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用于伤口愈合应用的3D打印、载新霉素聚-L-丙交酯垫的设计与表征

Design and characterization of 3D printed, neomycin-eluting poly-L-lactide mats for wound-healing applications.

作者信息

Singh Mahima, Jonnalagadda Sriramakamal

机构信息

Department of Pharmaceutical Sciences, Philadelphia College of Pharmacy, USciences 600 S 43rd St, Philadelphia, PA, 19143, USA.

出版信息

J Mater Sci Mater Med. 2021 Apr 8;32(4):44. doi: 10.1007/s10856-021-06509-7.

Abstract

This study evaluates the suitability of 3D printed biodegradable mats to load and deliver the topical antibiotic, neomycin, for up to 3 weeks in vitro. A 3D printer equipped with a hot melt extruder was used to print bandage-like wound coverings with porous sizes appropriate for cellular attachment and viability. The semicrystalline polyester, poly-l-lactic acid (PLLA) was used as the base polymer, coated (post-printing) with polyethylene glycols (PEGs) of MWs 400 Da, 6 kDa, or 20 kDa to enable manipulation of physicochemical and biological properties to suit intended applications. The mats were further loaded with a topical antibiotic (neomycin sulfate), and cumulative drug-release monitored for 3 weeks in vitro. Microscopic imaging as well as Scanning Electron Microscopy (SEM) studies showed pore dimensions of 100 × 400 µm. These pore dimensions were achieved without compromising mechanical strength; because of the "tough" individual fibers constituting the mat (Young's Moduli of 50 ± 20 MPa and Elastic Elongation of 10 ± 5%). The in vitro dissolution study showed first-order release kinetics for neomycin during the first 20 h, followed by diffusion-controlled (Fickian) release for the remaining duration of the study. The release of neomycin suggested that the ability to load neomycin on to PLLA mats increases threefold, as the MW of the applied PEG coating is lowered from 20 kDa to 400 Da. Overall, this study demonstrates a successful approach to using a 3D printer to prepare porous degradable mats for antibiotic delivery with potential applications to dermal regeneration and tissue engineering. Illustration of the process used to create and characterize 3D printed PLLA mats.

摘要

本研究评估了3D打印的可生物降解垫子在体外加载和递送局部用抗生素新霉素长达3周的适用性。使用配备热熔挤出机的3D打印机打印绷带样伤口覆盖物,其孔隙尺寸适合细胞附着和存活。半结晶聚酯聚-L-乳酸(PLLA)用作基础聚合物,在打印后用分子量为400 Da、6 kDa或20 kDa的聚乙二醇(PEG)进行涂层,以调节物理化学和生物学性质以适应预期应用。这些垫子进一步加载局部用抗生素(硫酸新霉素),并在体外监测3周的药物累积释放。显微镜成像以及扫描电子显微镜(SEM)研究显示孔隙尺寸为100×400 µm。在不损害机械强度的情况下实现了这些孔隙尺寸;这是因为构成垫子的单根纤维“坚韧”(杨氏模量为50±20 MPa,弹性伸长率为10±5%)。体外溶出研究表明,新霉素在前20小时内呈现一级释放动力学,在研究的剩余时间内为扩散控制(菲克)释放。新霉素的释放表明,随着所应用的PEG涂层的分子量从20 kDa降低到400 Da,将新霉素加载到PLLA垫子上的能力提高了三倍。总体而言,本研究展示了一种成功的方法,即使用3D打印机制备用于抗生素递送的多孔可降解垫子,其在皮肤再生和组织工程方面具有潜在应用。用于创建和表征3D打印PLLA垫子的过程示意图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17f6/8032582/445426cb8fff/10856_2021_6509_Figa_HTML.jpg

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