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Impact of Nanoparticles on Drug Delivery

A special issue of Molecules (ISSN 1420-3049). This special issue belongs to the section "Medicinal Chemistry".

Deadline for manuscript submissions: closed (31 August 2023) | Viewed by 3745

Special Issue Editors


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Guest Editor
Surgery department, Universidad de Zaragoza, Zaragoza, Spain
Interests: nanotechnology; cancer research; stem cells; extracellular vesicles; gene and cell therapy; imaging; viral vectors

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Guest Editor
Departamento de Física, Escuela Politécnica Nacional, Quito, Ecuador
Interests: materials chemistry; nanostructured materials; molecular electronics; graphene; 2D materials; self-assembled monolayers; scanning probe microscopies

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Guest Editor
Centro de Investigación Biomédica, Facultad de Ciencias de la Salud Eugenio Espejo, Universidad UTE, Quito, Ecuador
Interests: cancer research; stem cells; gene and cell therapy; drug delivery; adenoviral vectors; nanotechnology

Special Issue Information

Dear Colleagues,

Delivering drugs at a controlled rate, targeted delivery and other very attractive methods have been pursued in the last decade with the aim of controlling the bioavailability, pharmacodynamic and pharmacokinetic profile of therapeutics.

In this context, nanotechnology has presented efficient drug delivery systems (DDSs) based on both synthetic and natural sources. In fact, there is growing interest in the use of naturally occurring compounds as alternative strategies in the prevention and/or treatment of several pathologies thanks to their safety, which may avoid a portion of the side effects.

Nanotechnology has the potential to overcome the limitations of conventional drug delivery, from biodistribution and intracellular trafficking, thanks to the feasibility of engineering cell-specific targeting, to improving the stability and solubility of the cargo, molecular transport to specific parts of the cell, increasing safety and efficacy and more.

These delivery vehicles have been used since the 1990s, with many reaching clinical trials and some of them being approved for different indications. Although many clinically approved nanoparticle formulations are used in treating several types of cancers, other formulations are applied as iron‐replacement nanoparticle therapies, imaging agents, vaccines, anesthetics, fungal treatments and for treatment of macular degeneration. While the majority of nano-delivery systems in clinical trials are based on technologies that are long‐established or already approved, still, a fraction of these formulations is focused on chemical‐targeting or stimuli‐responsive therapeutic release. Thus, the development of new strategies of synthesis for more efficient and/or more complex systems is essential.

Despite the extensive research in this area, the number of nanomedicines available to patients is significantly below projections for the field, partially because of a translational gap between animal and human studies but also because of the heterogeneity amongst patients. Additionally, for the majority of these formulations in the pre-clinical and clinical setting, information regarding their bioaccumulation and toxicity is still insufficient, together with the biological and technological challenges that impact the clinical success of nanoparticle delivery systems. Nonetheless, the interest in and pursuit of successful nanoparticle technologies in the field of drug delivery continues.

For this Special Issue, we are looking for original research articles and state-of-the-art reviews on novel or established structures at nanoscale level that have been able to overcome barriers encountered in the field of drug delivery, focusing on the studies that have allowed defining their key beneficial activities and discussing their potential applications in the clinical field.

Dr. Pilar Martin-Duque
Dr. Henrry Osorio
Dr. Rebeca González-Pastor
Guest Editors

Manuscript Submission Information

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Keywords

  • drug delivery
  • nanoparticles
  • stimuli-responsive nanoparticles
  • functionalization
  • targeted delivery
  • novel nanomaterials
  • combinatorial therapy
  • nanostructures as vehicles
  • systemic toxicity

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Published Papers (2 papers)

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Research

12 pages, 4111 KiB  
Article
Toxicity Analysis of Mesoporous Polydopamine on Intestinal Tissue and Microflora
by Luoyijun Xie, Qiyan Li, Yingying Liao, Zihua Huang, Yulin Liu, Chutong Liu, Leilei Shi, Qingjiao Li and Miaomiao Yuan
Molecules 2022, 27(19), 6461; https://doi.org/10.3390/molecules27196461 - 30 Sep 2022
Cited by 7 | Viewed by 1538
Abstract
As a promising therapy, photothermal therapy (PTT) converts near-infrared (NIR) light into heat through efficient photothermal agents (PTAs), causing a rapid increase in local temperature. Considering the importance of PTAs in the clinical application of PTT, the safety of PTAs should be carefully [...] Read more.
As a promising therapy, photothermal therapy (PTT) converts near-infrared (NIR) light into heat through efficient photothermal agents (PTAs), causing a rapid increase in local temperature. Considering the importance of PTAs in the clinical application of PTT, the safety of PTAs should be carefully evaluated before their widespread use. As a promising PTA, mesoporous polydopamine (MPDA) was studied for its clinical applications for tumor photothermal therapy and drug delivery. Given the important role that intestinal microflora plays in health, the impacts of MPDA on the intestine and on intestinal microflora were systematically evaluated in this study. Through biological and animal experiments, it was found that MPDA exhibited excellent biocompatibility, in vitro and in vivo. Moreover, 16S rRNA analysis demonstrated that there was no obvious difference in the composition and classification of intestinal microflora between different drug delivery groups and the control group. The results provided new evidence that MPDA was safe to use in large doses via different drug delivery means, and this lays the foundation for further clinical applications. Full article
(This article belongs to the Special Issue Impact of Nanoparticles on Drug Delivery)
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10 pages, 1509 KiB  
Article
Compound Capecitabine Colon-Targeted Microparticle Prepared by Coaxial Electrospray for Treatment of Colon Tumors
by Ruiqi Chen, Ruidong Zhai, Chao Wang, Shulong Liang, Jing Wang, Zhepeng Liu and Wenlin Li
Molecules 2022, 27(17), 5690; https://doi.org/10.3390/molecules27175690 - 3 Sep 2022
Cited by 4 | Viewed by 1789
Abstract
To improve the antitumor effect of combined capecitabine (CAP) and osimertinib (OSI) therapy and quickly and efficiently reduce tumor volumes for preoperative chemotherapy, we designed a compound CAP colon-targeted microparticle (COPMP) prepared by coaxial electrospray. COPMP is a core–shell microparticle composed of a [...] Read more.
To improve the antitumor effect of combined capecitabine (CAP) and osimertinib (OSI) therapy and quickly and efficiently reduce tumor volumes for preoperative chemotherapy, we designed a compound CAP colon-targeted microparticle (COPMP) prepared by coaxial electrospray. COPMP is a core–shell microparticle composed of a Eudragit S100 outer layer and a CAP/OSI-loaded PLGA core. In this study, we characterized its size distribution, drug loading (DL), encapsulation efficiency (EE), differential scanning calorimetry (DSC), Fourier transform infrared spectra (FTIR), in vitro release, formula ratio, cellular growth inhibition, and in vivo antitumor efficacy. COPMP is of spherical appearance with a size of 1.87 ± 0.23 μm. The DLs of CAP and OSI are 4.93% and 4.95%, respectively. The DSC showed that the phase state of CAP and OSI changed after encapsulation. The FTIR results indicated good compatibility between the drug and excipients. The release curve showed that CAP and OSI were released in a certain ratio. They were barely released prior to 2 h (pH 1.0), less than 50% was released between 3 and 5 h (pH 6.8), and sustained release of up to 80% occurred between 6 and 48 h (pH 7.4). CAP and OSI demonstrated a synergistic effect on HCT-116 cells. In a colon tumor model, the tumor inhibition rate after oral administration of COPMP reached 94% within one week. All the data suggested that COPMP promotes the sustained release of CAP and OSI in the colon, which provides a preoperative chemotherapy scheme for the treatment of colon cancer. Full article
(This article belongs to the Special Issue Impact of Nanoparticles on Drug Delivery)
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