Non-invasive blood glucose in vivo detection based on photoacoustic spectroscopy

2019 ◽  
Vol 27 (6) ◽  
pp. 1301-1308
Author(s):  
吕鹏飞 L Peng-fei ◽  
陆志谦 LU Zhi-qian ◽  
何巧芝 HE Qiao-zhi ◽  
王 倩 WANG Qian ◽  
赵 辉 ZHAO Hui
Nanomaterials ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 2181
Author(s):  
Ryan D. Mellor ◽  
Andreas G. Schätzlein ◽  
Ijeoma F. Uchegbu

Gold nanoparticles (AuNPs) are used experimentally for non-invasive in vivo Raman monitoring because they show a strong absorbance in the phototherapeutic window (650–850 nm), a feature that is accompanied by a particle size in excess of 100 nm. However, these AuNPs cannot be used clinically because they are likely to persist in mammalian systems and resist excretion. In this work, clustered ultrasmall (sub-5 nm) AuNP constructs for in vivo Raman diagnostic monitoring, which are also suitable for mammalian excretion, were synthesized and characterized. Sub-5 nm octadecyl amine (ODA)-coated AuNPs were clustered using a labile dithiol linker: ethylene glycol bis-mercaptoacetate (EGBMA). Upon clustering via a controlled reaction and finally coating with a polymeric amphiphile, a strong absorbance in the phototherapeutic window was demonstrated, thus showing the potential suitability of the construct for non-invasive in vivo detection and monitoring. The clusters, when labelled with a biphenyl-4-thiol (BPT) Raman tag, were shown to elicit a specific Raman response in plasma and to disaggregate back to sub-5 nm particles under physiological conditions (37 °C, 0.8 mM glutathione, pH 7.4). These data demonstrate the potential of these new AuNP clusters (Raman NanoTheranostics—RaNT) for in vivo applications while being in the excretable size window.


2009 ◽  
Vol 8 (2) ◽  
pp. 279-286 ◽  
Author(s):  
Kim Anker Kristiansen ◽  
Anastassia Khrouchtchova ◽  
Anne Stenbaek ◽  
Alexander Schulz ◽  
Poul Erik Jensen

Author(s):  
Mitsuhiro Ogawa ◽  
Takehiro Yamakoshi ◽  
Kenta Matsumura ◽  
Kosuke Motoi ◽  
Ken-Ichi Yamakoshi

A recently proposed optical method for a non-invasive in vivo blood glucose level (BGL) measurement named “pulse glucometry” is introduced. This method is based on near-infrared living body spectroscopy to accurately obtain blood information. The remarkable feature of the method is the measurement of both the total transmitted radiation spectra in wavelength ? (I?) and the cardiac-related pulsatile component (?I?). When ?I? is superimposed on I?, the differential optical density (?OD?), which includes only arterial blood information, is obtained, thus avoiding interference from living tissues other than arterial blood. Another feature is the ability to measure the differential optical density (?OD?) in multiple wavelengths to avoid interference from blood constituents other than the target blood chemical (glucose). To support this methodology, a very fast near-infrared spectroscopic system was developed to obtain a photoplethysmographic cardiac signal with a resolution of 8 nm over a wavelength range of 900 to 1700 nm at a 100 Hz sampling frequency. An example of an in vivo BGL measurement is shown and indicates good prediction capabilities. This method can be expanded to the measurement of other blood constituents.


2009 ◽  
Vol 321 (10) ◽  
pp. 1658-1661 ◽  
Author(s):  
Maxim P. Nikitin ◽  
Petr M. Vetoshko ◽  
Nikolai A. Brusentsov ◽  
Petr I. Nikitin

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