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Engineering Better Treatments for Diabetes: From Next-Gen Insulin Drugs to Autonomous Insulin Delivery.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Engineering Better Treatments for Diabetes: From Next-Gen Insulin Drugs to Autonomous Insulin Delivery./
作者:
Maikawa, Caitlin L.
出版者:
Ann Arbor : ProQuest Dissertations & Theses, : 2021,
面頁冊數:
364 p.
附註:
Source: Dissertations Abstracts International, Volume: 83-05, Section: B.
Contained By:
Dissertations Abstracts International83-05B.
標題:
Biocompatibility. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=28812953
ISBN:
9798494455253
Engineering Better Treatments for Diabetes: From Next-Gen Insulin Drugs to Autonomous Insulin Delivery.
Maikawa, Caitlin L.
Engineering Better Treatments for Diabetes: From Next-Gen Insulin Drugs to Autonomous Insulin Delivery.
- Ann Arbor : ProQuest Dissertations & Theses, 2021 - 364 p.
Source: Dissertations Abstracts International, Volume: 83-05, Section: B.
Thesis (Ph.D.)--Stanford University, 2021.
This item must not be sold to any third party vendors.
Insulin was first isolated a century ago, yet commercial formulations of insulin and its analogues for hormone replacement therapy falls short of mimicking the endogenous glycemic control that occurs in non-diabetic individuals. Moreover, diabetes management is increasingly relying automated insulin delivery using closed-loop systems to improve glucose management and reduce patient burden. However improvements in insulin formulations, sensors, and algorithms are required to shift from hybrid systems to fully autonomous delivery. Insulin formulations that better mimic secretion from the beta-cells, by enabling more rapid insulin absorption kinetics and/or co-delivering complementary hormones (i.e. amylin), would improve diabetes management. However, formulation innovation is complicated by the poor stability of insulin monomers and amylin. During my time in the Appel lab, I have developed two polymeric excipient platforms (non-covalent PEGylation and amphiphilic copolymer excipients) that can be used to increase the stability of insulin in formulation. Using these designer excipients, I have developed three enhanced insulin formulations: (i) an ultrafast monomeric insulin lispro (ii) an insulin-amylin co-formulation and (iii) an ultra-stable insulin for improved global access. These three enhanced insulin formulations are promising candidates for improving glucose control and reducing burden for patients with diabetes. Beyond formulation engineering, through collaborations I have investigated the use of open-source algorithms in a full closed-loop setting as well as helped to develop a continuous real-time ELISA microfluidic device for continuous monitoring of insulin and glucose. Together, this collection of work describes the development of new technologies towards insulin delivery with the goal of improving glucose management in patients with diabetes.
ISBN: 9798494455253Subjects--Topical Terms:
656157
Biocompatibility.
Engineering Better Treatments for Diabetes: From Next-Gen Insulin Drugs to Autonomous Insulin Delivery.
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Insulin was first isolated a century ago, yet commercial formulations of insulin and its analogues for hormone replacement therapy falls short of mimicking the endogenous glycemic control that occurs in non-diabetic individuals. Moreover, diabetes management is increasingly relying automated insulin delivery using closed-loop systems to improve glucose management and reduce patient burden. However improvements in insulin formulations, sensors, and algorithms are required to shift from hybrid systems to fully autonomous delivery. Insulin formulations that better mimic secretion from the beta-cells, by enabling more rapid insulin absorption kinetics and/or co-delivering complementary hormones (i.e. amylin), would improve diabetes management. However, formulation innovation is complicated by the poor stability of insulin monomers and amylin. During my time in the Appel lab, I have developed two polymeric excipient platforms (non-covalent PEGylation and amphiphilic copolymer excipients) that can be used to increase the stability of insulin in formulation. Using these designer excipients, I have developed three enhanced insulin formulations: (i) an ultrafast monomeric insulin lispro (ii) an insulin-amylin co-formulation and (iii) an ultra-stable insulin for improved global access. These three enhanced insulin formulations are promising candidates for improving glucose control and reducing burden for patients with diabetes. Beyond formulation engineering, through collaborations I have investigated the use of open-source algorithms in a full closed-loop setting as well as helped to develop a continuous real-time ELISA microfluidic device for continuous monitoring of insulin and glucose. Together, this collection of work describes the development of new technologies towards insulin delivery with the goal of improving glucose management in patients with diabetes.
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