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Modified-release dosage

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When the drug is covered with some slow dissolving coat, it will eventually release the drug. Instead of diffusion, the drug release depends on the solubility and thickness of the coating. Because of this mechanism, the dissolution will be the rate limiting factor for drug release. Dissolution systems can be broken down to subcategories called reservoir devices and matrix devices.
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amount to maintain a prolonged effective dose. In this case, a broad therapeutic window is necessary to avoid toxicity; otherwise, the risk is unwarranted and another mode of administration would be recommended. Appropriate half-lives used to apply sustained methods are typically 3–4 hours and a drug dose greater than 0.5 grams is too high.
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to be higher than the rate at which it is released. The matrix device cannot achieve a zero-order release but higher molecular weight molecules can be used. The diffusion matrix device also tends to be easier to produce and protect from changing in the gastrointestinal tract, but factors such as food can affect the release rate.
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Spherical hydrogels, in micro-size (50-600 μm diameter) with 3-dimensional cross-linked polymer, can be used as drug carrier to control the release of the drug. These hydrogels are called microgels. They may possess a negative charge as example DC-beads. By ion-exchange mechanism, a large amount
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Dissolution systems must have the system dissolved slowly in order for the drug to have sustained release properties which can be achieved by using appropriate salts and/or derivatives as well as coating the drug with a dissolving material. It is used for drug compounds with high solubility in water.
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Matrix devices forms a matrix (drug(s) mixed with a gelling agent) where the drug is dissolved/dispersed. The drug is usually dispersed within a polymer and then released by undergoing diffusion. However, to make the drug SR in this device, the rate of dissolution of the drug within the matrix needs
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The earliest SR drugs are associated with a patent in 1938 by Israel Lipowski, who coated pellets which led to coating particles. The science of controlled release developed further with more oral sustained-release products in the late 1940s and early 1950s, the development of controlled release of
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Reservoir devices coat the drug with polymers and in order for the reservoir devices to have sustained-release effects, the polymer must not dissolve and let the drug be released through diffusion. The rate of reservoir devices can be altered by changing the polymer and is possible be made to have
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Most commonly it refers to time-dependent release in oral dose formulations. Timed release has several distinct variants such as sustained release where prolonged release is intended, pulse release, delayed release (e.g. to target different regions of the GI tract) etc. A distinction of controlled
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In the ion-exchange method, the resins are cross-linked water-insoluble polymers that contain ionisable functional groups that form a repeating pattern of polymers, creating a polymer chain. The drug is attached to the resin and is released when an appropriate interaction of ions and ion exchange
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The release technology scientific and industrial community is represented by the Controlled Release Society (CRS). The CRS is the worldwide society for delivery science and technologies. CRS serves more than 1,600 members from more than 50 countries. Two-thirds of CRS membership is represented by
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systems generally are meant to stick to mucus and can be favorable for mouth based interactions due to high mucus levels in the general area but not as simple for other areas. Magnetic materials can be added to the drug so another magnet can hold it from outside the body to assist in holding the
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of the drug refers to the drug's elimination from the bloodstream which can be caused by metabolism, urine, and other forms of excretion. If the active compound has a long half-life (over 6 hours), it is sustained on its own. If the active compound has a short half-life, it would require a large
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is also regarded as a more complete technology to produce complex dissolution profiles. Through coating an active pharmaceutical ingredient around an inert core and layering it with insoluble substances to form a microsphere, one can obtain more consistent and replicable dissolution rates in a
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A hydrophilic matrix will go back to the matrix as discussed before where a matrix is a mixture of a drug or drugs with a gelling agent. This system is well liked because of its cost and broad regulatory acceptance. The polymers used can be broken down into categories: cellulose derivatives,
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will allow the system to float to the top of the stomach and release at a slower rate without worry of excreting it. This system requires that there are enough gastric fluids present as well as food. Many types of forms of drugs use this method such as powders, capsules, and tablets.
611:, and differing intestinal environments. Using an osmotic pump to deliver drugs has additional inherent advantages regarding control over drug delivery rates. This allows for much more precise drug delivery over an extended period of time, which results in much more predictable 939:
Tarun Parashar, Soniya, Vishal Singh, Gaurav Singh, Satyanand Tyagi, Chirag Patel, and Anil Gupta. International Journal of Research and Development in Pharmacy and Life Sciences. Novel Oral Sustained Release Technology: A Concise Review. 2013. Accessed: May 30,
731:(HIT) that pharmacists use are medication safety tools to help manage this problem. For example, the ISMP "do not crush" list can be entered into the system so that warning stickers can be printed at the point of dispensing, to be stuck on the pill bottle. 81:
Extended-release dosage consists of either sustained-release (SR) or controlled-release (CR) dosage. SR maintains drug release over a sustained period but not at a constant rate. CR maintains drug release over a sustained period at a nearly constant rate.
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The matrix system is the mixture of materials with the drug, which will cause the drug to slow down. However, this system has several subcategories: hydrophobic matrices, lipid matrices, hydrophilic matrices, biodegradable matrices, and mineral matrices.
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There is no industry standard for these abbreviations, and confusion and misreading have sometimes caused prescribing errors. Clear handwriting is necessary. For some drugs with multiple formulations, putting the meaning in parentheses is advisable.
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over time in order to be released more slowly and steadily into the bloodstream, while having the advantage of being taken at less frequent intervals than immediate-release (IR) formulations of the same drug. For example, orally administered
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Diffusion systems' rate release is dependent on the rate at which the drug dissolves through a barrier which is usually a type of polymer. Diffusion systems can be broken into two subcategories, reservoir devices and matrix devices.
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The reservoir device coats the drug with an appropriate material which will dissolve slowly. It can also be used to administer beads as a group with varying thickness, making the drug release in multiple times creating a
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Some time release formulations do not work properly if split, such as controlled-release tablet coatings, while other formulations such as micro-encapsulation still work if the microcapsules inside are swallowed whole.
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van den Berg, G; van Steveninck, F; Gubbens-Stibbe, JM; Schoemaker, HC; de Boer, AG; Cohen, AF (1990). "Influence of food on the bioavailability of metoprolol from an OROS system; a study in healthy volunteers".
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also factors whether a drug can be used as a time release drug. A drug with a thin therapeutic range, or small therapeutic index, will be determined unfit for a sustained release mechanism in partial fear of
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in the 1970s where sustained and controlled delivery of nutrients was achieved following a single application to the soil. Delivery is usually effected by dissolution, degradation, or disintegration of an
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A hydrophobic matrix is a drug mixed with a hydrophobic polymer. This causes SR because the drug, after being dissolved, will have to be released by going through channels made by the hydrophilic polymer.
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A floating system is a system where it floats on gastric fluids due to low density. The density of the gastric fluids is about 1 g/mL; thus, the drug/tablet administered must have a smaller density. The
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of oppositely charged amphiphilic drugs can be loaded inside these microgels. Then, the release of these drugs can be controlled by a specific triggering factor like pH, ionic strength or temperature.
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Auiler, JF; Liu, K; Lynch, JM; Gelotte, CK (2002). "Effect of food on early drug exposure from extended-release stimulants: results from the Concerta, Adderall XR Food Evaluation (CAFE) Study".
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If the pharmacological activity of the active compound is not related to its blood levels, time releasing has no purpose except in some cases, such as bupropion, to reduce possible side effects.
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Examples of stimuli that may be used to bring about release include pH, enzymes, light, magnetic fields, temperature, ultrasonics, osmosis, cellular traction forces, and electronic control of
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Kapil Patil, Prashant Patil, Javesh Patil, and Sunil Pawar. A Basic Approach on Sustained Release Drug Delivery System. American Journal of PharmTech Research. 2011. Accessed: May 30, 2016.
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Pharmaceutical companies that do not supply a range of half-dose and quarter-dose versions of time-release tablets can make it difficult for patients to be slowly tapered off their drugs.
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Dusane Ratilal, Gaikwad D., Banker H., and Pawar P. A Review On: Sustained Release Technology. International Journal of Research in Ayurveda and Pharmacy. 2011. Accessed: May 30, 2016.
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Sampath Kumar, Debjit Bhowmik, Shweta Srivastava, Shravan Paswan, and A. Dutta. Sustained. Release Drug Delivery System Potential. The Pharma Innovation. 2012. Accessed: May 30, 2016.
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Navin Dixit, Sheo Dutt Maurya, and Bhanu Sagar. Sustained Release Drug Delivery System. Indian Journal of Research in Pharmacy and Biotechnology. 2013. Accessed: May 30, 2016.
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Lilesh Khalane, Atulal Kunte, and Arunadevi Blrajdar. Sustained Release Drug Delivery System: A Concise Review. Pharmatutor: pharmacy infopedia. 2016. Accessed: May 30, 2016.
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which can prove fatal at the conditions mentioned. For a drug that is made to be released over time, the objective is to stay within the therapeutic range as long as needed.
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Ratnaparkhi P. and Gupta P. Sustained Release Oral Drug Delivery System – An Overview. International Journal of Pharma Research & Review. 2013. Accessed: May 30, 2016.
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Jaimini Manish and Kothari Abhay. Sustained Release Matrix Type Drug Delivery System: A Review. Journal of Drug Delivery & Therapeutics. 2012. Accessed: May 30, 2016.
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The matrix device has the drug in a matrix and the matrix is dissolved instead of a coating. It can come either as drug-impregnated spheres or drug-impregnated tablets.
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In some SR formulations, the drug dissolves into the matrix, and the matrix physically swells to form a gel, allowing the drug to exit through the gel's outer surface.
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Modi, NB; Wang, B; Hu, WT; Gupta, SK (January 2000). "Effect of food on the pharmacokinetics of osmotic controlled-release methylphenidate HCl in healthy subjects".
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Conley, R; Gupta, SK; Sathyan, G (October 2006). "Clinical spectrum of the osmotic-controlled release oral delivery system (OROS), an advanced oral delivery form".
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groups occur. The area and length of the drug release and number of cross-link polymers dictate the rate at which the drug is released, determining the SR effect.
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A lipid matrix uses wax or similar materials. Drug release happens via diffusion through, and erosion of, the wax and tends to be sensitive to digestive fluids.
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Osmotic release systems have a number of major advantages over other controlled-release mechanisms. They are significantly less affected by factors such as
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Bass, DM; Prevo, M; Waxman, DS (2002). "Gastrointestinal safety of an extended-release, nondeformable, oral dosage form (OROS: a retrospective study".
52:(delayed-release dosage) or for a prolonged period of time (extended-release dosage) or to a specific target in the body (targeted-release dosage). 425:
A few other abbreviations are similar to these (in that they may serve as suffixes) but refer to dose rather than release rate. They include
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Malaterre, V; Ogorka, J; Loggia, N; Gurny, R (November 2009). "Oral osmotically driven systems: 30 years of development and clinical use".
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Biodegradable matrices are made with unstable, linked monomers that will erode by biological compounds such as enzymes and proteins.
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to avoid potentially hazardous peaks in drug concentration following ingestion or injection and to maximize therapeutic efficiency.
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has in fact defined most of these as different concepts. Sometimes the term "depot tablet" is used, by analogy to the term for an
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convenient format that can be mixed and matched with other instant release pharmaceutical ingredients into any two piece gelatin
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Perrie, Y., & Rades, T. Pharmaceutics: Drug delivery and targeting. London: Pharmaceutical Press. Accessed: May 30, 2016.
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at a predetermined rate in order to maintain a constant drug concentration for a specific period of time with minimum
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zero-order release; however, drugs with higher molecular weight have difficulty diffusing through the membrane.
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Theeuwes, F; Yum, SI; Haak, R; Wong, P (1991). "Systems for triggered, pulsed, and programmed drug delivery".
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Examples for cosmetic, personal care, and food science applications often centre on odour or flavour release.
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XL 150mg manufactured by Anchen Pharmaceuticals that was soaked in water overnight and then shaken.
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Ahnfelt, E.; Gernandt, J.; Al-Tikriti, Y.; Sjögren, E.; Lennernäs, H.; Hansson, P. (2018-12-28).
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release is that it not only prolongs action, but it attempts to maintain drug levels within the
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Verma, RK; Mishra, B; Garg, S (July 2000). "Osmotically controlled oral drug delivery".
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industry and one-third represents academia and government. CRS is affiliated with the
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There are certain considerations for the formation of sustained-release formulation:
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Stejskalová, Anna; Oliva, Nuria; England, Frances J.; Almquist, Benjamin D. (2019).
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A mineral matrix which generally means the polymers used are obtained in seaweed.
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Osmotic controlled-release oral delivery systems (OROS) have the form of a rigid
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Maloney JM, Uhland S, Polito B, Sheppard NF Jr, Pelta C, Santini JT Jr (2005).
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In addition to pills, the mechanism can also apply to capsules and injectable
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system in place. However, there is low patient compliance with this system.
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and other encapsulation technologies can further modify release profiles.
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through the opening(s) in the tablet. OROS is a trademarked name owned by
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ISMP "do not crush" list: Oral dosage forms that should not be crushed
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There are many different methods used to obtain a sustained release.
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Mechanism that delivers a drug with a delay after its administration
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Institute for Safe Medication Practices (ISMP) (20 November 2017),
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10.1002/1099-081x(200001)21:1<23::aid-bdd212>3.0.co;2-v
1084:"Osmotically controlled drug delivery system with associated drugs" 600:, which pioneered the use of osmotic pumps for oral drug delivery. 2282: 2007: 1909: 1868: 1747: 559: 445:
is embedded in a matrix of insoluble substance(s) (various: some
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Modified-release dosage and its variants are mechanisms used in
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injection formulation of a drug which releases slowly over time
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Gupta, BP; Thakur, N; Jain, NP; Banweer, J; Jain, S (2010).
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with a semi-permeable outer membrane and one or more small
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Today, most time-release drugs are formulated so that the
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5-day short course at MIT with Professor Robert Langer.
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United Kingdom & Ireland Controlled Release Society
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Pennsylvania Patient Safety Authority (December 2004),
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European Journal of Pharmaceutics and Biopharmaceutics
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A 54mg tablet of Concerta, which uses OROS technology.
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as is typical with standard-release morphine tablets.
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can enable certain chronic pain patients to take only
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is a mechanism that (in contrast to immediate-release
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If the absorption of the active compound involves an
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tablets per day, rather than needing to redose every
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non-cellulose natural, and polymers of acrylic acid.
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For the novel, see 1088:Journal of Pharmacy & Pharmaceutical Sciences 948: 946: 556:Osmotic controlled-release oral delivery system 89:are treated as synonyms, but the United States 858: 856: 854: 852: 850: 74:and drug-polymer conjugates (an example being 1697: 848: 846: 844: 842: 840: 838: 836: 834: 832: 830: 8: 1464:You JO, Almeda D, Ye GJ, Auguste DT (2010). 752:in which the active compound is formulated. 319:Ambiguous, can sometimes mean Short-Acting 2462: 2003: 1905: 1743: 1729: 1704: 1690: 1682: 990:Annals of the New York Academy of Sciences 900: 898: 896: 894: 892: 890: 888: 886: 795:Pharmaceutics: Drug Delivery and Targeting 86: 1619: 1600:Bosnian Journal of Basic Medical Sciences 1532: 1491: 1481: 1466:"Bioresponsive matrices in drug delivery" 1398: 1169:European Journal of Clinical Pharmacology 1099: 1125:Drug Development and Industrial Pharmacy 926: 924: 710: 175:Drug Delivery and Translational Research 1255:Biopharmaceutics & Drug Disposition 914: 912: 910: 790: 788: 786: 782: 743:marine anti-foulants in the 1950s, and 1594:Vranić, E; Uzunović, A (August 2009). 7: 1298:Current Medical Research and Opinion 1041:Current Medical Research and Opinion 226:Continuous Control, Constant Control 2061:Heated humidified high-flow therapy 1010:10.1111/j.1749-6632.1991.tb27262.x 25: 2503: 2029: 1790: 1784: 1224:10.2165/00002018-200225140-00004 580:, water is absorbed through the 1565:"Equasym XL (methylphenidate)" 56:Sustained-release dosage forms 1: 1829:Effervescent powder or tablet 1676:Controlled Release Technology 1571:. 24 May 2013. Archived from 1534:10.1016/j.jconrel.2018.11.011 1521:Journal of Controlled Release 1443:10.1016/j.jconrel.2005.09.035 1431:Journal of Controlled Release 745:controlled release fertilizer 729:health information technology 453:; these substances are often 170:Journal of Controlled Release 2613:Patient-controlled analgesia 1918:Orally disintegrating tablet 715:Empty half-shell of a split 91:Food and Drug Administration 592:is used to push the active 576:holes in it. As the tablet 2675: 2124:Relative analgesia machine 1666:Controlled Release Society 1310:10.1185/030079902125000840 967:10.1016/j.ejpb.2009.07.002 819:(4): 17–18, archived from 622: 553: 29: 2501: 2027: 1782: 813:PA PSRS Patient Saf Advis 119:extended-release morphine 64:release (liberate) a drug 2649:Routes of administration 1713:Routes of administration 1612:10.17305/bjbms.2009.2815 1053:10.1185/030079906x132613 687:Stimuli inducing release 2239:Extra-amniotic infusion 1844:Molecular encapsulation 1776:Osmotic delivery system 1771:Time release technology 578:passes through the body 48:with a delay after its 38:Modified-release dosage 2542:Central nervous system 2330: 2268: 2196:Mucoadhesive microdisc 2161: 1483:10.1186/1754-1611-4-15 1383:10.1002/adma.201806380 720: 582:semipermeable membrane 565: 357:Extended/Extra Release 2654:Drug delivery devices 2385:Transfersome vesicles 2329: 2267: 2244:Intravesical infusion 2160: 1137:10.1081/ddc-100101287 714: 563: 377:Lesser/Lower Strength 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1994:Respiratory tract 1988: 1987: 1882: 1881: 771:Tablet (pharmacy) 513:Diffusion systems 499:therapeutic index 443:active ingredient 423: 422: 327:Sustained Release 306:Prolonged Release 256:Immediate Release 18:Sustained release 16:(Redirected from 2666: 2659:Pharmacokinetics 2507: 2463: 2454: 2041: 2037: 2033: 2004: 1933:Sublingual drops 1906: 1794: 1788: 1744: 1730: 1706: 1699: 1692: 1683: 1653: 1652: 1651: 1640: 1634: 1633: 1623: 1591: 1585: 1584: 1582: 1580: 1561: 1555: 1554: 1536: 1512: 1506: 1505: 1495: 1485: 1461: 1455: 1454: 1437:(1–3): 244–255. 1428: 1419: 1413: 1412: 1402: 1354: 1348: 1345: 1339: 1336: 1330: 1329: 1293: 1287: 1286: 1250: 1244: 1243: 1207: 1201: 1200: 1163: 1157: 1156: 1120: 1114: 1113: 1103: 1079: 1073: 1072: 1036: 1030: 1029: 985: 979: 978: 950: 941: 937: 931: 928: 919: 916: 905: 902: 881: 878: 872: 869: 863: 860: 825: 824: 804: 798: 792: 634:Floating systems 613:pharmacokinetics 598:ALZA Corporation 590:osmotic pressure 483:active transport 316:Sustained Action 296:Modified Release 246:Extended Release 189: 132: 130: 124: 21: 2674: 2673: 2669: 2668: 2667: 2665: 2664: 2663: 2634: 2633: 2632: 2623: 2603:Intraperitoneal 2575:musculoskeletal 2573: 2564: 2536: 2532:Intra-articular 2508: 2499: 2459: 2453: 2452: 2428: 2309: 2247: 2200: 2145: 2128: 2086: 2042: 2039: 2038: 2035: 2034: 2025: 1984: 1953: 1878: 1795: 1789: 1780: 1734:Digestive tract 1719: 1710: 1662: 1657: 1656: 1649: 1642: 1641: 1637: 1593: 1592: 1588: 1578: 1576: 1569:netdoctor.co.uk 1563: 1562: 1558: 1514: 1513: 1509: 1463: 1462: 1458: 1426: 1421: 1420: 1416: 1356: 1355: 1351: 1346: 1342: 1337: 1333: 1295: 1294: 1290: 1252: 1251: 1247: 1218:(14): 1021–33. 1209: 1208: 1204: 1165: 1164: 1160: 1122: 1121: 1117: 1101:10.18433/j38w25 1081: 1080: 1076: 1047:(10): 1879–92. 1038: 1037: 1033: 987: 986: 982: 952: 951: 944: 938: 934: 929: 922: 917: 908: 903: 884: 879: 875: 870: 866: 861: 828: 806: 805: 801: 793: 784: 779: 766:Depot injection 762: 754:Enteric coating 740: 709: 689: 662: 650: 636: 627: 621: 607:, food intake, 558: 552: 550:Osmotic systems 534: 515: 439: 387:Double Strength 236:Delayed Release 183: 128: 126: 122: 35: 28: 23: 22: 15: 12: 11: 5: 2672: 2670: 2662: 2661: 2656: 2651: 2646: 2636: 2635: 2629: 2628: 2625: 2624: 2622: 2621: 2616: 2610: 2605: 2600: 2595: 2590: 2585: 2579: 2577: 2566: 2565: 2563: 2562: 2557: 2552: 2546: 2544: 2538: 2537: 2535: 2534: 2529: 2524: 2522:Intracavernous 2518: 2516: 2510: 2509: 2502: 2500: 2498: 2493: 2492: 2491: 2481: 2476: 2474: 2460: 2451: 2450: 2445: 2440: 2434: 2433: 2430: 2429: 2427: 2422: 2417: 2412: 2407: 2402: 2397: 2392: 2387: 2382: 2377: 2372: 2367: 2361: 2356: 2351: 2346: 2341: 2336: 2324: 2322: 2311: 2310: 2308: 2307: 2305:Nutrient enema 2302: 2297: 2296: 2295: 2290: 2280: 2275: 2262: 2260: 2249: 2248: 2246: 2241: 2236: 2230: 2225: 2220: 2215: 2210: 2208: 2202: 2201: 2199: 2198: 2193: 2188: 2183: 2178: 2173: 2168: 2155: 2153: 2138: 2137: 2134: 2133: 2130: 2129: 2127: 2126: 2121: 2116: 2111: 2106: 2096: 2094: 2088: 2087: 2085: 2084: 2079: 2074: 2068: 2063: 2058: 2052: 2050: 2044: 2043: 2028: 2026: 2024: 2023: 2018: 2012: 2010: 2001: 1990: 1989: 1986: 1985: 1983: 1982: 1979: 1974: 1969: 1963: 1961: 1955: 1954: 1952: 1951: 1946: 1940: 1935: 1930: 1925: 1920: 1914: 1912: 1903: 1884: 1883: 1880: 1879: 1877: 1876: 1871: 1866: 1861: 1856: 1851: 1846: 1841: 1836: 1831: 1826: 1821: 1816: 1811: 1805: 1803: 1797: 1796: 1783: 1781: 1779: 1778: 1773: 1768: 1763: 1758: 1752: 1750: 1741: 1727: 1721: 1720: 1711: 1709: 1708: 1701: 1694: 1686: 1680: 1679: 1673: 1668: 1661: 1660:External links 1658: 1655: 1654: 1635: 1586: 1556: 1507: 1456: 1414: 1369:(7): 1806380. 1349: 1340: 1331: 1288: 1245: 1202: 1158: 1131:(7): 695–708. 1115: 1074: 1031: 980: 942: 932: 920: 906: 882: 873: 864: 826: 823:on 2013-07-24. 799: 781: 780: 778: 775: 774: 773: 768: 761: 758: 739: 736: 708: 707:Pill splitting 705: 688: 685: 684: 683: 680: 677: 674: 670: 661: 660:Matrix systems 658: 649: 646: 635: 632: 623:Main article: 620: 617: 554:Main article: 551: 548: 547: 546: 543: 533: 530: 529: 528: 524: 514: 511: 487: 486: 479: 438: 435: 421: 420: 418: 417:Extra Strength 415: 411: 410: 408: 407:Extra Strength 405: 401: 400: 398: 395: 391: 390: 388: 385: 381: 380: 378: 375: 371: 370: 368: 365: 361: 360: 358: 355: 351: 350: 348: 345: 341: 340: 338: 335: 331: 330: 328: 325: 321: 320: 317: 314: 310: 309: 307: 304: 300: 299: 297: 294: 290: 289: 287: 284: 280: 279: 277: 274: 270: 269: 267: 264: 260: 259: 257: 254: 250: 249: 247: 244: 240: 239: 237: 234: 230: 229: 227: 224: 220: 219: 217: 214: 210: 209: 207: 204: 200: 199: 196: 193: 182: 179: 50:administration 26: 24: 14: 13: 10: 9: 6: 4: 3: 2: 2671: 2660: 2657: 2655: 2652: 2650: 2647: 2645: 2642: 2641: 2639: 2620: 2617: 2614: 2611: 2609: 2606: 2604: 2601: 2599: 2596: 2594: 2593:Intramuscular 2591: 2589: 2586: 2584: 2581: 2580: 2578: 2576: 2571: 2567: 2561: 2558: 2556: 2553: 2551: 2550:Intracerebral 2548: 2547: 2545: 2543: 2539: 2533: 2530: 2528: 2525: 2523: 2520: 2519: 2517: 2515: 2511: 2506: 2497: 2494: 2490: 2487: 2486: 2485: 2482: 2480: 2477: 2475: 2472: 2468: 2464: 2461: 2457: 2449: 2446: 2444: 2441: 2439: 2436: 2435: 2431: 2426: 2423: 2421: 2418: 2416: 2413: 2411: 2408: 2406: 2403: 2401: 2398: 2396: 2393: 2391: 2388: 2386: 2383: 2381: 2378: 2376: 2373: 2371: 2370:Iontophoresis 2368: 2365: 2362: 2360: 2357: 2355: 2352: 2350: 2347: 2345: 2342: 2340: 2339:Topical cream 2337: 2335: 2332: 2328: 2323: 2320: 2316: 2312: 2306: 2303: 2301: 2298: 2294: 2291: 2289: 2286: 2285: 2284: 2281: 2279: 2276: 2274: 2271: 2270: 2266: 2261: 2258: 2254: 2250: 2245: 2242: 2240: 2237: 2234: 2231: 2229: 2226: 2224: 2221: 2219: 2216: 2214: 2211: 2209: 2207: 2203: 2197: 2194: 2192: 2189: 2187: 2184: 2182: 2179: 2177: 2174: 2172: 2169: 2167: 2164: 2163: 2159: 2154: 2152: 2148: 2143: 2139: 2125: 2122: 2120: 2117: 2115: 2112: 2110: 2107: 2105: 2104:Nasal cannula 2101: 2098: 2097: 2095: 2093: 2089: 2083: 2080: 2078: 2075: 2072: 2069: 2067: 2064: 2062: 2059: 2057: 2054: 2053: 2051: 2049: 2045: 2032: 2022: 2019: 2017: 2014: 2013: 2011: 2009: 2005: 2002: 1999: 1995: 1991: 1980: 1978: 1975: 1973: 1970: 1968: 1965: 1964: 1962: 1960: 1956: 1950: 1947: 1944: 1941: 1939: 1936: 1934: 1931: 1929: 1926: 1924: 1921: 1919: 1916: 1915: 1913: 1911: 1907: 1904: 1901: 1897: 1893: 1889: 1885: 1875: 1872: 1870: 1867: 1865: 1862: 1860: 1857: 1855: 1852: 1850: 1847: 1845: 1842: 1840: 1837: 1835: 1832: 1830: 1827: 1825: 1822: 1820: 1817: 1815: 1812: 1810: 1807: 1806: 1804: 1802: 1798: 1793: 1787: 1777: 1774: 1772: 1769: 1767: 1764: 1762: 1759: 1757: 1754: 1753: 1751: 1749: 1745: 1742: 1739: 1735: 1731: 1728: 1726: 1722: 1718: 1714: 1707: 1702: 1700: 1695: 1693: 1688: 1687: 1684: 1677: 1674: 1672: 1669: 1667: 1664: 1663: 1659: 1648: 1647: 1639: 1636: 1631: 1627: 1622: 1617: 1613: 1609: 1605: 1601: 1597: 1590: 1587: 1574: 1570: 1566: 1560: 1557: 1552: 1548: 1544: 1540: 1535: 1530: 1526: 1522: 1518: 1511: 1508: 1503: 1499: 1494: 1489: 1484: 1479: 1475: 1471: 1467: 1460: 1457: 1452: 1448: 1444: 1440: 1436: 1432: 1425: 1418: 1415: 1410: 1406: 1401: 1396: 1392: 1388: 1384: 1380: 1376: 1372: 1368: 1364: 1360: 1353: 1350: 1344: 1341: 1335: 1332: 1327: 1323: 1319: 1315: 1311: 1307: 1303: 1299: 1292: 1289: 1284: 1280: 1276: 1272: 1268: 1264: 1260: 1256: 1249: 1246: 1241: 1237: 1233: 1229: 1225: 1221: 1217: 1213: 1206: 1203: 1198: 1194: 1190: 1186: 1182: 1178: 1174: 1170: 1162: 1159: 1154: 1150: 1146: 1142: 1138: 1134: 1130: 1126: 1119: 1116: 1111: 1107: 1102: 1097: 1094:(4): 571–88. 1093: 1089: 1085: 1078: 1075: 1070: 1066: 1062: 1058: 1054: 1050: 1046: 1042: 1035: 1032: 1027: 1023: 1019: 1015: 1011: 1007: 1003: 999: 996:(1): 428–40. 995: 991: 984: 981: 976: 972: 968: 964: 961:(3): 311–23. 960: 956: 949: 947: 943: 936: 933: 927: 925: 921: 915: 913: 911: 907: 901: 899: 897: 895: 893: 891: 889: 887: 883: 877: 874: 868: 865: 859: 857: 855: 853: 851: 849: 847: 845: 843: 841: 839: 837: 835: 833: 831: 827: 822: 818: 814: 810: 803: 800: 796: 791: 789: 787: 783: 776: 772: 769: 767: 764: 763: 759: 757: 755: 751: 746: 737: 735: 732: 730: 725: 718: 713: 706: 704: 700: 698: 694: 686: 681: 678: 675: 671: 668: 667: 666: 659: 657: 654: 647: 645: 642: 633: 631: 626: 618: 616: 614: 610: 606: 601: 599: 595: 591: 587: 583: 579: 575: 574:laser drilled 571: 562: 557: 549: 544: 540: 539: 538: 531: 525: 521: 520: 519: 512: 510: 507: 505: 500: 495: 492: 484: 480: 477: 476: 475: 472: 470: 465: 461: 458: 456: 452: 448: 444: 436: 434: 432: 428: 419: 416: 413: 412: 409: 406: 403: 402: 399: 397:Double Action 396: 393: 392: 389: 386: 383: 382: 379: 376: 373: 372: 369: 366: 363: 362: 359: 356: 353: 352: 349: 346: 343: 342: 339: 337:Timed Release 336: 333: 332: 329: 326: 323: 322: 318: 315: 312: 311: 308: 305: 302: 301: 298: 295: 292: 291: 288: 285: 282: 281: 278: 275: 272: 271: 268: 266:Initial Depot 265: 262: 261: 258: 255: 252: 251: 248: 245: 242: 241: 238: 235: 232: 231: 228: 225: 222: 221: 218: 215: 212: 211: 208: 205: 202: 201: 197: 194: 191: 190: 187: 180: 178: 176: 172: 171: 164: 161: 159: 155: 151: 147: 146:drug carriers 142: 140: 134: 120: 115: 111: 107: 103: 98: 96: 92: 88: 83: 79: 77: 73: 69: 65: 61: 57: 53: 51: 47: 44:) delivers a 43: 39: 33: 19: 2644:Dosage forms 2598:Intraosseous 2588:Intracardiac 2527:Intravitreal 2489:Injector pen 2484:Subcutaneous 2455: 2425:Jet injector 2410:Dermal patch 2223:Vaginal ring 2191:Insufflation 1943:Effervescent 1717:dosage forms 1645: 1638: 1606:(3): 245–9. 1603: 1599: 1589: 1577:. Retrieved 1573:the original 1568: 1559: 1524: 1520: 1510: 1473: 1469: 1459: 1434: 1430: 1417: 1366: 1362: 1352: 1343: 1334: 1304:(5): 311–6. 1301: 1297: 1291: 1261:(1): 23–31. 1258: 1254: 1248: 1215: 1211: 1205: 1175:(3): 315–6. 1172: 1168: 1161: 1128: 1124: 1118: 1091: 1087: 1077: 1044: 1040: 1034: 993: 989: 983: 958: 954: 935: 876: 867: 821:the original 816: 812: 802: 741: 733: 726: 722: 701: 690: 663: 653:Bio-adhesive 651: 637: 628: 602: 567: 535: 516: 508: 504:dose dumping 496: 488: 473: 462: 459: 440: 430: 426: 424: 192:Abbreviation 184: 174: 168: 165: 162: 150:vaginal ring 143: 135: 104:(pills) and 99: 84: 80: 68:side effects 62:designed to 60:dosage forms 55: 54: 37: 36: 2583:Intravenous 2570:Circulatory 2555:Intrathecal 2479:Intradermal 2471:transdermal 2438:Parenterals 2344:Topical gel 2300:Murphy drip 2278:Suppository 2166:Nasal spray 2100:Oxygen mask 1949:Chewing gum 1888:Oral mucosa 1527:: 235–247. 1212:Drug Safety 609:GI motility 276:Long-Acting 87:other terms 2638:Categories 2443:Injections 2206:Urogenital 2142:Ophthalmic 1998:inhalation 1972:Toothpaste 1900:sublingual 1864:Suspension 1834:Herbal tea 1470:J Biol Eng 727:Among the 347:Extra Long 2448:infusions 2380:Liposomes 2176:Eye drops 2171:Ear drops 2082:Vaporizer 2077:Nebulizer 1967:Mouthwash 1896:sublabial 1819:Electuary 1809:Decoction 1579:16 August 1543:0168-3659 1391:1521-4095 797:, p. 7-13 777:Footnotes 750:excipient 717:bupropion 76:hydrogels 72:liposomes 2619:PIC line 2560:Epidural 2400:Lip balm 2375:Hydrogel 2366:solution 2349:Liniment 2334:Ointment 2293:Hydrogel 2288:Solution 2273:Ointment 2213:Ointment 2186:Hydrogel 2181:Ointment 1977:Ointment 1938:Lozenges 1928:Lollipop 1874:Tincture 1859:Solution 1839:Hydrogel 1824:Emulsion 1766:Pastille 1630:19754482 1551:30419268 1502:21114841 1451:16278032 1409:30614086 1326:25994524 1318:12240794 1283:33413277 1275:11038435 1240:35424637 1232:12408733 1153:35670161 1145:10872087 1110:21486532 1069:42490425 1061:17022845 1026:31442663 975:19602438 760:See also 641:buoyancy 455:patented 447:acrylics 110:dissolve 106:capsules 2319:topical 2257:enteral 2218:Pessary 2048:Liquids 2021:Smoking 1959:Liquids 1854:Softgel 1801:Liquids 1761:Capsule 1738:enteral 1621:5632511 1493:3002303 1400:6375388 1371:Bibcode 1197:1838636 1189:2257873 1018:2006800 998:Bibcode 738:History 586:osmosis 469:capsule 449:, even 437:Methods 195:Meaning 102:tablets 2514:Organs 2395:Lotion 2315:Dermal 2253:Rectal 2228:Douche 2008:Solids 1945:tablet 1910:Solids 1892:buccal 1849:Powder 1814:Elixir 1756:Tablet 1748:Solids 1628:  1618:  1549:  1541:  1500:  1490:  1476:: 15. 1449:  1407:  1397:  1389:  1324:  1316:  1281:  1273:  1238:  1230:  1195:  1187:  1151:  1143:  1108:  1067:  1059:  1024:  1016:  973:  570:tablet 451:chitin 198:Notes 156:) and 129:  42:dosage 2390:Cream 2354:Paste 2283:Enema 2235:(IUD) 2151:nasal 2073:(MDI) 1981:Spray 1869:Syrup 1650:(PDF) 1427:(PDF) 1322:S2CID 1279:S2CID 1236:S2CID 1193:S2CID 1149:S2CID 1065:S2CID 1022:S2CID 940:2016. 131:hours 2615:pump 2467:Skin 2364:DMSO 2359:Film 2147:otic 2102:and 1923:Film 1725:Oral 1626:PMID 1581:2016 1547:PMID 1539:ISSN 1498:PMID 1447:PMID 1405:PMID 1387:ISSN 1314:PMID 1271:PMID 1228:PMID 1185:PMID 1141:PMID 1106:PMID 1057:PMID 1014:PMID 971:PMID 697:NEMS 695:and 693:MEMS 594:drug 584:via 497:The 489:The 429:and 173:and 152:and 114:drug 58:are 46:drug 2092:Gas 1616:PMC 1608:doi 1529:doi 1525:292 1488:PMC 1478:doi 1439:doi 1435:109 1395:PMC 1379:doi 1306:doi 1263:doi 1220:doi 1177:doi 1133:doi 1096:doi 1049:doi 1006:doi 994:618 963:doi 542:SR. 283:LAR 127:4–6 123:1–2 108:to 2640:: 2149:, 1898:, 1894:, 1715:, 1624:. 1614:. 1602:. 1598:. 1567:. 1545:. 1537:. 1523:. 1519:. 1496:. 1486:. 1472:. 1468:. 1445:. 1433:. 1429:. 1403:. 1393:. 1385:. 1377:. 1367:31 1365:. 1361:. 1320:. 1312:. 1302:18 1300:. 1277:. 1269:. 1259:21 1257:. 1234:. 1226:. 1216:25 1214:. 1191:. 1183:. 1173:39 1171:. 1147:. 1139:. 1129:26 1127:. 1104:. 1092:13 1090:. 1086:. 1063:. 1055:. 1045:22 1043:. 1020:. 1012:. 1004:. 992:. 969:. 959:73 957:. 945:^ 923:^ 909:^ 885:^ 829:^ 815:, 811:, 785:^ 699:. 605:pH 471:. 431:XS 427:ES 414:XS 404:ES 394:DA 384:DS 374:LS 364:XT 354:XR 344:XL 334:TR 324:SR 313:SA 303:PR 293:MR 273:LA 263:ID 253:IR 243:ER 233:DR 223:CC 213:CR 203:CD 160:. 112:a 2572:, 2473:) 2469:( 2321:) 2317:( 2259:) 2255:( 2144:, 2040:0 2036:0 2000:) 1996:( 1902:) 1890:( 1740:) 1736:( 1705:e 1698:t 1691:v 1632:. 1610:: 1604:9 1583:. 1553:. 1531:: 1504:. 1480:: 1474:4 1453:. 1441:: 1411:. 1381:: 1373:: 1328:. 1308:: 1285:. 1265:: 1242:. 1222:: 1199:. 1179:: 1155:. 1135:: 1112:. 1098:: 1071:. 1051:: 1028:. 1008:: 1000:: 977:. 965:: 817:1 34:. 20:)

Index

Sustained release
Time Release (novel)
dosage
drug
administration
dosage forms
release (liberate) a drug
side effects
liposomes
hydrogels
other terms
Food and Drug Administration
injection formulation of a drug which releases slowly over time
tablets
capsules
dissolve
drug
extended-release morphine
therapeutic window
drug carriers
vaginal ring
contraceptive implant
transdermal patches
Journal of Controlled Release
active ingredient
acrylics
chitin
patented
Micro-encapsulation
capsule

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