Red Blood Cells for Glucose-Responsive Insulin Delivery

被引:142
作者
Wang, Chao [1 ,2 ,3 ,4 ]
Ye, Yanqi [1 ,2 ,3 ,4 ]
Sun, Wujin [1 ,2 ,3 ,4 ]
Yu, Jicheng [1 ,2 ,3 ,4 ]
Wang, Jingqiang [1 ,2 ,3 ,4 ]
Lawrence, David S. [5 ,6 ,7 ]
Buse, John B. [8 ]
Gu, Zhen [1 ,2 ,3 ,4 ,8 ]
机构
[1] Univ North Carolina Chapel Hill, Joint Dept Biomed Engn, Raleigh, NC 27695 USA
[2] North Carolina State Univ, Raleigh, NC 27695 USA
[3] Univ N Carolina, Div Mol Pharmaceut, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Eshelman Sch Pharm, Ctr Nanotechnol Drug Delivery, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[6] Univ N Carolina, Div Chem Biol & Med Chem, Chapel Hill, NC 27599 USA
[7] Univ N Carolina, Dept Pharmacol, Chapel Hill, NC 27599 USA
[8] Univ N Carolina, Sch Med, Dept Med, Chapel Hill, NC 27599 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
CATIONIC COPOLYMER HYDROGELS; DRUG-DELIVERY; IN-VIVO; NANOPARTICLES; THERAPY; ERYTHROCYTES; TRANSPORTERS; PATCHES; SYSTEMS; RELEASE;
D O I
10.1002/adma.201606617
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Glucose-responsive delivery of insulin mimicking the function of pancreatic beta-cells to achieve meticulous control of blood glucose (BG) would revolutionize diabetes care. Here the authors report the development of a new glucose-responsive insulin delivery system based on the potential interaction between the glucose derivative-modified insulin (Glc-Insulin) and glucose transporters on erythrocytes (or red blood cells, RBCs) membrane. After being conjugated with the glucosamine, insulin can efficiently bind to RBC membranes. The binding is reversible in the setting of hyperglycemia, resulting in fast release of insulin and subsequent drop of BG level in vivo. The delivery vehicle can be further simplified utilizing injectable polymeric nanocarriers coated with RBC membrane and loaded with Glc-Insulin. The described work is the first demonstration of utilizing RBC membrane to achieve smart insulin delivery with fast responsiveness.
引用
收藏
页数:7
相关论文
共 51 条
[1]
American Diabetes Association, 2016, Clin Diabetes, V34, P3, DOI 10.2337/diaclin.34.1.3
[2]
Delivering Nanoparticles to Lungs while Avoiding Liver and Spleen through Adsorption on Red Blood Cells [J].
Anselmo, Aaron C. ;
Gupta, Vivek ;
Zern, Blaine J. ;
Pan, Daniel ;
Zakrewsky, Michael ;
Muzykantov, Vladimir ;
Mitragotri, Samir .
ACS NANO, 2013, 7 (12) :11129-11137
[3]
The functional importance of blood group-active molecules in human red blood cells [J].
Anstee, D. J. .
VOX SANGUINIS, 2011, 100 (01) :140-149
[4]
GLUCOSE-CONTROLLED INSULIN-DELIVERY SYSTEM - SEMI-SYNTHETIC INSULIN BOUND TO LECTIN [J].
BROWNLEE, M ;
CERAMI, A .
SCIENCE, 1979, 206 (4423) :1190-1191
[5]
Chopra A., 2004, MOL IMAGING CONTRAST
[6]
Glucose-responsive insulin activity by covalent modification with aliphatic phenylboronic acid conjugates [J].
Chou, Danny Hung-Chieh ;
Webber, Matthew J. ;
Tang, Benjamin C. ;
Lin, Amy B. ;
Thapa, Lavanya S. ;
Deng, David ;
Truong, Jonathan V. ;
Cortinas, Abel B. ;
Langer, Robert ;
Anderson, Daniel G. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (08) :2401-2406
[7]
NORMAL FUNCTIONS OF THE SPLEEN RELATIVE TO RED BLOOD CELLS - A REVIEW [J].
CROSBY, WH .
BLOOD, 1959, 14 (04) :399-408
[8]
Niosomes and polymeric chitosan based vesicles bearing transferrin and glucose ligands for drug targeting [J].
Dufes, C ;
Schätzlein, AG ;
Tetley, L ;
Gray, AI ;
Watson, DG ;
Olivier, JC ;
Couet, W ;
Uchegbu, IF .
PHARMACEUTICAL RESEARCH, 2000, 17 (10) :1250-1258
[9]
CHARACTERISTICS OF HUMAN ERYTHROCYTE INSULIN RECEPTORS [J].
GAMBHIR, KK ;
ARCHER, JA ;
BRADLEY, CJ .
DIABETES, 1978, 27 (07) :701-708
[10]
Glucose-Responsive Microgels Integrated with Enzyme Nanocapsules for Closed-Loop Insulin Delivery [J].
Gu, Zhen ;
Dang, Tram T. ;
Ma, Minglin ;
Tang, Benjamin C. ;
Cheng, Hao ;
Jiang, Shan ;
Dong, Yizhou ;
Zhang, Yunlong ;
Anderson, Daniel G. .
ACS NANO, 2013, 7 (08) :6758-6766