Abstract

BackgroundExternally controlling and monitoring drug release at a desired time and location is currently lacking in the gastrointestinal tract. The aim of the study was to develop a thermoresponsive wax-coated capsule and to trigger its release upon applying a magnetic resonance imaging (MRI)-guided high-intensity focused ultrasound (HIFU) pulse.MethodsCapsules containing a lyophilised gadolinium-based contrast agent (GBCA) were coated with a 1:1 (mass/mass) mixture of lanolin and cetyl alcohol (melting point ≈43 °C) and exposed to simulated gastric and intestinal fluids (United States Pharmacopoeia) at 37 °C for 2 and 24 h, respectively. In a HIFU gel phantom, wax-coated capsules (n = 3) were tracked based on their T1- and T2-hypointensity by 1.5-T T1- and T2-weighted MRI pre- and post-exposure to an MRI-guided HIFU pulse.ResultsLanolin/cetyl alcohol-coated capsules showed high resistance to simulated gastrointestinal fluids. In a gel phantom, an MRI-guided HIFU pulse punctured the wax coating, resulting in the hydration and release of the encapsulated lyophilised GBCA and yielding a T1-hyperintense signal close to the wax-coated capsule.ConclusionWe provide the proof-of-concept of applying a non-invasive MRI-guided HIFU pulse to actively induce the disintegration of the wax-coated capsule, and a method to monitor the release of the cargo via T1-weighted MRI based on the hydration of an encapsulated lyophilised GBCA. The wax-coated capsule platform enables temporally and spatially supertargeted drug release via the oral route and promises to address a currently unmet clinical need for personalised local therapy in gastrointestinal diseases such as inflammatory bowel diseases and cancer.

Highlights

  • Controlling and monitoring drug release at a desired time and location is currently lacking in the gastrointestinal tract

  • Michelangelo method for capsule coating In order to achieve a homogenous wax coating, the capsules were casted in a mixture of 50% (m/m) lanolin and 50% (m/m) cetyl alcohol and subsequently carved out in predefined dimensions

  • The increase in turbidity stemmed from the suspended barium sulphate from the capsule core which has a very low solubility in water

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Summary

Introduction

Controlling and monitoring drug release at a desired time and location is currently lacking in the gastrointestinal tract. Even though a variety of thermoresponsive systems have been described (e.g. hydrogels, metal or polymeric nanoparticles, liposomes, micelles), their application in harsh environments such as the GI tract or highly inflamed lesions is generally limited by their stability [8,9,10,11,12,13,14,15]. Such systems may be difficult to locate in dynamic body cavities such as the GI tract.

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