Effect of Surface Chemistry on Hemolysis, Thrombogenicity, and Toxicity of Carbon Nanotube Doped Thermally Sprayed Hydroxyapatite Implants

dc.contributor.authorShankar, D.
dc.contributor.authorJambagi, S.C.
dc.contributor.authorGowda, N.
dc.contributor.authorLakshmi, K.S.
dc.contributor.authorJayanthi, K.J.
dc.contributor.authorChaudhary, V.K.
dc.date.accessioned2026-02-04T12:25:04Z
dc.date.issued2024
dc.description.abstractAssessing blood compatibility is crucial before in vivo procedures and is considered more reliable than many in vitro tests. This study examines the physiochemical properties and blood compatibility of bioactive powders ((0.5-2 wt % carbon nanotube (CNT)/alumina)-20 wt %)) produced through a heterocoagulation colloidal technique followed by ball milling with hydroxyapatite (HAp). The 1 wt % CNT composite demonstrated a surface charge ∼5 times higher than HAp at pH 7.4, with a value of −11 mV compared to −2 mV. This increase in electrostatic charge is desirable for achieving hemocompatibility, as evidenced by a range of blood compatibility assessments, including hemolysis, blood clotting, platelet adhesion, platelet activation, and coagulation assays (prothrombin time (PT) and activated partial thrombin time (aPTT)). The 1 wt % CNT composite exhibited hemolysis ranging from 2 to 7%, indicating its hemocompatibility. In the blood clot investigation, the absorbance values for 1-2 wt % CNT samples were 0.927 ± 0.038 and 1.184 ± 0.128, respectively, indicating their nonthrombogenicity. Additionally, the percentage of platelet adhered on the 1 wt % CNT sample (∼5.67%) showed a ∼2.5-fold decrement compared to the clinically used negative control, polypropylene (∼13.73%). The PT and aPTT experiments showed no difference in the coagulation time for CNT samples even at higher concentrations, unlike HAC2 (80 mg). In conclusion, the 1 wt % CNT sample was nontoxic to human blood, making it more hemocompatible, nonhemolytic, and nonthrombogenic than other samples. This reliable study reduces the need for additional in vitro and in vivo studies before clinical trials, saving time and cost. © 2024 American Chemical Society.
dc.identifier.citationACS Biomaterials Science and Engineering, 2024, 10, 3, pp. 1403-1417
dc.identifier.urihttps://doi.org/10.1021/acsbiomaterials.3c00912
dc.identifier.urihttps://idr.nitk.ac.in/handle/123456789/21234
dc.publisherAmerican Chemical Society
dc.subjectBall milling
dc.subjectCoagulation
dc.subjectElectrostatics
dc.subjectHydroxyapatite
dc.subjectPlatelets
dc.subjectPolypropylenes
dc.subjectSols
dc.subjectSurface chemistry
dc.subjectBlood compatibility
dc.subjectCarbon nanotubes composites
dc.subjectHaemocompatibility
dc.subjectHaemolysis
dc.subjectHetero-coagulation
dc.subjectHigh velocity oxy fuel
dc.subjectHydroxyapatite implants
dc.subjectProthrombin time
dc.subjectThrombin time
dc.subjectThrombogenicity
dc.subjectCarbon nanotubes
dc.subjectbioceramics
dc.subjectcarbon nanotube
dc.subjecthydroxyapatite
dc.subjectpolypropylene
dc.subjectactivated partial thromboplastin time
dc.subjectArticle
dc.subjectblood clotting
dc.subjectblood compatibility
dc.subjectcontrolled study
dc.subjectcrystal structure
dc.subjectfield emission scanning electron microscopy
dc.subjectFourier transform infrared spectroscopy
dc.subjecthemolysis
dc.subjecthuman
dc.subjectin vitro study
dc.subjectin vivo study
dc.subjectnonhuman
dc.subjectplatelet count
dc.subjectprothrombin time
dc.subjectRaman spectrometry
dc.subjectstatic electricity
dc.subjectsurface area
dc.subjectsurface charge
dc.subjectsurface property
dc.subjectthrombin time
dc.subjectthrombocyte activation
dc.subjectthrombocyte adhesion
dc.subjectthrombocyte rich plasma
dc.subjectthrombogenicity
dc.subjecttoxicity
dc.subjectzeta potential
dc.subjectchemistry
dc.subjectthrombocyte
dc.subjectBlood Platelets
dc.subjectDurapatite
dc.subjectHemolysis
dc.subjectHumans
dc.subjectNanotubes, Carbon
dc.subjectPlatelet Adhesiveness
dc.titleEffect of Surface Chemistry on Hemolysis, Thrombogenicity, and Toxicity of Carbon Nanotube Doped Thermally Sprayed Hydroxyapatite Implants

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