11 research outputs found

    Interaction Studies of ACE Inhibitors with Statins

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    Twenty First Century- An Era of Infectious Diseases

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    Degradation study of different brands of amlodipine using UV spectrophotometer

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    Abstract There are several different brands available for Amlodipine as it is the most prescribed oral antihypertensive agents that is used for primary and secondary hypertension. The objective of this study develops the degradation studies of different brands of Amlodipine besylate 5 mg. This drug was subjected to different stress conditions as per International Conference on Harmonization guidelines (ICH). An ultraviolet UV spectroscopic method was developed for analysis of the drug in the presence of the degradation products. Distilled water was used as a solvents. The amount of degraded drugs was calculated by taking the absorbance at 238 nm. According to the assay limit of USP specified that the content should not be less than 95% and not more than 105% of labelled amount. Brand 1, 2 and 5 are degraded by UV light exposure and Brand 1 and 2 degraded after the heat exposure. On basic pH brand 1, 2 ,4 and 5 showed degradation after the addition of 1N NaOH while brand 3 do not degrade as the base has no impact on Amlodipine concentration. On addition of 1N HCL brands 1, 2, 4 and 5 showed heavy degradation and brand 3 is remain nondegradable in acidic pH. The method was found to be simple and less time consuming and cost effective

    Regimental and Diet-o-therapy during pregnancy and their effects

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    Prevention of health in the antenatal stage is essential for future generations' growth and development before entering this world. Care during pregnancy is called Tadbeer-e-Hamla from Unani perspective. According to the Tibb-e-Unani and ayurvedic medicine system, health restoration and maintenance in different conditions, even diseased or healthy, is achieved by managing lifestyle factors. This management is based on which type of condition you suffer and the signs and symptoms that diagnose this condition. Then this diagnosis is also confirmed by the Unani tools that are Pulse (Nabz), Urine (Baul), and Stool (Baraz). After securing the state of the body, treatment starts with four basic principles of management (Usool-e-Ilaj). These principles of management are regimental therapy (Ilaj-bil-tadbeer), Diet therapy (Ilaj-bil-ghiza), Pharmacotherapy (Ilaj-bil-dawa), and Surgery (Jarahat). In this paper, regimental treatments and diet therapy are described in detail during pregnancy

    Interaction Studies of ACE Inhibitors with Antidiabetic Drugs

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    Angiotensin converting enzyme (ACE)-inhibitors are effective in patients with mild to moderately severe hypertension, collagen vascular and cardiovascular disease. They are also used in the prevention and treatment of myocardial infarction and in the management of cardiac arrhythmias. Patients with cardiovascular diseases are generally on multiple medicines that’s why it is imperative to study drug–drug interactions of medicines which are commonly taken together in any given case, as combined administration of different medicines can significantly influence the availability of drugs. In the present study we investigated the “in vitro” interactions of ACE inhibitors (enalapril, captopril and lisinopril) with frequently prescribed and co-administered drugs in simulated human body environments. These interactions were monitored by means of UV spectrophotometry and separation technique as RP-HPLC. Prior to start of actual drug interactions, the method of analysis of each drug was established and its various parameters validated for considering its use in testing of drug in vitro as well as in human serum. For this purpose, an attempt was made to develop a number of new HPLC methods for determination of ACE inhibitors (enalapril, captopril and lisinopril) and simultaneously with interacting drugs. These methods were optimized, validated and then successfully employed for the quantitation of enalapril, captopril and lisinopril and selected drugs in interactions studies. As a result, new methods for the quantitation of individual as well as multiple drugs were developed. The interacting drugs selected were antidiabetic drugs (metformin, glibenclamide, glimepride and pioglitazone. Interaction consequences revealed that the availability of enalapril was not affected in presence of antidiabetic drugss whereas the availability of captopril and lisinopril were altered in presence of NIDDMs

    An in-vitro evaluation of skin protection factor of non-polar date seed extract from three different date varieties Ajwa, Aseel and Khapra by UV spectrophotometry

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    Objective: Skin is the primary layer of human body which act as protective barrier against exogenous chemicals, UV radiations as well as microorganisms. Maintaining the skin morphology under regular environmental stresses and controlling age related skin changes is one of the biggest challenges for modern science, pharmaceutical and cosmetics industry. These environmental stresses, such as excessive exposure to UV radiations, can even lead to the devastating skin disorders such as skin cancer. Dates seed has capability to protect skin against the damages caused by solar radiations, which mostly appear in the forms of wrinkles and some other skin related issues. Methods: Therefore, current research is focused on to analyze sun protection factor (SPF) of two non-polar fractions obtained from crushed seeds of three different varieties of i.e., Ajwa, Aseel and Khapra. Results: Results indicate that the highest value of SPF was found in AEA i.e., 15.061 at 200ppm while no difference was observed in the SPF values of KPPE. Conclusion: Hence, it could be concluded that the ethyl acetate fraction of all date seed varieties could be potential Ajwa, Aseel and Khapra could be a promising source of cosmetic and pharmaceutical preparations due to the potential SPF value except petroleum ether of Khapra extract

    SIMULTANEOUS DETERMINATION OF ENALAPRIL AND STATIN'S IN PHARMACEUTICAL FORMULATIONS BY RP-HPLC

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    Phytochemical characterization, antioxidant activity and antihypertensive evaluation of Ocimum basilicum L. in l-NAME induced hypertensive rats and its correlation analysis

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    Ocimum basilicum Linn. (basil) is an aromatic culinary herb that has shown a great potential in therapeutic world. It has many promising pharmacological activities that make it centre for investigations for many researchers. Current study has been planned to determine chemical constituents of basil leaves extracts and their in-vitro and ex-vivo antioxidant and in-vivo antihypertensive potential. GC-MS studies of non-polar extracts showed presence of 75 compounds including monoterpenes, hydrocarbons, sesquiterpenes, triterpenes, phyto-sterols and phthalates. Higher percentages of fatty acids were also identified. The major compounds include linalool (7.65%), terpineol (1.42%), tau-cadinol (13.55%), methyl palmitate (14.24%), palmitic acid (14.31%), linolenic acid (1.30%) and methyl linolenate (17.72%). Electron spray ionization mass spectrometry ESI-HRMS/MS of the polar extracts revealed the presence of alkaloids, phenolic acid, amino acid, coumarin, lignin, flavanoid and terpene derivative. Total phenolic content and total flavonoid content were determined using spectrophotometric technique and calculated as gallic acid equivalents GAE/g dry weight and rutin equivalent RE/g of dry weight respectively. The highest phenolic content and flavonoid content were found in ethyl acetate extract 9.40 mg GAE/g and 15.9 mg RE/g of dry weight. All the extracts showed significant antioxidant activity in DPPH and ABTS cation decolorization assays. Dichloromethane extract possess the highest DPPH scavenging activity, i.e., 64.12% ± 0.23 at concentration of 4 mg/ml. Moreover in ex-vivo studies all the extracts showed prominent effect by inhibiting AAPS induce oxidation in Human erythrocytes being 69.24% ± 0.18 in dichloromethane extract, 64.44% ± 0.04 in ethyl acetate and 53.33% ± 0.09 in acetone extract. The methanol extract of O. basilicum exhibited significant decrease in systolic blood pressure in l-Name induced hypertensive rats at the dose of 50 mg/kg for 28 days. Total phenolic content had a higher linear correlation (r = 0.678) with antihypertensive activity, with a level of significance 95% showing that phenolic compounds in the leaves of the plant has important role in inhibiting l –NAME induced hypertension while flavonoid compounds may play a key role in the antioxidant activities of the plant, through synergism. Conclusively, O. basilicum leaves with bioactive metabolites are a potential source for the development of antihypertensive drugs
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