Geigert J
J Parenter Sci Technol. 1989 Sep-Oct;43(5):220-4.
Recombinant protein products have now been added to the inventory of parenteral drugs, and because of their newness, there exists a certain mystique about how they need to be handled. This article describes how the manufacturer determines both the shelf life and the proper preparation procedures for administering these new drugs. It will be shown that some recombinant protein drugs have comparable shelf lives to other parenteral drugs on the market. Also, it will be shown that, as for any parenteral drug, the manufacturer's recommended procedure for handling and administration of a recombinant protein drug should be followed.
重组蛋白产品现已被纳入肠胃外用药的库存中,由于其新颖性,在如何处理这些产品方面存在一定的神秘感。本文描述了制造商如何确定这些新药的保质期以及正确的制备程序。结果将表明,一些重组蛋白药物的保质期与市场上其他肠胃外用药相当。此外,还将表明,对于任何肠胃外用药,都应遵循制造商推荐的重组蛋白药物处理和给药程序。