DETERMINATION OF ANNONACYN COMPOUND BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY ON THE EXTRACT OF Annona muricata LINN SEED FOR PESTICIDE FORMULA

https://doi.org/10.22146/ijc.21792

Freddy L Wurangian(1*)

(1) Chemistry Department, Faculty of Mathematics and Natural Sciences State University of Manado, Tondano-Minahasa, Sulawesi Utara, Indonesia 95618
(*) Corresponding Author

Abstract


Determination of annonacyn grade, a main insecticide compound has been done in the ethanolic and ethyl acetate extracts produced by soxhletation, and ethyl acetate extract produced by fractionation of ethanolic extract to find out the most active extract to be used as raw material of pesticide formulae. Analysis method used the reverse phase high performance liquid chromatography with column of Novapack ODS C-18 (waters; 3.9 x 150 nm), mobile phase was the mixture of acetonitrile-water. The result of this research showed the optimum condition as follows: the mobile phase was acetonitrile-water (60:40), flow rate of 0.2 mL min-1, injection volume of 5.0 μL, detector UV, wavelength (λ) at 220 nm with AUFS of 1.00. The limit detection of annonacyn was 0.01 μg, annonacyn grade in ethanolic extract produced by soxhletation: 0.0405 + 0.0021%, in ethyl acetate extract produced by soxhletation: 0.0293 + 0.0009%, in ethyl acetate extract produced by fractionation of ethanolic extract: 0.1003 + 0.0018%. The precision and accuracy of annonacyn in this research were respectively obtained 8.89% - 1.92%, and 4.91% - 7.28%, at the concentration of 5.00 μg mL-1 - 25.00 μg mL-1. The sensitivity was 0.75 < b < 1.13.


Keywords


Annona muricata Linn; Annonacyn; HPLC

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References

[1] Rupprecht, J.K.., Hui, Y.H., and McLaughlin, J.L. 1990, J. Nat. Prod., 53, 237-278.

[2] Gromek, D., Hocquemiller, R., and Cave, A., 1994, J.Phytochem. Anal., 5, 133-144.

[3] Wurangian, F.L., 2005, Teknik Isolasi dan Identifikasi Terkini Senyawa Insektisida Bahan Alam Annonasin Pada Biji Sirsak Annona muricata Linn. Laporan Jurusan Kimia, FMIPA- UNIMA, Manado.

[4] Bahti, H.H., Agma, M., and Tjokronegoro, R., 1991, Petunjuk Praktikum Kromatografi Cair Kinerja Tinggi Biomolekul, Pusat Antar Universitas - Bioteknologi, Bandung.

[5] Kantasubrata, J., 1986, Warta Kimia Analitik, 1, 2.

[6] Hovart, C., Melander, W., and Molnar, I., 1976, J. Chromatogr., 125, 129-156.

[7] Knox, J.H., 1978, High Performance Liquid Chromatography, Chapman and Hall, London.

[8] Leboeuf, M., Cave, A., and Mukherjee, R., 1982, J. Phytochem., 21, 2783-2813.

[9] Caulcutt, R., and Boddy, R., 1983, Statistic for Analytical Chemist. London, New York, Chapman and Hall.



DOI: https://doi.org/10.22146/ijc.21792

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Indonesian Journal of Chemistry (ISSN 1411-9420 /e-ISSN 2460-1578) - Chemistry Department, Universitas Gadjah Mada, Indonesia.

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