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. 2020 Feb 18;34(3):363–379. doi: 10.1007/s40259-020-00407-0

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

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Fig. 3 — Comparison of glycan structures released from HLX02, CN-Herceptin^®, and EU-Herceptin^® by PNGase F. a N-glycan profiles by HILIC UPLC-FLD; the major types of glycans are labelled beside the corresponding peaks in the top panel (HLX02). b–f Quantitative results of each glycoform subtype analyzed using tier 2 attribute criteria (mean ± 3 SD). CN China-sourced, EU Europe-sourced, HILIC UPLC-FLD hydrophilic interaction–ultra performance liquid chromatography–fluorescence detection, SD standard deviation