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负载地塞米松的用于软组织应用的3D打印与电纺混合支架

Hybrid 3D-Printed and Electrospun Scaffolds Loaded with Dexamethasone for Soft Tissue Applications.

作者信息

Pisani Silvia, Mauri Valeria, Negrello Erika, Friuli Valeria, Genta Ida, Dorati Rossella, Bruni Giovanna, Marconi Stefania, Auricchio Ferdinando, Pietrabissa Andrea, Benazzo Marco, Conti Bice

机构信息

Department of Drug Sciences, University of Pavia, Viale Taramelli, 12, 27100 Pavia, Italy.

SC General Surgery 2, Fondazione IRCCS Policlinico San Matteo, Viale Camillo Golgi, 19, 27100 Pavia, Italy.

出版信息

Pharmaceutics. 2023 Oct 17;15(10):2478. doi: 10.3390/pharmaceutics15102478.

Abstract

BACKGROUND

To make the regenerative process more effective and efficient, tissue engineering (TE) strategies have been implemented. Three-dimensional scaffolds (electrospun or 3D-printed), due to their suitable designed architecture, offer the proper location of the position of cells, as well as cell adhesion and the deposition of the extracellular matrix. Moreover, the possibility to guarantee a concomitant release of drugs can promote tissue regeneration.

METHODS

A PLA/PCL copolymer was used for the manufacturing of electrospun and hybrid scaffolds (composed of a 3D-printed support coated with electrospun fibers). Dexamethasone was loaded as an anti-inflammatory drug into the electrospun fibers, and the drug release kinetics and scaffold biological behavior were evaluated.

RESULTS

The encapsulation efficiency (EE%) was higher than 80%. DXM embedding into the electrospun fibers resulted in a slowed drug release rate, and a slower release was seen in the hybrid scaffolds. The fibers maintained their nanometric dimensions (less than 800 nm) even after deposition on the 3D-printed supports. Cell adhesion and proliferation was favored in the DXM-loading hybrid scaffolds.

CONCLUSIONS

The hybrid scaffolds that were developed in this study can be optimized as a versatile platform for soft tissue regeneration.

摘要

背景

为了使再生过程更有效率,已经实施了组织工程(TE)策略。三维支架(电纺或3D打印)由于其合适的设计结构,为细胞提供了合适的位置,以及细胞黏附和细胞外基质的沉积。此外,保证药物同时释放的可能性可以促进组织再生。

方法

使用聚乳酸/聚己内酯共聚物制造电纺支架和混合支架(由涂有电纺纤维的3D打印支架组成)。将地塞米松作为抗炎药物负载到电纺纤维中,并评估药物释放动力学和支架的生物学行为。

结果

包封率(EE%)高于80%。地塞米松嵌入电纺纤维导致药物释放速率减慢,在混合支架中释放更慢。即使沉积在3D打印支架上后,纤维仍保持其纳米尺寸(小于800nm)。载有地塞米松的混合支架有利于细胞黏附和增殖。

结论

本研究中开发的混合支架可以优化为软组织再生的通用平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e95d/10609822/c3ccaa06ec4f/pharmaceutics-15-02478-g001.jpg

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