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Ovicidal and adulticidal activities of Cinnamomum zeylanicum bark essential oil compounds and related compounds against Pediculus humanus capitis (Anoplura: Pediculicidae).
Int J Parasitol. 2005 Dec; 35(14):1595-600.IJ

Abstract

The toxicity of cinnamon, Cinnamomum zeylanicum, bark essential oil compounds against eggs and adult females of human head louse, Pediculus humanus capitis, was examined using direct contact and vapour phase toxicity bioassays and compared with the lethal activity of their related compounds, benzyl alcohol, cinnamic acid, cinnamyl acetate, 4-hydroxybenzaldehyde and salicylaldehyde, as well as two widely used pediculicides, d-phenothrin and pyrethrum. In a filter-paper contact toxicity bioassay with female lice at 0.25 mg/cm(2), benzaldehyde was 29- and 27-fold more toxic than pyrethrum and d-phenothrin, respectively, as judged by median lethal time (LT(50)) values. Salicylaldehyde was nine and eight times more active than pyrethrum and d-phenothrin, respectively. Pediculicidal activity of linalool was comparable with that of d-phenothrin and pyrethrum. Cinnamomum bark essential oil was slightly less effective than either d-phenothrin or pyrethrum. Benzyl alcohol and (E)-cinnamaldehyde exhibited moderate pediculicidal activity. After 24h of exposure, no hatching was observed with 0.063 mg/cm(2) salicylaldehyde, 0.125 mg/cm(2) benzaldehyde, 0.5mg/cm(2)Cinnamomum bark essential oil, 1.0 mg/cm(2) (E)-cinnamaldehyde, and 1.0 mg/cm(2) benzyl cinnamate. Little or no ovicidal activity was observed with d-phenothrin or pyrethrum. In vapour phase toxicity tests with female lice, benzaldehyde and salicylaldehyde were much more effective in closed containers than in open ones, indicating that the mode of delivery of these compounds was largely due to action in the vapour phase. Neither d-phenothrin nor pyrethrum exhibited fumigant toxicity. Cinnamomum bark essential oil and test compounds described merit further study as potential pediculicides or ovicides for the control of P. h. capitis.

Authors+Show Affiliations

Research Institute, Naturobiotech Co., Ltd., Suwon 441-744, South Korea.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

16188263

Citation

Yang, Young-Cheol, et al. "Ovicidal and Adulticidal Activities of Cinnamomum Zeylanicum Bark Essential Oil Compounds and Related Compounds Against Pediculus Humanus Capitis (Anoplura: Pediculicidae)." International Journal for Parasitology, vol. 35, no. 14, 2005, pp. 1595-600.
Yang YC, Lee HS, Lee SH, et al. Ovicidal and adulticidal activities of Cinnamomum zeylanicum bark essential oil compounds and related compounds against Pediculus humanus capitis (Anoplura: Pediculicidae). Int J Parasitol. 2005;35(14):1595-600.
Yang, Y. C., Lee, H. S., Lee, S. H., Clark, J. M., & Ahn, Y. J. (2005). Ovicidal and adulticidal activities of Cinnamomum zeylanicum bark essential oil compounds and related compounds against Pediculus humanus capitis (Anoplura: Pediculicidae). International Journal for Parasitology, 35(14), 1595-600.
Yang YC, et al. Ovicidal and Adulticidal Activities of Cinnamomum Zeylanicum Bark Essential Oil Compounds and Related Compounds Against Pediculus Humanus Capitis (Anoplura: Pediculicidae). Int J Parasitol. 2005;35(14):1595-600. PubMed PMID: 16188263.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Ovicidal and adulticidal activities of Cinnamomum zeylanicum bark essential oil compounds and related compounds against Pediculus humanus capitis (Anoplura: Pediculicidae). AU - Yang,Young-Cheol, AU - Lee,Hoi-Seon, AU - Lee,Si Hyeock, AU - Clark,J Marshall, AU - Ahn,Young-Joon, Y1 - 2005/09/15/ PY - 2005/04/18/received PY - 2005/06/27/revised PY - 2005/08/01/accepted PY - 2005/9/29/pubmed PY - 2006/9/12/medline PY - 2005/9/29/entrez SP - 1595 EP - 600 JF - International journal for parasitology JO - Int J Parasitol VL - 35 IS - 14 N2 - The toxicity of cinnamon, Cinnamomum zeylanicum, bark essential oil compounds against eggs and adult females of human head louse, Pediculus humanus capitis, was examined using direct contact and vapour phase toxicity bioassays and compared with the lethal activity of their related compounds, benzyl alcohol, cinnamic acid, cinnamyl acetate, 4-hydroxybenzaldehyde and salicylaldehyde, as well as two widely used pediculicides, d-phenothrin and pyrethrum. In a filter-paper contact toxicity bioassay with female lice at 0.25 mg/cm(2), benzaldehyde was 29- and 27-fold more toxic than pyrethrum and d-phenothrin, respectively, as judged by median lethal time (LT(50)) values. Salicylaldehyde was nine and eight times more active than pyrethrum and d-phenothrin, respectively. Pediculicidal activity of linalool was comparable with that of d-phenothrin and pyrethrum. Cinnamomum bark essential oil was slightly less effective than either d-phenothrin or pyrethrum. Benzyl alcohol and (E)-cinnamaldehyde exhibited moderate pediculicidal activity. After 24h of exposure, no hatching was observed with 0.063 mg/cm(2) salicylaldehyde, 0.125 mg/cm(2) benzaldehyde, 0.5mg/cm(2)Cinnamomum bark essential oil, 1.0 mg/cm(2) (E)-cinnamaldehyde, and 1.0 mg/cm(2) benzyl cinnamate. Little or no ovicidal activity was observed with d-phenothrin or pyrethrum. In vapour phase toxicity tests with female lice, benzaldehyde and salicylaldehyde were much more effective in closed containers than in open ones, indicating that the mode of delivery of these compounds was largely due to action in the vapour phase. Neither d-phenothrin nor pyrethrum exhibited fumigant toxicity. Cinnamomum bark essential oil and test compounds described merit further study as potential pediculicides or ovicides for the control of P. h. capitis. SN - 0020-7519 UR - https://www.unboundmedicine.com/medline/citation/16188263/Ovicidal_and_adulticidal_activities_of_Cinnamomum_zeylanicum_bark_essential_oil_compounds_and_related_compounds_against_Pediculus_humanus_capitis__Anoplura:_Pediculicidae__ DB - PRIME DP - Unbound Medicine ER -