By Satinder Ahuja, Stephen Scypinski
Handbook of contemporary Pharmaceutical Analysis, Second Edition, synthesizes the complicated learn and up to date alterations within the field, while protecting the techniques and technology required for latest laboratories. The work integrates technique, case reports, methodologies, and implications of latest regulatory buildings, supplying whole insurance of caliber coverage from the purpose of discovery to the purpose of use.
- Treats pharmaceutical research (PA) as an vital associate to the drug improvement technique instead of as a carrier to it
- Covers strategy improvement, validation, choice, checking out, modeling, and simulation experiences mixed with complex exploration of assays, impurity trying out, biomolecules, and chiral separations
- Features detailed coverage of QA, ethics, and regulatory suggestions (quality through layout, reliable production practice), in addition to high-tech methodologies and applied sciences from ''lab-on-a-chip'' to LC-MS, LC-NMR, and LC-NMR-MS
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Extra resources for Handbook of Modern Pharmaceutical Analysis
For instance, the sieve diameter is the width of the minimum square aperture through which the particle will pass. Other descriptors that have been used are the drag diameter (the diameter of a sphere having the same resistance to motion as the particle in a fluid of the same viscosity and at the same velocity), the free-falling diameter (the diameter of a sphere having the same density and the same free-falling speed as the particle in a fluid of the same density and viscosity), and the Stokes’ diameter (the free-falling diameter of a particle in the laminar flow region).
168 The nature of the enantiotropy was established by systematically changing the sample heating rates, where it was found that the heat of fusion of the lower melting form was greater than that of the higher melting form. 169,170 TG analysis is restricted to studies that involve either a mass gain or loss (usually loss), and is most commonly used to study desolvation processes and compound decomposition. The major use of TG analysis is in the quantitative determination of the total volatile content of a solid.
It is also true that reproducibility in all aspects of lot-to-lot behavior can be significantly improved through the implementation of properly designed specifications. The testing of raw materials is particularly important at this stage, since only those species passing appropriate challenges should be used for manufacturing processes. Once a given drug candidate has reached the latter stages of development, the physical characteristics associated with the other formulation ingredients assumes a high level of importance.
Handbook of Modern Pharmaceutical Analysis by Satinder Ahuja, Stephen Scypinski