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容器片剂的三维打印:含多种药物的生物活性自纳米乳化给药系统(Bio-SNEDDSs)的新范例。

Three-Dimensional Printing of a Container Tablet: A New Paradigm for Multi-Drug-Containing Bioactive Self-Nanoemulsifying Drug-Delivery Systems (Bio-SNEDDSs).

作者信息

Kulkarni Vineet R, Kazi Mohsin, Shahba Ahmad Abdul-Wahhab, Radhanpuri Aakib, Maniruzzaman Mohammed

机构信息

Pharmaceutical Engineering and 3D Printing (PharmE3D) Labs, Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, The University of Texas at Austin, Austin, TX 78705, USA.

Department of Pharmaceutics, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.

出版信息

Pharmaceutics. 2022 May 18;14(5):1082. doi: 10.3390/pharmaceutics14051082.

Abstract

This research demonstrates the use of fused deposition modeling (FDM) 3D printing to control the delivery of multiple drugs containing bioactive self-nano emulsifying drug-delivery systems (SNEDDSs). Around two-thirds of the new chemical entities being introduced in the market are associated with some inherent issues, such as poor solubility and high lipophilicity. SNEDDSs provide for an innovative and easy way to develop a delivery platform for such drugs. Combining this platform with FDM 3D printing would further aid in developing new strategies for delivering poorly soluble drugs and personalized drug-delivery systems with added therapeutic benefits. This study evaluates the performance of a 3D-printed container system containing curcumin (CUR)- and lansoprazole (LNS)-loaded SNEDDS. The SNEDDS showed 50% antioxidant activity (IC) at concentrations of around 330.1 µg/mL and 393.3 µg/mL in the DPPH and ABTS radical scavenging assay, respectively. These SNEDDSs were loaded with no degradation and leakage from the 3D-printed container. We were able to delay the release of the SNEDDS from the hollow prints while controlling the print wall thickness to achieve lag phases of 30 min and 60 min before the release from the 0.4 mm and 1 mm wall thicknesses, respectively. Combining these two innovative drug-delivery strategies demonstrates a novel option for tackling the problems associated with multi-drug delivery and delivery of drugs susceptible to degradation in, i.e., gastric pH for targeting disease conditions throughout the gastrointestinal tract (GIT). It is also envisaged that such delivery systems reported herein can be an ideal solution to deliver many challenging molecules, such as biologics, orally or near the target site in the future, thus opening a new paradigm for multi-drug-delivery systems.

摘要

本研究展示了使用熔融沉积建模(FDM)3D打印来控制含有生物活性自纳米乳化药物递送系统(SNEDDSs)的多种药物的递送。市场上引入的新化学实体中约三分之二存在一些固有问题,如溶解度差和高亲脂性。SNEDDSs为开发此类药物的递送平台提供了一种创新且简便的方法。将该平台与FDM 3D打印相结合将进一步有助于开发新策略,以递送难溶性药物和具有附加治疗益处的个性化药物递送系统。本研究评估了一种3D打印容器系统的性能,该系统含有负载姜黄素(CUR)和兰索拉唑(LNS)的SNEDDSs。在DPPH和ABTS自由基清除试验中,SNEDDSs分别在浓度约为330.1μg/mL和393.3μg/mL时显示出50%的抗氧化活性(IC)。这些SNEDDSs装载后在3D打印容器中无降解和渗漏。我们能够延缓SNEDDSs从空心打印物中的释放,同时控制打印壁厚,分别在壁厚为0.4mm和1mm的情况下,在释放前实现30分钟和60分钟的延迟期。将这两种创新的药物递送策略相结合,为解决与多药物递送以及在胃肠道(GIT)中易在胃pH值下降解的药物递送相关的问题展示了一种新选择。还设想本文报道的此类递送系统未来可能是口服或在靶位点附近递送许多具有挑战性的分子(如生物制品)的理想解决方案,从而为多药物递送系统开启新的范例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc98/9147480/b84abc025c76/pharmaceutics-14-01082-g001.jpg

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