Myeloid cell-mediated drug delivery: From nanomedicine to cell therapy

被引:10
|
作者
Zhang, Fan [1 ,2 ,3 ,4 ]
Xu, Zijing
Jolly, Kevon J. [1 ]
机构
[1] Univ Florida, Coll Pharm, Dept Pharmaceut, Gainesville, FL USA
[2] Univ Florida, Coll Engn, Dept Chem Engn, Gainesville, FL USA
[3] Univ Florida, Coll Med, Dept Pharmacol & Therapeut, Gainesville, FL USA
[4] 1345 Ctr Dr,POB 100494, Gainesville, FL 32610 USA
关键词
Myeloid cells; Cell migration; Chemotaxis; Nanoparticles; Nano-engineering; Targeted delivery; Cell-carriers; Cell-engineering; ANTIRETROVIRAL DRUG; MACROPHAGE DELIVERY; LEUKOCYTE ADHESION; SUPPRESSOR-CELLS; MURINE MODEL; BONE-MARROW; STEM-CELLS; IN-VIVO; NANOPARTICLES; CHEMOKINES;
D O I
10.1016/j.addr.2023.114827
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the presence of tissue inflammation, injury, or cancer, myeloid cells are recruited to disease regions through a multi-step process involving myelopoiesis, chemotaxis, cell migration, and diapedesis. As an emerging drug delivery approach, cell-mediated drug delivery takes advantage of the cell recruitment process to enhance the active transport of therapeutic cargo to disease regions. In the past few decades, a variety of nano-engineering methods have emerged to enhance interactions of nanoparticles with cells of interest, which can be adapted for cell-mediated drug delivery. Moreover, the drug delivery field can benefit from the recent clinical success of cell-based therapies, which created cell-engineering methods to engineer circulating leukocytes as 'living drug delivery vehicles' to target diseased tissues. In this review, we first provide an overview of myeloid cell recruitment and discuss how various factors within this process may affect cell-mediated delivery. In the second part of this review article, we summarize the status quo of nano-engineering and cell-engineering approaches and discuss how these engineering approaches can be adapted for cell-mediated delivery. Finally, we discuss future directions of this field, pointing out key challenges in the clinical translation of cell-mediated drug delivery.Published by Elsevier B.V.
引用
收藏
页数:17
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