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Shuang-Hua Wang

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Open access Oct 2026

Oleanolic Acid-Loaded Organosilica Nanoparticles for Synergistic Anti-Inflammatory and Antibacterial Therapy via Inducing Macrophage Polarization

Chronic inflammatory diseases caused by bacterial infections are notoriously difficult to treat due to the formation of a vicious cycle in which bacterial infection and immune dysregulation mutually reinforce each other at the lesion site. Current antibiotic therapies face the dual challenges of escalating drug resis...

Xiao-Peng Zhou, Hua-Fu Wang, Shuang-Hua Wang et al. · 0 citations
Open access Sep 2026

Dual-targeting by rotating magnetic field-driven superparamagnetic bionic nanorobots for enhanced triple-negative breast cancer therapy

Triple-negative breast cancer (TNBC) is a highly aggressive subtype of breast cancer with limited treatment options and poor prognosis due to the absence of estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 (HER2). Doxorubicin (DOX)-based chemotherapy remains the standard of care, y...

Wei Song, Zhong-Xin Liu, Jia Xu et al. · 1 citation
Aug 2026

RVG‐Functionalized Liposomal Mollugin: A Targeted Nanotherapy for Spinal Cord Injury

A RVG‐modified liposomal nanoplatform for targeted delivery of mollugin (Mol@Lip‐RVG) as a novel therapeutic strategy for SCI resulted in enhanced neuro‐preservation and substantial improvement in motor function recovery, achieved through dual modulation of microglial reprogramming and attenuation of oxidative stress.

Quan Zhou, I. Shaikh, Jian-Feng Wang et al. · 0 citations
Open access Sep 2026

Nano Engineered Chitosan-Based Delivery System for Vonoprazan Fumarate for Enhanced Bioavailability: Fabrication and Evaluation

This study showed that mucoadhesive polymeric nanoparticles of vonoprazan significantly enhanced solubility, pH-dependent release, and improved mucoadhesion, making it a promising approach to improve the oral bioavailability of drugs with poor water solubility.

S. Sajjad, U. Tulain, M. Asim et al. · 0 citations
Open access Jul 2026

PEG-g-(HEMA-co-AA) pH-responsive graft copolymer: A promising approach for the controlled oral delivery of acid-labile rabeprazole sodium.

Overall, the PEG (HEMA-co-AA) hydrogel represents a versatile vehicle for the controlled and local administration of acid-labile pharmaceuticals, thereby promoting increased therapeutic efficacy and safe for use in future therapeutic applications.

U. Tulain, N. Malik, Alia Erum et al. · 0 citations

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