Issue 12, 2023

Magnetic delivery and ultrasound-responsive release of chelating microcapsules for selective removal of urolithiasis

Abstract

A novel urolithiasis treatment in which a chelating solution encapsulated in poly(lactic-co-glycolic acid); PLGA-based microcapsules was delivered magnetically to specific urolithiasis sites and then subjected to ultrasound (US) to release the chelating solution and dissolve the stones. Using a double-droplet microfluidics method, a hexametaphosphate (HMP) chelating solution was encapsulated in an Fe3O4 nanoparticle (Fe3O4 NP)-loaded PLGA polymer shell with a thickness of <15 μm, forming homogenous microcapsules of 319 ± 14 μm in size. The obtained microcapsules (HMP/Fe3O4@PLGA) exhibited efficient magnetic mobility and US-responsive solution release. Moreover, in a Ψ-shaped flow chip, selective delivery of HMP from the microcapsules was achieved with high magnetic delivery efficiency (>90%), and an effective removal efficacy (>95%, 7 repeat cycles) of artificial calcium oxalate (5 mm in size) via a chelating effect. Eventually, the potential removal of urolithiasis in the body was verified using a PDMS-based kidney urinary flow-imitating chip with a human kidney stone (CaOx 100%, 5–7 mm in size) located in the minor calyx under an artificial urine counter flow (0.5 mL min−1). In the end, more than 50% of the stone, even in surgically tricky regions, was removed by 10 repeated treatments. Therefore, the selective approach of stone-dissolution capsules will help to develop alternative urolithiasis treatments to conventional surgical and systemic dissolution approaches.

Graphical abstract: Magnetic delivery and ultrasound-responsive release of chelating microcapsules for selective removal of urolithiasis

Supplementary files

Article information

Article type
Paper
Submitted
01 Nov 2022
Accepted
05 May 2023
First published
10 May 2023

Lab Chip, 2023,23, 2829-2837

Magnetic delivery and ultrasound-responsive release of chelating microcapsules for selective removal of urolithiasis

B. K. Kaang, S. Lee, J. Piao, H. J. Cho and D. Kim, Lab Chip, 2023, 23, 2829 DOI: 10.1039/D2LC01014C

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