CYTOTOXICITY AND CHARACTERISATION OF POLYMETHYL METHACRYLATE DENTURE BASE ENHANCED WITH LINSEED OIL (PMMA-L)

Nadiyah Abdullah Zawawi; Hazlina Abdul Ghani; Raja Azman Raja Awang; Nik Noor Idayu Nik Ibrahim; Nik Noor Idayu Nik Ibrahim

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CYTOTOXICITY AND CHARACTERISATION OF POLYMETHYL METHACRYLATE DENTURE BASE ENHANCED WITH LINSEED OIL (PMMA-L)

Author: Nadiyah Abdullah Zawawi ¹ ; Hazlina Abdul Ghani ¹ ; Raja Azman Raja Awang ² ; Nik Noor Idayu Nik Ibrahim ³ ; Nik Noor Idayu Nik Ibrahim ⁴
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1. Centre of Restorative Dentistry, Faculty of Dentistry, Universiti Teknologi MARA, 47000 Sg Buloh, Selangor.
2. School of Dental Sciences, Health Campus, Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan.
3. Centre of Chemical Synthesis and Polymer Technology, Institute of Science, Universiti Teknologi MARA, 40450 Shah Alam, Selangor.
4. Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam, Selangor.
Publication Type:Journal Article
Keywords: Polymethyl Methacrylate; Linseed Oil; Dentures; Plasticiser; Bio-based
From: Journal of University of Malaya Medical Centre 2024;27(Special Issue):302-310
CountryMalaysia
Language:English
Abstract: CYTOTOXICITY AND CHARACTERISATION OF POLYMETHYL METHACRYLATE DENTURE BASE ENHANCED WITH LINSEED OIL (PMMA-L):Objectives: Polymethyl methacrylate (PMMA) is a widely used polymer for a denture base material. Dibutyl phthalate was previously utilised as a synthetic plasticiser in PMMA, but concerns about ester leaching have raised awareness of using organic plasticisers, such as linseed oil. The objective of this research was to assess the cytotoxic effects of linseed oil and to characterise the experimental polymethyl methacrylate enhanced with linseed oil (PMMA-L). Method: The cytotoxicity of linseed oil (LO) was evaluated by exposing Human Gingival Fibroblast (HGF) cells to different linseed oil concentrations (1%, 3%, 5%, 7%, and 10%) for 24, 48, and 72 hours. Afterwards, cell viability was measured with the WST-1 assay, and a spectrophotometer was used for cell quantification. Five groups of PMMA-L were prepared, each containing different percentages of linseed oil (1%, 3%, 5%, 7%, and 10% by weight). These samples underwent an ageing process involving 5,000 cycles of thermocycling between 5°C and 55°C with a 30-second dwell time. Compositional and leaching analyses of PMMA-L were performed using attenuated total reflection fourier-transform infrared spectroscopy (ATR-FTIR). Results: The results from the WST-1 assay consistently showed cell viability exceeding 95% across all doses and incubation periods, indicating the non-cytotoxicity of LO. Composition analysis revealed that the ATR-FTIR spectra of PMMA-L and linseed oil were identical within the C=C stretching vibration range (1536-1652 cm-1), originating from unsaturated triglyceride compounds found in linseed oil but not in PMMA. Additionally, the leaching analysis did not detect any leaching of linseed oil from PMMA-L. Conclusions: The research offers proof of the non-cytotoxic nature of linseed oil. Moreover, the successful creation of PMMA-L is evident, as indicated by the incorporation of the linseed oil component in PMMA-L and the absence of linseed oil in the leaching analysis.
Full text:2026081116085905668CYTOTOXICITY.pdf