4.1 Article

In vitro delivery of mTOR inhibitors by kidney-targeted micelles for autosomal dominant polycystic kidney disease

Journal

SLAS TECHNOLOGY
Volume 28, Issue 4, Pages 223-229

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.slast.2023.02.001

Keywords

Micelles; ADPKD; Targeted; Rapalogs; mTOR

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Autosomal dominant polycystic kidney disease (ADPKD) is a common genetic kidney disease characterized by renal cyst formation. Inhibition of the mTOR pathway has been proposed as a potential treatment approach. This study focused on encapsulating mTOR inhibitors in drug delivery carriers that target the kidneys. The results show promising efficacy of the encapsulated drugs in inhibiting cell proliferation in vitro. Encapsulation in peptide amphiphile micelle (PAM) nanoparticles could be a potential strategy for delivering mTOR inhibitors to treat ADPKD.
Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic kidney disease and is characterized by the formation of renal cysts and the eventual development of end-stage kidney disease. One approach to treating ADPKD is through inhibition of the mammalian target of rapamycin (mTOR) pathway, which has been implicated in cell overproliferation, contributing to renal cyst expansion. However, mTOR inhibitors, including rapamycin, everolimus, and RapaLink-1, have off-target side effects including immunosuppression. Thus, we hypothesized that the encapsulation of mTOR inhibitors in drug delivery carriers that target the kidneys would provide a strategy that would enable therapeutic efficacy while minimizing off-target accumulation and associated toxicity. Toward eventual in vivo application, we synthesized cortical collecting duct (CCD) targeted peptide amphiphile micelle (PAM) nanoparticles and show high drug encapsulation efficiency ( > 92.6%). In vitro analysis indicated that drug encapsulation into PAMs enhanced the anti-proliferative effect of all three drugs in human CCD cells. Analysis of in vitro biomarkers of the mTOR pathway via western blotting confirmed that PAM encapsulation of mTOR inhibitors did not reduce their efficacy. These results indicate that PAM encapsulation is a promising way to deliver mTOR inhibitors to CCD cells and potentially treat ADPKD. Future studies will evaluate the therapeutic effect of PAM-drug formulations and ability to prevent off-target side effects associated with mTOR inhibitors in mouse models of ADPKD.

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