Development and verification of a high performance liquid chromatography method for determination of aluminium adjuvant content in vaccine
Objective To develop a high performance liquid chromatography(HPLC)method for determination of alumi-nium adjuvant content in vaccine,and verify and preliminarily apply the method.Methods The 8-hydroxyquinoline derivatization method was used for determination.The chromatographic column was phenyl-hexyl column[Luna 5u Phenyl-Hexyl(250 mm × 4.6 mm)],and the mobile phase was composed of ammonium acetate solution-acetonitrile(with 8-hydroxyquinoline)(60∶40)containing 20 mg/L ascorbic acid,while eluted at a flow rate of 1.0 mL/min with the isocratic eluent.The excitation wavelength and the emission wavelength of the fluorescence detector were 380 nm and 520 nm respectively.The column temperature was 40 ℃,and the sample injection was 50 μL.The developed method was verified for the specificity,linear range,accuracy,repeatability,stability and durability,and used to determine the aluminum content in 12 batches of vaccines.The results were compared with those determined by titration in general principle 3106 of Chinese Pharmacopoeia(Volume Ⅲ,2020 edition).Results No interference peaks appeared in the sample chromato-gram,and the non-aluminum adjuvant vaccine components and phosphate buffer had no interference with the determi-nation.The linearity of aluminum standard was good in the concentration range of 6.25～100 μg/mL,r=0.999 6.The average results of spike recoveries of aluminum content in inactivated hepatitis A vaccine,recombinant hepatitis B vaccine,adsorbed acellular DTP vaccine and inactivated enterovirus 71 vaccine were 98.32％,100.85％,101.09％and 99.31％,respectively in the verification for accuracy.The relative standard deviations(RSDs)of the determination results of aluminum content in the solution of six samples of the four vaccines in the same batch were 1.09％,1.42％,0.97％and 1.30％,respectively.The RSDs of aluminum content of four vaccine samples stored at room tempe-rature for 0,2,4,6 and 8 h were 0.82％,0.73％,0.40％and 0.48％,respectively.When the ratio of ammonium acetate solution to 8-hydroxyquinoline acetonitrile solution in mobile phase changed within 5％,the fluctuation range of aluminum content of four vaccines was less than 2％.There was no significant difference between the developed HPLC method and the titration method of Chinese Pharmacopoeia(Volume Ⅲ,2020 edition)for determination of aluminum content in the 12 batches of vaccine samples.Conclusion A HPLC method for determination of aluminum adjuvant content in vaccines has been successfully established with good specificity,linearity,accuracy,repeatability,stability and durability,simple operation,high degree of automation and less interference of manual factors.It can realize the determination of aluminium content in single dose,which provides an effective means for the rapid and large-scale determination of aluminum content in vaccine products and monitoring the dispensing of semi-final products in the production process.
万方数据
维普
