Mau Robert, Seitz Hermann
Microfluidics, Faculty of Mechanical Engineering and Marine Technology, University of Rostock, Justus-von-Liebig Weg 6, 18059 Rostock, Germany.
Department Life, Light & Matter, Interdisciplinary Faculty, University of Rostock, Albert-Einstein-Str. 25, 18059 Rostock, Germany.
Pharmaceutics. 2023 Jan 21;15(2):367. doi: 10.3390/pharmaceutics15020367.
Drop-on-demand (DOD) inkjet printing enables exact dispensing and positioning of single droplets in the picoliter range. In this study, we investigate the long-term reproducibility of droplet formation of piezoelectric inkjet printed drug solutions using solvents with different volatilities. We found inkjet printability of EtOH/ASA drug solutions is limited, as there is a rapid forming of drug deposits on the nozzle of the printhead because of fast solvent evaporation. Droplet formation of c = 100 g/L EtOH/ASA solution was affected after only a few seconds by little drug deposits, whereas for c = 10 g/L EtOH/ASA solution, a negative affection was observed only after t = 15 min, while prominent drug deposits form at the printhead tip. Due to the creeping effect, the crystallizing structures of ASA spread around the nozzle but do not clog it necessarily. When there is a negative affection, the droplet trajectory is affected the most, while the droplet volume and droplet velocity are influenced less. In contrast, no formation of drug deposits could be observed for highly concentrated, low volatile DMSO-based drug solution of c = 100 g/L even after a dispensing time of t = 30 min. Therefore, low volatile solvents are preferable to highly volatile solvents to ensure a reproducible droplet formation in long-term inkjet printing of highly concentrated drug solutions. Highly volatile solvents require relatively low drug concentrations and frequent printhead cleaning. The findings of this study are especially relevant when high droplet positioning precision is desired, e.g., drug loading of microreservoirs or drug-coating of microneedle devices.
按需滴注(DOD)喷墨打印能够精确地分配和定位皮升范围内的单个液滴。在本研究中,我们研究了使用具有不同挥发性的溶剂,通过压电喷墨打印药物溶液形成液滴的长期重现性。我们发现乙醇/阿司匹林(EtOH/ASA)药物溶液的喷墨打印性有限,因为溶剂快速蒸发,打印头喷嘴上会迅速形成药物沉积物。对于浓度为100 g/L的EtOH/ASA溶液,仅几秒钟后,少量药物沉积物就会影响液滴形成;而对于浓度为10 g/L的EtOH/ASA溶液,仅在15分钟后才观察到负面影响,同时在打印头尖端形成明显的药物沉积物。由于爬行效应,阿司匹林(ASA)的结晶结构在喷嘴周围扩散,但不一定会堵塞喷嘴。当出现负面影响时,液滴轨迹受到的影响最大,而液滴体积和液滴速度受到的影响较小。相比之下,即使在30分钟的滴注时间后,对于浓度为100 g/L的高浓度、低挥发性二甲亚砜(DMSO)基药物溶液,也未观察到药物沉积物的形成。因此,在高浓度药物溶液的长期喷墨打印中,为确保可重现的液滴形成,低挥发性溶剂优于高挥发性溶剂。高挥发性溶剂需要相对较低的药物浓度且频繁清洁打印头。当需要高液滴定位精度时,例如微储库的药物装载或微针装置的药物包被,本研究的结果尤其重要。