Antoprotozoal drugsuvufuguguvuvugug7.pptx

 Introduction
 Protozoal infections are common among people in underdeveloped
tropical and subtropical countries, where sanitary conditions, hygienic
practices, and control of the vectors of transmission are inadequate.
 However, with increased world travel, protozoal diseases, such as
malaria, amebiasis, leishmaniasis, trypanosomiasis,
trichomoniasis, and giardiasis, are no longer confined to specific
geographic locales.
 Because they are unicellular eukaryotes, the protozoal cells have
metabolic processes closer to those of the human host than to
prokaryotic bacterial pathogens. Therefore, protozoal diseases are less
easily treated than bacterial infections, and many of the antiprotozoal
drugs cause serious toxic effects in the host, particularly on cells
showing high metabolic activity.
 Mammals have developed very efficient mechanisms for defending
themselves against invading parasites, but many parasites have, in turn,
evolved sophisticated evasion tactics. One common parasite trick is to
take refuge within the cells of the host, where antibodies cannot reach
them. Most protozoa do this, for example Plasmodium species take up
residence in red cells, Leishmania species infect macrophages
exclusively, while Trypanosoma species invade many other cell types.
The host deals with these intracellular fugitives by spread out cytotoxic
CD8+ T cells and T helper (Th)1 pathway cytokines, such as
interleukin (IL)-2, tumour necrosis factor (TNF)-α and interferon-γ. These
cytokines activate macrophages, which can then kill intracellular
parasites.
 The Th1 pathway responses can be down regulated by Th2 pathway
cytokines (e.g. transforming growth factor-β, IL-4 and IL-10). Some

 CHEMOTHERAPY FOR AMEBIASIS
 Amebiasis (also called amebic dysentery) is
an infection of the intestinal tract caused by
Entamoeba histolytica. The disease can be
acute or chronic, with patients showing
varying degrees of illness, from no
symptoms to mild diarrhea to fulminating
dysentery, ameboma, liver abscess, and
other extraintestinal infections.
 Entamoeba histolytica exists in two forms:
cysts that can survive outside the body, and
labile but invasive trophozoites that do not
persist outside the body.
 Therapy is indicated for acutely ill patients
and asymptomatic carriers, since dormant E.
histolytica may cause future infections in the
carrier and be a potential source of infection
for others.

 Classification of amebicidal drugs
 Therapeutic agents are classified as luminal, systemic, or mixed
(luminal and systemic) amebicides according to the site where the
drug is effective.
1.Mixed amebicides (metronidazole and tinidazole)
 Metronidazole:
 Metronidazole, a nitroimidazole, is the mixed amebicide of choice for
treating amebic infections; it kills the E. histolytica trophozoites.It is
also effective for infections caused by Giardia lamblia, Trichomonas
vaginalis, anaerobic cocci, and anaerobic gram-negative bacilli (for
example, Bacteroides species which cause pelvic inflammatory
disease, intra-abdominal infection, etc.). Metronidazole is the drug of
choice for the treatment of pseudomembranous colitis caused by
the anaerobic, gram-positive bacillus Clostridium difficile.
 In the treatment of H. pylori infection, metronidazole is useful in
combination with clarithromycin or amoxicillin and a proton pump
inhibitor.
 Mechanism of action: anaerobic bacteria and some protozoal
parasites (including amebas) possess ferrodoxin-like electron-
transport proteins that participate in metabolic electron removal
reactions. The nitro group of metronidazole is able to serve as an
electron acceptor, forming reduced cytotoxic compounds that bind to

 Pharmacokinetics: Metronidazole is completely
and rapidly absorbed after oral administration. For
the treatment of amebiasis, it is usually
administered with a luminal amebicide, such as
iodoquinol or diloxanide furoate. This
combination provides cure rates of greater than 90
percent.
 Metronidazole distributes well throughout body
tissues and fluids. The half-life of unchanged drug is
7.5 hours for metronidazole and 12–14 hours for
tinidazole.
 Metabolism of the drug depends on hepatic
oxidation of the metronidazole side chain by mixed-
function oxidase, followed by glucuronidation. So it
is affected by enzyme inducers or inhibitors.
 The parent drug and its metabolites are excreted in
the urine.

 Adverse effects: The most common adverse
effects are those associated with the
gastrointestinal tract, including nausea, vomiting,
epigastric distress, and abdominal cramps.
 An unpleasant, metallic taste is often experienced.
Other effects include oral moniliasis (yeast infection
of the mouth) and, rarely, neurotoxicologic
problems.
 Metronidazole has a disulfiram-like effect, so that
nausea and vomiting can occur if alcohol is
ingested during therapy.
 Tinidazole has a similar adverse-effect profile,
although it appears to be somewhat better
tolerated than metronidazole.
 Resistance: Resistance to metronidazole is not a
therapeutic problem.

 Tinidazole:
 Tinidazole is a second-generation
nitroimidazole that is similar to
metronidazole in spectrum of activity,
mechanism of action, absorption, adverse
effects and drug interactions.
 Tinidazole is as effective as
metronidazole, with a shorter course of
treatment & low dosing frequancy, yet is
more expensive than generic
metronidazole.

 2. Luminal amebicides
 A luminal agent, such as iodoquinol, diloxanide furoate, or
paromomycin, should be administered for treatment of
asymptomatic carriers. It is also required in the treatment of
all other forms of amebiasis.
 Iodoquinol: a halogenated 8-hydroxyquinolone, is
amebicidal against E. histolytica, and is effective against the
luminal trophozoite and cyst forms. The mechanism of action
of iodoquinol against trophozoites is unknown .Side effects
from iodoquinol include rash, diarrhea, and dose-related
peripheral neuropathy, including a rare optic neuritis.
 Diloxanide furoate is a dichloroacetamide derivative. It is
an effective luminal amebicide. In the gut, diloxanide furoate
is split into diloxanide and furoic acid; the mechanism of
action of diloxanide furoate is unknown.
 Diloxanide furoate is considered by many the drug of choice
for asymptomatic luminal infections. It is used with a tissue
amebicide, usually metronidazole, to treat serious intestinal
and extraintestinal infections.
 Diloxanide furoate does not produce serious adverse effects.
Flatulence is common, but nausea and abdominal cramps
are infrequent and rashes are rare.

 Paromomycin: is an aminoglycoside antibiotic, is only effective
against the intestinal (luminal) forms of E. histolytica and
tapeworm, because it is not significantly absorbed from the
gastrointestinal tract. Its direct amebicidal action is through
effects it has on cell membranes, causing leakage, it also exerts
antiamebic actions by reducing the population of intestinal flora
(which are the ameba's major food source). Gastrointestinal
distress diarrhea are the principal adverse effects.
 3-Systemic amebicides
 These drugs are useful for treating liver abscesses or intestinal
wall infections caused by amebas.
 Chloroquine: Chloroquine is used in combination with
metronidazole (or as a substitute for one of the nitroimidazoles in
the case of intolerance) to treat amebic liver abscesses. It
eliminates trophozoites in liver abscesses, but it is not useful in
treating luminal amebiasis. Therapy should be followed with
aluminal amebicide.
 Dehydroemetine: Dehydroemetine is an alternative agent for the
treatment of amebiasis. The drug inhibits protein synthesis by
blocking chain elongation. Intramuscular injection is the
preferred route, since it is an irritant when taken orally.
 The use of this ipecac alkaloid is limited by its toxicity, and it has
largely been replaced by metronidazole. Adverse effects include
pain at the site of injection, nausea, cardiotoxicity (arrhythmias

 CHEMOTHERAPY FOR GIARDIASIS
 Giardia lamblia is one of the most commonly
diagnosed intestinal parasite in the world. It has only
two life-cycle stages: the binucleate trophozoite with
four flagellae, and the drug-resistant, four-nucleate
cyst.
 Although some infections are asymptomatic, severe
diarrhea can occur, which can be very serious in
immune-suppressed patients.
 The treatment of choice is metronidazole for 5 days.
One alternative agent is tinidazole, which is equally
effective as metronidazole in treatment of giardiasis
but with a much shorter course of treatment (2 g
given once).
 Nitazoxanide, a nitrothiazole derivative, is also
approved for the treatment of giardiasis. It is
administered as a 3-day course of oral therapy.
 The anthelmintic drug albendazole may also be
efficacious for giardiasis, and paromomycin is
sometimes used for treatment of giardiasis in

 CHEMOTHERAPY FOR MALARIA
 Malaria is an acute infectious disease caused by
four species of the protozoal genus
Plasmodium. The parasite is transmitted to
humans through the bite of a female Anopheles
mosquito, which lives in humid areas.
 Plasmodium falciparum is the most dangerous
species, causing an acute, rapidly fulminating
disease that is characterized by persistent high
fever, orthostatic hypotension, and massive
erythrocytosis. (an abnormal elevation in the
number of red blood cells accompanied by
swollen, reddish limbs). P. falciparum infection
can lead to capillary obstruction and death
without prompt treatment.
 Plasmodium vivax causes a milder form of the
disease. Plasmodium malariae is common to
many tropical regions, but Plasmodium ovale is
rarely encountered.

 Tissue schizonticide: Primaquine
 Primaquine, an 8-aminoquinoline, is an oral antimalarial drug
that eradicates primary exoerythrocytic (tissue) forms of
plasmodia and the secondary exoerythrocytic forms of
recurring malarias (P. vivax and P. ovale). [Note: Primaquine
is the only agent that prevents relapses of the P. vivax and
P. ovale malarias, which may remain in the liver in the
exoerythrocytic form after the erythrocytic form of the disease
is eliminated (hypnozoites)]
 The sexual (gametocytic) forms of all four plasmodia are
destroyed in the plasma or are prevented from maturing later
in the mosquito, thereby interrupting transmission of the
disease. [Note: Primaquine is not effective against the
erythrocytic stage of malaria and, therefore, is used in
conjunction with agents to treat the erythrocytic form (for
example, chloroquine and mefloquine).]
 Mechanism of action: This is not completely understood.
Metabolites of primaquine are believed to act as oxidants
that are responsible for the schizonticidal action as well as for
the hemolysis and methemoglobinemia encountered as
toxicities.

 Pharmacokinetics: The drug is well absorbed
orally. Primaquine is widely distributed to the
tissues, but only a small amount is bound there. It
is rapidly metabolized and excreted in the urine.
Its metabolites appear to have less antimalarial
activity but more potential for inducing hemolysis
than the parent compound.
 Adverse effects: Primaquine has a low incidence
of adverse effects, except for drug-induced
hemolytic anemia in patients with genetically low
levels of glucose-6-phosphate dehydrogenase.
It results from the drug’s ability to oxidize and
destroy erythrocyte membranes. Hemolysis
occurs because there is insufficient G6PD to
generate enough reduced nicotinamide adenine
dinucleotide phosphate (NADPH) to maintain
glutathione in its reduced form and prevent
oxidation of erythrocyte membranes.
 Others include: abdominal discomfort occasional
methemoglobinemia

 Blood schizonticides:
 1-Chloroquine
 Chloroquine is a synthetic 4-aminoquinoline that has been
the mainstay of antimalarial therapy, and it is the drug of
choice in the treatment of erythrocytic P. falciparum
malaria, except in resistant strains.
 Chloroquine is less effective against P. vivax malaria. It is
highly specific for the asexual form of plasmodia.
Chloroquine is the preferred chemoprophylactic agent in
malarious regions without resistant falciparum malaria.
 Chloroquine is also effective in the treatment of
extraintestinal amebiasis and has anti-inflammatory action
making it a disease modifying anti-rheumatic drug
(DMARD) in rheumatoid arthritis.

 Mechanism of action: Chloroquine probably acts by
concentrating in parasite food vacuoles, preventing the
polymerization of the hemoglobin breakdown product,
heme, into hemozoin(non- toxic product to the parasite),
and thus eliciting parasite toxicity due to the buildup of free
heme. The increased pH and the accumulation of heme
result in oxidative damage to the membranes, leading to
lysis of both the parasite and the red blood cell.

 Pharmacokinetics: Chloroquine is rapidly and completely
absorbed following oral administration. Usually, 4 days of
therapy suffice to cure the disease. The drug concentrates
in erythrocytes, liver, spleen, kidney, lung, melanin-
containing tissues, and leukocytes. Thus, it has a very
large volume of distribution. It persists in erythrocytes. The
drug also penetrates into the CNS and traverses the
placenta. Chloroquine is dealkylated by the hepatic mixed-
function oxidase system, but some metabolic products
retain antimalarial activity. Both parent drug and
metabolites are excreted predominantly in the urine.
 Adverse effects: Chloroquine is usually very well
tolerated, even with prolonged use. Pruritus is common,
primarily in Africans. Nausea, vomiting, abdominal pain,
headache, anorexia, malaise, blurring of vision, and
urticaria are uncommon.
 The long-term administration of high doses of chloroquine
for rheumatologic diseases can result in irreversible

 Chloroquine is contraindicated in patients
with psoriasis or porphyria. It should
generally not be used in those with retinal or
visual field abnormalities or myopathy.
 Chloroquine is considered safe in pregnancy
and for young children.
 Resistance: P. falciparum is now resistant to
chloroquine in most parts of the world.
Resistance appears to result from enhanced
efflux of the drug from parasitic vesicles as a
result of mutations in plasmodia transporter
genes
 Resistance of P. vivax to chloroquine is
growing problem in many parts of the world.

 Atovaquone–proguanil
 The combination of atovaquone–proguanil is
effective for chloroquine-resistant strains of P.
falciparum, and it is used in the prevention and
treatment of malaria. Atovaquone inhibits
mitochondrial processes such as electron
transport, as well as ATP and pyrimidine
biosynthesis. Cycloguanil, the active metabolite
of proguanil, inhibits plasmodial dihydrofolate
reductase, thereby preventing DNA synthesis.
Proguanil is metabolized via CYP2C19, an
isoenzyme that is known to exhibit a genetic
polymorphism resulting in poor metabolism of
the drug in some patients. The combination
should be taken with food or milk to enhance
absorption. Common adverse effects include
nausea, vomiting, abdominal pain, headache,
diarrhea, anorexia, and dizziness.

 Mefloquine
 Mefloquine hydrochloride is a synthetic 4-quinoline
methanol that is chemically related to quinine.
Mefloquine is now considered to be an alternative for
the prophylaxis and treatment of chloroquine-resistant
malaria in areas where it is known to be effective.
 Its exact mechanism of action remains to be
determined, but it can apparently damage the
parasite's membrane.
 Mefloquine is absorbed well after oral administration
and concentrates in the liver and lung. It has a long
half-life (20 days) because of its concentration in
various tissues and its continuous circulation through
the enterohepatic and enterogastric systems.
 Adverse reactions at high doses range from nausea,
vomiting, and dizziness to disorientation,
hallucinations, and depression. Because of the
potential for neuropsychiatric reactions, mefloquine is
usually reserved for treatment of malaria when other
agents cannot be used.

 Quinine
 Quinine (derived from cinchona tree) interferes with heme
polymerization, resulting in death of the erythrocytic form
of the plasmodial parasite. It is reserved for severe
infestations and for malarial strains that are resistant to
other agents, such as chloroquine.
 Quinine is usually administered in combination with
doxycycline, tetracycline, or clindamycin.
 Taken orally, quinine is well distributed throughout the
body. Quinine is primarily metabolized in the liver and
excreted in the urine.
 The major adverse effect of quinine is cinchonism (a
syndrome causing tinnitus, headache, nausea, dizziness,
flushing, and visual disturbances).Mild symptoms of
cinchonism do not warrant the discontinuation of therapy.
However, quinine treatment should be suspended if a
positive Coombs' test for hemolytic anemia occurs. QT
interval prolongation can occur with intravenous quinine.
 Drug interactions include potentiation of neuromuscular-
blocking agents and elevation of digoxin levels if taken
concurrently with quinine.

 Artemisinin
 Artemisinin is derived from the qinghao plant, which has been
used in Chinese medicine. Two derivatives of artemisinin called
artemether and artesunate were subsequently found to have
potent activity against the erythrocytic stages of malaria.
 Artemisinin (or one of its derivatives) is available for the treatment
of severe, multidrug-resistant P. falciparum malaria. Their short
half-lives prevents their use in chemoprophylaxis.
 To prevent the development of resistance, these agents should
not be used alone. For instance, artemether is coformulated with
lumefantrine (an antimalarial drug similar in action to quinine or
mefloquine) and used for the treatment of uncomplicated malaria.
Artesunate may be combined with sulfadoxine–pyrimethamine,
mefloquine, clindamycin, or others.
 Its antimalarial action may result from the production of free
radicals that follows the iron-catalyzed cleavage of the formed
artemisinin endoperoxide bridge in the parasite food vacuole. The
free radicals alkylate (add methyl groups to) heme and proteins in
malarial parasites and inhibit erythrocytic schizogony.
 Oral, rectal, and intravenous preparations are available. It is
metabolized in the liver and are excreted primarily in the bile.
 Adverse effects include nausea, vomiting, and diarrhea.
Extremely high doses may cause neurotoxicity and prolongation
of the QT interval.

 Pyrimethamine
 The antifolate agent pyrimethamine, a 2,4-diaminopyrimidine
related to trimethoprim, frequently employed as a blood
schizonticide. It also acts as a strong sporonticide in the
mosquito’s gut when the mosquito ingests it with the blood of the
human host.
 Pyrimethamine inhibits plasmodial dihydrofolate reductase at
much lower concentrations than those needed to inhibit the
mammalian enzyme. The inhibition deprives the protozoan of
tetrahydrofolate.
 Pyrimethamine, in combination with with sulfadoxine, is effective
against P. falciparum, P. malariae and Toxoplasma gondii. If
megaloblastic anemia occurs with pyrimethamine treatment, it
may be reversed with folinic acid.
 Antibiotics
 Tetracycline, doxycycline and clindamycin are active against
erythrocytic schizonts of all human malaria parasites. They can
be used in the treatment of falciparum malaria in conjunction with
quinine, allowing a shorter and better-tolerated course of that
drug.
 They appear to act against malaria parasites by inhibiting protein
synthesis in a plasmodial prokaryote-like organelle, the
apicoplast. None of the antibiotics should be used as single
agents in the treatment of malaria because their action is much

 TREATMENT OF LEISHMANIASIS
 There are three types of leishmaniasis: cutaneous,
mucocutaneous, and visceral. In the visceral type (liver and
spleen), the parasite is in the bloodstream and can cause very
serious problems.
 The treatment of leishmaniasis is difficult, because the effective
drugs are limited by their toxicities and failure rates.
 Pentavalent antimonials, such as sodium stibogluconate, are
the conventional therapy used in the treatment of leishmaniasis,
with pentamidine and amphotericin B as backup agents.
Allopurinol has also been reported to be effective.
 Sodium stibogluconate
 Sodium stibogluconate is not effective in vitro. Therefore, it has
been proposed that reduction to the trivalent antimonial
compound is essential for activity.
 The exact mechanism of action has not been determined.
Evidence for inhibition of glycolysis in the parasite at the
phosphofructokinase reaction has been found. Because it is not
absorbed on oral administration, sodium stibogluconate must be
administered parenterally, Metabolism is minimal, and the drug is
excreted in the urine.
 Adverse effects include pain at the injection site, gastrointestinal
upsets, and cardiac arrhythmias. Renal and hepatic function
should be monitored periodically.

 Pentamidine
 pentamidine is an aromatic diamidine used for
pneumocystosis ,african trypanosomiasis
(sleeping sickness) and leishmaniasis. It is only
administered parenterally. pentamidine is a
highly toxic drug causing many adverse effects
including pancreatic toxicity, reversible renal
insufficiency and others.
 Miltefosine
 Miltefosine is the first orally active drug for
visceral leishmaniasis. It may also have some
activity against cutaneous and mucocutaneous
forms of the disease.
 The precise mechanism of action is not known,
but miltefosine appears to interfere with
phospholipids in the parasitic cell membrane to
induce apoptosis.
 Nausea and vomiting are common adverse
reactions.

 TREATMENT OF TOXOPLASMOSIS
 One of the most common infections in humans is
caused by the protozoan Toxoplasma gondii. An
infected pregnant woman can transmit the organism
to her fetus. Cats are the only animals that shed
oocysts, which can infect other animals as well as
humans.
 Pyrimethamine, in combination with sulfadiazine, is
first-line therapy in the treatment of toxoplasmosis,
including acute infection, congenital infection, and
disease in immunocompromised patients. Folinic
acid is included to limit myelosuppression. Toxicity
from the combination is usually due primarily to
sulfadiazine.
 Alternative regimens combining azithromycin,
clarithromycin or clindamycin with either
trimethoprim– sulfamethoxazole or pyrimethamine
and folinic acid. Spiramycin(a macrolide antibiotic),
which concentrates in placental tissue, is used to
treat acute acquired toxoplasmosis in pregnancy to

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