Synthesis and characteristics of the human serum albumin-triazine chiral stationary phase


Autoria(s): Zhang, Q; Zou, HF; Chen, XM; Wang, HL; Luo, QZ; Ni, JY
Data(s)

2000

Resumo

Human serum albumin (HSA) was successfully bonded to silica with s-triazine as activator. The coupling reaction by this method was rapid and effective. The triazine-activated silica is relatively stable and can be installed for at least 1 month without obvious loss of reactivity when stored below 30 degreesC, pH below 7. It was observed that the amount of bound HSA reached 120 mg/g silica calculated from the UV absorbance difference of the HSA solution. d,l-tryptophan was selected as the probe solute to characterize the properties of HSA bonded s-triazine chiral stationary phase, and separation factor of 9.4 was obtained for d,l-tryptophan. Furthermore, the amount of effective HSA on silica was measured by high-performance frontal analysis, and only 16.8 mg/g silica was responsible for the resolution of d,l-tryptophan. These results indicate that the amount of both the bound and effective HSA on silica with triazine as activator was much higher than those by the Schiff base coupling method. Different kinds of enantiomers were resolved successfully on the aminopropylsilica-bonded HSA s-triazine chiral stationary phase. (C) 2000 Wiley-Liss, Inc.

Identificador

http://159.226.238.44/handle/321008/84053

http://www.irgrid.ac.cn/handle/1471x/139694

Idioma(s)

英语

Fonte

张强;邹汉法;陈小明;汪海林;罗权洲;倪坚毅.Synthesis and characteristics of the human serum albumin-triazine chiral stationary phase,Chirality,2000,10(12):714-719

Palavras-Chave #HSA chiral stationary phase #s-triazine activator #high-performance frontal analysis #resolution of enantiomers
Tipo

期刊论文