Implantable magnetically-actuated capsule for on-demand delivery
Journal of Controlled Release, ISSN: 0168-3659, Vol: 364, Page: 576-588
2023
- 8Citations
- 11Captures
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Article Description
Many implantable drug delivery systems (IDDS) have been developed for long-term, pulsatile drug release. However, they are often limited by bulky size, complex electronic components, unpredictable drug delivery, as well as the need for battery replacement and consequent replacement surgery. Here, we develop an implantable magnetically-actuated capsule (IMAC) and its portable magnetic actuator (MA) for on-demand and robust drug delivery in a tether-free and battery-free manner. IMAC utilizes the bistable mechanism of two magnetic balls inside IMAC to trigger drug delivery under a strong magnetic field (| B a | > 90 mT), ensuring precise and reproducible drug delivery (9.9 ± 0.17 μg per actuation, maximum actuation number: 180) and excellent anti-magnetic capability (critical trigger field intensity: ∼90 mT). IMAC as a tetherless robot can navigate to and anchor at the lesion sites driven by a gradient magnetic field (∇ B g = 3 T/m, | B g | < 60 mT), and on-demand release drug actuated by a uniform magnetic field (| B a | = ∼100 mT) within the gastrointestinal tract. During a 15-day insulin administration in vivo, the diabetic rats treated with IMAC exhibited highly similar pharmacokinetic and pharmacodynamic profiles to those administrated via subcutaneous injection, demonstrating its robust and on-demand drug release performance. Moreover, IMAC is biocompatible, batter-free, refillable, miniature (only Φ 6.3 × 12.3 mm 3 ), and lightweight (just 0.8 g), making it an ideal alternative for precise implantable drug delivery and friendly patient-centered drug administration.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0168365923007265; http://dx.doi.org/10.1016/j.jconrel.2023.11.009; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85178662962&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/37951475; https://linkinghub.elsevier.com/retrieve/pii/S0168365923007265; https://dx.doi.org/10.1016/j.jconrel.2023.11.009
Elsevier BV
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