Dipartimento di Scienze e Tecnologie Biologiche Chimiche e Farmaceutiche (STEBICEF), Università degli Studi di Palermo, Via Archirafi 32, 90123, Palermo, Italy.
Dipartimento di Scienze e Tecnologie Biologiche Chimiche e Farmaceutiche (STEBICEF), Università degli Studi di Palermo, Via Archirafi 32, 90123, Palermo, Italy.
Colloids Surf B Biointerfaces. 2021 Jan;197:111438. doi: 10.1016/j.colsurfb.2020.111438. Epub 2020 Nov 4.
The aim of the work was to determine the effects of the chemical functionalization of hyaluronic acid (HA) with pendant aliphatic tails at different lengths and free amino groups in terms of chemical reactivity, degradation rate, drug-eluting features, and surface properties when processed as electrospun membranes (EM) evaluating the osteoinductive potential for a possible application as guided bone regeneration (GBR). To this end, a series of HA derivatives with different aliphatic tails (DD-Cx mol% ≈ 12.0 mol%) and decreasing derivatization of free amino groups (DD mol% from 70.0 to 30.0 mol%) were first synthesized, namely Hn. Then dexamethasone-loaded Hn EM, i.e. HnX were prepared from aqueous polymeric solutions with polyvinyl alcohol (PVA), as a non-ionogenic linear flexible polymeric carrier, and the multifunctional 2-hydroxypropyl- cyclodextrin (HPCD) which acted as a rheological modifier, a stabilizer of Taylor's cone, and a solubilizing agent. A comprehensive characterization of the membranes was carried out through ATR-IR, XRD, and WCA measurements. According to the in vitro hydrolytic and enzymatic degradation and drug release in different aqueous media for two months, the insertion of alkyl pendant grafts and the crosslinking process provided tuneable additional resistance to the whole membrane suitably for the final application of the membranes. Cell culture showed the cytocompatibility and cell proliferation until 7 days. Osteogenic differentiation and mineralization of pre-osteoblastic MC3T3 cells occurred for most of membranes after 35 days as valued by measuring ALP activity (50 nmol 4-np/h/nf DNA) and the deposition of calcium (120-140 μg ml).
本工作旨在确定通过在不同长度的脂肪侧链和游离氨基上对透明质酸(HA)进行化学功能化,以及将其加工成电纺膜(EM)时,在化学反应性、降解速率、药物洗脱特性和表面性能方面的影响,评估其作为引导骨再生(GBR)的潜在应用的成骨诱导能力。为此,首先合成了一系列具有不同脂肪侧链(DD-Cx mol%≈12.0 mol%)和游离氨基逐渐降低的 HA 衍生物(DD mol%从 70.0 到 30.0 mol%),即 Hn。然后,从含有聚乙烯醇(PVA)的水性聚合物溶液中制备负载地塞米松的 Hn EM,即 HnX,PVA 是一种非离子型线性柔性聚合物载体,多功能 2-羟丙基-环糊精(HPCD)作为流变改性剂、泰勒锥的稳定剂和增溶剂。通过 ATR-IR、XRD 和 WCA 测量对膜进行了全面表征。根据两个月在不同水性介质中的体外水解和酶降解以及药物释放情况,烷基侧链接枝的插入和交联过程为整个膜提供了可调的额外阻力,非常适合膜的最终应用。细胞培养显示细胞相容性和细胞增殖至 7 天。预成骨 MC3T3 细胞的成骨分化和矿化在 35 天后发生在大多数膜上,通过测量碱性磷酸酶活性(50 nmol 4-np/h/nf DNA)和钙沉积(120-140 μg ml)来评估。