Chemical profiling and cytotoxicity screening of agarwood essential oil (Aquilaria sinensis) in brine shrimp nauplii and cancer cell lines

PLoS One. 2024 Nov 7;19(11):e0310770. doi: 10.1371/journal.pone.0310770. eCollection 2024.

Abstract

Agarwood essential oil (AEO) has gained attention from healthcare industries due to its numerous pharmacological properties. However, a comprehensive understanding of the chemical composition and its cytotoxic property is lacking. The objective of this study was to investigate the chemical profile as well as the cytotoxic concentration range of AEO derived from Aquilaria sinensis agarwood. Gas chromatography-mass spectrometry (GC-MS) was employed to identify the AEO components. Results showed that sesquiterpenes and sesquiterpenoids constitute 95.85% of the AEO. Among the major compounds identified are allo-aromadendrene (13.04%), dihydro-eudesmol (8.81%), α-eudesmol (8.48%), bulnesol (7.63%), τ-cadinol (4.95%), dehydrofukinone (3.83%), valerenol (3.54%), cis-nerolidol (2.75%), agarospirol (2.72%), dehydrojinkoh-eremol (2.53%), selina-3,11-dien-9-al (2.36%), guaiol (2.12%) and caryophyllene oxide (2.0%). The presence of volatile quality marker compounds such as 10-epi-ϒ-eudesmol, aromadendrane, β-agarofuran, α-agarofuran, γ-eudesmol, agarospirol and guaiol, with no contaminants detected, indicates that the extracted AEO is of high purity. Interestingly, the AEO displayed moderate to high toxicity in brine shrimp lethality test (BLST). All studied tumor cell lines (MDA-MB-231, HepG2, B16F10) exhibited varying degrees of sensitivity to AEO, which resulted in time and dose-dependent reduction of cell proliferation. Moreover, flow cytometry analysis revealed that AEO could induce apoptosis in treated HepG2 cells. Our findings showed that AEO contains bioactive components that may be exploited in future studies for the development of anti-cancer therapeutics.

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology
  • Artemia* / drug effects
  • Cell Line, Tumor
  • Gas Chromatography-Mass Spectrometry*
  • Hep G2 Cells
  • Humans
  • Oils, Volatile* / chemistry
  • Oils, Volatile* / pharmacology
  • Sesquiterpenes / chemistry
  • Sesquiterpenes / pharmacology
  • Thymelaeaceae* / chemistry

Substances

  • Oils, Volatile
  • Sesquiterpenes
  • Antineoplastic Agents

Grants and funding

This research was supported by the Ministry of Higher Education (MOHE) through the Fundamental Research Grant Scheme (FRGS/1/2024/STG01/TAYLOR/02/2). This research is also funded by the industrial grant (Project Code: DADVANCE/2023/SBS/001). The funders did not play any role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. In addition, we would like to acknowledge the provision of research materials by staff of DAdvance Agarwood Solutions Sdn. Bhd. in particular Mr. Liew Kien Meng, Mr. Lim Kok Seong, Mr. Tan Chen Wee, and Mr. Gan Yong Hao.