Nanoparticles for oral delivery: targeted nanoparticles with peptidic ligands for oral protein delivery.

Adv Drug Deliv Rev

Purdue University, Departments of Biomedical Engineering & Pharmaceutics, West Lafayette, IN, USA.

Published: June 2013

AI Article Synopsis

  • Advances in biotechnology have improved oral protein delivery, which is the most preferred method of drug administration due to its high patient acceptance.
  • Despite this preference, significant challenges remain in ensuring proteins are effectively absorbed, with issues like poor membrane permeability and enzymatic degradation still needing solutions.
  • Nanotechnology offers potential solutions, particularly through the use of nanoparticles that can enhance drug delivery by targeting specific areas in the gastrointestinal tract and improving drug absorption.

Article Abstract

As the field of biotechnology has advanced, oral protein delivery has also made significant progress. Oral delivery is the most common method of drug administration with high levels of patient acceptance. Despite the preference of oral delivery, administration of therapeutic proteins has been extremely difficult. Increasing the bioavailability of oral protein drugs to the therapeutically acceptable level is still a challenging goal. Poor membrane permeability, high molecular weight, and enzymatic degradation of protein drugs have remained unsolved issues. Among diverse strategies, nanotechnology has provided a glimpse of hope in oral delivery of protein drugs. Nanoparticles have advantages, such as small size, high surface area, and modification using functional groups for high capacity or selectivity. Nanoparticles with peptidic ligands are especially worthy of notice because they can be used for specific targeting in the gastrointestinal (GI) tract. This article reviews the transport mechanism of the GI tract, barriers to protein absorption, current status and limitations of nanotechnology for oral protein delivery system.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3574626PMC
http://dx.doi.org/10.1016/j.addr.2012.10.007DOI Listing

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