Paper Type |
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Research Paper |
Title |
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Pancreas Cancer: A Literary Review |
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Authors |
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Ana Paula Schneider Bruck || Bruna Fernandes da Silva || Camila da Silva Senna Barroso || Isadora Cristina Teixeira Bono || Leticia Margon Manzini de Souza || Michelle Lima Garcez || Orlando Chiarelli Neto |
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01-11 |
Introduction : Pancreatic cancer occurs as pancreatic adenocarcinoma, with a poor prognosis, which represents, in addition to pathophysiological changes, great psychosocial impacts on the patient's life, due to the fact that the disease presents itself, in most cases, late, making it difficult to early detection of tumor or pre-malignant tumors. Objective: To demonstrate updated data about the clinical aspects, diagnosis and treatments of the disease. Method: To obtain the data, 38 articles on the subject were used, researched in the main books and articles related to pancreatic cancer, from 2010 to 2021. Statistical were performed observing the equality between the understandings cited by each author, so that the thesis about each point of this article was confirmed Results : Mortality and incidence of pancreatic cancer are increasing rapidly.......
KEYWORDS: pancreas ; cancer ; surgery
[1]. McCain et al. Pancreatic cancer: A review of clinical diagnosis, epidemiology, treatment and outcomes . World Journal of Gastroenterology.DOI: 10.3748 / wjg.v24.i 43.4846 . 2018
[2]. Klein. APEpidemiology of pancreatic cancer: understanding the role of lifestyle and hereditary risk factors . Nature Reviews Gastroenterology & Hepatology. DOI https://doi.org/10.1038/s41575-021-00457-x. 2021 _
[3]. Cai et al . Advances in theepidemiologyofpancreaticcancer : Trends, riskfactors , screening, andprognosis https://doi.org/10.1016/j.canlet.2021.06.027 . 021 Elsevier BV Allrightsreserved . 2021.
[4]. Beg,Muhammad et al. Impact of Diabetes Mellitus on the Outcome of Pancreatic Cancer . Plosone.DOIhttps://doi.org/10.1371/journal.pone.0098511 https://doi.org/10.1371/journal.pone.0098511. _ 2014.
[5]. Lulu Zhang, Santosh Sanagapalli , and Alina Stoita . Challenges in diagnosis of pancreatic cancer . World Journal of Gastroenterology. DOI: https:// 10.3748/ https://dx.doi.org/10.3748%2Fwjg.v24.i19.2047wjg.v24.i https://dx.doi.org/10.3748%2Fwjg.v24.i19.204719.2047 . 2018
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Research Paper |
Title |
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Use of corticosteroids in medical practice: Pattern of prescription, adverse effects and pre-prescription counselling practices |
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Nigeria |
Authors |
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Ogundele SO || Dada AO || Olaosebikan BH || Amisu M || Cole-Adeife OM || Dr. Sunday O. Ogundele |
Page No. |
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12-16 |
Corticosteroids are a group of medications that are structurally and pharmacologically similar to the endogenous hormone cortisol. The mechanisms of action for the therapeutic effects and clinical improvement associated with corticosteroids are also responsible for most of the adverse effects associated with its chronic use or its use in high doses. Prescription of corticosteroids is on the increaseamong patients seen in our clinical practice. The increase in steroid prescription is associated with increasing frequency of complications associated with its chronic use. The main objective of this study is to review the prescription pattern of steroids in our practice and to also assess how patients are counselled before they are started on these agents.......
KEYWORDS: Corticosteroids, counselling, prescription, adverse effects, Lagos.
[1]. Yasir M, Goyal A, Bansal P, Sonthalia S. Corticosteroid Adverse Effects. (Updated 2021 Mar 3). In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2021 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK531462/
[2]. Liu, D., Ahmet, A., Ward, L, Krishnamoorthy P, Mandelcorm ED, Leigh R, Brown JP, Cohen A, Kim H. A practical guide to the monitoring and management of the complications of systemic corticosteroid therapy. All AsthClinImmun 2013; 9: 30. https://doi.org/10.1186/1710-1492-9-30.
[3]. Hengge UR, Ruzicka T, Schwartz RA, Cork MJ. Adverse effects of topical glucocorticosteroids. J Am AcadDermatol. 2006;54(1):1-15; quiz 16-8. DOI: 10.1016/j.jaad.2005.01.010. PMID: 16384751.
[4]. van Staa TP, Leufkens HG, Abenhaim L, Begaud B, Zhang B, Cooper C. Use of oral corticosteroids in the United Kingdom. QJMed. 2000;93(2):105-11. DOI: 10.1093/qjmed/93.2.105. PMID: 10700481.
[5]. Royal College of Physicians Guidelines Writing Group. Glucocorticoid-induced osteoporosis: Guidelines for prevention and treatment. London: Royal College of Physicians, 2002.
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Research Paper |
Title |
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Development and Validation of RP-HPLC Method For quantitative Estimation of Cetirizine HCL in Pharmaceutical Formulation as Per ICH Guideline |
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India |
Authors |
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Dr. Gayatri Barabde || Aarti Babu Kokate || Dr. Sushama Ambadekar |
Page No. |
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17-25 |
Background: A simple, specific, linear, precise and accurate reverse phase liquid chromatographic (RP-HPLC) method was developed to analysis speed by minimizing run time and retention timeof Cetirizine Hydrochloride in tablet dosage forms. The chromatographic separation was performed using Phenomenex Luna 5μ C18 100A (250 x 4.6 mm). Mobile phase composed of Acetonitrile and water (60:40 v/v) was selected and a flow rate of 1.000 ml/minute is monitored with injection volume of 20μl. Detection was carried out at 229 nm. The method was validated as per ICH guidelines. The retention time for CetirizineHydrochloride is observed as 2.3 minutes. Linearity range was observed in concentration of 50 - 150 μg/ml for Cetirizine Hydrochloride. The percentage recovery of Cetirizine Hydrochlorideis 100%. The correlation coefficients for both the components are close to 1. The proposed method was validated and successfully applied to the estimation of CetirizineHydrochloride in tablet dosage forms.
KEYWORDS: Cetirizine Hydrochloride, method development, Validation.
[1]. Rudaz. S., Souverain. S., Schelling. C.,andDeleersM.Anal. Chim. Acta,Development and validation of a heart-cutting liquid chromatography–mass spectrometry method for the determination of process-related substances in cetirizine tablets.2003, 492:271–282.
[2]. Nightingale, C.H. 1996. Treating allergic rhinitis with second-generation antihistamines. Pharmacotherapy, 1996, 16: 904-914.
[3]. P Beringer, A der Marderosian, L. Felton, et al, "Remington: The Science and Practice of Pharmacy" Lippincott Williams & Wilkins, Philadelphia, 21st ed., 2006.
[4]. European Medicines Agency, "Guideline on Excipients in the Dossier for Application for Marketing Authorisation of a Medicinal Product" Doc. Ref. EMEA/CHMP/QWP/396951 /2006, London, 6 November 2006.
[5]. Kuchekar BS, Shinde GS, Naikwadi IT, Todkar KJ, Kharade SV, "Specrtophotometric estimation of ambroxol hydrochloride in tablets" Indian J Pharm Sci, 2003; 65(2): 193-195.
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Research Paper |
Title |
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A Recent Review on Novel Derivatives of Hydroxychloroquine |
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India |
Authors |
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Aditi || Dr.Abhishek Soni || Ms.Pooja Devi |
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26-35 |
Malaria is an acute febrile disease that is caused due to the parasite infection, transmitted in humans by female anopheles mosquito bite. Malaria is one of the leading reasons of mortality worldwide, but the early detection and quick acting treatment can fend off these unpleasant results. In Africa and some Asian countries, malaria is the most common disease,while in other developed countries it occurs due to import from endemic countries. As early as the 2nd century BC Chinese people used sweet sagewort plant to cure malarial fever. Quinine began to be used as an anti-malarial drug much later..........
KEYWORDS: Malaria, Hydroxychloroquine, Nano-technological strategies and Nanoject.
[1]. Garcia LS. Malaria. Clin Lab Med. 2010 Mar;30(1):93-129. doi: 10.1016/j.cll.2009.10.001. PMID: 20513543.
[2]. Lover AA, Baird JK, Gosling R, Price RN. Malaria Elimination: Time to Target All Species. Am J Trop Med Hyg. 2018 Jul;99(1):17-23. doi: 10.4269/ajtmh.17-0869. Epub 2018 May 10. PMID: 29761762; PMCID: PMC6035869.
[3]. Ishtiaq F, Swain S, Kumar SS. Anopheles stephensi (Asian Malaria Mosquito). Trends Parasitol. 2021 Jun;37(6):571-572. doi: 10.1016/j.pt.2021.03.009. Epub 2021 Apr 14. PMID: 33865712.
[4]. Bilgin ZD, Evcil I, Yazgi D, Binay G, OkuyucuGenc C, Gulsen B, Huseynova A, Ozdemir AZ, Ozmen E, Usta Y, Ustun S, CaglarAndac S. Liquid Chromatographic Methods for COVID-19 Drugs, Hydroxychloroquine and Chloroquine. J Chromatogr Sci. 2021 Aug 18;59(8):748-757. doi: 10.1093/chromsci/bmaa110. PMID: 33336246; PMCID: PMC7799265.
[5]. Talapko J, Škrlec I, Alebić T, Jukić M, Včev A. Malaria: The Past and the Present. Microorganisms. 2019 Jun 21;7(6):179. doi: 10.3390/microorganisms7060179. PMID: 31234443; PMCID: PMC6617065.
Paper Type |
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Research Paper |
Title |
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Antimicrobial activity of ParkiaspeciosaHasskagainst Bacteria and Fungi using different Solvents Extractions |
Country |
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Indonesia |
Authors |
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Henny Rachdiati || Suci Sammulia || Delladari Mayefis || Nur Aqilla Mohd Zunaidi |
Page No. |
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36-38 |
Background: ParkiaspeciosaHassk is widely known as stink bean and one of the edible plants that have not been cultivated as medicinal plants yet Materials and Methods:Samples were collected randomly from the local market in Kemaman, Terengganu. The pods were separated from the seed and cleaned thoroughly using tap water. Extraction process by maceration using three solvents, n-hexane, ethyl acetate, and ethanol 95%. Qualitative phytochemical analysis of the extract was determined. Antimicrobial activity using Kirby-Bauer (KB) method. Results: Maceration of ethanol 95% had the highest percent yield of 17.57% among all extracts.The phytochemical analysis resulted in the three extracts containing flavonoids. The three extracts with different solvents produced antimicrobial activity......
KEYWORDS: Antimicrobial, Parkia speciose Hassk, Kirby-Bauer Disc Susceptibility Test.
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[2]. [2] Gan, C., &Latiff, A. A. (2011). Optimisation of the solvent extraction of bioactive compounds from Parkiaspeciosa pod using response surface methodology. Food Chemistry, 124(3), 1277–1283.
[3]. Harborne JB. Phytochemical methods. 2nd Edition,Chapman and Hall, New York, 1987.
[4]. Hasim, Faridah, D. N., &Kurniawati, D. A. (2015). Antibacterial activity of ParkiaspeciosaHassk. peel to Escherichia coli and Staphylococcus aureus bacteria. Journal of Chemical and Pharmaceutical Research, 7(4), 239–243.
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