A robotic pill for oral delivery of biotherapeutics: safety, tolerability, and performance in healthy subjects
Autor: | Laura Fusaro, Baber Syed, Shilpy Sharma, Radhika Korupolu, Anvesh Dasari, Betsy Gutierrez, Radia Abdul-Wahab, Padma Karamchedu, Mir Hashim, Delia Gratta, Shane Yen, April T Vo, Mir A. Imran, Anusha Garapaty, Simret Beraki, Asad Wasi, Mansoor Syed, Arvinder K. Dhalla, Kyle Horlen, Zachary Owyang, Alyson Yamaguchi, Chang Ong, Vasudha Salgotra, Leonard C Fung, Eric Liang, Ziad T. Al-Shamsie |
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Rok vydání: | 2021 |
Předmět: |
Drug
medicine.medical_specialty Oral biotherapeutics media_common.quotation_subject Administration Oral Biological Availability Pharmaceutical Science Octreotide Balloon Oral biologics delivery 030226 pharmacology & pharmacy Gastroenterology Intestinal absorption 03 medical and health sciences Robotic drug delivery platform Drug Delivery Systems 0302 clinical medicine Robotic Surgical Procedures Internal medicine Humans Medicine 030304 developmental biology media_common 0303 health sciences business.industry Reproducibility of Results Healthy Volunteers Bioavailability Tolerability Pill Drug delivery Original Article business medicine.drug |
Zdroj: | Drug Delivery and Translational Research |
ISSN: | 2190-3948 2190-393X |
DOI: | 10.1007/s13346-021-00938-1 |
Popis: | Biotherapeutics are highly efficacious, but the pain and inconvenience of chronic injections lead to poor patient compliance and compromise effective disease management. Despite innumerable attempts, oral delivery of biotherapeutics remains unsuccessful due to their degradation in the gastrointestinal (GI) environment and poor intestinal absorption. We have developed an orally ingestible robotic pill (RP) for drug delivery, which protects the biotherapeutic drug payload from digestion in the GI tract and auto-injects it into the wall of the small intestine as a safe, pain-free injection since the intestines are insensate to sharp stimuli. The payload is delivered upon inflation of a balloon folded within the RP, which deflates immediately after drug delivery. Here we present results from two clinical studies demonstrating the safety, tolerability and performance of the RP in healthy humans. In the first study, three versions of the RP (A, B and C) were evaluated, which were identical in all respects except for the diameter of the balloon. The RP successfully delivered a biotherapeutic (octreotide) in 3 out of 12 subjects in group A, 10 out of 20 subjects in group B and 16 out of 20 subjects in group C, with a mean bioavailability of 65 ± 9% (based on successful drug deliveries in groups A and B). Thus, reliability of drug delivery with the RP ranged from 25 to 80%, with success rate directly related to balloon size. In a separate study, the deployment of the RP was unaffected by fed or fasting conditions suggesting that the RP may be taken with or without food. These promising clinical data suggest that biotherapeutics currently administered parenterally may be safely and reliably delivered via this versatile, orally ingestible drug delivery platform. Graphical abstract |
Databáze: | OpenAIRE |
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