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  1. <?xml version='1.0' encoding='UTF-8'?><stnAnswers><answer><answer_number>1</answer_number><source>PQSCITECH</source><fields><field><fieldCode>LNUMBER</fieldCode><fieldDescription>Answer Line</fieldDescription><values><value>L12 </value></values></field><field><fieldCode>TI</fieldCode><fieldDescription>Title</fieldDescription><values><value> Preparation and Characterization of the <hit>Na2Ti3O7</hit>: ABS/<hit>Na2Ti3O7</hit> Composites
  2. </value></values></field><field><fieldCode>DT</fieldCode><fieldDescription>Document Type</fieldDescription><values><value> Journal; Article
  3. </value></values></field><field><fieldCode>AN</fieldCode><fieldDescription>Accession Number</fieldDescription><values><value> 2019:143971 PQSCITECH</value></values></field><field><fieldCode>ANSWER_COUNT</fieldCode><fieldDescription></fieldDescription><values><value>ANSWER 1 OF 4</value></values></field><field><fieldCode>FULL_TEXT_LINK</fieldCode><fieldDescription>Full-Text</fieldDescription><values><value> <link href="https://chemport.fiz-karlsruhe.de/BASScgi/3?Tm2y6TQo_eXbm1oOqdouz8H2g9jCeSSCjHMrhu2@_dGtgXqfy5CUEgCcMvYmyygNi5NXsYFG30gahBmsZ3r0pNguDNzX@OoLuiJyszXWi@um2skJB5GQkMO6STNgSS0mZUK@Tt9zWxuT9mTHxpNNUr3J_NGKgHHscGhkUaXm3pgtJt1">Full-text</link>
  4. </value></values></field><field><fieldCode>LA</fieldCode><fieldDescription>Language</fieldDescription><values><value> English
  5. </value></values></field><field><fieldCode>COPYRIGHT_INFO</fieldCode><fieldDescription></fieldDescription><values><value>PQSCITECH COPYRIGHT 2022 ProQuest LCC on STN. </value></values></field><field><fieldCode>AU</fieldCode><fieldDescription>Author/Inventor</fieldDescription><values><value> Sangkatip, Rittichai ; Sriseubsai, Wipoo ; Kiatkittipong, Kunlanan
  6. </value></values></field><field><fieldCode>DN</fieldCode><fieldDescription>Document Number</fieldDescription><values><value> 2198665384
  7. </value></values></field><field><fieldCode>SO</fieldCode><fieldDescription>Source</fieldDescription><values><value><![CDATA[ Key Engineering Materials, Vol. 753, No. International Symposium on Advanced Material Research, pp. 39-43, 20170801
  8. ISSN: 1013-9826 E-ISSN: 1662-9795
  9. DOI: 10.4028/]]><link href="http://www.scientific.net/KEM.753.39">http://www.scientific.net/KEM.753.39</link><![CDATA[
  10. Published by: Trans Tech Publications Ltd., Zurich
  11. ]]></value></values></field><field><fieldCode>AB</fieldCode><fieldDescription>Abstract</fieldDescription><values><value><![CDATA[ Titanate Ribbon (]]><hit>Na2Ti3O7</hit><![CDATA[) used in ABS plastic was synthesized to study the mechanical properties and to conduct test on the E-coli ]]><hit>bacteria</hit><hit>inhibition</hit><![CDATA[ performance. The polymer blends of ABS/]]><hit>Na2Ti3O7</hit><![CDATA[ by ]]><hit>Na2Ti3O7</hit><![CDATA[, was synthesized
  12. through alkaline hydrothermal reaction with 0.5 grams of titanium dioxide as a precursor with 20 ml. of sodium hydroxide (NaOH) at the concentration of 10 molar under the alkalinity at 200 ° c for 24 hours. The study on the
  13. microstructure by scanning electron microscope revealed that the Layered structure was shaped as a complete ribbon. The mechanical testing activities on the E-coli ]]><hit>bacteria</hit><hit>inhibition</hit><![CDATA[ polymer mixed ABS/]]><hit>Na2Ti3O7</hit><![CDATA[; it was found that the
  14. mechanical properties for ABS/]]><hit>Na2Ti3O7</hit><![CDATA[, The results showed that tensile modulus and tensile strength of blending ]]><hit>Na2Ti3O7</hit><![CDATA[ at 0.5 %wt was the highest. The result showed that E.coli could reduce up to 66.01%.
  15. ]]></value></values></field></fields></answer><answer><answer_number>2</answer_number><source>EMBASE</source><fields><field><fieldCode>LNUMBER</fieldCode><fieldDescription>Answer Line</fieldDescription><values><value>L12 </value></values></field><field><fieldCode>TI</fieldCode><fieldDescription>Title</fieldDescription><values><value> In vitro biological response of micro- And nano-sized monosodium titanates and titanate-metal compounds.
  16. </value></values></field><field><fieldCode>DT</fieldCode><fieldDescription>Document Type</fieldDescription><values><value> Journal; Article
  17. </value></values></field><field><fieldCode>AN</fieldCode><fieldDescription>Accession Number</fieldDescription><values><value> 2015662023 EMBASE </value></values></field><field><fieldCode>ANSWER_COUNT</fieldCode><fieldDescription></fieldDescription><values><value>ANSWER 2 OF 4 </value></values></field><field><fieldCode>FULL_TEXT_LINK</fieldCode><fieldDescription>Full-Text</fieldDescription><values><value> <link href="https://chemport.fiz-karlsruhe.de/BASScgi/3?mTqpk3jswgCWWbFu9lDfok6qiZCERRTfD4Em15UTwpog_YHegKcIsZMMVBTOZotFvtys6wNyrJBHcVmXU9Swp_YtYmeVgQDE8YPgQFOZpf4qtsp6EaWF@_nVuQdwKSybgz8tcFdYOSCJQPmoi_Gwgo2_6qJo7cjSpY9_LZqGq2">Full-text</link>
  18. </value></values></field><field><fieldCode>LA</fieldCode><fieldDescription>Language</fieldDescription><values><value> English
  19. </value></values></field><field><fieldCode>COPYRIGHT_INFO</fieldCode><fieldDescription></fieldDescription><values><value>EMBASE COPYRIGHT (c) 2022 Elsevier B.V. All rights reserved on STN </value></values></field><field><fieldCode>AU</fieldCode><fieldDescription>Author/Inventor</fieldDescription><values><value> Drury, Jeanie L. (correspondence); Jang, Yoonji; Wataha, John C.
  20. </value><value> Taylor-Pashow, Kathryn M. L.; Elvington, Mark; Hobbs, David T.
  21. </value></values></field><field><fieldCode>CS</fieldCode><fieldDescription>Patent Assignee/Corporate Source</fieldDescription><values><value> Department of Restorative Dentistry, University of Washington School of Dentistry, Seattle, WA, 98195-7456, United States. <link href="mailto:[email protected]">mailto:[email protected]</link>
  22. </value><value> Savannah River National Laboratory, US Department of Energy, Aiken, SC, 29808, United States.
  23. </value></values></field><field><fieldCode>DN</fieldCode><fieldDescription>Document Number</fieldDescription><values><value> 601209169 PMID: 24819184
  24. </value></values></field><field><fieldCode>PB</fieldCode><fieldDescription>Publisher</fieldDescription><values><value> John Wiley and Sons Inc., P.O.Box 18667, Newark, NJ 07191-8667, United States.
  25. </value></values></field><field><fieldCode>CS</fieldCode><fieldDescription>Patent Assignee/Corporate Source</fieldDescription><values><value> Department of Restorative Dentistry, University of Washington School of Dentistry, Seattle, WA, 98195-7456, United States. <link href="mailto:[email protected]">mailto:[email protected]</link>
  26. </value><value> Savannah River National Laboratory, US Department of Energy, Aiken, SC, 29808, United States.
  27. </value></values></field><field><fieldCode>SO</fieldCode><fieldDescription>Source</fieldDescription><values><value><![CDATA[ Journal of Biomedical Materials Research - Part B Applied Biomaterials, (]]><hit>1 Feb 2015</hit><![CDATA[) Vol. 103, No. 2, pp. 254-260.
  28. Refs: 20
  29. ISSN: 1552-4973; E-ISSN: 1552-4981 CODEN: JBMRGL
  30. ]]></value></values></field><field><fieldCode>AB</fieldCode><fieldDescription>Abstract</fieldDescription><values><value><![CDATA[ Previous studies report that microsized monosodium titanates (MSTs) deliver metal ions and species to mammalian cells and ]]><hit>bacteria</hit><![CDATA[ with cell-specific and metalspecific effects. In this study, we explored the use of MST and a new synthesized
  31. nanosized ]]><hit>monosodium</hit><hit>titanate</hit><![CDATA[ (nMST) to deliver gold(III), cisplatin, or platinum(IV) to two human cell lines with different population doubling times, in vitro. The effect was measured using a fluorescent mitochondrial activity assay
  32. (CellTiter-Blue® Assay). This fluorescence assay was implemented to mitigate optical density measurement errors owing to particulate titanate interference and allowed for the studies to be extended to higher titanate concentrations than
  33. previously possible. Overall, native MST significantly (p < 0.05) decreased mitochondrial activity of both cell types by 50% at concentrations of >50 mg/L. Native nMST significantly suppressed the rapidly dividing cell line (by 50%) over
  34. untreated cultures, but had no effect on the more slowly dividing cells. For both cell types, increased titanate concentrations resulted in increased effects from delivered metals. However, there was no difference in the effect of metal
  35. delivered from micro- versus nano-sized MST.
  36. ]]></value></values></field></fields></answer><answer><answer_number>3</answer_number><source>MEDLINE</source><fields><field><fieldCode>LNUMBER</fieldCode><fieldDescription>Answer Line</fieldDescription><values><value>L12 </value></values></field><field><fieldCode>TI</fieldCode><fieldDescription>Title</fieldDescription><values><value> Antibacterial activity of gold-titanates on Gram-positive cariogenic <hit>bacteria</hit>.
  37. </value></values></field><field><fieldCode>DT</fieldCode><fieldDescription>Document Type</fieldDescription><values><value> Journal; Article; (JOURNAL ARTICLE)
  38. </value></values></field><field><fieldCode>AN</fieldCode><fieldDescription>Accession Number</fieldDescription><values><value> 2018711029 MEDLINE</value></values></field><field><fieldCode>ANSWER_COUNT</fieldCode><fieldDescription></fieldDescription><values><value>ANSWER 3 OF 4 </value></values></field><field><fieldCode>FULL_TEXT_LINK</fieldCode><fieldDescription>Full-Text</fieldDescription><values><value> <link href="https://chemport.fiz-karlsruhe.de/BASScgi/3?kHn1oWF2c953Ap3ikS8y7qinWa2S04W9_BsDSKs2cA3cjZkXXbMcMMvrmppGhl6COR@1U00WKdmd4OHPQMprXxpe4ZTHAtjPXtZ0tS4GhDaFGRE2UsBtdxxr7C8J@puL5cJtgI4hdGZ7UI53kg8gcW3CjiBogxMuYTZVNvMugun">Full-text</link>
  39. </value></values></field><field><fieldCode>LA</fieldCode><fieldDescription>Language</fieldDescription><values><value> English
  40. </value></values></field><field><fieldCode>COPYRIGHT_INFO</fieldCode><fieldDescription></fieldDescription><values><value>MEDLINE ® on STN</value></values></field><field><fieldCode>AU</fieldCode><fieldDescription>Author/Inventor</fieldDescription><values><value> Eiampongpaiboon Trinuch
  41. </value><value> Chung Whasun O
  42. </value><value> Bryers James D
  43. </value><value> Chung Kwok-Hung; Chan Daniel C N
  44. </value></values></field><field><fieldCode>CS</fieldCode><fieldDescription>Patent Assignee/Corporate Source</fieldDescription><values><value> Department of Prosthodontics, Mahidol UniversityBangkokThailand.
  45. </value><value> Department of Oral Health Sciences, University of WashingtonSeattleWAUSA.
  46. </value><value> Department of Bioengineering, University of WashingtonSeattleWAUSA, and.
  47. </value><value> Department of Restorative Dentistry, University of WashingtonSeattleWAUSA.
  48. </value></values></field><field><fieldCode>DN</fieldCode><fieldDescription>Document Number</fieldDescription><values><value> PubMed ID: 28642901
  49. </value></values></field><field><fieldCode>CS</fieldCode><fieldDescription>Patent Assignee/Corporate Source</fieldDescription><values><value> Department of Prosthodontics, Mahidol UniversityBangkokThailand.
  50. </value><value> Department of Oral Health Sciences, University of WashingtonSeattleWAUSA.
  51. </value><value> Department of Bioengineering, University of WashingtonSeattleWAUSA, and.
  52. </value><value> Department of Restorative Dentistry, University of WashingtonSeattleWAUSA.
  53. </value></values></field><field><fieldCode>SO</fieldCode><fieldDescription>Source</fieldDescription><values><value><![CDATA[ Acta biomaterialia odontologica Scandinavica, ]]><hit>(2015 Dec)</hit><![CDATA[ Vol. 1, No. 2-4, pp. 51-58. Electronic Publication Date: 18 Sep 2015
  54. Journal code: 101681462. ISSN: 2333-7931. L-ISSN: 2333-7931.
  55. Report No.: PMC-PMC5433202.
  56. ]]></value></values></field><field><fieldCode>AB</fieldCode><fieldDescription>Abstract</fieldDescription><values><value><![CDATA[ Objective: Gram-positive cariogenic ]]><hit>bacteria</hit><![CDATA[ are etiological agents in dental caries; therefore, strategies to ]]><hit>inhibit</hit><![CDATA[ these ]]><hit>bacteria</hit><![CDATA[ to reduce the incident of this disease have intensified. In this study, we investigated antibacterial
  57. activities of titanates and gold-titanates against Lactobacillus casei (Lc) and Streptococcus mutans (Sm). Materials and methods: ]]><hit>Monosodium</hit><hit>titanate</hit><![CDATA[ (MST), nanomonosodium titanate (nMST) and amorphous peroxo-titanate (APT), which are
  58. inorganic compounds with high-binding affinity for specific metal ions, were used. Total bacterial proteins were measured to represent bacterial cell mass after 24 h incubation with gold-titanates. We further examined the effect of
  59. nMST-Au(III) concentrations (10,200,400 mg/L) on Lc and Sm cell viability over time via Live/Dead fluorescent staining and colony forming units (CFUs). Transmission electron microscopy (TEM) was used to determine specific locations on the
  60. bacterial cells affected by the nMST-Au(III). Results: We found all gold-titanates and APT alone reduced bacterial protein for Lc (p value <0.001) while only MST-Au(III) and nMST-Au(III) affected Sm growth (p value <0.001). Overall,
  61. nMST-Au(III) showed the most effectiveness against both Lc and Sm at 400 mg/L. The Live/Dead staining showed all concentrations of nMST-Au(III) affected Lc growth but only 200 and 400 mg/L nMST-Au(III) interrupted Sm growth. The growth curves
  62. based on CFUs/mL showed all nMST-Au(III) concentrations affected growth of both Lc and Sm. TEM images showed nMST-Au(III) attached to Lc and Sm cell wall and were internalized into both cells.Conclusions: nMST-Au(III) demonstrated potential
  63. antimicrobial activity against Gram-positive cariogenic ]]><hit>bacteria</hit><![CDATA[. These results support further development of nMST-Au(III) as a potential novel material to prevent dental caries.
  64. ]]></value></values></field></fields></answer><answer><answer_number>4</answer_number><source>MEDLINE</source><fields><field><fieldCode>LNUMBER</fieldCode><fieldDescription>Answer Line</fieldDescription><values><value>L12 </value></values></field><field><fieldCode>TI</fieldCode><fieldDescription>Title</fieldDescription><values><value> Peroxotitanate- and monosodium metal-titanate compounds as <hit>inhibitors</hit> of bacterial growth.
  65. </value></values></field><field><fieldCode>DT</fieldCode><fieldDescription>Document Type</fieldDescription><values><value><![CDATA[ Journal; Article; (JOURNAL ARTICLE)
  66. (RESEARCH SUPPORT, NON-U.S. GOV'T)
  67. (RESEARCH SUPPORT, U.S. GOV'T, NON-P.H.S.)
  68. ]]></value></values></field><field><fieldCode>AN</fieldCode><fieldDescription>Accession Number</fieldDescription><values><value> 2011445295 MEDLINE</value></values></field><field><fieldCode>ANSWER_COUNT</fieldCode><fieldDescription></fieldDescription><values><value>ANSWER 4 OF 4 </value></values></field><field><fieldCode>FULL_TEXT_LINK</fieldCode><fieldDescription>Full-Text</fieldDescription><values><value> <link href="https://chemport.fiz-karlsruhe.de/BASScgi/3?d@WinnGvx7tqL9@2yV__bBWWO7cyHb9uFIHya4mlxvFXDv_4HorXzU_4@93vep1gwAxTXmHmT5TTR3Pf4obHmJthRvjsjaF_mHv8aymvuoHyaAeSXH8q4rJMagNIhjCUoXaHJrmLvvmk0BIlWhBCxJFqDWJTm1rh@RvTCdU5C5g">Full-text</link>
  69. </value></values></field><field><fieldCode>LA</fieldCode><fieldDescription>Language</fieldDescription><values><value> English
  70. </value></values></field><field><fieldCode>COPYRIGHT_INFO</fieldCode><fieldDescription></fieldDescription><values><value>MEDLINE ® on STN DUPLICATE 1</value></values></field><field><fieldCode>AU</fieldCode><fieldDescription>Author/Inventor</fieldDescription><values><value> Chung Whasun O
  71. </value><value> Wataha John C; Hobbs David T; An Jonathan; Wong Jacqueline J; Park Christine H; Dogan Sami; Elvington Mark C; Rutherford R Bruce
  72. </value></values></field><field><fieldCode>CS</fieldCode><fieldDescription>Patent Assignee/Corporate Source</fieldDescription><values><value> Department of Oral Biology, University of Washington, Seattle, Washington 98195, USA.
  73. </value></values></field><field><fieldCode>DN</fieldCode><fieldDescription>Document Number</fieldDescription><values><value> PubMed ID: 21472975
  74. </value></values></field><field><fieldCode>CS</fieldCode><fieldDescription>Patent Assignee/Corporate Source</fieldDescription><values><value> Department of Oral Biology, University of Washington, Seattle, Washington 98195, USA.
  75. </value></values></field><field><fieldCode>SO</fieldCode><fieldDescription>Source</fieldDescription><values><value><![CDATA[ Journal of biomedical materials research. Part A, ]]><hit>(2011 Jun 01)</hit><![CDATA[ Vol. 97, No. 3, pp. 348-54. Electronic Publication Date: 5 Apr 2011
  76. Journal code: 101234237. E-ISSN: 1552-4965. L-ISSN: 1549-3296.
  77. ]]></value></values></field><field><fieldCode>AB</fieldCode><fieldDescription>Abstract</fieldDescription><values><value><![CDATA[ Sodium titanates are ion-exchange materials that effectively bind a variety of metal ions over a wide pH range. Sodium titanates alone have no known adverse biological effects but metal-exchanged titanates (or metal titanates) can deliver
  78. metal ions to mammalian cells to alter cell processes in vitro. In this work, we test a hypothesis that metal-titanate compounds ]]><hit>inhibit</hit><![CDATA[ bacterial growth; demonstration of this principle is one prerequisite to developing metal-based,
  79. titanate-delivered antibacterial agents. Focusing initially on oral diseases, we exposed five species of oral ]]><hit>bacteria</hit><![CDATA[ to titanates for 24 h, with or without loading of Au(III), Pd(II), Pt(II), and Pt(IV), and measuring bacterial growth in
  80. planktonic assays through increases in optical density. In each experiment, bacterial growth was compared with control cultures of titanates or ]]><hit>bacteria</hit><![CDATA[ alone. We observed no suppression of bacterial growth by the sodium titanates alone,
  81. but significant (p < 0.05, two-sided t-tests) suppression was observed with metal-titanate compounds, particularly Au(III)-titanates, but with other metal titanates as well. Growth ]]><hit>inhibition</hit><![CDATA[ ranged from 15 to 100% depending on the metal ion
  82. and bacterial species involved. Furthermore, in specific cases, the titanates ]]><hit>inhibited</hit><![CDATA[ bacterial growth 5- to 375-fold versus metal ions alone, suggesting that titanates enhanced metal-]]><hit>bacteria</hit><![CDATA[ interactions. This work supports further
  83. development of metal titanates as a novel class of antibacterials.
  84. Copyright © 2011 Wiley Periodicals, Inc.
  85.  
  86. ]]></value></values></field></fields></answer></stnAnswers>
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