A Solid Contribution to Spectroscopy - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

A Solid Contribution to Spectroscopy
A substantive book offers valuable information to spectroscopy veterans and neophytes alike.


Pharmaceutical Technology


Steve Doherty, PhD
In the preface to Spectroscopy of Pharmaceutical Solids, editor Harry Brittain states the rather lofty objective of providing "a greater degree of fundamental understanding ... necessary to obtain maximal use out of each [solid-state spectroscopy] technique." This text accomplishes its goal through the clear and cogent writing of Brittain and his coauthors, including Dave Bugay, James Drennen, Robert Cogdill, and Ales Medek. The book explores topics such as mid-infrared, near-infrared (NIR), and Raman spectroscopy, as well as solid-state nuclear magnetic resonance. Brittain himself contributes chapters about X-ray techniques, UV–vis, and luminescence spectroscopy.




The book opens with a brief primer about electromagnetic radiation and spectroscopy, showing the derivation of quantum theory and its implications for spectroscopy. Subsequent major sections focus, logically and sequentially, on core-electron, valence-electron, vibrational, and nuclear-spin spectroscopies. Each major section opens with a chapter describing the fundamental interactions behind particular spectroscopic techniques. These concepts are provided in a concise but detailed manner, analogous to the treatment in a college-level text. Each of the subsequent chapters lists many illustrative citations from the scientific literature. For example, the chapter on solid-state nuclear magnetic resonance spectrometry has 618 references that help demonstrate the applicability of the analytical methods while highlighting the pitfalls in using the techniques. In addition, relevant figures and tables are reproduced to illustrate some of the more important points.


Spectroscopy of Pharmaceutical Solids, Harry G. Brittain, Ed., Informa Healthcare, New York, NY, 2006, 592 pp., ISBN 9781574448931.
For each of the spectroscopic techniques, citations are provided from both the bulk-active and formulated product areas, as is perspective relevant to both the development and manufacturing environments. With the recent increased interest in pharmaceutical spectroscopy arising from the well-publicized FDA-sponsored process analytical technology and quality by design (QbD) initiatives, the appearance of this text is quite timely. Several of the technique chapters highlight on-line applications and show their relevance to fulfilling QbD objectives. Furthermore, fairly recent developments such as Raman and NIR imaging are described.

This generally well-written text has a few minor faults. It omits some relevant spectroscopic advances. For example, although the book describes using chalcogenide fiber-optic elements in infrared spectrometry, it does not mention silver-halide fibers. Some of the characteristic-absorbance tables and other data could have been compiled in appendices for ease of access. The text detailing the similarities and differences between spectroscopy in the laboratory and manufacturing settings could have been supplemented, even though, as stated previously, the book's focus is intended to be fundamental in nature.

All in all, this book is a handy reference that combines textbook-like theory with timely and illustrative citations. It would be a worthwhile resource for neophytes in the field of pharmaceutical spectroscopy, as well as practitioners wishing to refresh their understanding.

Steve Doherty, PhD, is a senior research scientist in the Process Analytical Technology Group at Eli Lilly and Company, DC 4210, Indianapolis, IN 46285, tel. 317.651.1580,

ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
How does your company apply quality-by-design (QbD) principles to manufacturing processes?
To all processes for both new and legacy products
To all process for new products only
To select process for new products only
To select processes for both new and legacy products
Do not use QbD
To all processes for both new and legacy products
18%
To all process for new products only
13%
To select process for new products only
22%
To select processes for both new and legacy products
22%
Do not use QbD
24%
View Results
UPCOMING CONFERENCES

Programs for Investigational and Pre-Launch Drugs
Philadelphia, PA
July 17-18, 2013
Request Brochure

Strategic Pipeline Planning & Portfolio Valuation
Philadelphia, PA
August 13-14, 2013
Request Brochure

MES 2013 - Forum on Manufacturing Execution Systems
Philadelphia, PA
August 14-15, 2013
Request Brochure

Mobile Innovation for the Life Sciences Industry
Philadelphia, PA
August 20-21, 2013
Request Brochure

See All Conferences >>

Eric Langer Outsourcing Outlook Eric LangerOutsourcing's Modest Role as a Cost-Containment Strategy
Patricia Van Arnum Ingredients Insider Patricia Van ArnumIntellectual Property Battles in Solid-State Chemistry
Nathan Jessop Industry Insider Nathan Jessop Campaign Against Counterfeit Drugs Continues
Lynn Torbeck Statistical Solutions Lynn D. TorbeckCompositing Samples and the Risk to Product Quality
 More
Inadequate Access to Medicines Puts EU at Risk
FDA Offers Insight on QbD for Modified-Release Products
Global Biosimilars Market to Reach $2.445 Billion in 2013
Adapting to Change
AstraZeneca and Exco InTouch Collaborate to Augment Current COPD Pathways
FindPharma Custom Search
Source: Pharmaceutical Technology,
Click here