Design and Control of a Dual-Drug-Chamber Drug Delivery Capsule Robot for Multi-Target Drug Delivery

With the advancement of capsule endoscopy technology, the treatment of gastrointestinal (GI) tract diseases has entered a new era. Capsule robots enable the diagnosis and treatment of lesions in a painless and minimally invasive manner. Research on highly controllable Drug Delivery Systems (DDSs) using capsule endoscopy is significant for treating GI tract diseases. Despite the variety and complexity of DDS designs, most systems lack the capability for multi-target drug delivery and simultaneous carriage of multiple drugs. This paper proposes a dual-drug-chamber drug delivery capsule robot (DDCR) that utilizes a single Internal Permanent Magnet (IPM) for both drug delivery and propulsion. The design of the dual-drug-chamber primarily aims to carry one or two drugs simultaneously for treating one or multiple target sites. The proposed DDCR uses a balloon mechanism for drug containment. An external magnetic drive system activates a needle attached to a piston, which punctures the balloon and, thereby, releases the medication. This mechanism ensures rapid and effective coverage of lesions by the drugs. Based on both theoretical and experimental results regarding balloon drug loading and the control distance of the external permanent magnet (EPM) control distance, it was established that a drug load of 0.3 ml per chamber was most suitable for the design, and the feasibility of the dosing method was demonstrated. The size (29mm in length and ~13mm in diameter) of the DDCR was also found to be suitable for biological experiments, including multi-target drug delivery. By continuously adjusting the distance between the DDCR and the EPM in porcine small intestine samples, the optimal driving distance and drug delivery distance were found to be 80mm and 140mm.

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Journal
IEEE Transactions on Automation Science and Engineering
Published
2025-01-01
DOI
https://doi.org/10.1109/tase.2025.3604374
Citations
1
Primary Topic
Innovative Microfluidic and Catalytic Techniques Innovation
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article
Field-Weighted Citation Impact
0.67
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article

Design and Control of a Dual-Drug-Chamber Drug Delivery Capsule Robot for Multi-Target Drug Delivery

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1 citations
IEEE Transactions on Automation Science and Engineering
Innovative Microfluidic and Catalytic Techniques Innovation
0.67
article

Design and Control of a Dual-Drug-Chamber Drug Delivery Capsule Robot for Multi-Target Drug Delivery

Princy Randhawa, Guangzheng Gao, Dai Sagata, Zhi Shu, Shufang Wang, Lalit Garg, Sixian Liu, Amit Krishna Dwivedi, Sheng Liu, Bo Ye, Yihan Xu, Bo Wang
article en
1 citations

Abstract

With the advancement of capsule endoscopy technology, the treatment of gastrointestinal (GI) tract diseases has entered a new era. Capsule robots enable the diagnosis and treatment of lesions in a painless and minimally invasive manner. Research on highly controllable Drug Delivery Systems (DDSs) using capsule endoscopy is significant for treating GI tract diseases. Despite the variety and complexity of DDS designs, most systems lack the capability for multi-target drug delivery and simultaneous carriage of multiple drugs. This paper proposes a dual-drug-chamber drug delivery capsule robot (DDCR) that utilizes a single Internal Permanent Magnet (IPM) for both drug delivery and propulsion. The design of the dual-drug-chamber primarily aims to carry one or two drugs simultaneously for treating one or multiple target sites. The proposed DDCR uses a balloon mechanism for drug containment. An external magnetic drive system activates a needle attached to a piston, which punctures the balloon and, thereby, releases the medication. This mechanism ensures rapid and effective coverage of lesions by the drugs. Based on both theoretical and experimental results regarding balloon drug loading and the control distance of the external permanent magnet (EPM) control distance, it was established that a drug load of 0.3 ml per chamber was most suitable for the design, and the feasibility of the dosing method was demonstrated. The size (29mm in length and ~13mm in diameter) of the DDCR was also found to be suitable for biological experiments, including multi-target drug delivery. By continuously adjusting the distance between the DDCR and the EPM in porcine small intestine samples, the optimal driving distance and drug delivery distance were found to be 80mm and 140mm.

IEEE Transactions on Automation Science and EngineeringVol. 22
University of Malta (MT), Wuhan University (CN), University of Warwick (GB), Manipal University Jaipur, Hubei University (CN)
Good health and well-being
Openalex Percentile: Top 27%
Innovative Microfluidic and Catalytic Techniques Innovation
0.67
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