Abstract
Drug manufacturers use filters widely in their manufacturing processes for bioburden reduction and sterility assurance. In implementing a pharmaceutical filtration, it is essential to determine and profile the filter extractables that could be introduced into the product. There is an ongoing industry effort to explore the analysis of extractables. Toward this end, the use of complementary analytical techniques was evaluated to aid in extractables identification by determining whether the analysis of filters in the form of components, rather than entire assemblies, facilitated the profiling of extractables. The study examines filter components of 10-inch, 0.22-μm Durapore® cartridge filters using Fourier transform infra-red spectroscopy (FTIR) and nuclear magnetic resonance spectroscopy (NMR), as well as determines the non-volatile residues (NVR) and total organic carbon contents (TOC) of the extractables. The complementary techniques of high performance liquid chromatography (HPLC/UV) and liquid chromatography nuclear magnetic resonance spectroscopy (LC/NMR) were also used. The results of the tests indicated very low levels of extractables.
Footnotes
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↵aThe term of extractables is sometimes used interchangeably with the term of leachables in the field. According to the definitions provided in “PDA Scientific Forum on Extractables” (2001), leachables refer to those compounds that migrate into the solutions under the use conditions, while the extractables refer to those that have the potential. Since in this study we selected conditions that were more aggressive than the actual use conditions for the extractions, we chose to use the term of extractables.
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