Glucose-responsive insulin by molecular and physical design

被引:1
作者
Bakh, Naveed A. [1 ]
Cortinas, Abel B. [1 ]
Weiss, Michael A. [2 ]
Langer, Robert S. [1 ]
Anderson, Daniel G. [1 ]
Gu, Zhen [3 ,4 ]
Dutta, Sanjoy [5 ,6 ,7 ]
Strano, Michael S. [1 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] Case Western Reserve Univ, Dept Biochem, Cleveland, OH 44106 USA
[3] Univ North Carolina Chapel Hill, Joint Dept Biomed Engn, Raleigh, NC 27695 USA
[4] North Carolina State Univ, Raleigh, NC 27695 USA
[5] Univ North Carolina Chapel Hill, Eshelman Sch Pharm, Pharmacoengn & Mol Pharmaceut Div, Chapel Hill, NC 27599 USA
[6] Univ N Carolina, Sch Med, Dept Med, Chapel Hill, NC 27599 USA
[7] JDRF Int, New York, NY 10004 USA
关键词
CATIONIC COPOLYMER HYDROGELS; CHEMICAL-SYNTHESIS; BORONIC ACIDS; ANALOGS; BINDING; CONSTANTS; PROFILES; OXIDASE; RELEASE; ROUTE;
D O I
10.1038/NCHEM.2857
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The concept of a glucose-responsive insulin (GRI) has been a recent objective of diabetes technology. The idea behind the GRI is to create a therapeutic that modulates its potency, concentration or dosing relative to a patient's dynamic glucose concentration, thereby approximating aspects of a normally functioning pancreas. From the perspective of the medicinal chemist, the GRI is also important as a generalized model of a potentially new generation of therapeutics that adjust potency in response to a critical therapeutic marker. The aim of this Perspective is to highlight emerging concepts, including mathematical modelling and the molecular engineering of insulin itself and its potency, towards a viable GRI. We briefly outline some of the most important recent progress toward this goal and also provide a forward-looking viewpoint, which asks if there are new approaches that could spur innovation in this area as well as to encourage synthetic chemists and chemical engineers to address the challenges and promises offered by this therapeutic approach.
引用
收藏
页码:937 / 943
页数:7
相关论文
共 87 条
[1]  
ALBIN G, 1985, Journal of Controlled Release, V2, P153, DOI 10.1016/0168-3659(85)90041-0
[2]   A D-glucose selective fluorescent assay [J].
Arimori, S ;
Ward, CJ ;
James, TD .
TETRAHEDRON LETTERS, 2002, 43 (02) :303-305
[3]   Fully Convergent Chemical Synthesis of Ester Insulin: Determination of the High Resolution X-ray Structure by Racemic Protein Crystallography [J].
Avital-Shmilovici, Michal ;
Mandal, Kalyaneswar ;
Gates, Zachary P. ;
Phillips, Nelson B. ;
Weiss, Michael A. ;
Kent, Stephen B. H. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (08) :3173-3185
[4]   Cell factories for insulin production [J].
Baeshen, Nabih A. ;
Baeshen, Mohammed N. ;
Sheikh, Abdullah ;
Bora, Roop S. ;
Ahmed, Mohamed Morsi M. ;
Ramadan, Hassan A. I. ;
Saini, Kulvinder Singh ;
Redwan, Elrashdy M. .
MICROBIAL CELL FACTORIES, 2014, 13
[5]   Insulin analogues [J].
Barnett, AH ;
Owens, DR .
LANCET, 1997, 349 (9044) :47-51
[6]  
Berenson D. F., 2012, ANN NY ACAD SCI, V1243, pE40
[7]   A Pharmacokinetic Model of a Tissue Implantable Insulin Sensor [J].
Bisker, Gili ;
Iverson, Nicole M. ;
Ahn, Jiyoung ;
Strano, Michael S. .
ADVANCED HEALTHCARE MATERIALS, 2015, 4 (01) :87-97
[8]   A critical review of mathematical models and data used in diabetology [J].
Boutayeb, A. ;
Chetouani, A. .
BIOMEDICAL ENGINEERING ONLINE, 2006, 5 (1)
[9]   GLUCOSE-CONTROLLED INSULIN-DELIVERY SYSTEM - SEMI-SYNTHETIC INSULIN BOUND TO LECTIN [J].
BROWNLEE, M ;
CERAMI, A .
SCIENCE, 1979, 206 (4423) :1190-1191
[10]   Exploiting the Reversible Covalent Bonding of Boronic Acids: Recognition, Sensing, and Assembly [J].
Bull, Steven D. ;
Davidson, Matthew G. ;
Van den Elsen, Jean M. H. ;
Fossey, John S. ;
Jenkins, A. Toby A. ;
Jiang, Yun-Bao ;
Kubo, Yuji ;
Marken, Frank ;
Sakurai, Kazuo ;
Zhao, Jianzhang ;
James, Tony D. .
ACCOUNTS OF CHEMICAL RESEARCH, 2013, 46 (02) :312-326