REVIEW ON: PULSATILE DRUG DELIVERY SYSTEMS
Journal Title: Journal of Pharmaceutical Sciences and Research - Year 2009, Vol 1, Issue 4
Abstract
Traditionally, drugs are released in an immediate or extended fashion. However, in recent years, pulsatile drug release systems are gaining growing interest. A pulsatile drug release, where the drug is released rapidly after a well defined lag-time, could be advantageous for many drugs or therapies. Pulsatile release systems can be classified in multiple-pulse and single-pulse systems. A popular class of single-pulse systems is that of rupturable dosage forms. Other systems consist of a drug-containing core, covered by a swelling layer and an outer insoluble, but semipermeable polymer coating or membrane. The lag time prior to the rupture is mainly controlled by: (i) the permeation and mechanical properties of the polymer coating and (ii) the swelling behavior of the swelling layer. As is frequently found in the living body, many vital functions are regulated by pulsed or transient release of bioactive substances at a specific site and time. Thus it is important to develop new drug delivery systems to achieve pulsed delivery of a certain amount of drugs in order to mimic the function of the living systems, while minimizing undesired side effects. Special attention has been given to the thermally responsive poly (N-isopropylacrylamide) and its derivative hydrogels. Thermal stimuli-regulated pulsed drug release is established through the design of drug delivery devices, hydrogels, and micelles. Therefore Pulsatile drug delivery is one such systems that, by delivering drug at the right time, right place and in right amounts, holds good promises of benefit to the patients suffering from chronic problems like arthritis, asthma, hypertension
Authors and Affiliations
J. Ravi Kumar Reddy , M. Veera Jyothsna , S. Mohamed Saleem , C. Madhu Sudhana Chetty
Development and Physiochemical, In-Vitro Evaluation of Antihypertensive Transdermal
Transdermal patches of Losartan with hydrophilic and hydrophobic polymers containing the drug reservoir were prepared by solvent evaporation method. In this experiment, the membranes of ethylcellose and eudragit RS...
HPTLC Determination of Amoxicillin Trihydrate and Bromhexine Hydrochloride in Oral Solid Dosage Forms
A simple, accurate, precise and rapid high-performance thin-layer chromatographic method for determination of Amoxicillin Trihydrate and Bromhexine Hydrochloride in Bulk and combined Pharmaceutical Dosage Form was develo...
Synthesis and Characterization of 2,6-Dihydroxy Substituted Chalcones Using PEG-400 as a Recyclable Solvent
A novel method for the synthesis of 2,6-dihydroxy substituted chalcones via Claisen-Schmidt is introduced using recyclable PEG-400 as an alternative reaction solvent. The reaction is clean with excellent yield, shorter r...
Production of a thermostable extracellular amylase from thermophilic Bacillus species
Isolation and identification of thermophilic Bacillus sp was carried out from a soil sample. The cells were cultivated in a medium containing soluble starch as sole carbon source. The addition of calcium (10 m...
Selection of better method for the preparation of microspheres by applying Analytic Hierarchy Process
One of the most effective approaches for achieving novel drug delivery dosage forms such as sustained release, controlled release is microencapsulation. A number of techniques are available for thepreparation...