Quantitative and qualitative control of antineoplastic preparations: Gravimetry versus HPLC

Abstract

This article compares gravimetry vs. high-performance liquid chromatography (HPLC) as quality control (QC) methods for paclitaxel, docetaxel and oxaliplatin preparations. We aimed at assessing the preparation method reliability in our hospital, evaluating compounding accuracy and estimating the influence of personnel training and standardized homogenization on compounding accuracy. Agreement, correlation, concordance, accuracy and precision between methods were evaluated for each drug. Conforming preparation percentages (CPs) at different tolerance limits (TLs) and compounding accuracy were calculated for each method and drug. Compounding accuracy was compared before and after personnel training and standardized homogenization implantation. SPSS v 20.0 and Ene v 2.0 were used. A total of 222 samples (58 docetaxel, 95 paclitaxel and 69 oxaliplatin) were analyzed. Gravimetry and HPLC are comparable methods. Overall CP was 81% for gravimetry at 10% TL and 85% for HPLC at 15% TL. Compounding accuracy is shown to be good for all methods and drugs. Homogenization optimization and personnel training make measurements more accurate for docetaxel and paclitaxel HPLC, but seem to worsen accuracy for docetaxel gravimetry. Gravimetry has shown to be a good alternative to HPLC for routine QC. Coupling with electronic methods should be considered in the future.

Amoxicillin and Favipiravir Bio-Degradation by Aspergillus Flavus Fungus

“…The rationale for using this relatively high concentration range was the possible application of fungal bioremediation technology in the treatment of drug manufacturing effluents. Previous studies indicated that Aspergillus species were able to depredate pollutants in aerobic or anaerobic environmental conditions and can produce a high quality of compost by degradation 15,17 . Aspergillus spp.…”

Qualification and impact of a video-assisted control system in a chemotherapy compounding unit

“…Visual control induces reliability problems because it is directly exposed to human error risk, and difficulties in traceability 12 13. Gravimetric control, if simple to implement without requiring expensive equipment, does not allow identification of the product 12 14. Among analytical methods used for preparations control, we can cite high-performance liquid chromatography (HPLC) with or without column (FIA: flow injection analysis) coupled with ultraviolet (UV) detection,11 15 16 high-performance thin-layer chromatography (HPTLC),17 spectrophotometer UV/IR (Multispec, Microdom Company),18 19 spectrophotometer UV used with or without Raman (QCRx, Icônes Services Company),20 21 and spectrophotometer UV/visible (DrugLog, Pharmacolog Company).…”