Metwally Walaa M, El-Habashy Salma E, El-Hosseiny Lobna S, Essawy Marwa M, Eltaher Hoda M, El-Khordagui Labiba K
Department of Pharmaceutics, Faculty of Pharmacy, Alexandria University, Alexandria 21521, Egypt.
Department of Environmental Studies, Institute of Graduate Studies and Research, Alexandria University, Alexandria 21526, Egypt.
Biofabrication. 2023 Oct 10;16(1). doi: 10.1088/1758-5090/acfd60.
There is a constant demand for novel materials/biomedical devices to accelerate the healing of hard-to-heal wounds. Herein, an innovative 3D-printed bioinspired construct was developed as an antibacterial/regenerative scaffold for diabetic wound healing. Hyaluronic/chitosan (HA/CS) ink was used to fabricate a bilayer scaffold comprising a dense plain hydrogel layer topping an antibacterial/regenerative nanofibrous layer obtained by incorporating the hydrogel with polylactic acid nanofibrous microspheres (MS). These were embedded with nano ZnO (ZNP) or didecyldimethylammonium bromide (DDAB)-treated ZNP (D-ZNP) to generate the antibacterial/healing nano/micro hybrid biomaterials, Z-MS@scaffold and DZ-MS@scaffold. Plain and composite scaffolds incorporating blank MS (blank MS@scaffold) or MS-free ZNP@scaffold and D-ZNP@scaffold were used for comparison. 3D printed bilayer constructs with customizable porosity were obtained as verified by SEM. The DZ-MS@scaffold exhibited the largest total pore area as well as the highest water-uptake capacity andantibacterial activity. Treatment of-infected full thickness diabetic wounds in rats indicated superiority of DZ-MS@scaffold as evidenced by multiple assessments. The scaffold afforded 95% wound-closure, infection suppression, effective regulation of healing-associated biomarkers as well as regeneration of skin structure in 14 d. On the other hand, healing of non-diabetic acute wounds was effectively accelerated by the simpler less porous Z-MS@scaffold. Information is provided for the first-time on the 3D printing of nanofibrous scaffolds using non-electrospun injectable bioactive nano/micro particulate constructs, an innovative ZNP-functionalized 3D-printed formulation and the distinct bioactivity of D-ZNP as a powerful antibacterial/wound healing promotor. In addition, findings underscored the crucial role of nanofibrous-MS carrier in enhancing the physicochemical, antibacterial, and wound regenerative properties of DDAB-nano ZnO. In conclusion, innovative 3D-printed DZ-MS@scaffold merging the MS-boosted multiple functionalities of ZNP and DDAB, the structural characteristics of nanofibrous MS in addition to those of the 3D-printed bilayer scaffold, provide a versatile bioactive material platform for diabetic wound healing and other biomedical applications.
对于新型材料/生物医学装置以加速难愈合伤口的愈合一直存在需求。在此,开发了一种创新的3D打印仿生构建体作为用于糖尿病伤口愈合的抗菌/再生支架。使用透明质酸/壳聚糖(HA/CS)墨水制造双层支架,该双层支架包括致密的普通水凝胶层,其顶部是通过将水凝胶与聚乳酸纳米纤维微球(MS)结合而获得的抗菌/再生纳米纤维层。这些微球嵌入纳米氧化锌(ZNP)或经二癸基二甲基溴化铵(DDAB)处理的ZNP(D-ZNP)以生成抗菌/愈合纳米/微杂化生物材料,即Z-MS@支架和DZ-MS@支架。使用包含空白MS的普通和复合支架(空白MS@支架)或不含MS的ZNP@支架和D-ZNP@支架进行比较。如通过扫描电子显微镜(SEM)验证的那样,获得了具有可定制孔隙率的3D打印双层构建体。DZ-MS@支架表现出最大的总孔面积以及最高的吸水能力和抗菌活性。对大鼠感染的全层糖尿病伤口的治疗表明DZ-MS@支架具有优越性,这通过多项评估得到证明。该支架在14天内实现了95%的伤口闭合、感染抑制、对愈合相关生物标志物的有效调节以及皮肤结构的再生。另一方面,更简单、孔隙率更低的Z-MS@支架有效地加速了非糖尿病急性伤口的愈合。首次提供了关于使用非静电纺丝可注射生物活性纳米/微颗粒构建体进行纳米纤维支架的3D打印、创新的ZNP功能化3D打印配方以及D-ZNP作为强大的抗菌/伤口愈合促进剂的独特生物活性的信息。此外,研究结果强调了纳米纤维-MS载体在增强DDAB-纳米氧化锌的物理化学、抗菌和伤口再生特性方面的关键作用。总之,创新的3D打印DZ-MS@支架融合了ZNP和DDAB的MS增强的多种功能、纳米纤维MS的结构特征以及3D打印双层支架的结构特征,为糖尿病伤口愈合和其他生物医学应用提供了一个多功能的生物活性材料平台。