Norepinephrine-loaded thermoresponsive hydrogel-like system for enhanced angiogenesis in tissue engineering

IF 4.5 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Tassia Joi Martins , Italo Rodrigo Calori , Ana Paula Pereira Guimaraes , Gabriel Henrique Ribeiro , Tiago Venâncio , Fiama Martins , Lucas da Silva Ribeiro , Emerson Camargo , Antonio Claudio Tedesco
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Abstract

Inadequate vascularization in thick biofabricated tissues and organs leads to hypoxia and graft failure, highlighting the critical role of angiogenesis in the clinical translation of tissue engineering. Norepinephrine (NE), a neurotransmitter and hormone, regulates vascular tone and modulates angiogenesis through proangiogenic factors, offering an option for improving vascularization and tissue integration. This study aimed to characterize an injectable and in situ forming hydrogel-like system made of poly(N-vinylcaprolactam) (PNVCL) loaded with NE, and evaluate its effects on endothelial cell models. PNVCL was successfully synthesized via free-radical polymerization, as indicated by 1H NMR and FTIR spectroscopy. The polymer exhibited a glass transition temperature (Tg) of 194 °C and thermoresponsive behavior with a lower critical solution temperature of 34 °C. NMR spectroscopy indicated through-space dipolar couplings between NE and PNVCL hydrogens, which suggest interaction groups within the NE-PNVCL system. This system protects NE from degradation, as indicated by absorption spectroscopy. The PNVCL system exhibited a burst release of NE followed by a controlled release profile, with approximately 80 % and 87 % of the NE released within 24 h and 72 h, respectively. In human umbilical vein endothelial cells (HUVEC) culture, NE reduced migration and enhanced tubulogenesis, indicating a dual role in angiogenesis. In addition, NE promoted sprout formation in endothelial cell spheroids. These findings highlight the potential of NE-loaded PNVCL systems to enhance angiogenesis and vascularization in tissue engineering.
组织工程中用于增强血管生成的去甲肾上腺素负载热响应水凝胶样系统
在厚的生物组织和器官中血管形成不足会导致缺氧和移植物失败,这突出了血管生成在组织工程临床转化中的关键作用。去甲肾上腺素(NE)是一种神经递质和激素,通过促血管生成因子调节血管张力和血管生成,为改善血管化和组织整合提供了一种选择。本研究旨在表征负载NE的可注射和原位形成的聚(n -乙烯基己内酰胺)(PNVCL)水凝胶样体系,并评估其对内皮细胞模型的影响。经1H NMR和FTIR光谱验证,采用自由基聚合法制备了PNVCL。该聚合物的玻璃化转变温度(Tg)为194℃,热响应性较低,临界溶液温度为34℃。核磁共振发现NE和PNVCL之间存在空间偶极耦合,表明NE-PNVCL体系中存在相互作用基团。正如吸收光谱所显示的那样,该系统保护NE免受降解。PNVCL系统表现出NE的爆发性释放,随后是可控释放,分别在24 h和72 h内释放约80%和87%的NE。在人脐静脉内皮细胞(HUVEC)培养中,NE减少了迁移并增强了小管生成,表明其在血管生成中的双重作用。此外,NE促进内皮细胞球体的芽形成。这些发现强调了ne负载PNVCL系统在组织工程中促进血管生成和血管化的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.00
自引率
8.00%
发文量
879
审稿时长
94 days
期刊介绍: The Journal of Drug Delivery Science and Technology is an international journal devoted to drug delivery and pharmaceutical technology. The journal covers all innovative aspects of all pharmaceutical dosage forms and the most advanced research on controlled release, bioavailability and drug absorption, nanomedicines, gene delivery, tissue engineering, etc. Hot topics, related to manufacturing processes and quality control, are also welcomed.
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