Publications by authors named "Honghua Guan"

Article Synopsis
  • Preterm birth (PTB) is a significant global health issue linked to changes in cervical collagen, and researchers have developed a flexible second harmonic generation (SHG) endomicroscope for non-invasive imaging of cervical tissue.
  • The study tested this technology on cervical tissues from normal and PTB mouse models to identify differences in collagen morphology.
  • Findings showed that PTB models had distinct collagen characteristics, suggesting SHG endomicroscopy could be a promising tool for early diagnosis and assessment of PTB risks in clinical settings.
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NADH intensity and fluorescence lifetime characteristics have proved valuable intrinsic biomarkers for profiling the cellular metabolic status of living biological tissues. To fully leverage the potential of NADH fluorescence lifetime imaging microscopy (FLIM) in (pre)clinical studies and translational applications, a compact and flexible endomicroscopic embodiment is essential. Herein we present our newly developed two-photon fluorescence (2PF) lifetime imaging endomicroscope (2p-FLeM) that features an about 2 mm diameter, subcellular resolution, and excellent emission photon utilization efficiency and can extract NADH lifetime parameters of living tissues and organs reliably using a safe excitation power (~30 mW) and moderate pixel dwelling time (≤10 s).

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  • Scanning two-photon (2P) fiberscopes offer a lightweight, high-resolution imaging solution for studying neural activity in freely-moving mice, which could help understand behavior.
  • Recent advancements achieved a significant boost in imaging speed (26 frames per second), thanks to a new scanner and deep learning (DL) techniques for image quality enhancement.
  • This DL-assisted 2P fiberscope allows researchers to observe activity changes in specific neuron populations in the primary motor cortex, paving the way for linking neural activity to behavioral changes.
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OCT-based quantitative tissue optical properties imaging is a promising technique for intraoperative brain cancer assessment. The attenuation coefficient analysis relies on the depth-dependent OCT intensity profile, thus sensitive to tissue surface positions relative to the imaging beam focus. However, it is almost impossible to maintain a steady tissue surface during intraoperative imaging due to the patient's arterial pulsation and breathing, the operator's motion, and the complex tissue surface geometry of the surgical cavity.

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Frozen section and smear preparation are the current standard for intraoperative histopathology during cancer surgery. However, these methods are time-consuming and subject to limited sampling. Multiphoton microscopy (MPM) is a high-resolution non-destructive imaging technique capable of optical sectioning in real time with subcellular resolution.

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Lightweight and head-mountable scanning nonlinear fiberscope technologies offer an exciting opportunity for enabling mechanistic exploration of ensemble neural activities with subcellular resolution on freely behaving rodents. The tether of the fiberscope, consisting of an optical fiber and scanner drive wires, however, restricts the mouse's movement and consequently precludes free rotation and limits the freedom of walking. Here we present the first twist-free two-photon fiberscope technology for enabling neuroimaging on freely rotating/walking mice.

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Visualizing activity patterns of distinct cell types during complex behaviors is essential to understand complex neural networks. It remains challenging to excite multiple fluorophores simultaneously so that different types of neurons can be imaged. In this Letter, we report a multicolor fiber-optic two-photon endomicroscopy platform in which two pulses from a Ti:sapphire laser and an optical parametric oscillator were synchronized and delivered through a single customized double-clad fiber to excite multiple chromophores.

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Compactness, among several others, is one unique and very attractive feature of a scanning fiber-optic two-photon endomicroscope. To increase the scanning area and the total number of resolvable pixels (i.e.

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Article Synopsis
  • Fiber-optic two-photon fluorescence endomicroscopy is becoming a key technology for imaging internal organs and studying neuronal functions in live animals.
  • High imaging speeds are needed, especially in neuroscience for tracking quick changes, but miniaturizing technology has been costly and inefficient until now.
  • This study introduces a fast fiber-optic scanning endomicroscope capable of 26 frames per second, successfully capturing real-time neural activity in a mouse's motor cortex using a specialized calcium indicator.
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An ultra-sensitive, wide-range force loading scheme is proposed for compression optical coherence elastography (OCE) that allows for the quantitative analysis of cervical tissue elasticity . We designed a force loading apparatus featuring a water sink for minuscule incremental loading through a volume-controlled water droplet, from which the Young's modulus can be calculated by fitting the stress-strain curve. We validated the performance of the proposed OCE system on homogenous agar phantoms, showing the Young's modulus can be accurately estimated using this scheme.

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Background: The objective of this survey was to explore the association between pregnancy complications and perinatal outcome from regionally total birth population.

Methods: In this prospectively collected data of complete birth registries from all level I-III hospitals in Huai'an in 2015, perinatal morbidity and mortality in relation to pregnancy complications and perinatal outcome were analyzed using international definitions. The results were compared with that of 2010 survey in the same region.

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In this work, we report a biopsy-needle compatible rigid probe, capable of performing three-dimensional (3D) two-photon optical biopsy. The probe has a small outer diameter of 1.75 mm and fits inside a gauge-14 biopsy needle to reach internal organs.

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Fiber-optic endomicroscopes open new avenues for the application of non-linear optics to novel applications. To achieve focus scanning , shape memory alloy (SMA) wires have been used to move optical elements in miniature endomicroscopes. However, this method has various limitations, making it difficult to achieve accurate and reliable depth scanning.

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