List Of Local Anesthetics
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List Of Local Anesthetics
This is a list of local anesthetic agents. Not all of these drugs are still used in clinical practice and in research. Some are primarily of historical interest. See also * 4-Aminobenzoic acid * Amino amide * Amino esters * Anesthesia * Anesthetic * Brachial plexus block * Cocaine analogues: local anesthetics * Dental anesthesia * Dibucaine number * Epidural * Intravenous regional anesthesia * Local anesthesia * Local anesthetic with vasoconstrictor * Local anesthetic toxicity * Methemoglobin * Sodium channel blocker * Spinal anesthesia * Topical anesthesia * Veterinary anesthesia Veterinary anesthesia is anesthesia performed on non-human animals by a veterinarian or a Registered Veterinary Technician. Anesthesia is used for a wider range of circumstances in animals than in people, due to animals' inability to cooperate with ... References {{reflist Local anesthetics ...
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Local Anesthetic
A local anesthetic (LA) is a medication that causes absence of pain sensation. In the context of surgery, a local anesthetic creates an absence of pain in a specific location of the body without a loss of consciousness, as opposed to a general anesthetic. When it is used on specific nerve pathways (local anesthetic nerve block), paralysis (loss of muscle power) also can be achieved. Examples Short Duration & Low Potency Procaine Chloroprocaine Medium Duration & Potency Lidocaine Prilocaine High Duration & Potency Tetracaine Bupivacaine Cinchocaine Ropivacaine Clinical LAs belong to one of two classes: aminoamide and aminoester local anesthetics. Synthetic LAs are structurally related to cocaine. They differ from cocaine mainly in that they have a very low abuse potential and do not produce hypertension or (with few exceptions) vasoconstriction. They are used in various techniques of local anesthesia such as: * Topical anesthesia (surface) * Topical administration ...
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Butanilicaine
Butanilicaine is a local anesthetic. It is also known by the name Hostacaine. Synthesis The amide formation between 2-Chloro-6-Methylaniline 7-63-8(1) and Chloroacetyl chloride (2) gives 2-Chloro-n-(2-chloro-6-methylphenyl)acetamide 307-67-1(3). Alkylation with N-Butylamine ''n''-Butylamine is an organic compound (specifically, an amine) with the formula CH3(CH2)3NH2. This colourless liquid is one of the four isomeric amines of butane, the others being ''sec''-butylamine, ''tert''-butylamine, and isobutylamine. It ... (4) completed the synthesis of ''Butanilicaine'' (5). References Local anesthetics Acetanilides Chloroarenes {{nervous-system-drug-stub ...
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Dibucaine
Cinchocaine (INN/ BAN) or dibucaine (USAN) is an amide local anesthetic. Among the most potent and toxic of the long-acting local anesthetics, current use of cinchocaine is generally restricted to spinal and topical anesthesia. It is sold under the brand names Cincain, Nupercainal, Nupercaine and Sovcaine. Medical use Cinchocaine is the active ingredient in some topical hemorrhoid creams such as Proctosedyl. It is also a component of the veterinary drug Somulose, used for euthanasia of horses and cattle. Physical properties Cinchocaine is relatively insoluble in alkaline aqueous solutions. See also * Dibucaine number Dibucaine, also known as cinchocaine, is an amino amide local anesthetic. When administered to humans intravenously, it is capable of inhibiting the plasma cholinesterase (butyrylcholinesterase) enzyme. The dibucaine number is used to differentiate ... References Further reading * * * * Local anesthetics Quinolines Phenol ethers Carboxamides Dieth ...
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Cyclomethycaine
Cyclomethycaine is a local anesthetic A local anesthetic (LA) is a medication that causes absence of pain sensation. In the context of surgery, a local anesthetic creates an absence of pain in a specific location of the body without a loss of consciousness, as opposed to a general an .... References Benzoate esters Piperidines {{nervous-system-drug-stub ...
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Cyclomethycaine
Cyclomethycaine is a local anesthetic A local anesthetic (LA) is a medication that causes absence of pain sensation. In the context of surgery, a local anesthetic creates an absence of pain in a specific location of the body without a loss of consciousness, as opposed to a general an .... References Benzoate esters Piperidines {{nervous-system-drug-stub ...
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William Stewart Halsted
William Stewart Halsted, M.D. (September 23, 1852 – September 7, 1922) was an American surgeon who emphasized strict aseptic technique during surgical procedures, was an early champion of newly discovered anesthetics, and introduced several new operations, including the radical mastectomy for breast cancer. Along with William Osler (Professor of Medicine), Howard Atwood Kelly (Professor of Gynecology) and William H. Welch (Professor of Pathology), Halsted was one of the "Big Four" founding professors at the Johns Hopkins Hospital. His operating room at Johns Hopkins Hospital is in Ward G, and was described as a small room where medical discoveries and miracles took place. According to an intern who once worked in Halsted's operating room, Halsted had unique techniques, operated on the patients with great confidence and often had perfect results which astonished the interns. Throughout his professional life, he was addicted to cocaine and later also to morphine, which were no ...
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Karl Koller (ophthalmologist)
Karl Koller (December 3, 1857 – March 21, 1944) was an Austrian ophthalmologist who began his medical career as a surgeon at the Vienna General Hospital and a colleague of Sigmund Freud. Koller introduced cocaine as a local anaesthetic for eye surgery. Prior to this discovery, he had tested solutions such as chloral hydrate and morphine as anaesthetics in the eyes of laboratory animals without success. Freud was fully aware of the pain-killing properties of cocaine, but Koller recognized its tissue-numbing capabilities, and in 1884 demonstrated its potential as a local anaesthetic to the medical community. Koller's findings were a medical breakthrough. Prior to his discovery, performing eye surgery was difficult because the involuntary reflex motions of the eye to respond to the slightest stimuli. Later, cocaine was also used as a local anaesthetic in other medical fields such as dentistry. In the 20th century, other agents such as lidocaine have replaced cocaine as a local anae ...
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Richard Willstätter
Richard Martin Willstätter FRS(For) HFRSE (, 13 August 1872 – 3 August 1942) was a German organic chemist whose study of the structure of plant pigments, chlorophyll included, won him the 1915 Nobel Prize for Chemistry. Willstätter invented paper chromatography independently of Mikhail Tsvet. Life Willstätter was born into a Jewish family in Karlsruhe. He was the son of Maxwell (Max) Willstätter, a textile merchant, and his wife, Sophie Ulmann. He went to school at the Karlsruhe Gymnasium and, when his family moved to Nuremberg, he attended the Technical School there. At age 18 he entered the University of Munich to study science and stayed for the next fifteen years. He was in the Department of Chemistry, first as a student of Alfred Einhorn—he received his doctorate in 1894 – then as a faculty member. His doctoral thesis was on the structure of cocaine. Willstätter continued his research into other alkaloids and synthesized several of them. In 1896 he was named Lec ...
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Friedrich Gaedcke
Friedrich Georg Carl (Friedrich) Gaedcke (5 June 1828 – 19 September 1890) was a German chemist. He was the first person to isolate the cocaine alkaloid in 1855. Gaedcke named the alkaloid “erythroxyline,” and published a description in the journal Archiv der Pharmazie. Gaedcke worked in a pharmacy in Rostock and studied in Rostock between 1850 and 1851. In 1856, he took over a pharmacy in Dömitz Dömitz () is a municipality in the Ludwigslust-Parchim district, in Mecklenburg-Western Pomerania, Germany. It is situated on the right bank of the Elbe, 25 km southwest of Ludwigslust, and 37 km northwest of Wittenberge. It was grant ... which he ran for 3 4 years. References 1828 births 1890 deaths 19th-century German chemists People from Rostock {{Germany-chemist-stub ...
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Cocaine
Cocaine (from , from , ultimately from Quechuan languages, Quechua: ''kúka'') is a central nervous system (CNS) stimulant mainly recreational drug use, used recreationally for its euphoria, euphoric effects. It is primarily obtained from the leaves of two Coca species native to South America, ''Erythroxylum coca'' and ''Erythroxylum novogranatense''. After extraction from coca leaves and further processing into cocaine hydrochloride (powdered cocaine), the drug is often Insufflation (medicine), snorted, applied topical administration, topically to the mouth, or dissolved and injection (medicine), injected into a vein. It can also then be turned into free base form (crack cocaine), in which it can be heated until sublimated and then the vapours can be smoking, inhaled. Cocaine stimulates the mesolimbic pathway, reward pathway in the brain. Mental effects may include an euphoria, intense feeling of happiness, sexual arousal, psychosis, loss of contact with reality, or psychomo ...
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Cinchocaine
Cinchocaine (INN/ BAN) or dibucaine (USAN) is an amide local anesthetic. Among the most potent and toxic of the long-acting local anesthetics, current use of cinchocaine is generally restricted to spinal and topical anesthesia. It is sold under the brand names Cincain, Nupercainal, Nupercaine and Sovcaine. Medical use Cinchocaine is the active ingredient in some topical hemorrhoid creams such as Proctosedyl. It is also a component of the veterinary drug Somulose, used for euthanasia of horses and cattle. Physical properties Cinchocaine is relatively insoluble in alkaline aqueous solutions. See also * Dibucaine number Dibucaine, also known as cinchocaine, is an amino amide local anesthetic. When administered to humans intravenously, it is capable of inhibiting the plasma cholinesterase (butyrylcholinesterase) enzyme. The dibucaine number is used to differentiate ... References Further reading * * * * Local anesthetics Quinolines Phenol ethers Carboxamides Diethyl ...
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