• Study Resource
  • Explore
    • Arts & Humanities
    • Business
    • Engineering & Technology
    • Foreign Language
    • History
    • Math
    • Science
    • Social Science

    Top subcategories

    • Advanced Math
    • Algebra
    • Basic Math
    • Calculus
    • Geometry
    • Linear Algebra
    • Pre-Algebra
    • Pre-Calculus
    • Statistics And Probability
    • Trigonometry
    • other →

    Top subcategories

    • Astronomy
    • Astrophysics
    • Biology
    • Chemistry
    • Earth Science
    • Environmental Science
    • Health Science
    • Physics
    • other →

    Top subcategories

    • Anthropology
    • Law
    • Political Science
    • Psychology
    • Sociology
    • other →

    Top subcategories

    • Accounting
    • Economics
    • Finance
    • Management
    • other →

    Top subcategories

    • Aerospace Engineering
    • Bioengineering
    • Chemical Engineering
    • Civil Engineering
    • Computer Science
    • Electrical Engineering
    • Industrial Engineering
    • Mechanical Engineering
    • Web Design
    • other →

    Top subcategories

    • Architecture
    • Communications
    • English
    • Gender Studies
    • Music
    • Performing Arts
    • Philosophy
    • Religious Studies
    • Writing
    • other →

    Top subcategories

    • Ancient History
    • European History
    • US History
    • World History
    • other →

    Top subcategories

    • Croatian
    • Czech
    • Finnish
    • Greek
    • Hindi
    • Japanese
    • Korean
    • Persian
    • Swedish
    • Turkish
    • other →
 
Profile Documents Logout
Upload
Misoprostol
Misoprostol

... • high variability of plasma levels between and within studies • mean plasma levels after single oral doses show a linear relationship with dose over the range of 200-400 mcg • no accumulation of misoprostol noted in multiple dose studies • serum protein binding less than 90%, concentration-independ ...
Slides
Slides

... dose in an office or clinic for S/S bradycardia / heart block. If med stopped > 2 weeks then restart monitoring as new therapy ...
DESIGN AND CHARACTERIZATION OF MODIFIED RELEASE ISONIAZID AND SALBUTAMOL
DESIGN AND CHARACTERIZATION OF MODIFIED RELEASE ISONIAZID AND SALBUTAMOL

... The objective of the present study was to improve the therapeutic efficacy of a formulation which contains two drugs i.e. Isoniazid and Salbutamol sulphate. The present invention is to provide a dosage form comprising of an active ingredient (Isoniazid) as modified release and another active ingredi ...
$doc.title

... abnormalities,  and  problems  with  atten-­‐ tion  and  memory,  although  it  is  possible   that  some  of  these  effects  may  be  due  to   the  use  of  other  drugs  in  combination   with  MDMA  (especially  marijuana).     ...
Properties of Ingredients in Dasanga Guggulu
Properties of Ingredients in Dasanga Guggulu

... century. It is defined as elevated concentrations of any or all the lipids in the plasma, including hypertriglyceridemia, hypercholesterolemia, etc1.Less physical activities, sedentary life style and mental stress are negatively influenced on increasing serum lipids level. Due to modernization of th ...
FDA Warning Letter to SR Burzynski Manufacturing Facility 2016
FDA Warning Letter to SR Burzynski Manufacturing Facility 2016

... described above. For example, there are inherent flaws in your facility design that promote the influx of poor quality air into the aseptic processing (ISO 5) zone where the sterile product is exposed. These and other conditions observed at your firm and discussed in this Warning Letter create conta ...
DESIGN AND OPTIMISATION OF EXTENDED RELEASE METOPROLOL SUCCINATE
DESIGN AND OPTIMISATION OF EXTENDED RELEASE METOPROLOL SUCCINATE

... reproducibility and stability of dosage forms, process validation and industrial feasibility due to easy scale-up [2]. A wide miscellanea of polymers employed as release retardants can broadly be classified into three categories: Plastic matrix systems/insoluble or skeleton matrices where drug relea ...
H.M. Garraffo, T.F. Spande, M. Williams, Heterocycles, 79, (2009)
H.M. Garraffo, T.F. Spande, M. Williams, Heterocycles, 79, (2009)

... biomedical research environment, being replaced with superficiality. Daly's reduction to practice of the concept of nicotinic analgesia, proposed in 193232 and some 62 years later in 1994,8 is a prime example of what Black termed commitment - never giving up on a new concept. Thus Daly's perseveranc ...
Coated balloons
Coated balloons

... • These data compare favourable to the data from the same investigators in a similar group of 58 patients that were treated with non-coated balloons: at 3 month angiographic follow-up restenosis of more than 50% was seen in 69% of cases, with restenosis of the whole treated segment in 56% of cases ...
Bridging Studies
Bridging Studies

...  To describe the characteristics of foreign clinical data that will facilitate their extrapolation to different populations and support their acceptance as a basis for registration of a medicine in a new region  To describe regulatory strategies that minimize duplication of clinical data and facil ...
Use of Heparin HyperD® M Affinity Resin for Batch Mode Protein
Use of Heparin HyperD® M Affinity Resin for Batch Mode Protein

... proteins that bind, as seen in the eluate fractions in Figure 4 compared to eluate fractions in Figure 3. Albumin lower salt elution buffer (e.g., 0.5 M), but in this case it is easier to prevent binding of impurities than to selectively ...
The Rational Use of Drugs - Part 4
The Rational Use of Drugs - Part 4

... When the assumption of linearity does not hold, the EC50 no longer approximates the KD. For example, the EC50 will be much smaller than the KD when “spare receptors” are present. A tissue is said to express “spare receptors” when only a small fraction of the receptor population must be occupied by d ...
127 - Chimica
127 - Chimica

... (CO),] (compound 4), identified spectroscopically (IR and 'H NMR), which was previously synthesized'" by photochemical hydrogenation of [Re2(CO)lo].The new method parallels that recently discovered8for the transformation of [Re4H6(CO)12]2into the unsaturated [Re4H5(CO),,]-. As in that case, the proc ...
Drug Effects on the Fetus and Breast-Fed Infant
Drug Effects on the Fetus and Breast-Fed Infant

... pregnancy experience, so the estimation of pregnancy risk is difficult at best. Three methods to reduce the risks arising from treating pregnant women with drugs are readily apparent: try to use only those agents considered relatively safe in pregnancy; if a drug known to be toxic must be used, avoi ...
View slide set - Mayo Clinic Center for Tuberculosis
View slide set - Mayo Clinic Center for Tuberculosis

... • TDM (after 3 weeks) on her TB medications show the following: • 2h post dose levels: • PZA – below the lower limit of detection • EMB – below the lower limit of detection • INH – below the lower limit of detection • RIF – below the lower limit of detection ...
ANTHELMINTIC DRUGS
ANTHELMINTIC DRUGS

...  mechanism of action: similar to other benzimidazoles.It is ovicidal for some paracites  clinical uses:  should be given after meals .and tablets should be chewed  for strongyloides(thread worms) infections: 25 mg /kg ( not more than 1.5 grams) twice daily for 2 days ,can be repeated after 2 wee ...
Bulletin #90
Bulletin #90

... renal dialysis. Note: Coverage for dialysis patients is provided under the Saskatchewan Aids to Independent Living (SAIL) Program. Exception Drug Status coverage is NOT required for SAIL patients. (b) For management of hypocalcemia and clinical manifestations associated with post-surgical hypoparath ...
Epidural and CSF pharmacokinetics of drugs
Epidural and CSF pharmacokinetics of drugs

... large number of different drugs (local anesthetics, opioids, a2-agonists, baclofen, ketamine, midazolam, neostigmine, adenosine, steroids, ziconotide) to provide anesthesia, but also analgesia and treatment of spasticity in a variety of acute and chronic settings. However, ...
Beware: Clinically Significant Drug Interactions in the Treatment of HIV
Beware: Clinically Significant Drug Interactions in the Treatment of HIV

... Mechanism of ARV Drug Interactions • Most clinically relevant antiretroviral (ARV) drug ...
Document
Document

... of the Australian response to heroin dependence, typically implemented as a long-term treatment option which reflects the evidence of improved outcomes with longer treatment duration (>19 months).46 The second pathway can be broadly referred to as abstinence-oriented treatment. Detoxification is the ...
`Let Them Eat Prozac` - Introduction: The SSRI Issues
`Let Them Eat Prozac` - Introduction: The SSRI Issues

... first of the proton-pump inhibitors, omeprazolexii, which in 1990 was on its way to becoming one of the best-selling drugs on the market. Despite the revenues from omeprazole, Astra were forced into a merger later in the decade. This story indicates how big the stakes can be. A troublesome side effe ...


... competitive binding. Drugs that may be present in the oral fluid specimen compete against their respective drug conjugate for binding sites on their specific antibody. ...
Introduction - Let them Eat Prozac
Introduction - Let them Eat Prozac

... first of the proton-pump inhibitors, omeprazolexii, which in 1990 was on its way to becoming one of the best-selling drugs on the market. Despite the revenues from omeprazole, Astra were forced into a merger later in the decade. This story indicates how big the stakes can be. A troublesome side effe ...
Dose translation from animal to human studies revisited
Dose translation from animal to human studies revisited

... to exist regarding the appropriate method for allometric dose translations, especially when starting new animal or clinical studies. The need for education regarding appropriate translation is evident from the media response regarding some recent studies where authors have shown that resveratrol, a ...
Precipitation and complex formation reactions based titrimetric and
Precipitation and complex formation reactions based titrimetric and

... an
< 1 ... 111 112 113 114 115 116 117 118 119 ... 391 >

Drug design



Drug design, sometimes referred to as rational drug design or simply rational design, is the inventive process of finding new medications based on the knowledge of a biological target. The drug is most commonly an organic small molecule that activates or inhibits the function of a biomolecule such as a protein, which in turn results in a therapeutic benefit to the patient. In the most basic sense, drug design involves the design of molecules that are complementary in shape and charge to the biomolecular target with which they interact and therefore will bind to it. Drug design frequently but not necessarily relies on computer modeling techniques. This type of modeling is often referred to as computer-aided drug design. Finally, drug design that relies on the knowledge of the three-dimensional structure of the biomolecular target is known as structure-based drug design. In addition to small molecules, biopharmaceuticals and especially therapeutic antibodies are an increasingly important class of drugs and computational methods for improving the affinity, selectivity, and stability of these protein-based therapeutics have also been developed.The phrase ""drug design"" is to some extent a misnomer. A more accurate term is ligand design (i.e., design of a molecule that will bind tightly to its target). Although design techniques for prediction of binding affinity are reasonably successful, there are many other properties, such as bioavailability, metabolic half-life, side effects, etc., that first must be optimized before a ligand can become a safe and efficacious drug. These other characteristics are often difficult to predict with rational design techniques. Nevertheless, due to high attrition rates, especially during clinical phases of drug development, more attention is being focused early in the drug design process on selecting candidate drugs whose physicochemical properties are predicted to result in fewer complications during development and hence more likely to lead to an approved, marketed drug. Furthermore, in vitro experiments complemented with computation methods are increasingly used in early drug discovery to select compounds with more favorable ADME (absorption, distribution, metabolism, and excretion) and toxicological profiles.
  • studyres.com © 2025
  • DMCA
  • Privacy
  • Terms
  • Report