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Fish oil-based microemulsion can efficiently deliver oral peptide blocking PD-1/PD-L1 and simultaneously induce
Xin Yang1, Wanqiong Li1, Shuzhen Li1
1School of Pharmaceutical Sciences (Shenzhen), Shenzhen Campus of Sun Yat-sen University, Shenzhen 518107, China.
Abstract:
Peptide immune checkpoint inhibitors in cancer immunotherapy have attracted great attention recently, but oral delivery of these peptides remains a huge challenge due to the harsh gastrointestinal environment, large molecular size, high hydrophilic, and poor transmembrane permeability. Here, for the first time, a fish oil-based microemulsion was developed for oral delivery of programmed death-1/programmed cell death-ligand 1 (PD-1/PD-L1) blocking model peptide, OPBP-1. The delivery system was characterized, in vitro and in vivo studies were conducted to evaluate its overall implication. As a result, this nutraceutical microemulsion was easily formed without the need of co-surfactants, and it appeared light yellow, transparent, good flowability with a particle size of 152 ± 0.73 nm, with a sustained drug release manner of 56.45 ± 0.36% over 24 h and a great stability within the harsh intestinal environment. It enhanced intestinal drug uptake and transportation over human intestinal epithelial Caco-2 cells, and drastically elevated the oral peptide bioavailability of 4.1-fold higher than that of OPBP-1 solution. Meanwhile, the mechanism of these dietary droplets permeated over the intestinal enterocytic membrane was found via clathrin and caveolae-mediated endocytic pathways. From the in vivo studies, the microemulsion facilitated the infiltration of CD8+ T lymphocytes in tumors, with increased interferon-γ (IFN-γ) secretion. Thus, it manifested a promising immune anti-tumor effect and significantly inhibited the growth of murine colonic carcinoma (CT26). Furthermore, it was found that the fish oil could induce ferroptosis in tumor cells and exhibited synergistic effect with OPBP-1 for cancer immunotherapy. In conclusion, this fish oil-based formulation demonstrated great potential for oral delivery of peptides with its natural property in reactive oxygen species (ROS)-related ferroptosis of tumor cells, which provides a great platform for functional green oral delivery system in cancer immunotherapy.
Insights
A novel fish oil microemulsion effectively delivers peptide immune checkpoint inhibitors orally. This approach enhances bioavailability and anti-tumor immunity by facilitating T-cell infiltration and inducing ferroptosis in cancer cells.
Area of Science:
- Pharmaceutical Sciences
- Nanotechnology
- Cancer Immunotherapy
Background:
- Oral delivery of peptide drugs is challenging due to poor stability and permeability.
- Peptide immune checkpoint inhibitors show promise in cancer immunotherapy but face delivery hurdles.
Purpose of the Study:
- To develop a fish oil-based microemulsion for oral delivery of a peptide immune checkpoint inhibitor (OPBP-1).
- To evaluate the stability, bioavailability, and anti-tumor efficacy of the developed formulation.
Main Methods:
- Formulation of a fish oil-based microemulsion without co-surfactants.
- Characterization of particle size, drug release, and stability.
- In vitro studies using Caco-2 cells for drug uptake.
- In vivo studies in a murine colon carcinoma model (CT26).
Main Results:
- The microemulsion exhibited excellent stability in the intestinal environment and sustained drug release.
- Enhanced intestinal uptake and a 4.1-fold increase in oral peptide bioavailability were observed.
- In vivo studies showed increased CD8+ T lymphocyte infiltration, interferon-γ secretion, and significant tumor growth inhibition.
- Fish oil demonstrated synergistic anti-tumor effects by inducing ferroptosis.
Conclusions:
- The fish oil-based microemulsion is a promising system for oral peptide delivery in cancer immunotherapy.
- The formulation leverages natural properties for enhanced drug delivery and synergistic anti-tumor effects.
- This approach offers a green and effective platform for oral peptide-based cancer therapies.
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