Todd L. Cecil

Office of Science — United States

Pharmacology, Toxicology and Pharmaceutics · Life Sciences

12h-index558citations30works0.02yr avg
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Research Topics

Drug Solubulity and Delivery Systems(6), Spectroscopy and Chemometric Analyses(6), Analytical Chemistry and Chromatography(5), Analytical Methods in Pharmaceuticals(5), Pharmaceutical studies and practices(5)

Publications30 total

Carbonyl Yields in Cigars under Three Smoking Regimens Using a Linear Smoking Machine
Chemical Research in Toxicology·2023· 3 citedOpen Access
Characterization of aerosols generated by high-power electronic nicotine delivery systems (ENDS): Influence of atomizer, temperature and PG:VG ratios
PLoS ONE·2022· 16 citedOpen Access
Development and Validation Of A Discriminatory Dissolution Method for Portioned Moist Snuff and Snus
Journal of Pharmaceutical Sciences·2021· 5 cited
Acrolein Yields in Mainstream Smoke From Commercial Cigarette and Little Cigar Tobacco Products
Nicotine & Tobacco Research·2017· 24 cited
Establishment of Measurement Requirements – Performance‐Based Specifications
2014· 2 cited
Progressively Reducing Regulatory Burden
The AAPS Journal·2014· 5 citedOpen Access
Biorelevant In Vitro Performance Testing of Orally Administered Dosage Forms—Workshop Report
Pharmaceutical Research·2014· 21 cited
Validation of procedures for elemental impurities
Elsevier eBooks·2013· 2 cited
List of Contributors
Elsevier eBooks·2013
FIP/AAPS Joint Workshop Report: Dissolution/In Vitro Release Testing of Novel/Special Dosage Forms
AAPS PharmSciTech·2011· 117 cited
Meeting Report: FIP/AAPS Joint Workshop Report: Dissolution/In Vitro Release Testing of Novel/Special Dosage Forms
Dissolution Technologies·2011· 9 citedOpen Access
FIP/AAPS Joint Workshop Report: Dissolution/In Vitro Release Testing of Novel/Special Dosage Forms
PubMed Central·2011· 6 citedOpen Access
Metal Impurities in Food and Drugs
Pharmaceutical Research·2010· 146 cited
Performance-based monographs
2009· 8 cited
Acceptable, Equivalent, or Better: Approaches for Alternatives to Official Compendial Procedures
2009· 12 cited
USP Responses to Comments on Stimuli Article, “Proposed Change to Acceptance Criteria for Dissolution Performance Verification Testing”
Dissolution Technologies·2008· 6 citedOpen Access
The US Pharmacopeia near Infrared System Suitability Reference Standard
Journal of Near Infrared Spectroscopy·2008· 1 cited
Proposed Change to Acceptance Criteria for Dissolution Performance Verification Testing
Dissolution Technologies·2007· 11 citedOpen Access
Oral Dosage Form Performance Tests: New Dissolution Approaches
Pharmaceutical Research·2005· 11 cited
14 Impurity evaluations
Separation science and technology·2005· 2 cited
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Frequent Co-authors

Roger Williams(7), Vinod P. Shah(5), Cynthia K. Brown(4), Amy R. Barker(4), Lucinda F. Buhse(4), Susanne Keitel(4), Johannes Kraemer(4), John Morris(4), Christos Reppas(4), Mary P. Stickelmeyer(4), Chikako Yomota(4), Sarah C. Rutan(4), Eric B. Sheinin(4), Walter W. Hauck(4), Nicholas M. P. King(3), Horst Dieter Friedel(3), Mimy Young(3), Vivian A. Gray(3), Anthony J. DeStefano(2), Jeffrey R. Wyatt(2)