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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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