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There are 17118 results for: content related to: Forced degradation of therapeutic proteins

  1. Effects of surfaces and leachables on the stability of biopharmaceuticals

    Journal of Pharmaceutical Sciences

    Volume 100, Issue 10, October 2011, Pages: 4158–4170, Jared S. Bee, Theodore W. Randolph, John F. Carpenter, Steven M. Bishop and Mariana N. Dimitrova

    Version of Record online : 26 APR 2011, DOI: 10.1002/jps.22597

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    Impact of product-related factors on immunogenicity of biotherapeutics

    Journal of Pharmaceutical Sciences

    Volume 100, Issue 2, February 2011, Pages: 354–387, Satish Kumar Singh

    Version of Record online : 25 AUG 2010, DOI: 10.1002/jps.22276

  3. Analytical Leachables Studies

    Leachables and Extractables Handbook: Safety Evaluation, Qualification, and Best Practices Applied to Inhalation Drug Products

    Andrew D. Feilden, Andy Rignall, Pages: 417–447, 2012

    Published Online : 28 FEB 2012, DOI: 10.1002/9781118147672.ch17

  4. Identification of pharmaceutical impurities in formulated dosage forms

    Journal of Pharmaceutical Sciences

    Volume 100, Issue 4, April 2011, Pages: 1228–1259, Changkang Pan, Frances Liu and Michael Motto

    Version of Record online : 26 OCT 2010, DOI: 10.1002/jps.22376

  5. Forced degradation studies of corticosteroids with an alumina–steroid–ethanol model for predicting chemical stability and degradation products of pressurized metered-dose inhaler formulations

    Journal of Pharmaceutical Sciences

    Volume 101, Issue 6, June 2012, Pages: 2109–2122, Zheng-zhi Wu, Matthew L. Thatcher, James K. Lundberg, Mark K. Ogawa, Cliffton B. Jacoby, John L. Battiste and Katherine A. Ledoux

    Version of Record online : 12 MAR 2012, DOI: 10.1002/jps.23111

  6. Focus on Emerging Concepts

    Compatibility of Pharmaceutical Products and Contact Materials: Safety Considerations Associated with Extractables and Leachables

    Dennis Jenke, Pages: 319–346, 2008

    Published Online : 1 OCT 2008, DOI: 10.1002/9780470459416.ch12

  7. Degradation of amine-based solvents in CO2 capture process by chemical absorption

    Greenhouse Gases: Science and Technology

    Volume 4, Issue 6, December 2014, Pages: 707–733, Fernando Vega, Aimaro Sanna, Benito Navarrete, M. Mercedes Maroto-Valer and Vicente J. Cortés

    Version of Record online : 10 JUL 2014, DOI: 10.1002/ghg.1446

  8. Product Stability and Accelerated Degradation Studies

    Medicines from Animal Cell Culture

    P Matejtschuk, P Phillips, Pages: 503–522, 2007

    Published Online : 6 SEP 2007, DOI: 10.1002/9780470723791.ch27

  9. Effect of Packaging on Stability of Drugs and Drug Products

    Pharmaceutical Manufacturing Handbook: Regulations and Quality

    Shayne Cox Gad, Pages: 641–686, 2007

    Published Online : 28 AUG 2007, DOI: 10.1002/9780470259832.ch19

  10. Accelerated stability studies of abatacept formulations: Comparison of freeze–thawing- and agitation-induced stresses

    Journal of Pharmaceutical Sciences

    Volume 101, Issue 7, July 2012, Pages: 2307–2315, Amanda A. Cordes, John F. Carpenter and Theodore W. Randolph

    Version of Record online : 4 APR 2012, DOI: 10.1002/jps.23150

  11. On developing a process for conducting extractable–leachable assessment of components used for storage of biopharmaceuticals

    Journal of Pharmaceutical Sciences

    Volume 99, Issue 5, May 2010, Pages: 2209–2218, Aditya A. Wakankar, Y. John Wang, Eleanor Canova-Davis, Stacey Ma, Dieter Schmalzing, Josh Grieco, Terry Milby, Theresa Reynolds, Kellen Mazzarella, Ed Hoff, Stephen Gomez and Sherry Martin-Moe

    Version of Record online : 28 DEC 2009, DOI: 10.1002/jps.22012

  12. Impact of Residual Impurities and Contaminants on Protein Stability

    Journal of Pharmaceutical Sciences

    Volume 103, Issue 5, May 2014, Pages: 1315–1330, Wei Wang, Arun Alphonse Ignatius and Santosh V. Thakkar

    Version of Record online : 12 MAR 2014, DOI: 10.1002/jps.23931

  13. Role of HPLC During Formulation Development

    HPLC for Pharmaceutical Scientists

    Tarun S. Patel, Rosario LoBrutto, Pages: 679–734, 2006

    Published Online : 18 MAY 2006, DOI: 10.1002/9780470087954.ch15

  14. Late-Stage Formulation Development and Characterization of Biopharmaceuticals

    Formulation and Process Development Strategies for Manufacturing Biopharmaceuticals

    Feroz Jameel, Susan Hershenson, Pages: 161–171, 2010

    Published Online : 5 AUG 2010, DOI: 10.1002/9780470595886.ch7

  15. Product Maintenance

    Compatibility of Pharmaceutical Products and Contact Materials: Safety Considerations Associated with Extractables and Leachables

    Dennis Jenke, Pages: 271–313, 2008

    Published Online : 1 OCT 2008, DOI: 10.1002/9780470459416.ch10

  16. Analytical Best Practices for the Evaluation and Management of Extractables and Leachables in Orally Inhaled and Nasal Drug Products

    Leachables and Extractables Handbook: Safety Evaluation, Qualification, and Best Practices Applied to Inhalation Drug Products

    Daniel L. Norwood, Cheryl L. M. Stults, Lee M. Nagao, Pages: 153–183, 2012

    Published Online : 28 FEB 2012, DOI: 10.1002/9781118147672.ch10

  17. Development and validation of a stability indicating isocratic HPLC method for gemcitabine with application to drug release from poly lactic-co-glycolic acid nanoparticles and enzymatic degradation studies

    Journal of Pharmacy and Pharmacology

    Volume 67, Issue 11, November 2015, Pages: 1528–1536, Guanyu Chen, Darren Svirskis and Jingyuan Wen

    Version of Record online : 15 SEP 2015, DOI: 10.1111/jphp.12470

  18. Effect of Packaging on Stability of Drugs and Drug Products

    Standard Article

    Pharmaceutical Sciences Encyclopedia

    Emmanuel O. Akala

    Published Online : 15 MAR 2010, DOI: 10.1002/9780470571224.pse392

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    Index

    Biopharmaceutical Production Technology, Volume 1 & Volume 2

    Ganapathy Subramanian, Pages: 859–883, 2012

    Published Online : 15 OCT 2012, DOI: 10.1002/9783527653096.index

  20. Analytical Techniques for Identification and Quantitation of Extractables and Leachables

    Leachables and Extractables Handbook: Safety Evaluation, Qualification, and Best Practices Applied to Inhalation Drug Products

    Daniel L. Norwood, Thomas N. Feinberg, James O. Mullis, Scott J. Pennino, Pages: 241–287, 2012

    Published Online : 28 FEB 2012, DOI: 10.1002/9781118147672.ch13