Naturally Derived Materials-Based Drug Delivery Systems and Their Biomedical Applications

A special issue of Pharmaceutics (ISSN 1999-4923). This special issue belongs to the section "Drug Delivery and Controlled Release".

Deadline for manuscript submissions: 20 May 2025 | Viewed by 317

Special Issue Editors

Department of Pharmaceutics, School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai 201203, China
Interests: drug formulation and delivery; design of functional drug delivery systems; biomedical materials; visible drug delivery; disease diagnose and theranostics; mechanism investigation in drug delivery

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Guest Editor
Department of Health Sciences, University “Magna Græcia” of Catanzaro, Campus Universitario “S. Venuta”—Building of BioSciences, Viale S. Venuta, Germaneto, 88100 Catanzaro, Italy
Interests: nanomedicine; drug delivery; HPLC; microemulsions; skin; lyotropic liquid crystals; rheology; biomaterials; functional biomaterials; bioengineeing

Special Issue Information

Dear Colleagues,

Naturally derived materials-based drug delivery systems (DDS) represent a crucial and sustainable approach in modern biomedical research. These materials, which include alginate, chitosan, hyaluronic acid, collagen, and silk proteins, offer the advantages of biocompatibility, biodegradability, and minimal toxicity. They align with circular economy principles by transforming waste from natural sources into valuable therapeutic platforms. Through the development of hydrogels, nanoparticles, and micelles, these materials have been applied to enhance controlled drug release, providing versatile tools for improving therapeutic outcomes. However, the transition from preclinical studies to industrial production presents significant challenges. These include scalability, reproducibility, and compliance with GMP and ISO standards, ensuring consistent quality and functionality in large-scale production.

Beyond drug delivery, naturally derived systems are increasingly being explored for applications in regenerative medicine, leveraging advanced cellular models like spheroids, organoids, and extracellular vesicles (EVs). These models offer enhanced physiological relevance and therapeutic precision in several research fields of biomedical interest. However, integrating these cutting-edge tools into scalable, reproducible, and compliant manufacturing pipelines requires multidisciplinary efforts, combining materials science, bioengineering, pharmacology, and clinical research expertise.

Natural-derived materials can solve problems in tissue engineering and regenerative medicine because of their inherent biocompatibility and ability to mimic the body's natural extracellular matrix. This allows for better integration with host tissues and reduced immune responses, which are critical for the success of any implanted biomaterial. Additionally, the biodegradability of these materials ensures that they can be safely metabolized and replaced by the body's cells over time, avoiding long-term complications associated with permanent implants.

The match between clinical needs and solution strategies is achieved through engineering means by tailoring the properties of these materials to specific therapeutic requirements. For instance, the degradation rate of a biomaterial can be adjusted to match the tissue regeneration rate, and a drug's release profile can be controlled to coincide with the healing process. This requires a deep understanding of the materials' biological and mechanical properties, as well as the ability to manipulate them at the molecular level to achieve desired outcomes. Such collaborations are essential to overcoming the current limitations, such as maintaining cell viability and product stability during scale-up processes.

This Special Issue focuses on drug delivery systems, but contributions derived from the use of DDS in extended areas of tissue engineering and regenerative medicine are also welcome. In particular, submissions that address the sustainable and scalable production of these materials, including their use in combination with cellular models and advanced therapies, will contribute to bridging the gap between academic research and industrial translation, ultimately promoting the multidisciplinary development of sustainable therapeutic platforms for clinical use.

Dr. Tao Sun
Dr. Martine Tarsitano
Guest Editors

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Keywords

  • naturally derived material
  • drug delivery systems
  • tissue engineering
  • regenerative medicine

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Published Papers (1 paper)

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Research

13 pages, 1054 KiB  
Article
Self-Assembled Cannabigerol-Based Nanoparticles: Design, Synthesis, and Antiproliferative Activity
by Arianna Amenta, Giulia Nordio, Francesco Piazzola, Maria Luisa Di Paolo, Fabio Milani, Martina Giacomini, Andrea Citarella, Umberto Ciriello, Giuseppe Paladino, Sara Pellegrino, Federica Silvestri, Valerio Fasano, Lisa Dalla Via and Daniele Passarella
Pharmaceutics 2025, 17(5), 636; https://doi.org/10.3390/pharmaceutics17050636 (registering DOI) - 11 May 2025
Abstract
Background/Objectives: Cannabigerol (CBG) is a non-psychoactive phytocannabinoid with significant therapeutic potential, showing emerging applications in drug delivery. This study aimed to develop and evaluate CBG-conjugated nanoparticles (NPs) incorporating tubulin-targeting drugs to enhance anticancer activity. Methods: CBG was conjugated with N-desacetylthiocolchicine, paclitaxel, and [...] Read more.
Background/Objectives: Cannabigerol (CBG) is a non-psychoactive phytocannabinoid with significant therapeutic potential, showing emerging applications in drug delivery. This study aimed to develop and evaluate CBG-conjugated nanoparticles (NPs) incorporating tubulin-targeting drugs to enhance anticancer activity. Methods: CBG was conjugated with N-desacetylthiocolchicine, paclitaxel, and camptothecin using sebacic acid and 4,4′-dithiodibutyric acid as linkers, and nanoparticles were obtained. The NPs were characterized by their stability and size (hydrodynamic diameters <90 nm). Their antiproliferative activity was assessed in three human tumor cell lines and non-tumorigenic cells. Their cellular uptake and mechanisms of action were investigated via confocal microscopy and cell cycle analysis. Results: The chemical composition of the linkers significantly influenced the antiproliferative effect, with the NPs containing 4,4′-dithiodibutyric acid demonstrating higher activity. Notably, NP3b, formulated with this linker, exhibited up to an 80-fold increase in antiproliferative potency compared to its sebacic acid counterpart (NP3a). In mesothelioma cells (MSTO-211H), NP3b displayed significantly higher cytotoxicity than in non-tumorigenic mesothelial cells (MeT-5A), indicating selectivity for cancer cells. Further analysis in glioblastoma cells confirmed that the NPs retained the microtubule-disrupting effects of their parent drugs. Conclusions: These findings highlight the potential of CBG-based NPs as versatile nanomedicine platforms for targeted cancer therapy. This study underscores the importance of linker chemistry in modulating therapeutic efficacy and supports the development of multifunctional drug delivery systems. Full article
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