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采用数字光处理技术制备用于口腔给药的 3D 打印中空微针。

Fabrication of 3D Printed Hollow Microneedles by Digital Light Processing for the Buccal Delivery of Actives.

机构信息

Department of Pharmacy Division of Pharmaceutical Technology, Aristotle University of Thessaloniki, Thessaloniki 54124, Greece.

Center for Interdisciplinary Research and Innovation (CIRI-AUTH), Thessaloniki 57001, Greece.

出版信息

ACS Biomater Sci Eng. 2023 Aug 14;9(8):5072-5083. doi: 10.1021/acsbiomaterials.3c00116. Epub 2023 Aug 1.

DOI:10.1021/acsbiomaterials.3c00116
PMID:37528336
Abstract

In the present study, two different microneedle devices were produced using digital light processing (DLP). These devices hold promise as drug delivery systems to the buccal tissue as they increase the permeability of actives with molecular weights between 600 and 4000 Da. The attached reservoirs were designed and printed along with the arrays as a whole device. Light microscopy was used to quality control the printability of the designs, confirming that the actual dimensions are in agreement with the digital design. Non-destructive volume imaging by means of microfocus computed tomography was employed for dimensional and defect characterization of the DLP-printed devices, demonstrating the actual volumes of the reservoirs and the malformations that occurred during printing. The penetration test and finite element analysis showed that the maximum stress experienced by the needles during the insertion process (10 N) was below their ultimate compressive strength (240-310 N). Permeation studies showed the increased permeability of three model drugs when delivered with the MN devices. Size-exclusion chromatography validated the stability of all the actives throughout the permeability tests. The safety of these printed devices for buccal administration was confirmed by histological evaluation and cell viability studies using the TR146 cell line, which indicated no toxic effects.

摘要

在本研究中,使用数字光处理(DLP)制造了两种不同的微针装置。这些装置有望成为向颊组织递送药物的系统,因为它们可以增加分子量在 600 至 4000 Da 之间的活性剂的通透性。附着的储液器与阵列一起设计和打印为整体装置。使用光学显微镜进行质量控制,以确认设计的可印刷性,实际尺寸与数字设计一致。使用微焦点计算机断层扫描进行无损体积成像,对 DLP 打印设备进行尺寸和缺陷特征分析,展示了储液器的实际体积以及打印过程中发生的畸形。穿透测试和有限元分析表明,在插入过程中(10 N)针所经历的最大应力低于其极限抗压强度(240-310 N)。渗透研究表明,当使用 MN 装置输送三种模型药物时,它们的渗透性增加。尺寸排阻色谱法验证了所有活性剂在整个渗透试验过程中的稳定性。使用 TR146 细胞系进行组织学评估和细胞活力研究,证实了这些用于颊部给药的打印装置的安全性,表明没有毒性作用。

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