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  4. Type I collagen hydrogels as a delivery matrix for royal jelly derived extracellular vesicles
Details

Type I collagen hydrogels as a delivery matrix for royal jelly derived extracellular vesicles

Journal
Drug Delivery
ISSN
1071-7544
1521-0464
Date Issued
2020
Author(s)
Orlando J. Ramírez
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Simón Alvarez
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Pamina Contreras-Kallens
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Nelson P. Barrera
Sebastian Aguayo
Christina M. A. P. Schuh
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Type
Resource Types::text::journal::journal article
Scopus ID
2-s2.0-85090865603
WoS ID
WOS:000568862400001
DOI
10.1080/10717544.2020.1818880
URL
https://investigadores.udd.cl/handle/123456789/5819
URL Institutional Repository
http://hdl.handle.net/11447/4148
Cite this document
Ramírez, O. J., Alvarez, S., Contreras-Kallens, P., Barrera, N. P., Aguayo, S., & Schuh, C. M. A. P. (2020). Type I collagen hydrogels as a delivery matrix for royal jelly derived extracellular vesicles. Drug Delivery, 27(1), 1308-1318. https://doi.org/10.1080/10717544.2020.1818880
Project(s)
Influence of age-derived dental collagen glycation on bacterial adhesion and initial biofilm formation of oral streptococci  
Analysis of antimicrobial and pro-regenerative properties of exosomes derived from Apis mellifera Royel Jelly  
Subjects
apis mellifera

; 

drug delivery

; 

extracellular vesicle delivery

; 

regenerative medicine

; 

wound healing

; 

cell movement

; 

collagen type i

; 

dose-response relationship, drug

; 

drug delivery systems

; 

extracellular vesicles

; 

fatty acids

; 

fibroblasts

; 

humans

; 

hydrogels

; 

collagen type 1

; 

hydrogel

; 

royal jelly

; 

collagen type 1

; 

fatty acid

; 

royal jelly

; 

apis mellifera

; 

article

; 

atomic force microscopy

; 

biofilm

; 

brdu assay

; 

cell migration

; 

drug delivery system

; 

exosome

; 

fibroblast

; 

membrane microparticle

; 

mesenchymal stem cell

; 

nonhuman

; 

priority journal

; 

skin injury

; 

staphylococcus aureus

; 

wound healing

; 

wound healing assay

; 

administration and dosage

; 

cell motion

; 

chemistry

; 

dose response

; 

drug delivery system

; 

drug effect

; 

human

; 

hydrogel

; 

physiology

; 

procedures

; 

synthesis
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