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Editorial

Nanotechnology in Targeted Drug Delivery

by
Antonio Di Stefano
Department of Pharmacy, University of “G. d’Annunzio” Chieti-Pescara, Via dei Vestini, 66100 Chieti, Italy
Int. J. Mol. Sci. 2023, 24(9), 8194; https://doi.org/10.3390/ijms24098194
Submission received: 13 April 2023 / Accepted: 21 April 2023 / Published: 3 May 2023
(This article belongs to the Special Issue Nanotechnology in Targeted Drug Delivery)
The use of large sized materials in drug delivery raises several challenges, including in vivo stability, poor bioavailability/solubility/absorption, and issues with target-specific delivery, in addition to the side effects of the delivered drugs. Therefore, using new drug delivery systems for targeting drugs to a specific area in the body could be an opportunity to solve these critical issues.
The area of nanotechnology develops nanoscale-sized materials that consist of natural, synthetic/semisynthetic polymers, lipids, or metallic materials. Nanoparticles [NPS] can be used in targeted drug delivery to improve the bioavailability, biodistribution, and accumulation of therapeutics, preferentially in the targeted diseased area, acting as stability enhancers. These colloidal systems can deliver drugs to target sites to improve therapeutic efficiency, reduce toxicity, and reduce side effects, protecting the drug from biological degradation, achieving temporal and spatial control of therapeutics in the specific location of a disease [1,2,3]. The first implementation of nanocarriers for use in drug delivery was based on a passive targeting mechanism that aimed to increase efficiency over traditional free-drug formulations. However, a new approach has been introduced that consists of active targeting through the incorporation of specific ligands to enhance drug delivery to target sites using conjugation strategies or magnetic fields. Hence, nanotechnology has the potential to generate innovation in drug formulations and delivery systems.
Reaching a therapeutic outcome that is able to fight neurodegenerative disorders, tumoral diseases, or immunological disorders is facilitated by an efficient and site-specific delivery of compounds. For these reasons, this Special Issue collates different aspects of research into nanotechnology in order to identify new therapeutic targets and strategies, including review papers [4,5], mathematical models to calculate the trajectories of magnetic NPs in the body or clarify the structures of metal-decorated fullerenes [6,7], the drug delivery systems of different antitumoral agents [8,9,10,11], and the biocompatibilities of stealth liposomes and hybrid nanosystems containing surfactant agents [12,13].
The Editor wishes to thank the researchers who contributed to organize the present issue, who made their knowledge available to the scientific community. I also would like to thank all the Reviewers who have revised the submitted articles; thanks to their deep knowledge of the topics covered, they provided suggestions that have improved the quality of each manuscript reported in this Special Issue.

Conflicts of Interest

The author declares no conflict of interest.

References

  1. Marinelli, L.; Ciulla, M.; Ritsema, J.A.S.; van Nostrum, C.F.; Cacciatore, I.; Dimmito, M.P.; Palmerio, F.; Orlando, G.; Robuffo, I.; Grande, R.; et al. Preparation, Characterization, and Biological Evaluation of a Hydrophilic Peptide Loaded on PEG-PLGA Nanoparticles. Pharmaceutics 2022, 14, 1821. [Google Scholar] [CrossRef] [PubMed]
  2. Ben Khalifa, R.; Cacciatore, I.; Dimmito, M.P.; Ciulla, M.; Grande, R.; Puca, V.; Robuffo, I.; De Laurenzi, V.; Chekir-Ghedira, L.; Di Stefano, A.; et al. Multiple lipid nanoparticles as antimicrobial drug delivery systems. J. Drug Deliv. Sci. Technol. 2022, 67, 102887. [Google Scholar] [CrossRef]
  3. Cortesi, R.; Esposito, E.; Drechsler, M.; Pavoni, G.; Cacciatore, I.; Sguizzato, M.; Di Stefano, A. L-dopa co-drugs in nanostructured lipid carriers: A comparative study. Mater. Sci. Eng. C 2017, 72, 168–176. [Google Scholar] [CrossRef] [PubMed]
  4. Petrisor, G.; Motelica, L.; Craciun, L.N.; Oprea, O.C.; Ficai, D.; Ficai, A. Melissa officinalis: Composition, Pharmacological Effects and Derived Release Systems-A Review. Int. J. Mol. Sci. 2022, 23, 3591. [Google Scholar] [CrossRef] [PubMed]
  5. Winifred, N.; Simelane, N.; Abrahamse, H. Nanoparticle-Mediated Delivery Systems in Photodynamic Therapy of Colorectal Cancer. Int. J. Mol. Sci. 2021, 22, 12405. [Google Scholar]
  6. Yuan, T.; Yang, Y.; Zhan, W.; Dini, D. Mathematical Optimisation of Magnetic Nanoparticle Diffusion in the Brain White Matter. Int. J. Mol. Sci. 2023, 24, 2534. [Google Scholar] [CrossRef] [PubMed]
  7. Katin, K.P.; Kochaev, A.I.; Kaya, S.; El-Hajjaji, F.; Maslov, M.M. Ab Initio Insight into the Interaction of Metal-Decorated Fluorinated Carbon Fullerenes with Anti-COVID Drugs. Int. J. Mol. Sci. 2022, 23, 2345. [Google Scholar] [CrossRef] [PubMed]
  8. Longo, R.; Raimondo, M.; Vertuccio, L.; Vertuccio, M.; Ciardulli, M.C.; Sirignano, M.; Mariconda, A.; Della Porta, G.; Guadagno, L. Bottom-Up Strategy to Forecast the Drug Location and Release Kinetics in Antitumoral Electrospun Drug Delivery Systems. Int. J. Mol. Sci 2023, 24, 1507. [Google Scholar] [CrossRef] [PubMed]
  9. Peira, E.; Chirio, D.; Sapino, S.; Chegaev, K.; Chindamo, G.; Salaroglio, I.C.; Riganti, C.; Gallarate, M. Naked and Decorated Nanoparticles Containing H2S-Releasing Doxorubicin: Preparation; Characterization and Assessment of Their Antitumoral Efficiency on Various Resistant Tumor Cells. Int. J. Mol. Sci. 2022, 23, 11555. [Google Scholar] [CrossRef] [PubMed]
  10. Varon, E.; Blumrosen, G.; Sinvani, M.; Haimov, E.; Polani, S.; Natan, M.; Shoval, I.; Jacob, A.; Atkins, A.; Zitoun, D.; et al. An Engineered Nanocomplex with Photodynamic and Photothermal Synergistic Properties for Cancer Treatment. Int. J. Mol. Sci. 2022, 23, 228. [Google Scholar] [CrossRef] [PubMed]
  11. Yoon, H.-M.; Kang, M.-S.; Choi, G.-E.; Kim, Y.-J.; Bae, C.-H.; Yu, Y.-B.; Jeong, Y.-I. Stimuli-Responsive Drug Delivery of Doxorubicin Using Magnetic Nanoparticle Conjugated Poly(ethylene glycol)-g-Chitosan Copolymer. Int. J. Mol. Sci. 2021, 22, 13169. [Google Scholar] [CrossRef] [PubMed]
  12. Mesquita, B.S.; Fens, M.H.A.M.; Di Maggio, A.; Bosman, E.D.C.; Hennink, W.E.; Heger, M.; Oliveira, S. The Impact of Nanobody Density on the Targeting Efficiency of PEGylated Liposomes. Int. J. Mol. Sci 2022, 23, 14974. [Google Scholar] [CrossRef] [PubMed]
  13. Kontogiannis, O.; Selianitis, D.; Perinelli, D.R.; Bonacucina, G.; Pippa, N.; Gazouli, M.; Pispas, S. Non-Ionic Surfactant Effects on Innate Pluronic 188 Behavior: Interactions; and Physicochemical and Biocompatibility Studies. Int. J. Mol. Sci. 2022, 23, 13814. [Google Scholar] [PubMed]
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MDPI and ACS Style

Di Stefano, A. Nanotechnology in Targeted Drug Delivery. Int. J. Mol. Sci. 2023, 24, 8194. https://doi.org/10.3390/ijms24098194

AMA Style

Di Stefano A. Nanotechnology in Targeted Drug Delivery. International Journal of Molecular Sciences. 2023; 24(9):8194. https://doi.org/10.3390/ijms24098194

Chicago/Turabian Style

Di Stefano, Antonio. 2023. "Nanotechnology in Targeted Drug Delivery" International Journal of Molecular Sciences 24, no. 9: 8194. https://doi.org/10.3390/ijms24098194

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