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AI-Guided Design of pH- and Redox-Responsive Lignin@GO@ZIF-8 Nanocarriers for Targeted Co-Delivery of 5-Fluorouracil and Metformin in Prostate Cancer Therapy.

Small (Weinheim an der Bergstrasse, Germany) 2026 Vol.22(19) p. e13085

Gorish BMT, Abdelmula WIY, Wenqian D, Yue B, Yahu L, Zhu D

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Prostate cancer therapy is limited by systemic toxicity and inefficient tumor-selective delivery.

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BibTeX ↓ RIS ↓
APA Gorish BMT, Abdelmula WIY, et al. (2026). AI-Guided Design of pH- and Redox-Responsive Lignin@GO@ZIF-8 Nanocarriers for Targeted Co-Delivery of 5-Fluorouracil and Metformin in Prostate Cancer Therapy.. Small (Weinheim an der Bergstrasse, Germany), 22(19), e13085. https://doi.org/10.1002/smll.202513085
MLA Gorish BMT, et al.. "AI-Guided Design of pH- and Redox-Responsive Lignin@GO@ZIF-8 Nanocarriers for Targeted Co-Delivery of 5-Fluorouracil and Metformin in Prostate Cancer Therapy.." Small (Weinheim an der Bergstrasse, Germany), vol. 22, no. 19, 2026, pp. e13085.
PMID 41627184

Abstract

Prostate cancer therapy is limited by systemic toxicity and inefficient tumor-selective delivery. Here we report a multi-stimuli-responsive nanocomposite, Lignin@GO@ZIF-8, that co-delivers 5-Fluorouracil (5-FU) and metformin and couples pH- and redox-responsive release. We integrate machine learning (ML) to guide formulation: trained on 500 formulation property pairs with cross-validation and a held-out test set, XGBoost achieved the highest predictive performance (R = 0.86-0.89) for drug loading, encapsulation efficiency, and release rate, with influential features including the ZIF-8 fraction, graphene oxide (GO) content, particle size, zeta potential, pH, and glutathione concentration. ML-optimized Lignin@GO@ZIF-8 exhibited improved loading and tunable release relative to pre-optimized controls. In vitro, the platform sustained drug release and produced potent anticancer activity, reducing LNCaP viability to 18 ± 3% at 72 h, while showing low cytotoxicity toward non-malignant cells. These results support a data-driven framework for rational design of multifunctional, stimuli-responsive nanomedicine platforms and may help inform future translational strategies for prostate cancer.

MeSH Terms

Metformin; Male; Prostatic Neoplasms; Humans; Fluorouracil; Graphite; Oxidation-Reduction; Hydrogen-Ion Concentration; Drug Carriers; Lignin; Cell Line, Tumor; Drug Delivery Systems; Drug Liberation; Nanocomposites; Nanoparticles