Lactosylated lipid calcium phosphate-based nanoparticles: A promising approach for efficient DNA delivery to hepatocytes

• Published in: Iranian journal of basic medical sciences Vol. 27; no. 8; pp. 952 - 958
• Main Authors: Khalifeh, Masoomeh, Badiee, Ali, Ramezanian, Navid, Sahebkar, Amirhossein, Farahpour, Atena, Kazemi Oskuee, Reza
• Format: Journal Article
• Language: English
• Published: Iran Mashhad University of Medical Sciences 01-01-2024
• Subjects: calcium phosphates; dna delivery; Fourier transforms; hepatocytes; Lactose; Microscopy; nanoparticle; Nanoparticles; NMR; Nuclear magnetic resonance; Original; polyethylenimine; Calcium Phosphates; Polyethylenimine; DNA delivery; Hepatocytes; Nanoparticle
• ISSN: 2008-3866; 2008-3874
• DOI: 10.22038/IJBMS.2024.76683.16602

For safe and effective gene therapy, the ability to deliver the therapeutic nucleic acid to the target sites is crucial. In this study, lactosylated lipid phosphate calcium nanoparticles (lac-LCP) were developed for targeted delivery of pDNA to the hepatocyte cells. The lac-LCP formulation contained lactose-modified cholesterol (CHL), a ligand that binds to the asialoglycoprotein receptor (ASGR) expressed on hepatocytes, and polyethyleneimine (PEI) in the core.
Fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance (NMR) were used to monitor the chemical modification, and the physicochemical properties of NPs were studied using dynamic light scattering (DLS) and transmission electron microscopy (TEM). To evaluate transfection efficiency, cellular uptake and GFP expression were assessed using fluorescence microscopy and flow cytometry.
The results revealed that lactose-targeted particles (lac-LCP) had a significant increase in cellular uptake by hepatocytes. The inclusion of a low molecular weight PEI (1.8 KDa) with a low PEI/pDNA ratio of 1 in the core of LCP, elicited high degrees of GFP protein expression (by 5 and 6-fold), which exhibited significantly higher efficiency than PEI 1.8 KDa and Lipofectamine.
The successful functionalization and nuclear delivery of LCP NPs described here indicate its promise as an efficient delivery vector to hepatocyte nuclei.