You are here

FORMULATION AND EVALUATION OF PULSATILE DRUG DELIVERY SYSTEM OF METOPROLOL TARTRATE

Journal Name:

Publication Year:

Abstract (2. Language): 
The objective of present investigation was to prepare and evaluate a pulsatile drugdelivery system of metoprolol tartrate. The prepared pulsatile delivery system consists of two different parts: a core tablet, containing the active ingredient, an erodible . The rapid release core tablet (RRCT) was prepared by using superdisintegrants along with active ingredient metoprolol tartrate. press coating of optimized RRCT was done by using different ratios of hydroxy propyl methyl cellulose (HPMC K100) and ethyl cellulose 5Cps. Developed formulations were evaluated for their physical characteristics, in vitro disintegration time and in vitro drug release profile (lag time).On the basis of these evaluation parameters it was found that optimized pulsatile release formulation (P3F3) showed time of 2hrs and in-vitro drug relrease time of 8hrs with97.8%released drug. The P3F3 formulation showed compliance with chronotherapeutic objective of hypertension.
246
257

REFERENCES

References: 

1. Gothaskar, AV, Joshi AM, Joshi, NH,
2004. Pulsatile drug deliverysystem a
review. Drug Del. Technol. 4,
http://www.drugdeliverytech.com/id
article=250.
2. Sharma S, Pawar SA, Low density
multiparticulate system for pulsatilerelease
of meloxicam. Int J Pharm 2006; 313: 150-
158.
3. Bhavana V, Khopade AJ, Jain VVD, Jain
NK. Oral pulsatile drugdelivery.Eastern
pharmacist 1996 Aug; 39 (464):21-6.
4. Sachin Survase, Neeraj Kumar. Pulsatile
drug delivery: Current scenario crips 2007;
8:33
5. Bi-Botti CY. Chronopharmaceutics:
Gimmick or clinically relevant approach to
drug delivery a review. J Control Rel 2004;
98(3):337-353
6. Bjorn, L. 1996. The clinical relevance
of chronopharmacology intherapeutics.
Pharmacological Res.1996; 33:107-115.
7. Suresh S, Pathak S.
Chronopharmaceutics: Emerging role of
rhythms in optimizing drug therapy. Indian j
Pharm Sci 2005; 67(2):135-140.
8. Schafer M, Frischkopf K, Taimor G, Piper
HM, Schluter KD: Hypertrophic effect of
selective beta(1)-adrenoceptor stimulation
on ventricular cardiomyocytes from adult
rat. Am J Physiol Cell Physiol. 2000
Aug;279(2):C495-503. Pubmed.
9. K Flory. Analytical profile of drug
substances, Academic Press Elsevier, New
York, 2005; PP : 325.
10. Chaudhari S. P., Chaudhari P. D., Mistry
C.J., Patil M. J., Barhate N. S., The effect of
core and coating composition on drug
release from directly compressed timecontrolled
release tablets, Pharm. Tech.,
2007, 31, 132-144.
11. RC Rowe; P Sheskey; P Weller.
Handbook of Pharmaceutical Excipients,
Fourth Edition, Pharmaceutical Press
Publishers, Great Britain, 2005; pp. 139-146.
12. Ghimire M., McInnes F., Watson D.,
Mullen A.,Stevens N., In-vitro/in-vivo
correlation of pulsatile drug release from
press-coated tablet formulations: A
pharmacoscintigraphic study in the beagle
dogs, Eur. J. Pharm. Biopharm., 2007, 67 (2)
515-523.
13. Government of India, Ministry of health
and welfare. Indian Pharmacopoeia,
Controller of Publications, Delhi, 1996;
pp. A-80-81.
14. http://www.uspharmacist.com/oldform
at.asp?url=newlook/files/Feat/ACF2F15.cfm
&pub_id.
15. Spvyas and RK Khar, Controlled drug
Delivery – Fundamentals and application,
Vallabh Prakashan – New Delhi, First
Edition 2002.
16. Joseph R. Robinson, Controlled drug
delivery, fundamentals and application, 2nd
edition, pp 4, 5, and 6,373,379.
Research Article CODEN: IJPRNK ISSN: 2277-8713
K. Surendra Kumar, IJPRBS, 2013; Volume 2(5):246-257 IJPRBS
Available Online at www.ijprbs.com
257
17. International Conferences on
Harmonization. Stability Testing of new
Drug Substances and Products. Q 1 A (R2).
2003 [cited 2009 Sept 10]; Available from:
http://www.emea.europa.eu.

Thank you for copying data from http://www.arastirmax.com