Method for the Determination of Pd-Catalyst Residues in Active Pharmaceutical Ingredients by Means of High-Energy Polarized-Beam Energy Dispersive X-Ray Fluorescence-Reference-Cited by-同舟云学术

Method for the Determination of Pd-Catalyst Residues in Active Pharmaceutical Ingredients by Means of High-Energy Polarized-Beam Energy Dispersive X-Ray Fluorescence

Published:2009-01-22 Issue:4 Volume:81 Page:1404-1410
ISSN:0003-2700
Container-title:Analytical Chemistry
language:en
Short-container-title:Anal. Chem.

Author:

Marguí E.¹,Van Meel K.¹,Van Grieken R.¹,Buendía A.¹,Fontàs C.¹,Hidalgo M.¹,Queralt I.¹

Affiliation:

1. Laboratory of X-Ray Analytical Applications, Institute of Earth Sciences “Jaume Almera”, CSIC, Solé Sabarís s/n, 08028 Barcelona, Spain, Department of Chemistry, University of Antwerp, Universiteitsplein 1, 2610 Antwerp, Belgium, Department of Quality Control, Medichem, S.A. Pol. Ind. Celrà, 17460 Celrà, Spain, and Department of Chemistry, University of Girona, Campus Montilivi, 17071 Girona, Spain

Publisher

American Chemical Society (ACS)

Subject

Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ac8021373

Reference22 articles.

1. The impact of low-level inorganic impurities on key physicochemical properties of paracetamol

2. An overview of recent applications of inductively coupled plasma-mass spectrometry (ICP-MS) in determination of inorganic impurities in drugs and pharmaceuticals

3. The Art of Meeting Palladium Specifications in Active Pharmaceutical Ingredients Produced by Pd-Catalyzed Reactions

4. Committee for medicinal products for human use (CHMP).Guideline on the Specification Limits for Residues of Metal Catalysts or Metal Reagents; Doc. No. EMEA/CHMP/SWP/4446/2000);European Medicines Agency:London, U.K., February2008.

5. The United States Pharmacopoeia, USP30.Chemical Tests. Limit Tests. Heavy Metals; 2007, pp146−147.

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