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Development and Biophysical Characterization of a Humanized FSH–Blocking Monoclonal Antibody Therapeutic Formulated at an Ultra–High Concentration

Highly concentrated antibody formulations are oftentimes required for subcutaneous, self-administered biologics. Here, we report the creation of a unique formulation for our first–in–class FSH–blocking humanized antibody, MS-Hu6, which we propose to move to the clinic for osteoporosis, obesity, and...

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Autores principales: Rojekar, Satish, Pallapati, Anusha R., Gimenez–Roig, Judit, Korkmaz, Funda, Sultana, Farhath, Sant, Damini, Haeck, Clement, Macdonald, Anne, Kim, Se-Min, Rosen, Clifford J., Barak, Orly, Meseck, Marcia, Caminis, John, Lizneva, Daria, Yuen, Tony, Zaidi, Mone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197643/
https://www.ncbi.nlm.nih.gov/pubmed/37214886
http://dx.doi.org/10.1101/2023.05.11.540323
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author Rojekar, Satish
Pallapati, Anusha R.
Gimenez–Roig, Judit
Korkmaz, Funda
Sultana, Farhath
Sant, Damini
Haeck, Clement
Macdonald, Anne
Kim, Se-Min
Rosen, Clifford J.
Barak, Orly
Meseck, Marcia
Caminis, John
Lizneva, Daria
Yuen, Tony
Zaidi, Mone
author_facet Rojekar, Satish
Pallapati, Anusha R.
Gimenez–Roig, Judit
Korkmaz, Funda
Sultana, Farhath
Sant, Damini
Haeck, Clement
Macdonald, Anne
Kim, Se-Min
Rosen, Clifford J.
Barak, Orly
Meseck, Marcia
Caminis, John
Lizneva, Daria
Yuen, Tony
Zaidi, Mone
author_sort Rojekar, Satish
collection PubMed
description Highly concentrated antibody formulations are oftentimes required for subcutaneous, self-administered biologics. Here, we report the creation of a unique formulation for our first–in–class FSH–blocking humanized antibody, MS-Hu6, which we propose to move to the clinic for osteoporosis, obesity, and Alzheimer’s disease. The studies were carried out using our Good Laboratory Practice (GLP) platform, compliant with the Code of Federal Regulations (Title 21, Part 58). We first used protein thermal shift, size exclusion chromatography, and dynamic light scattering to examine MS-Hu6 concentrations between 1 and 100 mg/mL. We found that thermal, monomeric, and colloidal stability of formulated MS-Hu6 was maintained at a concentration of 100 mg/mL. The addition of the antioxidant L–methionine and chelating agent disodium EDTA improved the formulation’s long–term colloidal and thermal stability. Thermal stability was further confirmed by Nano differential scanning calorimetry (DSC). Physiochemical properties of formulated MS-Hu6, including viscosity, turbidity, and clarity, conformed with acceptable industry standards. That the structural integrity of MS-Hu6 in formulation was maintained was proven through Circular Dichroism (CD) and Fourier Transform Infrared (FTIR) spectroscopy. Three rapid freeze–thaw cycles at −80°C/25°C or −80°C/37°C further revealed excellent thermal and colloidal stability. Furthermore, formulated MS-Hu6, particularly its Fab domain, displayed thermal and monomeric storage stability for more than 90 days at 4°C and 25°C. Finally, the unfolding temperature (T(m)) for formulated MS-Hu6 increased by >4.80°C upon binding to recombinant FSH, indicating highly specific ligand binding. Overall, we document the feasibility of developing a stable, manufacturable and transportable MS-Hu6 formulation at a ultra–high concentration at industry standards. The study should become a resource for developing biologic formulations in academic medical centers.
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spelling pubmed-101976432023-05-20 Development and Biophysical Characterization of a Humanized FSH–Blocking Monoclonal Antibody Therapeutic Formulated at an Ultra–High Concentration Rojekar, Satish Pallapati, Anusha R. Gimenez–Roig, Judit Korkmaz, Funda Sultana, Farhath Sant, Damini Haeck, Clement Macdonald, Anne Kim, Se-Min Rosen, Clifford J. Barak, Orly Meseck, Marcia Caminis, John Lizneva, Daria Yuen, Tony Zaidi, Mone bioRxiv Article Highly concentrated antibody formulations are oftentimes required for subcutaneous, self-administered biologics. Here, we report the creation of a unique formulation for our first–in–class FSH–blocking humanized antibody, MS-Hu6, which we propose to move to the clinic for osteoporosis, obesity, and Alzheimer’s disease. The studies were carried out using our Good Laboratory Practice (GLP) platform, compliant with the Code of Federal Regulations (Title 21, Part 58). We first used protein thermal shift, size exclusion chromatography, and dynamic light scattering to examine MS-Hu6 concentrations between 1 and 100 mg/mL. We found that thermal, monomeric, and colloidal stability of formulated MS-Hu6 was maintained at a concentration of 100 mg/mL. The addition of the antioxidant L–methionine and chelating agent disodium EDTA improved the formulation’s long–term colloidal and thermal stability. Thermal stability was further confirmed by Nano differential scanning calorimetry (DSC). Physiochemical properties of formulated MS-Hu6, including viscosity, turbidity, and clarity, conformed with acceptable industry standards. That the structural integrity of MS-Hu6 in formulation was maintained was proven through Circular Dichroism (CD) and Fourier Transform Infrared (FTIR) spectroscopy. Three rapid freeze–thaw cycles at −80°C/25°C or −80°C/37°C further revealed excellent thermal and colloidal stability. Furthermore, formulated MS-Hu6, particularly its Fab domain, displayed thermal and monomeric storage stability for more than 90 days at 4°C and 25°C. Finally, the unfolding temperature (T(m)) for formulated MS-Hu6 increased by >4.80°C upon binding to recombinant FSH, indicating highly specific ligand binding. Overall, we document the feasibility of developing a stable, manufacturable and transportable MS-Hu6 formulation at a ultra–high concentration at industry standards. The study should become a resource for developing biologic formulations in academic medical centers. Cold Spring Harbor Laboratory 2023-05-11 /pmc/articles/PMC10197643/ /pubmed/37214886 http://dx.doi.org/10.1101/2023.05.11.540323 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Rojekar, Satish
Pallapati, Anusha R.
Gimenez–Roig, Judit
Korkmaz, Funda
Sultana, Farhath
Sant, Damini
Haeck, Clement
Macdonald, Anne
Kim, Se-Min
Rosen, Clifford J.
Barak, Orly
Meseck, Marcia
Caminis, John
Lizneva, Daria
Yuen, Tony
Zaidi, Mone
Development and Biophysical Characterization of a Humanized FSH–Blocking Monoclonal Antibody Therapeutic Formulated at an Ultra–High Concentration
title Development and Biophysical Characterization of a Humanized FSH–Blocking Monoclonal Antibody Therapeutic Formulated at an Ultra–High Concentration
title_full Development and Biophysical Characterization of a Humanized FSH–Blocking Monoclonal Antibody Therapeutic Formulated at an Ultra–High Concentration
title_fullStr Development and Biophysical Characterization of a Humanized FSH–Blocking Monoclonal Antibody Therapeutic Formulated at an Ultra–High Concentration
title_full_unstemmed Development and Biophysical Characterization of a Humanized FSH–Blocking Monoclonal Antibody Therapeutic Formulated at an Ultra–High Concentration
title_short Development and Biophysical Characterization of a Humanized FSH–Blocking Monoclonal Antibody Therapeutic Formulated at an Ultra–High Concentration
title_sort development and biophysical characterization of a humanized fsh–blocking monoclonal antibody therapeutic formulated at an ultra–high concentration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197643/
https://www.ncbi.nlm.nih.gov/pubmed/37214886
http://dx.doi.org/10.1101/2023.05.11.540323
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