Harris Johnisha, Gurumoorthy Kaarthikeyan
Department of Periodontics, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, Tamil Nadu, India.
J Indian Soc Periodontol. 2024 Sep-Oct;28(5):522-528. doi: 10.4103/jisp.jisp_554_23. Epub 2025 Feb 26.
Although a lot of commercially available guided tissue regeneration (GTR) membranes are used, none of them could actually ensure complete bone regeneration so far and they also have certain limitations. This study aims to explore further and develop a membrane that might overcome these limitations and aid in bone regeneration for the treatment of bony defects.
Magnesium oxide nanoparticles (MgONPs) were prepared from magnesium nitrate prepared by calcination at different temperatures and dried using filter paper under specific temperature. Later, 0.3 ml of 0.2 M 1% acetic acid was added to water and placed in the stirrer for at least 1 h. Chitosan (CS) (2%) of two different concentrations containing 0.588 g and 0.576 g of CS, respectively, was prepared and added to the previous mixture. To these concentrations, the prepared MgONPs were added and stirred using a magnetic stirrer for 1 h. Later, it was cast in the mold and dried. The prepared membrane was immersed in 1 M sodium hydroxide to neutralize acetic acid. After preparation, they were subjected to scanning electron microscope (SEM) analysis, energy-dispersive X-ray (EDAX), Fourier transform infrared spectroscopy (FTIR), and contact angle test.
In SEM analysis, spherical in size, uniformly dense, and porous agglomeration was noticed. EDAX and FTIR revealed the formation of MgONPs (magnesium oxide) in the membrane. The average contact angles of the CS with MgONPs and control membranes were 85.48° and 80.80°, respectively. Degradation analysis showed that test membrane showed a slower degradation rate than control collagen membrane at the end of the 28 day.
On comparing membranes with pure CS, membranes with nanoparticles, and control collagen membranes, the membrane incorporated with nanoparticles showed more favorable positive outcomes.
尽管目前使用了许多市售的引导组织再生(GTR)膜,但到目前为止,没有一种膜能够真正确保完全的骨再生,并且它们也存在一定的局限性。本研究旨在进一步探索并开发一种可能克服这些局限性并有助于骨再生以治疗骨缺损的膜。
通过在不同温度下煅烧硝酸镁制备氧化镁纳米颗粒(MgONPs),并在特定温度下用滤纸干燥。随后,将0.3 ml 0.2 M 1%的醋酸加入水中,并置于搅拌器中搅拌至少1小时。制备两种不同浓度的壳聚糖(CS)(2%),分别含有0.588 g和0.576 g的CS,并加入到先前的混合物中。向这些浓度的混合物中加入制备好的MgONPs,并用磁力搅拌器搅拌1小时。之后,将其浇铸在模具中并干燥。将制备好的膜浸入1 M氢氧化钠中以中和醋酸。制备完成后,对其进行扫描电子显微镜(SEM)分析、能量色散X射线(EDAX)分析、傅里叶变换红外光谱(FTIR)分析和接触角测试。
在SEM分析中,观察到尺寸呈球形、均匀致密且多孔团聚。EDAX和FTIR显示膜中形成了MgONPs(氧化镁)。CS与MgONPs膜和对照膜的平均接触角分别为85.48°和80.80°。降解分析表明,在第28天结束时,测试膜的降解速率比对照胶原膜慢。
与纯CS膜、含纳米颗粒的膜和对照胶原膜相比,含纳米颗粒的膜显示出更有利的积极结果。