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High drug-loading gold nanoclusters for responsive glucose control in type 1 diabetes

BACKGROUND: Diabetes is one of the biggest medical challenges worldwide. The key to efficiently treat type 1 diabetes is to accurately inject insulin according to the blood glucose levels. In this study, we aimed to develop an intelligent insulin-releasing gold nanocluster system that responds to en...

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Autores principales: Zhang, Yujie, Wu, Mingxin, Dai, Wubin, Chen, Min, Guo, Zhaoyang, Wang, Xin, Tan, Di, Shi, Kui, Xue, Longjian, Liu, Sheng, Lei, Yifeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547569/
https://www.ncbi.nlm.nih.gov/pubmed/31159842
http://dx.doi.org/10.1186/s12951-019-0505-z
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author Zhang, Yujie
Wu, Mingxin
Dai, Wubin
Chen, Min
Guo, Zhaoyang
Wang, Xin
Tan, Di
Shi, Kui
Xue, Longjian
Liu, Sheng
Lei, Yifeng
author_facet Zhang, Yujie
Wu, Mingxin
Dai, Wubin
Chen, Min
Guo, Zhaoyang
Wang, Xin
Tan, Di
Shi, Kui
Xue, Longjian
Liu, Sheng
Lei, Yifeng
author_sort Zhang, Yujie
collection PubMed
description BACKGROUND: Diabetes is one of the biggest medical challenges worldwide. The key to efficiently treat type 1 diabetes is to accurately inject insulin according to the blood glucose levels. In this study, we aimed to develop an intelligent insulin-releasing gold nanocluster system that responds to environmental glucose concentrations. RESULTS: We employed gold nanoclusters (AuNCs) as a novel carrier nanomaterial by taking advantage of their high drug-loading capacity. We prepared AuNCs in the protection of bovine serum albumin, and we decorated AuNCs with 3-aminophenylboronic acid (PBA) as a glucose-responsive factor. Then we grafted insulin onto the surface to obtain the glucose-responsive insulin-releasing system, AuNC-PBA-Ins complex. The AuNC-PBA-Ins complex exhibited high sensitivity to glucose concentration, and rapidly released insulin in high glucose concentration in vitro. In the type 1 diabetic mouse model in vivo, the AuNC-PBA-Ins complex effectively released insulin and regulated blood glucose level in the normoglycemic state for up to 3 days. CONCLUSIONS: We successfully developed a phenylboronic acid-functionalized gold nanocluster system (AuNC-PBA-Ins) for responsive insulin release and glucose regulation in type 1 diabetes. This nanocluster system mimics the function of blood glucose regulation of pancreas in the body and may have potential applications in the theranostics of diabetes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-019-0505-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-65475692019-06-06 High drug-loading gold nanoclusters for responsive glucose control in type 1 diabetes Zhang, Yujie Wu, Mingxin Dai, Wubin Chen, Min Guo, Zhaoyang Wang, Xin Tan, Di Shi, Kui Xue, Longjian Liu, Sheng Lei, Yifeng J Nanobiotechnology Research BACKGROUND: Diabetes is one of the biggest medical challenges worldwide. The key to efficiently treat type 1 diabetes is to accurately inject insulin according to the blood glucose levels. In this study, we aimed to develop an intelligent insulin-releasing gold nanocluster system that responds to environmental glucose concentrations. RESULTS: We employed gold nanoclusters (AuNCs) as a novel carrier nanomaterial by taking advantage of their high drug-loading capacity. We prepared AuNCs in the protection of bovine serum albumin, and we decorated AuNCs with 3-aminophenylboronic acid (PBA) as a glucose-responsive factor. Then we grafted insulin onto the surface to obtain the glucose-responsive insulin-releasing system, AuNC-PBA-Ins complex. The AuNC-PBA-Ins complex exhibited high sensitivity to glucose concentration, and rapidly released insulin in high glucose concentration in vitro. In the type 1 diabetic mouse model in vivo, the AuNC-PBA-Ins complex effectively released insulin and regulated blood glucose level in the normoglycemic state for up to 3 days. CONCLUSIONS: We successfully developed a phenylboronic acid-functionalized gold nanocluster system (AuNC-PBA-Ins) for responsive insulin release and glucose regulation in type 1 diabetes. This nanocluster system mimics the function of blood glucose regulation of pancreas in the body and may have potential applications in the theranostics of diabetes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12951-019-0505-z) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-03 /pmc/articles/PMC6547569/ /pubmed/31159842 http://dx.doi.org/10.1186/s12951-019-0505-z Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zhang, Yujie
Wu, Mingxin
Dai, Wubin
Chen, Min
Guo, Zhaoyang
Wang, Xin
Tan, Di
Shi, Kui
Xue, Longjian
Liu, Sheng
Lei, Yifeng
High drug-loading gold nanoclusters for responsive glucose control in type 1 diabetes
title High drug-loading gold nanoclusters for responsive glucose control in type 1 diabetes
title_full High drug-loading gold nanoclusters for responsive glucose control in type 1 diabetes
title_fullStr High drug-loading gold nanoclusters for responsive glucose control in type 1 diabetes
title_full_unstemmed High drug-loading gold nanoclusters for responsive glucose control in type 1 diabetes
title_short High drug-loading gold nanoclusters for responsive glucose control in type 1 diabetes
title_sort high drug-loading gold nanoclusters for responsive glucose control in type 1 diabetes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547569/
https://www.ncbi.nlm.nih.gov/pubmed/31159842
http://dx.doi.org/10.1186/s12951-019-0505-z
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