In Vitro Characterizations of Poly(Ethylene Glycol) Dimethacrylate)-Nanofibrillated Cellulose as an Injectable Biomaterial Substitute for Herniated Nucleus Pulposus

P. Widiyanti, Yurituna Firda, Aminatun, Herry Wibowo
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Abstract

Highlights: Novel synthetic biopolymer hydrogels were successfully prepared using photopolymerization method based on pristine PEGDMA and pristine NFC. Biocomposite hydrogel based on pristine PEGDMA: pristine NFC can be developed as a substitute biomaterial for the nucleus pulposus in cases of herniated nucleus pulposus which can afford for clinical application standards   Abstract As many as 30-80% of cases low back pain (LBP) is frequently attributed to herniated nucleus pulposus (HNP) with 18-29% of instances reported in Indonesia. HNP can cause in motor weakness, sensory disturbances and decreased physiological reflexes. HNP occurs due to protrusion of the intervertebral disc through the annulus fibrosus which can be caused by the rupture of the annulus fibrosus or decreased proteoglycans (PGs). Hydrogel implant material is injected into the disc space, which can restore disc thickness caused by disc degeneration with minimal invasive. This study utilizes  poly(ethylene glycol) dimethacrylate (PEGDMA):nanofibrillated cellulose (NFC) used to treat first-degree HNP using photopolymerization method. PEGDMA is very hydrophilic and is able to produce hydrogel. The addition of NFC to the PEGDMA precursor that forms a hydrogel was able to show mechanical properties as a hydrogel biocomposite candidate. This research to characterize of PEGDMA:NFC for biomaterial substitute of HNP. Characterizations involves Fourier Transform Infrared (FTIR) test, viscosity assessment and in vitro injection model test.  PEGDMA:NFC concentrations explored include 1:0 (control), 1:0.5 (K1 sample), 1:0.75 (K2 sample) and 1:1 (K3 sample). FTIR test can indicating each functional group for hydrogel biomaterial of PEGDMA:NFC. Based on characterization results, the K3 sample has the best results with a concentration of 1:1. The viscosity value was 74,67 dPa.s and in vitro injection model test showed the addition of NFC indicates the hydrogel state when released from the mold will be not ruptured. Hydrogels can be injected with syringe 18 gauge. Consequently, the study concludes that the PEGDMA:NFC biocomposite hydrogel can be effectively applied in cases of  herniated nucleus pulposus.
聚(乙二醇)二甲基丙烯酸酯-纳米纤维素作为疝核髓注射生物材料替代物的体外特性分析
研究亮点:基于原始PEGDMA和原始NFC,采用光聚合法成功制备了新型合成生物聚合物水凝胶。基于原生 PEGDMA 和原生 NFC 的生物复合水凝胶可作为髓核突出病例的髓核替代生物材料,并可用于临床应用标准 摘要多达 30-80% 的腰背痛(LBP)病例经常归因于髓核突出(HNP),在印度尼西亚有 18-29% 的病例报告。髓核突出可导致运动无力、感觉障碍和生理反射减弱。HNP 的发生是由于椎间盘穿过纤维环突出,而纤维环的破裂或蛋白聚糖(PGs)的减少都可能导致 HNP 的发生。将水凝胶植入材料注入椎间盘间隙,可在微创的情况下恢复因椎间盘退变造成的椎间盘厚度。本研究利用聚乙二醇二甲基丙烯酸酯(PEGDMA):纳米纤维素(NFC),采用光聚合法治疗一级 HNP。PEGDMA 具有很强的亲水性,能够生成水凝胶。在形成水凝胶的 PEGDMA 前体中加入 NFC,可显示出作为水凝胶生物复合材料候选材料的机械性能。这项研究旨在表征 PEGDMA:NFC 作为 HNP 生物材料替代品的特性。表征包括傅立叶变换红外(FTIR)测试、粘度评估和体外注射模型试验。 探讨的 PEGDMA:NFC 浓度包括 1:0(对照组)、1:0.5(K1 样品)、1:0.75(K2 样品)和 1:1(K3 样品)。傅立叶变换红外光谱测试可显示 PEGDMA:NFC 水凝胶生物材料的各官能团。根据表征结果,浓度为 1:1 的 K3 样品效果最好。粘度值为 74,67 dPa.s,体外注射模型试验表明,添加 NFC 表明水凝胶在脱模时不会破裂。水凝胶可用 18 号注射器注射。因此,研究得出结论,PEGDMA:NFC 生物复合水凝胶可有效用于髓核突出的病例。
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