GAS CHROMATOGRAPH-MASS SPECTROMETER ANALYSIS AND ACUTE ORAL TOXICITY OF CINNAMOMUM BURMANNII., NESS EX BL. ESSENTIAL OIL

Authors

  • HERDWIANI W Institute of Technology Bandung
  • Soemardji Aa
  • El-fahmi
  • Tan Mi

Abstract

ABSTRACT
Objective: Cinnamomum burmannii Nees Ex Bl. essential oil has cytotoxic effect on a lot of cancer cell lines. An investigation was carried out to analyze
the possible chemical components from C. burmannii essential oil and evaluate its acute toxicity, before an effective formulation of C. burmannii
essential oil as anticancer drugs.
Methods: This study was analyzed chemical components from C. burmannii essential oil by gas chromatograph-mass spectrometer (GC-MS) and
evaluated the acute oral toxicities of C. burmannii essential oil in strain Balb/C mice.
Results: This analysis revealed that C. burmannii essential oil contains the active compound cinnamaldehyde (71.814%), trans-cinnamyl acetate
(11.09%), coumarin (3.41%), and cineol (1.77%). Acute oral toxicity of C. burmannii essential oil with lethal dose 50 3679.11 mg/kg BW.
Conclusion: C. burmannii essential oil contains the active compound cinnamaldehyde, trans-cinnamyl acetate, coumarin and cineol. Acute oral toxicity
conclusively indicates C. burmannii essential oil includes category 5 practically non-toxic.
Keywords: Gas chromatograph-mass spectrometer, Cinnamomum burmannii, Essential oil, Acute toxicity.

Downloads

Download data is not yet available.

References

REFERENCES

Mir AH, Sexena M, Malla MY. An acute oral toxicity study of

methanolic extract from tridex procumbens in sprague dawley’s rats as

per OECD guidelines 423. Asian J Plant Sci Res 2013;3:16-20.

Annonim. OECD Guidance Document on the Recognition Assessment

and Use of Clinical Signs as Humane Endpoints for Experimental

Animals Used in Safety Evaluation Environmental Health and Safety

Monograph Series on Testing and Assessment No 19; 2013.

Chan PK, Hayes AW. Acute Toxicity and Eye Irritancy Principles and

Methods of Toxicology. 3

ed. New York: Raven Press; 1994.

Annonim. OECD Guideline For Testing of Chemicals Acute Oral

rd

Toxicity - Acute Toxic Class Method No 423. Paris: OECD; 1994.

Mohamed Sham Shihabudeen H, Hansi Priscilla D, Thirumurugan K.

Cinnamon extract inhibits a-glucosidase activity and dampens

postprandial glucose excursion in diabetic rats. Nutr Metab (Lond)

;8(1):46.

Singh R, Koppikar SJ, Paul P, Gilda S, Paradkar AR, Kaul-Ghanekar R.

Comparative analysis of cytotoxic effect of aqueous cinnamon extract

from Cinnamomum zeylanicum bark with commercial cinnamaldehyde

on various cell lines. Pharm Biol 2009;47:1174-9.

Herdwiani W, Soemardji AA, Elfahmi, Tan MI. A review of cinnamon

as a potent anticancer. Asian J Pharm Clin Res 2016;9(1):41-6.

Cory S, Adams JM. The Bcl 2 family: Regulators of the cellular life-ordeath

switch. Nat Rev Cancer 2002;2:647-56.

Yu W, Sanders BG, Kline K. RRR-alpha-tocopheryl succinate-induced

apoptosis of human breast cancer cells involves bax translocation to

mitochondria. Cancer Res 2003;63(10):2483-91.

EPA. Health Effects Test Guidelines: OPPTS 870.1100. Acute Oral

Toxicity. Washington DC: EPA; 2014.

Budin SB, Siti Nor Ain SM, Omar B, Taib IS, Hidayatulfathi O. Acute

and subacute oral toxicity of Litsea elliptica blume essential oil in rats.

J Zhejiang Univ Sci B 2012;13:783-90.

Konan NA, Bacchi EM, Lincopan N, Varela SD, Varanda EA. Acute,

subacute toxicity and genotoxic effect of a hydroethanolic extract

of the cashew (Anacardium occidentale L.). J Ethnopharmacol

;110(1):30-8.

Soemardji AA, Kumolosasi E, Aisyah C. Toksisitas akut dan penentuan

DL50 oral ekstrak air daun gandarusa (Justicia gendarussa Burm. F.)

pada mencit swiss webster. J Matematika dan Sains 2002;7(2):57-62.

Gossel JB. Priciples of Clinical Toxicology. 2

ed. New York: Taylor

and Francis; 1995.

nd

ILO. Acute Toxicity; 2000. Available from: http://www.ilo.org/legacy.

Cliff MA, Green BG. Sensory irritation and coolness produced by

menthol: Evidence for selective desensitization of irritation. Physiol

Behav 1994;56(5):1021-9.

Cliff MA, Green BG. Sensitization and desensitization to capsaicin

and menthol in the oral cavity: Interactions and individual differences.

Physiol Behav 1996;59(3):487-94.

Prescott J, Swain-Campbell N. Responses to repeated oral irritation

by capsaicin, cinnamaldehyde and ethanol in PROP tasters and nontasters.

Chem Senses 2000;25(3):239-46.

Dessirier JM, O’Mahony M, Carstens E. Oral irritant effects of nicotine:

Psychophysical evidence for decreased sensation following repeated

application and lack of cross-desensitization to capsaicin. Chem Senses

;22:483-92.

Namer B, Seifert F, Handwerker HO, Maihöfner C. TRPA1 and

TRPM8 activation in humans: Effects of cinnamaldehyde and menthol.

Neuroreport 2005;16(9):955-9.

Carstens E, Mitsuyo T. Neural correlates of oral irritation by

mustard oil and other pungent chemicals: A hot topic. Chem Senses

;30 Suppl 1:i203-4.

Zanotto KL, Iodi Carstens M, Carstens E. Cross-desensitization

of responses of rat trigeminal subnucleus caudalis neurons to

cinnamaldehyde and menthol. Neurosci Lett 2008;430(1):29-33.

Zanotto KL, Merrill AW, Carstens MI, Carstens E. Neurons in

superficial trigeminal subnucleus caudalis responsive to oral cooling,

menthol, and other irritant stimuli. J Neurophysiol 2007;97(2):966-78.

Simons CT, Carstens MI, Carstens E. Oral irritation by mustard oil:

Self-desensitization and cross-desensitization with capsaicin. Chem

Senses 2003;28(6):459-65.

Klein AH, Carstens MI, Zanotto KL, Sawyer CM, Ivanov M, Cheung S,

et al. Self- and cross-desensitization of oral irritation by menthol and

cinnamaldehyde (CA) via peripheral interactions at trigeminal sensory.

Neurons Chem Senses 2011;36:199-208.

Stolz DR, Scott PM. Mutagenicity of coumarin and related compounds

for Salmonella typhimurium. Can J Genet Cytol 1980;22:679.

Norman RL, Wood JB. Assessment of the mutagenic potential of

coumarin in histidine-dependent strains of Salmonella typhimurium.

Proc Am Assoc Cancer Res 1981;22:Abs433.

Haworth S, Lawlor T, Mortelmans K, Speck W, Zeiger E. Salmonella

Asian J Pharm Clin Res, Vol 9, Issue 3, 2016, 240-245

Herdwiani et al.

mutagenicity test results for 250 chemicals. Environ Mutagen

;5 Suppl 1:1-142.

NTP, 1993. Toxicology and Carcinogenesis Studies of Coumarin (CAS

No. 91-64-5) in F344/N Rats and B6C3F1 Mice (gavage studies), 422.

US Department of Health and Human Services.

Edwards AJ, Price RJ, Renwick AB, Lake BG. Lack of effect of

coumarin on unscheduled DNA synthesis in the in vivo rat hepatocyte

DNA repair assay. Food Chem Toxicol 2000;38(5):403-9.

Api AM. Lack of effect of coumarin on the formation of micronuclei

in an in vivo mouse micronucleus assay. Food Chem Toxicol

;39:837-41.

Swenberg JA. Covalent binding index study on coumarin, Report of

Laboratory of Molekular Carcinogenesis and Mutagenesis, University

of North Carolina, Chapel Hill, NC 27599. Brussels: Submitted by

European Flavour and Fragrance Association (EFFA); 2003.

Fotland TØ, Paulsen JE, Sanner T, Alexander J, Husøy T. Risk

assessment of coumarin using the bench mark dose (BMD) approach:

Children in Norway which regularly eat oatmeal porridge with

cinnamon may exceed the TDI for coumarin with several folds. Food

Chem Toxicol 2012;50:903-12.

Lake BG. Coumarin metabolism, toxicity and carcinogenicity:

Relevance for human risk assessment. Food Chem Toxicol

;37(4):423-53.

Mielke H, Abraham K, Götz M, Vieth B, Lampen A, Luch A, et al.

Physiologically based toxicokinetic modelling as a tool to assess target

organ toxicity in route-to-route extrapolation – The case of coumarin.

Toxicol Lett 2011;202(2):100-10.

Lipnick RL, Cotruvo JA, Hill RN, Bruce RD, Stitzel KA, Walker AP,

et al. Comparison of the up-and-down, conventional LD50, and fixeddose

acute toxicity

procedures.

Food Chem Toxicol

;33(3):223-31.

Published

01-05-2016

How to Cite

W, H., S. Aa, El-fahmi, and T. Mi. “GAS CHROMATOGRAPH-MASS SPECTROMETER ANALYSIS AND ACUTE ORAL TOXICITY OF CINNAMOMUM BURMANNII., NESS EX BL. ESSENTIAL OIL”. Asian Journal of Pharmaceutical and Clinical Research, vol. 9, no. 3, May 2016, pp. 240-5, https://journals.innovareacademics.in/index.php/ajpcr/article/view/11136.

Issue

Section

Original Article(s)