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Potency definition

Lead structure According to Valler and Green s definition a lead structure is a representative of a compound series with sufficient potential (as measured by potency, selectivity, pharmacokinetics, physicochemical properties, absence of toxicity and novelty) to progress to a full drug development program [12]. [Pg.599]

But in order to understand what needs to be changed, we first need to understand the current situation. In order for a pharmaceutical company to use any analytical method for certifying the properties (efficacy, potency, etc.) of their products, the analytical method has to be validated. Validation , in the parlance of the FDA, is a far cry from what we usually call validation when developing a multivariate spectroscopic method. In fact, what we call validation in spectroscopic calibration (which usually means calculating an SEP, or an SECV) is a far cry from the dictionary definition of validate , which is to make legally valid , where valid is defined as having legal efficacy or force [11],... [Pg.423]

For definitive references on the cultivation and chemistry of marijuana, see MARIJUANA GROWERS GUIDE, And/Or Press (1978) and MARIJUANA POTENCY, And/Or Press (1977). [Pg.24]

A few other official antibiotics in BP (1993) may also be assayed by adopting the method stated above, but using specific micro-organism, definite final pH of the medium, pH of the phosphate buffer, potency of solution (U per ml) and the incubation temperature. A few typical examples are given in Table 20.1 below ... [Pg.288]

The usual definitions of maximal effect (E ) and potency EC or IC50) require another look at this stage before proceeding to developing mathemahcal relationship between drug concentration, dose, and body fxmchons using a PK/PD approach. ... [Pg.361]

What do the terms potency and effectiveness of a drug mean Explain the definitions of therapeutic index and safety margin. [Pg.172]

Some articles, for example, include an identical table of effective and lethal doses of high potency Fentanyl derivatives. The estimated safety margins are as high as 30,000. I could find no source for these data. I sent out several inquiries but thus far have received no definitive answers. I also discussed the questions with Harry Salem, who continues to study the toxicology of opioids at Edgewood. He is hopeful that the concomitant use of drugs tailored to suppress the effect of potent opioids on respiration may produce much safer agents. [Pg.265]

A competitive inhibition screen is often the first step in understanding the DDI potential of a NCE. The definitive assessment of inhibition is the inhibition constant (K ), which provides not only the inhibition potency but also information on the mechanism of inhibition (competitive, non-competitive). However in the hit to lead profiling environment this approach is over-complex for the question being asked, and generates far too many samples to enable rapid screening of compound series. DDI assays based upon the IC50 principle are therefore favored. The relationship between K and IC50 for a competitive inhibitor is ... [Pg.169]


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See also in sourсe #XX -- [ Pg.284 ]




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Potency

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