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Updated: Sep 19, 2025

Targeted Plasma Membrane Delivery of a Hydrophobic Cargo Encapsulated in a Liquid Crystal Nanoparticle Carrier
Published on: February 8, 2017
Mechanically Responsive Organic-Inorganic Hybrid as Advanced Delivery Vehicle for Targeted Cancer Treatment
Swapan Maity1, Dipesh Kumar Dubey1, Akshita Upreti2
1School of Materials Science and Technology, Indian Institute of Technology (Banaras Hindu University), Varanasi, 221005, India.
Abstract:
Clinical oncology grapples with a daunting challenge therapy resistance in tumors evolves rapidly, undermining treatment efficacy. Chemotherapy, while inducing specific cancer cell death, often falls short due to intrinsic cellular defences. This underscores the urgent need for precision and controlled therapeutic strategies. A breakthrough emerges in tumor targeted drug delivery through interlamellar surface modification of hydroxyl groups in pristine Li-Al-based layered double hydroxide (LDH). Grafting polyurethane (PU) onto LDH enhances its mechanical integrity, achieving an extraordinary elongation at break of 1230%. This exceptional flexibility enables the material to withstand substantial deformation, ensuring adaptability within dynamic physiological environments - critical for injectable and implantable drug carriers navigating complex biological structures. The polyurethane graft fine-tunes the hydrophilic hydrophobic balance, orchestrating synchronized drug delivery. First principle density functional theory (DFT) analyses reveal intricate molecular interactions between the nanohybrid and doxorubicin (Dox)In vitro and in vivo studies, particularly in luciferase - expressing melanoma-bearing mice, demonstrate remarkable biocompatibility and synergistic anticancer efficacy. Furthermore, an injectable hydrogel beneath the tumor site mitigates chemotherapy's toxic side effects by precisely regulating drug release. This pioneering nanohybrid heralds a new era in multifunctional nanomedicine, offering enhanced precision, stability, and patient compatibility, transforming the landscape of next generation cancer therapies.
Insights
This study introduces a flexible nanohybrid material for targeted cancer drug delivery. The engineered material shows enhanced biocompatibility and anticancer efficacy, offering a promising new therapy.
Area of Science:
- Biomaterials Science
- Nanomedicine
- Oncology
Background:
- Cancer therapy resistance necessitates advanced drug delivery systems.
- Current chemotherapy faces limitations due to intrinsic cellular defenses and systemic toxicity.
- Precision-controlled drug release is crucial for improving treatment efficacy and patient outcomes.
Purpose of the Study:
- To develop a novel, flexible nanohybrid for targeted tumor drug delivery.
- To enhance the mechanical properties and drug release kinetics of layered double hydroxide (LDH) materials.
- To evaluate the anticancer efficacy and biocompatibility of the modified nanohybrid in vitro and in vivo.
Main Methods:
- Surface modification of Li-Al-based layered double hydroxide (LDH) with polyurethane (PU).
- Characterization of mechanical properties (elongation at break) and drug loading/release profiles.
- In vitro and in vivo studies using doxorubicin (Dox) in melanoma models, including DFT analysis.
Main Results:
- The polyurethane-grafted LDH (PU-LDH) nanohybrid exhibited exceptional flexibility (1230% elongation at break).
- PU grafting optimized the hydrophilic-hydrophobic balance for synchronized drug delivery.
- In vivo studies demonstrated significant biocompatibility and synergistic anticancer effects with reduced toxicity.
Conclusions:
- The flexible PU-LDH nanohybrid represents a significant advancement in injectable and implantable drug delivery systems.
- This multifunctional nanomedicine platform offers enhanced precision, stability, and patient compatibility for next-generation cancer therapies.
- The injectable hydrogel formulation effectively localized drug release, mitigating systemic chemotherapy side effects.
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