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使用胰腺和细胞方法在胰岛递送方面的前沿生物技术进展。

Cutting-edge biotechnological advancement in islet delivery using pancreatic and cellular approaches.

作者信息

Elnashar Magdy, Vaccarezza Mauro, Al-Salami Hani

机构信息

Biotechnology & Drug Development Research Laboratory, School of Pharmacy & Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Perth, Western Australia, Australia.

Centre of Excellence, Department of Polymers, National Research Centre, Cairo, Egypt.

出版信息

Future Sci OA. 2020 Nov 23;7(3):FSO660. doi: 10.2144/fsoa-2020-0105.

DOI:10.2144/fsoa-2020-0105
PMID:33552541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7849926/
Abstract

There are approximately 1 billion prediabetic people worldwide, and the global cost for diabetes mellitus (DM) is estimated to be $825 billion. In regard to Type 1 DM, transplanting a whole pancreas or its islets has gained the attention of researchers in the last few decades. Recent studies showed that islet transplantation (ILT) containing insulin-producing β cells is the most notable advancement cure for Type 1 DM. However, this procedure has been hindered by shortage and lack of sufficient islet donors and the need for long-term immunosuppression of any potential graft rejection. The strategy of encapsulation may avoid the rejection of stem-cell-derived allogeneic islets or xenogeneic islets. This review article describes various biotechnology features in encapsulation-of-islet-cell therapy for humans, including the use of bile acids.

摘要

全球约有10亿人处于糖尿病前期,全球糖尿病(DM)的成本估计为8250亿美元。关于1型糖尿病,在过去几十年中,移植整个胰腺或其胰岛已引起研究人员的关注。最近的研究表明,含有产生胰岛素的β细胞的胰岛移植(ILT)是治疗1型糖尿病最显著的进展性疗法。然而,该手术受到胰岛供体短缺和不足以及对任何潜在移植物排斥进行长期免疫抑制的需求的阻碍。封装策略可能避免干细胞衍生的同种异体胰岛或异种胰岛的排斥。这篇综述文章描述了用于人类的胰岛细胞治疗封装中的各种生物技术特性,包括胆汁酸的使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a287/7849926/ab3aaa83790b/fsoa-07-660-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a287/7849926/c955474681de/fsoa-07-660-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a287/7849926/ab3aaa83790b/fsoa-07-660-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a287/7849926/c955474681de/fsoa-07-660-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a287/7849926/ab3aaa83790b/fsoa-07-660-g2.jpg

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本文引用的文献

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Bile acid bio-nanoencapsulation improved drug targeted-delivery and pharmacological effects via cellular flux: 6-months diabetes preclinical study.胆酸生物纳米囊泡通过细胞内流改善药物靶向递送和药效:6 个月糖尿病临床前研究。
Sci Rep. 2020 Jan 9;10(1):106. doi: 10.1038/s41598-019-53999-1.
2
Islet Autotransplantation in Diabetic Patients.糖尿病患者的胰岛自体移植
Transplant Proc. 2019 Oct;51(8):2781-2786. doi: 10.1016/j.transproceed.2019.04.080. Epub 2019 Aug 19.
3
Therapies for Type 1 Diabetes: Current Scenario and Future Perspectives.
1型糖尿病的治疗:现状与未来展望
Clin Med Insights Endocrinol Diabetes. 2019 May 3;12:1179551419844521. doi: 10.1177/1179551419844521. eCollection 2019.
4
Islet Transplantation Alone Versus Solitary Pancreas Transplantation: an Outcome-Driven Choice?单纯胰岛移植与单纯胰腺移植:基于结局的选择?
Curr Diab Rep. 2019 Apr 25;19(5):26. doi: 10.1007/s11892-019-1145-2.
5
Mathematical predictions of oxygen availability in micro- and macro-encapsulated human and porcine pancreatic islets.微囊化和大囊化的人及猪胰岛中氧可用性的数学预测。
J Biomed Mater Res B Appl Biomater. 2020 Feb;108(2):343-352. doi: 10.1002/jbm.b.34393. Epub 2019 Apr 23.
6
An in vivo pharmacological study: Variation in tissue-accumulation for the drug probucol as the result of targeted microtechnology and matrix-acrylic acid optimization and stabilization techniques.体内药理学研究:靶向微技术和基质-丙烯酸优化及稳定技术导致药物普罗布考在组织中的蓄积变化。
PLoS One. 2019 Apr 4;14(4):e0214984. doi: 10.1371/journal.pone.0214984. eCollection 2019.
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J Korean Neurosurg Soc. 2019 Mar;62(2):153-165. doi: 10.3340/jkns.2018.0035. Epub 2019 Feb 27.
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OPTN/SRTR 2017 Annual Data Report: Pancreas.OPTN/SRTR 2017 年度数据报告:胰腺。
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