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Lecture 12 Gastrointestinal Agents Chapters 41 & 42
Lecture 12 Gastrointestinal Agents Chapters 41 & 42

... • Main function = Digestion of food particles & absorption of digestive contents (nutrients, electrolytes, minerals, & fluids) - into circulatory system for cellular use • Undigested material passes through the lower intestinal tract w/ aid of peristalsis to rectum & anus - excreted as feces or stoo ...
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Company Description

... When Pfizer introduced Viagra at the end of the 1990s, they broke completely new ground. They offered a medicinal product that resulted in millions of men – and their partners – regaining the ability to have a functional sex life. Thus, they were responsible for injecting new life, lust and vitality ...
Using Terahertz Pulse Spectroscopy to Study the Crystalline
Using Terahertz Pulse Spectroscopy to Study the Crystalline

... a time-gated technique, which minimizes background noise and enhances the signal-to-noise ratio. This allows a spectrum to be acquired in less than 100 ms, and because it is a transform technique there is no requirement for an expensive grating spectrometer. TPS selection rules are the same dipole s ...
The IGF-I Generation Test Revisited: A Marker of GH Sensitivity
The IGF-I Generation Test Revisited: A Marker of GH Sensitivity

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Table of Contents - International College of Health Sciences
Table of Contents - International College of Health Sciences

... Discuss the effect of food on drug absorption, on drug metabolism (e.g., grapefruit juice), and on drug toxicity and action, as well as the timing of drug administration with respect to meals. Give examples of inhibitory interaction of drugs that can produce dangerous effects and those that are bene ...
Drug Coated Balloons
Drug Coated Balloons

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Design and Characterization of Fast Dissolving Films of Valsartan

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mind altering… synthetic (designer) and naturally occuring

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IN VIVO TABLETS BY HYDROXY PROPYL BETA CYCLODEXTRIN COMPLEXATION Research Article
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... The treatment regimens, approved TB drugs and the dosage of anti-TB drugs recommended by the evidence-based WHO guidelines ( presently under revision) are summarised in tables 1 and 2. “New” and “retreatment” cases are clearly separated, 30 days of previous anti-TB treatment being the cut-off [17]. ...
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... and process control technology can lead to products with different therapeutic performance. The complete characterisation of the stability, pharmacokinetics (including tissue distribution) of a new liposomal product is critical to establish safe and effective use. This is because differences between ...
Original Article Inhibitory effects of 19 antiprotozoal drugs and
Original Article Inhibitory effects of 19 antiprotozoal drugs and

... mice infected with Babesia microti. The aims of the present study were to find a preferable method for drug screening and to re-evaluate the activity of several drugs against B. microti. Methodology: The activity of 19 drugs on B. microti-infected BALB/c mice was evaluated. The study was built on Pe ...
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... Figure 3–5 Effervescent tablet. This large tablet needs to be dissolved before the drug can be taken orally. This generic drug is a combination antacid and pain reliever. Another well-known effervescent tablet is Alka-Seltzer, which is used to treat head colds and pain. Understanding Pharmacology f ...
title of topic
title of topic

... Long-term control (as in chronic asthma) is most effectively achieved with an antiinflammatory agent such as an inhaled corticosteroid. It can also be achieved, though less effectively, with a leukotriene pathway antagonist or an inhibitor of mast cell degranulation, such as cromolyn or nedocromil. ...
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Chemical resistance of UHMWPE fiber from DSM

... UHMWPE fibers from DSM Dyneema are produced from ultrahigh-molecular weight polyethylene. It is highly crystalline and does not contain any chemical groups as aromatic rings, amide, hydroxyl or other that are susceptible to attack by aggressive agents. The result is that UHMWPE fibers are very resis ...
LIPOSOMES FOR THE DELIVERY OF NUCLEIC ACID DRUGS A
LIPOSOMES FOR THE DELIVERY OF NUCLEIC ACID DRUGS A

... liposomes have received attention not only for their utility as model membrane systems, but also for use in drug delivery. Typically, liposomes are used as drug carriers, with the solubilized drug encapsulated in the internal aqueous space formed by the liposomal lamellae. Liposomal drug formulation ...
Prescription Medication Misuse and Abuse
Prescription Medication Misuse and Abuse

... As a preventive intervention strategy we are conservatively setting the drinking limit at a slightly higher level than recommended by the NIAAA. This study sets the limit to enter the study at: ...
Herb-Drug Interactions: What Clinicians Need to Know.
Herb-Drug Interactions: What Clinicians Need to Know.

... The majority of data on herb-drug interactions are theoretical and based on case reports, in vitro assays, animal studies, and/or speculation.6 Case reports are frequently cited as unequivocal evidence of dangerous interactions, despite the fact that “published case reports are often incomplete” and ...
Background: This experiment involves analysis of a hypothetical
Background: This experiment involves analysis of a hypothetical

... analgesic, and owe their activity to metabolic breakdown to paracetamol, better known as acetaminophen (the active ingredient in Tylenol). Note that acetaminophen, unlike aspirin, is not anti-inflammatory, but it has the benefit of not irritating the stomach lining. Acetaminophen has fewer side effe ...
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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.
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