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Praziquantel

Praziquantel is an antihelminthic drug used to treat a variety of parasitic infections, including schistosomiasis, clonorchiasis, and opisthorchiasis.
It works by damaging the tegument of the parasites, causing them to detach from the host's intestinal wall or other tissues.
Praziquantel is considered the drug of choice for the treatment of schistosomiasis, a neglected tropical disease affecting millions of people worldwide.
Its efficacy, safety profile, and ease of administration have made it an important tool in the global effort to control and eliminate schistosomiasis.
Reserach on optimizing praziquantel protocols can help improve the reproducibility, accuracy, and efficiency of studies involving this important antihelminthic medication.

Most cited protocols related to «Praziquantel»

Case studies are in-depth investigations of a single instance of a phenomenon in its real-life context (Yin 1994 ). They are to be distinguished from other research designs, such as controlled comparisons, formal modelling, quantitative analyses and randomized-controlled experiments. A substantial body of work offers guidance on case study methodology (Yin 1994 ; Brady and Collier 2004 ; George and Bennett 2004 ; McKeown 2004 ; Yin 2004 ).
Case study methodologists argue that asking just a few basic questions about the case can improve the value of the study considerably. First, what is it a case of (George and Bennett 2004 )? Is it, say, an example of health policy implementation failure, of effective transfer of a health policy from one country to another, of health policy network influence on agenda setting, of the influence of political factors on health policy evaluation? Sometimes cases may be clearly identifiable by the researcher at the start of the study, sometimes they may be constructed or re-constructed during the course of the research as the analysis reveals their defining characteristics (Ragin and Becker 1992 ). The process of clarifying ‘the case’ enables the researcher to specify a body of knowledge to which he or she may make a contribution. Second, why is this case a useful one to study (George and Bennett 2004 )? Does it offer the possibility of comparing the explanatory value of alternative theories? Is it an unusual example of policy effectiveness, potentially offering insight into factors that facilitate policy impact? It is consideration of these issues that help the researcher to select the tools and theories that might frame a study, and to determine which methods will be used.
A study on the global availability of praziquantel, a drug for the tropical disease schistosomiasis, offers clear answers to both questions (Reich and Govindaraj 1998 (link)). The researchers document how the discovery of this effective drug did not automatically result in it reaching the poor in developing countries. They identify this as a case of the gap between drug development and drug availability for the poor—an issue of concern for many tropical disease pharmaceuticals—and highlight the usefulness of this case in revealing the influence of political and economic factors on this gap. Their careful case selection and classification enable them to suggest a set of policy prescriptions on surmounting the drug development–availability gap, recommendations that apply well beyond the case itself.
Another means of facilitating generalization is increasing the number of cases. Doing so is not always easy, since investigating even a single case is a time and resource intensive process that requires careful consideration of historical and contextual influences. Comparative case studies may introduce the further challenges of working across multiple languages and cultures. It can also be difficult to find sufficient funds for undertaking such research. Yet there are several strong examples in the health policy field.
Lee et al. (1998 (link)) used matched country comparisons to investigate factors influencing the development of strong national family planning programmes. They conducted four country comparisons: Bangladesh/Pakistan, Tunisia/Algeria, Zimbabwe/Zambia and Thailand/Philippines. Each pair was matched on socio-economic characteristics, but differed on the strength of the family planning programme. The comparisons enabled the researchers to point to three factors that shaped the development of effective programmes: the formation of coalitions among policy elites, the spread of policy risk, and the country's financial and institutional stability. Walt et al. (1999 (link)) considered individual cases of donor aid coordination in the aid-dependent countries of Bangladesh, Cambodia, Mozambique, South Africa and Zambia to develop generalizations concerning the origins and effectiveness of aid coordination mechanisms. Shiffman (2007 (link)) explored agenda-setting for maternal mortality reduction in five countries: Guatemala, Honduras, India, Indonesia and Nigeria. He identified nine factors that shaped the degree to which this issue emerged as a political priority. He found that while international donors played a role, even more critical were efforts by national champions.
Collectively, these different examples highlight the value of cross-country comparative study approaches, where comparisons between similar (and different) country contexts can help disentangle generalizable from country context-specific effects in policy adaptation, evolution and implementation. Comparisons can be incorporated into study design, ad-hoc, as in the case of Lee et al. (1998 (link)) above; researchers can select as case studies several countries with a shared feature (Brugha et al. 2005 ), see Box 1; or comparison can be made post-hoc, as in the case of Walt et al. (1999 (link)). Clearly, multi-country studies are more time and resource intensive.
Publication 2008
Acclimatization Biological Evolution Donors Family Planning Programs Generalization, Psychological Human Body Pharmaceutical Preparations Political Factors Praziquantel Prescriptions Reading Frames Schistosomiasis

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Publication 2001
Praziquantel
Seven ‘population’ isolates were collected from schoolchildren in the Hoima district of Uganda in June 2004; 4 consisted of pooled isolates from 20 children at 4 randomly selected primary schools and the remaining 3 were isolates from individual children. Miracidia were also collected from a fourth infected child, but isolate establishment in the laboratory host failed in this case (Table 2: see Fig. 1 for location of schools). Infected children were identified by positive Kato-Katz smears and all examined children were treated with praziquantel at 40 mg/kg. Miracidia were hatched from faecal samples in bottled spring water. Samples were divided and 48 to 150 miracidia used for the immediate exposure of laboratory bred Biomphalaria glabrata (strain NHM2), at a dose of 6 miracidia per snail. The remaining samples were stored on Whatman FTA® Indicator cards (Whatman plc, Maidstone, UK). The number of snails exposed varied according to the number of miracidia hatched (Table 2). Snails were transported to the UK, where they were maintained in the laboratory in bottled spring water (Sainsburys Supermarkets plc, London, UK) and fed ad libitum on freshly washed lettuce. The laboratory was maintained at 27 °C and subject to a light regime of 12 h light and 12 h darkness, with a 30-min gradual transition at ‘dawn’ and ‘dusk’. Snails were maintained for 35-40 days, the pre-patent period during which larval development to the cercarial stage takes place. Following this time, cercariae from each snail were induced to shed by placing snails in the dark for 24 h and subsequently exposing them, at 10 am to an overhead light source (100 W) for 2 h in vials containing 16 ml of water. Cercariae from the snails representing one isolate were pooled and used to infect 5-10 laboratory mice (strain TO) per isolate at a dose of 220 cercariae per animal by paddling for 0·5 h in 30 ml of infected water. At 7 weeks post-infection, before signs of pathology had occurred, mice were asphyxiated using a rising concentration of carbon dioxide. Adult schistosomes (which varied in number from 24 to several hundred established worms per 4-mouse isolate) were recovered by a modified hepatic perfusion technique (Smithers and Terry, 1965 (link)). Thirty randomly selected adult worms were stored in 100% ethanol until required for genetic analysis, except for isolate Run-1 where only 24 adult worms were recovered and stored. Miracidia from eggs in each of the livers were stimulated to hatch by maceration through a sieve and exposure to a bright light (100 W) source for 30 min in 100 ml of deionized water. Liver samples of each isolate separately, were pooled and 30-50 miracidia per isolate stored for PCR analysis on Whatman FTA® Indicator cards (Whatman plc, Maidstone, UK), with the exception again of isolate Run-1 where a total of only 25 miracidia were successfully hatched.
DNA was extracted from the 30 (or 24 for Run-1) adult worms using phenol chloroform and ethanol precipitation (Davies et al. 1999 (link)) and from 30 field and 30 laboratory miracidial samples (25 for Run-1) as described above. All samples were subject to multiplex PCR for 7 microsatellite loci as described above. A sample size of 30 was selected as this represented the smallest field miracidial sample (isolate Kib-P).
Publication 2006
Adult Animals Australorbis glabratus Carbon dioxide Cercaria Child Chloroform Darkness Eggs Ethanol Feces Helminths Infection Lactuca sativa Larva Light Liver Mice, House Mice, Laboratory Multiplex Polymerase Chain Reaction Perfusion Phenols Praziquantel Schistosoma Short Tandem Repeat Snails Strains

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Publication 2002
Child Pharmacy Distribution Praziquantel

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Publication 2011
Albendazole Anthelmintics Antibody Formation Antiretroviral Therapy, Highly Active Birth BLOOD Child Childbirth Clinic Visits Communicable Diseases Cytokine Diarrhea Hemoglobin Hookworm Infections Immunization Infant Malaria Maternal Inheritance Measles Mothers Patients Physicians Placebos Pneumonia Praziquantel Response, Immune Schistosomiasis Toxoid, Tetanus Tuberculosis Twins Vertical Infection Transmission Vision Youth

Most recents protocols related to «Praziquantel»

We used two separate tools (See https://tinyurl.com/mkudxmsw) and (See https://tinyurl.com/mudvvh7t) to document responses from female MPMS and HCPs, respectively. For HCPs, demographic information including age, gender, profession, year of practice and place of work were documented. In addition, we collected information on HCPs expertise on a range of symptoms/condition that overlaps with FGS pathology. These included; (i) if the practitioner performs pelvic examination, (ii) treat venereal diseases, (ii) lower abdominal pain, (iv) dysuria or (v) hematuria. Knowledge of HCPs about schistosomiasis and FGS were also documented, with emphasis on (i) awareness, (ii) source of information, (iii) transmission routes, (iv) preventive practices, (v) treatment choices with emphasis on pregnant women, and (vi) dosage requirements for children and adult. HCPs were also asked if FGS patients should be quarantined and if care commodities for FGS patients are available in their place of work (See S1 File)
Similarly for female MPMS, we collected information on age, religion, parents’ occupation and income. In addition, knowledge about schistosomiasis and FGS were documented, with emphasis on awareness and source of information. We also documented if MPMS (i) have ever been treated with praziquantel, (ii) had contact with freshwater, or (iii) had experienced any of the following symptoms that overlaps with FGS pathology; hematuria, painful urination, lower abdominal pain and venereal diseases (See S1 File).
Publication 2023
1-methyl-1-piperidinomethane sulfonate Abdominal Pain Adult Awareness Child Dysuria Gender Hematuria Parent Patients Pelvic Examination Praziquantel Pregnant Women Schistosomiasis Selection for Treatment Sexually Transmitted Diseases Transmission, Communicable Disease Woman
Spironolactone (SPL) was obtained from Sigma-Aldrich, St. Louis, MO, USA. Poly(lactic-co-glycolic acid) (PLGA) (lactide–glycolide 50:50 (ester terminated) and 75:25 (acid terminated), Viscosity 1 and 0.2 dL/g, respectively) was kindly supplied by Purac Biomaterials, Holland. Polyvinyl alcohol (87.0–89.0% hydrolyzed, molecular weight 31,000–50,000 Da) was obtained from Acros Organics, Belgium. Acetone, methylene chloride, dimethylsulfoxide (DMSO), and methanol were bought from Adwic, EL Nasr Pharmaceutical Chemicals, Co., Egypt. All other materials were of fine analytical grades. Praziquantel (PZQ) was supplied from Alexandria Company for Pharmaceuticals & Chemical Industries, Egypt.
Publication 2023
Acetone Acids Biomaterials dilactide Esters glycolic acid Methanol Methylene Chloride Pharmaceutical Preparations Poly A Polylactic Acid-Polyglycolic Acid Copolymer Polyvinyl Alcohol Praziquantel Spironolactone Sulfoxide, Dimethyl Viscosity
The study protocol was approved by the Federal University of Ceará (UFC) Ethical Committee (Opinion N. 3.706.472) and was conducted with adherence to the Resolution N. 466/12 of the Brazilian Health Council and to the Declaration of Helsinki, as revised in 1975, 1983, 1989, 1996, and 2000.
Treatment with praziquantel (PZQ) (Farmanguinhos, Ministry of Health, Brazil) was offered to all individuals free of charge, regardless of infection status at baseline. It was performed with a single dose of 60 mg/kg for children (≤15 years old) and 50 mg/kg for adults, as recommended by the Brazilian Ministry of Health37.
Publication 2023
Adult Child Infection Praziquantel
We manipulated food availability and the intensity of helminthic infections by provisioning with bananas, and by supplying antiparasitic drugs, respectively. Both groups were provisioned during winter (i.e. the season of food shortage for capuchins in Iguazú), but with different regimes: a high provisioning (3 bananas/platform × 3 platforms/site × 3 sites = 27 bananas), and a low provisioning regime (2–3 bananas/platform × 1 platform/site × 1–3 sites = 2–9 bananas). The low provisioning functioned as a control, reducing the chances of potential differences attributable to banana consumption/provisioning itself. To reduce the intensity of helminthic infections, we supplied approximately a randomly selected half of adults/subadults each year within each group with antiparasitic drugs, using a cocktail of ivermectin, which reduces infections by nematodes and ectoparasites, and praziquantel, which removes cestodes. Details of both experimental treatments, provisioning and parasite removal, are described in our previous study36 (link) and Supplementary Tables S1S2.
Publication 2023
Adult Antiparasitic Agents Banana Capuchin Monkey Cestode Infections Food Helminthiasis Ivermectin Nematode Infections Parasites Praziquantel Therapies, Investigational
All experiments were conducted on samples from Icelandic horses with and without clinical allergy (Table 1). All horses lived together in the same environment with similar natural exposure to Cul midges from mid-April to mid-October. Cul were absent from the environment during winter months. Vaccination and deworming were synchronized. All horses were annually vaccinated against rabies, tetanus, West Nile virus and Eastern and Western Encephalitis virus, as well as dewormed with moxidectin and praziquantel (Zoetis, Parsipanny, NJ, USA) once a year in December. All horses were on the same diet. They were kept full time on large pastures with run-in-sheds, free access to water, mineral salt blocks, were grazing in the summer and fed grass hay in the winter.
Icelandic horses in this study were either clinically healthy or had seasonal, recurrent Cul hypersensitivity. Cul hypersensitivity was confirmed, as previously described (19 (link)), by intradermal skin testing with Cul whole body extract (WBE; Stallergenes Greer Inc., Cambridge, MA, USA) in comparison to injections with saline and histamine as negative and positive controls, respectively. Allergic horses developed immediate reactions to Cul WBE, while healthy horses did not. Allergic horses (n=7) included 5 mares (12-18 years, median 17 years), 1 gelding (age 10) and 1 stallion (age 9). All 7 allergic horses and 6 of the healthy horses were also used in our previous study which characterized IgE+ plasmablasts in horses (17 (link)). The prior study took place in the summer and winter preceding the year of this study. Allergic horses had a history of seasonal Cul hypersensitivity for at least 3 years (median 8, range 3-8 years) before this study took place. Healthy horses (n=10) included 5 mares (ages 8-10 years, median 8 years) and 5 geldings (8-10 years, median 9 years).
Blood samples were obtained from the V. jugularis using the BD Vacutainer system (Becton Dickinson, Franklin Lakes, NJ). Samples were collected from all horses weekly from March 22-April 26, twice weekly from May 3-June 10, twice monthly from June 17- November 15, and once in February and December. Midges were first observed in the environment for a few days during the weeks of April 5 and April 19. April 26 was the last day in the spring when the temperature dropped to freezing temperature. Daily minimum and maximum temperatures were recorded from wunderground.com at a weather station <1 mile from the horse pasture.
At every blood collection day, clinical allergy scores were assigned to each horse as previously described (29 (link)). Scores were given based on pruritis (0-3), alopecia (0-4), and dermatitis (0-3) and total scores ≥3 represent horses with clinical allergy. Allergic horses developed clinical allergy and had clinical scores above 3 on average 15 timepoints (standard deviation 3.7) during the summer. Healthy horses never developed clinical signs or scores above 3. The first day when any allergic horse had clinical signs with a score above 3 was May 24.
All animal procedures were carried out in accordance with the recommendation in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The animal protocol was approved by the Institutional Animal Care and Use Committee at Cornell University (protocol #2011–0011). The study also followed the Guide for Care and Use of Animals in Agricultural Research and Teaching.
Publication 2023
Allergic Reaction Alopecia Animals Animals, Laboratory BLOOD Dermatitis Diet Encephalitis Viruses Equus caballus Histamine Human Body Hypersensitivity Institutional Animal Care and Use Committees Minerals moxidectin Poaceae Praziquantel Pruritus Rabies Vaccines Saline Solution Sodium Chloride, Dietary Specimen Collection Toxoid, Tetanus Vaccination West Nile virus

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Praziquantel is a pharmaceutical compound primarily used as an antiparasitic agent. It is a crystalline solid and is used in the treatment of various parasitic infections, particularly those caused by trematodes and cestodes. Praziquantel acts by disrupting the calcium homeostasis of the parasites, leading to their death or expulsion from the host.
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DMSO is a versatile organic solvent commonly used in laboratory settings. It has a high boiling point, low viscosity, and the ability to dissolve a wide range of polar and non-polar compounds. DMSO's core function is as a solvent, allowing for the effective dissolution and handling of various chemical substances during research and experimentation.
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Acetonitrile is a colorless, volatile, flammable liquid. It is a commonly used solvent in various analytical and chemical applications, including liquid chromatography, gas chromatography, and other laboratory procedures. Acetonitrile is known for its high polarity and ability to dissolve a wide range of organic compounds.
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Biltricide is a pharmaceutical product manufactured by Bayer. It is a type of lab equipment used for medical and scientific purposes. Biltricide is designed to perform specific functions within a laboratory setting.
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HEPES buffer is a widely used buffer solution that maintains a stable pH environment. It is commonly used in cell culture, biochemical assays, and various laboratory applications to maintain the desired pH conditions for experiments and analyses.
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Penicillin is a type of antibacterial drug that is widely used in medical and laboratory settings. It is a naturally occurring substance produced by certain fungi, and it is effective against a variety of bacterial infections. Penicillin works by inhibiting the growth and reproduction of bacteria, making it a valuable tool for researchers and medical professionals.
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Penicillin G sodium salt is a white crystalline powder that is a common antibiotic compound. It functions as a bactericidal agent by inhibiting the synthesis of bacterial cell walls.
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Albendazole is a laboratory product used for the detection and measurement of certain parasitic worms. It functions as an anthelmintic, which means it is effective against parasitic worms. The core function of Albendazole is to aid in the diagnosis and management of parasitic infections.
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Praziquantel tablets are a pharmaceutical product manufactured by Merck Group. They are used as an antiparasitic medication. The core function of these tablets is to treat infections caused by various types of parasitic worms.
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Thiazolyl blue tetrazolium bromide (MTT) is a yellow tetrazolium salt that can be reduced to a purple formazan product by dehydrogenase enzymes, primarily those found in the mitochondria of living cells. This reduction process is used as a widely accepted method for assessing cell viability and proliferation in various cell-based assays.

More about "Praziquantel"

Praziquantel is a versatile antihelminthic medication used to treat a variety of parasitic infections, including schistosomiasis, clonorchiasis, and opisthorchiasis.
This drug works by damaging the tegument, or outer layer, of the parasites, causing them to detach from the host's intestinal wall or other tissues.
As the drug of choice for treating schistosomiasis, a neglected tropical disease affecting millions worldwide, praziquantel's efficacy, safety profile, and ease of administration make it an invaluable tool in the global effort to control and eliminate this debilitating condition.
Optimizing praziquantel protocols is crucial for improving the reproducibility, accuracy, and efficiency of studies involving this important antihelminthic.
Researchers can utilize tools like PubCompare.ai to locate protocols from literature, preprints, and patents, and leverage AI-driven comparisons to identify the best protocols and products.
This innovative solution can help enhance research efficiency and accuracy.
In addition to praziquantel, other compounds like DMSO, acetonitrile, and HEPES buffer may be used in conjunction with praziquantel protocols.
Penicillin and penicillin G sodium salt are also commonly employed as antimicrobial agents.
Albendazole, another antihelminthic drug, may be used in combination with praziquantel for certain parasitic infections.
Praziquantel tablets, a convenient dosage form, are widely available for treating pateints.
The thiazolyl blue tetrazolium bromide (MTT) assay is a common method used to assess the efficacy of praziquantel and other antihelminthic compounds.
By optimizing praziquantel protocols and leveraging these related compounds and techniques, researchers can improve the reproducibility, accuracy, and efficiency of their studies on this crucial antihelminthic medication.