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Inhalable Dry Powder of Bedaquiline for Pulmonary Tuberculosis: In Vitro Physicochemical Characterization Antimicrobial Activity and Safety Studies

机译:贝达喹啉可吸入性干粉用于肺结核:体外理化特性抗菌活性和安全性研究

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摘要

Bedaquiline is a newly developed anti-tuberculosis drug, conditionally approved by the United States Food and Drug Administration (USFDA) for treating drug-resistant tuberculosis in adults. Oral delivery of bedaquiline causes severe side effects such as increased hepatic aminotransferase levels and cardiac arrhythmias (prolongation of QT-interval). This study aimed to develop inhalable dry powder particles of bedaquiline with high aerosolization efficiency to reduce the side-effects of oral bedaquiline. Bedaquiline (with or without -leucine) powders were prepared using a Buchi Mini Spray-dryer. The powders were characterized for physicochemical properties and for their in vitro aerosolization efficiency using a next-generation impactor (NGI). The formulation with maximum aerosolization efficiency was investigated for physicochemical and aerosolization stability after one-month storage at 20 ± 2 °C/30 ± 2% relative humidity (RH) and 25 ± 2 °C/75% RH in an open Petri dish. The cytotoxicity of the powders on A549 and Calu-3 cell-lines was evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The powders were also evaluated for antimicrobial activity against The aerodynamic diameter of the -leucine-containing powder was 2.4 µm, and the powder was amorphous in nature. The aerosolization efficiency (fine-particle fraction) of -leucine-containing powder (fine-particle fraction (FPF): 74.4%) was higher than the bedaquiline-only powder (FPF: 31.3%). -leucine containing powder particles were plate-shaped with rough surfaces, but the bedaquiline-only powder was spherical and smooth. The optimized powder was stable at both storage conditions during one-month storage and non-toxic (up to 50 µg/mL) to the respiratory cell-lines. Bedaquiline powders were effective against and had a minimal inhibitory concentration (MIC) value of 0.1 µg/mL. Improved aerosolization may help to combat pulmonary tuberculosis by potentially reducing the side-effects of oral bedaquiline. Further research is required to understand the safety of the optimized inhalable powder in animal models.
机译:Bedaquiline是一种新开发的抗结核药,已获得美国食品和药物管理局(USFDA)的有条件批准,可用于治疗成人的耐药性结核病。苯达喹啉的口服给药会引起严重的副作用,例如肝转氨酶水平升高和心律不齐(QT间隔延长)。这项研究旨在开发具有高雾化效率的苯达喹啉可吸入干粉颗粒,以减少口服苯达喹啉的副作用。使用Buchi Mini喷雾干燥器制备贝达喹啉(有或没有亮氨酸)粉末。使用下一代撞击器(NGI)对粉末的理化性质和体外雾化效率进行了表征。在开放培养皿中,在20±2°C / 30±2%相对湿度(RH)和25±2°C / 75%RH储存一个月后,研究了具有最大雾化效率的制剂的理化和雾化稳定性。使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物(MTT)分析评估了粉末对A549和Calu-3细胞系的细胞毒性。还评估了这些粉末对抗菌的活性。含亮氨酸的粉末的空气动力学直径为2.4μm,并且该粉末本质上是无定形的。含亮氨酸的粉末(微粒分数(FPF):74.4%)的雾化效率(微粒分数)高于仅苯达喹啉的粉末(FPF:31.3%)。含亮氨酸的粉末颗粒为具有粗糙表面的板状,而仅苯达喹啉的粉末为球形且光滑。经过优化的粉末在一个月的储存条件下均稳定,并且对呼吸道细胞系无毒(最高50 µg / mL)。贝达喹啉粉对0.1克/毫升有效,最小抑菌浓度(MIC)值为0.1 µg / mL。改善的雾化作用可能通过减少口服苯达喹啉的副作用来帮助抗击肺结核。需要进一步研究以了解优化的可吸入粉剂在动物模型中的安全性。

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