Jia Guan1, Zhi-ming Bi, Ping Li. 1. Department of Pharmacognosy, China Pharmaceutical University, Nanjing 210038, China.
Abstract
OBJECTIVE: To develop an HPLC method for fingerprint determination of the astragalosides injection. METHOD: Analyses were carried out at 25 degrees C on a Zorbax SB-C18 column (4.6 mm x 250 mm,5 microm). Mobile phase A was water, and B was acetonitrile. The analysis followed a linear gradient program. Initial conditions were 15% B; 0 to approximately 65 min, changed to 60% B. The flow rate was 0.8 mL x min(-1). The drift tube temparature of the ELSD was 105 degrees C, and gas flowrate was 2.7 L x min(-1). RESULT: The RSD of relative retention time of the common peaks in the plant material, the extract and the injection fingerprints was less than 0.1%, and there was good similarity among 10 batches of samples. CONCLUSION: The method was reliable and simple which could be used for quality control of the injection.
OBJECTIVE: To develop an HPLC method for fingerprint determination of the astragalosides injection. METHOD: Analyses were carried out at 25 degrees C on a Zorbax SB-C18 column (4.6 mm x 250 mm,5 microm). Mobile phase A was water, and B was acetonitrile. The analysis followed a linear gradient program. Initial conditions were 15% B; 0 to approximately 65 min, changed to 60% B. The flow rate was 0.8 mL x min(-1). The drift tube temparature of the ELSD was 105 degrees C, and gas flowrate was 2.7 L x min(-1). RESULT: The RSD of relative retention time of the common peaks in the plant material, the extract and the injection fingerprints was less than 0.1%, and there was good similarity among 10 batches of samples. CONCLUSION: The method was reliable and simple which could be used for quality control of the injection.