PubMed · 12567867
[Quality control methods for recombinant human endostatin].
Abstract
AIM: To establish the quality control methods for recombinant human endostatin. METHODS: Biological activity was determined by endothelial cell migration assays. Peptide mapping was tested by trypsin digestion and RP-HPLC. Purity was determined by non-reduced SDS-PAGE and RP-HPLC. Other tests including molecular weight, isoelectrical point, etc. were done according to the National Requirements for Biological Products (2000). RESULTS: The method of bioassay was established and used for determining activity of endostatin. Specific activity of the three batchs of drug substance was 1.45 x 10(6), 1.57 x 10(6) and 2.73 x 10(6) u.mg-1 proteins. Peptide mappings of the three batches of drug substance were completely identified. Both purity results of the products tested by SDS-PAGE and RP-HPLC were more than 99%. CONCLUSION: The established methods can effectively control the quality of recombinant human endostatin.
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Yong-Hong Li, Jun-zhi Wang, Chun-mei Han, Yi Zhang, Chun-ming Rao. 2002. [Quality control methods for recombinant human endostatin].. https://pubmed.ncbi.nlm.nih.gov/12567867/
Cite the original work for its findings. Save a collection to share your selection of sources.