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    LIANG Qiuxia, CHEN Han, HUANG Lili, ZHU Jianping, LU Rigang. HPLC Determination of Vitamin B12 in Gentamicin Sulfate, Procaine Hydrochloride and Vitamin B12 Capsules and Evaluation of Content Uniformity[J]. PHYSICAL TESTING AND CHEMICAL ANALYSIS PART B:CHEMICAL ANALYSIS, 2021, 57(3): 199-203. DOI: 10.11973/lhjy-hx202103002
    Citation: LIANG Qiuxia, CHEN Han, HUANG Lili, ZHU Jianping, LU Rigang. HPLC Determination of Vitamin B12 in Gentamicin Sulfate, Procaine Hydrochloride and Vitamin B12 Capsules and Evaluation of Content Uniformity[J]. PHYSICAL TESTING AND CHEMICAL ANALYSIS PART B:CHEMICAL ANALYSIS, 2021, 57(3): 199-203. DOI: 10.11973/lhjy-hx202103002

    HPLC Determination of Vitamin B12 in Gentamicin Sulfate, Procaine Hydrochloride and Vitamin B12 Capsules and Evaluation of Content Uniformity

    • A HPLC method was introduced to determine the content of Vitamin B12 in 47 batches of gentamicin sulfate, procaine hydrochloride and Vitamin B12 capsules from 4 manufacturers including factory A, factory B, factory C, factory D, and the content uniformity was evaluated for Vitamin B12 in the same batch or different bathes of samples from 4 manufactures. Vitamin B12 in capsules was extracted with water. CAPCELL PAK ACR C18 chromatographic column was used as separation column, the mixtures of methanol and 0.028 mol·L-1 sodium dihydrogen phosphate solution (pH 3.2) with various volume ratios were used as mobile phase for gradient elution, and the content of Vitamin B12 was determined at the detection wavelength of 362 nm. The results showed that the linearity range of Vitamin B12 standard curve was in the range of 0.2-5.0 mg·L-1, with lower limit of determination (10S/N) of 0.12 mg·L-1. The spiked recovery was made on capsule samples at three concentration levels, giving recoveries in the range of 96.9%-102%, and RSD of measured values of Vitamin B12 in 6 sample solutions was 1.5%. This method was used to analyze the 47 batches of samples, and values of Vitamin B12 obtained were in the range of 55.4%-137.0% of the labelled values of the samples from factory D, exceeding the range (80.0%-120.0%) set by the second part of Chinese Pharmacopoeia and actual samples. Therefore, the content uniformity evaluation was made, and the results showed that the vitomin B12 content in the samples within and between batches was uneven, finding that it may be related to the dry mixing process used in factory D.
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