2015
DOI: 10.1016/j.progpolymsci.2014.10.004
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Polymers for cell/tissue anti-adhesion

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Cited by 137 publications
(76 citation statements)
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“…PEG has been widely used to treat PMMA surfaces to promote cell adhesion and minimize nonspecific adsorption. [36,[43][44][45] The X-ray photoelectron spectroscopy (XPS) results in Figure 3c onfirm that hydrophilic PEG chains have been successfully grafted onto the PMMA surface. The survey spectra of unmodified PMMA,P EG, and PMMA-g-PEG in Figure 3a indicatet he presence of oxygen and carbon.…”
Section: Resultsmentioning
confidence: 74%
“…PEG has been widely used to treat PMMA surfaces to promote cell adhesion and minimize nonspecific adsorption. [36,[43][44][45] The X-ray photoelectron spectroscopy (XPS) results in Figure 3c onfirm that hydrophilic PEG chains have been successfully grafted onto the PMMA surface. The survey spectra of unmodified PMMA,P EG, and PMMA-g-PEG in Figure 3a indicatet he presence of oxygen and carbon.…”
Section: Resultsmentioning
confidence: 74%
“…However, the leakage from incisions, edema formation, and allergic response (by cornstarch) in some patients was curtained in its clinical uses . The high viscous aqueous solutions [hyaluronic acid (HA) solution (Sepracoat, Genzyme, Cambridge, MA), HA/carboxymethylcellulose (CMC) solution (Sepragel, Genzyme and Guardix‐SL, Genewel, Republic of Korea), PEG/CMC solution (Oxiplex, FzioMed, San Luis Obispo, CA and Intercoat, Ethicon), and poly(vinyl alcohol) (PVA)/CMC solution (A‐part Gel, B. Braun, Germany)], which can improve residence time on the defect site and thus reduce the apply volume compared to the low viscous one, were also applied for human. However, their effectiveness to prevent tissue adhesion is still controversial because of their dilution by body fluid which may lead to the rapid absorption in the body and/or flowing away from target region.…”
Section: Discussionmentioning
confidence: 99%
“…However, their effectiveness to prevent tissue adhesion is still controversial because of their dilution by body fluid which may lead to the rapid absorption in the body and/or flowing away from target region. Recently, the use of crosslinked hydrogels [esterified (auto crosslinked) HA (ACP gel, Fidia Advanced Biopolymers, Italy) or ferric HA (Lubricoat, Ethicon and Intergel, Lifecore, Chaska, MN)] or in situ gel forming hydrogels [PEG precursors with reactive end groups (SprayGel, Confluent Surgical, Waltham, MA and Coseal, Baxter) or chemically modified HA and PEG system (Carbylan‐SX, Carbylan Biosurgery, Palo Alto, CA)] have been accepted as a promising strategy to the prolonged residence time of the tissue adhesion barriers on the applied site. However, the potential toxicity caused by the crosslinking agent (that is, ferric ion) and chemically modified polymers continue as a pending question for their wide application in clinical practices.…”
Section: Discussionmentioning
confidence: 99%
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