Delivery of cancer therapeutics to extracellular and intracellular targets: Determinants, barriers, challenges and opportunities

被引:122
作者
Au, Jessie L. -S. [1 ,2 ,3 ,4 ]
Yeung, Bertrand Z. [2 ]
Wientjes, Michael G. [1 ]
Lu, Ze [1 ]
Wientjes, M. Guillaume [1 ]
机构
[1] Optimum Therapeut LLC, 1815 Aston Ave, Carlsbad, CA 92008 USA
[2] Univ Oklahoma, Dept Pharmaceut Sci, Hlth Sci Ctr, Oklahoma City, OK 73014 USA
[3] Med Univ S Carolina, Charleston, SC 29425 USA
[4] Taipei Med Univ, Taipei, Taiwan
关键词
Computational modeling; Extracellular matrix; Immune checkpoint therapy; Interstitial and transvascular transport; Intracellular trafficking; Nanoparticles; Tumor microenvironment; Spatiokinetics; PLASMA-PROTEIN ADSORPTION; CELL-PENETRATING PEPTIDES; TRANSCAPILLARY PRESSURE-GRADIENT; PEGYLATED-LIPOSOMAL DOXORUBICIN; MACROMOLECULAR DRUG-DELIVERY; SENSITIVE FUSOGENIC PEPTIDE; INTERSTITIAL FLUID PRESSURE; ENHANCED ENDOSOMAL ESCAPE; PHASE-III TRIAL; IN-VIVO;
D O I
10.1016/j.addr.2015.12.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Advances in molecular medicine have led to identification of worthy cellular and molecular targets located in extracellular and intracellular compartments. Effectiveness of cancer therapeutics is limited in part by inadequate delivery and transport in tumor interstitium. Parts I and II of this report give an overview on the kinetic processes in delivering therapeutics to their intended targets, the transport barriers in tumor microenvironment and extracellular matrix (TME/ECM), and the experimental approaches to overcome such barriers. Part III discusses new concepts and findings concerning nanoparticle-biocorona complex, including the effects of TME/ECM. Part IV outlines the challenges in animal-to-human translation of cancer nanotherapeutics. Part V provides an overview of the background, current status, and the roles of TME/ECM in immune checkpoint inhibition therapy, the newest cancer treatment modality. Part VI outlines the development and use of multiscale computational modeling to capture the unavoidable tumor heterogeneities, the multiple nonlinear kinetic processes including interstitial and transvascular transport and interactions between cancer therapeutics and TME/ECM, in order to predict the in vivo tumor spatiokinetics of a therapeutic based on experimental in vitro biointerfacial interaction data. Part VII provides perspectives on translational research using quantitative systems pharmacology approaches. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:280 / 301
页数:22
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