GPAT-2012 PAPER
... regulators in inflammation and are the targets for antiinflammatory agents used in rheumatoid arthritis? (A) Tumor necrosis factor-a and Interleukin-1 (B) Acetylcholine esterase and Eicosanoids (C) Leukotrienes and Isoprostanes (D) Adhesion factor and Monoamine oxidase A Q.16 Which one of the follow ...
... regulators in inflammation and are the targets for antiinflammatory agents used in rheumatoid arthritis? (A) Tumor necrosis factor-a and Interleukin-1 (B) Acetylcholine esterase and Eicosanoids (C) Leukotrienes and Isoprostanes (D) Adhesion factor and Monoamine oxidase A Q.16 Which one of the follow ...
GPAT-2012 PAPER
... regulators in inflammation and are the targets for antiinflammatory agents used in rheumatoid arthritis? (A) Tumor necrosis factor-a and Interleukin-1 (B) Acetylcholine esterase and Eicosanoids (C) Leukotrienes and Isoprostanes (D) Adhesion factor and Monoamine oxidase A Q.16 Which one of the follow ...
... regulators in inflammation and are the targets for antiinflammatory agents used in rheumatoid arthritis? (A) Tumor necrosis factor-a and Interleukin-1 (B) Acetylcholine esterase and Eicosanoids (C) Leukotrienes and Isoprostanes (D) Adhesion factor and Monoamine oxidase A Q.16 Which one of the follow ...
Synthesis and Evaluation of Antifungal Activity of Benzothiazole
... dolastatin. Due to their important pharmaceutical utilities, the synthesis of these compounds is of considerable interests. Being a heterocyclic compound, benzothiazole finds its use in research as a starting material for the synthesis of bioactive molecules. Its aromaticity makes it relatively stab ...
... dolastatin. Due to their important pharmaceutical utilities, the synthesis of these compounds is of considerable interests. Being a heterocyclic compound, benzothiazole finds its use in research as a starting material for the synthesis of bioactive molecules. Its aromaticity makes it relatively stab ...
Benazepril to lisinopril conversion
... Benazepril to lisinopril conversion Benazepril to lisinopril conversion Lisinopril is classified as FDA pregnancy risk category D. Once pregnancy is detected, every effort should be made to discontinue lisinopril therapy. Lisinopril Conversion to ACE-Is and ARBs *Approximate dosing was based off of ...
... Benazepril to lisinopril conversion Benazepril to lisinopril conversion Lisinopril is classified as FDA pregnancy risk category D. Once pregnancy is detected, every effort should be made to discontinue lisinopril therapy. Lisinopril Conversion to ACE-Is and ARBs *Approximate dosing was based off of ...
An overview of interactions between grapefruit juice and drugs ReView Abstract
... Because grapefruit contains fibre, vitamin C, antioxidants and phytochemicals, the fruit and its juice are consumed widely to help meet daily nutritional requirements. However, in the past 15 years, studies have shown that grapefruit juice can induce a several-fold increase in the plasma levels of p ...
... Because grapefruit contains fibre, vitamin C, antioxidants and phytochemicals, the fruit and its juice are consumed widely to help meet daily nutritional requirements. However, in the past 15 years, studies have shown that grapefruit juice can induce a several-fold increase in the plasma levels of p ...
TECTONA GRANDIS Research Article NEHA KHERA
... However, there was highly significant increase in the T/C ratio in the group of animals treated with lapachol in combination with radiation. The change in the T/C ration was concentration and dose dependent. There was significant change in the percentage of body weight [38]. Anti-metastatic activity ...
... However, there was highly significant increase in the T/C ratio in the group of animals treated with lapachol in combination with radiation. The change in the T/C ration was concentration and dose dependent. There was significant change in the percentage of body weight [38]. Anti-metastatic activity ...
Research Article EVALUATION OF A NEW TABLET DISINTEGRANT
... generally considered acceptable. The mechanical strength of tablets can also be measured by the crushing strength – friability ratio (CSFR) 18. Generally, the higher the CSFR, the stronger the tablet. Okra powders formed strong tablets. ...
... generally considered acceptable. The mechanical strength of tablets can also be measured by the crushing strength – friability ratio (CSFR) 18. Generally, the higher the CSFR, the stronger the tablet. Okra powders formed strong tablets. ...
as a PDF
... performed, because specific substrate can be useful for profiling CYP2J2 inhibition of drug candidates in vitro in liver microsome with use of cocktail method, and specific potent CYP2J2 inhibitor can also facilitate the evaluation of the role that CYP2J2 plays in liver microsomal metabolism and DDI ...
... performed, because specific substrate can be useful for profiling CYP2J2 inhibition of drug candidates in vitro in liver microsome with use of cocktail method, and specific potent CYP2J2 inhibitor can also facilitate the evaluation of the role that CYP2J2 plays in liver microsomal metabolism and DDI ...
pharmacology basic principles
... There is a lag-time before effect as it takes time to make proteins; effects can persist long after drug eliminated from system 2Y to slow turnover of enzymes and proteins Eg. Corticosteroids (binding to receptor triggers release of Hsp90 which was covering DNAbinding portion of receptor), mineraloc ...
... There is a lag-time before effect as it takes time to make proteins; effects can persist long after drug eliminated from system 2Y to slow turnover of enzymes and proteins Eg. Corticosteroids (binding to receptor triggers release of Hsp90 which was covering DNAbinding portion of receptor), mineraloc ...
MAXIDOL® Liquid Gels
... or any of the excipients in the caplets. For a complete listing, see the Dosage Forms, Composition and Packaging section of the product monograph with a history of asthma, urticaria, or allergic-type reactions after taking acetylsalicylic acid (ASA) or other NSAIDs (i.e. complete or partial syndrome ...
... or any of the excipients in the caplets. For a complete listing, see the Dosage Forms, Composition and Packaging section of the product monograph with a history of asthma, urticaria, or allergic-type reactions after taking acetylsalicylic acid (ASA) or other NSAIDs (i.e. complete or partial syndrome ...
1 Spironolactone Tablets, USP WARNING
... performed in rats, with its proliferative effects manifested on endocrine organs and the liver. In an 18-month study using doses of about 50, 150 and 500 mg/kg/day, there were statistically significant increases in benign adenomas of the thyroid and testes and, in male rats, a dose-related increase ...
... performed in rats, with its proliferative effects manifested on endocrine organs and the liver. In an 18-month study using doses of about 50, 150 and 500 mg/kg/day, there were statistically significant increases in benign adenomas of the thyroid and testes and, in male rats, a dose-related increase ...
TRIS AMINO Technical Data Sheet
... anti-allergy drug (Figure 5). It is a biologue of disodium cromoglycate (DSCG), but lodoxamide trometamol has been shown to have much greater intravenous activity than does DSCG, as well as possessing significant oral activity.9 It acts by preventing histamine release, through inhibiting the calcium ...
... anti-allergy drug (Figure 5). It is a biologue of disodium cromoglycate (DSCG), but lodoxamide trometamol has been shown to have much greater intravenous activity than does DSCG, as well as possessing significant oral activity.9 It acts by preventing histamine release, through inhibiting the calcium ...
Antiatherogenic Properties of Naringenin, a Citrus Flavonoid
... plasma (3,29) following oral doses of pure naringin (3,50) or grapefruit juice (3,29,64,92). Hesperetin has been detected also in human urine (3,92) and plasma (3) following doses of pure compound or orange juice. These results showed that naringenin and hesperetin can be absorbed from the diet. In ...
... plasma (3,29) following oral doses of pure naringin (3,50) or grapefruit juice (3,29,64,92). Hesperetin has been detected also in human urine (3,92) and plasma (3) following doses of pure compound or orange juice. These results showed that naringenin and hesperetin can be absorbed from the diet. In ...
Severe Intoxication with the Veterinary Tranquilizer Xylazine in
... before the mass spectrometer was turned on. Because the urine sample was collected very early, the concentration of the metabolites was too small. Pharmacokinetic studies in animals found an exponential decline of xylazine concentration after i.m. dosage. The data were described by an open one-compa ...
... before the mass spectrometer was turned on. Because the urine sample was collected very early, the concentration of the metabolites was too small. Pharmacokinetic studies in animals found an exponential decline of xylazine concentration after i.m. dosage. The data were described by an open one-compa ...
an-update-of-taste-m.. - Scholars Research Library
... polymeric network used is a copolymer of styrene and divinylbenzene (DVB). Apart from this other polymers such as those of acrylic and methacrylic acid cross linked with DVB and containing appropriate functional groups, have been used as ion exchange drug carriers.[42,43] Types of resins (table 4) I ...
... polymeric network used is a copolymer of styrene and divinylbenzene (DVB). Apart from this other polymers such as those of acrylic and methacrylic acid cross linked with DVB and containing appropriate functional groups, have been used as ion exchange drug carriers.[42,43] Types of resins (table 4) I ...
TASTE MASKING TECHNOLOGIES: A REVIEW Review Article SHALINI SHARMA AND SHAILA LEWIS*
... by coating is selection of coating polymers. Ideally, the coating polymers should be such that it prevents the release of active agent in the oral cavity, following per oral intake, but allows it in stomach or small intestine where the drug is expected to be absorbed. Polyme ...
... by coating is selection of coating polymers. Ideally, the coating polymers should be such that it prevents the release of active agent in the oral cavity, following per oral intake, but allows it in stomach or small intestine where the drug is expected to be absorbed. Polyme ...
Cucurbit[n]urils as excipients in pharmaceutical dosage forms
... Cucurbit[n]urils (CB[n], where n = 5, 6, 7, 8, 10 or 14, Figure 1) are a family of synthetic macrocycles that are able to form host-guest complexes with a variety of molecules (1). They have a range of applications, including: waste remediation, chromatography, molecular switches and handcuffs, diag ...
... Cucurbit[n]urils (CB[n], where n = 5, 6, 7, 8, 10 or 14, Figure 1) are a family of synthetic macrocycles that are able to form host-guest complexes with a variety of molecules (1). They have a range of applications, including: waste remediation, chromatography, molecular switches and handcuffs, diag ...
Introduction
... Ranitidine is a drug used in the treatment of digestive tract bleeding, primarily in the upper segment, due to mucus alteration during neonatal stage. In addition, it is highly used in the prevention of gastric bleeding in children requiring therapeutic management in intensive care unities. However, ...
... Ranitidine is a drug used in the treatment of digestive tract bleeding, primarily in the upper segment, due to mucus alteration during neonatal stage. In addition, it is highly used in the prevention of gastric bleeding in children requiring therapeutic management in intensive care unities. However, ...
Gamma Hydroxybutyric Acid (GHB) Intoxication Abstract 730
... infarction, stroke, sepsis, small bowel ischemia, hypovolemic shock, ionizing radiation, and oxygen free radicals.2,5,6 Despite promising beneficial effects in basic science research, GHB has not found widespread clinical use. In the 1960–70’s, GHB was used as a general anesthetic agent but fell out ...
... infarction, stroke, sepsis, small bowel ischemia, hypovolemic shock, ionizing radiation, and oxygen free radicals.2,5,6 Despite promising beneficial effects in basic science research, GHB has not found widespread clinical use. In the 1960–70’s, GHB was used as a general anesthetic agent but fell out ...
sertraline is metabolized by multiple cytochrome p450 enzymes
... N-desmethyl metabolite or via initial deamination of the methylamino substituent (data on file, Pfizer, Inc.). Also, sertraline undergoes N-carbamoyl glucuronidation, an unusual reaction in drug metabolism, albeit that this pathway appears to be minor in human but major in the dog (Tremaine et al., ...
... N-desmethyl metabolite or via initial deamination of the methylamino substituent (data on file, Pfizer, Inc.). Also, sertraline undergoes N-carbamoyl glucuronidation, an unusual reaction in drug metabolism, albeit that this pathway appears to be minor in human but major in the dog (Tremaine et al., ...
10 Rocuronium for Tracheal Intubation
... seconds) and 1.2 mg/kg of rocuronium (33+5 seconds); both were significantly less than the 0.8 mg/kg group (46+8 seconds). Time to 25% recovery from 1.2 mg/kg of rocuronium was nearly 8 times longer than after succinylcholine (41+13 compared to 5.2+1.9 minutes). Another study by Mazurek and coworker ...
... seconds) and 1.2 mg/kg of rocuronium (33+5 seconds); both were significantly less than the 0.8 mg/kg group (46+8 seconds). Time to 25% recovery from 1.2 mg/kg of rocuronium was nearly 8 times longer than after succinylcholine (41+13 compared to 5.2+1.9 minutes). Another study by Mazurek and coworker ...
Madhuca Indica JF Gmel. (Sapotaceae): An Overview
... standard. Ulcerated area was measured by Image J software. Various antioxidant parameter like SOD, GSH, MDA, MPO, NO and histamine were also determined. After 4 week treatment period, aqueous extract of plant of M. indica at the dose of 200 and 400 mg/kg, p.o. (P <0.01, P <0.001) showed significant ...
... standard. Ulcerated area was measured by Image J software. Various antioxidant parameter like SOD, GSH, MDA, MPO, NO and histamine were also determined. After 4 week treatment period, aqueous extract of plant of M. indica at the dose of 200 and 400 mg/kg, p.o. (P <0.01, P <0.001) showed significant ...
nitropress
... When the Fe+++ of cytochromes is bound to cyanide, the cytochromes are unable to participate in oxidative metabolism. In this situation, cells may be able to provide for their energy needs by utilizing anaerobic pathways, but they thereby generate an increasing body burden of lactic acid. Other cell ...
... When the Fe+++ of cytochromes is bound to cyanide, the cytochromes are unable to participate in oxidative metabolism. In this situation, cells may be able to provide for their energy needs by utilizing anaerobic pathways, but they thereby generate an increasing body burden of lactic acid. Other cell ...
DIPYRIDAMOLE TABLETS USP 25 MG, 50 MG AND 75 MG
... In these trials, the coumarin anticoagulant was begun between 24 hours and 4 days postoperatively, and the dipyridamole tablets were begun between 24 hours and 10 days postoperatively. The length of follow-up in these trials varied from 1 to 2 years. Dipyridamole tablets do not influence prothrombi ...
... In these trials, the coumarin anticoagulant was begun between 24 hours and 4 days postoperatively, and the dipyridamole tablets were begun between 24 hours and 10 days postoperatively. The length of follow-up in these trials varied from 1 to 2 years. Dipyridamole tablets do not influence prothrombi ...
opioid codrugs for pain management - UKnowledge
... treating moderate to severe pain, but opioid alone therapy is associated with several adverse effects, development of tolerance and addiction potential. One way to solve these problems is to administer opioids with adjuvant drugs. In this project several opioid molecules were combined with other adj ...
... treating moderate to severe pain, but opioid alone therapy is associated with several adverse effects, development of tolerance and addiction potential. One way to solve these problems is to administer opioids with adjuvant drugs. In this project several opioid molecules were combined with other adj ...
Discovery and development of proton pump inhibitors
Proton pump inhibitors (PPIs) block the gastric hydrogen potassium ATPase (H+,K+-ATPase) and inhibit gastric acid secretion. These drugs have emerged as the treatment of choice for acid-related diseases, including gastroesophageal reflux disease (GERD) and peptic ulcer disease.PPIs also can bind to other types of proton pumps such as those that occur in cancer cells and are finding applications in the reduction of cancer cell acid efflux and reduction of chemotherapy drug resistance.