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  4. Functional reservoir microcapsules generated: via microfluidic fabrication for long-term cardiovascular therapeutics
 
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Functional reservoir microcapsules generated: via microfluidic fabrication for long-term cardiovascular therapeutics

Journal
Lab on a Chip
Journal Volume
20
Journal Issue
15
Pages
2756-2764
Date Issued
2020
Author(s)
Dinh N.-D.
Kukumberg M.
Nguyen A.-T.
Keramati H.
Guo S.
Phan D.-T.
Ja'afar N.B.
Birgersson E.
Leo H.L.
RUBY YUN-JU HUANG  
Kofidis T.
Rufaihah A.J.
Chen C.-H.
DOI
10.1039/d0lc00296h
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85088846449&doi=10.1039%2fd0lc00296h&partnerID=40&md5=202e3091dc9834d5854b1f23f669e102
https://scholars.lib.ntu.edu.tw/handle/123456789/567397
Abstract
Cardiovascular disease is a chronic disease that leads to impaired cardiac function and requires long-term management to control its progression. Despite the importance of hydrogels for therapeutic applications, a contradiction between the size of a hydrogel and the amount of loaded drug has been encountered when using conventional fabrication methods. In this study, biocompatible reservoir microcapsules (diameter ?100 μm) with a large liquid core and polymeric shell were fabricated via a one-step phase separation of poly(ethylene glycol)diacrylate (PEGDA) and dextran within pre-gel droplets through microfluidics. By controlling the process of phase separation, high drug-loading efficiency (?80%) for long-term release (30 days) of vascular endothelial growth factor (VEGF) and platelet-derived growth factor (PDGF) was achieved. Drug molecules were dispersed within the liquid core at a concentration above saturation solubility for sustained delivery via regulation of the shells. Effective therapeutic enhancement of human umbilical vein endothelial cell (HUVEC) and umbilical artery smooth muscle cell (SMC) proliferation and tube formation in vitro promoted rapid cell proliferation and increased the number of migrated cells by ?1.7 times. Moreover, in vivo blood vessel regeneration for cardiovascular control induced by sustained dual-drug (VEGF and PDGF) delivery to the rat heart was achieved, showing the effectiveness of long-term protein delivery in improving cardiac function and significantly reducing ventricular wall thickness and fibrosis of the infarct region. The ratio of heart tissue scarring was reduced to 11.2% after microcapsule treatment compared with 21.4% after saline treatment in the rat model. By using these reservoir microcapsules, similar sustained delivery of proteins, mRNAs and biologic drugs could be developed for the treatment of a range of long-term chronic diseases and regenerative medicine. This journal is ? 2020 The Royal Society of Chemistry.
SDGs

[SDGs]SDG3

Other Subjects
Biocompatibility; Blood vessels; Cell engineering; Cell proliferation; Cytology; Disease control; Diseases; Endothelial cells; Fabrication; Heart; Hydrogels; Microfluidics; Microstructure; Muscle; Phase separation; Polyethylene glycols; Proteins; Rat control; Rats; Targeted drug delivery; Cardio-vascular disease; Cardiovascular control; Human umbilical vein endothelial (HUVEC) cells; Platelet-derived growth factors; Polyethylene glycol diacrylate; Saturation solubility; Therapeutic Application; Vascular endothelial growth factor; Controlled drug delivery; biomaterial; dextran; hydrogel; platelet derived growth factor BB; poly(ethylene glycol)diacrylate; polymer; sodium chloride; unclassified drug; vasculotropin; vasculotropin A; acute heart infarction; angiogenesis; animal experiment; animal model; animal tissue; arterial smooth muscle cell; Article; biocompatibility; cardiovascular disease; cell migration; cell proliferation; combination drug therapy; concentration (parameter); controlled study; dispersity; drug delivery system; drug efficacy; drug solubility; heart; heart function; heart muscle fibrosis; heart protection; heart tissue; heart ventricle hypertrophy; human; human cell; in vitro study; liquid; male; microcapsule; microencapsulation; microfluidics; microtechnology; nonhuman; particle size; phase separation; priority journal; rat; sustained drug release; umbilical artery; umbilical artery smooth muscle cell; umbilical vein endothelial cell; animal; cardiovascular disease; hydrogel; microcapsule; umbilical vein endothelial cell; Animals; Capsules; Cardiovascular Diseases; Human Umbilical Vein Endothelial Cells; Humans; Hydrogels; Microfluidics; Rats; Vascular Endothelial Growth Factor A
Publisher
Royal Society of Chemistry
Type
journal article

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