Abstract
The development of controlled biodegradable materials is of fundamental importance in immunodrug delivery to spatiotemporally controlled immune stimulation but avoid systemic inflammatory side effects. Based on this, polycarbonate nanogels are developed as degradable micellar carriers for transient immunoactivation of lymph nodes. An imidazoquinoline-type TLR7/8 agonist is covalently conjugated via reactive ester chemistry to these nanocarriers. The nanogels not only provide access to complete disintegration by the hydrolysable polymer backbone, but also demonstrate a gradual disintegration within several days at physiological conditions (PBS, pH 6.4–7.4, 37 °C). These intrinsic properties limit the lifetime of the carriers but their payload can still be successfully leveraged for immunological studies in vitro on primary immune cells as well as in vivo. For the latter, a spatiotemporal control of immune cell activation in the draining lymph node is found after subcutaneous injection. Overall, these features render polycarbonate nanogels a promising delivery system for transient activation of the immune system in lymph nodes and may consequently become very attractive for further development toward vaccination or cancer immunotherapy. Due to the intrinsic biodegradability combined with the high chemical control during the manufacturing process, these polycarbonate-based nanogels may also be of great importance for clinical translation.
| Original language | English |
|---|---|
| Article number | 2203490 |
| Journal | Advanced Functional Materials |
| Volume | 32 |
| Issue number | 35 |
| Early online date | 26 Jun 2022 |
| DOIs | |
| Publication status | Published - 25 Aug 2022 |
Bibliographical note
AcknowledgementsThe authors thank Dieter Schollmeyer for X-ray diffraction analysis,
Jutta Schnee and Stephan Türk for MALDI measurements, Christine Rosenauer for multi-angle DLS measurements,
and Manfred Wagner for NMR measurements. Moreover, the authors kindly acknowledge financial support by the DFG through the
Emmy Noether program (to L.N.) as well as the SFB 1066 projects B03, B04, Q02 and Q04 (to L.N., S.G., H.S., M.B., and K.K.). C.C. and
L.N. would also like to thank Tanja Weil for providing access to excellent laboratory facilities.
Open access funding enabled and organized by Projekt DEAL