Non-ionic surfactants for stabilization of polymeric nanoparticles for biomedical uses

H Cortés, H Hernández-Parra, SA Bernal-Chávez… - Materials, 2021 - mdpi.com
Surfactants are essential in the manufacture of polymeric nanoparticles by emulsion
formation methods and to preserve the stability of carriers in liquid media. The deposition of …

Factors affecting the physical stability (aggregation) of peptide therapeutics

KL Zapadka, FJ Becher… - Interface …, 2017 - royalsocietypublishing.org
The number of biological therapeutic agents in the clinic and development pipeline has
increased dramatically over the last decade and the number will undoubtedly continue to …

Protein aggregation–mechanisms, detection, and control

W Wang, CJ Roberts - International journal of pharmaceutics, 2018 - Elsevier
Protein aggregation has been recognized as one of the major challenges in the
development and commercialization of successful protein-based drug products because of …

Oxidation and deamidation of monoclonal antibody products: potential impact on stability, biological activity, and efficacy

S Gupta, W Jiskoot, C Schöneich, AS Rathore - Journal of pharmaceutical …, 2022 - Elsevier
The role in human health of therapeutic proteins in general, and monoclonal antibodies
(mAbs) in particular, has been significant and is continuously evolving. A considerable …

Protein–excipient interactions: Mechanisms and biophysical characterization applied to protein formulation development

TJ Kamerzell, R Esfandiary, SB Joshi… - Advanced drug delivery …, 2011 - Elsevier
The purpose of this review is to demonstrate the critical importance of understanding protein–
excipient interactions as a key step in the rational design of formulations to stabilize and …

Key interactions of surfactants in therapeutic protein formulations: a review

TA Khan, HC Mahler, RSK Kishore - European journal of pharmaceutics …, 2015 - Elsevier
Proteins as amphiphilic, surface-active macromolecules, demonstrate substantial interfacial
activity, which causes considerable impact on their multifarious applications. A commonly …

Developability assessment during the selection of novel therapeutic antibodies

A Jarasch, H Koll, JT Regula, M Bader… - Journal of …, 2015 - Elsevier
Therapeutic antibodies and antibody derivatives comprise the majority of today's
biotherapeutics. Routine methods to generate novel antibodies, such as immunization and …

Polysorbate degradation in biotherapeutic formulations: identification and discussion of current root causes

M Dwivedi, M Blech, I Presser, P Garidel - International journal of …, 2018 - Elsevier
Biotherapeutic protein formulations are often high concentration liquid protein solutions,
which are required to be stable under pharmaceutically relevant storage conditions and …

[图书][B] Chemical reagents for protein modification

RL Lundblad - 2004 - taylorfrancis.com
Revised and updated, Chemical Reagents for Protein Modification, Third Edition is an
encyclopedic work describing the many approaches to the site-specific modification of …

Particles in therapeutic protein formulations, Part 1: overview of analytical methods

S Zölls, R Tantipolphan, M Wiggenhorn… - Journal of …, 2012 - Elsevier
The presence of particles is a major issue during therapeutic protein formulation
development. Both proteinaceous and nonproteinaceous particles need to be analyzed not …