Keyword search (4,163 papers available)

"Singh D" Authored Publications:

Title Authors PubMed ID
1 Shear Stress and Microbubble-Mediated Modulation of Endothelial Cell Immunobiology Memari E; Singh D; Alkins R; Helfield B; 40657183
PHYSICS
2 Flow rate modulates focused ultrasound-mediated vascular delivery of microRNA He S; Singh D; Helfield B; 39850318
BIOLOGY
3 Focused Ultrasound and Microbubble-Mediated Delivery of CRISPR-Cas9 Ribonucleoprotein to Human Induced Pluripotent Stem Cells Hazel K; Singh D; He S; Guertin Z; Husser MC; Helfield B; 39797397
BIOLOGY
4 Immunomodulation of human T cells by microbubble-mediated focused ultrasound Baez A; Singh D; He S; Hajiaghayi M; Gholizadeh F; Darlington PJ; Helfield B; 39502696
BIOLOGY
5 Cardiac gene delivery using ultrasound: State of the field Singh D; Memari E; He S; Yusefi H; Helfield B; 38983873
BIOLOGY
6 Stable Cavitation-Mediated Delivery of miR-126 to Endothelial Cells He S; Singh D; Yusefi H; Helfield B; 36559150
BIOLOGY
7 An Overview of Cell Membrane Perforation and Resealing Mechanisms for Localized Drug Delivery He S; Singh D; Helfield B; 35456718
BIOLOGY

 

Title:An Overview of Cell Membrane Perforation and Resealing Mechanisms for Localized Drug Delivery
Authors:He SSingh DHelfield B
Link:https://pubmed.ncbi.nlm.nih.gov/35456718/
DOI:10.3390/pharmaceutics14040886
Publication:Pharmaceutics
Keywords:cytoskeletal remodelingendocytosisexocytosismembrane permeabilityplasma membrane repairporesonoporationwound healing
PMID:35456718 Category: Date Added:2022-04-23
Dept Affiliation: BIOLOGY
1 Department of Biology, Concordia University, Montreal, QC H4B 1R6, Canada.
2 Department of Physics, Concordia University, Montreal, QC H4B 1R6, Canada.

Description:

Localized and reversible plasma membrane disruption is a promising technique employed for the targeted deposition of exogenous therapeutic compounds for the treatment of disease. Indeed, the plasma membrane represents a significant barrier to successful delivery, and various physical methods using light, sound, and electrical energy have been developed to generate cell membrane perforations to circumvent this issue. To restore homeostasis and preserve viability, localized cellular repair mechanisms are subsequently triggered to initiate a rapid restoration of plasma membrane integrity. Here, we summarize the known emergency membrane repair responses, detailing the salient membrane sealing proteins as well as the underlying cytoskeletal remodeling that follows the physical induction of a localized plasma membrane pore, and we present an overview of potential modulation strategies that may improve targeted drug delivery approaches.





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