Previous Page  8 / 15 Next Page
Information
Show Menu
Previous Page 8 / 15 Next Page
Page Background

Volume 8, Issue 6 (Suppl)

J Bioequiv Availab

ISSN: 0975-0851 JBB, an open access journal

Page 33

Notes:

Biopharma 2016

September 14-16, 2016

conferenceseries

.com

September 14-16, 2016 San Antonio, USA

2

nd

International Conference & Expo on

Biopharmaceutics and Biologic Drugs

Design and evaluation of press coated pulsatile release tablets of Prednisolone

Upendra L Patel

Arihant School of Pharmacy and Bio-Research Institute, India

T

o formulate and evaluate a press coated pulsatile release tablets of prednisolone using an admixture of hydrophilic polymer,

i.e., low substituted hydroxy propyl cellulose (L-HPC) and hydrophobic polymer, i.e., ethyl cellulose (Ethocel 10 cps) in order

to achieve a pre-determined lag time for chronotherapy of rheumatoid arthritis. The press coated pulsatile tablets containing

prednisolone in the inner core were prepared by compression coating with L-HPC and Ethocel 10 cps as the outer layer in different

ratios. The effect of polymer ratio and weight gain of the outer layer on lag time of drug release was investigated using 3

2

full factorial

design. The parameters determined were tablet hardness, friability, drug content, lag time,

dissolution. The release profile

of the press coated tablet exhibited a distinct lag time before burst release of prednisolone. Lag time was dependent on the ratio of

L-HPC/Ethocel 10 cps and weight gain in outer shell. The lag time was from 1 to 10 hr and could be modulated as it decreased as the

amount of L-HPC in the outer layer increased. A surface plots are also presented to graphically represent the effect of independent

variables on the lag time. The validity of generated mathematical model was tested by preparing checkpoint formulation. Formulation

PCPT7 with L-HPC/Ethocel 10 cps (10:90) and weight gain 300 mg showing predetermined lag time of 5 hr prior to burst release of

the drug from the press coated tablet was taken as the optimized formulation.

Biography

Upendra L Patel has completed his PhD from Sardar Patel University, Anand, Gujarat, India in 2010. He is the Head of Department & Associate Professor in

Department of Pharmaceutics & Pharmaceutical Technology in Arihant School of Pharmacy & BRI, Gujarat, India. His area of research is formulation and evaluation

of controlled drug delivery formulations. He has guided more than 25 MPharm students. He has published more than 40 papers in reputed journals and one book

“Dispensing Pharmacy & Drug Store Management”.

He is life time member of Gujarat Pharmacy Teacher Associations.

upendra_patel01@rediffmail.com

Upendra L Patel, J Bioequiv Availab 2016, 8:6 (Suppl)

http://dx.doi.org/10.4172/0975-0851.C1.027