From Bench to Bedside: Material Selection and Clinical Translation of Nanocarrier Systems for Anticancer Drug Delivery
Research Article
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From Bench to Bedside: Material Selection and Clinical Translation of Nanocarrier Systems for Anticancer Drug Delivery

Hongyuan Yang 1*
1 HD Qingdao Wanda School
*Corresponding author: 13376472855@163.com
Published on 28 October 2025
Journal Cover
TNS Vol.147
ISSN (Print): 2753-8826
ISSN (Online): 2753-8818
ISBN (Print): 978-1-80590-489-2
ISBN (Online): 978-1-80590-490-8
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Abstract

This study examines how material selection governs the design, performance, and clinical translation of nanocarrier systems for anticancer drug delivery. By comparatively analyzing organic (e.g., liposomes, polymeric micelles, protein-based carriers) and inorganic platforms (e.g., gold nanoparticles, mesoporous silica, carbon-based materials), we delineate how biocompatibility, drug‐loading mechanisms, surface chemistry, and stimuli responsiveness shape pharmacokinetics, tumor accumulation, and release profiles. We highlight design rules that connect physicochemical parameters—size, charge, morphology, and ligand density—to biological outcomes such as enhanced permeability and retention, receptor-mediated uptake, and intracellular trafficking. Beyond single-material systems, we evaluate hybrid and core–shell architectures that integrate complementary strengths (biodegradability, structural robustness, imaging/theranostic capability) to enable controlled, site-specific delivery and real-time monitoring. Translational considerations—including scalable synthesis, Good Manufacturing Practice readiness, batch-to-batch quality attributes, and safety/clearance pathways—are discussed as co-equal constraints with efficacy. This paper maps these considerations to clinical use-cases, noting where liposomes remain the regulatory benchmark, polymers offer programmable targeting and release, and inorganic or hybrid constructs unlock multifunctional therapies (photothermal, photoacoustic, or immuno-combination regimens). Finally, the author outlines a decision framework that aligns tumor biology (biomarkers, microenvironment, prior resistance) with nanocarrier typology to support personalized medicine. Collectively, the analysis provides practical guidance for matching material classes to therapeutic objectives, accelerating the trajectory from bench formulation to bedside impact in oncology.

Keywords:

Nanocarrier, Anticancer Drugs, Material Selection, Targeted Delivery, Side Effects

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Yang,H. (2025). From Bench to Bedside: Material Selection and Clinical Translation of Nanocarrier Systems for Anticancer Drug Delivery. Theoretical and Natural Science,147,55-65.

References

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Cite this article

Yang,H. (2025). From Bench to Bedside: Material Selection and Clinical Translation of Nanocarrier Systems for Anticancer Drug Delivery. Theoretical and Natural Science,147,55-65.

Data availability

The datasets used and/or analyzed during the current study will be available from the authors upon reasonable request.

About volume

Volume title: Proceedings of ICBioMed 2025 Symposium: AI for Healthcare: Advanced Medical Data Analytics and Smart Rehabilitation

ISBN: 978-1-80590-489-2(Print) / 978-1-80590-490-8(Online)
Editor: Alan Wang
Conference date: 17 October 2025
Series: Theoretical and Natural Science
Volume number: Vol.147
ISSN: 2753-8818(Print) / 2753-8826(Online)