Molecular imaging and disease theranostics with renal-clearable optical agents

被引:307
作者
Cheng, Penghui [1 ]
Pu, Kanyi [1 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, Singapore, Singapore
关键词
GLOMERULAR-FILTRATION-RATE; REAL-TIME; SILICA NANOPARTICLES; TRANSCUTANEOUS MEASUREMENT; GOLD NANOPARTICLES; POLYFRUCTOSAN-S; CAPILLARY WALL; GUIDED SURGERY; KIDNEY INJURY; CANCER-CELLS;
D O I
10.1038/s41578-021-00328-6
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Optical imaging in disease diagnosis and treatment benefits from high spatiotemporal resolution and the availability of numerous optical agents. However, many optical imaging probes are cleared by the reticuloendothelial system, which can lead to probe accumulation in the liver and spleen and hence organ toxicity. By contrast, renal-clearable optical agents (RCOAs) are rapidly excreted from the body via the kidneys, undergoing minimal metabolism. In this Review, we discuss the design principles of RCOAs, with a focus on imaging and disease theranostics (the combination of diagnosis and therapy). Renal excretion of RCOAs makes them intrinsically suitable for targeted kidney imaging, including passive monitoring of the glomerular filtration rate and detection of early kidney injury biomarkers. The pharmacokinetics of RCOAs can further be tailored to prolong their circulation in the blood, allowing deep tumour penetration and high-contrast tumour imaging. Finally, we discuss intraoperative image-guided surgery and optical urinalysis, and suggest future applications of RCOAs. Intravenously injected renal-clearable optical agents (RCOAs) are rapidly cleared by the kidneys, allowing disease diagnosis and treatment by optical imaging, while avoiding unwanted tissue accumulation and adverse effects. This Review discusses the design of RCOAs for kidney imaging, kidney injury detection, cancer theranostics, intraoperative image-guided surgery and optical urinalysis.
引用
收藏
页码:1095 / 1113
页数:19
相关论文
共 167 条
[1]  
Antaris AL, 2016, NAT MATER, V15, P235, DOI [10.1038/NMAT4476, 10.1038/nmat4476]
[2]  
ARISZ L, 1969, ACTA MED SCAND, V186, P393
[3]   INTRAVASCULAR PERSISTENCE AND RENAL CLEARANCE OF DEXTRAN OF DIFFERENT MOLECULAR SIZES IN NORMAL CHILDREN [J].
ARTURSON, G ;
GRANATH, K ;
GROTTE, G .
ARCHIVES OF DISEASE IN CHILDHOOD, 1966, 41 (216) :168-&
[4]   Pathophysiology of Acute Kidney Injury [J].
Basile, David P. ;
Anderson, Melissa D. ;
Sutton, Timothy A. .
COMPREHENSIVE PHYSIOLOGY, 2012, 2 (02) :1303-1353
[5]   RENAL CLEARANCES OF INULIN POLYFRUCTOSAN-S AND A POLYETHYLENE GLYCOL (PEG 1000) IN RAT [J].
BERGLUND, F .
ACTA PHYSIOLOGICA SCANDINAVICA, 1965, 64 (03) :238-&
[6]   Principles of nanoparticle design for overcoming biological barriers to drug delivery [J].
Blanco, Elvin ;
Shen, Haifa ;
Ferrari, Mauro .
NATURE BIOTECHNOLOGY, 2015, 33 (09) :941-951
[7]   PERMSELECTIVITY OF GLOMERULAR CAPILLARY WALL - FACILITATED FILTRATION OF CIRCULATING POLYCATIONS [J].
BOHRER, MP ;
BAYLIS, C ;
HUMES, HD ;
GLASSOCK, RJ ;
ROBERTSON, CR ;
BRENNER, BM .
JOURNAL OF CLINICAL INVESTIGATION, 1978, 61 (01) :72-78
[8]   Next-generation biomarkers for detecting kidney toxicity [J].
Bonventre, Joseph V. ;
Vaidya, Vishal S. ;
Schmouder, Robert ;
Feig, Peter ;
Dieterle, Frank .
NATURE BIOTECHNOLOGY, 2010, 28 (05) :436-440
[9]   Clinically-translated silica nanoparticles as dual-modality cancer-targeted probes for image-guided surgery and interventions [J].
Bradbury, Michelle S. ;
Phillips, Evan ;
Montero, Pablo H. ;
Cheal, Sarah M. ;
Stambuk, Hilda ;
Durack, Jeremy C. ;
Sofocleous, Constantinos T. ;
Meester, Richard J. C. ;
Wiesner, Ulrich ;
Patel, Snehal .
INTEGRATIVE BIOLOGY, 2013, 5 (01) :74-86
[10]   Fluorescent core-shell silica nanoparticles: towards "Lab on a Particle" architectures for nanobiotechnology [J].
Burns, Andrew ;
Ow, Hooisweng ;
Wiesner, Ulrich .
CHEMICAL SOCIETY REVIEWS, 2006, 35 (11) :1028-1042