Ontology highlight
ABSTRACT: Background
The application of combination therapy for cancer treatment is limited due to poor tumor-specific drug delivery and the abscopal effect.Methods
Here, PD-L1- and CD44-responsive multifunctional nanoparticles were developed using a polymer complex of polyethyleneimine and oleic acid (PEI-OA) and loaded with two chemotherapeutic drugs (paclitaxel and chloroquine), an antigen (ovalbumin), an immunopotentiator (CpG), and an immune checkpoint inhibitor (anti-PD-L1 antibody).Results
PEI-OA greatly improved the drug loading capacity and encapsulation efficiency of the nanoplatform, while the anti-PD-L1 antibody significantly increased its cellular uptake compared to other treatment formulations. Pharmacodynamic experiments confirmed that the anti-PD-L1 antibody c
SUBMITTER: Cheng Y
PROVIDER: S-EPMC9615197 | biostudies-literature | 2022 Oct
REPOSITORIES: biostudies-literature