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Analysis of Protein Aggregates Hydrodynamic Diameter by Size Exclusion Chromatography (SEC) (CAT#: STEM-B-0304-CJ)

Introduction

The generic term 'aggregates' refers to species characterized by a wide size range, diverse morphologies and structures. Protein aggregates may start in the low nanometer size range but then can grow into the micrometer and even visible size range.<br /><br />Most protein therapeutics and many other biopharmaceutical compounds are inherently unstable and can undergo aggregation through various pathways. Aggregates of various kinds can be formed, such as reversible and non-reversible, soluble, and non-soluble etc. In addition,Aggregation maybe occur because of exposure to air-liquid or liquid-solid interfaces, e.g., during mixing, during filling and shipping, during reconstitution of lyophilized products, or through contact with chromatography columns, pumps, pipes, vessels, filters, etc. Aggregation can directly influence the efficacy of the therapy by reducing the number of functional molecules, but also indirectly influence efficacy as well as safety of a therapy by inducing side-effects, such as unwanted immunogenicity.<br /><br />The hydrodynamic diameter (Dh) of a molecule is defined as the diameter of a perfect solid sphere that would exhibit the same hydrodynamic friction as the molecule of interest. Thus, the Dh value reflects primarily the hydrodynamic friction but is usually also a good estimation of the absolute size of the molecule.




Principle

Size exclusion chromatography (SEC) is used for the analysis and quantitation of soluble aggregates that are noncovalent and irreversible in nature. Separation is based on the hydrodynamic size of the protein in solution. SEC is suitable for the analysis of aggregates in the size range of 1–50 nm and is considered robust and accurate when the method induces no changes to the aggregation state, and nonspecific interactions with the column packing media are eliminated. The analysis of mAbs by SEC is typically performed under non-denaturing conditions at near-physiological pH range. Using volatile buffers such as 20 mM ammonium formate, SEC columns can also be directly coupled to a high resolution mass spectrometer for native SEC-MS analysis . Separation of mAb dimer aggregates and monomer can be optimized through careful choice of the UHPLC system employed, the

Applications

Biopharmaceutica

Procedure

SEC resins consist of a porous matrix of spherical particles (beads) that lack reactivity and adsorptive properties. After sample has entered the column, molecules larger than the pores are unable to diffuse into the beads, so they elute first. Molecules that range in size between the very big and very small can penetrate the pores to varying degrees based on their size. If a molecule is smaller than the smallest of the pores in the resin, it will be able to enter the total pore volume. Molecules that enter the total pore volume are eluted last. Samples are eluted isocratically so there is no need to use different buffers during the separation.

Materials

• Sample: Proteins
• Equipment: Size Exclusion Chromatography (SEC)

Notes

• The formation of aggregates in your biopharmaceutical product can have a negative effect on safety, efficacy and function. Regulatory authorities expect that orthogonal characterization techniques are used to fully understand the aggregation profile of any molecule.
• Measurable range: 5–50 nm