• Study Resource
  • Explore Categories
    • 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
EFFECT OF ECLIPTA ALBA ON FRUCTOSE INDUCED HYPERTENSION IN ALBINO...
EFFECT OF ECLIPTA ALBA ON FRUCTOSE INDUCED HYPERTENSION IN ALBINO...

... administration standard & test drugs by non invasive BP system for rodents. Results- A rise in blood pressure was found on day 16th of fructose diet. EEEA decreased the rise in B.P significantly in a dose dependent manner comparable to Quinapril. Conclusion- Eclipta alba Hassk was found to posses si ...
Prescribing Information
Prescribing Information

... buspirone, and St. John’s Wort [see Drug Interactions (7.1)]. Amphetamines and amphetamine derivatives are known to be metabolized, to some degree, by cytochrome P450 2D6 (CYP2D6) [see Clinical Pharmacology 12.3]. The potential for a pharmacokinetic interaction exists with the coadministration of CY ...
Slides generic guide - Gerontological Nursing Association
Slides generic guide - Gerontological Nursing Association

... Always need to use the lowest possible dose and review frequently Most patients need these medications only for short periods (few months) ...
2. Basic Principles of Stability Testing
2. Basic Principles of Stability Testing

... ¹Only for semi-quantitative procedures instead of quantitation limit. ²At this stage only for drug products and not for drug substance. The extend of validation reflects the objective of the analysis in the six steps of development. At the beginning of the stress testing with the drug substance no i ...
2.1 - Powerpoint D
2.1 - Powerpoint D

... commonly used drugs in sport. They mimic testosterone, a male ...
Biophytis presents preliminary clinical data of SARA
Biophytis presents preliminary clinical data of SARA

... Sarcopenia is defined as a loss of muscle mass and strength with ageing leading to severe decline in mobility and physical ability. Although no candidate drug has received yet marketing authorization for this geriatric condition, Sarcopenia was recently recognized as an independent geriatric conditi ...
Vol 20 No 5 2014 (PDF 659Kb)
Vol 20 No 5 2014 (PDF 659Kb)

... are not all free from DDIs (Tables 1 and 2).25,30 Many of the new AEDs are cleared fully or partly by inducible enzymes and are a target for interactions mediated by enzyme induction (Table 1).26 Overall, levetiracetam, gabapentin, lacosamide, tiagabine, vigabatrin and zonisamide are associated with ...
LONGRANGE® (eprinomectin) and IVOMEC® (ivermectin) Brand
LONGRANGE® (eprinomectin) and IVOMEC® (ivermectin) Brand

... The macrocyclic lactones have a unique mode of action. Compounds of this class bind selectively and with high affinity to glutamate-gated chloride ion channels that are present in invertebrate nerve and muscle cells. This leads to an increase in the permeability of the cell membrane to chloride ions ...
contaminantion in herbal drug and preparations
contaminantion in herbal drug and preparations

... integrate phytotherapy into their doctrines even though they are based on different cultural models. Pharmacist and physicians should be more aware about safety of herbal preparation as use of these preparations is increasing by patients day by day. Chemical compounds of herbal drugs could also be h ...
DOPAMINE ANTAGONISTS: PHENOTHIAZINE/THIOXANTHENE SAR
DOPAMINE ANTAGONISTS: PHENOTHIAZINE/THIOXANTHENE SAR

... symptoms) or tuberoinfundibular (prolactin release). They also bind with varying affinities on nondopaminergic sites, such as cholinergic (muscarinic), alpha-1adrenergic and histamine-1 receptors, which can partially explain the varied side effect profiles for each agent. Typical antipsychotics have ...
15-002 – February 24, 2015
15-002 – February 24, 2015

... oxycodone CR products on the market. In April 2013, the U.S. Food and Drug Administration rejected approval of generic versions of oxycodone CR that were not tamper resistant due to concerns of potential misuse. In June 2014, Health Canada initiated public consultation on proposed regulations, under ...
Towards early inclusion of children in tuberculosis drugs trials: a
Towards early inclusion of children in tuberculosis drugs trials: a

... morbidity and mortality in children in the middleincome and low-income countries. The proportions of people infected probably underestimate the global disease burden, with childhood cases accounting for an estimated 6% of all reported cases,1 and at least double this percentage in tuberculosis endem ...
bicalutamide - Cancer Care Ontario
bicalutamide - Cancer Care Ontario

... breach of contract or tort (including negligence), and even if advised of the possibility thereof. Anyone using the  information in the Formulary does so at his or her own risk, and by using such information, agrees to indemnify CCO  and its content providers from any and all liability, loss, damage ...
Americas
Americas

... kits containing sterile syringes, condoms and basic medical supplies to prevent the transmission of blood-borne diseases such as HIV/AIDS and hepatitis C. ...
Treatment of Cough
Treatment of Cough

... Treatment of Cough 1. Antitussive a. Opioid i. Codeine (methylmorphine) b. Non – opioid i. Dextromethorphan 2. Expectorant a. Guaifenesin 3. Mucolytics a. N – actylcysteine b. Bromhexine c. Ambroxol (active metabolite of Bromhexine) ...
Non Compartmental Pharmacokinetics
Non Compartmental Pharmacokinetics

... Sem,UCPSc,KU ...
An introduction to Phase 1 dual
An introduction to Phase 1 dual

... If a prior ordering of the dose combinations can be assumed then a 1-dimensional CRM can be applied. 2 Alternatively, the likelihood of each possible ordering can be assessed after each patient is recruited. 3 Can become problematic if many dose levels are used (many possible orderings). ...
Modelling and simulation to help define MABEL and Starting
Modelling and simulation to help define MABEL and Starting

... • Extrapolate model to humans using all relevant data (literature, in vitro human etc) • Perform simulations considering both uncertainty in model parameters and in scale-up • This approach should help select a more rational starting dose for FIH within the minimum anticipated biological effect leve ...
PowerPoint Presentation - Lecture 7
PowerPoint Presentation - Lecture 7

... • Candidiasis = opportunistic infection - body’s defense mechanism impaired allowing overgrowth of fungus • Drugs - antibiotics, contraceptives & immunosuppressives may alter body’s defense mechanisms ...
Toxic epidermal necrolysis: an update
Toxic epidermal necrolysis: an update

... TEN is a rare, mostly drug-induced, severe mucocutoneous reaction with various complications and high mortality[7]. TEN are rare but serious dermatologic disorders. I t gave rise to such conditions which are of medical emergency in nature requiring prompt diagnosis and management. These are often dr ...
Comprehensive Translational Assessment of Human Induced
Comprehensive Translational Assessment of Human Induced

... correlation for clinically arrhythmogenic compounds (Clements and Thomas 2014; Harris et al. 2013). With these technologies, we focus on their ability to measure prolonged repolarization – action potential duration (APD) with VSD and field potential duration (FPD) by MEA – and detect the presence of ...
ANALYSIS  OF COMPARTMENT  MODELS, KINETICS  OF
ANALYSIS OF COMPARTMENT MODELS, KINETICS OF

... Clearance can be defined as the volume of plasma which is completely cleared of drug per unit time. The symbol is CL and the units are ml/min, L/hr, i.e. volume per time. Another way of looking at Clearance is to consider the drug being eliminated from the body ONLY via the kidneys. [If we were to a ...
Vioxx Report.indd - The Physicians Committee
Vioxx Report.indd - The Physicians Committee

... events were likely with Vioxx unless patients were also allowed to take low-dose aspirin, but that doing so would likely negate the GI toxicity advantage for Vioxx. Merck appears to have attempted to circumvent this issue by limiting clinical evaluations to low-risk patients, promoting alternative e ...
Exhibit B
Exhibit B

... Docket No.2001P-0574/CP1 and 2005P-0061/CP1 FDA disagrees with Novartis' conclusions. By their very nature, bioequivalence studies are designed to determine if the same doses of two different products provide the same plasma concentrations of the active ingredient over time .' While data on symptom ...
our conference presentation
our conference presentation

... that includes hydroxyproline is elastin and so for this reason, hydroxyproline content can be used as an indicator to determine collagen level. ...
< 1 ... 200 201 202 203 204 205 206 207 208 ... 707 >

Drug discovery



In the fields of medicine, biotechnology and pharmacology, drug discovery is the process by which new candidate medications are discovered. Historically, drugs were discovered through identifying the active ingredient from traditional remedies or by serendipitous discovery. Later chemical libraries of synthetic small molecules, natural products or extracts were screened in intact cells or whole organisms to identify substances that have a desirable therapeutic effect in a process known as classical pharmacology. Since sequencing of the human genome which allowed rapid cloning and synthesis of large quantities of purified proteins, it has become common practice to use high throughput screening of large compounds libraries against isolated biological targets which are hypothesized to be disease modifying in a process known as reverse pharmacology. Hits from these screens are then tested in cells and then in animals for efficacy.Modern drug discovery involves the identification of screening hits, medicinal chemistry and optimization of those hits to increase the affinity, selectivity (to reduce the potential of side effects), efficacy/potency, metabolic stability (to increase the half-life), and oral bioavailability. Once a compound that fulfills all of these requirements has been identified, it will begin the process of drug development prior to clinical trials. One or more of these steps may, but not necessarily, involve computer-aided drug design. Modern drug discovery is thus usually a capital-intensive process that involves large investments by pharmaceutical industry corporations as well as national governments (who provide grants and loan guarantees). Despite advances in technology and understanding of biological systems, drug discovery is still a lengthy, ""expensive, difficult, and inefficient process"" with low rate of new therapeutic discovery. In 2010, the research and development cost of each new molecular entity (NME) was approximately US$1.8 billion. Drug discovery is done by pharmaceutical companies, with research assistance from universities. The ""final product"" of drug discovery is a patent on the potential drug. The drug requires very expensive Phase I, II and III clinical trials, and most of them fail. Small companies have a critical role, often then selling the rights to larger companies that have the resources to run the clinical trials.Discovering drugs that may be a commercial success, or a public health success, involves a complex interaction between investors, industry, academia, patent laws, regulatory exclusivity, marketing and the need to balance secrecy with communication. Meanwhile, for disorders whose rarity means that no large commercial success or public health effect can be expected, the orphan drug funding process ensures that people who experience those disorders can have some hope of pharmacotherapeutic advances.
  • studyres.com © 2026
  • DMCA
  • Privacy
  • Terms
  • Report