Тірі тіндердің фотондар шығаруы және биофотоника ғылымы

the spontaneous low level emission of photons from living tissues

The term biophotonics denotes a combination of biology and photonics, with photonics being the science and technology of generation, manipulation, and detection of photons, quantum units of light. Photonics is related to electronics and photons. Photons play a central role in information technologies, such as fiber optics, the way electrons do in electronics. Biophotonics can also be described as the "development and application of optical techniques, particularly imaging, to the study of biological molecules, cells and tissue". One of the main benefits of using the optical techniques which make up biophotonics is that they preserve the integrity of the biological cells being examined. Biophotonics has therefore become the established general term for all techniques that deal with the interaction between biological items and photons. This refers to emission, detection, absorption, reflection, modification, and creation of radiation from biomolecular, cells, tissues, organisms, and biomaterials. Areas of application are life science, medicine, agriculture, and environmental science. Similar to the differentiation between "electric" and "electronics," a difference can be made between applications such as therapy and surgery, which use light mainly to transfer energy, and applications such as diagnostics, which use light to excite matter and to transfer information back to the operator. In most cases, the term biophotonics refers to the latter type of application.

Biophotonics is an interdisciplinary field involving the interaction between electromagnetic radiation and biological materials including: tissues, cells, sub cellular structures, and molecules in living organisms. Recent biophotonics research has created new applications for clinical diagnostics and therapies involving fluids, cells, and tissues. These advances are allowing scientists and physicians opportunities for superior, non invasive diagnostics for vascular and blood flow, as well as tools for better examination of skin lesions. In addition to new diagnostic tools, the advancements in biophotonics research have provided new photothermal, photodynamic, and tissue therapies.

By observing the numerous and complex interactions between light and biological materials, the field of biophotonics presents a unique set of diagnostic techniques that medical practitioners can utilize. Biophotonic imaging provides the field of dermatology with the only non invasive technique available for diagnosing skin cancers. Traditional diagnostic procedures for skin cancers involve visual assessment and biopsy, but a new laser induced fluorescence spectroscopy technique allow dermatologists to compare spectrographs of a patient's skin with spectrographs known to correspond with malignant tissue. This provides doctors with earlier diagnosis and treatment options.

Laser micro scalpels are a combination of fluorescence microscopy and a femtosecond laser "can penetrate up to 250 micrometers into tissue and target single cells in 3 D space." The technology, which was patented by researchers at the University of Texas at Austin, means that surgeons can excise diseased or damaged cells without disturbing or damaging healthy surrounding cells in delicate surgeries involving areas such as the eyes and vocal chords. Researchers have also been able to use PAM to diagnose endometriosis in rats.

Photodynamic therapy (PT) uses photosynthesizing chemicals and oxygen to induce a cellular reaction to light. It can be used to kill cancer cells, treat acne, and reduce scarring. PT can also kill bacteria, viruses, and fungi. The technology provides treatment with little to no long term side effects, is less invasive than surgery and can be repeated more often than radiation. Treatment is limited, however, to surfaces and organs that can be exposed to light, which eliminates deep tissue cancer treatments.

Photothermal therapy most commonly uses nanoparticles made of a noble metal to convert light into heat. The nanoparticles are engineered to absorb light in the 700 1000 nm range, where the human body is optically transparent. When the particles are hit by light they heat up, disrupting or destroying the surrounding cells via hyperthermia. Because the light used does not interact with tissue directly, photothermal therapy has few long term side effects and it can be used to treat cancers deep within the body.

Fluorescence resonance energy transfer, also known as Förster resonance energy transfer (FRET in both cases) is the term given to the process where two excited "fluorophores" pass energy one to the other non radiatively (i. e., without exchanging a photon). By carefully selecting the excitation of these fluorophores and detecting the emission, FRET has become one of the most widely used techniques in the field of biophotonics, giving scientists the chance to investigate sub cellular environments.

Biofluorescence describes the absorption of ultraviolet or visible light and the sub sequential emission of photons at a lower energy level (S 1 excited state relaxes to S 0 ground state) by intrinsically fluorescent proteins or by synthetic fluorescent molecules covalently attached to a biomarker of interest. Biomarkers are molecules indicative or disease or distress and are a typically monitored systemically in a living organism, or by using an ex vivo tissue sample for microscopy, or in vitro: in the blood, urine, sweat, saliva, interstitial fluid, aqueous humor, or sputum. Stimulating light excites an electron, raising energy to an unstable level. This instability is unfavorable, so the energized electron is returned to a stable state almost as immediately as it becomes unstable. The time delay between excitation and re emission that occurs when returning to the stable ground state causes the photon that is re emitted to be a different color (i. e. it relaxes to a lower energy and thus the photon emitted is at a shorter wavelength, as governed by the Plank Einstein relation) than the excitation light that was absorbed. This return to stability corresponds with the release of excess energy in the form of fluorescent light. This emission of light is only observable whilst the excitation light is still providing photons to the fluorescent molecule and is typically excited by blue or green light and emits purple, yellow, orange, green, cyan, or red. Biofluorescence is often confused with the following forms of biotic light: bioluminescence and biophosphorescence.

Bioluminescence differs from biofluorescence in that it is the natural production of light by chemical reactions within an organism, whereas biofluorescence and biophosphorescence are the absorption and reemission of light from the natural environment.

Biophosphorescence is similar to biofluorescence in its requirement of light at specified wavelengths as a provider of excitation energy. The difference here lies in the relative stability of the energized electron. Unlike with biofluorescence, here the electron retains stability in the forbidden triplet state (unpaired spins), with a longer delay in emitting light resulting in the effect that it continues to “glow in the dark” even long after the stimulating light source has been removed.

A biolaser is when laser light is generated by or from within a living cell. Imaging in biophotonics often relies on laser light, and integration with biological systems is seen as a promising route to enhancing sensing and imaging techniques. Biolasers, like any lasers, require three components: a gain medium, an optical feedback structure and a pump source. For the gain medium, a variety of naturally produced fluorescent proteins can be used in different laser structure. Enclosing an optical feedback structure in a cell has been demonstrated using cell vacuoles, as well as using fully enclosed laser systems such as dye doped polymer microspheres, or semiconductor nanodisks lasers.

The predominantly used light sources are beam lights. LEDs and superluminescent diodes also play an important role. Typical wavelengths used in biophotonics are between 600 nm (Visible) and 3000 nm (near IR).

Lasers play an increasingly important role in biophotonics. Their unique intrinsic properties like precise wavelength selection, widest wavelength coverage, highest focusability and thus best spectral resolution, strong power densities and broad spectrum of excitation periods make them the most universal light tool for a wide spectrum of applications. As a consequence a variety of different laser technologies from a broad number of suppliers can be found in the market today.

Solid state lasers are lasers based on solid state gain media such as crystals or glasses doped with rare earth or transition metal ions, or semiconductor lasers. (Although semiconductor lasers are of course also solid state devices, they are often not included in the term solid state lasers.) Ion doped solid state lasers (also sometimes called doped insulator lasers) can be made in the form of bulk lasers, fiber lasers, or other types of waveguide lasers. Solid state lasers may generate output powers between a few milliwatts and (in high power versions) many kilowatts.

Many advanced applications in biophotonics require individually selectable light at multiple wavelengths. As a consequence a series of new laser technologies has been introduced, which currently looks for precise wording. The most commonly used terminology are supercontinuum lasers, which emit visible light over a wide spectrum simultaneously. This light is then filtered e. g. via acousto optic modulators (AOM, AOTF) into 1 or up to 8 different wavelengths. Typical suppliers for this technology was NKT Photonics or Fianium. Recently NKT Photonics bought Fianium, remaining the major supplier of the supercontinuum technology on the market. In another approach the supercontinuum is generated in the infrared and then converted at a single selectable wavelength into the visible regime. This approach does not require AOTF's and has a background free spectral purity. Since both concepts have major importance for biophotonics the umbrella term "ultrachrome lasers" is often used.

Swept sources are designed to continuously change ('sweep') emitted light frequency in time. They typically continuously circle through a pre defined range of frequencies (e. g., 800 +/ 50 nm). Swept sources in the terahertz regime have been demonstrated. A typical application of swept sources in biophotonics is optical coherence tomography (OCT) imaging.

Vibrational spectroscopy in the terahertz (THz) frequency range, 0.1–10 THz, is a fast emerging technique for fingerprinting biological molecules and species. For more than 20 years, theoretical studies predicted multiple resonances in absorption (or transmission) spectra of biological molecules in this range. THz radiation interacts with the low frequency internal molecular vibrations by exciting these vibrations.

Single photon sources are novel types of light sources distinct from coherent light sources (lasers) and thermal light sources (such as incandescent light bulbs and mercury vapor lamps) that emit light as single particles or photons.