Literature DB >> 33789155

A review of Formulations of Commercially Available Antibodies.

Robert G Strickley1, William J Lambert2.   

Abstract

This review identified 126 commercially available antibodies approved globally between 1986 and February 2021 including 10 antibody drug conjugates, 16 biosimilars, and 3 antibody fragments. Prior to 2014 there were ≤ 5 approved each year, but after 2014 there have been ≥ 7 approved each year with the years 2017, 2019 and 2020 having the most at 17 each. A total of 136 products were identified of which 36 are lyophilized powders and 100 are solutions. The routes of administration are mainly subcutaneous or intravenous infusion with three intravenous bolus, two intravitreal, and one intramuscular. The subcutaneous products are ready-to-use solutions or reconstituted lyophilized powders that do not require dilution while most intravenous products are concentrates that require dilution into saline or another intravenous fluid prior to infusion. Most are packaged in single-dose units and the exception of multi-use is Herceptin® and its biosimilars. The package configurations are vials, prefilled autoinjectors, or prefilled syringes. A typical antibody formulation contains an antibody, an excipient to adjust tonicity or osmolality for solutions or a lyoprotectant for lyophilized powders, a buffer, and a surfactant. The ionic tonicity-adjusting excipient is mainly sodium chloride and the non-ionic osmolality-adjusting excipients include sucrose, trehalose, mannitol, maltose, and sorbitol. The lyoprotectants are trehalose and sucrose. The pH range is 4.8-8.0 and the buffers or pH-modifying agents include histidine, citrate, succinate, acetate, phosphate, glutamate, adipic acid, aspartic acid, lactic acid, tromethamine, and 2-(N-morpholino)-ethanesulfonic acid. The surfactants include mostly polysorbate 20 or polysorbate 80, with four containing poloxamer 188, and one that does not contain a surfactant but contains PEG 3350. One product does not contain a buffer, and 12 do not contain a surfactant. The viscosity-lowering excipients are sodium chloride and the amino acids arginine, glycine, proline, and lysine. Arginine may also function to adjust ionic strength and minimize aggregation. Human serum albumin is used in 2 products for intravenous infusion. Other excipients include methionine as an anti-oxidant, and EDTA or DTPA as chelating agents. The maximum volume of subcutaneous injection is 15 mL administered over 3-5 minutes, but the typically volume is 0.5-2 mL. Five fixed-dose combinations have recently been approved and four contain hyaluronidase to assist the large volume subcutaneous injection of up to 15 mL, while one is a fixed-dose combination for intravenous with three antibodies. Prefilled autoinjectors and syringes are becoming more common and many come affixed with a needle of 27-gauge or 29-gauge, while a few have a 26-gauge or a 30-gauge needle. Recent advancements include hyaluronidase to assist the large subcutaneous injection volume of 5-15 mL, fixed-dose combinations, buffer-free formulation, and smaller subcutaneous injection volume (0.1 mL).
Copyright © 2021 American Pharmacists Association. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Antibody; Antibody drug conjugates; Biosimilars; Formulation

Year:  2021        PMID: 33789155     DOI: 10.1016/j.xphs.2021.03.017

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  13 in total

1.  Characterization of Grinding-Induced Subvisible Particles and Free Radicals in a Freeze-Dried Monoclonal Antibody Formulation.

Authors:  Zhen-Yi Jing; Guo-Li Huo; Min-Fei Sun; Bin-Bin Shen; Wei-Jie Fang
Journal:  Pharm Res       Date:  2022-01-26       Impact factor: 4.200

2.  Investigation of native and aggregated therapeutic proteins in human plasma with asymmetrical flow field-flow fractionation and mass spectrometry.

Authors:  Ingrid Ramm; Mats Leeman; Herje Schagerlöf; Ileana Rodríguez León; Alejandra Castro; Lars Nilsson
Journal:  Anal Bioanal Chem       Date:  2022-10-05       Impact factor: 4.478

3.  Antibodies with Weakly Basic Isoelectric Points Minimize Trade-offs between Formulation and Physiological Colloidal Properties.

Authors:  Priyanka Gupta; Emily K Makowski; Sandeep Kumar; Yulei Zhang; Justin M Scheer; Peter M Tessier
Journal:  Mol Pharm       Date:  2022-02-02       Impact factor: 5.364

Review 4.  US FDA-approved therapeutic antibodies with high-concentration formulation: summaries and perspectives.

Authors:  Shawn Shouye Wang; Yifei Susie Yan; Kin Ho
Journal:  Antib Ther       Date:  2021-11-18

Review 5.  Hybridoma technology; advancements, clinical significance, and future aspects.

Authors:  Sanchita Mitra; Pushpa Chaudhary Tomar
Journal:  J Genet Eng Biotechnol       Date:  2021-10-18

Review 6.  Computational models for studying physical instabilities in high concentration biotherapeutic formulations.

Authors:  Marco A Blanco
Journal:  MAbs       Date:  2022 Jan-Dec       Impact factor: 5.857

Review 7.  Advanced Oxidation Processes in Pharmaceutical Formulations: Photo-Fenton Degradation of Peptides and Proteins.

Authors:  Christian Schöneich
Journal:  Int J Mol Sci       Date:  2022-07-27       Impact factor: 6.208

8.  A New Alternative Tool to Analyse Glycosylation in Monoclonal Antibodies Based on Drop-Coating Deposition Raman imaging: A Proof of Concept.

Authors:  Sabrina Hamla; Pierre-Yves Sacré; Allison Derenne; Ben Cowper; Erik Goormaghtigh; Philippe Hubert; Eric Ziemons
Journal:  Molecules       Date:  2022-07-09       Impact factor: 4.927

9.  Nano Differential Scanning Fluorimetry-Based Thermal Stability Screening and Optimal Buffer Selection for Immunoglobulin G.

Authors:  Soo Hyun Kim; Han Ju Yoo; Eun Ji Park; Dong Hee Na
Journal:  Pharmaceuticals (Basel)       Date:  2021-12-25

10.  DELOS Nanovesicles-Based Hydrogels: An Advanced Formulation for Topical Use.

Authors:  Lídia Ballell-Hosa; Elisabet González-Mira; Hector Santana; Judit Morla-Folch; Marc Moreno-Masip; Yaima Martínez-Prieto; Albert Revuelta; Primiano Pio Di Mauro; Jaume Veciana; Santi Sala; Lidia Ferrer-Tasies; Nora Ventosa
Journal:  Pharmaceutics       Date:  2022-01-15       Impact factor: 6.321

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