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Kiran Sonaje

Researcher at National Tsing Hua University

Publications -  25
Citations -  3083

Kiran Sonaje is an academic researcher from National Tsing Hua University. The author has contributed to research in topics: Insulin & Oral administration. The author has an hindex of 18, co-authored 24 publications receiving 2760 citations. Previous affiliations of Kiran Sonaje include University of Lausanne & University of Geneva.

Papers
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Journal ArticleDOI

A review of the prospects for polymeric nanoparticle platforms in oral insulin delivery.

TL;DR: The gastrointestinal barriers to oral insulin delivery, including chemical, enzymatic and absorption barriers, are described and the potential transport mechanisms of insulin delivered by nanoparticles across the intestinal epithelium are discussed.
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Recent advances in chitosan-based nanoparticles for oral delivery of macromolecules.

TL;DR: The synthesis of CS derivatives and their characteristics, as well as their potential transport mechanisms of macromolecular therapeutics across the intestinal biological membrane, are described.
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In vivo evaluation of safety and efficacy of self-assembled nanoparticles for oral insulin delivery

TL;DR: Oral administration of insulin-loaded NPs demonstrated a significant hypoglycemic action for at least 10h in diabetic rats and the corresponding relative bioavailability of insulin was found to be 15.1+/-0.9%, suggesting that the NPs prepared in the study are a promising vehicle for oral delivery of insulin.
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Enteric-coated capsules filled with freeze-dried chitosan/poly(γ-glutamic acid) nanoparticles for oral insulin delivery

TL;DR: The results suggest that the formulation developed in the study might be employed as a potential approach for the oral delivery of insulin and provide a prolonged reduction in blood glucose levels.
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Opening of epithelial tight junctions and enhancement of paracellular permeation by chitosan: microscopic, ultrastructural, and computed-tomographic observations

TL;DR: In vivo fluorescence-microscopic results demonstrate that insulin could be absorbed into the systemic circulation, while most CS was retained in the microvilli scaffolds, and that CS is a safe permeation enhancer and is an effective carrier for oral protein delivery.