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Long-term Effect of Biomineralized Insulin Nanoparticles on Type 2 Diabetes Treatment

Intracellular insulin may exhibit a long-term effect in regulating protein synthesis, DNA synthesis, and gene transcription. However, the intracellular delivery of insulin is a great challenge. Here, we describe how a simple biomineralization modification of insulin can transport it into intact cell...

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Detalles Bibliográficos
Autores principales: Xiao, Yun, Wang, Xiaoyu, Wang, Ben, Liu, Xueyao, Xu, Xurong, Tang, Ruikang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695014/
https://www.ncbi.nlm.nih.gov/pubmed/29158827
http://dx.doi.org/10.7150/thno.21450
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author Xiao, Yun
Wang, Xiaoyu
Wang, Ben
Liu, Xueyao
Xu, Xurong
Tang, Ruikang
author_facet Xiao, Yun
Wang, Xiaoyu
Wang, Ben
Liu, Xueyao
Xu, Xurong
Tang, Ruikang
author_sort Xiao, Yun
collection PubMed
description Intracellular insulin may exhibit a long-term effect in regulating protein synthesis, DNA synthesis, and gene transcription. However, the intracellular delivery of insulin is a great challenge. Here, we describe how a simple biomineralization modification of insulin can transport it into intact cells on a large scale, leading to a long-term therapeutic effect on diabetes mellitus. Using insulin-resistant HepG2 cell and diabetic KKAy mice as models, in vitro and in vivo assessments have demonstrated that biomineralized insulin nanoparticles can trigger glucose metabolism, and this improvement extends after the treatment. The potential exists to improve the current treatment of type 2 diabetes mellitus through biomineralized modifications of insulin. This study provides a new paradigm of biomimetic nanotechnology for biomedical applications.
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spelling pubmed-56950142017-11-20 Long-term Effect of Biomineralized Insulin Nanoparticles on Type 2 Diabetes Treatment Xiao, Yun Wang, Xiaoyu Wang, Ben Liu, Xueyao Xu, Xurong Tang, Ruikang Theranostics Research Paper Intracellular insulin may exhibit a long-term effect in regulating protein synthesis, DNA synthesis, and gene transcription. However, the intracellular delivery of insulin is a great challenge. Here, we describe how a simple biomineralization modification of insulin can transport it into intact cells on a large scale, leading to a long-term therapeutic effect on diabetes mellitus. Using insulin-resistant HepG2 cell and diabetic KKAy mice as models, in vitro and in vivo assessments have demonstrated that biomineralized insulin nanoparticles can trigger glucose metabolism, and this improvement extends after the treatment. The potential exists to improve the current treatment of type 2 diabetes mellitus through biomineralized modifications of insulin. This study provides a new paradigm of biomimetic nanotechnology for biomedical applications. Ivyspring International Publisher 2017-09-26 /pmc/articles/PMC5695014/ /pubmed/29158827 http://dx.doi.org/10.7150/thno.21450 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Xiao, Yun
Wang, Xiaoyu
Wang, Ben
Liu, Xueyao
Xu, Xurong
Tang, Ruikang
Long-term Effect of Biomineralized Insulin Nanoparticles on Type 2 Diabetes Treatment
title Long-term Effect of Biomineralized Insulin Nanoparticles on Type 2 Diabetes Treatment
title_full Long-term Effect of Biomineralized Insulin Nanoparticles on Type 2 Diabetes Treatment
title_fullStr Long-term Effect of Biomineralized Insulin Nanoparticles on Type 2 Diabetes Treatment
title_full_unstemmed Long-term Effect of Biomineralized Insulin Nanoparticles on Type 2 Diabetes Treatment
title_short Long-term Effect of Biomineralized Insulin Nanoparticles on Type 2 Diabetes Treatment
title_sort long-term effect of biomineralized insulin nanoparticles on type 2 diabetes treatment
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5695014/
https://www.ncbi.nlm.nih.gov/pubmed/29158827
http://dx.doi.org/10.7150/thno.21450
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