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    SYNTHETIC DRUGS 1

    SULPHA DRUGS (SULPHONAMIDES)

    In 1932 , Prontosil,ie, 4-sulphonamide 24 - diamino benzene a dye intermediate was suggested to have antibacterial

    property . Prontosil breaks dwn in the tissues to sulphanilamide and suggested that antibacterial property is resided in

    this part of the molecule.

    In 1937 sulphapyredene which was the structural analogue of sulphanilamide proved tremendous success in curing

    pneumonia was first discovered. Many structural modification of sulphanilamide were then prepared which have been

    extensively used against many common bacterial infections.

    CLASSIFICATION OF SULPHONAMIDES :-

    Sulphonamides may be classified broadly on the basis of their site of action as

    Suplhonamide for general infections:-These are invariably employed against the streptococcal, meningococcal ,

    gonococcal,and pneumococcal infections . Examples : Sulfanilamide, sulphapyredene, sulpha thiazole,sulfadiazine etc.

    Sulpphonamides for urenary infections:-Examples:- Sulfacetamide,sulfafurazole etc

    Sulphonamides for intestenal infection :-Examples:- Sulfaguanidene, pthalyl sulfathiazole etc

    Sulphonamide for local infections:-Examples:- sulfacetamide sodium,Mafenide etc

    MODE OF ACTION OF SULPHONAMIDES :-Sulphanomides are bacteriostatic in nature.However in large doses they

    may also act as bactericidal. Sulphanomide sensitive microorganism require p-aminobenzoic acid(PABA),for

    the synthesis of folic acid,which is essential for the synthesis of DNA and RNA and there for for the growth and

    multiplication of bacteria. Sulphanomides can compete with PABA and prevent the utilization of PABA and

    thereby the synthesis of bacterial DNA and RNA,thus the sulphanomides have selective effect on the sensitive bacteria.

    ANTI BACTERIALS

    ANTIBIOTICS:-Antibitics are medication used to treat bacterial infections either by killing bacteria (bactericidal

    or by inhibiting the growth of susceptible bacteria (bactereostatic) . Examples : Sulpha drugs, Penicillines,

    Ciphalosporin, Tetracyclin etc

    PENICILLINS:- Penicillins are first introduced in 1940 Alexander Fleming . These are bactericidal and inhibit cell wall

    synthesis in bacteria, kill a wide variety of them. The basic structure in penicillin contains lactum ring and are called

    lactum eg: Penicilline-G , Amoxycilline , Ampicilline etc

    MECHANISM OF ACTION

    Penicillins enter the bacteria via the cell wall. Inside the cell, they bind to penicillin-binding protein. Once bound,

    normal cell wall synthesis is disrupted. As a result: bacteria cells die from cell lysis

    USES:- For the Prevention and treatment of infections caused by susceptible bacteria, such as: gram-positive

    bacteria -Streptococcus, Enterococcus, Staphylococcus species

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    Antipyretics , Analgesics and Anti-inflammatory agents 2Anti inflammatory agents are drugs used to diminish or reduce inflammations and pain arising from it. Non narcotic

    analgesic differ from narcotic analgesic in the way that they do not depress the CNS(central nervous system) and are

    divoid of addiction liability

    General mode of action:-

    Prostaglandins play an important role in radiating pain , fever and inflammation . Antipyretics , Analgesics and Anti-

    inflammatory effects of drugs are due to inhibition of synthesis and release of prostaglandins. Release of prostaglandin

    is reduced by stablilsing the cell membrane and the synthesis is reduced by blocking the enzyme prostaglandin

    synthetase.

    Antiinflamatory action:- These drug stabilize cell membranes so that the cells become less permeable thus

    decreasing the formation of edema, Irritating substances are inhibited from affecting nerve endings and prostaglandin

    synthesis is blocked.

    Examples and uses of antipyretics , analgesics and anti-inflammatory agents:-

    Asprin:- Used as antipyretic, Antirheumatic and antithrombolytic agent

    Paracetamol (Aceteminophen):- Used as antipyretic and mild analgesic

    Analgin(Novalgin):- Used to relieve mild to moderate pain

    Mefenamic acid:- Used in the relief of head ache, tooth ache, muscular pain and stomach pain

    Ibuprofen:- Used to relief muscular pain, tooth ache and joint pain.Diclofenac:- Used in the treatment of rheumatoid arthritis,spondylitis and acute musculoskeletal disorders.

    Antihistamines

    - Histamine is a biological amine widely distributed in the body tissues especially in the mast calls.It is synthesized in th

    body from histidine by decarboxylation.When present in the cell it is inert, but when released it produces a number of

    biological actions such as allergic manifestations,oedema,bronchiole constriction and gastric acid secretion.

    Drug which antagonize the effect of histamine are called antihistamines.There are two groups of antihistamines H1

    receptor antagonists and H2receptor antogonists.When not specified the term antihistamine refer to H1receptor

    antagonists

    Mechanism of action.:-

    i. H1blockers:- They competitively inhibit the interaction of histamines with H1 receptors. Blockade of these

    receptors significantly reduces the secretion of acids and pepsin outputs from the target tissues

    ii. Mast cell stabilizers:- Act by stabilizing the cell membrane of mast cell so that the release of histamine is

    blocked.

    Examples and uses of antihistamines:-

    i. Pheniramines:- Used in the treatment of allergic dermatitis, rhinitis and food allergy

    ii. Clorpheniramine:- Used in the treatment of allergic dermatitis, rhinitis and Urticaria

    iii. Diphenhydramine:- Used in the treatment of all kinds of allergies , cough and cold.

    iv. Doxylamine:- Used as an anti emetic to arrest nausea and vomiting concerned with pregnancy and travelingH2receptor blockers:- As stated earlier histamines activate two types of receptor H1and H2receptors. The activation of

    H2receptors leads to increased gastric acid secretion, increased contraction of the isolated atria and inhibition of

    isolated uterus. These effects are blocked by H2receptor antagonists

    Examples and uses of histamines H2receptor blockers:-

    i. Famotidine :- Used in the treatment of gastric and duodenal ulcer and in the treatment of hyper acidity and

    reflex usophagitis.

    ii. Cimetidine:- Used in the treatment of gastric and duodenal ulcer and in the treatment of hyper acidity.

    iii. Ranitidine:- Used in the treatment of gastric ulcer and reflex eusophagitis

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    Expectorants and antitussives:- Expectorants are drugs employed to aid in the relief of congestions in the

    lower respiratory tract below the epiglottis, in the trachea, bronchi or lungs and therefore they are helpful in the

    treatment of cough

    Expectoration may be caused by :-

    i. Enhancing bronchial secretion

    ii. Making secretion less viscous

    iii. Suppressing cough

    Anti tussives are agents that normally depress the area in the CNS which usually controls the cough reflex

    Examples and uses of expectorants and antitussives:-

    i. Guaifensin:- It is used as an expectorant

    ii. Terpinhydrates:- used as an expectorant in bronchitis

    iii. Benzonatate:-It is used asantitussives

    iv. Levopropoxyphene:- It is used asantitussivesand cough suppressant

    MUSCLE RELAXANT :- Drugs which blocks the transmission of nerve impulses at the neuromuscular junction and

    thereby producing relaxation of the skeletal muscles are known as skeletal muscle relaxants. They are also known as

    neuromuscular blocking agents.

    The skeletal muscles may be relaxed by two different groups of drugs, namely : first, by those exerting an action on the

    CNS and used mainly for the relief of painful muscle spasms in neuromuscular or musculoskeletal disorders; Secondly,

    those affecting neuro muscular transmission that are employed as adjuncts in anaestesia inorder to modify the muscle

    relaxation ability.

    Examples and uses :-

    1) Pancuronium- Used in anaesthesia in surgeries 2) Mephenesin- Used in the relief of muscular spasms

    3) Galamine triethiodide- Used in the treatment of muscular rigidity. 4) Methocarbamol- Used in the treatemen

    of muscular spasm

    ANTIMALARIAL DRUGS:-Malaria is a disease caused by plasmodium parasites which are spreaded by a female mosquit

    from a malaria patient to a normal person.More than one million people die of malaria and most of these peoplebelong to the third world countries . Antimalarials are chemotherapeutic agents which are used for the prevention and

    treatment of malaria . Some of the alkaloids extracted from cinchona bark like quinidine , cinchonine, are found to be

    effective . Soon after II world war a large number of compounds were synthesized and tested for antimalarial actions

    which leads to the discovery of antimalarials such as Chloroquine,Proguanil,Camoquineetc

    ANTISYCOTICS (Tranquilizers):- Antisycortics are primarily employed for the treatment of symptoms in mental

    diseases,their overall influence being to free the mind from passion or disturbance and thus calm the mind ,ie theycause sedation without indusing sleep.

    Tranquilers are drugs essentially used in the management and treatment of sycosis and neurosis.They specifically

    exerts their action on the lower brain area to produce emotional calmness and relaxation without appreciable

    hypnosis,sedation,euphoria or minor impairement. They are used to control the effects of stress and feeling of

    discomfort, tension and disforia in patients with neurosis and mild depressive statesExamples : Chlorpromazine ,

    Chlozapine , Diazepam

    Antiulcer drugs:upper GI tract drugs:The most common problem associated with the stomach is the secretion of excess acid. the stomach is well protected

    with the mucosal cells from the acid and proteinase pepsin.

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    When there is a damage of the mucosal layer erosion can occur in the gastric mucosa leading to a gastric ulcer. Whenthis acid enters the duodenum it can cause duodenal ulcer. In some cases there can be furthererosion and the fluid can leak into the peritoneal cavity leading to life threatening peritonitis. When the acid enter theoesophagus a burning sensation is felt and this is commonly termed as a heart burn and is treated with an antacid.

    Antacids:Mechanism of action: are weak bases which readily combine with the HCl and neutralize it. They also raise the pH of thestomach and over a pH of 4 pepsin is inactive. There are usually basic compounds of Al, Na, Ca, Mg and K. normallyused are AlOH and MgCO3 in combination. These are mixed in a correct

    proportion to nullify the effect of Al causing constipation and mg acting as a laxative. E.g. hydrotalcite.

    Peptic Ulcer:There are three receptors in the stomach that needs to be stimulated for the production of acid they are H2 histaminereceptor, muscarinic cholinergic receptors and gastrin receptors. Gastric ulcers are mainly due to a defect in mucusproduction whereas duodenal ulcers are due to excessive acid production. The use of colloidal bismuth in combination oftwo antibacterials for the treatment of gastric ulcer due to the cause of a bacteria is known as triple therapy.

    Example:-H2 receptor antagonist cimetidine, nizatidine, ranitidine ; Proton pump inhibitor omeprazoleAntacids Aluminium Hydroxide, Magnesium Hydroxide .; Bismuth compoundsSucralfate ; Antibiotics necessary for the treatment against H. Pyroli

    ANTI EMETIC:-Drugs used to treat Nausea and vomiting:To treat vomiting suppositories are convenient whereas in the case of nausea the cause is determined and is preventedthen being cured. When nausea and vomiting is due to the psychogenic factors involving the cortical center of the brainthe use of benzodiazepine is useful as a sedative.

    Antimuscarinic drugs:The only antimuscarinic drug used to treat against emetics is hyoscine and is used in the treatment of motion sickness. Iis available in various forms and is an effective way of treatment. It has a long lasting effect.

    Metoclopramide and domperidone:They reduce the stimulation of the CTZ (Chemoreceptor trigger zone) and as a result prevent nausea and vomiting, theyalso inc the rate of gastric emptying and dec the sensitivity of the receptors in the pharynx and upper gut to noxiousstimuli.

    CANCER & CHAEMOTHERAPY

    Cancer is the uncontrolled growth ofcells coupled withmalignant behavior: invasion andmetastasis.Cancer is thought to

    be caused by the interaction betweengenetic susceptibility and environmental toxins.

    In the broad sense, most chemotherapeuticdrugs work by impairingmitosis (cell division), effectively targetingfast-

    dividing cells.As these drugs cause damage to cells, they are termed cytotoxic. Some drugs cause cells to

    undergoapoptosis (so-called "self-programmed cell death").

    Scientists have yet to identify specific features of malignant and immune cells that would make them uniquely

    targetable. This means that other fast-dividing cells, such as those responsible forhair growth and for replacement of

    theintestinalepithelium (lining), are also often affected. However, some drugs have a betterside effect profile than others

    enablingdoctors to adjust treatment regimens to the advantage of patients in certain situations.

    As chemotherapy affects cell division, tumors with high growth fractionsare more sensitive to chemotherapy, as a larger

    proportion of the targeted cells are undergoingcell division at any time. Malignancies with slower growth rates, such as

    indolent lymphomas, tend to respond to chemotherapy much more modestly.

    Drugs affect "younger" tumors (i.e., more differentiated) more effectively, because mechanisms regulating cell growth are

    usually still preserved. With succeeding generations of tumor cells, differentiation is typically lost, growth becomes less

    regulated, and tumors become less responsive to most chemotherapeutic agents. Near the center of some solid tumors,

    cell division has effectively ceased, making them insensitive to chemotherapy. Another problem with solid tumors is the

    fact that the chemotherapeutic agent often does not reach the core of the tumor. Solutions to this problem

    includeradiation therapy andsurgery.

    http://en.wikipedia.org/wiki/Cell_(biology)http://en.wikipedia.org/wiki/Malignanthttp://en.wikipedia.org/wiki/Metastasishttp://en.wikipedia.org/wiki/Genehttp://en.wikipedia.org/wiki/Mitosishttp://en.wikipedia.org/wiki/Cell_divisionhttp://en.wikipedia.org/wiki/Fast-dividing_cellshttp://en.wikipedia.org/wiki/Fast-dividing_cellshttp://en.wikipedia.org/wiki/Apoptosishttp://en.wikipedia.org/wiki/Hairhttp://en.wikipedia.org/wiki/Intestinehttp://en.wikipedia.org/wiki/Epitheliumhttp://en.wikipedia.org/wiki/Adverse_effect_(medicine)http://en.wikipedia.org/wiki/Physicianhttp://en.wikipedia.org/wiki/Cell_divisionhttp://en.wikipedia.org/wiki/Radiation_therapyhttp://en.wikipedia.org/wiki/Surgeryhttp://en.wikipedia.org/wiki/Surgeryhttp://en.wikipedia.org/wiki/Radiation_therapyhttp://en.wikipedia.org/wiki/Cell_divisionhttp://en.wikipedia.org/wiki/Physicianhttp://en.wikipedia.org/wiki/Adverse_effect_(medicine)http://en.wikipedia.org/wiki/Epitheliumhttp://en.wikipedia.org/wiki/Intestinehttp://en.wikipedia.org/wiki/Hairhttp://en.wikipedia.org/wiki/Apoptosishttp://en.wikipedia.org/wiki/Fast-dividing_cellshttp://en.wikipedia.org/wiki/Fast-dividing_cellshttp://en.wikipedia.org/wiki/Cell_divisionhttp://en.wikipedia.org/wiki/Mitosishttp://en.wikipedia.org/wiki/Genehttp://en.wikipedia.org/wiki/Metastasishttp://en.wikipedia.org/wiki/Malignanthttp://en.wikipedia.org/wiki/Cell_(biology)