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朝着基于明胶的 3D 贴片的个性化方向发展:一种用于局部应用的可调多孔载体。

Towards the personalization of gelatin-based 3D patches: a tunable porous carrier for topical applications.

机构信息

Research Institute for Medicines (iMed.ULisboa), Faculty of Pharmacy, Universidade de Lisboa, Lisbon, 1649-003, Portugal.

CQE, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, Lisbon, 1049-001, Portugal.

出版信息

Drug Deliv Transl Res. 2023 Jun;13(6):1799-1812. doi: 10.1007/s13346-023-01294-y. Epub 2023 Jan 12.

Abstract

Cell-free based therapies, for example, the use of the cell secretome, have emerged as a promising alternative to conventional skin therapies using bioactive and, when combined with 3D printing technologies, allow the development of personalized dosage forms. This research work aimed to develop gelatin-based patches with controlled network topology via extrusion 3D printing, loaded with cell culture medium as a model of the secretome, and applicable as vehicles for topical delivery. Inks were optimized through rheological and printing assays, and the incorporation of medium had minor effects in printability. Regarding network topology, grid infills rendered more defined structures than the triangular layout, depicting clearer pores and pore area consistency. Release studies showed that filament spacing and infill pattern influenced the release of rhodamine B (model bioactive) and bovine serum albumin (model protein). Moreover, the grid patches (G-0.7/1/0.7), despite having around a seven-fold higher mean pore area than 0.7-mm triangular ones (T-0.7), showed a similar release profile, which can be linked to the network topology of the printed structures This work provided insight on employing (bio)printing in the production of carriers with reproducible and controlled pore area, able to incorporate cell-derived secretome and to be quickly tailored to the patient's lesions.

摘要

无细胞的治疗方法,例如细胞外泌体的应用,已成为一种有前途的替代传统生物活性皮肤治疗的方法,与 3D 打印技术结合,可以开发出个性化的剂量形式。这项研究工作旨在通过挤出 3D 打印开发基于明胶的具有受控网络拓扑结构的贴片,该贴片负载细胞培养基作为外泌体的模型,并可作为局部递送的载体。通过流变学和打印试验优化了油墨,并且介质的掺入对可印刷性的影响较小。关于网络拓扑结构,网格填充比三角形布局产生的结构更清晰,显示出更清晰的孔和孔面积一致性。释放研究表明,丝间距和填充模式影响着罗丹明 B(模型生物活性物质)和牛血清白蛋白(模型蛋白质)的释放。此外,尽管网格贴片(G-0.7/1/0.7)的平均孔径比 0.7mm 三角形贴片(T-0.7)大约七倍,但仍显示出相似的释放曲线,这可以与打印结构的网络拓扑结构联系起来。这项工作为(生物)打印在生产具有可重复和可控孔面积的载体方面提供了新的见解,这些载体能够结合细胞来源的外泌体,并能快速适应患者的病变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b17/10125939/bf4b69f01ac2/13346_2023_1294_Fig1_HTML.jpg

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