Effect of Andrographis paniculata extract and Andrographolide on the pharmacokinetics of Aceclofenac and Celecoxib in rats

• Published in: Future journal of pharmaceutical sciences Vol. 9; no. 1; p. 1
• Main Authors: More, S. J., Tandulwadkar, S. S., Balap, Aishwarya R., Lohidasan, S., Sinnathambi, A., Mahadik, K. R.
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.01.2023; Springer Nature B.V; SpringerOpen
• Subjects: Accuracy; Aceclofenac; Acids; Analgesics; Andrographis Paniculata Nees; Andrographolide; Animals; Calibration; Celecoxib; Drug dosages; Herb drug Interaction; Medicine; Medicine & Public Health; Methods; Nonsteroidal anti-inflammatory drugs; Oral administration; Pharmaceutical sciences; Pharmacokinetics; Plasma; Quality control; Sensors; Solvents; United States > US; Mumbai India; India; Aceclofenac; Celecoxib; Andrographolide; Pharmacokinetics; Herb drug Interaction; Andrographis Paniculata Nees
• ISSN: 2314-7253; 2314-7245; 2314-7253
• DOI: 10.1186/s43094-022-00450-4

Background In India, for the treatment of cold, fever and inflammation, people consume herbal remedies containing Andrographis paniculata Nees (APE) as main ingredient, along with NSAIDs. So the purpose of this study is to investigate the effect of APE and pure andrographolide (AN) on the pharmacokinetic of with aceclofenac (ACF) and celecoxib (CXB) after oral co-administration in wistar rats. After co-administration of APE (equivalent to 20 mg/kg of AN) and AN (20 mg/kg) with ACF (5 mg/kg) and CXB (5 mg/kg) in rats, orally, drug concentrations in plasma were determined using HPLC method. Non-compartment model was used to calculate pharmacokinetic parameters like Cmax, Tmax, t 1/2, MRT, Vd, CL, and AUC. Results Co-administration of ACF and CXB with APE and pure AN altered the systemic exposure level of each compound in vivo. The Cmax, Tmax, MRT of CXB were increased whereas Vd and Cl of CXB were decreased significantly after co-administration of CXB with APE. Whereas co-administration of CXB with AN significantly decreased Vd, CL, and MRT of CXB. The concentration of ACF was increased significantly in co-administered groups with pure AN and APE. The AUC0-∞, AUMC0-∞, MRT, Vd and t 1/2 of ACF were also significantly decreased in co-administered groups, hence CL of ACF was increased significantly. Conclusion This study concludes that APE and pure AN have effect on pharmacokinetic of CXB and ACF in rat. Not only patients but medical practitioners using Andrographis paniculata should have awareness regarding probable herb–drug interactions with ACF and CXB.