TY - JOUR
T1 - Artificial Dense Granules
T2 - A Procoagulant Liposomal Formulation Modeled after Platelet Polyphosphate Storage Pools
AU - Donovan, Alexander J.
AU - Kalkowski, Joseph
AU - Szymusiak, Magdalena
AU - Wang, Canhui
AU - Smith, Stephanie A.
AU - Klie, Robert F.
AU - Morrissey, James H.
AU - Liu, Ying
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/8/8
Y1 - 2016/8/8
N2 - Granular platelet-sized polyphosphate nanoparticles (polyP NPs) were encapsulated in sterically stabilized liposomes, forming a potential, targeted procoagulant nanotherapy resembling human platelet dense granules in both structure and functionality. Dynamic light scattering (DLS) measurements reveal that artificial dense granules (ADGs) are colloidally stable and that the granular polyP NPs are encapsulated at high efficiencies. High-resolution scanning transmission electron microscopy (HR-STEM) indicates that the ADGs are monodisperse particles with a 150 nm diameter dense core consisting of P, Ca, and O surrounded by a corrugated 25 nm thick shell containing P, C, and O. Further, the ADGs manifest promising procoagulant activity: Detergent solubilization by Tween 20 or digestion of the lipid envelope by phospholipase C (PLC) allows for ADGs to trigger autoactivation of Factor XII (FXII), the first proteolytic step in the activation of the contact pathway of clotting. Moreover, ADGs' ability to reduce the clotting time of human plasma in the presence of PLC further demonstrate the feasibility to develop ADGs into a potential procoagulant nanomedicine.
AB - Granular platelet-sized polyphosphate nanoparticles (polyP NPs) were encapsulated in sterically stabilized liposomes, forming a potential, targeted procoagulant nanotherapy resembling human platelet dense granules in both structure and functionality. Dynamic light scattering (DLS) measurements reveal that artificial dense granules (ADGs) are colloidally stable and that the granular polyP NPs are encapsulated at high efficiencies. High-resolution scanning transmission electron microscopy (HR-STEM) indicates that the ADGs are monodisperse particles with a 150 nm diameter dense core consisting of P, Ca, and O surrounded by a corrugated 25 nm thick shell containing P, C, and O. Further, the ADGs manifest promising procoagulant activity: Detergent solubilization by Tween 20 or digestion of the lipid envelope by phospholipase C (PLC) allows for ADGs to trigger autoactivation of Factor XII (FXII), the first proteolytic step in the activation of the contact pathway of clotting. Moreover, ADGs' ability to reduce the clotting time of human plasma in the presence of PLC further demonstrate the feasibility to develop ADGs into a potential procoagulant nanomedicine.
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U2 - 10.1021/acs.biomac.6b00577
DO - 10.1021/acs.biomac.6b00577
M3 - Article
C2 - 27405511
AN - SCOPUS:84981215085
SN - 1525-7797
VL - 17
SP - 2572
EP - 2581
JO - Biomacromolecules
JF - Biomacromolecules
IS - 8
ER -