Assessment of the Quality of Injectable Antibiotics in Benin
| Autor: | Dohou, Angèle Modupè, Yémoa, Achille Loconon, Guidan, Dodji Boris Aurel, Ahouandjinou, Seyive Hélène Solange, Amoussa, Ahmed, Dossou, Francis Moïse, Marini Djang’eing’a, Roland, Dalleur, Olivia |
|---|---|
| Přispěvatelé: | UCL - SSS/LDRI - Louvain Drug Research Institute, UCL - (SLuc) Département de pharmacie |
| Rok vydání: | 2022 |
| Předmět: | |
| Zdroj: | The American Journal of Tropical Medicine and Hygiene, Vol. 107, no.1, p. 24-31 (2022) Am J Trop Med Hyg |
| ISSN: | 1476-1645 0002-9637 |
| Popis: | Substandard and falsified medicines are an enormous threat to global health. Poor quality antibiotic preparations contribute to the development of antimicrobial resistance. In surgery, where the occurrence of healthcare-associated infections is high, healthcare teams need to rely on the quality of antibiotic prophylaxis to prevent infections. We assessed the quality of antibiotics used for surgical infection prophylaxis in Benin. Thirty-three samples were collected from six hospitals located in various departments in Benin. The antibiotics (powders for injection: amoxicillin + clavulanic acid, ampicillin, ceftriaxone; solutions for injection: ciprofloxacin, gentamicin, metronidazole) were assessed using visual inspection, pharmacotechnical tests (including uniformity of mass, pH measure, sterility test, and active pharmaceutical ingredient identification), and assay tests (including a simple analytical method thin layer chromatography) and complex analytical techniques (ultraviolet-visible spectrophotometry, high-performance liquid chromatography—diode-array detection, conductometry). Because the material needed for the methods recommended by the pharmacopeias to assess the dosage of gentamicin was not available, we developed and validated a conductometry method. Results showed that 97% (n = 32) of the samples passed visual inspection; 100% (n = 33) of the samples passed the pharmacotechnical tests, identification of active ingredients, and sterility test; 88% (n = 29) passed the test for percentage of active pharmaceutical ingredients. Overall, 15% of the samples did not pass the quality test (3% on visual inspection and 12% for excess active ingredients). Although most of the samples passed the quality tests, it appears important to perform routine quality control for intravenous medicines. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|