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Updated: Sep 21, 2025

Direct Drug Delivery to Kidney via the Renal Artery
Published on: April 17, 2021
Novel Drug Delivery Technologies and Targets for Renal Disease
Alejandro R Chade1,2,3, Gene L Bidwell4,5,6
1The Department of Physiology and Biophysics (A.R.C.), University of Mississippi Medical Center, Jackson.
Abstract:
The burden of acute and chronic kidney diseases to the health care system is exacerbated by the high mortality that this disease carries paired with the still limited availability of comprehensive therapies. A reason partially resides in the complexity of the kidney, with multiple potential target cell types and a complex structural environment that complicate strategies to protect and recover renal function after injury. Management of both acute and chronic renal disease, irrespective of the cause, are mainly focused on supportive treatments and renal replacement strategies when needed. Emerging preclinical evidence supports the feasibility of drug delivery technology for the kidney, and recent studies have contributed to building a robust catalog of peptides, proteins, nanoparticles, liposomes, extracellular vesicles, and other carriers that may be fused to therapeutic peptides, proteins, nucleic acids, or small molecule drugs. These fusions can display a precise renal uptake, an enhanced circulating time, and a directed intraorgan biodistribution while protecting their cargo to improve therapeutic efficacy. However, several hurdles that slow the transition towards clinical applications are still in the way, such as solubility, toxicity, and sub-optimal renal targeting. This review will discuss the feasibility and current limitations of drug delivery technologies for the treatment of renal disease, offering an update on their potential and the future directions of these promising strategies.
Insights
Novel drug delivery technologies show promise for treating kidney diseases, offering enhanced uptake and targeted delivery. Overcoming challenges like solubility and toxicity is key for clinical translation of these advanced renal therapies.
Area of Science:
- Nephrology and Pharmacology
- Biomedical Engineering and Drug Delivery Systems
Background:
- Acute and chronic kidney diseases pose a significant health burden due to high mortality and limited therapeutic options.
- The kidney's complex cellular and structural environment complicates strategies for protecting and recovering renal function post-injury.
- Current management relies primarily on supportive care and renal replacement therapies.
Purpose of the Study:
- To review the feasibility and limitations of drug delivery technologies for treating kidney diseases.
- To provide an update on the potential of advanced carriers for renal therapy.
- To discuss future directions for overcoming clinical translation hurdles.
Main Methods:
- Review of emerging preclinical evidence on drug delivery systems for renal applications.
- Analysis of various carriers including peptides, proteins, nanoparticles, liposomes, and extracellular vesicles.
- Examination of therapeutic cargo such as peptides, proteins, nucleic acids, and small molecules.
Main Results:
- Drug delivery systems demonstrate potential for precise renal uptake, extended circulation time, and targeted intraorgan biodistribution.
- These systems can protect therapeutic cargo, potentially improving efficacy for kidney disease treatment.
- Key challenges include drug solubility, toxicity, and suboptimal renal targeting, hindering clinical application.
Conclusions:
- Drug delivery technologies offer promising strategies to enhance the treatment of acute and chronic kidney diseases.
- Further research is needed to address current limitations and facilitate the clinical translation of these advanced renal therapies.
- Optimizing targeting and formulation will be crucial for realizing the full therapeutic potential in nephrology.
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