Institute for Medicines and Medical Devices of Montenegro, Ivana Crnojevića 64a, 81000 Podgorica, Montenegro.
Department of Pharmaceutical Technology and Cosmetology, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11221 Belgrade, Serbia.
Molecules. 2020 Dec 29;26(1):111. doi: 10.3390/molecules26010111.
Various three-dimensional printing (3DP) technologies have been investigated so far in relation to their potential to produce customizable medicines and medical devices. The aim of this study was to examine the possibility of tailoring drug release rates from immediate to prolonged release by varying the tablet thickness and the drug loading, as well as to develop artificial neural network (ANN) predictive models for atomoxetine (ATH) release rate from DLP 3D-printed tablets. Photoreactive mixtures were comprised of poly(ethylene glycol) diacrylate (PEGDA) and poly(ethylene glycol) 400 in a constant ratio of 3:1, water, photoinitiator and ATH as a model drug whose content was varied from 5% to 20% (/). Designed 3D models of cylindrical shape tablets were of constant diameter, but different thickness. A series of tablets with doses ranging from 2.06 mg to 37.48 mg, exhibiting immediate- and modified-release profiles were successfully fabricated, confirming the potential of this technology in manufacturing dosage forms on demand, with the possibility to adjust the dose and release behavior by varying drug loading and dimensions of tablets. DSC (differential scanning calorimetry), XRPD (X-ray powder diffraction) and microscopic analysis showed that ATH remained in a crystalline form in tablets, while FTIR spectroscopy confirmed that no interactions occurred between ATH and polymers.
迄今为止,已经研究了各种三维打印(3DP)技术,以探讨它们在生产定制药物和医疗器械方面的潜力。本研究的目的是通过改变片剂厚度和药物负载来研究从即刻释放到延长释放调节药物释放速率的可能性,以及开发用于从 DLP 3D 打印片剂中释放阿托西汀(ATH)的人工神经网络(ANN)预测模型。光反应混合物由聚乙二醇二丙烯酸酯(PEGDA)和聚乙二醇 400 以 3:1 的恒定比例组成,水、光引发剂和 ATH 作为模型药物,其含量从 5%变化到 20%(/)。设计的圆柱形片剂 3D 模型具有相同的直径,但厚度不同。成功制造了一系列具有从 2.06 毫克到 37.48 毫克剂量的片剂,具有即刻和改良释放的特征,证实了这项技术在按需制造剂型方面的潜力,通过改变药物负载和片剂的尺寸来调整剂量和释放行为。DSC(差示扫描量热法)、XRPD(X 射线粉末衍射)和微观分析表明,ATH 在片剂中保持结晶形式,而 FTIR 光谱证实 ATH 和聚合物之间没有相互作用。