Highly selective separation and purification of lincomycin by macroporous adsorption resin column chromatography

被引:0
|
作者
Yu, Xue [1 ,2 ]
Chen, Houmao [1 ]
Sha, Zigan [3 ]
Hu, Yawen [1 ]
Yan, Mengxia [2 ]
Xin, Jianhui [2 ]
Cao, Xuejun [1 ]
Wan, Junfen [1 ]
机构
[1] East China Univ Sci & Technol, Dept Bioengn, State Key Lab Bioreactor Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China
[2] Dezhou Univ, Inst Biophys, Shandong Key Lab Biophys, Dezhou 253023, Peoples R China
[3] Shanghai Jiao Tong Univ, Shanghai Ctr Syst Biomed, Key Lab Syst Biomed, Minist Educ, Shanghai 200240, Peoples R China
关键词
Lincomycin; Separation; Macroporous adsorption resin; Column chromatography; FIXED-BED COLUMN; ABSORPTION;
D O I
10.1016/j.chroma.2024.465282
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this study, lincomycin was successfully purified by macroporous adsorption resin column chromatography using the HZ3 resin. The optimal separation parameters were set as follows: the column bed height was 33 cm, sample loading capacity was 48 mg/mL and flow rate of loading was 1 mL/min. A mixture of 0.02 mol/L of Na2HPO4 center dot 12H2O 2 HPO 4 center dot 12H 2 O (pH = 8.5, adjusted using H3PO4) 3 PO 4 ) and acetone (80:20, v/v) was used as the eluent. The elution flow rate was maintained at 3 mL/min. Under these parameters, the purity of lincomycin calculated using the standard curve was 99.00 %, with the yield being 97.84 %. This enrichment and separation method of lincomycin is highly regarded owing to its remarkable efficiency and straightforward operation. Thus, the proposed method for the separation and purification of lincomycin holds considerable promise for pharmaceutical applications.
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页数:8
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