Green Analytical Method for Simultaneous Determination of Glucosamine and Calcium in Dietary Supplements by Capillary Electrophoresis with Capacitively Coupled Contactless Conductivity Detection

被引:5
|
作者
Do, Yen Nhi [1 ]
Kieu, Thi Lan Phuong [1 ,2 ]
Dang, Thi Huyen My [1 ]
Nguyen, Quang Huy [1 ,3 ]
Dang, Thu Hien [2 ]
Tran, Cao Son [2 ]
Vu, Anh Phuong [4 ]
Do, Thi Trang [4 ]
Nguyen, Thi Ngan [4 ]
Dinh, Son Luong [4 ]
Nguyen, Thi Minh Thu [1 ]
Pham, Thi Ngoc Mai [1 ]
Hoang, Anh Quoc [1 ]
Pham, Bach [1 ]
Nguyen, Thi Anh Huong [1 ]
机构
[1] Vietnam Natl Univ, Univ Sci, Fac Chem, 19 Le Thanh Tong, Hanoi 10000, Vietnam
[2] Natl Inst Food Control NIFC, 65 Pham Duat, Hanoi 10000, Vietnam
[3] Thai Nguyen Univ, Univ Med & Pharm, Fac Pharm, 284 Luong Ngoc Quyen, Thai Nguyen 24000, Vietnam
[4] Bach Mai Hosp, Poison Control Ctr, 78 Giai Phong, Hanoi 10000, Vietnam
关键词
PERFORMANCE LIQUID-CHROMATOGRAPHY; KNEE OSTEOARTHRITIS; CHONDROITIN SULFATE; FUNDAMENTAL-ASPECTS; RAW-MATERIALS; PART II; MANAGEMENT; DERIVATIZATION; HYDROCHLORIDE; EFFICACY;
D O I
10.1155/2023/2765508
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The need for analytical methods that are fast, affordable, and ecologically friendly is expanding. Because of its low solvent consumption, minimal waste production, and speedy analysis, capillary electrophoresis is considered a "green " choice among analytical separation methods. With these "green " features, we have utilized the capillary electrophoresis method with capacitively coupled contactless conductivity detection (CE-(CD)-D-4) to simultaneously determine glucosamine and Ca2+ in dietary supplements. The CE analysis was performed in fused silica capillaries (50 mu m inner diameter, 40 cm total length, 30 cm effective length), and the analytical time was around 5 min. After optimization, the CE conditions for selective determination of glucosamine and Ca2+ were obtained, including a 10 mM tris (hydroxymethyl) aminomethane/acetic acid (Tris/Ace) buffer of pH 5.0 as the background electrolyte; separation voltage of 20 kV; and hydrodynamic injection (siphoning) at 25 cm height for 30 s. The method illustrated good linearity over the concentration range of 5.00 to 200 mg/L of for glucosamine (R-2 = 0.9994) and 1.00 to 100 mg/L for Ca2+ (R-2 = 0.9994). Under the optimum conditions, the detection limit of glucosamine was 1.00 mg/L, while that of Ca2+ was 0.05 mg/L. The validated method successfully analyzed glucosamine and Ca2+ in seven dietary supplement samples. The measured concentrations were generally in line with the values of label claims and with cross-checking data from reference methods (HPLC and ICP-OES).
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页数:10
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