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Development of A New HPLC Method for Separation and Determination 25(OH)- Cholecalciferol (Vitamin D3). | ||
| journal of al-qadisiyah for pure science(quarterly) | ||
| Article 1, Volume 16, Issue 4, 2016, Pages 101-111 PDF (0 K) | ||
| Author | ||
| Sarmad B. Dikran | ||
| Abstract | ||
| Vitamin D3 was found interference with other fat soluble vitamins (especially vitamin A and E) that are commonly present with vitamin D, in Serum & pharmaceutical preparation. In the present study, a rapid, simple and economical reversed phase-HPLC procedure has been fixed optimization of condition and developed for the separation and determination of vitamin D3 in mixture standard of Vitamin D3and Vitamin A. Anew method were developed in HPLC ,based method with a UV detector by examining various conditions including mobile phase, flow rate, volume inject and temperature, we have also proposed a very simple method of isolation of these vitamins. The vitamins were separated isocratically on a Knauer C18 column (250×4.6mm, 5μm particle size) with a mobile phase consisting of isocratic acetonitrile and methanol (75:25, v/v) operated at 40ºC with retention times less than 10 min. and the detection limit of our developed HPLC method is 0.01μg/ml. The eluted vitamins were identified and monitored on a UV-Detector at 265 nm with optimum flow rate 1.5 mL/min and 50μL Injection volume. The linearity of the method was excellent (r2 > 0.999), over the concentration range of 10-200ng/ml. Vitamin D3 was found interference with other fat soluble vitamins (especially vitamin A and E) that are commonly present with vitamin D, in Serum & pharmaceutical preparation. In the present study, a rapid, simple and economical reversed phase-HPLC procedure has been fixed optimization of condition and developed for the separation and determination of vitamin D3 in mixture standard of Vitamin D3and Vitamin A. Anew method were developed in HPLC ,based method with a UV detector by examining various conditions including mobile phase, flow rate, volume inject and temperature, we have also proposed a very simple method of isolation of these vitamins. The vitamins were separated isocratically on a Knauer C18 column (250×4.6mm, 5μm particle size) with a mobile phase consisting of isocratic acetonitrile and methanol (75:25, v/v) operated at 40ºC with retention times less than 10 min. and the detection limit of our developed HPLC method is 0.01μg/ml. The eluted vitamins were identified and monitored on a UV-Detector at 265 nm with optimum flow rate 1.5 mL/min and 50μL Injection volume. The linearity of the method was excellent (r2 > 0.999), over the concentration range of 10-200ng/ml. Key Words: 25(OH) Cholecalciferol (Vitamin D3) , HPLC.. | ||
| Keywords | ||
| Vitamin D; in Serum; In the present study; a rapid; simple and economical reversed phase; HPLC procedure has been fixed optimization of condition and developed for the separation and determination of vitamin D; Anew method were developed in HPLC; based method with a UV detector by examining various conditions including mobile phase; flow rate; volume inject and temperature; we have also proposed a very simple method of isolation of these vitamins; The vitamins were separated isocratically on a Knauer C; m particle size; operated at; and the detection limit of our developed HPLC method is; The eluted vitamins were identified and monitored on a UV; Detector at; min and; The linearity of the method was excellent; over the concentration range of; Key Words; HPLC | ||
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