三维生物打印黏液支架治疗口腔黏膜病变一项体外研究。

IF 3.2 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Maryam Koopaie, Duha Hayder Mohammad Ali Nassar, Mahvash Shokrolahi
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引用次数: 2

摘要

背景:慢性口腔病变可能是某些疾病的一部分,包括皮肤粘膜疾病、免疫大疱性疾病、胃肠道疾病和移植物抗宿主病。全身类固醇是一种有效的治疗方法,但它们会引起不利的甚至严重的全身副作用。停用全身性皮质类固醇或其他免疫抑制药物会导致复发,这证实了长期使用皮质类固醇的重要性。本研究旨在利用三维(3D)生物打印技术制造一种粘膜粘附支架,用于口腔粘膜病变的持续药物递送,以满足临床对替代治疗的需求,特别是对那些常规治疗无效的患者。方法:采用生物3D打印技术制备支架。支架分为三层;粘合剂/含药层、衬层和中间层。为评价药物的释放特性,采用人工唾液作为释放介质。采用扫描电镜(SEM)和扫描电镜(SEM)表面重建对黏附支架进行了分析。用pH计测定黏附支架的pH值,用Enslin dipositive测定支架的溶胀效果。用微处理器测力仪测量拉伸强度。用MTT法测定口腔角质形成细胞的存活率,评价其细胞毒性。使用稳定微系统织构分析仪和分析探针微型拉伸握把进行折叠耐久性测试。结果:所有支架的释药趋势一致;在最初的12小时内开始快速释放,然后逐渐释放。支架持续释放药物,并持续到第4天。支架表面pH为5.3 ~ 6.3,5 h后肿胀率为28±3.2%。含药支架的抗拉强度为7.8±0.12 MPa。该支架对粘膜无刺激性,支架的折叠耐力在300次以上。结论:采用生物3D打印技术制备的支架可用于口腔黏膜病变的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Three-dimensional bioprinting of mucoadhesive scaffolds for the treatment of oral mucosal lesions; an in vitro study.

Three-dimensional bioprinting of mucoadhesive scaffolds for the treatment of oral mucosal lesions; an in vitro study.

Three-dimensional bioprinting of mucoadhesive scaffolds for the treatment of oral mucosal lesions; an in vitro study.

Three-dimensional bioprinting of mucoadhesive scaffolds for the treatment of oral mucosal lesions; an in vitro study.

Background: Chronic oral lesions could be a part of some diseases, including mucocutaneous diseases, immunobullous diseases, gastrointestinal diseases, and graft versus host diseases. Systemic steroids are an effective treatment, but they cause unfavorable and even severe systemic side effects. Discontinuation of systemic corticosteroids or other immunosuppressive drugs leads to relapse, confirming the importance of long-term corticosteroid use. The present study aims to fabricate a mucoadhesive scaffold using three-dimensional (3D) bioprinting for sustained drug delivery in oral mucosal lesions to address the clinical need for alternative treatment, especially for those who do not respond to routine therapy.

Methods: 3D bioprinting method was used for the fabrication of the scaffolds. Scaffolds were fabricated in three layers; adhesive/drug-containing, backing, and middle layers. For evaluation of the release profile of the drug, artificial saliva was used as the release medium. Mucoadhesive scaffolds were analyzed using a scanning electron microscope (SEM) and SEM surface reconstruction. The pH of mucoadhesive scaffolds and swelling efficacy were measured using a pH meter and Enslin dipositive, respectively. A microprocessor force gauge was used for the measurement of tensile strength. For the evaluation of the cytotoxicity, oral keratinocyte cells' survival rate was evaluated by the MTT method. Folding endurance tests were performed using a stable microsystem texture analyzer and analytic probe mini tensile grips.

Results: All scaffolds had the same drug release trend; An initial rapid explosive release during the first 12 h, followed by a gradual release. The scaffolds showed sustained drug release and continued until the fourth day. The pH of the surface of the scaffolds was 5.3-6.3, and the rate of swelling after 5 h was 28 ± 3.2%. The tensile strength of the scaffolds containing the drug was 7.8 ± 0.12 MPa. The scaffolds were non-irritant to the mucosa, and the folding endurance of the scaffolds was over three hundred times.

Conclusion: The scaffold fabricated using the 3D bioprinting method could be suitable for treating oral mucosal lesions.

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