Engineering mesoporous silica nanoparticles towards oral delivery of vancomycin. Issue 35 (18th August 2021)

• Record Type: Journal Article
• Authors: Ndayishimiye, John; Cao, Yuxue; Kumeria, Tushar; Blaskovich, Mark A. T.; Falconer, James Robert; Popat, Amirali
• Is Part Of: Journal of materials chemistry. Volume 9:Issue 35(2021)
• Page Start: 7145
• Page End: 7166
• Publication Date: 2021-08-18
• Subjects: Materials -- Periodicals; Chemistry, Analytic -- Periodicals; Biomedical materials -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d1tb01430g
• Languages: English
• ISSNs: 2050-750X

Abstract

Abstract : Vancomycin (Van) is an antibiotic of choice for many drug resistant infections but cannot be given orally due to its poor permeability. Encapsulation of Vancomycin within MSNs improved its gastrointestinal permeation and provided controlled release. Abstract : Vancomycin (Van) is a key antibiotic of choice for the treatment of systemic methicillin resistant Staphylococcus aureus (MRSA) infections. However, due to its poor membrane permeability, it is administered parenterally, adding to the cost and effort of treatment. The poor oral bioavailability of Van is mainly due to its physico-chemical properties that limit its paracellular and transcellular transport across gastrointestinal (GI) epithelium. Herein we report the development of silica nanoparticles (SNPs)-based formulations that are able to enhance the epithelial permeability of Van. We synthesized SNPs of different pore sizes (2 nm and 9 nm) and modified their surface charge and polarity by attaching different functional groups (–NH2, –PO3, and –CH3 ). Van was loaded within these SNPs at a loading capacity in the range of ca. 18–29 wt%. The Van-loaded SNPs exhibited a controlled release behaviour when compared to un-encapsulated Van which showed rapid release due to its hydrophilic nature. Among Van-loaded SNPs, SNPs with large pores showed a prolonged release compared to SNPs with small pores while SNPs functionalised with -CH3 groups exhibited a slowest release among the functionalised SNPs. Importantly, Van-loaded SNPs, especially the large pore SNPs with negative charge, enhanced the permeability of Van across an epithelial cell monolayer (Caco-2 cell model) by up to 6-fold, with P app values up to 1.716 × 10 −5 cm s −1 ( vs. 0.304 × 10 −5 cm s −1 for un-encapsulated Van) after 3 h. The enhancement was dependent on both the type of SNPs and their surface functionalisation. The permeation enhancing effect of SNPs was due to its ability to transiently open the tight junctions measured by decrease in transepithelial resistance (TEER) which was reversible after 3 h. All in all, our data highlights the potential of SNPs (especially SNPs with large pores) for oral delivery of Van or other antimicrobial peptides.