» Articles » PMID: 24786098

Potential for Layered Double Hydroxides-based, Innovative Drug Delivery Systems

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2014 May 3
PMID 24786098
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Layered Double Hydroxides (LDHs)-based drug delivery systems have, for many years, shown great promises for the delivery of chemical therapeutics and bioactive molecules to mammalian cells in vitro and in vivo. This system offers high efficiency and drug loading density, as well as excellent protection of loaded molecules from undesired degradation. Toxicological studies have also found LDHs to be biocompatible compared with other widely used nanoparticles, such as iron oxide, silica, and single-walled carbon nanotubes. A plethora of bio-molecules have been reported to either attach to the surface of or intercalate into LDH materials through co-precipitation or anion-exchange reaction, including amino acid and peptides, ATPs, vitamins, and even polysaccharides. Recently, LDHs have been used for gene delivery of small molecular nucleic acids, such as antisense, oligonucleotides, PCR fragments, siRNA molecules or sheared genomic DNA. These nano-medicines have been applied to target cells or organs in gene therapeutic approaches. This review summarizes current progress of the development of LDHs nanoparticle drug carriers for nucleotides, anti-inflammatory, anti-cancer drugs and recent LDH application in medical research. Ground breaking studies will be highlighted and an outlook of the possible future progress proposed. It is hoped that the layered inorganic material will open up new frontier of research, leading to new nano-drugs in clinical applications.

Citing Articles

LDH-Indomethacin Nanoparticles Antitumoral Action: A Possible Coadjuvant Drug for Cancer Therapy.

Alves K, Costa C, Remedios C, Calcagno D, de Oliveira Lima M, Silva J Molecules. 2024; 29(14).

PMID: 39064929 PMC: 11279815. DOI: 10.3390/molecules29143353.


Carbon supported ternary layered double hydroxide nanocomposite for Fluoxetine removal and subsequent utilization of spent adsorbent as antidepressant.

Mahgoub S, Essam D, Eldin Z, Abdel Moaty S, Shehata M, Farghali A Sci Rep. 2024; 14(1):3990.

PMID: 38368467 PMC: 10874413. DOI: 10.1038/s41598-024-53781-y.


Deep eutectic solvent-assisted facile synthesis of copper hydroxide nitrate nanosheets as recyclable enzyme-mimicking colorimetric sensor of biothiols.

Munyemana J, Chen J, Wei X, Chand Ali M, Han Y, Qiu H Anal Bioanal Chem. 2020; 412(19):4629-4638.

PMID: 32436032 DOI: 10.1007/s00216-020-02712-7.


Sol-Gel Synthesis and Characterization of Coatings of Mg-Al Layered Double Hydroxides.

Smalenskaite A, Kaba M, Grigoraviciute-Puroniene I, Mikoliunaite L, Zarkov A, Ramanauskas R Materials (Basel). 2019; 12(22).

PMID: 31766177 PMC: 6888420. DOI: 10.3390/ma12223738.


The Impact of Magnesium-Aluminum-Layered Double Hydroxide-Based Polyvinyl Alcohol Coated on Magnetite on the Preparation of Core-Shell Nanoparticles as a Drug Delivery Agent.

Ebadi M, Buskaran K, Saifullah B, Fakurazi S, Hussein M Int J Mol Sci. 2019; 20(15).

PMID: 31374834 PMC: 6695672. DOI: 10.3390/ijms20153764.


References
1.
Xu Z, Stevenson G, Lu C, Lu G, Bartlett P, Gray P . Stable suspension of layered double hydroxide nanoparticles in aqueous solution. J Am Chem Soc. 2006; 128(1):36-7. DOI: 10.1021/ja056652a. View

2.
Liu W, Zhu L . Environmental microbiology-on-a-chip and its future impacts. Trends Biotechnol. 2005; 23(4):174-9. DOI: 10.1016/j.tibtech.2005.02.004. View

3.
Choi S, Choy J . Layered double hydroxide nanoparticles as target-specific delivery carriers: uptake mechanism and toxicity. Nanomedicine (Lond). 2011; 6(5):803-14. DOI: 10.2217/nnm.11.86. View

4.
Canel C, Moraes R, Dayan F, Ferreira D . Podophyllotoxin. Phytochemistry. 2000; 54(2):115-20. DOI: 10.1016/s0031-9422(00)00094-7. View

5.
Campbell L, Abulrob A, Kandalaft L, Plummer S, Hollins A, Gibbs A . Constitutive expression of p-glycoprotein in normal lung alveolar epithelium and functionality in primary alveolar epithelial cultures. J Pharmacol Exp Ther. 2002; 304(1):441-52. DOI: 10.1124/jpet.102.042994. View