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Modified-release dosage is a mechanism that (in contrast to immediate-release dosage) delivers a drug with a delay after its administration (delayed-release dosage) or for a prolonged period of time (extended-release [ER, XR, XL] dosage) or to a specific target in the body (targeted-release dosage). [1] Sustained-release dosage forms are dosage ...
The drug is expelled via the laser-drilled hole visible on the left side of the tablet. The osmotic-controlled release oral delivery system (OROS) is an advanced controlled release oral drug delivery system in the form of a rigid tablet with a semi-permeable outer membrane and one or more small laser drilled holes in it.
Tablets to swallow, chew or dissolve in water or under the tongue; Capsules and chewable capsules (with a coating that dissolves in the stomach or bowel to release the medication there) Time-release or sustained-release tablets and capsules (which release the medication gradually) Powders or granules; and oral liquid dosage forms: [5] Teas; Drops
Biovail's sustained-release tablets will compete with AstraZeneca's Seroquel XR. In December 2008, AstraZeneca notified shareholders that the FDA had asked for additional information on the company's application to expand the use of sustained-release quetiapine for treatment of depression.
The dissolution time can be modified for a rapid effect or for sustained release. Special coatings can make the tablet resistant to the stomach acids such that it only disintegrates in the duodenum, jejunum and colon as a result of enzyme action or alkaline pH. Pills can be coated with sugar, varnish, or wax to disguise the taste ...
It can be directed to the location of cancer cells with sustained release behavior. Studies have also been done on gold nanoparticle responses to local near-infrared (NIR) light as a stimuli for drug release. In one study, gold nanoparticles functionalized with double-stranded DNA encapsulated with drug molecules, were irradiated with NIR light.
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In September 2014, a sustained release formulation of the drug was approved for marketing in the United States under the brand name Contrave. [8] [9] The combination was subsequently approved in the European Union in the spring of 2015, where it is sold under the name Mysimba. [5] [10] It was approved in Canada under the Contrave brand name in ...