| Literature DB >> 31173789 |
Ruolin Lu1, Chad Groer2, Peter A Kleindl1, K Ryan Moulder1, Aric Huang1, Jordan R Hunt1, Shuang Cai3, Daniel J Aires4, Cory Berkland5, M Laird Forrest6.
Abstract
The toll-like receptor 7 and 8 (TLR7/8) agonist Resiquimod (R848) has been recognized as a promising immunostimulator for the treatment of cutaneous cancers in multiple clinical trials. However, systemic administration of R848 often results in strong immune-related toxicities while having limited therapeutic effects to the tumor. In the present study, a prodrug-based nanocarrier delivery system was developed that exhibited high therapeutic efficiency. R848 was conjugated to α-tocopherol to constitute an R848-Toco prodrug, followed by formulating with a tocopherol-modified hyaluronic acid (HA-Toco) as a polymeric nano-suspension. In vitro evaluation showed that the delivery system prolonged the release kinetics while maintaining TLR agonist activities. When administered subcutaneously, the nano-suspension formed a depot at the injection site, inducing localized immune responses without systemic expansion. This formulation also suppressed tumor growth and recruited immune cells to the tumor in a murine model of head and neck cancer. In a preclinical canine study of spontaneous mast cell tumors, the treatment led to a 67% response rate (three partial remissions and one complete remission).Entities:
Keywords: Cancer immunotherapy; Depot effect; Nanotherapeutic formulation; Sustained delivery; Toll-like receptor agonists
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Year: 2019 PMID: 31173789 PMCID: PMC6679596 DOI: 10.1016/j.jconrel.2019.06.003
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776