lllin000_PaperForge/audit/28ALPCY7/block_trace.csv

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412headerSubscriber access provided by University of Glasgow Library[685.0, 195.0, 1120.0, 216.0]noise0.9["header label"]noise0.9frontmatter_main_zonesupport_likenoneFalseFalse
513textTissue Engineering and Regenerative Medicine[86.0, 219.0, 640.0, 251.0]authors0.8["page-1 zone author_zone: Tissue Engineering and Regenerative Medicine"]authors0.8frontmatter_main_zonesupport_likenoneTrueTrue
614doc_title3D-printed #- tricalcium phosphate scaffold combined with a pulse electromagnetic field promotes the repair of skull defects in rats[134.0, 263.0, 1055.0, 328.0]paper_title0.8["page-1 zone title_zone: 3D-printed #- tricalcium phosphate scaffold combined with a "]paper_title0.8frontmatter_main_zonesupport_likenoneTrueTrue
715textHaifeng Liang, Xiao Liu, Ying Pi, Qiang Yu, Yukun Yin, Xian Li, Yipei Yang, and Jing Tian[153.0, 335.0, 1036.0, 364.0]authors0.8["page-1 zone author_zone: Haifeng Liang, Xiao Liu, Ying Pi, Qiang Yu, Yukun Yin, Xian "]authors0.8frontmatter_main_zonesupport_likenoneTrueTrue
816textACS Biomater. Sci. Eng., Just Accepted Manuscript • DOI: 10.1021/acsbiomaterials.9b00858 • Publication Date (Web): 03 Sep 2019[308.0, 369.0, 874.0, 414.0]frontmatter_noise0.8["page-1 zone journal_furniture_zone: ACS Biomater. Sci. Eng., Just Accepted Manuscript \u2022 DOI: 10."]frontmatter_noise0.8frontmatter_main_zonesupport_likenoneFalseFalse
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1018paragraph_titleJust Accepted[124.0, 515.0, 281.0, 541.0]frontmatter_noise0.8["page-1 zone journal_furniture_zone: Just Accepted"]frontmatter_noise0.8frontmatter_main_zoneheading_likeshort_fragmentFalseFalse
1119abstract“Just Accepted” manuscripts have been peer-reviewed and accepted for publication. They are posted online prior to technical editing, formatting for publication and author proofing. The American Chemic[132.0, 564.0, 1058.0, 883.0]unknown_structural0.85["abstract label from Paddle OCR"]abstract_body0.85frontmatter_main_zonesupport_likenoneFalseTrue
12110footeris published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036[591.0, 1562.0, 1071.0, 1595.0]noise0.9["footer label"]noise0.9frontmatter_main_zonesupport_likenoneFalseFalse
13111footerPublished by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth[590.0, 1597.0, 1113.0, 1665.0]noise0.9["footer label"]noise0.9frontmatter_main_zonesupport_likenoneFalseFalse
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1622headerACS Biomaterials Science & Engineering[426.0, 18.0, 764.0, 45.0]noise0.9["header label"]noise0.9frontmatter_side_zonesupport_likenoneFalseFalse
1723doc_title3D-printed $ \beta $-tricalcium phosphate scaffold combined with a pulse electromagnetic field promotes the repair of skull defects in rats[191.0, 182.0, 1000.0, 344.0]unknown_structural0.8["page-1 zone title_zone: 3D-printed $ \\beta $-tricalcium phosphate scaffold combined"]paper_title0.8body_zonebody_likenoneFalseTrue
1824textHaifeng Liang $ ^{a} $, Xiao Liu $ ^{b} $, Ying Pi $ ^{a} $, Qiang Yu $ ^{a} $, Yukun Yin $ ^{a} $, Xian Li $ ^{a} $, Yipei Yang $ ^{a} $, Jing Tian $ ^{*a} $[174.0, 380.0, 946.0, 408.0]unknown_structural0.8["page-1 zone author_zone: Haifeng Liang $ ^{a} $, Xiao Liu $ ^{b} $, Ying Pi $ ^{a} $,"]authors0.8body_zonebody_likenoneFalseTrue
1925texta Department of Orthopedics, Zhujiang Hospital, Southern Medical University, No. 253 Industrial Avenue, Haizhu, Guangzhou 510280, People's Republic of China[174.0, 443.0, 1015.0, 533.0]affiliation0.8["page-1 zone affiliation_zone: a Department of Orthopedics, Zhujiang Hospital, Southern Med"]affiliation0.8body_zonebody_likenoneTrueTrue
2026text $ ^{b} $ School of Materials Science and Engineering, South China University of Technology, Wushan, Guangzhou 510640, People's Republic of China[173.0, 568.0, 1015.0, 657.0]affiliation0.8["page-1 zone affiliation_zone: $ ^{b} $ School of Materials Science and Engineering, South "]affiliation0.8body_zonebody_likeaffiliation_markerTrueTrue
2127text*Corresponding author: Jing Tian, Email: tianjing_ortho@163.com[176.0, 693.0, 748.0, 720.0]frontmatter_support0.78["first-surviving-page support text: *Corresponding author: Jing Tian, Email: tianjing_ortho@163."]frontmatter_support0.78frontmatter_side_zonesupport_likenoneTrueTrue
2228paragraph_titleABSTRACT[175.0, 815.0, 277.0, 842.0]abstract_heading0.95["abstract heading"]abstract_heading0.95frontmatter_side_zoneheading_likeshort_fragmentTrueTrue
2329abstractTrauma, infection, cancer and congenital diseases can lead to bone defects. The combination of 3D printing with biomaterials is of great significance in the treatment of bone defects. In addition, pul[174.0, 880.0, 1017.0, 1533.0]abstract_body0.85["abstract label from Paddle OCR"]abstract_body0.85body_zonebody_likenoneTrueTrue
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2833textproliferation and differentiation of rADSCs and the repair of a critical defect in the rat skull. Therefore, the combination of $ \beta $-TCP and PEMF with 3D printing technology can provide better t[175.0, 164.0, 1015.0, 316.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
2934textKEYWORDS: 3D printing; $ \beta $-tricalcium phosphate; pulse electromagnetic field; bone defect[175.0, 476.0, 953.0, 502.0]structured_insert0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneFalseFalse
3035paragraph_titleINTRODUCTION[176.0, 664.0, 311.0, 687.0]section_heading0.9["explicit scholarly heading: INTRODUCTION"]section_heading0.9body_zoneheading_likecanonical_section_nameTrueTrue
3136textPulse electromagnetic fields (PEMFs) are transient electromagnetic fields produced in a coil when a pulse current generated by a pulse generator passes through the coil. The strength and frequency of [173.0, 726.0, 1017.0, 1503.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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3643textPEMFs have a "window effect" $ ^{39} $; that is, the field strength, frequency and action time of PEMFs do not have linear relationships with the biological effects observed in cells. The field streng[171.0, 162.0, 1019.0, 1504.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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4153textnonunion and other orthopedic diseases, it is rarely used to treat bone defects. Prior to this study, we demonstrated that PEMF therapy (50 Hz, 1 mT) can promote the proliferation and osteogenic diffe[174.0, 166.0, 1017.0, 441.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
4254textThe treatment of bone defects has always been a clinical problem, and the gold standard for treatment is autografts. However, bone transplantation has disadvantages such as few available sources, a la[173.0, 476.0, 1017.0, 1504.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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4763textalso contains a porous structure design and rapid prototyping technology to provide space for osteoblast growth and vascular formation and to shorten the whole transplantation process. The combination[175.0, 166.0, 1016.0, 380.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
4864paragraph_titleMATERIALS AND METHODS[176.0, 539.0, 423.0, 562.0]section_heading0.9["explicit scholarly heading: MATERIALS AND METHODS"]section_heading0.9body_zoneheading_likecanonical_section_nameTrueTrue
4965paragraph_titleFabrication and characterization of $ \beta $-TCP scaffolds[176.0, 601.0, 626.0, 625.0]subsection_heading0.6["unnumbered paragraph_title, inferred level subsection_heading: Fabrication and characterization of $ \\beta $-TCP scaffolds"]subsection_heading0.6body_zoneheading_likenoneTrueTrue
5066textThe β-TCP scaffolds were fabricated as previously described $ ^{33} $. Briefly, β-TCP powder was prepared using the chemical precipitation method. Then, ammonium polyacrylate (PAA-NH4) and hydroxyprop[174.0, 663.0, 1016.0, 1502.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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5573textvolume of the $ \beta $-TCP scaffolds was reduced to 90% after sintering. The design of the scaffold was completed by the CAD software SolidWorks (Massachusetts, USA). The scaffold was coated with go[174.0, 164.0, 1015.0, 317.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
5674paragraph_titleCell culture and PEMF treatment[176.0, 352.0, 470.0, 376.0]subsection_heading0.6["unnumbered paragraph_title, inferred level subsection_heading: Cell culture and PEMF treatment"]subsection_heading0.6body_zoneheading_likenoneTrueTrue
5775textADSCs were obtained from the groin of 3-day-old Sprague Dawley rats. The cells were cultured on Dulbecco's minimum Eagle's medium (DMEM, Gibco) with 10% fetal bovine serum (FBS, Gibco) and 5% antibiot[174.0, 415.0, 1016.0, 628.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
5876textThe prepared cells were randomly divided into four groups and seeded on tissue culture plates (TCPS) or $ \beta $-TCP scaffolds. The LIVE/DEAD Cell Staining Kit (BioVision, Inc.) was applied to rADSC[173.0, 665.0, 1016.0, 940.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
5977textThe PEMF device (Yongyikeji, Hunan, China) consisted of a generator and its connected coils. When the generator produces a pulse current of a certain intensity, a PEMF will be generated between the co[173.0, 977.0, 1016.0, 1377.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
6078paragraph_titleCCK-8 and LIVE/DEAD cell staining[176.0, 1475.0, 480.0, 1499.0]subsection_heading0.6["unnumbered paragraph_title, inferred level subsection_heading: CCK-8 and LIVE/DEAD cell staining"]subsection_heading0.6body_zoneheading_likenoneTrueTrue
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6583textThe CCK-8 assay was performed to evaluate the proliferation of ADSCs under the influence of PEMF and the scaffolds. rADSCs were cultured in basic culture medium for 1, 4 or 7 days on TCPS and $ \beta[173.0, 165.0, 1016.0, 563.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
6684textLIVE/DEAD cell staining was performed to evaluate the cytotoxicity of the $ \beta $-TCP scaffolds. Each scaffold was washed twice with PBS after 24, 48 and 72 hours, before the working solution was a[174.0, 601.0, 1016.0, 878.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
6785paragraph_titleALP activity and osteogenesis - related gene expression[175.0, 913.0, 661.0, 938.0]subsection_heading0.6["unnumbered paragraph_title, inferred level subsection_heading: ALP activity and osteogenesis - related gene expression"]subsection_heading0.6body_zoneheading_likenoneTrueTrue
6886textTo evaluate the osteogenic differentiation of ADSCs, cellular ALP activity was accessed with an alkaline phosphatase assay kit (A059-1, Nanjing Jiancheng Bioengineering Institute, China) after 7 or 14[174.0, 978.0, 1017.0, 1503.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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7393textwas completed with the cALP Stain Kit (D001-1-1, Nanjing Jiancheng Bioengineering Institute, China).[174.0, 164.0, 1015.0, 254.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
7494textThe expression of osteogenesis-related genes in the four groups was evaluated by SYBR Green Real-Time PCR (Thermo Fisher Scientific, Waltham, MA, USA). Total RNA of the ADSCs of the four groups was is[173.0, 289.0, 1017.0, 818.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
7595figure_titleTable 1. Primer sequences used for qRT-PCR.[197.0, 851.0, 587.0, 877.0]table_caption0.9["table prefix matched: Table 1. Primer sequences used for qRT-PCR."]table_caption0.9display_zonetable_caption_liketable_numberTrueTrue
7696table<table><tr><td>Gene</td><td>Forward(5-3)</td><td>Reverse(5-3)</td></tr><tr><td>ALP</td><td>ACCATTCCCACGTCTTCACATTT</td><td>AGACATTCTCTCGTTCACCGCC</td></tr><tr><td>RUNX2</td><td>ACTTCCTGTGCTCGGTGCT[204.0, 911.0, 979.0, 1110.0]table_html0.85["media label: table"]media_asset0.85body_zoneunknown_likenoneTrueTrue
7797paragraph_titleSurgical operation and PEMF treatment[175.0, 1163.0, 529.0, 1188.0]subsection_heading0.6["unnumbered paragraph_title, inferred level subsection_heading: Surgical operation and PEMF treatment"]subsection_heading0.6body_zoneheading_likenoneTrueTrue
7898textAll the surgical operations were approved by the Ethics Committee of Southern Medical University. Eighteen female Sprague-Dawley rats (180-200 g) were anesthetized with chloral hydrate (300 mg/kg body[173.0, 1225.0, 1017.0, 1502.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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83103textmm, on both sides of the parietal bone; physiological saline was added dropwise to help reduce the increase in temperature from the drill. A size matched scaffold, with a diameter of 4.8 mm and a heig[173.0, 166.0, 1017.0, 441.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
84104textOn the third day after the operation, the 18 SD rats were randomly divided into 2 groups. One group was treated with PEMF (50 Hz, 1 mT, 2 hours per day), and the other group, as a control, did not rec[173.0, 476.0, 1017.0, 877.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
85105paragraph_titleMicro-CT[175.0, 912.0, 264.0, 936.0]sub_subsection_heading0.6["unnumbered paragraph_title, inferred level sub_subsection_heading: Micro-CT"]sub_subsection_heading0.6body_zoneheading_likeshort_fragmentTrueTrue
86106textThe skulls were placed into an X-ray CT scanner for experimental animals (Latheta LCT-200) and scanned with a resolution of 18 $ \mu $m. DICOM images were obtained. Bone mineral density was analyzed [173.0, 975.0, 1017.0, 1249.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
87107paragraph_titleHistological examination[176.0, 1288.0, 400.0, 1313.0]subsection_heading0.6["unnumbered paragraph_title, inferred level subsection_heading: Histological examination"]subsection_heading0.6body_zoneheading_likenoneTrueTrue
88108textThe free skulls were fixed with formalin for 24 hours and then decalcified with EDTA decalcifying solution (Solarbio, China) for 14 days. The decalcified samples were dehydrated by gradient alcohol an[173.0, 1349.0, 1017.0, 1502.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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93113texttissue sections. Hematoxylin-eosin staining of the sections was used to stain the nucleus blue and the cytoplasm red.[174.0, 164.0, 1014.0, 253.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
94114paragraph_titleStatistics[176.0, 289.0, 262.0, 312.0]sub_subsection_heading0.6["unnumbered paragraph_title, inferred level sub_subsection_heading: Statistics"]sub_subsection_heading0.6body_zoneheading_likeshort_fragmentTrueTrue
95115textThe statistical analyses of this study were completed with SPSS software (Version 20.0). All biological experiments in this study were repeated at least three times. The data were analyzed by one-way [174.0, 352.0, 1015.0, 568.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
96116paragraph_titleRESULTS AND DISCUSSION[176.0, 725.0, 415.0, 749.0]section_heading0.9["explicit scholarly heading: RESULTS AND DISCUSSION"]section_heading0.9body_zoneheading_likecanonical_section_nameTrueTrue
97117paragraph_titleβ-TCP scaffold characterization[176.0, 788.0, 454.0, 812.0]subsection_heading0.6["unnumbered paragraph_title, inferred level subsection_heading: \u03b2-TCP scaffold characterization"]subsection_heading0.6body_zoneheading_likenoneTrueTrue
98118textThe surface morphology of the fritted β-TCP scaffolds was observed by SEM (Figure 1a and 1b.), which showed that the structure of the scaffolds was arranged regularly with a bar that was 170±10 μm in [173.0, 851.0, 1017.0, 1252.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
99119textThe $ \beta $-TCP scaffolds produced by 3D printing technology had great porosity. This property can provide a large number of adhesion areas for cells. When used as a graft, high porosity scaffolds [174.0, 1289.0, 1015.0, 1502.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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103122headerACS Biomaterials Science & Engineering[426.0, 18.0, 764.0, 45.0]noise0.9["header label"]noise0.9body_zonebody_likenoneFalseFalse
104123vision_footnotebeneficial for osteogenesis and angiogenesis.[177.0, 163.0, 566.0, 189.0]footnote0.7["vision_footnote label: beneficial for osteogenesis and angiogenesis."]footnote0.7body_zonebody_likenoneTrueTrue
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109128figure_titleFigure 1. SEM images of 3D-printed β-TCP scaffolds: the top panels are (a) 100×, (b) 240× and show that the diameter of the bar is approximately 170±10 microns. The bars are arranged vertically, which[173.0, 943.0, 1016.0, 1159.0]figure_caption0.92["figure_title label: Figure 1. SEM images of 3D-printed \u03b2-TCP scaffolds: the top "]figure_caption0.92display_zonelegend_likefigure_numberTrueTrue
110129paragraph_titleLIVE/DEAD staining[175.0, 1256.0, 354.0, 1283.0]subsection_heading0.6["unnumbered paragraph_title, inferred level subsection_heading: LIVE/DEAD staining"]subsection_heading0.6body_zoneheading_likeshort_fragmentTrueTrue
1111210textTo determine the cytocompatibility and cytotoxicity of the scaffolds, we performed the LIVE/DEAD cell staining assay. As the results show (Figure 2.), living cells were dyed green, and dead cells were[173.0, 1319.0, 1017.0, 1534.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
1121211footerACS Paragon Plus Environment[462.0, 1601.0, 728.0, 1627.0]noise0.9["footer label"]noise0.9body_zonebody_likenoneFalseFalse
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115132numberPage 12 of 36[1059.0, 18.0, 1178.0, 44.0]noise0.9["page number label"]noise0.9body_zonebody_likeshort_fragmentFalseFalse
116133textmorphology of the rADSCs attached to the scaffold was observed. The ratios of live/dead rADSCs at 24, 48 and 72 hours were 4.36 (Figure 2a, 109/25), 5.81 (Figure 2b, 343/59) and 7.60 (Figure 2c, 251/3[172.0, 164.0, 1017.0, 441.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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1231310figure_titleFigure 2. LIVE/DEAD staining of rADSCs cultured on scaffolds in ordinary medium for 24, 48 or 72 hours. Live cells are stained green and dead cells are stained red. In the low power field of vision, t[173.0, 1318.0, 1019.0, 1533.0]figure_caption0.92["figure_title label: Figure 2. LIVE/DEAD staining of rADSCs cultured on scaffolds"]figure_caption0.92display_zonelegend_likefigure_numberTrueTrue
1241311footerACS Paragon Plus Environment[462.0, 1601.0, 728.0, 1627.0]noise0.9["footer label"]noise0.9body_zonebody_likenoneFalseFalse
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127142headerACS Biomaterials Science & Engineering[425.0, 18.0, 764.0, 45.0]noise0.9["header label"]noise0.9body_zonebody_likenoneFalseFalse
128143textof culture time. In the high-power field of vision, the living cells exhibit a state of expansion in the early stage (b) and elongation in the later stage (f).[173.0, 164.0, 1015.0, 254.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
129144paragraph_titleCCK-8 assay[175.0, 351.0, 288.0, 378.0]subsection_heading0.6["unnumbered paragraph_title, inferred level subsection_heading: CCK-8 assay"]subsection_heading0.6body_zoneheading_likeshort_fragmentTrueTrue
130145textAs shown in Figure 3, after one day of culture, the proliferation rate of the rADSCs cultured on the scaffold was significantly higher than that of the cells cultured on TCPS, but PEMF treatment had n[172.0, 415.0, 1018.0, 1317.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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133151headerACS Biomaterials Science & Engineering[425.0, 18.0, 764.0, 45.0]noise0.9["header label"]noise0.9body_zonebody_likenoneFalseFalse
134152numberPage 14 of 36[1059.0, 18.0, 1178.0, 43.0]noise0.9["page number label"]noise0.9body_zonebody_likeshort_fragmentFalseFalse
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136154figure_titleFigure 3. CCK-8 analysis after culture for 1, 4, or 7 days on TCPS or $ \beta $-TCP scaffolds. After 1 day of culture, the proliferation rate of rADSCs cultured on $ \beta $-TCP scaffolds was signif[172.0, 631.0, 1016.0, 1037.0]figure_caption0.92["figure_title label: Figure 3. CCK-8 analysis after culture for 1, 4, or 7 days o"]figure_caption0.92display_zonelegend_likefigure_numberTrueTrue
137155paragraph_titleALP activity and osteogenesis-related gene expression[175.0, 1132.0, 656.0, 1157.0]subsection_heading0.6["unnumbered paragraph_title, inferred level subsection_heading: ALP activity and osteogenesis-related gene expression"]subsection_heading0.6body_zoneheading_likenoneTrueTrue
138156textALP activity and ALP staining were used to assess the osteogenic differentiation of rADSCs in the four groups after 14 days of culture. As shown in Figure 4., the ALP activity of the $ \beta $-TCP+PE[173.0, 1194.0, 1018.0, 1472.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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144164figure_titleFigure 4. ALP activity analysis of rADSCs after culture in osteogenic induction medium for 14 days. The activity of ALP in the TCPS+PEMF and $ \beta $-TCP groups was similar, and a significant differ[173.0, 693.0, 1017.0, 973.0]figure_caption0.92["figure_title label: Figure 4. ALP activity analysis of rADSCs after culture in o"]figure_caption0.92display_zonelegend_likefigure_numberTrueTrue
145165textAreas of positive ALP staining are shown as purple. As seen from Figure 5a and 5c, the positive area of the TCPS+PEMF group is more disperse than that of the TCPS group, and the coloration is deeper. [174.0, 1070.0, 1016.0, 1344.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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154177figure_titleβ-TCP[348.0, 688.0, 421.0, 720.0]figure_caption_candidate0.85["figure_title label: \u03b2-TCP"]figure_caption0.85body_zoneunknown_likeshort_fragmentFalseFalse
155178figure_titleβ-TCP+PEMF[742.0, 687.0, 890.0, 720.0]figure_caption0.85["figure_title label: \u03b2-TCP+PEMF"]figure_caption0.85body_zoneunknown_likeshort_fragmentTrueTrue
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1571710image[610.0, 750.0, 1011.0, 1157.0]figure_asset0.85["media label: image"]media_asset0.85body_zoneunknown_likeemptyTrueTrue
1581711figure_titleFigure 5. ALP staining of rADSCs after culture in osteogenic induction medium for 14 days. (a), (b) rADSCs exposed to PEMF and cultured on TCPS. (c), (d) rADSCs not exposed to PEMF and cultured on TCP[172.0, 1192.0, 1016.0, 1408.0]figure_caption0.92["figure_title label: Figure 5. ALP staining of rADSCs after culture in osteogenic"]figure_caption0.92display_zonelegend_likefigure_numberTrueTrue
1591712textqRT-PCR was performed to detect the expression of osteoblast-related genes in cells. As[216.0, 1504.0, 1016.0, 1534.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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163182headerACS Biomaterials Science & Engineering[426.0, 18.0, 764.0, 45.0]noise0.9["header label"]noise0.9body_zonebody_likenoneFalseFalse
164183textshown in Figure 6a, the mean values of ALP and Runx2 expression were the highest in the $ \beta $-TCP+PEMF group after 7 days of culture, and there were significant differences among the groups. Ther[174.0, 166.0, 1017.0, 503.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
165184textOn the 14th day (Figure 6b.), the expression of ALP, Runx2 and OPN was highest in the $ \beta $-TCP+PEMF group and was significantly higher than that in the other three groups. The expression of OPN [174.0, 540.0, 1016.0, 753.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
166185textOn the 21st day (Figure 6c.), the expression of ALP, Runx2 and OPN in the $ \beta $-TCP+PEMF group was significantly higher than that in the other three groups, and the expression of ALP and Runx2 in[174.0, 788.0, 1016.0, 1004.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
167186textThe ALP activity assay showed that the ALP activity of the cells treated with PEMF was significantly increased, and the ALP activity of the cells treated with PEMF was similar to that of the cells tre[173.0, 1039.0, 1016.0, 1252.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
168187textA study by LeGeros, R $ Z^{32} $ et al. showed that calcium phosphate compounds have the following characteristics: similarity to the composition of bone minerals, ability to form a unique bone-calci[174.0, 1289.0, 1016.0, 1502.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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172192numberPage 18 of 36[1059.0, 18.0, 1178.0, 43.0]noise0.9["page number label"]noise0.9body_zonebody_likeshort_fragmentFalseFalse
173193textmechanism by which PEMFs can promote osteogenic differentiation is not completely clear. Wang et al. showed that PEMFs could stimulate osteoblast differentiation by stimulating the sAC-cAMP-PKA-CREB s[174.0, 165.0, 1017.0, 754.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
174194figure_titleALP[393.0, 796.0, 440.0, 822.0]figure_caption0.85["figure_title label: ALP"]figure_caption0.85body_zoneunknown_likeshort_fragmentTrueTrue
175195chart[196.0, 824.0, 587.0, 1134.0]media_asset0.85["media label: chart"]media_asset0.85body_zoneunknown_likeemptyTrueTrue
176196figure_titleRunx2[788.0, 796.0, 860.0, 823.0]figure_caption_candidate0.85["figure_title label: Runx2"]figure_caption0.85body_zoneunknown_likeshort_fragmentFalseFalse
177197chart[610.0, 828.0, 993.0, 1133.0]media_asset0.85["media label: chart"]media_asset0.85body_zoneunknown_likeemptyTrueTrue
178198figure_titleOPN[401.0, 1160.0, 451.0, 1187.0]figure_caption0.85["figure_title label: OPN"]figure_caption0.85body_zoneunknown_likeshort_fragmentTrueTrue
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184203figure_titleFigure 6. qRT-PCR analysis was used to evaluate the expression of osteogenesis-related genes in rADSCs cultured in osteogenic induction medium for 7, 14 or 21 days. (a) The expression of ALPin the $ [173.0, 165.0, 1017.0, 817.0]figure_caption0.92["figure_title label: Figure 6. qRT-PCR analysis was used to evaluate the expressi"]figure_caption0.92display_zonelegend_likefigure_numberTrueTrue
185204paragraph_titleMicro CT scanning and hematoxylin-eosin staining[175.0, 913.0, 621.0, 938.0]subsection_heading0.6["unnumbered paragraph_title, inferred level subsection_heading: Micro CT scanning and hematoxylin-eosin staining"]subsection_heading0.6body_zoneheading_likenoneTrueTrue
186205textAs shown in Figure 7, the bone defect site of the SD rats not treated with PEMF, especially the side without the scaffold, grew slowly and new bone appeared at the edge of the defect site at the eight[173.0, 978.0, 1016.0, 1441.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
187206textOsteogenic differentiation and angiogenesis are essential for bone regeneration. In addition[216.0, 1474.0, 1014.0, 1501.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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192213textto promoting the osteogenic differentiation of stem cells, PEMF therapy can also promote angiogenesis. Yen-Patton, G P $ ^{43} $ et al. used PEMFs to treat endothelial cells of the human umbilical vei[174.0, 165.0, 1017.0, 567.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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198224figure_titleFigure 7. 3D reconstruction of the imaging data of SD rats after 0, 4, 8 and 12 weeks of rearing. The rats in the PEMF group were treated with PEMFs for 2 hours per day, whereas the rats in the withou[173.0, 1161.0, 1015.0, 1315.0]figure_caption0.92["figure_title label: Figure 7. 3D reconstruction of the imaging data of SD rats a"]figure_caption0.92display_zonelegend_likefigure_numberTrueTrue
199225textBone mineral density (BMD) measurements of the new bone were determined in SD rats after 12 weeks. As shown in Figure 8, the highest BMD values were found in the cranial defects[172.0, 1412.0, 1017.0, 1502.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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201230aside_text1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60[9.0, 84.0, 42.0, 1531.0]noise0.95["margin-band narrow/tall geometry; treated as noise"]noise0.95reference_likereference_numeric_dotFalseFalse
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204233textof rats treated with the scaffold and PEMFs. The cranial defect of rats with the scaffold but without PEMF treatment followed closely. The blank group, which did not receive any treatments, had the lo[174.0, 164.0, 1016.0, 317.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
205234chart[208.0, 370.0, 988.0, 986.0]figure_asset0.85["media label: chart"]media_asset0.85body_zoneunknown_likeemptyTrueTrue
206235figure_titleFigure 8. Bone mineral density analysis based on micro-CT data was used to detect the growth of skull defects in SD rats after 12 weeks of rearing. The BMD values of the defect site of rats in the $ [173.0, 1038.0, 1016.0, 1314.0]figure_caption0.92["figure_title label: Figure 8. Bone mineral density analysis based on micro-CT da"]figure_caption0.92display_zonelegend_likefigure_numberTrueTrue
207236textThe results of the HE staining (Figure 9) showed that the implanted scaffold defects possessed good bone mass; however, the rats treated with PEMFs grew thicker bone tissue than[173.0, 1412.0, 1016.0, 1502.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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212243textthe rats who had not been treated with PEMFs. In the defect sites without $ \beta $-TCP scaffold implantation, the amount of new bone tissue was reduced, and the new bone tissue structure was more di[173.0, 164.0, 1016.0, 380.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
213244textThe BMD results of this study indicate that the BMD values of the defect sites of the rats treated with PEMFs were higher than those of the rats who did not receive PEMF treatment, regardless of wheth[174.0, 415.0, 1017.0, 878.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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234275figure_titleFigure 9. HE staining of the cranial defects of rats after 12 weeks of rearing. (A), (E) Rats[173.0, 1504.0, 1014.0, 1532.0]figure_caption0.92["figure_title label: Figure 9. HE staining of the cranial defects of rats after 1"]figure_caption0.92tail_nonref_hold_zonelegend_likefigure_numberTrueTrue
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239283textimplanted with a $ \beta $-TCP scaffold and exposed to PEMFs. (B), (F) Rats implanted with a $ \beta $-TCP scaffold and not exposed to PEMFs. (C), (G) Rats exposed to PEMFs. (D), (H) Rats not expose[175.0, 163.0, 1017.0, 314.0]body_paragraph0.6["default body_paragraph for text label", "promoted in tail spread from body_paragraph"]body_paragraph0.6body_zonebody_likenoneTrueTrue
240284paragraph_titleCONCLUSION[176.0, 475.0, 301.0, 500.0]section_heading0.9["explicit scholarly heading: CONCLUSION"]section_heading0.9body_zoneheading_likecanonical_section_nameTrueTrue
241285textTo summarize, 3D-printed $ \beta $-TCP porous scaffolds have excellent performance in the treatment of skull defects in rats. These scaffolds solve the problems associated with complications and limi[173.0, 541.0, 1018.0, 1253.0]body_paragraph0.6["default body_paragraph for text label", "promoted in tail spread from body_paragraph"]body_paragraph0.6body_zonebody_likenoneTrueTrue
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261303texttibial non-union. Interim results of a double-blind trial. LANCET 1984, 1, (8384), 994-6 (10) de Haas, W. G.;Beaupre, A.;Cameron, H.;English, E., The Canadian experience with pulsed magnetic fields in[175.0, 166.0, 1014.0, 374.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_likenoneTrueTrue
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306343textbioactive glass nanolayer-functionalized 3D-printed scaffolds for accelerating osteogenesis and angiogenesis. NANOSCALE 2015, 7, (45), 19207-21. DOI:10.1039/c5nr05421d[175.0, 165.0, 1013.0, 253.0]body_paragraph0.6["default body_paragraph for text label"]body_paragraph0.6body_likenoneTrueTrue
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320355text(44) Tepper, O. M.; Callaghan, M. J.; Chang, E. I.; Galiano, R. D.; Bhatt, K. A.; Baharestani, S.; Gan, J.; Simon, B.; Hopper, R. A.; Levine, J. P.; Gurtner, G. C., Electromagnetic fields increase in [175.0, 415.0, 1014.0, 626.0]reference_item0.82["default body_paragraph for text label", "late role resolution: reference_like family + reference zone", "style_family_authority=reference_marker", "context_source=block"]body_paragraph0.6reference_zonereference_likereference_numeric_parenthesisTrueTrue
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