81 research outputs found

    In vivo anti-malarial activity of hydroalcoholic extracts from Asparagus africanus Lam. in mice infected with Plasmodium berghei

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    Background: Malaria is a major public health problem in the world in general and developing countries in particular, causing an estimated 1-2 million deaths per year, an annual incidence of 300-500 million clinical cases and more than 2 billion people are at risk of infection from it. But it is also becoming more difficult to treat malaria due to the increasing drug resistance. Therefore, the need for alternative drugs is acute. Objective: The This study aims at investigating the in vivo antiplasmodial activity of extracts of the roots and area parts from traditionally used medicinal plant, named Asparagus africanus (Liliaceae). Methods: A rodent malaria parasite, Plasmodium berghei, which was maintained at the Ethiopian Health and Nutrition Research Institute (EHNRI) laboratory, was inoculated into Swiss albino mice. The mice were infected with 1x107 parasites intraperitoneally. The extracts were administered by an intra gastric tube daily for four days starting from the day of parasite inoculation. The control groups received the same amount of solvent (vehicle) used to suspend each dose of the herbal drug. Chloroquine was used as a standard drug, and was administered through the same route. Results: Extracts from the roots and aerial parts of A.africanus were observed to inhibit Plasmodium berghei parasitaemia in the Swiss albino mice by 46.1% and 40.7% respectively. Conclusion: The study could partly confirm the claim in Ethiopian traditional medicine that the plant has therapeutic values in human malaria. There is, thus, the need to initiate further in-depth investigation by using different experimental models. The Ethiopian Journal of Health Development Vol. 20 (2) 2006: 112-11

    Neurofibromatosis: chronological history and current issues

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    In Vitro anthelmintic activity of crude bark extracts of Albizia gummifera on Haemonchus contortus

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    No Abstract. BAHPA Vol. 54 (3) 2006: pp. 168-17

    Short Communication: Comparative Quality Evaluation of Some Brands of Paracetamol Tablets, Suppositories and Syrups

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    The present study assesses the quality and the physicochemical properties of paracetamol dosage forms (tablet, suppository and syrup samples) from different drug outlets in Addis Ababa. Identity, weight uniformity, disintegration and dissolution times, assay for active ingredient content and pH test (for syrup) were performed. Hardness and drug release (t50% and t90%) of the different brands of paracetamol tablets were also evaluated and compared. The study showed that none of the tablet samples did meet the USP specification for assay of active ingredient content. One of the syrup samples (Efferalgan®) tested, contained less than the specified amount of the active principle. Keywords: quality evaluation, physicochemical properties, paracetamol dosage forms, drug outlets, Addis AbabaEthiopian Pharmaceutical Journal Vol. 26 (1) 2008: pp. 59-6

    Comparative In Vitro Quality Evaluation of Ciprofloxacin Tablets from Drug Retail Outlets in Addis Ababa, Ethiopia

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    Ciprofloxacin is a fluoroquinolone derivative having a broader spectrum of antibacterial activity against Gram-negative and Gram-positive aerobic and anaerobic organisms. It is the drug of choice for treating urinary tract infections and enteric typhoid fever. Quality assurance and evaluation of antibiotics has paramount importance to monitor the distribution of counterfeit and substandard medicines in the drug retail outlets and ensure the desired therapeutic efficacy on susceptible microorganisms. This investigation was carried out to assess the quality of eight brands of ciprofloxacin 500 mg tablets marketed by different drug retail outlets in Addis Ababa. At the time of this sampling, most of the tablets had a shelf-life of at least two years and they were in their original packages. Identity, weight uniformity, disintegration and dissolution tests as well as assay for the content of active ingredients were performed using the methods described in the British Pharmacopoeia. Hardness and equivalence of drug release at t50% and t90% of the different brands of ciprofloxacin tablets were also evaluated and compared. All the samples passed the identity, disintegration, and dissolution tests. Among the eight brands, ciprokin® failed the weight uniformity test. Eight of the ciprofloxacin brands examined passed the assay for content of active ingredient and also assured the minimum requirement for the test in crushing strength of the tablets. The eight brands were found to be bio-inequivalent for their drug release compared at t50% and t90% indicating significant difference in the in vitro drug release. Keywords: ciprofloxacin tablets, comparative study, In Vitro quality evaluation, physicochemical Ethiopian Pharmaceutical Journal Vol. 25 (1) 2007: pp. 1-

    Qualitative laboratory analysis for teh detaction of conventional drugs in herbal preparations supplied by healers in major towns of Ethiopia

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    No Abstract. Ethiopian Journal of Health Development Vol. 22 (1) 2008: pp. 55-6

    PAIN MANAGEMENT IN MICE USING THE AQUEOUS AND ETHANOL EXTRACTS OF FOUR MEDICINAL PLANTS

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    ABSTRACTBackground: There are many traditionally used analgesic plants in Ethiopia. They, however,have not been subject to scientific investigation for their efficacy and safety.Objective: To evaluate both prophylactic and relieving effects of aqueous and ethanolextracts of four traditionally used medicinal plants in Ethiopia.Design: An experimental design in which five group of albino mice weighing 30-35 gramsrepresenting positive and negative control, and extract treated groups respectively. Theextracts, standard drugs and normal saline were administered into GIT by gavage to evaluatethe analgesic effect.Setting: Department of Drug Research at Ethiopian Health and Nutrition Research Instituteand Department of Pharmacology at Faculty of Medicine, Addis Ababa university.Methods: Analgesic effects of water and ethanol extracts of four plants were evaluatedagainst distilled water and standard analgesics (morphine and acetylsalicylic acid) withacetic acid induced writhing tests in mice. The four plants used for this screening wereOcimum sauve, Ocimum lamiifolium, Lippia adoensis and Ajuga remota.Results: All extracts of the four plant materials were observed to possess both inhibiting andtreatment activities against acetic acid induced pain. Dose related analgesic effect was alsoobserved with all extracts of all plants with different potencies. Ethanol extracts of all the fourplant materials were more potent than their water extracts at all dose levels except O. sauve,and L. adoensis whose water extracts seem to be a bit more potent at low dose. The analgesicpotencies of both extracts of all the four plants were shown to be less than those of thestandard analgesics. Of all the extracts, the ethanol extract of O. lamiifolium was found to bethe most potent, while its water extract was the least. Acetic acid induced writhing wasrelieved with medium dose of both extracts in most cases and with low dose in few. Hundredpercent relief was achieved with both standard analgesics at a very low dose.Conclusion: The present study show that all the extracts of all the plant materials have gotboth inhibiting and relieving effects of pain
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