GASTRORETENTIVE DRUG DELIVERY SYSTEM PDF

8 Jun 1 gastroretentive drug delivery systems. 1. Presented By: Akash Aher( – 2nd semester)Guided by: Dr.G.S Asane(Dept. of. (gastro retentive drug delivery system). Dosage forms that can be retained in the stomach are called GRDDs. GRDDSs can improve the controlled delivery of. 1 Apr GASTRORETENTIVE DRUG DELIVERY SYSTEM: AN APPROACH TO ENHANCE GASTRIC RETENTION FOR PROLONGED DRUG.

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One should also consider viscosity of the plasticizer, its influence on the final coating solution, its effect on film permeability, tackiness, flexibility, solubility and taste and its toxicity, compatibility with other coating solution components and stability of the film and the final coated product3. The study was done at room temperature.

Hence, these dosage forms have been referred to as prolonged release or sustained release dosage forms as well1. Drugs having low solubility at high pH values.

Gastro-retentive drug delivery systems and their in vivo success: A recent update – ScienceDirect

Recent approaches to increase the gastric residence time of drug delivery systems include bioadhesive systems, floating systems low density systemsnon-floating systems high density systemsmagnetic systems, swelling systems, unfoldable and expandable systems, raft forming systems and superporous systems, biodegradable hydrogel systems 5. Reported in vivo studies with beagle dogs, rabbits, and human subjects are only a handful in spite of a large number of encouraging in vitro results.

A metaanalysis of randomized controlled trials suggests alginic acid may be the most effective of nonprescription treatments.

High Density Systems 31, 32 These systems possess density greater than the gastric fluids due to which the system sinks to the bottom and remains in the stomach. There is a possibility of triple layer matrix tablet. Oral route has been the most convenient gaztroretentive accepted route of drug delivery. Stabilization of quinapril using Magnesium oxide. Either round or spherical shaped dosage form exhibit better property related to other sstem.

In spite of the many advantages, high subject variations in gastrointestinal physiological condition, effect of food, and variable rate of gastric emptying time are the challenges that limit the drut of yastroretentive GRDDS in the market.

The following methods have been devised to improve period of retainment of oral dosage form in the stomach viz. The emptying of residual system is followed by the drug release, from the stomach. Indian Journal of Pharmaceutical Sciences ; Asian Journal of Pharmacy and Life Science ; 1: These systems are further classified as below: The release is followed by removal of the residual system from the stomach.

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Gastro-resistant tablet dosage form is intended to release a drug after some time that is delay or after the tablet has passed through one part of the GI tract in to another. Jurecic R, Jaklic M, Inventors. PyloriAmoxicillin Trihydrate. Controlledrelease formulations coated with aqueous dispersions of ethylcellulose, US 5,, December Unsuitable for such drugs as: Drugs with narrow absorption window inGastrointestinal tract GIT. Stabilized pharmaceutical compositions containing benzimidazole compounds.

Drug release studies were carried out using a USP type II dissolution test apparatus at rpm for 2hr in 0. Drug Development and Industrial Pharmacy, May However, there is still enough acidity to irritate the esophagus.

International Journal of Pharma and Bio Sciences ; 2: However the two states are varied upon pattern of motility.

Dgug Journal of Pharmaceutical and Clinical Research ; 4: Its attributed to the fact that gastroretentive drug delivery sustains drug release and hence, avail local therapy in these organs.

Secondly, it is helpful in providing easy dosage administration to the patient, that further provides patient compliance on the part of the patient and ultimately providing an array of options in the final formulation.

Related article at DelivefyScholar Google. Abstract A controlled drug delivery system with prolonged residence time in the stomach is of particular interest for drugs that i are locally active in the stomach, ii have an absorption window in the stomach or in the upper small intestine, iii are unstable in the intestinal or colonic environment, or iv exhibit low solubility at high pH values.

Pharmacokinetics following continuous intragastric mode of administration in a rat model.

A comprehensive review on floating drug delivery system. Sampling was done at regular intervals. The 4 phases are enumerated below and also shown in Figure 1.

Drug treatment9, 10, 11 A number of drugs are prescribed for GERD treatment and they are among gastroretenitve most oftenprescribed forms of medication in most Western countries. International Journal of Pharma Sciences ; 3: Unpredictable adherence owing to state of constant renewal of mucus wall of stomach. Formulation and evaluation of gastroretentive floating drug delivery system of metoprolol tartarate. Advancements in controlled release gastroretentive drug delivery syste, Another paradoxical cause of GERD-like symptoms is not enough stomach acid hypochlorhydria.