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University of Kansas

Pure Insulin Nanoparticle Agglomerates for Pulmonary Delivery

Abstract

dc:description.abstract

Diabetes is a disease characterized by defects in insulin utilization, either through autoimmune destruction of insulin-producing cells (Type I) or insulin resistance (Type II). Treatment includes regular insulin injections, which can be painful and inconvenient, often leading to low patient compliance. To overcome this problem, novel formulations of insulin are being investigated, such as inhaled aerosols. Sufficient deposition of powder in the distal regions of the lung to maximize systemic absorption requires precise control over particle size, with particles between 1 and 5 microns in aerodynamic diameter being within the respirable range. Insulin nanoparticles were produced by titrating insulin dissolved at low pH to the pI of the native protein, and were then processed into microparticles using solvent displacement. Particle size, crystallinity, dissolution properties, stability, and powder density were characterized. This work demonstrates that pure insulin microparticles can be produced from nanosuspensions with minimal processing steps and with suitable properties for deposition in the peripheral lung.

Degree

thesis:*
Grantor dc:publisher
University of Kansas
Year dc:date.issued
2008

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Bailey, Mark Michael
Advisor dc:contributor.advisor
  • Berkland, Cory J

Subjects

dc:subject × 7

Rights

dc:rights
Statement dc:rights
  • This item is protected by copyright and unless otherwise specified the copyright of this thesis/dissertation is held by the author.
Language dc:language.iso
EN

Identifiers

dc:identifier.*
OAI identifier oai:identifier
oai:kuscholarworks.ku.edu:1808/3945

Chain of custody

source
Harvested from
University of Kansas
Base URL
kuscholarworks.ku.edu/server/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Bailey, Mark Michael. Pure Insulin Nanoparticle Agglomerates for Pulmonary Delivery. University of Kansas, 2008. http://hdl.handle.net/1808/3945