Shankar, D.Jambagi, S.C.Gowda, N.Lakshmi, K.S.Jayanthi, K.J.Chaudhary, V.K.2026-02-042024ACS Biomaterials Science and Engineering, 2024, 10, 3, pp. 1403-1417https://doi.org/10.1021/acsbiomaterials.3c00912https://idr.nitk.ac.in/handle/123456789/21234Assessing 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.Ball millingCoagulationElectrostaticsHydroxyapatitePlateletsPolypropylenesSolsSurface chemistryBlood compatibilityCarbon nanotubes compositesHaemocompatibilityHaemolysisHetero-coagulationHigh velocity oxy fuelHydroxyapatite implantsProthrombin timeThrombin timeThrombogenicityCarbon nanotubesbioceramicscarbon nanotubehydroxyapatitepolypropyleneactivated partial thromboplastin timeArticleblood clottingblood compatibilitycontrolled studycrystal structurefield emission scanning electron microscopyFourier transform infrared spectroscopyhemolysishumanin vitro studyin vivo studynonhumanplatelet countprothrombin timeRaman spectrometrystatic electricitysurface areasurface chargesurface propertythrombin timethrombocyte activationthrombocyte adhesionthrombocyte rich plasmathrombogenicitytoxicityzeta potentialchemistrythrombocyteBlood PlateletsDurapatiteHemolysisHumansNanotubes, CarbonPlatelet Adhesiveness