI) flow test. Results of this experiment indicated that Riluzole 5 mg/mL oral suspension would basically fall under the “mildly thick” IDDSI descriptors. This is an important feature because thick fluids facilitate a safer swallow in patients with dysphagia. As a second objective, we evaluated for scientific purposes the compatibility of Riluzole 5 mg/mL oral suspension with some of the most common food thickeners available on the market. Intimate mixtures of the Riluzole 5 mg/mL oral suspension with thickeners were evaluated for appearance, pH, Riluzole assay and Riluzole related substances immediately after preparation and after two hours at room temperature. Riluzole 5 mg/mL oral suspension resulted to be compatible with all the marketed thickeners tested.
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