Wednesday, February 01, 2012
Sigrid Pieters Ph.D., Thomas De Beer, Ph.D, Yvan Vander Heyden, Ph.D.
For many biopharmaceutical drug products the last manufacturing step involves freeze-drying. As freeze-drying may be hazardous for the protein’s ...
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Wednesday, February 01, 2012
Michael Adler, Ph.D.
Pre-filled syringes (PFS) are well-established, functional container closure systems for biological products. Examples for marketed biological ...
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Wednesday, February 01, 2012
Zai-qing Wen, Guoxiang Chen, Ying Luo, Guiyang Li, Peter Masatani, Pavel Bondarenko, Joseph Phillips
This work focused on the assessment of the capability and suitability of several spectroscopic techniques for detecting adulteration of raw materials ...
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Wednesday, February 01, 2012
Dan Klees, Joshua Froimson, Michelle Calhoun, Anurag S. Rathore, Parrish Galliher, William Whitford, Juliette Schick, Ph.D.
One of the emerging trends that we see is in the area of single-use, disposable processing systems. But, “if you can’t measure it, you can’t
control ...
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Tuesday, January 17, 2012
Frederick T. Mattrey, Sarah Dolman, Jason Nyrop, Peter J. Skrdla
Chantland Material Handling Systems
Flow chemistry (FC) provides key advantages over traditional batch-mode processing by facilitating scale-up [1] and enabling automation [2]. FC also ...
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Patrick J. Marroum, Ph.D.
The release of the drug substance from the solid dosage form has a major impact on its rate and extent of absorption.
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Ben J. Boyd, Ph.D.
The performance of functional foods and pharmaceutical products is highly dependent on nano-scale self assembly of lipids and other substances in the ...
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Scott Sutton, Luis Jimenez
An analysis was conducted of 642 microbiologically-related recalls over the years 2004-2011.
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Mino R. Caira, Ph.D.
Polymorphs, solvates, inclusion complexes and co-crystals of active pharmaceutical ingredients (APIs) are four established classes of ‘...
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Jessica Kogan, Christopher T. John, Brian Kozlowski
In today’s pharmaceutical environment, a generic, automated sample preparation method is imperative to meeting compressed analytical timelines.
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Sheldon F. Oppenheim, Ph.D., Norbert Schuelke, Ph.D.
The harvest process most often used during the primary recovery of cell-based biopharmaceuticals is continuous centrifugation followed by depth ...
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Yong Liu, Ph.D., Tim Nowak, Jolanta Plewa, Xiaoyi Gong, Ph.D.
Potentiometric titration is a common laboratory method for quantitative chemical analysis that is routinely used in the pharmaceutical industry.
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Anthony L. Young
X-ray crystallography has been employed in research and development of small molecules pharmaceuticals for many years. Small molecule active ...
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Tuesday, November 01, 2011
Vineet Kumar, Ph.D., Nitin Dixit, Shubhadra N. Singh, Ph.D, Devendra S. Kalonia, Ph.D.
Polyethylene glycols (a-Hydroxy-?-hydroxy-poly(oxy-1,2ethanediyl)
abbreviated PEGs, are a family of non-ionic synthetic polymers with
an empirical ...
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Tuesday, November 01, 2011
Arn Malliett
In the current economic environment many companies are more rapidly identifying and implementing cost cutting and cost savings measures. One method of...
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