Simulation of metabolism-based herb-drug interaction: towards safe and efficacious use of NIPRD-AM1 | ||
| Avicenna Journal of Phytomedicine | ||
| مقاله 1، دوره 3، شماره 3، 2013، صفحه 201-204 اصل مقاله (224.93 K) | ||
| نوع مقاله: Short communication | ||
| شناسه دیجیتال (DOI): 10.22038/ajp.2013.233 | ||
| نویسندگان | ||
| Bulus Adzu* 1؛ Kudirat Bola Mustapha2؛ Collen Masimirembwa3؛ Obiageri Obodozie2؛ Rukaiyatu Abdullahi Kirim2؛ Karniyus Shingu Gamaniel4 | ||
| 1Department of Pharmacology and Toxicology, National Institute for Pharmaceutical Research and Development, PMB 21, Abuja, Nigeria | ||
| 2Department of Medicinal Chemistry and Quality Control, National Institute for Pharmaceutical Research and Development, PMB 21, Abuja, Nigeria | ||
| 3African Institute of Biomedical Science and Technology (AiBST), Cnr Chinhoyi Str./Jason Moyo Ave. No. 9 at LAPF Centre, Harare, Zimbabwe | ||
| 4Director General/Chief Executive Officer, National Institute for Pharmaceutical Research and Development, PMB 21, Abuja, Nigeria | ||
| چکیده | ||
| Objective: To evaluate the effect of NIPRD-AM1 on CYP3A4 in order to generate clinically significant data for its safe and efficacious use. Materials and Methods: NIPRD-AM1 is a phytomedicine developed from aqueous root extracts of Nauclea latifolia Smith (Rubiaceae) for the treatment of uncomplicated malaria. The effect of NIPRD-AM1 on CYP3A4 was measured with and without the addition of NIPRD-AM1, by testing different concentrations of the product at 37 °C in reactive mixtures with ketoconazole (2.5 µM) as the positive control. Results: Results showed a very low IC50 value of 0.01 mg/ml similar to that of ketoconazole (0.016 mg/ml). Conclusion: Metabolic processes of NIPRD-AM1 are likely to inhibit CYP3A4, with potential implication on drugs that are CYP3A4 substrates. This is a promising approach for guidance towards the safe and efficacious use of NIPRD-AM1. | ||
| کلیدواژهها | ||
| CYP3A4؛ Herb-Drug Interactions؛ Nauclea latifolia؛ NIPRD-AM1 | ||
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