Oh Ye Chan, Ong Jun Jie, Alfassam Haya, Díaz-Torres Eduardo, Goyanes Alvaro, Williams Gareth R, Basit Abdul W
Department of Pharmaceutics, UCL School of Pharmacy, University College London, 29-39 Brunswick Square, London, WC1N 1AX, UK.
Advanced Diagnostics and Therapeutics Institute, King Abdulaziz City for Science and Technology (KACST), Health Sector, Riyadh, 11442, Saudi Arabia.
Drug Deliv Transl Res. 2025 May;15(5):1595-1608. doi: 10.1007/s13346-024-01697-5. Epub 2024 Aug 23.
Mutable devices and dosage forms have the capacity to dynamically transform dimensionally, morphologically and mechanically upon exposure to non-mechanical external triggers. By leveraging these controllable transformations, these systems can be used as minimally invasive alternatives to implants and residence devices, foregoing the need for complex surgeries or endoscopies. 4D printing, the fabrication of 3D-printed structures that evolve their shape, properties, or functionality in response to stimuli over time, allows the production of such devices. This study explores the potential of volumetric printing, a novel vat photopolymerisation technology capable of ultra-rapid printing speeds, by comparing its performance against established digital light processing (DLP) printing in fabricating hydrogel-based drug-eluting devices. Six hydrogel formulations consisting of 2-(acryloyloxy)ethyl]trimethylammonium chloride solution, lithium phenyl-2,4,6-trimethylbenzoylphosphinate, varying molecular weights of the crosslinking monomer, poly(ethylene glycol) diacrylate, and paracetamol as a model drug were prepared for both vat photopolymerisation technologies. Comprehensive studies were conducted to investigate the swelling and water sorption profiles, drug release kinetics, and physicochemical properties of each formulation. Expandable drug-eluting 4D devices were successfully fabricated within 7.5 s using volumetric printing and were shown to display equivalent drug release kinetics to prints created using DLP printing, demonstrating drug release, swelling, and water sorption properties equivalent to or better than those of DLP-printed devices. The reported findings shed light on the advantages and limitations of each technology for creating these dynamic drug delivery systems and provides a direct comparison between the two technologies, while highlighting the promising potential of volumetric printing and further expanding the growing repertoire of pharmaceutical printing.
可变装置和剂型能够在暴露于非机械外部触发因素时,在尺寸、形态和机械性能方面进行动态转变。通过利用这些可控的转变,这些系统可以用作植入物和留置装置的微创替代品,无需进行复杂的手术或内窥镜检查。4D打印,即制造能随时间响应刺激而改变形状、性能或功能的3D打印结构,使得此类装置的生产成为可能。本研究通过将其性能与成熟的数字光处理(DLP)打印在制造水凝胶基药物洗脱装置方面进行比较,探索了体积打印(一种能够实现超快速打印速度的新型光固化3D打印技术)的潜力。为两种光固化3D打印技术制备了六种水凝胶配方,其由[2-(丙烯酰氧基)乙基]三甲基氯化铵溶液、苯基-2,4,6-三甲基苯甲酰基膦酸锂、不同分子量的交联单体聚乙二醇二丙烯酸酯以及作为模型药物的对乙酰氨基酚组成。进行了全面的研究,以调查每种配方的溶胀和吸水情况、药物释放动力学以及物理化学性质。使用体积打印在7.5秒内成功制造出可膨胀的药物洗脱4D装置,结果表明其药物释放动力学与使用DLP打印制作的装置相当,显示出与DLP打印装置相当或更好的药物释放、溶胀和吸水性能。所报告的研究结果揭示了每种技术在创建这些动态药物递送系统方面的优缺点,并对这两种技术进行了直接比较,同时突出了体积打印的广阔潜力,并进一步扩展了不断增长的药物打印技术种类。