The matrix of SDS integrated with linear hydrophilic polymer for resolution of high- and low-molecular weight hyaluronic acids in MEKC

被引:9
|
作者
Lin, Kung-Hung [1 ]
Kou, Hwang-Shang [2 ]
Lin, Yi-Hui [3 ]
Wang, Chun-Chi [2 ,4 ,5 ]
机构
[1] Kaohsiung Armed Forces Gen Hosp, Dept Surg, Div Gen Surg, Zuoying Branch, Kaohsiung, Taiwan
[2] Kaohsiung Med Univ, Coll Pharm, Sch Pharm, 100,Shi Chuan 1st Rd, Kaohsiung 807, Taiwan
[3] China Med Univ, Coll Pharm, Sch Pharm, Taichung, Taiwan
[4] Kaohsiung Med Univ Hosp, Dept Med Res, Kaohsiung, Taiwan
[5] Kaohsiung Med Univ Hosp, Drug Dev & Value Creat Res Ctr, Kaohsiung, Taiwan
关键词
Hyaluronic acids; LHA; HHA; MEKC; SDS micelles; PEG sieving matrix; ASSISTED CARBOHYDRATE ELECTROPHORESIS; CAPILLARY-ELECTROPHORESIS; CHONDROITIN SULFATE; SENSITIVITY; INJECTION; DELIVERY; RECEPTOR; MARKERS; ASSAY;
D O I
10.1016/j.jfda.2019.10.005
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Hyaluronic acid (HA), a multi-functional material, has a high dispersion in molecular weight, and the functions of HA are determined through the size. Nevertheless, hyaluronic acid mixtures are not easily separated due to their polydispersity. In this study, a capillary electrophoresis strategy was developed for resolution of different molecular-weight HA without enzymatic digestion. Here, hyaluronic acid mixtures with low molecular weight (380 kD; LHA) and high molecular weight (2180 kD; HHA) were successfully resolved by the SDS integrated with low molecular-weight polymer in capillary electrophoresis. By optimizing experimental conditions, the separation of LHA and HHA was completed within 14 min. The optimal conditions were as follows: the running buffer was 25 mM borate buffer (pH 9.75) containing 30 mM SDS and 10% polyethylene glycol (MW: 8000); applied voltage was 20 kV (detector at cathode side) and separation temperature was set at 25 degrees C. The data of method validation showed that calibration plots were linear (r >= 0.9977) over a range of 10-50 mu g/mL for LHA, and 40-200 mu g/mL for HHA. In the evaluation of precision and accuracy for this method, the RSD and RE values were all less than 4.2%. This fascinating technique was successfully applied to the quality control of cosmetic and pharmaceutical containing different ratios of LHA and HHA, and it was feasible for serving as a tool to quantitatively analyze different sizes of HA for clinical survey. Copyright (C) 2019, Food and Drug Administration, Taiwan. Published by Elsevier Taiwan LLC.
引用
收藏
页码:159 / 166
页数:8
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