In vitro- In vivo Correlation Studies of Modified Release Tolterodine Tablet Dosage form in Rabbits

P. Srinivasa Babu *

Department of Pharmaceutics, Vignan Pharmacy College, Vadlamudi, Guntur, Andhra Pradesh, 522213, India.

S. K. Rihana Parveen

Department of Pharmaceutics, Vignan Pharmacy College, Vadlamudi, Guntur, Andhra Pradesh, 522213, India and Research and Development, Jawaharlal Nehru Technological University Anantapur Andhra Pradesh, 515002, India.

K. B. Chandrasekar

Research and Development, Jawaharlal Nehru Technological University Anantapur Andhra Pradesh, 515002, India.

B. R. Challa

Department of Pharmaceutical Analysis, Vagdevi College of Pharmacy, Guntur, Andhra Pradesh, 522415, India.

*Author to whom correspondence should be addressed.


Abstract

Tolterodine is an antimuscarnic drug that is used for sympathetic treatment of urinary incontinence. Tolterodine modified release tablet, was investigated in rabbit for pharmacokinetic and in vitro–in vivocorrelation studies. Tablets were prepared and in vitro release was studied in simulated gastric fluid at 150RPMs. New Zealand albino male rabbits have been used as animal model for in vivo study. A sensitive and simple HPLC method was developed for the determination of Tolterodine content in rabbit plasma. In vitro release studies showed that release patterns followed zero order for around 24h. The in vivo–in vitro correlation coefficients obtained from point-to-point analysis were greater than 99% between concentrations at certain time points obtained from release study in simulated gastric fluid and HPLC analysis of rabbit’s plasma.
From the in vitro–in vivo correlation prediction it was evident that the Tolterodine matrix assisted tablet is a good for controlled delivery of Tolterodine.

Keywords: Tolterodine, modified release, In vitro–In vivo correlation.


How to Cite

Babu, P. S., Parveen, S. K. R., Chandrasekar, K. B. and Challa, B. R. (2014) “In vitro- In vivo Correlation Studies of Modified Release Tolterodine Tablet Dosage form in Rabbits”, Journal of Pharmaceutical Research International, 4(15), pp. 1861–1872. doi: 10.9734/BJPR/2014/9950.