Comprehensive determination of extractables from five different brands of stoppers used for injectable products.
PDA J Pharm Sci Technol
; 63(6): 527-36, 2009.
Article
in En
| MEDLINE
| ID: mdl-20169859
Five commonly used stopper formulations were tested for extractables using three different vehicles (pH 3 citrate buffer with 20% w/v sulfobutylether-beta-cyclodextrin, pH 8 phosphate buffer and 50/50 v/v polyoxyethylated castor oil/dehydrated alcohol). The stoppers, made from butyl and halobutyl rubbers, coated and uncoated with proprietary films, were stored in contact with each vehicle for up to 6 months at 40 degrees C/75% relative humidity (RH) or for up to 24 months at 25 degrees C/60% RH. Samples were analyzed for the presence of extractables using inductively coupled plasma-atomic emission spectroscopy, ion chromatography, high-performance liquid chromatography, and gas chromatography. Extractables were observed at greater than 10 ppm for only one of the five stoppers that were tested. Based on these results, a standardized protocol for stopper extractable testing was developed. This protocol has been used to satisfy stopper extractable testing regulatory requirements for a number of different new injectable products.
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Pharmaceutical Vehicles
/
Elastomers
/
Drug Packaging
Language:
En
Journal:
PDA J Pharm Sci Technol
Journal subject:
FARMACIA
/
FARMACOLOGIA
Year:
2009
Type:
Article
Affiliation country:
United States