Loading…

pH-temperature Responsive Hydrogel-Mediated Delivery of Exendin-4 Encapsulated Chitosan Nanospheres for Sustained Therapeutic Efficacy in Type 2 Diabetes Mellitus

Type 2 Diabetes Mellitus (T2D) is a chronic, obesity-related, and inflammatory disorder characterize by insulin resistance, inadequate insulin secretion, hyperglycemia, and excessive glucagon secretion. Exendin-4 (EX), a clinically established antidiabetic medication that acts as a glucagon-like pep...

Full description

Saved in:
Bibliographic Details
Published in:Macromolecular bioscience 2023-11, Vol.23 (11), p.e2300221-e2300221
Main Authors: Trinh, Thuy An, Le, Thai Minh Duy, Nguyen, Hien Thi-Thanh, Nguyen, Thanh Loc, Kim, Jaeyun, Huynh, Dai Phu, Lee, Doo Sung
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c323t-10d174d37023eb186bca8b891ffe48b4dbf0d077f668f0275edc6ea6abbc2cf3
cites cdi_FETCH-LOGICAL-c323t-10d174d37023eb186bca8b891ffe48b4dbf0d077f668f0275edc6ea6abbc2cf3
container_end_page e2300221
container_issue 11
container_start_page e2300221
container_title Macromolecular bioscience
container_volume 23
creator Trinh, Thuy An
Le, Thai Minh Duy
Nguyen, Hien Thi-Thanh
Nguyen, Thanh Loc
Kim, Jaeyun
Huynh, Dai Phu
Lee, Doo Sung
description Type 2 Diabetes Mellitus (T2D) is a chronic, obesity-related, and inflammatory disorder characterize by insulin resistance, inadequate insulin secretion, hyperglycemia, and excessive glucagon secretion. Exendin-4 (EX), a clinically established antidiabetic medication that acts as a glucagon-like peptide-1 receptor agonist, is effective in lowering glucose levels and stimulating insulin secretion while significantly reducing hunger. However, the requirement for multiple daily injections due to EX's short half-life is a significant limitation in its clinical application, leading to high treatment costs and patient inconvenience. To address this issue, an injectable hydrogel system is developed that can provide sustained EX release at the injection site, reducing the need for daily injections. In this study, the electrospray technique is examine to form EX@CS nanospheres by electrostatic interaction between cationic chitosan (CS) and negatively charged EX. These nanospheres are uniformly dispersed in a pH-temperature responsive pentablock copolymer, which forms micelles and undergoes sol-to-gel transition at physiological conditions. Following injection, the hydrogel gradually degraded, exhibiting excellent biocompatibility. The EX@CS nanospheres are subsequently released, maintaining therapeutic levels for over 72 h compared to free EX solution. The findings demonstrate that the pH-temperature responsive hydrogel system containing EX@CS nanospheres can be a promising platform for the treatment of T2D.
doi_str_mv 10.1002/mabi.202300221
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2830213471</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2886149742</sourcerecordid><originalsourceid>FETCH-LOGICAL-c323t-10d174d37023eb186bca8b891ffe48b4dbf0d077f668f0275edc6ea6abbc2cf3</originalsourceid><addsrcrecordid>eNpdkcluFDEQhluIiITAlSOyxIVLD156bM8RTQYGKYsU5t7yUiaOuu3Gdkf06_CkOCTMgVNtX_0q1d807wheEYzpp1Fpv6KYslpQ8qI5I5zwdk0265fHXIrT5nXO9xgTITf0VXPKBONrQulZ83vatwXGCZIqcwJ0C3mKIfsHQPvFpvgDhvYKrFcFLLqAoQ7SgqJDu18QrA9th3bBqCnPw19ke-dLzCqgaxVinu4gQUYuJvR9zkX5UJFDbaoJ5uIN2jnnjTIL8gEdlgkQRRdeaSh16wqGwZc5v2lOnBoyvH2O583hy-6w3beXN1-_bT9ftoZRVlqCLRGdZaI-AzSRXBsltdwQ56CTurPaYYuFcJxLh6lYgzUcFFdaG2ocO28-PslOKf6cIZd-9NnUG1SAOOeeSoYpYZ0gFf3wH3of5xTqcZWSnHQb0dFKrZ4ok2LOCVw_JT-qtPQE94_m9Y_m9Ufz6sL7Z9lZj2CP-D-32B_U-ZhE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2886149742</pqid></control><display><type>article</type><title>pH-temperature Responsive Hydrogel-Mediated Delivery of Exendin-4 Encapsulated Chitosan Nanospheres for Sustained Therapeutic Efficacy in Type 2 Diabetes Mellitus</title><source>Wiley-Blackwell Read &amp; Publish Collection</source><creator>Trinh, Thuy An ; Le, Thai Minh Duy ; Nguyen, Hien Thi-Thanh ; Nguyen, Thanh Loc ; Kim, Jaeyun ; Huynh, Dai Phu ; Lee, Doo Sung</creator><creatorcontrib>Trinh, Thuy An ; Le, Thai Minh Duy ; Nguyen, Hien Thi-Thanh ; Nguyen, Thanh Loc ; Kim, Jaeyun ; Huynh, Dai Phu ; Lee, Doo Sung</creatorcontrib><description>Type 2 Diabetes Mellitus (T2D) is a chronic, obesity-related, and inflammatory disorder characterize by insulin resistance, inadequate insulin secretion, hyperglycemia, and excessive glucagon secretion. Exendin-4 (EX), a clinically established antidiabetic medication that acts as a glucagon-like peptide-1 receptor agonist, is effective in lowering glucose levels and stimulating insulin secretion while significantly reducing hunger. However, the requirement for multiple daily injections due to EX's short half-life is a significant limitation in its clinical application, leading to high treatment costs and patient inconvenience. To address this issue, an injectable hydrogel system is developed that can provide sustained EX release at the injection site, reducing the need for daily injections. In this study, the electrospray technique is examine to form EX@CS nanospheres by electrostatic interaction between cationic chitosan (CS) and negatively charged EX. These nanospheres are uniformly dispersed in a pH-temperature responsive pentablock copolymer, which forms micelles and undergoes sol-to-gel transition at physiological conditions. Following injection, the hydrogel gradually degraded, exhibiting excellent biocompatibility. The EX@CS nanospheres are subsequently released, maintaining therapeutic levels for over 72 h compared to free EX solution. The findings demonstrate that the pH-temperature responsive hydrogel system containing EX@CS nanospheres can be a promising platform for the treatment of T2D.</description><identifier>ISSN: 1616-5187</identifier><identifier>EISSN: 1616-5195</identifier><identifier>DOI: 10.1002/mabi.202300221</identifier><identifier>PMID: 37365122</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Biocompatibility ; Chitosan ; Copolymers ; Diabetes ; Diabetes mellitus ; Diabetes mellitus (non-insulin dependent) ; Electrostatic properties ; Glucagon ; Hunger ; Hydrogels ; Hyperglycemia ; Inflammatory diseases ; Injection ; Insulin ; Insulin resistance ; Insulin secretion ; Micelles ; Nanospheres ; pH effects ; Secretion ; Sol-gel processes</subject><ispartof>Macromolecular bioscience, 2023-11, Vol.23 (11), p.e2300221-e2300221</ispartof><rights>2023 Wiley-VCH GmbH.</rights><rights>2023 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c323t-10d174d37023eb186bca8b891ffe48b4dbf0d077f668f0275edc6ea6abbc2cf3</citedby><cites>FETCH-LOGICAL-c323t-10d174d37023eb186bca8b891ffe48b4dbf0d077f668f0275edc6ea6abbc2cf3</cites><orcidid>0000-0002-8483-9641 ; 0000-0002-4687-6732 ; 0000-0002-6618-2084 ; 0000-0002-3788-7181 ; 0000-0002-8104-8094</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37365122$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Trinh, Thuy An</creatorcontrib><creatorcontrib>Le, Thai Minh Duy</creatorcontrib><creatorcontrib>Nguyen, Hien Thi-Thanh</creatorcontrib><creatorcontrib>Nguyen, Thanh Loc</creatorcontrib><creatorcontrib>Kim, Jaeyun</creatorcontrib><creatorcontrib>Huynh, Dai Phu</creatorcontrib><creatorcontrib>Lee, Doo Sung</creatorcontrib><title>pH-temperature Responsive Hydrogel-Mediated Delivery of Exendin-4 Encapsulated Chitosan Nanospheres for Sustained Therapeutic Efficacy in Type 2 Diabetes Mellitus</title><title>Macromolecular bioscience</title><addtitle>Macromol Biosci</addtitle><description>Type 2 Diabetes Mellitus (T2D) is a chronic, obesity-related, and inflammatory disorder characterize by insulin resistance, inadequate insulin secretion, hyperglycemia, and excessive glucagon secretion. Exendin-4 (EX), a clinically established antidiabetic medication that acts as a glucagon-like peptide-1 receptor agonist, is effective in lowering glucose levels and stimulating insulin secretion while significantly reducing hunger. However, the requirement for multiple daily injections due to EX's short half-life is a significant limitation in its clinical application, leading to high treatment costs and patient inconvenience. To address this issue, an injectable hydrogel system is developed that can provide sustained EX release at the injection site, reducing the need for daily injections. In this study, the electrospray technique is examine to form EX@CS nanospheres by electrostatic interaction between cationic chitosan (CS) and negatively charged EX. These nanospheres are uniformly dispersed in a pH-temperature responsive pentablock copolymer, which forms micelles and undergoes sol-to-gel transition at physiological conditions. Following injection, the hydrogel gradually degraded, exhibiting excellent biocompatibility. The EX@CS nanospheres are subsequently released, maintaining therapeutic levels for over 72 h compared to free EX solution. The findings demonstrate that the pH-temperature responsive hydrogel system containing EX@CS nanospheres can be a promising platform for the treatment of T2D.</description><subject>Biocompatibility</subject><subject>Chitosan</subject><subject>Copolymers</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Electrostatic properties</subject><subject>Glucagon</subject><subject>Hunger</subject><subject>Hydrogels</subject><subject>Hyperglycemia</subject><subject>Inflammatory diseases</subject><subject>Injection</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Insulin secretion</subject><subject>Micelles</subject><subject>Nanospheres</subject><subject>pH effects</subject><subject>Secretion</subject><subject>Sol-gel processes</subject><issn>1616-5187</issn><issn>1616-5195</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkcluFDEQhluIiITAlSOyxIVLD156bM8RTQYGKYsU5t7yUiaOuu3Gdkf06_CkOCTMgVNtX_0q1d807wheEYzpp1Fpv6KYslpQ8qI5I5zwdk0265fHXIrT5nXO9xgTITf0VXPKBONrQulZ83vatwXGCZIqcwJ0C3mKIfsHQPvFpvgDhvYKrFcFLLqAoQ7SgqJDu18QrA9th3bBqCnPw19ke-dLzCqgaxVinu4gQUYuJvR9zkX5UJFDbaoJ5uIN2jnnjTIL8gEdlgkQRRdeaSh16wqGwZc5v2lOnBoyvH2O583hy-6w3beXN1-_bT9ftoZRVlqCLRGdZaI-AzSRXBsltdwQ56CTurPaYYuFcJxLh6lYgzUcFFdaG2ocO28-PslOKf6cIZd-9NnUG1SAOOeeSoYpYZ0gFf3wH3of5xTqcZWSnHQb0dFKrZ4ok2LOCVw_JT-qtPQE94_m9Y_m9Ufz6sL7Z9lZj2CP-D-32B_U-ZhE</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Trinh, Thuy An</creator><creator>Le, Thai Minh Duy</creator><creator>Nguyen, Hien Thi-Thanh</creator><creator>Nguyen, Thanh Loc</creator><creator>Kim, Jaeyun</creator><creator>Huynh, Dai Phu</creator><creator>Lee, Doo Sung</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-8483-9641</orcidid><orcidid>https://orcid.org/0000-0002-4687-6732</orcidid><orcidid>https://orcid.org/0000-0002-6618-2084</orcidid><orcidid>https://orcid.org/0000-0002-3788-7181</orcidid><orcidid>https://orcid.org/0000-0002-8104-8094</orcidid></search><sort><creationdate>20231101</creationdate><title>pH-temperature Responsive Hydrogel-Mediated Delivery of Exendin-4 Encapsulated Chitosan Nanospheres for Sustained Therapeutic Efficacy in Type 2 Diabetes Mellitus</title><author>Trinh, Thuy An ; Le, Thai Minh Duy ; Nguyen, Hien Thi-Thanh ; Nguyen, Thanh Loc ; Kim, Jaeyun ; Huynh, Dai Phu ; Lee, Doo Sung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c323t-10d174d37023eb186bca8b891ffe48b4dbf0d077f668f0275edc6ea6abbc2cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Biocompatibility</topic><topic>Chitosan</topic><topic>Copolymers</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Electrostatic properties</topic><topic>Glucagon</topic><topic>Hunger</topic><topic>Hydrogels</topic><topic>Hyperglycemia</topic><topic>Inflammatory diseases</topic><topic>Injection</topic><topic>Insulin</topic><topic>Insulin resistance</topic><topic>Insulin secretion</topic><topic>Micelles</topic><topic>Nanospheres</topic><topic>pH effects</topic><topic>Secretion</topic><topic>Sol-gel processes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Trinh, Thuy An</creatorcontrib><creatorcontrib>Le, Thai Minh Duy</creatorcontrib><creatorcontrib>Nguyen, Hien Thi-Thanh</creatorcontrib><creatorcontrib>Nguyen, Thanh Loc</creatorcontrib><creatorcontrib>Kim, Jaeyun</creatorcontrib><creatorcontrib>Huynh, Dai Phu</creatorcontrib><creatorcontrib>Lee, Doo Sung</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Macromolecular bioscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Trinh, Thuy An</au><au>Le, Thai Minh Duy</au><au>Nguyen, Hien Thi-Thanh</au><au>Nguyen, Thanh Loc</au><au>Kim, Jaeyun</au><au>Huynh, Dai Phu</au><au>Lee, Doo Sung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>pH-temperature Responsive Hydrogel-Mediated Delivery of Exendin-4 Encapsulated Chitosan Nanospheres for Sustained Therapeutic Efficacy in Type 2 Diabetes Mellitus</atitle><jtitle>Macromolecular bioscience</jtitle><addtitle>Macromol Biosci</addtitle><date>2023-11-01</date><risdate>2023</risdate><volume>23</volume><issue>11</issue><spage>e2300221</spage><epage>e2300221</epage><pages>e2300221-e2300221</pages><issn>1616-5187</issn><eissn>1616-5195</eissn><abstract>Type 2 Diabetes Mellitus (T2D) is a chronic, obesity-related, and inflammatory disorder characterize by insulin resistance, inadequate insulin secretion, hyperglycemia, and excessive glucagon secretion. Exendin-4 (EX), a clinically established antidiabetic medication that acts as a glucagon-like peptide-1 receptor agonist, is effective in lowering glucose levels and stimulating insulin secretion while significantly reducing hunger. However, the requirement for multiple daily injections due to EX's short half-life is a significant limitation in its clinical application, leading to high treatment costs and patient inconvenience. To address this issue, an injectable hydrogel system is developed that can provide sustained EX release at the injection site, reducing the need for daily injections. In this study, the electrospray technique is examine to form EX@CS nanospheres by electrostatic interaction between cationic chitosan (CS) and negatively charged EX. These nanospheres are uniformly dispersed in a pH-temperature responsive pentablock copolymer, which forms micelles and undergoes sol-to-gel transition at physiological conditions. Following injection, the hydrogel gradually degraded, exhibiting excellent biocompatibility. The EX@CS nanospheres are subsequently released, maintaining therapeutic levels for over 72 h compared to free EX solution. The findings demonstrate that the pH-temperature responsive hydrogel system containing EX@CS nanospheres can be a promising platform for the treatment of T2D.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>37365122</pmid><doi>10.1002/mabi.202300221</doi><orcidid>https://orcid.org/0000-0002-8483-9641</orcidid><orcidid>https://orcid.org/0000-0002-4687-6732</orcidid><orcidid>https://orcid.org/0000-0002-6618-2084</orcidid><orcidid>https://orcid.org/0000-0002-3788-7181</orcidid><orcidid>https://orcid.org/0000-0002-8104-8094</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1616-5187
ispartof Macromolecular bioscience, 2023-11, Vol.23 (11), p.e2300221-e2300221
issn 1616-5187
1616-5195
language eng
recordid cdi_proquest_miscellaneous_2830213471
source Wiley-Blackwell Read & Publish Collection
subjects Biocompatibility
Chitosan
Copolymers
Diabetes
Diabetes mellitus
Diabetes mellitus (non-insulin dependent)
Electrostatic properties
Glucagon
Hunger
Hydrogels
Hyperglycemia
Inflammatory diseases
Injection
Insulin
Insulin resistance
Insulin secretion
Micelles
Nanospheres
pH effects
Secretion
Sol-gel processes
title pH-temperature Responsive Hydrogel-Mediated Delivery of Exendin-4 Encapsulated Chitosan Nanospheres for Sustained Therapeutic Efficacy in Type 2 Diabetes Mellitus
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T12%3A49%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=pH-temperature%20Responsive%20Hydrogel-Mediated%20Delivery%20of%20Exendin-4%20Encapsulated%20Chitosan%20Nanospheres%20for%20Sustained%20Therapeutic%20Efficacy%20in%20Type%202%20Diabetes%20Mellitus&rft.jtitle=Macromolecular%20bioscience&rft.au=Trinh,%20Thuy%20An&rft.date=2023-11-01&rft.volume=23&rft.issue=11&rft.spage=e2300221&rft.epage=e2300221&rft.pages=e2300221-e2300221&rft.issn=1616-5187&rft.eissn=1616-5195&rft_id=info:doi/10.1002/mabi.202300221&rft_dat=%3Cproquest_cross%3E2886149742%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c323t-10d174d37023eb186bca8b891ffe48b4dbf0d077f668f0275edc6ea6abbc2cf3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2886149742&rft_id=info:pmid/37365122&rfr_iscdi=true