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Anthelmintic drugs presentation
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- 2. o Introduction oHelminths oTypes ofHelminths oHelminths infection o Anthelmintics drugs /anti helminths o Classification of Anthelmintic Drugs o Description
- 3. Helminth isa general term meaning “worm” macroscopic, multicellular, eukaryotic invertebrates characterized by elongated, flat or round bodies Life cycles are complex Intermediate hosts are often needed to support larval stages
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- 5. Based onthe external and internal morphology of egg, larval, and adult stages. Three groups of helminthes ◦ Cestodes (tapeworm) ◦ Trematodes (fluke) ◦ Nematodes (roundworm)………… (STHs or Geohelminths)
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- 7. o Adult tapeworms Elongated Segmented inhabit the intestinal lumen o Larval forms Cystic or Solid Inhabit extraintestinal tissues.
- 8. o Adult worms leaf-shaped flatworms Prominent oral and ventral suckers help maintain position in situ. Flukes are hermaphroditic
- 9. o Adult roundworms clindrical bisexual inhabitintestinal& extrintestinal tissues o Larval forms clindrical bisexual inhabit intestinal& extrintestinal tissues
- 10. Infections withhelminths, or parasitic worms. affect more than two billion people worldwide Human is the primary host In the human body GIT is the abode of many helminths, but some also live in tisues, or their larvae migrates into tissues. They harm the host by depriving him of food, causing blood loss, injury to organs, intestinal or lymphatic obstruction and by secreting toxins Helminthiasis is rarely fatal, but is amajor cause of ill health
- 11. oTapeworms (cestodes) • Echinococcusgranulosus………………………Hydatid Disease •T. solium………………………………………..…. Cysticercosis o Flukes (trematodes) • Schistzoma (Schistozomes)………………….. Schistosomiasis oRoundworms (nematodes) • Enterobius vermicularis(pinworm)………..…Enterobiasis • Ascaris lumbricoid(Roundworm)….………......Ascariasis • Trichuris trichiura (whipworm)………….…..Trichuriasis • Necator americanus (hookworm)……………Nectariasis • Wuchereria bancrofti ……......………………..(Elephantiasis)
- 12. Lippincott's Illustrated Reviews:Pharmacology, 4th Edition
- 13. Anthelmintics area group of antiparasitic drugs that • Expel parasitic worms (helminths) & • Other internal parasites from the body by • Either stunning Or killing them
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- 15. Affect metabolic processes eitherdifferent in worms than human hosts are not found in humans Cause death of the worm by interfering with normal functioning
- 16. Lippincott's Illustrated Reviews:Pharmacology, 4th Edition
- 17. Anthelmintics are classifiedbased upon their chemical structures. i) Piperazines: eg. Diethylcarbamazine citrate, Piperazine citrate. ii) Benzimidazoles: eg. Albendazole, Mebendazole, Thiabendazole. iii) Heterocyclics: eg. Oxamniquine, Praziquantel. iv) Natural products: eg. Ivermectin, Avermectin. v) Vinyl pyrimidines: eg. Pyrantel, Oxantel. vi) Amide: eg. Niclosamide . vii) Nitro derivative: eg. Niridazole. viii) Imidazo thiazole:eg. Levamisole.
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- 20. The discoveryof the anthelmintic properties of piperazine usually is credited to Fayard (1949), Piperazine was first introduced as an anthelmintic in 1953.
- 21. organic compound 6-membered ring containing two nitrogen atoms Moderate oral absorption Partly metabolized in liver & excreted in urine
- 22. GABA agonistic actionopening CL channels Flaccid paralysis & Expel alive worms Hyperpolarization & Relaxation of worms muscle Anthelmintic Actions
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- 24. Highly effective against Ascaris lumbricoides Enterobius vermicularis 4gO.D * 2 day 50mg/kg/day * 7 day Clinical Uses
- 25. Nausea, vomiting,abd.discomfort, urticaria High Dose- dizzines,excitement Toxic Dose- convulsions, pralysis due to resp.failure Adverse effects occur as a result of the release of proteins from dying adult worms. Adverse Reactions
- 26. Pregnancy Renalinsuffiency epiliptics Contraindications & Cautions
- 27. Piperazine (Vermizine) Oral: piperazinecitrate tablets 250 mg piperazine citrate syrup 500mg/5 mL
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- 29. The discoveryby Brown and coworkers(1962) that thiabendazole possessed potent activity against gastrointestinal nematodes sparked Development of the BZAs as broad-spectrum anthelmintic agent Of the hundreds of derivatives tested, those most therapeutically useful have modifications at the 2 and/or 5 positions of the benzimidazole ring system Three compounds, thiabendazole, mebendazole, and albendazole, have been used extensively for the treatment of human helminth infections
- 30. Mebendazole isthe prototype, synthetic benzimidazole that has a wide spectrum of anthelmintic activity and a low incidence of adverse effects. Highly effective against gastrointestinal nematode infections Mebendazole came into use in 1971
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- 32. BZAs haveonly limited solubility in water Less than 10% of orally administered mebendazole is absorbed Rapidly converted to inactive metabolites(1st pass metabolism) The absorbed drug is protein-bound (> 90%) Abs. With fatty meal & co-adm. With Cimitidine
- 33. Blocks Glucose uptake InhibitsMicrotubule Synthesis By binding to b-tubulin &
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- 35. whipworm (Trichuris trichiura), pinworm (Enterobius vermicularis) 100mgBD * 3 Day Clinical Uses hookworms (Necator americanus) roundworm (Ascaris lumbricoides) 100mg BD * 3 Day 100mg BD * 3 Day 100mg BD * 3 Day Drug of Choice for STH Infection
- 36. Overall, theBZAs have excellent safety profiles Overall, the incidence of side effects, primarily mild GI symptoms, occurs in only 1% of treated children Rare side effects, usually with high-dose therapy, are hypersensitivity reactions (rash, urticaria), abdominal pain distention and Diarrhea (in cases of massive infestation and expulsion of gastrointestinal worms) Adverse Reactions
- 37. Not givenduring pregnancy ( potent embryotoxin and teratogen in laboratory animals; effects may occur in pregnant rats at single oral doses as low as 10 mg/kg.) hypersensitive peoples children under 2 years (No safety data)
- 38. free-living nematodeCaenorhabditis elegans and the sheep nematode Haemonchus contortus, displays reduced high-affinity drug binding to b-tubulin alterations in b-tubulin isotype gene expression correlate with drug resistance
- 39. Mebendazole (Vermox) Oral: 100mg chewable tablets, 100 mg/5 mL suspension
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- 42. Pyrazin isoquinolinederivative Praziquantel developed after this class of compounds was discovered to have anthelmintic activity in 1972 In animals and humans, infections with many different cestodes and trematodes respond favorably to this agent, whereas nematodes generally are unaffected
- 43. rapidly absorbed bioavailability 80% after oral administration serum conc. are reached in 1-3h About 80% of the drug is protein bound Excretion is mainly via the kidneys (60-80%) and bile (15-35%). Abs. With fatty meal & co-adm. With Cimitidine
- 44. cell membranes permeabilityto Ca++ spastic paralysis contraction Anthelmintic Actions
- 45. Schistomiasis (Blood fkukes) Liver flukes 20mg/kg TID* 4-6 hr apart Clinical Uses Intestinal flukes 25 mg/kg TID *4-8 hrs apart 25 mg/kg TID *4-8 hrs apart Drug of Choice for all forms of schistosomiasis
- 46. Mild andtransient adverse effects are common headache, dizziness, drowsines, nausea, vomiting, abdominal pain, loose stools, pruritus, urticaria, arthralgia, myalgia, and low-grade fever Such side effects and increases in eosinophilia often relate to parasite burden.
- 47. safe inchildren over 4 years of age Praziquantel is contraindicated for the treatment of ocular cysticercosis, because destruction of the organism in the eye may damage the organ.
- 48. Praziquantel (Biltricide) Oral: 600mg tablets
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- 51. In themid-1970s Isolation of the anthelmintic components from soil actinomycete Streptomyces avermitilis led to discovery of the avermectins, a novel class of 16-membered lactones Ivermectin is a semisynthetic analog of avermectin (macrocyclic lactone) In 1996, the FDA approved the use of ivermectin in humans for treatment of onchocerciasis, the filarial infection responsible for river blindness, and for therapy of intestinal strongyloidiasis.
- 52. Ivermectin isused only orally in humans Rapidly absorbed following oral administration with meals Reaching maximum plasma concentrations in 4 hours Excretion of the drug and its metabolites is almost exclusively in the feces.
- 53. targets the parasite'sglutamate-gated Cl- channel receptors paralysis of the worm Chloride influx is enhanced hyperpolarization Anthelmintic Actions
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- 55. ONCHOCERCIASIS STRONGYLOIDIASIS 150mcg/kg*every 6-12 months ClinicalUses Cutaneous larva migrans 200 mcg/kg BD *once monthly single 200-mcg/kg oral dose drug of choice in strongyloidiasis and onchocerciasis
- 56. Ivermectin toxicitynearly always results from Mazzotti-like reactions to dying Helminths (fever, headache, dizziness, somnolence, and hypotension).
- 57. Meningitis (because theirblood-brain barrier is more permeable and CNS effects might be expected) pregnancy
- 58. Ivermectin (Mectizan, Stromectol) Oral:3, 6 mg tablets
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- 61. First introducedinto veterinary practice as a broad-spectrum anthelmintic directed against pinworm, roundworm, and hookworm infections Its effectiveness and lack of toxicity led to its trial against related intestinal helminths in humans
- 62. Pyrantel pamoateis a tetrahydropyrimidine derivative Poorly absorbed orally Exerts its effects in the intestinal tract
- 63. Depolarizing neuromuscular blockingagents Contraction & Paralysis & expulsion of worms Causes release of Ach and inhibition of cholinesterase Anthelmintic Actions
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- 65. ascariasis enterobiasis standard dose is11 mg /kg (maximum 1 g) Clinical Uses hookworm infections 200 mcg/kg BD *once monthly single 200-mcg/kg oral dose Pyrantel pamoate is an alternative to mebendazole
- 66. Mild andInclude: Nausea, Vomiting, and Diarrhea
- 67. Some liverdysfunction patient showed low, transient aminotransferase elevations Pegnancy & Children (No Safety data)
- 68. Pyrantel pamoate (Antiminth,Combantrin) Oral: 180 mg tablets 50 mg/ml suspension 62.5 mg capsules
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- 71. Niclosamide isa salicylamide derivative A second-choice drug to praziquantel for treating human intestinal infections with Taenia saginata and most other Cestodes Introduced in the 1960s for human use as a taeniacide
- 72. Minimally absorbedfrom the gastrointestinal tract Neither the drug nor its metabolites have been recovered from the blood or urine.
- 73. Inhibit the parasite'smitochondrial phosphorylation of ADP Also inhibit Anaerobic metabolism which produces usable energy in the form of ATP Anthelmintic Actions
- 75. TAENIA SAGINATA (BEEF TAPEWORM) T.SOLIUM (PORK TAPEWORM), A single 2 g dose Clinical Uses OTHER TAPEWORMS A single 2 g dose 7-day course of treatment Niclosamide is an alternative to Praziquantel
- 76. Infrequent, mild: nausea,vomiting, diarrhea, and abdominal discomfort Therapy with niclosamide poses a risk to people infected with T. solium,( because ova released from drug-damaged gravid worms develop into larvae that can cause cysticercosis).
- 77. Niclosamide, alongwith oxyclozanide, another anti-tapeworm drug, was found in a 2015 study to display "strong in vivo and in vitro activity against methicillin-resistant Staphylococcus aureus (MRSA)". A 2016 drug repurposing screening study suggested that niclosamide may inhibit Zika virus replication in vitro.
- 78. Niclosamide (Niclocide) Oral: 500mg chewable tablets
- 79. 1)Goodman & GilmanThe Pharmacological Basis of Therapeutics 11th Edition 2)Katzung Pharmacology 10th Edition 3)Lippincott's Illustrated Reviews: Pharmacology, 4th Edition 4)www.google.com