Local and Systemic In Vivo Responses to Osseointegrative Titanium Nanotube Surfaces
Orthopedic implants requiring osseointegration are often surface modified; however, implants may shed these coatings and generate wear debris leading to complications. Titanium nanotubes (TiNT), a new surface treatment, may promote osseointegration. In this study, in vitro (rat marrow-derived bone m...
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Published in: | Nanomaterials (Basel, Switzerland) Vol. 11; no. 3; p. 583 |
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Abstract | Orthopedic implants requiring osseointegration are often surface modified; however, implants may shed these coatings and generate wear debris leading to complications. Titanium nanotubes (TiNT), a new surface treatment, may promote osseointegration. In this study, in vitro (rat marrow-derived bone marrow cell attachment and morphology) and in vivo (rat model of intramedullary fixation) experiments characterized local and systemic responses of two TiNT surface morphologies, aligned and trabecular, via animal and remote organ weight, metal ion, hematologic, and nondecalcified histologic analyses. In vitro experiments showed total adherent cells on trabecular and aligned TiNT surfaces were greater than control at 30 min and 4 h, and cells were smaller in diameter and more eccentric. Control animals gained more weight, on average; however, no animals met the institutional trigger for weight loss. No hematologic parameters (complete blood count with differential) were significantly different for TiNT groups vs. control. Inductively coupled plasma mass spectrometry (ICP-MS) showed greater aluminum levels in the lungs of the trabecular TiNT group than in those of the controls. Histologic analysis demonstrated no inflammatory infiltrate, cytotoxic, or necrotic conditions in proximity of K-wires. There were significantly fewer eosinophils/basophils and neutrophils in the distal region of trabecular TiNT-implanted femora; and, in the midshaft of aligned TiNT-implanted femora, there were significantly fewer foreign body giant/multinucleated cells and neutrophils, indicating a decreased immune response in aligned TiNT-implanted femora compared to controls. |
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AbstractList | Orthopedic implants requiring osseointegration are often surface modified; however, implants may shed these coatings and generate wear debris leading to complications. Titanium nanotubes (TiNT), a new surface treatment, may promote osseointegration. In this study, in vitro (rat marrow-derived bone marrow cell attachment and morphology) and in vivo (rat model of intramedullary fixation) experiments characterized local and systemic responses of two TiNT surface morphologies, aligned and trabecular, via animal and remote organ weight, metal ion, hematologic, and nondecalcified histologic analyses. In vitro experiments showed total adherent cells on trabecular and aligned TiNT surfaces were greater than control at 30 min and 4 h, and cells were smaller in diameter and more eccentric. Control animals gained more weight, on average; however, no animals met the institutional trigger for weight loss. No hematologic parameters (complete blood count with differential) were significantly different for TiNT groups vs. control. Inductively coupled plasma mass spectrometry (ICP-MS) showed greater aluminum levels in the lungs of the trabecular TiNT group than in those of the controls. Histologic analysis demonstrated no inflammatory infiltrate, cytotoxic, or necrotic conditions in proximity of K-wires. There were significantly fewer eosinophils/basophils and neutrophils in the distal region of trabecular TiNT-implanted femora; and, in the midshaft of aligned TiNT-implanted femora, there were significantly fewer foreign body giant/multinucleated cells and neutrophils, indicating a decreased immune response in aligned TiNT-implanted femora compared to controls. |
Author | Baker, Erin A Fortin, Paul T Vara, Alexander D Fleischer, Mackenzie M Friedrich, Craig R Salisbury, Meagan R Baker, Kevin C |
AuthorAffiliation | 2 Department of Mechanical Engineering-Engineering Mechanics, Michigan Technological University, Houghton, MI 49931, USA; craig@mtu.edu 3 Department of Orthopaedic Surgery, Oakland University William Beaumont School of Medicine, Rochester, MI 48309, USA 1 Departments of Orthopaedic Research and Surgery, Beaumont Health, Royal Oak, MI 48073, USA; mackenzie.fleischer@beaumont.org (M.M.F.); alexdvara@gmail.com (A.D.V.); meagan.salisbury@beaumont.org (M.R.S.); kevin.baker@beaumont.org (K.C.B.); paul.fortin@beaumont.org (P.T.F.) |
AuthorAffiliation_xml | – name: 2 Department of Mechanical Engineering-Engineering Mechanics, Michigan Technological University, Houghton, MI 49931, USA; craig@mtu.edu – name: 3 Department of Orthopaedic Surgery, Oakland University William Beaumont School of Medicine, Rochester, MI 48309, USA – name: 1 Departments of Orthopaedic Research and Surgery, Beaumont Health, Royal Oak, MI 48073, USA; mackenzie.fleischer@beaumont.org (M.M.F.); alexdvara@gmail.com (A.D.V.); meagan.salisbury@beaumont.org (M.R.S.); kevin.baker@beaumont.org (K.C.B.); paul.fortin@beaumont.org (P.T.F.) |
Author_xml | – sequence: 1 givenname: Erin A orcidid: 0000-0003-2415-6053 surname: Baker fullname: Baker, Erin A organization: Department of Orthopaedic Surgery, Oakland University William Beaumont School of Medicine, Rochester, MI 48309, USA – sequence: 2 givenname: Mackenzie M surname: Fleischer fullname: Fleischer, Mackenzie M organization: Departments of Orthopaedic Research and Surgery, Beaumont Health, Royal Oak, MI 48073, USA – sequence: 3 givenname: Alexander D surname: Vara fullname: Vara, Alexander D organization: Departments of Orthopaedic Research and Surgery, Beaumont Health, Royal Oak, MI 48073, USA – sequence: 4 givenname: Meagan R surname: Salisbury fullname: Salisbury, Meagan R organization: Departments of Orthopaedic Research and Surgery, Beaumont Health, Royal Oak, MI 48073, USA – sequence: 5 givenname: Kevin C surname: Baker fullname: Baker, Kevin C organization: Department of Orthopaedic Surgery, Oakland University William Beaumont School of Medicine, Rochester, MI 48309, USA – sequence: 6 givenname: Paul T surname: Fortin fullname: Fortin, Paul T organization: Department of Orthopaedic Surgery, Oakland University William Beaumont School of Medicine, Rochester, MI 48309, USA – sequence: 7 givenname: Craig R surname: Friedrich fullname: Friedrich, Craig R organization: Department of Mechanical Engineering-Engineering Mechanics, Michigan Technological University, Houghton, MI 49931, USA |
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CitedBy_id | crossref_primary_10_3390_nano12111923 crossref_primary_10_3390_app12136793 crossref_primary_10_1186_s43088_023_00363_y crossref_primary_10_1016_j_msec_2021_112513 |
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Keywords | nanomedicine nanomodified surfaces orthopedic animal model immune response |
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Title | Local and Systemic In Vivo Responses to Osseointegrative Titanium Nanotube Surfaces |
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