|
Review Article
Orally Disintegrating
Tablets: A Review
Jaysukh J Hirani1*, Dhaval A Rathod1,
Kantilal R Vadalia2
1Smt.
R.D.Gardi B. Pharmacy College, Rajkot-360110, 2Shri
H.N.Shukla College of Pharmacy, Rajkot, Gujarat, India.
Email:
jay_2150@yahoo.com
Tel: + 91 9925062150, +91 (0)281 2488613; Fax:
+91 (0)281 2488614
Received:
30 June 2008
Revised accepted:
02 November 2008
Tropical
Journal of Pharmaceutical Research, April
2009; 8(2):
161-172
Abstract
Drug delivery systems are
becoming increasingly sophisticated as pharmaceutical
scientists acquire a better understanding of the
physicochemical and biochemical parameters pertinent to
their performance. Over the past three decades, orally
disintegrating tablets (ODTs) have gained considerable
attention as a preferred alternative to conventional
tablets and capsules due to better patient compliance.
ODTs are solid dosage forms containing medicinal
substances which disintegrate rapidly, usually in a
matter of seconds, when placed on the tongue. Products
of ODT technologies entered the market in the 1980s,
have grown steadily in demand, and their product
pipelines are rapidly expanding. New ODT technologies
address many pharmaceutical and patient needs, ranging
from enhanced life-cycle management to convenient dosing
for paediatric, geriatric, and psychiatric patients with
dysphagia. This has encouraged both academia and
industry to generate new orally disintegrating
formulations and technological approaches in this field.
The aim of this article is to review the development of
ODTs, challenges in formulation, new ODT technologies
and evaluation methodologies, suitability of drug
candidates, and future prospects.
Keywords:
Orally disintegrating tablet, Improved
bioavailability, Texture analyser, NanomeltTM |