scholarly journals Study on ruminant tick infestation, phytochemical analysis and in vitro acaricidal effect of Calpurnia aurea and Otostegia integrifolia extracts on Amblyomma variegatum

2020 ◽  
Vol 24 (1) ◽  
Author(s):  
Jelalu Kemal ◽  
Sisay Alemu ◽  
Biniam Tsegaye ◽  
Nateneal Tamerat

Ticks limit the productivity of livestock through decreased production, reproduction, increased mortality, downgrading and rejection of hides and skin. A cross-sectional study was conducted to estimate the prevalence of tick infestation in ruminant while experimental study was used to evaluate the in-vitro acaricidal efficacy of methanolic extracts: Calpurnia aurea and Otostegia integrifolia and the phytochemicals present in those extracts at different concentrations (200, 100, 50, 25, 12.5 and 6.25 mg/ml) against Amblyomma variegatum. Adult immersion was used for the in-vitro acaricidal efficacy test and plant extracts were subjected to qualitative phytochemical screening for the presence or absence of secondary metabolites using standard procedures. Out of the 160 goats, 152 sheep and 121 cattle, 23 (14.4%), 44 (28.9%) and 28 (23.1%) were found to be positive for tick infestation, respectively. The incidence of tick infestation was significantly different (p<0.01) among ruminants. Five tick spp. were identified: A. variegatum, A. gemma, R. decoloratus, R. evertsi evertsi and R. pulchellus. Extract of C. aurea and O. integrifolia was found to contain alkaloids, saponins, phlobatannin, steroids, phenolic, flavonoids, glycosides and tannins. However, both plants were found negative for triterpens. Extracts of C. aurea and O. integrifolia at 200 and 100 mg/ml concentrations showed a significantly higher (p<0.05) acaricidal activities compared to other treatments at 24 hrs post exposure. Mortality of ticks was increased with the increased dosage (concentration) and exposure time after treatment. Extracts of C. aurea showed a significantly higher (p<0.05) tick mortality (52%) compared to those of O. integrifolia (27%). This is a promising finding to have alternative means of treatment and to substitute the use of synthetic drugs which have a wide spread drug resistance especially in developing countries like Ethiopia. Key words: Calpurnia aurea; in-vitro test; Otostegia integrifolia; Phytochemical screening; Tick infestation

Author(s):  
Marcella Tari Joshua ◽  
Edna O. Nwachukwu ◽  
N. Boisa ◽  
Nsirim Nduka

Aim: This study focused on the phytochemical screening of aqueous, ethanolic and methanolic leaf extracts on the species Morus mesozygia linn. Study Design: This study was a cross-sectional study. Place and Duration of Study: This study was carried out at the Plant Anatomy and Physiology Research Laboratory, University of Port Harcourt, between July, 2018 and November, 2018. Methodology: Morus mesozygia linn leaves were collected and washed with distilled water, air dried for seven days and milled into fine powder. Maceration method was use to extract the powdered leaf into a brownish paste using three different solvents; distilled water, ethanol and methanol. The different plant extracts were subjected to qualitative phytochemical screening for alkaloids, flavonoids, saponins, carbohydrates, tannins and anthraquinones. Quantitative phytochemical analysis was done using a Gas chromatography – Mass Spectroscopy machine. Results: Results showed that the powdered Morus mesozygia linn leaves contained alkaloids, flavonoids, saponins, carbohydrates, tannins, but not anthraquinones. The methanolic and aqueous leaf extracts contained high amounts of alkaloids, flavonoids, saponins, carbohydrates and tannins, while the ethanolic extract also contained high amounts of the aforementioned phytochemicals in the same proportion, but had saponins in moderate amounts. The result of the GC-MS analysis showed that the three extracts contained complex compounds in varying amounts. Conclusion: Phytochemical screening test of Morus mesozygia has revealed the presence of the substances like alkaloids, saponins, flavonoids, oils, phenolic compounds, tannins and some complex compounds discovered using GC-MS technique.


2016 ◽  
Vol 64 (4) ◽  
Author(s):  
Alexis Buitrago ◽  
Janne Del Carmen Rojas ◽  
Yonel Peñalosa

Vismia genus is distributed mainly in tropical and subtropical regions of Central, South America and some areas of Africa. According to previous investigations, antioxidant potential of Vismia species might be related to anthrones, anthraquinones, flavonoids and phenol derivatives biosynthesized by these plants. The aim of present study is to evaluate the free radical scavenging capacity, total phenolic and flavonoids content as well as the qualitative phytochemical screening of methanol extracts obtained from Vismia macrophylla (VM) and Vismia baccifera (VB) collected in Táchira and Mérida state, Venezuela. Phytochemical screening of VB and VM methanolic extracts carried out using various chemical assays revealed an abundant presence of anthraquinones in both species analyzed. Glycosides were also present while flavones and dehydroflavones were observed abundantly in VB but moderated in VM. Triterpenes were also detected and steroids showed to be abundant in VM but moderate in VB. On the other hand, antioxidant capacity measured by the DPPH radical scavenging assay showed that VM possesses a stronger antioxidant activity than VB with IC50 5.50 µg/mL. Phenol and flavonoid assays also revealed that methanol extracts of both VM and VB contain high concentrations of these metabolites. A relationship between the antioxidant activity, total phenol and flavonoids content of the extracts analyzed was demonstrated in present investigation since those samples with higher phenolic concentrations showed likewise higher antioxidant activity.


2021 ◽  
Vol 2021 ◽  
pp. 1-7
Author(s):  
Idris Mohammed Idris ◽  
Diyae Nesredin Hassan ◽  
Hanan Abdelkadir Hassen ◽  
Rahwa Zerabruk Araya ◽  
Dawit G. Weldemariam

Generic medicines are clinically equivalent and can be used interchangeably for their intended use. Globally, the usage of generic medicines is highly recommended because of their affordability and accessibility. However, consumers hold a negative perception and attitude of using generic medicine as they consider it poor and having inferior quality compared to branded medicines. This study was conducted to assess the consumers’ general view of generic medicines and in vitro evaluation of a locally produced generic medicine, paracetamol. An analytical and cross-sectional study was conducted in three selected hospitals, and in vitro quality control evaluation was done in National Drug Quality Control Laboratory between October 26 and November 21, 2017, in Asmara, Eritrea. A systematic random sampling design was employed, and the data was collected using a questionnaire and a check-list for recording the quality control parameters of paracetamol tablets. A total of 403 respondents were included in the study. The majority of the study participants were females (61.8%). Generally, about half (49.1%) of the respondents choose locally manufactured paracetamol over the imported ones. More than half (68.5%) of the respondents did not believe expensive medicines are of better quality. The main reason consumers prefer the local paracetamol (Azemol) tablet to the imported one was due to their good experience (62.1%). About three-fourths (78.1%) of the consumers also believed that medicines manufactured abroad confer higher quality. At the multivariate level, having educational backgrounds such as elementary ( AOR = 4.19 , 95% CI: 1.251, 14.035) and junior ( AOR = 2.4 , 95% CI: 1.146, 5.028) was associated with preferability to local paracetamol as a pain killer over the brand ones. The in vitro test of the local paracetamol met the standard specification for the identification test, weight variation test, pharmacopeial test, friability test, disintegration test, and dissolution test. In conclusion, the majority of the consumers considered local paracetamol as having an inferior quality when compared with brand paracetamol. However, the reality revealed that the local paracetamol was of the same quality as the brand ones. To facilitate widespread use of generic medicines, healthcare professionals should educate consumers on the advantages of these medicines.


Author(s):  
Marcella Tari Joshua ◽  
Edna O. Wachuku ◽  
N. Boisa ◽  
Nsirim Nduka

Aim: The aim of this study was to phytochemically analyze the aqueous, ethanolic and methanolic twig extracts of the species Morus mesozygia Linn. Stapf. Study Design: This is a cross-sectional study. Place and Duration of Study: This study was carried out at the Plant Anatomy and Physiology Research Laboratory, University of Port Harcourt, between July, 2018 and November, 2018. Methodology: Morus mesozygia linn twigs were collected and washed with distilled water, air dried for seven days and milled into fine powder. Maceration method was used to extract the powdered twig into a brownish paste using three different solvents; distilled water, ethanol and methanol. The different plant extracts were subjected to qualitative phytochemical screening for alkaloids, flavonoids, saponins, carbohydrates, tannins and anthraquinones. Quantitative phytochemical analysis was done using a Gas chromatography – Mass Spectroscopy machine. Results: The results of this study showed that the powdered Morus mesozygia linn twigs contained flavonoids, saponins, carbohydrates, alkaloids, tannins, but not anthraquinones. The methanolic and aqueous twig extracts contained high amounts of alkaloids, flavonoids, saponins, carbohydrates and tannins, while the ethanolic extract also contained high amounts of the aforementioned phytochemicals in the same proportion, but had saponins in moderate amounts. It also showed that the methanolic twig extract had more carbohydrate than the other two extracts. The result of the GC-MS analysis showed that the three extracts contained complex compounds in varying amounts. Conclusion: The qualitative and quantitative phytochemical analyses test results of Morus mesozygia Linn Stapf. revealed the presence of the substances like alkaloids, saponins, flavonoids, oils, phenolic compounds, tannins and some complex compounds discovered using GC-MS technique, in their varying concentrations for the three different extracts.


Author(s):  
JAGTAP SUPRIYA ◽  
GUJAR KISHOR ◽  
GHARE ANIKET

Objective: The objective of the study was to investigate in vitro antimicrobial activity against enterotoxigenic Escherichia coli and Bacillus subtilis and preliminary phytochemical screening of the leaves of Portulaca quadrifida (Linn.). Methods: The solvent extract such as petroleum ether, methanol, and water on the leaves of P. quadrifida (Linn) was prepared by Soxhlet extraction (continuous hot percolation method). These solvent extracts were screened for antimicrobial activity against enterotoxigenic E. coli and B. subtilis at various concentrations and were measured by observing zone of inhibition in mm by disc diffusion method (cup plate method). Results: The preliminary phytochemical screening revealed the flavonoids, fats, and oils in all extracts. Similarly, the presence of alkaloids and tannins was obtained in the petroleum ether and methanolic extracts, while the presence of glycosides was obtained in the methanolic and water extracts. Further, proteins and sterols were found in petroleum extracts. The results of antimicrobial activity shown that methanolic extracts of the plant leaf showed good antimicrobial activity and petroleum ether and water extract showed similar activity but less antimicrobial activity than methanolic extract. The antimicrobial activities of extracts were compared with standard antibiotic such as chloramphenicol. Conclusion: P. quadrifida (Linn.) has broad-spectrum antimicrobial activity and a potential source of new classes of antibiotics that could be useful for infectious disease chemotherapy and control. The phytochemical analysis of the crude extracts of this plant indicates the presence of major phytoconstituents which may have been responsible for the observed antimicrobial property.  


2018 ◽  
Vol 24 (2) ◽  
Author(s):  
GITA MISHRA ◽  
HEMESHWER KUMAR CHANDRA ◽  
NISHA SAHU ◽  
SATENDRA KUMAR NIRALA ◽  
MONIKA BHADAURIA

Pergularia daemia belongs to the family Asclepiadaceae, known to have anticancer, anti-inflammatory activity. Aim of the present study was to evaluate qualitative and quantitative phytochemical and antioxidant properties of ethanolic extracts of leaf, stem and root parts of P. daemia . Preliminary phytochemical analysis and in vitro antioxidant properties were evaluated by standard methods. The qualitative phytochemical analysis of P. daemia showed presence of flavonoids, tannins, alkaloid, phytosterol, carbohydrate, phenol, saponin, glycosides, terpenoids, steroids proteins and reducing sugars. Quantitative analysis showed polyphenol, flavonoid, flavonone, flavone and flavonol in P. daemia leaves, stem and root in considerable quantity. The in vitro antioxidant activity of P. daemia clearly demonstrated that leaf, stem and root parts have prominent antioxidant properties and was effective in scavenging free radicals.


Author(s):  
Michael Russelle Alvarez ◽  
Paolo Robert Bueno ◽  
Raymond Oliver Cruz ◽  
Richard Macapulay ◽  
Francis Jayson Vallesfin ◽  
...  

Plant-derived digestive enzyme inhibitors particularly those targeted to carbohydrate metabolism has been the focus of recent studies as natural supplements for weight control and diabetes. The present study explores the salivary amylase inhibition activity of Garcinia mangostana (Linn.) pericarp extracts and Carica papaya (Linn.) leaf extracts and fractions, as well as perform phytochemical screening and quantification, and thin layer – and high performance liquid chromatographic profiling. ­Results show that crude extracts and purified fractions were able to inhibit salivary amylase, with C. papaya fraction 1 being the most active at 30.89% inhibition. Phytochemical screening of all extracts tested ­positive for tannins, glycosides, phenolics, flavonoids and alkaloids. Quantification of phenolics showed that extracts contained high levels of phenolics, with C. papaya crude extract having the highest content with 219.0±12.7 mg GAE/g extract followed by G. mangostana crude extract with 247.1±18.0 mg GAE/g extract. Quantification of total flavonoids also showed C. papaya crude extract to contain the highest content with 55.12±0.679 mg QE/g extract. All extracts contained negligible alkaloid content, though. HPLC and TLC profiling showed several peaks and bands, when viewed in 210 nm and UV light, respectively. These results demonstrate in vitro the salivary amylase inhibitory activity of both plants and their potential as antidiabetic drug candidates; however, further studies need to be done, like isolation and structure elucidation of active components and toxicity assays. Keywords: Amylase inhibition, phytochemical quantification, Carica papaya, Garcinia mangostana


2017 ◽  
Vol 37 (3) ◽  
pp. 342-344
Author(s):  
Roberta M. Katzap ◽  
Vany Elisa Pagnussatti ◽  
Ana Elizabeth Figueiredo ◽  
Julia Gabriela Motta ◽  
Domingos O. d'Avila ◽  
...  

Patients with chronic kidney disease on peritoneal dialysis (PD) are susceptible to infections, with peritonitis being the primary cause of dropout. Peritoneal fluid culture is one of the essential elements for proper diagnosis and peritonitis treatment. The aim of this study was to compare the time required to obtain a positive culture using different laboratory methods. An in vitro cross-sectional study was conducted comparing different techniques for preparation and culture of bacteria in peritoneal fluid. The research was carried out with 21 sterile dialysis bags and 21 PD bags containing peritoneal fluid drained from patients without peritonitis. Fluids from the 42 PD bags were contaminated by injecting a coagulase-negative Staphylococcus suspension and then prepared for culture using 4 distinct techniques: A - direct culture; B - post-centrifugation culture; C - direct culture after 4 h sedimentation; and D - culture after 4 h sedimentation and centrifugation. This was followed by seeding. In the 21 contaminated sterile bags, mean times to obtain a positive culture with techniques D (19.6 h ± 2.6) and C (19.1 h ± 2.3) were longer than with technique A (15.8 h ± 3.0; p < 0.01), but not statistically different from group B (19.0 h ± 3.2). The same occurred in the 21 bags drained from patients, with mean times for techniques D (14.0 h ± 1.9) and C (14.5 h ± 1.7) being longer than technique A (12.22 h ± 1.94; p < 0.05) but not statistically different from technique B (13.2 h ± 1.3). The sedimentation and centrifugation steps seem to be unnecessary and may delay antibiotic sensitivity test results by approximately 8 hours.


2010 ◽  
Vol 33 (6) ◽  
pp. 384 ◽  
Author(s):  
Courtney L Bryan ◽  
K Scott Beard ◽  
Gregory B Pott ◽  
Jeremy Rahkola ◽  
Edward M Gardner ◽  
...  

Purpose: Several observations suggest the presence of HIV-suppressive factors in the fluid phase of blood. Alpha-1-antitrypsin (AAT), the most abundant serine protease inhibitor in the circulation, has potent anti-HIV activity in vitro, and may function as an endogenous HIV suppressor. Therefore, we assessed serum AAT concentrations for association with HIV infection. Methods: In this cross-sectional study, serum AAT concentrations were measured in 66 persons with HIV infection and in 45 healthy persons (Controls). In the HIV-infected group, antiretroviral therapy (ART) use was assessed and CD4+ T cell levels and plasma HIV RNA were quantified. Results: Median AAT concentration was significantly lower in the HIV-infected group (1.64 mg/mL) in comparison with Controls (1.94 mg/mL; p=0.001). AAT reduction was most pronounced in the HIV-infected subgroup with CD4+ T cell levels > 200 cells/µL in comparison with Controls (p < 0.01). Serum AAT concentrations < 1.0 mg/mL are clinically significant, and concentrations below this level were identified in 4.5% of the HIV-infected group and in no Control subjects. No association between AAT levels and viral load or use of ART was observed in HIV-infected subjects. Conclusion: The association between reduced serum AAT concentration and HIV infection is consistent with a role for AAT as an endogenous HIV suppressor.


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