Synthesis, Characterization and In-vivo Testing of Photoactivatable Insulin Depots for Continuously Variable and Minimally Invasive Insulin Delivery

Proteins are macromolecules involved in a diverse array of functions. Mutations or abnormal levels of proteins are indicated in several diseases. Despite showing early promise, the translation of protein therapeutics into the clinics has been challenging. The stability of these macromolecules, their delivery, and penetration inside the cells have been the main hurdles limiting their true potential. In the dissertation, various strategies to overcome such protein delivery challenges are discussed. Insulin is a lifesaving peptide for millions of diabetics around the world. Despite significant progress in insulin therapies, the quality of life in diabetics is constrained by the burden of multiple daily injections, invasive nature of therapy and inability to control the blood glucose tightly. To address these concerns, we constructed a photoactivatable insulin depot (PAD). In the approach, an insoluble depot of modified insulin was created by linking insulin covalently to photolabile caging moieties. Transcutaneous irradiation breaks the bond to release insulin from the depot into the systemic circulation. Chapter 3 describes the first successful testing on our PAD technology in diabetic animal models. In Chapters 2 and 4, I describe second-generation materials incorporating more efficient photolabile groups utilizing visible light wavelengths and PAD material with greater insulin loading. These changes improved the overall performance by several folds when tested in-vivo. Chapter 5 discusses the strategies addressed to deliver siRNA inside cells for effective light-activated RNA interference (LARI). LARI can be used for studying biology and cellular processes. Once administered, proteins are prone to degradation by ubiquitous proteases, limiting their circulation time and therapeutic effect significantly. Chapter 6 discusses prodrug strategies to temporarily modify proteins to shield them against proteases. We envisioned cross-linking amino acid residues on the surface via small crosslinkers. The tight bridges would hinder proteases from binding to proteins and unwinding the helices preventing their proteolysis. We also attempted integration of this approach to achieve intracellular protein delivery which is another obstacle in protein delivery. Here, the cross linking was performed via disulfide linkages. The disulfide groups would be reduced once inside the cells, yielding native proteins.

Name thesis:degree_name

Ph. D. (Doctor of Philosophy)

Level thesis:degree_level

Doctoral

Discipline thesis:degree_discipline

Pharmaceutical Sciences (UMKC)

Grantor dc:publisher

University of Missouri -- Kansas City

Year dc:date.issued

2019

Author dc:creator

• Sarode, Bhagyesh R.

Advisor dc:contributor.advisor

• Friedman, Simon H. (Simon Hilary), 1966-

Language dc:language.iso

en_US

Handle dc:identifier.uri

https://hdl.handle.net/10355/73362

OAI identifier oai:identifier

oai:mospace.umsystem.edu:10355/73362