Analysis of tablets containing the antihistamine loratadine: A contribution to the identification of impurities;Analýza tabliet s obsahom loratadínu (antihistaminikum) príspevok k identifikácii nečistôt

Ceska a Slovenska Farmacie

Volumn 53, Issue 4, 2004, Pages 192-196

  Issa, N ^a   Mlynárová, Marie ^a,b  

^a Statny ustav pre Kontrolu Lieciv   (Slovakia)

^b NONE   (Slovakia)

Author keywords

Impurities; Laratadine; Thin layer chromatography (TLC); Validation

Indexed keywords

ACETIC ACID ETHYL ESTER; ANTIHISTAMINIC AGENT; CELLULOSE; CHLOROFORM; DIPHENHYDRAMINE; FLONIDAN; LACTOSE; LORATADINE; SILICA GEL;

ARTICLE; DRUG IDENTIFICATION; DRUG IMPURITY; SPECTROPHOTOMETRY; TABLET; THIN LAYER CHROMATOGRAPHY; VALIDATION PROCESS;

CHROMATOGRAPHY, THIN LAYER; DRUG CONTAMINATION; HISTAMINE H1 ANTAGONISTS, NON-SEDATING; LORATADINE; TABLETS;

EID: 3543026326     PISSN: 12107816     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (8)

1. El Ragehy, N. A., Badawey, A. M., El Khateeb, S. Z.: Analytical Letters, 1995; 28, 2363-2378.
2. Ivanovic, D., Medenica, M., Markovic, S., Mandic, G.: Arzneim.-Forsch./Drug Resd 50, (II), (2000), 1004-1008.
3. Directive 2001/83/EC of the European Parliament and of the Council (6 November 2001).
4. Americký liekopis (USP 24).
5. Večerková, J.: Postup při záchytu a identifikaci léčiv a jejich metabolitů v biologickém materiálu pomocí chromatografie na tenkých vrstvách. Praha, SPN, 1983.
6. Rupérez, F. J., Fernández, H., Barbas, C.: Journal of Pharmaceutical and Biomedical Analysis, 2002; 29, 35-41.
7. Pharmeuropa Vol. 15, No. 3, July 2003.
8. ICH TOPIC Q 3 B: Impurities in New Medicinal Products, valid from 18 June 1997, The European Agency for the Evaluation of Medicinal Products, London.