热塑性聚氨酯抗菌材料的制备及药物释放控制研究。

IF 5.7 3区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Drug Delivery and Translational Research Pub Date : 2025-07-01 Epub Date: 2024-12-02 DOI:10.1007/s13346-024-01751-2
Chengzhi Cui, Jinxing Cao, Jianlan Liu, Hui Zhang
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引用次数: 0

摘要

随着人们希望生活得更健康,材料的抗菌性能越来越重要。本工作的目的是利用热塑性聚氨酯(TPU)作为基质,生产具有可调药物释放率的抗菌材料。以TPU、改性剂聚氧聚乙烯(PEO)和盐酸环丙沙星一水合物(CPFX)为原料,采用热熔加工技术制备了直径为1.75±0.08 mm的长丝。然后使用熔融沉积型(FDM) 3D打印打印相应的模型以进行性能测试。结果表明,不同组分配比的四种样品均具有均匀的纤维形态和较强的力学性能。PEO的加入改变了药物的释放机制,提高了材料的亲水性,并在溶解过程中产生了额外的孔隙。通过体外溶出度和区域抑制试验表明,即使在旋转浸泡21天后,该复合材料仍具有持续的抗菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Research on the preparation of antimicrobial material based on thermoplastic polyurethane and drug release control.

It's crucial of antimicrobial properties in materials is growing as people desire to live healthier. The purpose of this work was to use thermoplastic polyurethane (TPU) as a matrix to produce an antimicrobial material with a tunable drug release rate. Filaments with a diameter of 1.75 ± 0.08 mm were prepared by hot-melt processing technology utilizing TPU, the modifier polyethylene oxide (PEO) and ciprofloxacin hydrochloride monohydrate (CPFX) as raw materials. The corresponding models were then printed using fused deposition type (FDM) 3D printing for performance testing. Results demonstrate the uniform fiber morphology and strong mechanical properties of the four samples, each of which was composed of a different ratio of components. The addition of PEO caused a change to the drug release mechanism, increased the material hydrophilicity, and generated extra pores during the dissolution process. This composite exhibited sustained antimicrobial activity even after 21 days of rotary immersion, as shown by in vitro dissolution and zone inhibition tests.

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来源期刊
Drug Delivery and Translational Research
Drug Delivery and Translational Research MEDICINE, RESEARCH & EXPERIMENTALPHARMACOL-PHARMACOLOGY & PHARMACY
CiteScore
11.70
自引率
1.90%
发文量
160
期刊介绍: The journal provides a unique forum for scientific publication of high-quality research that is exclusively focused on translational aspects of drug delivery. Rationally developed, effective delivery systems can potentially affect clinical outcome in different disease conditions. Research focused on the following areas of translational drug delivery research will be considered for publication in the journal. Designing and developing novel drug delivery systems, with a focus on their application to disease conditions; Preclinical and clinical data related to drug delivery systems; Drug distribution, pharmacokinetics, clearance, with drug delivery systems as compared to traditional dosing to demonstrate beneficial outcomes Short-term and long-term biocompatibility of drug delivery systems, host response; Biomaterials with growth factors for stem-cell differentiation in regenerative medicine and tissue engineering; Image-guided drug therapy, Nanomedicine; Devices for drug delivery and drug/device combination products. In addition to original full-length papers, communications, and reviews, the journal includes editorials, reports of future meetings, research highlights, and announcements pertaining to the activities of the Controlled Release Society.
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