Introduction: With a wealth of knowledge on the effect of nanoparticle properties, including size, shape, charge and composition, on intracellular delivery, little has been reported on the effect of the cell cycle on the intracellular delivery and activity of nanomedicines including non-viral gene delivery systems. The aim of this review is to shed a light on this topic. Areas covered: It is now evident that nanoparticle cell uptake varies with the cell cycle phase. This review addresses this variation by dissecting the effect of cell population heterogeneity on the intracellular delivery and activity of nanomedicines with a special focus on non-viral gene delivery and combination therapy modalities that utilize cell cycle inhibitors as co-targets for therapy. In addition, the importance of three-dimensional (3D) culture systems in the drug delivery field within the context of the cell cycle will be addressed. Expert opinion: The understanding of the cell cycle machinery has improved dramatically over the last few decades. Developing combination therapy modalities that target the cell cycle to achieve better cancer patient outcome should now be the focus. Furthermore, more effort should be placed on developing a reliable, consistent, high throughput 3D cell culture system since these systems more closely resemble the cell cycle status of in vivo tumors. A switch from 2D to 3D culture systems, to more accurately predict the in vivo efficacy of nanoparticle drug delivery systems, is desirable.
机构:
Univ Illinois, Dept Bioengn, Chicago, IL 60612 USAUniv Illinois, Dept Bioengn, Chicago, IL 60612 USA
Cesur, Hacer
;
Rubinstein, Israel
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Univ Illinois, Dept Biopharmaceut Sci, Chicago, IL 60612 USA
Univ Illinois, Dept Med, Chicago, IL 60612 USA
Jesse Brown VA Med Ctr, Chicago, IL USAUniv Illinois, Dept Bioengn, Chicago, IL 60612 USA
Rubinstein, Israel
;
Pai, Ashwini
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机构:
Univ Illinois, Dept Biopharmaceut Sci, Chicago, IL 60612 USAUniv Illinois, Dept Bioengn, Chicago, IL 60612 USA
Pai, Ashwini
;
Oenyueksel, Hayat
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Univ Illinois, Dept Bioengn, Chicago, IL 60612 USA
Univ Illinois, Dept Biopharmaceut Sci, Chicago, IL 60612 USAUniv Illinois, Dept Bioengn, Chicago, IL 60612 USA
机构:
Vet Affairs Med Ctr, Lab Cell Growth, San Francisco, CA 94121 USA
Univ Calif San Francisco, Dept Surg, San Francisco, CA 94143 USAVet Affairs Med Ctr, Lab Cell Growth, San Francisco, CA 94121 USA
Chang, Tammy T.
;
Hughes-Fulford, Millie
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机构:
Vet Affairs Med Ctr, Lab Cell Growth, San Francisco, CA 94121 USA
Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USAVet Affairs Med Ctr, Lab Cell Growth, San Francisco, CA 94121 USA
机构:
Univ Illinois, Dept Bioengn, Chicago, IL 60612 USAUniv Illinois, Dept Bioengn, Chicago, IL 60612 USA
Cesur, Hacer
;
Rubinstein, Israel
论文数: 0引用数: 0
h-index: 0
机构:
Univ Illinois, Dept Biopharmaceut Sci, Chicago, IL 60612 USA
Univ Illinois, Dept Med, Chicago, IL 60612 USA
Jesse Brown VA Med Ctr, Chicago, IL USAUniv Illinois, Dept Bioengn, Chicago, IL 60612 USA
Rubinstein, Israel
;
Pai, Ashwini
论文数: 0引用数: 0
h-index: 0
机构:
Univ Illinois, Dept Biopharmaceut Sci, Chicago, IL 60612 USAUniv Illinois, Dept Bioengn, Chicago, IL 60612 USA
Pai, Ashwini
;
Oenyueksel, Hayat
论文数: 0引用数: 0
h-index: 0
机构:
Univ Illinois, Dept Bioengn, Chicago, IL 60612 USA
Univ Illinois, Dept Biopharmaceut Sci, Chicago, IL 60612 USAUniv Illinois, Dept Bioengn, Chicago, IL 60612 USA
机构:
Vet Affairs Med Ctr, Lab Cell Growth, San Francisco, CA 94121 USA
Univ Calif San Francisco, Dept Surg, San Francisco, CA 94143 USAVet Affairs Med Ctr, Lab Cell Growth, San Francisco, CA 94121 USA
Chang, Tammy T.
;
Hughes-Fulford, Millie
论文数: 0引用数: 0
h-index: 0
机构:
Vet Affairs Med Ctr, Lab Cell Growth, San Francisco, CA 94121 USA
Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USAVet Affairs Med Ctr, Lab Cell Growth, San Francisco, CA 94121 USA