Zhang K - Search Results

1

Compatibility study of a parenteral microdose polyethylene glycol formulation in medical devices and identification of degradation impurity by 2D-LC/MS.

Dai L, Yeh GK, Ran Y, Yehl P, Zhang K. Dai L, et al. Among authors: zhang k. J Pharm Biomed Anal. 2017 Apr 15;137:182-188. doi: 10.1016/j.jpba.2017.01.036. Epub 2017 Jan 18. J Pharm Biomed Anal. 2017. PMID: 28131057

2

Analysis of pharmaceutical impurities using multi-heartcutting 2D LC coupled with UV-charged aerosol MS detection.

Zhang K, Li Y, Tsang M, Chetwyn NP. Zhang K, et al. J Sep Sci. 2013 Sep;36(18):2986-92. doi: 10.1002/jssc.201300493. Epub 2013 Jul 31. J Sep Sci. 2013. PMID: 23821312

3

Limiting degradation of reactive antibody drug conjugate intermediates in HPLC method development.

Li Y, Medley CD, Zhang K, Wigman L, Chetwyn N. Li Y, et al. Among authors: zhang k. J Pharm Biomed Anal. 2014 Apr;92:114-8. doi: 10.1016/j.jpba.2014.01.004. Epub 2014 Jan 10. J Pharm Biomed Anal. 2014. PMID: 24503199

4

Characterization and stability study of polysorbate 20 in therapeutic monoclonal antibody formulation by multidimensional ultrahigh-performance liquid chromatography-charged aerosol detection-mass spectrometry.

Li Y, Hewitt D, Lentz YK, Ji JA, Zhang TY, Zhang K. Li Y, et al. Among authors: zhang ty, zhang k. Anal Chem. 2014 May 20;86(10):5150-7. doi: 10.1021/ac5009628. Epub 2014 May 2. Anal Chem. 2014. PMID: 24749737

5

A size exclusion-reversed phase two dimensional-liquid chromatography methodology for stability and small molecule related species in antibody drug conjugates.

Li Y, Gu C, Gruenhagen J, Zhang K, Yehl P, Chetwyn NP, Medley CD. Li Y, et al. Among authors: zhang k. J Chromatogr A. 2015 May 8;1393:81-8. doi: 10.1016/j.chroma.2015.03.027. Epub 2015 Mar 16. J Chromatogr A. 2015. PMID: 25818558

6

Sensitive and direct determination of lithium by mixed-mode chromatography and charged aerosol detection.

Dai L, Wigman L, Zhang K. Dai L, et al. Among authors: zhang k. J Chromatogr A. 2015 Aug 21;1408:87-92. doi: 10.1016/j.chroma.2015.06.063. Epub 2015 Jul 2. J Chromatogr A. 2015. PMID: 26184708 Free article.

7

A simple and sensitive method to analyze genotoxic impurity hydrazine in pharmaceutical materials.

Wang J, Yang S, Zhang K. Wang J, et al. Among authors: zhang k. J Pharm Biomed Anal. 2016 Jul 15;126:141-7. doi: 10.1016/j.jpba.2016.04.038. Epub 2016 Apr 27. J Pharm Biomed Anal. 2016. PMID: 27208624 Free article.

8

Mixed-mode chromatography in pharmaceutical and biopharmaceutical applications.

Zhang K, Liu X. Zhang K, et al. J Pharm Biomed Anal. 2016 Sep 5;128:73-88. doi: 10.1016/j.jpba.2016.05.007. Epub 2016 May 6. J Pharm Biomed Anal. 2016. PMID: 27236100 Free article. Review.

9

Reprint of "Mixed-mode chromatography in pharmaceutical and biopharmaceutical applications".

Zhang K, Liu X. Zhang K, et al. J Pharm Biomed Anal. 2016 Oct 25;130:19-34. doi: 10.1016/j.jpba.2016.09.013. Epub 2016 Sep 16. J Pharm Biomed Anal. 2016. PMID: 27645457 Free article. Review.

10

Validation of a two-dimensional liquid chromatography method for quality control testing of pharmaceutical materials.

Yang SH, Wang J, Zhang K. Yang SH, et al. Among authors: zhang k. J Chromatogr A. 2017 Apr 7;1492:89-97. doi: 10.1016/j.chroma.2017.02.074. Epub 2017 Mar 1. J Chromatogr A. 2017. PMID: 28284763

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