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. 2021 Sep;38(9):1563-1583.
doi: 10.1007/s11095-021-03087-9. Epub 2021 Sep 8.

Evaluating a Modified High Purity Polysorbate 20 Designed to Reduce the Risk of Free Fatty Acid Particle Formation

Nidhi Doshi #  1 , Kyle Ritchie #  2 , Tamanna Shobha  3 , Jamie Giddings  2 , Kathrin Gregoritza  4 , Rosalynn Taing  2 , Stephen Rumbelow  5 , Jeff Chu  6 , Anthony Tomlinson  2 , Aadithya Kannan  2 , Miguel Saggu  2 , Si Kai Cai  4 , Victor Nicoulin  4 , Wenqiang Liu  2 , Steve Russell  6 , Lin Luis  2 , Sandeep Yadav  3
Affiliations

Evaluating a Modified High Purity Polysorbate 20 Designed to Reduce the Risk of Free Fatty Acid Particle Formation

Nidhi Doshi et al. Pharm Res. 2021 Sep.

Abstract

Purpose: To evaluate a modified high purity polysorbate 20 (RO HP PS20)-with lower levels of stearate, palmitate and myristate esters than the non-modified HP PS20-as a surfactant in biopharmaceutical drug products (DP). RO HP PS20 was designed to provide functional equivalence as a surfactant while delaying the onset of free fatty acid (FFA) particle formation upon hydrolytic degradation relative to HP PS20.

Methods: Analytical characterization of RO HP PS20 raw material included fatty acid ester (FAE) distribution, higher order ester (HOE) fraction, FFA levels and trace metals. Functional assessments included 1) vial and intravenous bag agitation; 2) oxidation via a placebo and methionine surrogate study; and 3) hydrolytic PS20 degradation studies to evaluate FFA particle formation with and without metal nucleation.

Results: Interfacial protection and oxidation propensity were comparable between the two polysorbates. Upon hydrolytic degradation, FFA particle onset was delayed in RO HP PS20. The delay was more pronounced when HOEs of PS20 were preferentially degraded. Furthermore, the hydrolytic degradants of RO HP PS20 formed fewer particles in the presence of spiked aluminum.

Conclusion: This work highlights the criticality of having tighter control on long chain FAE levels of PS20 to reduce the occurrence of FFA particle formation upon hydrolytic degradation and lower the variability in its onset. By simultaneously meeting compendial PS20 specifications while narrowing the allowable range for each FAE and shifting its composition towards the shorter carbon chain species, RO HP PS20 provides a promising alternative to HP PS20 for biopharmaceutical DPs.

Keywords: Drug product stability; Free fatty acids; Particles; Polysorbate 20; Polysorbate degradation; Surfactants.

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