Untangling the Impact of Plastics on Pharmaceuticals

USP 661.1, USP 661.2, and More! – Untangling the Impact of Plastics on Pharmaceuticals

By now you are probably aware of the changes made to USP <661> in 2016 and the addition of USP <661.1> and USP <661.2> this year. In short, these changes required more in-depth analytical investigations on plastic packaging and materials. They also demonstrate how the USP is leading the charge to ensure polymer materials do not impact human health regardless of how or when those materials come in contact with a pharmaceutical product.

Additional guidance under development includes the new USP general chapter <665> (formerly <661.3>) titled “Polymeric Components and Systems Used in the Manufacturing of Pharmaceutical and Biopharmaceutical Drug Products”, which recently finished receiving comments. It is accompanied by informational chapter <1665> “Plastic Components and Systems Used to Manufacture Pharmaceutical Drug Products”. <665> and <1665> are expected to be posted by the end of this month (Sept. 29th) and will become official on November 1.

This new chapter emphasizes analysis of organic extractables and extractable metals on plastic manufacturing materials and components that assist in converting raw material into APIs, drug substances, and drug products. The polymers used in these manufacturing systems may contain additives of concern such as antioxidants, stabilizers, lubricants, plasticizers, and colorants. Once implemented, the new testing could encompass anything involved in solution transfer and transport, mixing and reacting, storage, and processing including:

  • Tubing and connectors
  • Tank liners and mixing bags
  • Raw material containers
  • Production reagents
  • Filters and chromatography columns

With the increasing influence of the USP on polymers in the pharmaceutical industry, new chapters, and frequent changes, it can be difficult to stay up-to-date with the latest recommendations. Fortunately, EKG Labs takes pride in keeping up-to-date with the latest USP revisions and is able to provide appropriate consulting and analytical services for companies seeking to conform to USP standards. Our team understands the complex interactions between pharmaceutical products and polymers, and we have years of experience guiding companies through the analytical portion of their product development.

Some of our services include:

Extractables and Leachables Analysis
Impurity Identification
Characterization
Failure Analysis
Material Compatibility Testing.

To find out more about the continual USP changes and how they may impact your product development, contact EKG Labs at info@ekglabs.com or at 810-354-5229.

About EKG Labs

EKG Labs is an analytical service provider for the medical device and pharmaceutical industries. Our analytical services support regulatory filings, product development, and analytical chemistry investigations. Specialty analytical services include: extractables, leachables, biocompatibility, characterization, impurity identification, method development, method validation, deformulation, and other investigational activities. EKG Labs is a certified woman-owned business enterprise that operates out of Innovative Technology Enterprises (ITE) at the University of Missouri, St. Louis (UMSL).