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A novel in vitro method to model the fate of subcutaneously administered biopharmaceuticals and associated formulation components

Kinnunen, Hanne M.; Sharma, Vikas; Contreras-Rojas, Luis Rodrigo; Yu, Yafei; Alleman, Chlöe; Sreedhara, Alavattam; Fischer, Stefan; Khawli, Leslie; Yohe, Stefan T.; Bumbaca, Daniela; Patapoff, Thomas W.; Daugherty, Ann L.; Mrsny, Randall J.

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Authors

Hanne M. Kinnunen

Vikas Sharma

Luis Rodrigo Contreras-Rojas

Yafei Yu

Chlöe Alleman

Alavattam Sreedhara

Stefan Fischer

Leslie Khawli

Stefan T. Yohe

Daniela Bumbaca

Thomas W. Patapoff

Ann L. Daugherty

Randall J. Mrsny



Contributors

H Bown (née Kinnunen) kwmd75@durham.ac.uk
Other

Abstract

Subcutaneous (SC) injection is becoming a more common route for the administration of biopharmaceuticals. Currently, there is no reliable in vitro method that can be used to anticipate the in vivo performance of a biopharmaceutical formulation intended for SC injection. Nor is there an animal model that can predict in vivo outcomes such as bioavailability in humans. We address this unmet need by the development of a novel in vitro system, termed Scissor (Subcutaneous Injection Site Simulator). The system models environmental changes that a biopharmaceutical could experience as it transitions from conditions of a drug product formulation to the homeostatic state of the hypodermis following SC injection. Scissor uses a dialysis-based injection chamber, which can incorporate various concentrations and combinations of acellular extracellular matrix (ECM) components that may affect the release of a biopharmaceutical from the SC injection site. This chamber is immersed in a container of a bicarbonate-based physiological buffer that mimics the SC injection site and the infinite sink of the body. Such an arrangement allows for real-time monitoring of the biopharmaceutical within the injection chamber, and can be used to characterize physicochemical changes of the drug and its interactions with ECM components. Movement of a biopharmaceutical from the injection chamber to the infinite sink compartment simulates the drug migration from the injection site and uptake by the blood and/or lymph capillaries. Here, we present an initial evaluation of the Scissor system using the ECM element hyaluronic acid and test formulations of insulin and four different monoclonal antibodies. Our findings suggest that Scissor can provide a tractable method to examine the potential fate of a biopharmaceutical formulation after its SC injection in humans and that this approach may provide a reliable and representative alternative to animal testing for the initial screening of SC formulations.

Citation

Kinnunen, H. M., Sharma, V., Contreras-Rojas, L. R., Yu, Y., Alleman, C., Sreedhara, A., …Mrsny, R. J. (2015). A novel in vitro method to model the fate of subcutaneously administered biopharmaceuticals and associated formulation components. Journal of Controlled Release, 214, 94-102. https://doi.org/10.1016/j.jconrel.2015.07.016

Journal Article Type Article
Acceptance Date Jul 15, 2015
Publication Date Sep 28, 2015
Deposit Date Oct 21, 2015
Publicly Available Date Jul 22, 2016
Journal Journal of Controlled Release
Print ISSN 0168-3659
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 214
Pages 94-102
DOI https://doi.org/10.1016/j.jconrel.2015.07.016
Keywords Subcutaneous injection, Biopharmaceuticals, In vitro model, Formulation design.

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