Materials in manufacturing and packaging systems as sources of elemental impurities in packaged drug products: a literature review

DR Jenke, CLM Stults, DM Paskiet, DJ Ball… - PDA journal of …, 2015 - journal.pda.org
Elemental impurities in drug products can arise from a number of different sources and via a
number of different means, including the active pharmaceutical ingredient, excipients, the …

[BOOK][B] Pharmaceutical packaging technology

DA Dean, ER Evans, IH Hall - 2005 - books.google.com
Pharmaceutical packaging requires a greater knowledge of materials and a greater intensity
of testing than most other packed products, not to mention a sound knowledge of …

UV and UV derivative spectrophotometric determination of two-component mixtures

H Salem, M El-Maamli, M El-Sadek… - Spectroscopy letters, 1991 - Taylor & Francis
In this paper, two-component mixtures (spironolactone with hydrochlorothiazide, captopril
with hydrochlorothiazide, and spironolactone with furosemide) were assayed by UV (A), first …

Pharmaceuticals and related drugs

RK Gilpin, LA Pachla - Analytical chemistry, 1989 - ACS Publications
This is the twenty-third biennial review dealing with the inorganic and organic analytical
chemistry of water. The format of this review is essentially the same, but with some minor …

Considerations for elastomeric closures for parenteral biopharmaceutical drugs

JA Bontempo - Development of Biopharmaceutical Parenteral …, 1997 - api.taylorfrancis.com
This chapter is essentially an overview on the interactions of proteins and peptides with
elastomeric closures rather than with glass containers. However, what is highly …