Selective solid-phase extraction of aloe emodin from aloe by molecularly imprinted polymers

Ming-lei Tian , Yu-ri Lee , Dong-wha Park , Kyung-ho Row

Chemical Research in Chinese Universities ›› 2013, Vol. 29 ›› Issue (4) : 663 -666.

PDF
Chemical Research in Chinese Universities ›› 2013, Vol. 29 ›› Issue (4) : 663 -666. DOI: 10.1007/s40242-013-2357-7
Article

Selective solid-phase extraction of aloe emodin from aloe by molecularly imprinted polymers

Author information +
History +
PDF

Abstract

The extraction and separation of aloe emodin were optimized via selective molecularly imprinted solid-phase extraction. Molecularly imprinted polymer was prepared from the functional monomer, methacrylic acid and a mixture of ethanol/dodecanol(90/10, volume ratio) as porogen. It overcomes the common problems of imprinting biological polar compounds and shows high selectivity compared favorably with those of non-imprinted polymer and commercially available C18 and silica cartridges in similar aloe emodin tests. Good linearity was obtained between 0.002 and 2.5 mg/mL (r 2=0.998) with relative standard deviations below 3.3%.

Keywords

Aloe emodin / Molecularly imprinted polymer / Solid-phase extraction / High performance liquid chromatography

Cite this article

Download citation ▾
Ming-lei Tian, Yu-ri Lee, Dong-wha Park, Kyung-ho Row. Selective solid-phase extraction of aloe emodin from aloe by molecularly imprinted polymers. Chemical Research in Chinese Universities, 2013, 29(4): 663-666 DOI:10.1007/s40242-013-2357-7

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Thomson R H. Naturally Occurring Quinines, 1971, New York: Academic Press.

[2]

Shen L, Ji H, Zhang H. J. Mol. Struc., THEOCHEM, 2006, 758: 221.

[3]

Wamer W G, Vath P, Falvey D E. Free Radical Bio. Med., 2003, 34: 233.

[4]

Reynolds T. Botanical J. Linnean Soc., 1985, 90: 157.

[5]

Grindlay D, Reynolds T J. Ethnopharmacology, 1986, 16: 117.

[6]

Imanishi K, Ishiguro T, Saito H, Suzuki I. Experimentia, 1981, 37: 1186.

[7]

Beppu H, Nagamura Y, Fujita K. Phytotherapy Res., 1993, 7: 37.

[8]

Yagi A, Kanbara T, Morinobu N. Planta Medica, 1987, 53: 509.

[9]

Teradaira R, Shinzato M, Beppu H, Fujita H. Phytotherapy Res., 1993, 7: 34.

[10]

Davis R H, Rosental K Y, Cesario L R, Rouw G A. J. Am. Podiatric Med. Association, 1989, 79: 395.

[11]

Hutter J A, Salman M, Stavinoha W B, Satsangi N, Williams R F, Streeper R T, Weintraub S T. J. Nat. Prod., 1996, 59: 541.

[12]

Lee K Y, Weintraub S T, Yu B P. Free Radical Bio. Med., 2000, 28: 261.

[13]

Pyrzynska K, Trojanowicz M. Critical Rev. Anal. Chem., 1999, 29: 313.

[14]

Cai Y Q, Jiang G B, Liu J F, Zhou Q X. Anal. Chem., 2003, 75: 2517.

[15]

Zhuang Y, Luo H, Duan D, Chen L, Xu X. Anal. Bioanal. Chem., 2007, 389: 1177.

[16]

Tian M, Yan H, Row K H. J. Chromatogr. B, 2009, 877: 738.

[17]

Bjarnason B, Chimuka L, Ramström O. Anal. Chem., 1999, 71: 2152.

[18]

Lu C H, Zhou W H, Han B, Yang H H, Chen X, Wang X R. Anal. Chem., 2007, 79: 5457.

[19]

Scorrano S, Longo L, Vasapollo G. Anal. Chimica Acta, 2010, 659: 171.

[20]

Puoci F, Curcio M, Cirillo G, Iemma F, Spizzirri U G, Picci N. Food Chem., 2008, 106: 836.

[21]

Javanbakht M, Attaran A M, Namjumanesh M H, Esfandyari-Manesh M, Akbari-Adergani B. J. Chromatogr. B, 2010, 878: 1700.

[22]

Yan H, Tian M, Row K H. Chin. J. Chem., 2009, 27: 2212.

[23]

Yan H, Tian M, Row K H. Sep. Sci. Tech., 2009, 44: 359.

[24]

Beltran A, Borrull F, Marcé R M, Cormack P A G. Trends in Anal. Chem., 2010, 29: 1363.

[25]

Dong J, Liu Y, Liang Z, Wang W. Ultra. Sonochem., 2010, 17: 61.

AI Summary AI Mindmap
PDF

147

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/