Noninvasive and Noncontact Sequential Imaging of the Iridocorneal Angle and the Cornea of the Eye.

Purpose: High-resolution imaging of the critical anatomic structures of the eye, especially of the anterior chamber, in vivo, remains a challenge, even with currently available state-of-the-art medical imaging techniques. This study aims for the noninvasive and noncontact sequential imaging of the iridocorneal angle, especially the trabecular meshwork (TM) and the cornea of the eye in high-resolution using a newly developed imaging platform.

Methods: Bessel beam scanned light sheet fluorescence microscopy is used to attain high-resolution images of the TM.

Influence of p-n junction mechanism and alumina overlayer on the photocatalytic performance of TiO nanotubes.

Modified hybrid structures of TiO nanotubes (TONT), p-Al doped TONT/n-TONT with an additional overlayer of alumina, are constructed to achieve 99.57% photodegradation of the stable organic pollutant methylene blue (MB) within 180 min, a degradation rate 17 times higher than pure TONTs. The anodization at three different temperatures 2, 28 and 40 °C followed by impregnation of Al is used for their preparation.

Particle free optical imaging of flow field by liquid crystal polarization.

This paper proposes and demonstrates a particle free method for flow field visualizations by analyzing liquid crystal polarizations. The proposed concept is implemented by imaging of liquid crystal flow under microfluidic environment using a crossed polarization microscopy configuration. Fringe patterns give good representation of flow characterizations for different nozzle/diffuser microchannel designs.

Preclinical imaging of iridocorneal angle and fundus using a modified integrated flexible handheld probe.

A flexible handheld imaging probe consisting of a [Formula: see text] charge-coupled device camera, light-emitting diode light sources, and near-infrared laser source is designed and developed. The imaging probe is designed with specifications to capture the iridocorneal angle images and posterior segment images. Light propagation from the anterior chamber of the eye to the exterior is considered analytically using Snell's law.

A simple and non-contact optical imaging probe for evaluation of corneal diseases.

Non-contact imaging techniques are preferred in ophthalmology. Corneal disease is one of the leading causes of blindness worldwide, and a possible way of detection is by analyzing the shape and optical quality of the cornea. Here, a simple and cost-effective, non-contact optical probe system is proposed and illustrated.

Integrated flexible handheld probe for imaging and evaluation of iridocorneal angle.

An imaging probe is designed and developed by integrating a miniaturized charge-coupled diode camera and light-emitting diode light source, which enables evaluation of the iridocorneal region inside the eye. The efficiency of the prototype probe instrument is illustrated initially by using not only eye models, but also samples such as pig eye. The proposed methodology and developed scheme are expected to find potential application in iridocorneal angle documentation, glaucoma diagnosis, and follow-up management procedures.

Note: A gel based imaging technique of the iridocorneal angle for evaluation of angle-closure glaucoma.

Noninvasive medical imaging techniques have high potential in the field of ocular imaging research. Angle closure glaucoma is a major disease causing blindness and a possible way of detection is the examination of the anterior chamber angle in eyes. Here, a simple optical method for the evaluation of angle-closure glaucoma is proposed and illustrated.

Design, fabrication, and characterization of thermoplastic microlenses for fiber-optic probe imaging.

Microlens-ended fibers could find great usefulness in future biomedical applications, particularly in endoscopic imaging applications. In this context, this paper focuses on microlens-attached specialty optical fibers such as imaging fiber that can be used for probe imaging applications. Stand-alone self-aligned polymer microlenses have been fabricated by microcompression molding.

Hollow-core photonic crystal fiber based multifunctional optical system for trapping, position sensing, and detection of fluorescent particles.

We demonstrate a novel multifunctional optical system that is capable of trapping, imaging, position sensing, and fluorescence detection of micrometer-sized fluorescent test particles using hollow-core photonic crystal fiber (HC-PCF). This multifunctional optical system for trapping, position sensing, and fluorescent detection is designed such that a near-IR laser light is used to create an optical trap across a liquid-filled HC-PCF, and a 473 nm laser is employed as a source for fluorescence excitation. This proposed system and the obtained results are expected to significantly enable an efficient integrated trapping platform employing HC-PCF for diagnostic biomedical applications.

Characteristics of stand-alone microlenses in fiber-based fluorescence imaging applications.

Microlens-ended fibers, which have found tremendous interest in the recent past, find potential biomedical applications, in particular, in endoscopic imaging. The work presented in this paper focuses on the stand-alone microlenses along with custom-fabricated specialty optical fiber, such as imaging fiber, for probe imaging applications. Stand-alone self-aligned microlenses have been fabricated employing microcompression molding and then attached at the end facet of imaging fiber.

Highly sensitive optical detection of specific protein in breast cancer cells using microstructured fiber in extremely low sample volume.

A simple optical method using hollow-core photonic crystal fiber for protein detection has been described. In this study, estrogen receptor (ER) from a MCF-7 breast carcinoma cell lysates immobilized inside a hollow-core photonic crystal fiber was detected using anti-ER primary antibody with either Alexa Fluor 488 (green fluorescent dye) or 555 (red Fluorescent dye) labeled Goat anti-rabbit IgG as the secondary antibody. The fluorescence fingerprints of the ERalpha protein were observed under fluorescence microscope, and its optical characteristics were analyzed.