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Osteoporosis risk assessment using multilayered gold-nanoparticle thin film via SALDI-MS measurement

  • Xi-Yu Pan
  • Chih-Hwa Chen
  • Yi-Hsuan Chang
  • Di-Yan Wang
  • Yi-Cheng Lee
  • Chien-Chung Liou
  • Yu-Xian Wang
  • Cho-Chun Hu
  • Tsung-Rong KuoEmail author
Paper in Forefront

Abstract

A powerful technique to detect bone biomarkers has been developed for assessment of osteoporosis at the early stage. Two-dimensional multilayered gold-nanoparticle thin film (MTF-AuNPs) was demonstrated as a promising test platform for detection of bone biomarker, hydroxyproline (HYP), measured by surface-assisted laser desorption/ionization mass spectrometry (SALDI-MS). With strong surface plasmon resonance and excellent homogeneity, facilely prepared, highly ordered, and large-scale MTF-AuNPs revealed high sensitivity of HYP in the SALDI-MS measurement without additional matrixes, such as α-cyano-4-hydroxycinnamic acid (CHCA) and 2,5-dihydroxybenzoic acid (DHB). Furthermore, the mass spectrum of HYP with MTF-AuNPs was significantly improved in signal intensity enhancement, background noise reduction, and signal-to-noise ratio amplification. The excellent reproducibility of HYP spectra with only 9.3% relative signal variation could be attributed to MTF-AuNPs’ high absorbance at a wavelength of 337 nm, low heat capacity, superior thermal conductivity, and outstanding homogeneity. The calibration curve showed high linear correlation between mass spectrum intensity and HYP concentration in the range of 1 to 100 μM, covering the whole level in healthy people and osteoporosis patients. In particular, the serum sample was directly deposited onto the MTF-AuNP sample substrate without any pretreatment and its HYP concentration was then successfully determined. We believe that the combination of SALDI-MS and MTF-AuNP sample substrates would be a potential approach for bone biomarker detection in the osteoporosis risk assessment.

Graphical abstract

Keywords

Osteoporosis Biomarker Gold nanoparticles Multilayered thin film Sample substrate Serum 

Notes

Acknowledgments

We would like to acknowledge Mr. Chi-Ming Lee for his excellent technical support at TMU Core Facility.

Funding information

This work was supported by MOST 107-2113-M-038-004, MOST 105-2119-M-038-002-MY2, MOST 107-2622-E-038-001-CC2, and Taipei Medical University.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Informed consent

Informed consent was obtained from all individual participants included in the study.

Supplementary material

216_2019_1759_MOESM1_ESM.pdf (1.2 mb)
ESM 1 (PDF 1215 kb)

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2019

Authors and Affiliations

  1. 1.Graduate Institute of Nanomedicine and Medical Engineering, College of Biomedical EngineeringTaipei Medical UniversityTaipeiTaiwan
  2. 2.School of Biomedical Engineering, College of Biomedical Engineering, School of Medicine, College of MedicineTaipei Medical UniversityTaipeiTaiwan
  3. 3.Department of Orthopedics, Shuang Ho HospitalTaipei Medical UniversityNew Taipei CityTaiwan
  4. 4.Department of ChemistryTunghai UniversityTaichungTaiwan
  5. 5.Department of Applied ScienceNational Taitung UniversityTaitungTaiwan
  6. 6.International Ph.D. Program in Biomedical Engineering, College of Biomedical EngineeringTaipei Medical UniversityTaipeiTaiwan

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