Department of Pharmaceutical & Biomedical Sciences, College of Pharmacy, California Northstate University, Elk Grove, CA 95757, USA.
Biosensors (Basel). 2022 Mar 22;12(4):186. doi: 10.3390/bios12040186.
3D printing (3DP) can serve not only as an excellent platform for producing solid dosage forms tailored to individualized dosing regimens but can also be used as a tool for creating a suitable 3D model for drug screening, sensing, testing and organ-on-chip applications. Several new technologies have been developed to convert the conventional dosing regimen into personalized medicine for the past decade. With the approval of Spritam, the first pharmaceutical formulation produced by 3DP technology, this technology has caught the attention of pharmaceutical researchers worldwide. Consistent efforts are being made to improvise the process and mitigate other shortcomings such as restricted excipient choice, time constraints, industrial production constraints, and overall cost. The objective of this review is to provide an overview of the 3DP process, its types, types of material used, and the pros and cons of each technique in the application of not only creating solid dosage forms but also producing a 3D model for sensing, testing, and screening of the substances. The application of producing a model for the biosensing and screening of drugs besides the creation of the drug itself, offers a complete loop of application for 3DP in pharmaceutics.
3D 打印(3DP)不仅可以作为定制个体化给药方案的固体剂型的绝佳平台,还可以作为用于药物筛选、传感、测试和器官芯片应用的合适 3D 模型的创建工具。在过去的十年中,已经开发了几种新技术将常规给药方案转化为个体化药物。随着 3DP 技术生产的第一种药物制剂 Spritam 的批准,这项技术引起了全球制药研究人员的关注。人们一直在努力改进该工艺并减轻其他缺点,如赋形剂选择受限、时间限制、工业生产限制和总成本。本综述的目的是概述 3DP 工艺、其类型、使用的材料类型以及每种技术在不仅创建固体剂型而且还创建用于传感、测试和筛选物质的 3D 模型的应用中的优缺点。除了药物本身的制备外,生产用于药物生物传感和筛选的模型为 3DP 在药剂学中的应用提供了完整的循环。