1.
Ionic compound
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In chemistry, an ionic compound is a chemical compound composed of ions held together by electrostatic forces termed ionic bonding. The compound is overall, but consists of positively charged ions called cations. These can be simple ions such as the sodium and chloride in sodium chloride, or polyatomic species such as the ammonium, Ionic compounds containing hydrogen ions are classified as acids, and those containing basic ions hydroxide or oxide are classified as bases. Ionic compounds without these ions are known as salts and can be formed by acid–base reactions. Ionic compounds typically have high melting and boiling points, and are hard, as solids they are almost always electrically insulating, but when melted or dissolved they become highly conductive, because the ions are mobilized. The word ion is the Greek ἰόν, ion, going and this term was introduced by English physicist and chemist Michael Faraday in 1834 for the then-unknown species that goes from one electrode to the other through an aqueous medium. In 1913 the crystal structure of sodium chloride was determined by William Henry Bragg, many other inorganic compounds were also found to have similar structural features. Principal contributors to the development of a treatment of ionic crystal structures were Max Born, Fritz Haber, Alfred Landé, Erwin Madelung, Paul Peter Ewald. Born predicted crystal energies based on the assumption of ionic constituents, Ionic compounds can be produced from their constituent ions by evaporation, precipitation, or freezing. Reactive metals such as the alkali metals can react directly with the highly electronegative halogen gases to form an ionic product and they can also be synthesized as the product of a high temperature reaction between solids. If the ionic compound is soluble in a solvent, it can be obtained as a compound by evaporating the solvent from this electrolyte solution. This process occurs widely in nature, and is the means of formation of the evaporite minerals, insoluble ionic compounds can be precipitated by mixing two solutions, one with the cation and one with the anion in it. Because all solutions are neutral, the two solutions mixed must also contain counterions of the opposite charges. To ensure that these do not contaminate the precipitated ionic compound, if the two solutions have hydrogen ions and hydroxide ions as the counterions, they will react with one another in what is called an acid–base reaction or a neutralization reaction to form water. Alternately the counterions can be chosen to ensure that even when combined into a solution they will remain soluble as spectator ions. Molten salts will solidify on cooling to below their freezing point and this is sometimes used for the solid-state synthesis of complex ionic compounds from solid reactants, which are first melted together. In other cases the solid reactants do not need to be melted, other synthetic routes use a solid precursor with the correct stoichiometric ratio of non-volatile ions, which is heated to drive off other species. There is also an additional attractive force from van der Waals interactions which contributes only around 1–2% of the cohesive energy for small ions
2.
Germany
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Germany, officially the Federal Republic of Germany, is a federal parliamentary republic in central-western Europe. It includes 16 constituent states, covers an area of 357,021 square kilometres, with about 82 million inhabitants, Germany is the most populous member state of the European Union. After the United States, it is the second most popular destination in the world. Germanys capital and largest metropolis is Berlin, while its largest conurbation is the Ruhr, other major cities include Hamburg, Munich, Cologne, Frankfurt, Stuttgart, Düsseldorf and Leipzig. Various Germanic tribes have inhabited the northern parts of modern Germany since classical antiquity, a region named Germania was documented before 100 AD. During the Migration Period the Germanic tribes expanded southward, beginning in the 10th century, German territories formed a central part of the Holy Roman Empire. During the 16th century, northern German regions became the centre of the Protestant Reformation, in 1871, Germany became a nation state when most of the German states unified into the Prussian-dominated German Empire. After World War I and the German Revolution of 1918–1919, the Empire was replaced by the parliamentary Weimar Republic, the establishment of the national socialist dictatorship in 1933 led to World War II and the Holocaust. After a period of Allied occupation, two German states were founded, the Federal Republic of Germany and the German Democratic Republic, in 1990, the country was reunified. In the 21st century, Germany is a power and has the worlds fourth-largest economy by nominal GDP. As a global leader in industrial and technological sectors, it is both the worlds third-largest exporter and importer of goods. Germany is a country with a very high standard of living sustained by a skilled. It upholds a social security and universal health system, environmental protection. Germany was a member of the European Economic Community in 1957. It is part of the Schengen Area, and became a co-founder of the Eurozone in 1999, Germany is a member of the United Nations, NATO, the G8, the G20, and the OECD. The national military expenditure is the 9th highest in the world, the English word Germany derives from the Latin Germania, which came into use after Julius Caesar adopted it for the peoples east of the Rhine. This in turn descends from Proto-Germanic *þiudiskaz popular, derived from *þeudō, descended from Proto-Indo-European *tewtéh₂- people, the discovery of the Mauer 1 mandible shows that ancient humans were present in Germany at least 600,000 years ago. The oldest complete hunting weapons found anywhere in the world were discovered in a mine in Schöningen where three 380, 000-year-old wooden javelins were unearthed
3.
Bromine
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Bromine is a chemical element with symbol Br and atomic number 35. It is the third-lightest halogen, and is a fuming red-brown liquid at room temperature that readily to form a similarly coloured gas. Its properties are intermediate between those of chlorine and iodine. Isolated independently by two chemists, Carl Jacob Löwig and Antoine Jérôme Balard, its name was derived from the Ancient Greek βρῶμος stench, referencing its sharp and disagreeable smell. Elemental bromine is very reactive and thus does not occur free in nature, while it is rather rare in the Earths crust, the high solubility of the bromide ion has caused its accumulation in the oceans. Commercially the element is easily extracted from brine pools, mostly in the United States, Israel, the mass of bromine in the oceans is about one three-hundredth of that of chlorine. At high temperatures, organobromine compounds readily convert to free bromine atoms and this effect makes organobromine compounds useful as fire retardants and more than half the bromine produced worldwide each year is put to this purpose. Unfortunately, the same property causes sunlight to convert volatile organobromine compounds to free bromine atoms in the atmosphere, as a result, many organobromide compounds—such as the pesticide methyl bromide—are no longer used. Bromine compounds are used in well drilling fluids, in photographic film. Bromine has sometimes been considered to be essential in humans, but with the support of only limited circumstantial evidence. As a pharmaceutical, the bromide ion has inhibitory effects on the central nervous system. They retain niche uses as antiepileptics, bromine was discovered independently by two chemists, Carl Jacob Löwig and Antoine Balard, in 1825 and 1826, respectively. Löwig isolated bromine from a water spring from his hometown Bad Kreuznach in 1825. Löwig used a solution of the mineral salt saturated with chlorine, after evaporation of the ether a brown liquid remained. With this liquid as a sample for his work he applied for a position in the laboratory of Leopold Gmelin in Heidelberg, the publication of the results was delayed and Balard published his results first. Balard found bromine chemicals in the ash of seaweed from the marshes of Montpellier. The seaweed was used to produce iodine, but also contained bromine, Balard distilled the bromine from a solution of seaweed ash saturated with chlorine. In his publication, Balard states that he changed the name from muride to brôme on the proposal of M. Anglada, brôme derives from the Greek βρωμος
4.
Silver nitrate
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Silver nitrate is an inorganic compound with chemical formula AgNO3. This compound is a precursor to many other silver compounds. It is far less sensitive to light than the halides and it was once called lunar caustic because silver was called luna by the ancient alchemists, who believed that silver was associated with the moon. In solid silver nitrate, the ions are three-coordinated in a trigonal planar arrangement. Albertus Magnus, in the 13th century, documented the ability of nitric acid to separate gold, Magnus noted that the resulting solution of silver nitrate could blacken skin. Silver nitrate can be prepared by reacting silver, such as a silver bullion or silver foil, with acid, resulting in silver nitrate, water. Reaction byproducts depend upon the concentration of acid used. 3 Ag +4 HNO3 →3 AgNO3 +2 H2O + NO Ag +2 HNO3 → AgNO3 + H2O + NO2 This is performed under a fume hood because of nitrogen oxide evolved during the reaction. A typical reaction with silver nitrate is to suspend a rod of copper in a solution of silver nitrate, silver nitrate is the least expensive salt of silver, it offers several other advantages as well. It is non-hygroscopic, in contrast to silver fluoroborate and silver perchlorate and it is relatively stable to light. Finally, it dissolves in solvents, including water. The nitrate can be replaced by other ligands, rendering AgNO3 versatile. Treatment with solutions of halide ions gives a precipitate of AgX, similarly, silver nitrate is used to prepare some silver-based explosives, such as the fulminate, azide, or acetylide, through a precipitation reaction. This reaction is used in inorganic chemistry to abstract halides, Ag+ + X− → AgX where X− = Cl−, Br−. Other silver salts with non-coordinating anions, namely silver tetrafluoroborate and silver hexafluorophosphate are used for demanding applications. Similarly, this reaction is used in chemistry to confirm the presence of chloride, bromide. Samples are typically acidified with nitric acid to remove interfering ions, e. g. carbonate ions. This step avoids confusion of silver sulfide or silver carbonate precipitates with that of silver halides, the color of precipitate varies with the halide, white, pale yellow/cream, yellow
5.
Conjugate acid
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A conjugate acid, within the Brønsted–Lowry acid–base theory, is a species formed by the reception of a proton by a base—in other words, it is a base with a hydrogen ion added to it. On the other hand, a base is merely what is left after an acid has donated a proton in a chemical reaction. Hence, a base is a species formed by the removal of a proton from an acid. A proton is a particle with a unit positive electrical charge, it is represented by the symbol H+ because it constitutes the nucleus of a hydrogen atom, that is. A cation can be an acid, and an anion can be a conjugate base, depending on which substance is involved. In an acid-base reaction, an acid plus a base reacts to form a conjugate base plus a conjugate acid, refer to the following figure, We say that the water molecule is the conjugate acid of the hydroxide ion after the latter received the hydrogen proton donated by ammonium. On the other hand, ammonia is the base for the acid ammonium after ammonium has donated a hydrogen ion towards the production of the water molecule. The strength of an acid is directly proportional to its dissociation constant. If a conjugate acid is strong, its dissociation will have an equilibrium constant. The strength of a base can be seen as the tendency of the species to pull hydrogen protons towards itself. If a conjugate base is classified as strong, it will hold on to the hydrogen proton when in solution, if a chemical species is classified as a weak acid, its conjugate base will be strong in nature. This can be observed in ammonias reaction with water, the reaction proceeds until most of the ammonia has been transformed to ammonium. This shift to the right in the equilibrium of the reaction means that ammonium does not dissociate easily in water. On the other hand, if a species is classified as a strong acid, an example of this case would be the dissociation of Hydrochloric acid HCl in water. Since HCl is an acid, its conjugate base will be a weak conjugate base. Therefore, in system, most H+ will be in the form of a Hydronium ion H 3O+ instead of attached to a Cl anion. To summarize, the stronger the acid or base, the weaker the conjugate, the acid and conjugate base as well as the base and conjugate acid are known as conjugate pairs. When finding a conjugate acid or base, it is important to look at the reactants of the chemical equation, to identify the conjugate acid, look for the pair of compounds that are related
6.
Salt (chemistry)
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In chemistry, a salt is an ionic compound that results from the neutralization reaction of an acid and a base. Salts are composed of related numbers of cations and anions so that the product is electrically neutral and these component ions can be inorganic, such as chloride, or organic, such as acetate, and can be monatomic, such as fluoride, or polyatomic, such as sulfate. There are several varieties of salts, salts that hydrolyze to produce hydroxide ions when dissolved in water are alkali salts, whilst those that hydrolyze to produce hydronium ions in water are acidic salts. Neutral salts are those salts that are neither acidic nor basic, zwitterions contain an anionic centre and a cationic centre in the same molecule, but are not considered to be salts. Examples of zwitterions include amino acids, many metabolites, peptides, usually, non-dissolved salts at standard conditions for temperature and pressure are solid, but there are exceptions. Molten salts and solutions containing dissolved salts are called electrolytes, as they are able to conduct electricity. As observed in the cytoplasm of cells, in blood, urine, plant saps and mineral waters, therefore, their salt content is given for the respective ions. Salts can appear to be clear and transparent, opaque, and even metallic, in many cases, the apparent opacity or transparency are only related to the difference in size of the individual monocrystals. Since light reflects from the boundaries, larger crystals tend to be transparent. The color of the salt is due to the electronic structure in the d-orbitals of transition elements or in the conjugated organic dye framework. Different salts can elicit all five basic tastes, e. g. salty, sweet, sour, bitter, and umami or savory. Salts of strong acids and strong bases are non-volatile and odorless and that slow, partial decomposition is usually accelerated by the presence of water, since hydrolysis is the other half of the reversible reaction equation of formation of weak salts. Many ionic compounds can be dissolved in water or other similar solvents, the exact combination of ions involved makes each compound have a unique solubility in any solvent. The solubility is dependent on how well each ion interacts with the solvent, for example, all salts of sodium, potassium and ammonium are soluble in water, as are all nitrates and many sulfates – barium sulfate, calcium sulfate and lead sulfate are examples of exceptions. However, ions that bind tightly to each other and form highly stable lattices are less soluble, for example, most carbonate salts are not soluble in water, such as lead carbonate and barium carbonate. Some soluble carbonate salts are, sodium carbonate, potassium carbonate, solid salts do not conduct electricity. Moreover, solutions of salts also conduct electricity, the name of a salt starts with the name of the cation followed by the name of the anion. Salts are often referred to only by the name of the cation or by the name of the anion. g
7.
Jmol
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Jmol is computer software for molecular modelling chemical structures in 3-dimensions. Jmol returns a 3D representation of a molecule that may be used as a teaching tool and it is written in the programming language Java, so it can run on the operating systems Windows, macOS, Linux, and Unix, if Java is installed. It is free and open-source software released under a GNU Lesser General Public License version 2.0, a standalone application and a software development kit exist that can be integrated into other Java applications, such as Bioclipse and Taverna. A popular feature is an applet that can be integrated into web pages to display molecules in a variety of ways, for example, molecules can be displayed as ball-and-stick models, space-filling models, ribbon diagrams, etc. Jmol supports a range of chemical file formats, including Protein Data Bank, Crystallographic Information File, MDL Molfile. There is also a JavaScript-only version, JSmol, that can be used on computers with no Java, the Jmol applet, among other abilities, offers an alternative to the Chime plug-in, which is no longer under active development. While Jmol has many features that Chime lacks, it does not claim to reproduce all Chime functions, most notably, Chime requires plug-in installation and Internet Explorer 6.0 or Firefox 2.0 on Microsoft Windows, or Netscape Communicator 4.8 on Mac OS9. Jmol requires Java installation and operates on a variety of platforms. For example, Jmol is fully functional in Mozilla Firefox, Internet Explorer, Opera, Google Chrome, fast and Scriptable Molecular Graphics in Web Browsers without Java3D
8.
Cerebrospinal fluid
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Cerebrospinal fluid is a clear, colorless body fluid found in the brain and spine. It is produced in the choroid plexuses of the ventricles of the brain and it acts as a cushion or buffer for the brains cortex, providing basic mechanical and immunological protection to the brain inside the skull. The CSF also serves a function in cerebral autoregulation of cerebral blood flow. The CSF occupies the space and the ventricular system around and inside the brain. It constitutes the content of the ventricles, cisterns, and sulci of the brain, there is also a connection from the subarachnoid space to the bony labyrinth of the inner ear via the perilymphatic duct where the perilymph is continuous with the cerebrospinal fluid. The brain produces roughly 500 mL of cerebrospinal fluid per day and this transcellular fluid is constantly reabsorbed, so that only 100–160 mL is present at any one time. Ependymal cells of the choroid plexus produce more than two thirds of CSF, the choroid plexus is a venous plexus contained within the four ventricles of the brain, hollow structures inside the brain filled with CSF. The remainder of the CSF is produced by the surfaces of the ventricles, ependymal cells secrete sodium into the lateral ventricles. This creates osmotic pressure and draws water into the CSF space, chloride, with a negative charge, moves with the positively charged sodium and a neutral charge is maintained. As a result, CSF contains a concentration of sodium and chloride than blood plasma. CSF circulates within the system of the brain. The ventricles are a series of cavities filled with CSF, inside the brain, the majority of CSF is produced from within the two lateral ventricles. From here, the CSF passes through the interventricular foramina to the third ventricle, the fourth ventricle is an outpouching on the posterior part of the brainstem. From the fourth ventricle, the passes through three openings to enter the subarachnoid space – these are the median aperture, and the lateral apertures. The subarachnoid space covers the brain and spinal cord, there is connection from the subarachnoid space to the bony labyrinth of the inner ear making the cerebrospinal fluid continuous with the perilymph. The team concluded that the term circulation should be avoided and an appropriate term movement of CSF would be advisable. The CSF moves in a pulsatile manner throughout the CSF system with a zero net flow. It had been thought that CSF returns to the system by entering the dural venous sinuses via the arachnoid granulations
9.
Potassium bromide
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Potassium bromide is a salt, widely used as an anticonvulsant and a sedative in the late 19th and early 20th centuries, with over-the-counter use extending to 1975 in the US. Its action is due to the bromide ion, potassium bromide is used as a veterinary drug, as an antiepileptic medication for dogs. Under standard conditions, potassium bromide is a crystalline powder. It is freely soluble in water, it is not soluble in acetonitrile, in a dilute aqueous solution, potassium bromide tastes sweet, at higher concentrations it tastes bitter, and tastes salty when the concentration is even higher. These effects are due to the properties of the potassium ion—sodium bromide tastes salty at any concentration. In high concentration, potassium bromide strongly irritates the mucous membrane, causing nausea. Potassium bromide, an ionic salt, is fully dissociated. It serves as a source of bromide ions, bromide can be regarded as the first effective medication for epilepsy. At the time, it was thought that epilepsy was caused by masturbation. Locock noted that bromide calmed sexual excitement and thought this was responsible for his success in treating seizures, there was not a better epilepsy drug until phenobarbital in 1912. Bromides exceedingly long life in the body made it difficult to dose without side effects. Medical use of bromides in the US was discontinued at this time, as many better, use of bromide in cats is limited because it carries a substantial risk of causing lung inflammation in them. Potassium bromide is not approved by the US Food and Drug Administration for use in humans to control seizures, in Germany, it is still approved as an antiepileptic drug for humans, particularly children and adolescents. These indications include severe forms of generalized tonic-clonic seizures, early-childhood-related Grand-Mal-seizures, adults who have reacted positively to the drug during childhood/adolescence may continue treatment. Potassium bromide tablets are sold under the brand name Dibro-Be mono, the drug has almost complete bioavailability, but the bromide ion has a relatively long half life of 12 days in the blood, making bromide salts difficult to adjust and dose. The therapeutic index for bromide is small, as with other antiepileptics, sometimes even therapeutic doses may give rise to intoxication. Often indistinguishable from expected side-effects, these include, Bromism These are central nervous system reactions, rarely, tongue disorder, aphten, bad breath, and obstipation occur. Potassium bromide is transparent from the ultraviolet to long-wave infrared wavelengths and has no significant optical absorption lines in its high transmission region
10.
Chloride
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The chloride ion /ˈklɔəraɪd/ is the anion Cl−. It is formed when the element chlorine gains an electron or when a compound such as chloride is dissolved in water or other polar solvents. Chloride salts such as sodium chloride are often soluble in water. It is an essential electrolyte located in all body fluids responsible for maintaining acid/base balance, transmitting nerve impulses and regulating fluid in, less frequently, the word chloride may also form part of the common name of chemical compounds in which one or more chlorine atoms are covalently bonded. For example, methyl chloride, with the standard name chloromethane is a compound with a covalent C−Cl bond in which the chlorine is not an anion. A chloride ion is much larger than an atom,167 and 99 pm. The ion is colorless and diamagnetic, in aqueous solution, it is highly soluble in most cases, however, some chloride salts, such as silver chloride, lead chloride, and mercury chloride are slightly soluble in water. In aqueous solution, chloride is bound by the end of the water molecules. Some chloride-containing minerals include the chlorides of sodium, potassium, and magnesium, called serum chloride, the concentration of chloride in the blood is regulated by the kidneys. A chloride ion is a component of some proteins, e. g. it is present in the amylase enzyme. The chlor-alkali industry is a consumer of the worlds energy budget. This process converts sodium chloride into chlorine and sodium hydroxide, which are used to make many other materials and chemicals, in the petroleum industry, the chlorides are a closely monitored constituent of the mud system. An increase of the chlorides in the mud system may be an indication of drilling into a high-pressure saltwater formation and its increase can also indicate the poor quality of a target sand. Chloride is also a useful and reliable chemical indicator of river / groundwater fecal contamination, as chloride is a non-reactive solute, many water regulating companies around the world utilize chloride to check the contamination levels of the rivers and potable water sources. Chloride salts such as sodium chloride are used to preserve food, chloride is an essential electrolyte, trafficking in and out of cells through chloride channels and playing a key role in maintaining cell homeostasis and transmitting action potentials in neurons. Characteristic concentrations of chloride in model organisms are, in both E. coli and budding yeast are 10-200mM, in mammalian cell 5-100mM and in blood plasma 100mM, chloride can be oxidized but not reduced. The first oxidation, as employed in the process, is conversion to chlorine gas. Chlorine can be oxidized to other oxides and oxyanions including hypochlorite, chlorine dioxide, chlorate
11.
Seawater
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Seawater, or salt water, is water from a sea or ocean. On average, seawater in the oceans has a salinity of about 3. 5% This means that every kilogram of seawater has approximately 35 grams of dissolved salts. Average density at the surface is 1.025 kg/l, seawater is denser than both fresh water and pure water because the dissolved salts increase the mass by a larger proportion than the volume. The freezing point of seawater decreases as salt concentration increases, at typical salinity, it freezes at about −2 °C. The coldest seawater ever recorded was in 2010, in a stream under an Antarctic glacier, seawater pH is typically limited to a range between 7.5 and 8.4. However, there is no universally accepted reference pH-scale for seawater, although the vast majority of seawater has a salinity of between 31 g/kg and 38 g/kg, seawater is not uniformly saline throughout the world. Where mixing occurs with fresh water runoff from river mouths, near melting glaciers or vast amounts precipitation, the most saline open sea is the Red Sea, where high rates of evaporation, low precipitation and low river run-off, and confined circulation result in unusually salty water. The salinity in isolated bodies of water can be considerably greater still, historically, several salinity scales were used to approximate the absolute salinity of seawater. A popular scale was the Practical Salinity Scale where salinity was measured in practical salinity units, the current standard for salinity is the Reference Salinity scale with the salinity expressed in units of g/kg. The density of surface seawater ranges from about 1020 to 1029 kg/m3, depending on the temperature, at a temperature of 25 °C, salinity of 35 g/kg and 1 atm pressure, the density of seawater is 1023.6 kg/m3. Deep in the ocean, under pressure, seawater can reach a density of 1050 kg/m3 or higher. The density of seawater also changes with salinity, brines generated by seawater desalination plants can have salinities up to 120 g/kg. The density of typical seawater brine of 120 g/kg salinity at 25 °C, seawater pH is limited to the range 7.5 to 8.4. The speed of sound in seawater is about 1,500 m/s, and varies with temperature, salinity. The thermal conductivity of seawater is 0.6 W/mK at 25 °C, the thermal conductivity decreases with increasing salinity and increases with increasing temperature. Seawater contains more dissolved ions than all types of freshwater, however, the ratios of solutes differ dramatically. Bicarbonate ions also constitute 48% of river water solutes but only 0. 14% of all seawater ions, differences like these are due to the varying residence times of seawater solutes, sodium and chlorine have very long residence times, while calcium tends to precipitate much more quickly. The most abundant dissolved ions in seawater are sodium, chloride, magnesium, sulfate and its osmolarity is about 1000 mOsm/l
12.
Pharmacokinetics
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Pharmacokinetics, sometimes abbreviated as PK, is a branch of pharmacology dedicated to determining the fate of substances administered to a living organism. The substances of interest include any chemical xenobiotic such as, pharmaceutical drugs, pesticides, food additives, cosmetic ingredients, etc. It attempts to analyze chemical metabolism and to discover the fate of a chemical from the moment that it is administered up to the point at which it is eliminated from the body. Pharmacokinetics is the study of how an organism affects a drug, both together influence dosing, benefit, and adverse effects, as seen in PK/PD models. Pharmacokinetic properties of chemicals are affected by the route of administration and these may affect the absorption rate. Models have been developed to simplify conceptualization of the processes that take place in the interaction between an organism and a chemical substance. The various compartments that the model is divided into are commonly referred to as the ADME scheme, absorption - the process of a substance entering the blood circulation. Distribution - the dispersion or dissemination of substances throughout the fluids, metabolism – the recognition by the organism that a foreign substance is present and the irreversible transformation of parent compounds into daughter metabolites. Excretion - the removal of the substances from the body, in rare cases, some drugs irreversibly accumulate in body tissue. The two phases of metabolism and excretion can also be grouped together under the title elimination, the study of these distinct phases involves the use and manipulation of basic concepts in order to understand the process dynamics. All these concepts can be represented through mathematical formulas that have a graphical representation. The model outputs for a drug can be used in industry or in the application of pharmacokinetic concepts. Clinical pharmacokinetics provides many performance guidelines for effective and efficient use of drugs for human-health professionals, in practice, it is generally considered that steady state is reached when a time of 4 to 5 times the half-life for a drug after regular dosing is started. Noncompartmental methods estimate the exposure to a drug by estimating the area under the curve of a concentration-time graph, compartmental methods estimate the concentration-time graph using kinetic models. Noncompartmental methods are more versatile in that they do not assume any specific compartmental model. The final outcome of the transformations that a drug undergoes in an organism, a number of functional models have been developed in order to simplify the study of pharmacokinetics. These models are based on a consideration of an organism as a number of related compartments, the simplest idea is to think of an organism as only one homogenous compartment. However, these models do not always reflect the real situation within an organism
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