2003
DOI: 10.1016/s0006-291x(03)00943-4
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Hemostatic effects of polymerized albumin particles bearing rGPIa/IIa in thrombocytopenic mice

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Cited by 25 publications
(16 citation statements)
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“…To prepare the PLT substitutes enhancing the hemostatic ability, we also conjugated fibrinogen 17 to biocompatible carriers such as polymerized albumin particles (polyAlb) 18,19 and phospholipid vesicles (liposomes) 20‐24 . These fibrinogen conjugates were shown to facilitate PLT aggregation on an activated PLT‐immobilized surface in vitro by recruitment of the flowing PLTs in the aggregates after their attachment 17 .…”
mentioning
confidence: 99%
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“…To prepare the PLT substitutes enhancing the hemostatic ability, we also conjugated fibrinogen 17 to biocompatible carriers such as polymerized albumin particles (polyAlb) 18,19 and phospholipid vesicles (liposomes) 20‐24 . These fibrinogen conjugates were shown to facilitate PLT aggregation on an activated PLT‐immobilized surface in vitro by recruitment of the flowing PLTs in the aggregates after their attachment 17 .…”
mentioning
confidence: 99%
“…14,15 This is because fibrinogen contains three putative binding sites to GPIIb/IIIa, namely, a tetrapeptide containing an RGD sequence, for example, RGDF and RGDS at a95-98 and a572-575, respectively, and a dodecapeptide (HHLGGAKQAGDV, H12) at a a-chain carboxyterminal segment (a400-411). 16 To prepare the PLT substitutes enhancing the hemostatic ability, we also conjugated fibrinogen 17 to biocompatible carriers such as polymerized albumin particles (polyAlb) 18,19 and phospholipid vesicles (liposomes). [20][21][22][23][24] These fibrinogen conjugates were shown to facilitate PLT aggregation on an activated PLT-immobilized surface in vitro by recruitment of the flowing PLTs in the aggregates after their attachment.…”
mentioning
confidence: 99%
“…Some research groups have focused on developing hemostatic materials based on functionalized nanoparticles capable of aggregating platelets from blood flow [108111]. For example, Ravikumar et al created hemostatic nanomaterials through the surface functionalization of liposomes with 150 nm diameters with three peptides including von Willebrand factor (vWF)-binding peptide (VBP), collagen-binding peptide (CBP) and cyclic-Arg-Gly-Asp (cRGD) peptide [109].…”
Section: Nanoparticle Incorporated Surgical Materialsmentioning
confidence: 99%
“…We have developed biocompatible and biodegradable nanoparticles such as albumin-based nanoparticles [2][3][4][5] and phospholipid vesicles 6,7 carrying recombi-nant fragments of platelet membrane proteins 3,4,6,8 and dodecapeptide as a recognition site for fibrinogen. 2,5,7,9 These nanoparticles specifically recognized the site of bleeding injury or activated platelets.…”
Section: Introductionmentioning
confidence: 99%