Flyer

International Journal of Drug Development and Research

  • ISSN: 0975-9344
  • Journal h-index: 49
  • Journal CiteScore: 11.20
  • Journal Impact Factor: 8.24
  • Average acceptance to publication time (5-7 days)
  • Average article processing time (30-45 days) Less than 5 volumes 30 days
    8 - 9 volumes 40 days
    10 and more volumes 45 days
Awards Nomination 20+ Million Readerbase
Indexed In
  • Genamics JournalSeek
  • China National Knowledge Infrastructure (CNKI)
  • CiteFactor
  • Scimago
  • Directory of Research Journal Indexing (DRJI)
  • OCLC- WorldCat
  • Publons
  • MIAR
  • University Grants Commission
  • Euro Pub
  • Google Scholar
  • J-Gate
  • SHERPA ROMEO
  • Secret Search Engine Labs
  • ResearchGate
  • International Committee of Medical Journal Editors (ICMJE)
Share This Page

Investigation of possible pharmacokinetic interaction between ivabradine and carvedilol in rats using high performance liquid chromatography/mass spectroscopy

8th Edition of International Conference on Mass Spectrometry
March 12-13, 2018 London, UK

Saif S Abbas, Israa H Al-Ani and Wael A Abu Dayyih

Al-Ahliyya Amman University, Jordan University of Petra, Jordan

Posters & Accepted Abstracts: Int J Drug Dev & Res

Abstract:

Ivabradine is a new hyperpolarization-activated cyclic nucleotidegated channel blocker. It has been approved by the FDA in 2015 in management of stable angina and congestive heart failure. The aim of this study was to investigate the possibility of pharmacokinetic interaction of a proposed combination of ivabradine and the �?²-blocker carvedilol in rats using spectroscopy technique. A simple, rapid and sensitive method for validation and determination of ivabradine and carvedilol in the rats�?¼ plasma was developed using HPLC/MS. The method was successfully developed and validated in terms of linearity, precision and accuracy which were within the values accepted by EMEA and ICH. Ivabradine and carvedilol were given both intravenously and orally, each alone and as oral combination to fasting Sprague-Dawley rats. Blood samples were withdrawn on scheduled time intervals up to 36 hours and analyzed for each drug. Both compartmental and non-compartmental kinetic analyses were performed on plasma level-time data and the kinetic parameters were calculated from non-compartmental analysis. Results showed significant increase in bioavailability of both drugs in combination (94% for carvedilol and 58% for ivabradine. Also, Cmax was changed significantly by 165% for carvedilol and 56% for ivabradine, when given in combination. There was also a significant decrease in elimination of both drugs expressed as 48% decrease in clearance and 41% increase in the half-life for carvedilol and 32% decrease in clearance and 37% increase of the half-life of ivabradine when given in combination. These changes suggested an interaction on metabolic function of the liver on both drugs by some kind of enzyme inhibition. Also, the rate of absorption of ivabradine was slowed by concomitant administration of carvedilol suggesting an interaction on absorption level. In conclusion, a significant kinetic interaction occurred when ivabradine was given orally with carvedilol which makes dose adjustment of both drugs of much importance.

Biography :

Saif S Abbas is pursuing his Master’s Degree in Pharmaceutics/Pharmacokinetics in Al-Ahliyya Amman University in Jordan. He graduated from the Faculty of Pharmacy and Medical Sciences in Al-Ahliyya Amman University, Jordan in 2013. He has worked as a Senior Pharmacist in retail pharmacies and drug stores in Amman, Jordan.

Email:saif_s_abbas90@yahoo.com