Analytical Similarity of a Proposed Biosimilar BVZ-BC to Bevacizumab
BVZ-BC (bevacizumab-biosimilar candidate) is a proposed biosimilar to bevacizumab. Bevacizumab binds to vascular endothelial growth factor (VEGF) type A and prevents the interaction of VEGF with its receptors on the surface of endothelial cells, neutralizing angiogenesis required for the growth, per...
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Veröffentlicht in: | Analytical chemistry (Washington) 2020-02, Vol.92 (4), p.3161-3170 |
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description | BVZ-BC (bevacizumab-biosimilar candidate) is a proposed biosimilar to bevacizumab. Bevacizumab binds to vascular endothelial growth factor (VEGF) type A and prevents the interaction of VEGF with its receptors on the surface of endothelial cells, neutralizing angiogenesis required for the growth, persistence, and metastases of solid tumors. An analytical comparison of BVZ-BC and bevacizumab was performed using state-of-the-art analytical techniques, including biochemical and biophysical characterization, biological activity, and immunological properties. Multiple attributes of the molecules were evaluated, including amino acid sequence, disulfide structure, glycan profiles, free thiol content, isoelectric point, protein content, subvisible particles, higher-order structure such as near- and far-ultraviolet circular dichroism and differential scanning calorimetry, product purity and product-related impurities, and process-related impurities. Biological activity assessment employed orthogonal assays such as the VEGF cell-based bioassay and the VEGF enzyme-linked immunosorbent assay, and Fc functional assays to interrogate all expected biological activities. An accumulation of 18 batches of bevacizumab (sourced in China, manufactured in Europe, Roche) and 10 batches of BVZ-BC representing unique drug product lots from each individual drug substance lot were utilized in this study. The analytical similarity between BVZ-BC and bevacizumab was assessed and demonstrated the similarities of all of the quality attributes between BVZ-BC and bevacizumab. |
doi_str_mv | 10.1021/acs.analchem.9b04871 |
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Bevacizumab binds to vascular endothelial growth factor (VEGF) type A and prevents the interaction of VEGF with its receptors on the surface of endothelial cells, neutralizing angiogenesis required for the growth, persistence, and metastases of solid tumors. An analytical comparison of BVZ-BC and bevacizumab was performed using state-of-the-art analytical techniques, including biochemical and biophysical characterization, biological activity, and immunological properties. Multiple attributes of the molecules were evaluated, including amino acid sequence, disulfide structure, glycan profiles, free thiol content, isoelectric point, protein content, subvisible particles, higher-order structure such as near- and far-ultraviolet circular dichroism and differential scanning calorimetry, product purity and product-related impurities, and process-related impurities. Biological activity assessment employed orthogonal assays such as the VEGF cell-based bioassay and the VEGF enzyme-linked immunosorbent assay, and Fc functional assays to interrogate all expected biological activities. An accumulation of 18 batches of bevacizumab (sourced in China, manufactured in Europe, Roche) and 10 batches of BVZ-BC representing unique drug product lots from each individual drug substance lot were utilized in this study. The analytical similarity between BVZ-BC and bevacizumab was assessed and demonstrated the similarities of all of the quality attributes between BVZ-BC and bevacizumab.</description><identifier>ISSN: 0003-2700</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/acs.analchem.9b04871</identifier><identifier>PMID: 31983199</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Amino acid sequence ; Amino acids ; Analytical chemistry ; Angiogenesis ; Bevacizumab ; Bioaccumulation ; Bioassays ; Biological activity ; Biological Assay ; Biological properties ; Biosimilar Pharmaceuticals - chemistry ; Biosimilar Pharmaceuticals - metabolism ; Biosimilar Pharmaceuticals - pharmacology ; Calorimetry ; Chemistry ; Circular dichroism ; Dichroism ; Differential scanning calorimetry ; Endothelial cells ; Enzyme-linked immunosorbent assay ; Glycan ; Growth factors ; Immunology ; Immunotherapy ; Impurities ; Mathematical analysis ; Metastases ; Monoclonal antibodies ; Polysaccharides - chemistry ; Quality management ; Receptors ; Similarity ; Solid tumors ; Targeted cancer therapy ; Vascular endothelial growth factor ; Vascular Endothelial Growth Factor A - metabolism</subject><ispartof>Analytical chemistry (Washington), 2020-02, Vol.92 (4), p.3161-3170</ispartof><rights>Copyright American Chemical Society Feb 18, 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a376t-eac8f2ae809440388737eb0ceb57a2ea574bdd721aa3c42a76a82a6b712963243</citedby><cites>FETCH-LOGICAL-a376t-eac8f2ae809440388737eb0ceb57a2ea574bdd721aa3c42a76a82a6b712963243</cites><orcidid>0000-0003-0588-4899</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.analchem.9b04871$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.analchem.9b04871$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31983199$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Chuanfei</creatorcontrib><creatorcontrib>Zhang, Feng</creatorcontrib><creatorcontrib>Xu, Gangling</creatorcontrib><creatorcontrib>Wu, Gang</creatorcontrib><creatorcontrib>Wang, Wenbo</creatorcontrib><creatorcontrib>Liu, Chunyu</creatorcontrib><creatorcontrib>Fu, Zhihao</creatorcontrib><creatorcontrib>Li, Meng</creatorcontrib><creatorcontrib>Guo, Sha</creatorcontrib><creatorcontrib>Yu, Xiaojuan</creatorcontrib><creatorcontrib>Wang, Lan</creatorcontrib><title>Analytical Similarity of a Proposed Biosimilar BVZ-BC to Bevacizumab</title><title>Analytical chemistry (Washington)</title><addtitle>Anal. Chem</addtitle><description>BVZ-BC (bevacizumab-biosimilar candidate) is a proposed biosimilar to bevacizumab. Bevacizumab binds to vascular endothelial growth factor (VEGF) type A and prevents the interaction of VEGF with its receptors on the surface of endothelial cells, neutralizing angiogenesis required for the growth, persistence, and metastases of solid tumors. An analytical comparison of BVZ-BC and bevacizumab was performed using state-of-the-art analytical techniques, including biochemical and biophysical characterization, biological activity, and immunological properties. Multiple attributes of the molecules were evaluated, including amino acid sequence, disulfide structure, glycan profiles, free thiol content, isoelectric point, protein content, subvisible particles, higher-order structure such as near- and far-ultraviolet circular dichroism and differential scanning calorimetry, product purity and product-related impurities, and process-related impurities. Biological activity assessment employed orthogonal assays such as the VEGF cell-based bioassay and the VEGF enzyme-linked immunosorbent assay, and Fc functional assays to interrogate all expected biological activities. An accumulation of 18 batches of bevacizumab (sourced in China, manufactured in Europe, Roche) and 10 batches of BVZ-BC representing unique drug product lots from each individual drug substance lot were utilized in this study. The analytical similarity between BVZ-BC and bevacizumab was assessed and demonstrated the similarities of all of the quality attributes between BVZ-BC and bevacizumab.</description><subject>Amino acid sequence</subject><subject>Amino acids</subject><subject>Analytical chemistry</subject><subject>Angiogenesis</subject><subject>Bevacizumab</subject><subject>Bioaccumulation</subject><subject>Bioassays</subject><subject>Biological activity</subject><subject>Biological Assay</subject><subject>Biological properties</subject><subject>Biosimilar Pharmaceuticals - chemistry</subject><subject>Biosimilar Pharmaceuticals - metabolism</subject><subject>Biosimilar Pharmaceuticals - pharmacology</subject><subject>Calorimetry</subject><subject>Chemistry</subject><subject>Circular dichroism</subject><subject>Dichroism</subject><subject>Differential scanning calorimetry</subject><subject>Endothelial cells</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Glycan</subject><subject>Growth factors</subject><subject>Immunology</subject><subject>Immunotherapy</subject><subject>Impurities</subject><subject>Mathematical analysis</subject><subject>Metastases</subject><subject>Monoclonal antibodies</subject><subject>Polysaccharides - chemistry</subject><subject>Quality management</subject><subject>Receptors</subject><subject>Similarity</subject><subject>Solid tumors</subject><subject>Targeted cancer therapy</subject><subject>Vascular endothelial growth factor</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><issn>0003-2700</issn><issn>1520-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kD1PwzAQhi0EoqXwDxCKxMKScrYT2xnb8ilVAomPgSW6OI5IldTFTpDKrydV2g4MDNYNft73dA8h5xTGFBi9Ru3HuMRKf5p6nGQQKUkPyJDGDEKhFDskQwDgIZMAA3Li_QKAUqDimAw4TVT3kiG5mXQV66bUWAUvZV1W6MpmHdgiwODZ2ZX1Jg-mpfX9XzB9_wins6CxwdR8oy5_2hqzU3JUYOXN2XaOyNvd7evsIZw_3T_OJvMQuRRNaFCrgqFRkEQRcKUklyYDbbJYIjMYyyjLc8koItcRQylQMRSZpCwRnEV8RK763pWzX63xTVqXXpuqwqWxrU8ZjwQHypno0Ms_6MK2rrt1QwkAFscCOirqKe2s984U6cqVNbp1SiHdWE47y-nOcrq13MUutuVtVpt8H9pp7QDogU18v_jfzl_k6Yng</recordid><startdate>20200218</startdate><enddate>20200218</enddate><creator>Yu, Chuanfei</creator><creator>Zhang, Feng</creator><creator>Xu, Gangling</creator><creator>Wu, Gang</creator><creator>Wang, Wenbo</creator><creator>Liu, Chunyu</creator><creator>Fu, Zhihao</creator><creator>Li, Meng</creator><creator>Guo, Sha</creator><creator>Yu, Xiaojuan</creator><creator>Wang, Lan</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7U5</scope><scope>7U7</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0588-4899</orcidid></search><sort><creationdate>20200218</creationdate><title>Analytical Similarity of a Proposed Biosimilar BVZ-BC to Bevacizumab</title><author>Yu, Chuanfei ; 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Chem</addtitle><date>2020-02-18</date><risdate>2020</risdate><volume>92</volume><issue>4</issue><spage>3161</spage><epage>3170</epage><pages>3161-3170</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><abstract>BVZ-BC (bevacizumab-biosimilar candidate) is a proposed biosimilar to bevacizumab. Bevacizumab binds to vascular endothelial growth factor (VEGF) type A and prevents the interaction of VEGF with its receptors on the surface of endothelial cells, neutralizing angiogenesis required for the growth, persistence, and metastases of solid tumors. An analytical comparison of BVZ-BC and bevacizumab was performed using state-of-the-art analytical techniques, including biochemical and biophysical characterization, biological activity, and immunological properties. Multiple attributes of the molecules were evaluated, including amino acid sequence, disulfide structure, glycan profiles, free thiol content, isoelectric point, protein content, subvisible particles, higher-order structure such as near- and far-ultraviolet circular dichroism and differential scanning calorimetry, product purity and product-related impurities, and process-related impurities. Biological activity assessment employed orthogonal assays such as the VEGF cell-based bioassay and the VEGF enzyme-linked immunosorbent assay, and Fc functional assays to interrogate all expected biological activities. An accumulation of 18 batches of bevacizumab (sourced in China, manufactured in Europe, Roche) and 10 batches of BVZ-BC representing unique drug product lots from each individual drug substance lot were utilized in this study. The analytical similarity between BVZ-BC and bevacizumab was assessed and demonstrated the similarities of all of the quality attributes between BVZ-BC and bevacizumab.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>31983199</pmid><doi>10.1021/acs.analchem.9b04871</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-0588-4899</orcidid></addata></record> |
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subjects | Amino acid sequence Amino acids Analytical chemistry Angiogenesis Bevacizumab Bioaccumulation Bioassays Biological activity Biological Assay Biological properties Biosimilar Pharmaceuticals - chemistry Biosimilar Pharmaceuticals - metabolism Biosimilar Pharmaceuticals - pharmacology Calorimetry Chemistry Circular dichroism Dichroism Differential scanning calorimetry Endothelial cells Enzyme-linked immunosorbent assay Glycan Growth factors Immunology Immunotherapy Impurities Mathematical analysis Metastases Monoclonal antibodies Polysaccharides - chemistry Quality management Receptors Similarity Solid tumors Targeted cancer therapy Vascular endothelial growth factor Vascular Endothelial Growth Factor A - metabolism |
title | Analytical Similarity of a Proposed Biosimilar BVZ-BC to Bevacizumab |
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