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羟基磷灰石整合、肝素和甘油功能化壳聚糖基可注射水凝胶,具有改善的机械性能和促血管生成性能。

Hydroxyapatite-Integrated, Heparin- and Glycerol-Functionalized Chitosan-Based Injectable Hydrogels with Improved Mechanical and Proangiogenic Performance.

机构信息

Engineering-Architecture Faculty, Metallurgy and Material Engineering, Nevsehir Haci Bektas Veli University, Nevsehir 50300, Turkey.

Engineering Department, Lancaster University, Lancaster LA1 4YW, UK.

出版信息

Int J Mol Sci. 2022 May 11;23(10):5370. doi: 10.3390/ijms23105370.

Abstract

The investigation of natural bioactive injectable composites to induce angiogenesis during bone regeneration has been a part of recent minimally invasive regenerative medicine strategies. Our previous study involved the development of in situ-forming injectable composite hydrogels (Chitosan/Hydroxyapatite/Heparin) for bone regeneration. These hydrogels offered facile rheology, injectability, and gelation at 37 °C, as well as promising pro-angiogenic abilities. In the current study, these hydrogels were modified using glycerol as an additive and a pre-sterile production strategy to enhance their mechanical strength. These modifications allowed a further pH increment during neutralisation with maintained solution homogeneity. The synergetic effect of the pH increment and further hydrogen bonding due to the added glycerol improved the strength of the hydrogels substantially. SEM analyses showed highly cross-linked hydrogels (from high-pH solutions) with a hierarchical interlocking pore morphology. Hydrogel solutions showed more elastic flow properties and incipient gelation times decreased to just 2 to 3 min at 37 °C. Toluidine blue assay and SEM analyses showed that heparin formed a coating at the top layer of the hydrogels which contributed anionic bioactive surface features. The chick chorioallantoic membrane (CAM) assay confirmed significant enhancement of angiogenesis with chitosan-matrixed hydrogels comprising hydroxyapatite and small quantities of heparin (33 µg/mL) compared to basic chitosan hydrogels.

摘要

研究天然生物活性可注射复合材料在骨再生过程中诱导血管生成一直是微创再生医学策略的一部分。我们之前的研究涉及开发原位形成的可注射复合水凝胶(壳聚糖/羟基磷灰石/肝素)用于骨再生。这些水凝胶具有易于流变、可注射性和在 37°C 下凝胶化的特点,并且具有有前途的促血管生成能力。在当前的研究中,通过添加甘油和预灭菌生产策略对这些水凝胶进行了改性,以提高其机械强度。这些改性允许在中性化过程中进一步增加 pH 值,同时保持溶液的均一性。由于添加了甘油,pH 值的增加和进一步的氢键作用产生协同效应,大大提高了水凝胶的强度。SEM 分析显示,具有分级互锁孔形态的高度交联水凝胶(来自高 pH 值溶液)。水凝胶溶液显示出更弹性的流动特性,初始凝胶化时间在 37°C 下缩短至仅 2 至 3 分钟。甲苯胺蓝测定和 SEM 分析表明,肝素在水凝胶的顶层形成涂层,这为水凝胶提供了带负电荷的生物活性表面特征。鸡胚绒毛尿囊膜(CAM)试验证实,与基本壳聚糖水凝胶相比,包含羟基磷灰石和少量肝素(33μg/mL)的壳聚糖基质水凝胶可显著增强血管生成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7769/9140455/d6b0bc7cc177/ijms-23-05370-g001.jpg

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