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Title: | Pharmaceutical Quality of Selected Metronidazole and Ciprofloxacin Infusions Marketed in South Eastern Nigeria |
Authors: | Oli, Angus Nnamdi Ibeabuchi, MaryRose Ukamaka Enweani, Ifeoma Bessie Emencheta, Stephen Chijioke |
Keywords: | intravenous infusions quality assessment ciprofloxacin metronidazole quality medicines |
Issue Date: | 2020 |
Publisher: | Dovepress |
Citation: | Drug, Healthcare and Patient Safety:12; 103-111 |
Abstract: | Background:Pharmaceutical products need to be of good quality and it is even morecritical when it comes to life saving medicaments like infusions. Objective:This research surveyed the qualityfitness of some ciprofloxacin and metronidazole infusion samples marketed in South-eastern of Nigeria. Methods:Using Official Compendial methods, microbiological quality, active pharmaceutical ingredients quantitation, pH and particle count tests were evaluated on eighty infusionbottles (from eight pharmaceutical companies) of each of the two drugs. Results: Out of the sixteen brands tested, 2 metronidazole brands and 1 ciprofloxacin brand (representing 18.75% of the total 16 brands/makes) were contaminated while the remaining13 brands (81.25%) were found sterile. The active pharmaceutical ingredients quantitativeassay showed that all the brands of ciprofloxacin infusion were between the 95% and 105%limit of label claim while one metronidazole brand has <95–110% limit label claim. Six brands each of the two drugs evaluated fall below the acceptable pH range [ciprofloxacin (3.5–4.6) and metronidazole (4.8–5.2)], while the other two brands of both drugs passed the test. In the antibacterial study, Pseudomonas aeruginosaandEscherichia coliwere susceptible to the ciprofloxacin (5 µg). However, Salmonella typhi recorded inhibition zonediameters within resistant and intermediate range.Peptostrepococcusspp was susceptible(at minimum inhibitory concentrations of 100 µg/mL) to all the brands of metronidazole, while none of the brands were effective onLactobacillusspp. All the brands passed the test for particulate contamination. The particles size range was <10µm. Conclusion: About eighty-one percent (81.25%) of the infusions have acceptable good microbiological quality. However, 18.75% that failed the tests is a concern knowing that these are lifesaving products. |
Description: | Scholarly Work |
URI: | https://doi.org/10.2147/DHPS.S246050 http://repository.unizik.edu.ng/handle/123456789/543 |
Appears in Collections: | Scholarly Works |
Files in This Item:
File | Description | Size | Format | |
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OLI ANGUS NNAMDI 22.pdf | 738.17 kB | Adobe PDF | View/Open |
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