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. Author manuscript; available in PMC: 2024 Dec 4.
Published in final edited form as: Adv Drug Deliv Rev. 2023 Sep 9;202:115083. doi: 10.1016/j.addr.2023.115083

Table 2.

Preclinical study examples demonstrating the use of in situ-forming hydrogels for delivery of cancer vaccines.

Hydrogel Injection location Gelation-stimuli Antigen Other loaded drugs/immunotherapy Tumor model Citation
PEG crosslinked melittin-peptide i.t. Self-assembly Ultrafiltered retentate from irradiated cells Doxorubicin, melittin B16F10; LLC; MC38 [64]
self-assembled poly(L-valine) s.c. Self-assembly Tumor cell lysates TLR3 agonist (poly(I:C) B16 [203]
PEG-b-poly(L-alanine) s.c. Self-assembly Tumor cell lysates GM-CSF; Anti-CTL-A-4; anti-PD-1 (encapsulated in hydrogel) B16F10; 4T-1 [111]
polymerized phenylboronic acid (pPBA)-based Contralateral flank Mixture of components from two syringes Tumor cell lysate Mannan 4T1 [204]
Silk hydrogel s.c. Ultrasound Hepa1−6 liver cancer-specific neoantigen TLR9 agonist (CPG-ODN); STING; Hepa1−6 [113]
mPEG-OVApeptide-AuNPs + ⍺-cyclodextrin s.c. Complexation between alpha-CD and PEG before injection. Shear thinning OVApeptide CPG B16-OVA [108]
PDLLA-PEG-PDLLA s.c. Temperature Tumor cell lysates GM-CSF, CpG-ODN B16F10; CT26 [55]