In vitro capacity of different grades of chitosan derivatives to induce platelet adhesion and aggregation

► Chitosan. ► Platelet adhesion. ► Platelet count. ► Morphology. ► Platelet aggregation. Chitosan-derived hemostatic agents with various formulations may have distinct potential in hemostasis. This study assessed the ability of different grades and forms of chitosan derivatives as hemostatic agents...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of biological macromolecules 2013-01, Vol.52, p.244-249
Hauptverfasser: Periayah, Mercy Halleluyah, Halim, Ahmad Sukari, Hussein, Abdul Rahim, Mat Saad, Arman Zaharil, Abdul Rashid, Ahmad Hazri, Noorsal, Kartini
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:► Chitosan. ► Platelet adhesion. ► Platelet count. ► Morphology. ► Platelet aggregation. Chitosan-derived hemostatic agents with various formulations may have distinct potential in hemostasis. This study assessed the ability of different grades and forms of chitosan derivatives as hemostatic agents to enhance platelet adhesion and aggregation in vitro. The chitosan derivatives utilized were 2% NO-CMC, 7% NO-CMC (with 0.45mL collagen), 8% NO-CMC, O-C 52, 5% O-CMC-47, NO-CMC-35, and O-C 53. Samples of chitosan derivatives weighing 5mg were incubated at 37°C with 50μL of phosphate buffer saline (PBS) (pH 7.4) for 60min. The morphological features of the platelets upon adherence to the chitosan were viewed using scanning electron microscope (SEM), and the platelet count was analyzed with an Automated Hematology Analyzer. For platelet aggregation, we added an adenosine diphosphate (ADP) agonist to induce the chitosan-adhered platelets. O-C 52 bound with platelets exhibited platelet aggregates and clumps on the surface of the membrane layer with approximately 70–80% coverage. A statistically significant correlation (p
ISSN:0141-8130
1879-0003
DOI:10.1016/j.ijbiomac.2012.10.001