Simultaneous Estimation of Berberine and Piperine in a Novel Nanoformulation for Epilepsy Control via HPLC

Author:

El-Nahas Amira E12ORCID,Elbedaiwy Heba M12,Helmy Maged W324,El-Kamel Amal H56

Affiliation:

1. Department of Pharmaceutics , Faculty of Pharmacy, , El Gomhouria street, Damanhour Post Office PO Box 22511, Damanhour , Egypt

2. Damanhour University , Faculty of Pharmacy, , El Gomhouria street, Damanhour Post Office PO Box 22511, Damanhour , Egypt

3. Department of Pharmacology and Toxicology , Faculty of Pharmacy, , El Gomhouria street, Damanhour Post Office PO Box 22511, Damanhour , Egypt

4. Department of Pharmacology and Toxicology, College of Pharmacy, Arab Academy for Science, Technology and Maritime Transport , Abu Qier, PO Box 1029, Alexandria , Egypt

5. Department of Pharmaceutics , Faculty of Pharmacy, , 1 Khartoum Square, Azarita, Mesalla Post office PO Box 21521, Alexandria , Egypt

6. Alexandria University , Faculty of Pharmacy, , 1 Khartoum Square, Azarita, Mesalla Post office PO Box 21521, Alexandria , Egypt

Abstract

Abstract Berberine (Brb) and piperine (Pip) are salient examples of bioactive nutraceuticals possessing a promising role in controlling epilepsy. However, during the development of novel nanoformulation that augments their effects, an adequate determination of each one separately was a challenge since they have nearly the same detection wavelength and diverse solubility profiles. Consequently, a tailored high-performance liquid chromatography technique was developed for their simultaneous detection in routine analyses. The chromatographic separation was achieved using a C18 column. The linear gradient flow of acetonitrile: 0.1%v/v aqueous phosphoric acid was altered from 55:45 to 80:20 v/v over 3 min at a 1.2 mL/min flow rate until the end of the run. Brb and Pip were eluted at 1.6 and 3.4 min, respectively. The linearity of the standard curves was found to be ≥0.999, and the mean % recovery for Brb and Pip lay within the accepted limit. Moreover, the percentage coefficient of variation was <2% for intra- and inter-day precision. Consequently, the developed assay was successfully applied for the quantification of both drugs rapidly with high resolution and minimum interference from each other during the different steps conducted during the nanoformulation development.

Publisher

Oxford University Press (OUP)

Subject

General Medicine,Analytical Chemistry

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