Frontiers in cancer nanomedicine: directing mass transport through biological barriers

被引:208
作者
Ferrari, Mauro [1 ,2 ,3 ]
机构
[1] UTHSC H, Dept NanoMed & Biomed Engn, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Houston, TX 77030 USA
[3] Rice Univ, Dept Bioengn, Houston, TX 77005 USA
关键词
PEGYLATED LIPOSOMAL DOXORUBICIN; RECEPTOR-MEDIATED ENDOCYTOSIS; LABELED MONOCLONAL-ANTIBODIES; ALBUMIN-BOUND PACLITAXEL; METASTATIC BREAST-CANCER; HUMAN TUMOR XENOGRAFT; SOLID TUMORS; DRUG-DELIVERY; IN-VIVO; THERAPEUTIC APPLICATIONS;
D O I
10.1016/j.tibtech.2009.12.007
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
The physics of mass transport within body compartments and across biological barriers differentiates cancers from healthy tissues. Variants of nanoparticles can be manufactured in combinatorially large sets, varying by only one transport-affecting design parameter at a time. Nanoparticles can also be used as building blocks for systems that perform sequences of coordinated actions, in accordance with a prescribed logic. We refer to these as Logic-Embedded Vectors (LEVs). Nanoparticles and LEVs are ideal probes for the determination of mass transport laws in tumors, acting as imaging contrast enhancers, and can be employed for lesion-selective delivery of therapy. Their size, shape, density and surface chemistry dominate convective transport in the bloodstream, margination, cell adhesion, selective cellular uptake, as well as sub-cellular trafficking and localization. As argued here, the understanding of transport differentials in cancer, termed 'transport oncophysics', reveals a promising new frontier in oncology: the development of lesion-specific delivery particulates that exploit mass transport differentials to deploy treatment of greater efficacy and reduced side effects.
引用
收藏
页码:181 / 188
页数:8
相关论文
共 106 条
[1]
In vivo diagnosis of epidermal growth factor receptor expression using molecular imaging with a cocktail of optically labeled monoclonal antibodies [J].
Barrett, Tristan ;
Koyama, Yoshinori ;
Hama, Yukihiro ;
Ravizzini, Gregory ;
Shin, In Soo ;
Jang, Beom-Su ;
Paik, Chang H. ;
Urano, Yasuteru ;
Choyke, Peter L. ;
Kobayashi, Hisataka .
CLINICAL CANCER RESEARCH, 2007, 13 (22) :6639-6648
[2]
Dynamic imaging of collagen and its modulation in tumors in vivo using second-harmonic generation [J].
Brown, E ;
McKee, T ;
diTomaso, E ;
Pluen, A ;
Seed, B ;
Boucher, Y ;
Jain, RK .
NATURE MEDICINE, 2003, 9 (06) :796-800
[3]
A tense situation: forcing tumour progression [J].
Butcher, Darci T. ;
Alliston, Tamara ;
Weaver, Valerie M. .
NATURE REVIEWS CANCER, 2009, 9 (02) :108-122
[4]
Pharmacokinetic and biodistribution properties of poly(ethylene glycol)-protein conjugates [J].
Caliceti, P ;
Veronese, FM .
ADVANCED DRUG DELIVERY REVIEWS, 2003, 55 (10) :1261-1277
[5]
Campos S, 2003, ONCOLOGIST, V8, P10
[6]
Biological applications of dendrimers [J].
Cloninger, MJ .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2002, 6 (06) :742-748
[7]
Radiofrequency ablation of malignant liver tumors [J].
Curley, SA .
ANNALS OF SURGICAL ONCOLOGY, 2003, 10 (04) :338-347
[8]
The receptor-mediated endocytosis of nonspherical particles [J].
Decuzzi, P. ;
Ferrari, M. .
BIOPHYSICAL JOURNAL, 2008, 94 (10) :3790-3797
[9]
The role of specific and non-specific interactions in receptor-mediated endocytosis of nanoparticles [J].
Decuzzi, P. ;
Ferrari, M. .
BIOMATERIALS, 2007, 28 (18) :2915-2922
[10]
The adhesive strength of non-spherical particles mediated by specific interactions [J].
Decuzzi, P. ;
Ferrari, M. .
BIOMATERIALS, 2006, 27 (30) :5307-5314