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A novel nano delivery system targeting different stages of osteoclasts

Zhang, B. (author)
Zhao, J. (author)
Yan, Hongji (author)
Karolinska Institutet,KTH,Glykovetenskap,Center for the Advancement of Integrated Medical and Engineering Sciences, AIMES,Department of Neuroscience, Karolinska Institutet, SE-171 77 Stockholm, Sweden
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Zhao, Y. (author)
Tian, H. (author)
Wang, C. (author)
Wang, R. (author)
Jin, J. (author)
Chen, Y. (author)
Yang, C. (author)
LI, C. (author)
Jiao, Y. (author)
Zheng, K. (author)
Zhu, F. (author)
Tian, W. (author)
Li, CF (author)
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 (creator_code:org_t)
2022
2022
English.
In: Biomaterials Science. - : Royal Society of Chemistry (RSC). - 2047-4830 .- 2047-4849. ; 10:7, s. 1821-1830
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Osteoclast (OC) abnormalities represent osteoporosis's critical mechanism (OP). OCs undergo multiple processes that range from monocytic to functional. Different drugs target OCs at different developmental stages; however, almost no Suitable drug-targeted delivery systems exist. Therefore, we designed two dual-targeting nanoparticles to target OCs at different functional stages. Using the calcitonin gene-related peptide receptor (CGRPR), which OC precursors highly express, and specific TRAPpeptides screened in the bone resorption lacuna, where mature OCs function, respectively, two types of dual-targeted nanoparticles were constructed. Afterwards, nanoparticles were grafted with hyaluronic acid (HA), which specifically binds to CD44 on the surface of the OCs. In vivo and in vitro experiments show that both nanoparticles have noticeable targeting effects on OCs. This suggests that dual-targeting nanoparticles designed for different functional periods of OC can be well targeted to the corresponding OC, and further promote the more precise delivery of drugs used to treat OP. 

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine (hsv//eng)

Keyword

Bone
Controlled drug delivery
Hyaluronic acid
Targeted drug delivery
Calcitonin gene-related peptides
Developmental stage
Different stages
Drug targets
Functional stages
Multiple process
Nano-delivery systems
Osteoclast precursor
Peptide receptor
Targeted delivery systems
Nanoparticles
acid phosphatase tartrate resistant isoenzyme
alkaline phosphatase
calcitonin
calcitonin gene related peptide
calcitonin gene related peptide receptor
calcitonin receptor like receptor
cathepsin K
colony stimulating factor 1
Hermes antigen
hyaluronic acid binding protein
layilin
membrane protein
nanoparticle
osteoclast differentiation factor
rhodamine 6G
scleroprotein
toll like receptor 4
unclassified drug
animal cell
animal experiment
animal tissue
Article
bone tissue
controlled study
drug delivery system
in vitro study
in vivo study
mouse
nanotechnology
newborn
nonhuman
osteoclast
osteolysis
osteoporosis
protein expression
human
metabolism
monocyte
Bone Resorption
Humans
Monocytes
Nanoparticle Drug Delivery System
Osteoclasts

Publication and Content Type

ref (subject category)
art (subject category)

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