Smart approaches to glucose-responsive drug delivery

被引:78
作者
Webber, Matthew J. [1 ,2 ]
Anderson, Daniel G. [1 ,2 ,3 ,4 ,5 ]
机构
[1] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[2] Boston Childrens Hosp, Dept Anesthesiol, Boston, MA USA
[3] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[4] MIT, Inst Med Engn & Sci, Cambridge, MA 02139 USA
[5] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
Artificial pancreas; diabetes; insulin; smart drug delivery; INSULIN DELIVERY; CONTROLLED-RELEASE; CONCANAVALIN-A; POLYMER MATRICES; HYDROGEL; SYSTEM; TYPE-1; OXIDASE; COMPLEX; GEL;
D O I
10.3109/1061186X.2015.1055749
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A grand challenge in the field of "smart" drug delivery has been the quest to create formulations that can sense glucose and respond by delivering an appropriate dose of insulin. This approach, referred to as the "fully synthetic pancreas", envisions closed-loop insulin therapy. The strategies for incorporating glucose sensing into formulations can be broadly categorized into three subsets: enzymatic sensing, natural glucose-binding proteins and synthetic molecular recognition. Here, we highlight some examples of each of these approaches. The challenges remaining en route to the realization of closed-loop insulin therapy are substantial, and include improved response time, more authentic fidelity in glycemic control, improved biocompatibility for delivery materials and assurance of both safety and efficacy. The ubiquitous existence of glucose, combined with the unstable and toxic properties of insulin, further compound efforts towards the generation of a fully synthetic pancreas. However, given the growing incidence of both type-1 and type-2 diabetes, there is significant potential impact from the realization of such an approach on improving therapeutic management of the disease.
引用
收藏
页码:651 / 655
页数:5
相关论文
共 77 条
[1]  
ALBIN G, 1985, Journal of Controlled Release, V2, P153, DOI 10.1016/0168-3659(85)90041-0
[2]  
Amer Diabet Assoc, 2011, DIABETES CARE, V34, pS11, DOI [10.2337/dc11-S062, 10.2337/dc14-S081, 10.2337/dc11-S011, 10.2337/dc13-S067, 10.2337/dc12-s011, 10.2337/dc10-S011, 10.2337/dc10-S062, 10.2337/dc13-S011, 10.2337/dc12-s064]
[3]  
[Anonymous], SELF REGULATED PEPTI
[4]   Glucose oxidase - An overview [J].
Bankar, Sandip B. ;
Bule, Mahesh V. ;
Singhal, Rekha S. ;
Ananthanarayan, Laxmi .
BIOTECHNOLOGY ADVANCES, 2009, 27 (04) :489-501
[5]   Materials for Diabetes Therapeutics [J].
Bratlie, Kaitlin M. ;
York, Roger L. ;
Invernale, Michael A. ;
Langer, Robert ;
Anderson, Daniel G. .
ADVANCED HEALTHCARE MATERIALS, 2012, 1 (03) :267-284
[6]   CONTROLLED RELEASE OF INSULIN FROM POLYMER MATRICES - INVITRO KINETICS [J].
BROWN, L ;
SIEMER, L ;
MUNOZ, C ;
LANGER, R .
DIABETES, 1986, 35 (06) :684-691
[7]   CONTROLLED RELEASE OF INSULIN FROM POLYMER MATRICES - CONTROL OF DIABETES IN RATS [J].
BROWN, L ;
MUNOZ, C ;
SIEMER, L ;
EDELMAN, E ;
LANGER, R .
DIABETES, 1986, 35 (06) :692-697
[8]   GLUCOSE-CONTROLLED INSULIN-DELIVERY SYSTEM - SEMI-SYNTHETIC INSULIN BOUND TO LECTIN [J].
BROWNLEE, M ;
CERAMI, A .
SCIENCE, 1979, 206 (4423) :1190-1191
[9]   GLUCOSE-SENSITIVE MEMBRANE COATED POROUS FILTERS FOR CONTROL OF HYDRAULIC PERMEABILITY AND INSULIN DELIVERY FROM A PRESSURIZED RESERVOIR [J].
CARTIER, S ;
HORBETT, TA ;
RATNER, BD .
JOURNAL OF MEMBRANE SCIENCE, 1995, 106 (1-2) :17-24
[10]   Drug Delivery Interfaces in the 21st Century: From Science Fiction Ideas to Viable Technologies [J].
Chertok, Beata ;
Webber, Matthew J. ;
Succi, Marc D. ;
Langer, Robert .
MOLECULAR PHARMACEUTICS, 2013, 10 (10) :3531-3543