Chitosan nanoparticle encapsulated pentoxifylline improves renal protection and reduces oxidative stress in amikacin induced nephrotoxicity

Theodor Bilharz Research Institute

Bibliographic Information

Authors: Moustafa N.; Abd El-latif M.B.; Farid A.

Journal: Discover Nano

Publisher: Springer

Publication Date: 18 April 2026

Volume / Issue: Volume 21 / Issue 1

Article No.: 128

ISSN: 27319229

DOI: 10.1186/s11671-026-04515-8

Scopus: View on Scopus

Document Type: Article

Access: All Open Access; Gold Open Access; Green Open Access


Authors and Affiliations

Moustafa N., Biotechnology Department, Faculty of Science, Cairo University, Giza, Egypt; Abd El-latif M.B., Environmental Research Department, Theodor Bilharz Research Institute, Giza, Egypt; Farid A., Biotechnology Department, Faculty of Science, Cairo University, Giza, Egypt


Abstract

Amikacin (AMK)-induced nephrotoxicity remains a clinical challenge, necessitating innovative therapeutic strategies. This study developed pentoxifylline-loaded chitosan nanoparticles (PTX-CSNPs) to enhance PTX’s renoprotective effects while minimizing its side effects. PTX-CSNPs were synthesized via ionic gelation, exhibiting high entrapment efficiency (89.53%) and sustained release (87% at 48 h). Characterization revealed spherical nanoparticles (30-50 nm by TEM and 79.05 nm by DLS) with positive zeta potential (+ 32.77 mV), confirmed by FTIR and XRD analyses. In vitro, PTX-CSNPs demonstrated superior antioxidant (98.73% DPPH scavenging), anti-inflammatory (76.46% RBCs membrane stabilization), and anticoagulant activity compared to free PTX. In vivo, AMK-induced nephrotoxic rats treated with PTX-CSNPs showed normalization of renal function biomarkers (BUN, creatinine, uric acid) and oxidative stress markers (MDA, SOD, GSH), alongside reduced inflammatory markers levels outperforming free PTX or CSNPs alone. Histopathology revealed preserved glomerular and tubular architecture. The nanoformulation’s efficacy was attributed to chitosan-mediated targeted delivery and PTX’s anti-inflammatory/antioxidant synergy. These findings highlighted PTX-CSNPs as a promising nanotherapeutic for drug-induced kidney injury, offering enhanced bioavailability and reduced systemic toxicity. © The Author(s) 2026.


Keywords

Chitosan nanoparticles; Nephrotoxicity; Pentoxifylline; Chitosan; Controlled drug delivery; Drug products; Nanoparticles; Oxidative stress; Amikacin; Anti-inflammatories; High entrapment efficiencies; Ionic gelations; Side effect; Synthesised; Therapeutic strategy; Gelation; Targeted drug delivery


Citation Information

Scopus Citations: 0


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