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Anti-inflammatory and antipyretic properties of Kang 601 heji,a traditional Chinese oral liquid dosage form

Asian Pacific Journal of Tropical Biomedicine 2015年第11期5卷 921-927页

作者： Raphael Nammahime Alolga Sarah Wambui Amadi Vitus Onoja assogba gabin assanhou Moses Muyaba Said Abasse Kassim State Key Laboratory of Natural Medicines China Pharmaceutical University Department of Pharmacology China Pharmaceutical University Joint Key Laboratory for Drug Development Department of PharmaceuticsChina Pharmaceutical University Department of Medicinal Chemistry China Pharmaceutical University

Objective: To evaluate the scientific basis for the use of Kang 601 heji(K-601) as an anti-in flammatory and antipyretic agent using appropriate animal ***: Carrageenan-induced rat paw and xylene-induced ear oedemas were models used to investigate anti-in flammatory actions of K-601. Lipopolysaccharide-induced pyrexia model was used to evaluate antipyretic activity in Wistar rats. The antiin flammatory and antipyretic mechanisms were evaluated by detecting prostaglandins E2, nitric oxide, interleukin-1b and tumour necrosis factora levels using appropriate reagents and ELISA ***: The results revealed that K-601 reduced the level of in flammations in both antiin flammatory models in a dose-dependent manner. The same was true for the antipyretic model. The possible mechanisms of actions were through the inhibition of prostaglandins E2, interleukin-1b, tumour necrosis factora and nitric ***: K-601 has proven anti-in flammatory and antipyretic actions. The findings provide a scientific basis for the use of K-601 as anti-in flammatory and antipyretic agent in traditional Chinese medicinal practice.

关键词： Kang 601 heji Anti-in flammatory Antipyretic Model

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Simultaneous Determination by HPLC-UV Vis of Tartrazine and Sunset Yellow in Soft Drinks Sold in Benin

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American Journal of Analytical Chemistry 2022年第8期13卷 277-288页

作者： Janvier Engelbert Agbokponto André Philippe S. Kpaibe Loconon Achille Yemoa assogba gabin assanhou Habib Ganfon Gildas Komenan Gbassi Michèle Aké N’cho Christoph Amin Laboratoire de Chimie Analytique et d’Analyse des Médicaments UFR Pharmacie Faculté des Sciences de la Santé Université d’Abomey-Calavi Cotonou Bénin UFR Pharmacie Faculté des Sciences de la Santé Université d’Abomey-Calavi Cotonou Bénin Département de Chimie Analytique Bromatologie Chimie Générale et Minérale UFR des Sciences Pharmaceutiques et Biologiques Université Félix Houphou&euml t-Boigny Abidjan C&ocirc te d’Ivoire

The use of dyes such as tartrazine (E102) and sunset yellow (E102) in food, beverages and health products for technological and commercial purposes is common. The adverse effects caused by these dyes, such as allergies and hyperactivity disorder have been reported, especially in children. In the present study, a chromatographic method was developed and validated for simultaneous determination of tartrazine and sunset yellow. The chromatographic separation was performed on a Lichrocart® C18 column (125 × 4.6 mm;5 μm) with a security Guard-C18 column (4 × 2.0 mm, 5 μm;Phenomenex, Torrance, CA, USA) maintained at 30°C. The mobile phase consisted of a mixture of acetonitrile/ammonium acetate buffer pH 6.8 in gradient mode with a flow rate of 1 mL/min. The injection volume was 10 μL. The detection wavelength was set at 455 nm. The parameters of specificity, linearity, precision, repeatability, accuracy and sensitivity were examined for validation. The developed method is linear in the range of 1 μg/mL to 100 μg/mL with a R2> 0.998. The intra-day and inter-day precisions (RSD) were less than 0.6% and 3.1% respectively. The detection limit was 0.03 μg/mL and the quantification limit was 0.1 μg/mL. The retention time of tartrazine was 2.86 min, while sunset yellow was detected at 5.67 min. A simple, rapid, accurate and robust HPLC/UV-Visible method was developed and validated for simultaneous identification and quantification of tartrazine and sunset yellow. This developed method was successfully applied for the simultaneous determination of tartrazine and sunset yellow in soft drinks sold in Benin.

关键词： Tartrazine Sunset Yellow HPLC-UV Food Dyes

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Quality Control of Paracetamol Generic Tablets Marketed in Benin and Search of Its Two Impurities P-Aminophenol and P-Nitrophenol by HPLC-UV/Visible

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American Journal of Analytical Chemistry 2022年第11期13卷 449-460页

作者： Yemoa Loconon Achille Agbokponto Janvier Engelbert assanhou assogba gabin Adetona Pauline Doffon Parfait Ganfon Habib Roland Marini Djang’eing’a Laboratoire de Chimie analytique et Analyse des Médicaments Unité de Formation et de Recherche en Pharmacie Faculté des Sciences de la Santé. Université d’Abomey Calavi Cotonou Bénin Laboratoire de Pharmacie Galénique et de Technologie Pharmaceutique Unité de Formation et de Recherche en Pharmacie Faculté des Sciences de la Santé Université d’Abomey Calavi Cotonou Bénin Laboratoire de Pharmacognosie et de de Phytothérapie Unité de Formation et de Recherche en Pharmacie Faculté des Sciences de la Santé Université d’Abomey Calavi Cotonou Bénin Laboratoire de Chimie Analytique Pharmaceutique Departement de Pharmacie Université de Liège (ULiège) Liège Belgium

In this work, we evaluated the quality of paracetamol generic tablets while seeking its two main impurities namely 4-para-aminophenol (4-AP) and 4-para-nitrophenol (4-NP) which have nephrotoxic and teratogenic properties. Ninety-four (94) samples were collected at various levels of the medicine supply chain and illegal markets in Benin for quality control tests such as visual inspection, pharmacotechnical tests as mass variation, disintegration test, dissolution test, followed by HPLC UV-Vis identification and assay of paracetamol, 4-AP and 4-NP. The analytes were separated on C18 Lichrocart column (250 mm × 4.0 mm i.d, 5 μm);the mobile phase was MeOH:10 mM ammonium acetate buffer pH 6.8 (35:65) pumped at a flow rate of 1 ml/min. The detection was done at 245 nm. Analysis of our results shows that 77.7% of the samples did not comply with the visual inspection test requirements, 2.1% did not pass the mass variation test, 24.3% of the sample batches didn’t comply with the disintegration test requirements. In addition none of these uncomply batches passed the dissolution test, even if the identification test indicated that all samples contained paracetamol. None contained 4-NP (acceptance limit < 0.05% m/m;BP), while 3 of 94 samples contained 4-AP but within acceptance limit (4-AP < 0.1% m/m;BP). As for the paracetamol assay, 80.9% complied with the specifications of the pharmacopoeias taken as reference (90% - 110%;USP). Further, broader studies should be conducted according to the same rules of good practice for a more comprehensive analysis of the situation. Generally the quality control of paracetamol in most African countries, particularly in Benin, is based on pharmacotechnical tests and paracetamol assay. This work, in addition to the usual tests, showed the importance to search for paracetamol and other drugs’ impurities during their routine quality control.

关键词： Quality Control Substandard Medicines Paracetamol P-Aminophenol P-Nitrophenol Benin

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