Original Research Article
Aug. 30, 2018
Preliminary Phytochemical Screening and Evaluation of Anti-Arthritic Potential of Ledum Pal Mother Tincture using Macrophage Raw 264.7 Cell Lines
Athira KA, Jayachandran TP
Sch Acad J Pharm | 354-364
DOI : 10.21276/sajp.2018.7.8.1
Abstract
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Rheumatoid arthritis is a chronic inflammatory disease affecting joints
manifesting as pain, stiffness, and synovitis leading to articular destruction. Current
medical treatments do not consistently halt the long-term progression of this disease, and
surgery may still be needed to restore mechanical function in large joint. Patients with
rheumatic syndromes often seek alternative therapies, with homeopathy being one of the
most frequent. So the necessity of this study gains more interest to prove the efficacy of
alternative system of medicine. Objective of the present study is to carry out preliminary
phytochemical screening followed by the evaluation of anti-arthritic potential of Ledum
Pal mother tincture (LPMT) in lipopolysaccharide (LPS) stimulated RAW 264.7
macrophage cell lines. Phytochemical screening was done to find the presence of various
primary and secondary metabolites of the plant. In-vitro anti-arthritic activity was
evaluated by assessing the inhibitory property of LPMT on LPS stimulated cell lines
using several assays like cyclooxygenase-2 (COX-2), 5-lipoxygenase (5-LOX), inducable
nitric oxide synthase (iNOS), and estimation of cellular nitrite level, myeloperoxidase
(MPO) activity using diclofenac as standard. Phytochemical tests of LPMT indicated the
presence of flavonoids, alkaloids, steroids, terpenoids, carbohydrates, proteins, tannins,
saponins, and glycosides. Macrophages produce COX-2, 5-LOX, iNOS, cellular nitrite
and myeloperoxidase etc.
Original Research Article
Aug. 30, 2018
The Antibiotic and Garlic Susceptibility of Escherichia coli Strains and Their Ability of Attachment and Biofilm Formation
Ameyapoh, Nakpane Fankibe
Sch Acad J Pharm | 365-371
DOI : 10.21276/sajp.2018.7.8.2
Abstract
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This study consisted on the impact of antimicrobial agents on Escherichia coli
(E. coli) isolates and their power to adhere to surface for biofilms formation. Sixty two E.
coli isolated from patients urines were then used for standard antibiograms on Mueller
Hinton (MH) agar associated with garlic juice antimicrobial activity. The attachment of
three E. coli strains selected according to their susceptibility to antibiotics was
experimentally performed on glass slides and the adhesion profiles were determined to
assess their power of biofilm formation. As results, even though, the dominant types of
resistance were respectively to amoxicillin, tetracycline, ampicillin and nalidixic acid in
more than 80% of all the E. coli isolates, the highest sensitivity were observed with
Gentamycin in 81% and imipenem in 97% of all the samples. In addition, the tests of
adhesion revealed that, significantly (p <0.0001), the three E. coli attachment to surface
increased with their resistance to antibiotics. However, none of them resisted the garlic
juice as well as isogenic planctonic-growing bacteria as biofilm-ones.
Original Research Article
Aug. 30, 2018
Importance of the Quality Control of Herbal Teas: Evaluation of Two Senna Leaf Tisanes Brands Commercialized in Costa Rica through Physicochemical and Microbiological Assays Stipulated in the Central American Technical Regulation 11.03.56.09
Juan José Mora Román, Kattia Bermúdez Carvajal, Yuliana Cordero Menéndez, Raquel Hernández Vega, Diana Porras León, Rodolfo Vargas González, Arlene Loría Gutiérrez, Jeimy Blanco Barrantes
Sch Acad J Pharm | 372-380
DOI : 10.21276/sajp.2018.7.8.3
Abstract
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The senna leaf contains a powerful natural laxative called anthraquinone.
Despite this indication, the quality control of this raw material is not strict, compared to
other substances with pharmacological properties, which is unacceptable. Therefore, the
present investigation sought to evaluate physicochemical and microbiological quality
aspects of the senna leaf tisanes from two brands commercialized in Costa Rica, through
various assays established in the current Central American Technical Regulation (RTCA)
11.03.56.09. The aforementioned was made in order to identify and compare whether
these aspects are constant or not for the different batches of the same product for each of
the brands. For that reason, the following assays were done for three batches of two
different brands: Labeling, minimum fill, organoleptic, foreign organic matter,
identification, loss on drying, total ash, acid-insoluble ash, microbial enumerations and
determination of specific microorganisms. The results show that the batches of both
brands are in compliance for all the assays, except for the labeling assay (six of the 23
items required for primary and secondary packaging labeling were not found). For all of
the above,
Original Research Article
Aug. 30, 2018
Formulation and Evaluation of Dispersible Tablet of Ornidazole
Nikhil Bhujbal, Aishwarya Shinde, Sneha Abnave, Ashwini Jadhav
Sch Acad J Pharm | 381-386
DOI : 10.21276/sajp.2018.7.8.4
Abstract
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This Present research with dispersible tablet can compromise the efficacy and
safety of thetreatment to children’s and geriatric patients with masking the bitter taste of
drug and developing its dispersible tablet.The purpose of this research work was to
develop Dispersible tablet of Ornidazole by masking the bitter taste. Tablet containing
drug and excipients were prepared by direct compression method. Excipients in
combinations were incorporated to achieve the aim. Effect of different combinations was
studied to optimize the ideal formulation. Drug excipients interaction studies were carried
out by FTIR spectral analysis. The tablets were evaluated for their hardness, wetting time,
disintegrating time and dissolution parameters. It was concluded that the tablets having
the combination of Dried Mucilage (obtained from dried seeds of ocimum bacilicum) and
Sodium starch glycolate met all the evaluation parameters and thus selected as the
optimized formulation. Optimized formulation was undergone for stability testing as a
parameter to predict the shelf life as per ICH guidelines and proved for its adequate shelf
life.
Original Research Article
Aug. 30, 2018
Comparison of the Antihypertensive activity of Telmisartan Versus Valsartan in Queen Alia Heart Institute/Royal Medical Services
Hadeel H. Alzayaat, Wafa M. Abu-Roman, Nawal H. Al-Abbadi, Ma’aali M. Al-Maseeb, Abeer A. Jibreen
Sch Acad J Pharm | 387-391
DOI : 10.21276/sajp.2018.7.8.5
Abstract
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Hypertension is a major risk factor for stroke, myocardial infarction, vascular
disease, and chronic kidney disease. The goal of antihypertensive therapy is to maintain
blood pressures of < 140/90 mmHg for most people. All international guidelines for the
management of hypertension recommend angiotensin receptor blockers (ARBs) as an
initial or add-on antihypertensive therapy. The ARBs are very well tolerated as
monotherapy as well as in combination with other anti-hypertensive medications that
improve adherence to therapy and have become a mainstay in the treatment of stage 1 and
2 hypertension. The 8 available ARBs have variable clinical efficacy when used for
control of hypertension. Assessment of the efficacy and safety of Telmisartan (80 mg
once daily) versus valsartan (160 mg once daily) for the management of blood pressure
(BP) in patients with essential hypertension. A cross sectional retrospective single center,
parallel-group study. Patients will be recruited from Queen Alia Heart Institute. Data will
be gathered by reviewing the medical records. Baseline characteristics were not
significantly different between the two study groups. After 12 weeks, BP had fallen to a
greater extent in the Telmisartan group compared to Valsartan group in terms of mean
reductions in the systolic and diastolic BP of 126.2/80.4 (Adjusted change from baseline-
26.8/-20.9) and 133.3/ 86.8 mm Hg (Adjusted change from baseline--18 /-12.7)
(p<0.0021). In Stage 2 hypertensive patients once daily Telmisartan 80 mg provides
significantly greater BP lowering compared to Valsartan 160 mg
Original Research Article
Aug. 30, 2018
Chalcones in the Therapeutics of Diabetes Mellitus
Swati Paliwal, DP Pathak
Sch Acad J Pharm | 392-401
DOI : 10.21276/sajp.2018.7.8.6
Abstract
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Diabetes mellitus is a metabolic disorder which affects the wide range of the
population worldwide. Most of the pharmacotherapeutic agents available today might
provide the symptomatic relief, but do not cure the disease completely. Further their
limitations make the researcher look forward to the newer and the safer
pharmacotherapeutic agents. Aim of the present work is to describe the role of the
chalcones in the treatment of diabetes mellitus. Information regarding the chalcones was
collected from the various site such as PubMed, Google, google scholars and science
direct. It has been concluded that the chalcones have the key potential due to their
structural property that might exert the beneficial effects of diabetes and the associated
pathological conditions.