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15개의 게시물을 찾았습니다.

  1. 2008/12/09
    kary mullis
    olfactory
  2. 2008/12/09
    Scent of strawberry
    olfactory
  3. 2008/12/09
    ACDLABS 11.0
    olfactory
  4. 2008/12/09
    Scent of Strawberry
    olfactory
  5. 2008/12/08
    The Good Scents Company
    olfactory
  6. 2008/12/02
    pleasure of eating
    olfactory
  7. 2008/12/02
    strawberry
    olfactory
  8. 2008/12/02
    butter
    olfactory
  9. 2008/12/02
    digital smell camera
    olfactory
  10. 2008/12/02
    How people can smell - smell process
    olfactory

kary mullis

kary mullis
진보블로그 공감 버튼트위터로 리트윗하기페이스북에 공유하기딜리셔스에 북마크

Scent of strawberry

 

 

 

 

진보블로그 공감 버튼트위터로 리트윗하기페이스북에 공유하기딜리셔스에 북마크

ACDLABS 11.0

진보블로그 공감 버튼트위터로 리트윗하기페이스북에 공유하기딜리셔스에 북마크

Scent of Strawberry

진보블로그 공감 버튼트위터로 리트윗하기페이스북에 공유하기딜리셔스에 북마크

The Good Scents Company

pleasure of eating

진보블로그 공감 버튼트위터로 리트윗하기페이스북에 공유하기딜리셔스에 북마크

strawberry

Esters

   Methyl Acetate

   Ethyl Acetate

   Methyl Butanoate

   Ethyl Butanoate

   Ethyl-2-Methyl Butanoate

   Ethyl-3-Methyl Butanoate

   3-Methyl Butyl Acetate

   Methyl Hexanoate

   Ethyl Hexanoate

   Hexyl Acetate

   (E)-2-Hexenyl Acetate

   Ethyl Octanoate

Aldehydes

   Hexanal

Acids

   Acetic Acid

Alcohols

   (Z)-3-Hexenol

   (E)-2-Hexenol

   Hexyl Alcohol

Ketones

   2-Pentanone

   3-Hydroxy-2-Butanone

Hydrocarbons

   Limonene

   γ-Terpinene

Sulfur-Containing Compounds

   s-Methyl Thioacetate

   Dimethyl Disulfide

Furans

   Furaneol

Lactones

   γ-Dodecalactone

진보블로그 공감 버튼트위터로 리트윗하기페이스북에 공유하기딜리셔스에 북마크

butter

Ethyl Formate

Ethyl Butyrate

Methyl Ethyl Ketone

Ethyl Alcohol

Aldehyde C-6 (Hexanal)

Methyl Amyl Ketone

2-Methylthio Acetaldehyde

Methyl Heptyl Ketone

Aldehyde C-9 (Nonanal)

Acetic Acid

Ethyl Octanoate

2-Ethyl Hexanol

Aldehyde C-10 (Decanal)

Alcohol C-8 (Octanol)

Methyl Octanoate

Methyl Nonyl Ketone

Butyric Acid

Methyl Benzoate

Ethyl Hexanoate

Furfuryl Alcohol

Isovaleric Acid

Valeric Acid

Alcohol C-10 (Decanol)

Methyl Laureate

Methyl Undecyl Ketone

Ethyl Laureate

Dimethyl Sulfone

Heptanoic Acid

δ-Octalactone

Alcohol C-12

(Dodecanol, Lauryl Alcohol)

Methyl Myristate

Methyl Tridecyl Ketone

Hexanoic Acid

δ-Nonalactone

Nonanoic Acid

δ-Decalactone

Octanoic Acid

δ-Undecalactone

γ-Dodecalactone

δ-Dodecalactone

Indole

Lauric Acid

Skatole

Myristic Acid

진보블로그 공감 버튼트위터로 리트윗하기페이스북에 공유하기딜리셔스에 북마크

digital smell camera

Smelling in Color: A Rainbow of Possibilities

A sensor that detects odors better than the human nose may be able to smell dangerous air pollutants, soil contaminants, insecticides, food pathogens, biological warfare neurotoxins, and body odors associated with illness and disease. At the University of Illinois at Urbana-Champaign, chemistry professor Kenneth S. Suslick and graduate student Neal A. Rakow have spent four years developing a sensor that sniffs out odors by "seeing" them. Called "smell-seeing" by its inventors, the method relies on color changes that occur in an array of vapor-sensitive dyes in response to exposure. This newest version of an artificial nose is simple, fast, and inexpensive.

Smell-Seeing

The new technology uses materials and concepts that have been available for at least 50 years. It's basically as simple as using litmus paper to see if a solution is acidic or basic by observing whether the paper changes color. In smell-seeing, the dyes are vapor-sensitive metalloporphyrins that are closely related to hemoglobin, which transports oxygen in blood, and chlorophyll, the green pigment in plants. When the metalloporphyrins come in contact with vapors containing chemical groups common to environmental contaminants, they change color. By measuring the color change pattern, the researchers can identify a contaminant both qualitatively and quantitatively.

The structure of a metalloporphyrin consists of large rings with loosely held electrons arranged around a metal ion in the center. Anything that perturbs the loosely held electrons and moves them produces a color change. A common example is the difference in color between bright red arterial blood and darker venous blood. "That's the result of oxygen binding to hemoglobin, an iron porphyrin," explains Suslick.

The researchers pursued the idea of seeing smells after observing that many of the most toxic--and foul-smelling--compounds readily bind metals. Although little is known about the structures of the olfactory receptor proteins in the human nose, Suslick and Rakow speculated that many of the nose's sensors are likely to contain metal ions at their active sites. Their smell-seeing technology somewhat mimics the physiology of the nose because "the olfactory system is based on a combination, or array, of receptor proteins that gives you a net response," says Rakow. He adds that within the nose there are probably specialized receptors that respond to and warn about chemicals that are toxic and harmful to the human body, similar to the device he and Suslick are developing.

Proof of Concept

To create an array, the researchers paint a series of tiny dots, each containing a different metalloporphyrin, on an inert backing such as silica gel. The array is scanned with an ordinary flatbed scanner or an inexpensive digital camera before and after exposure to chemical vapors. "By subtracting the 'before' image from the 'after' image, we obtain the color change pattern of the odorant," says Suslick. By comparing that pattern to a library of color fingerprints, the researchers can quickly identify and quantify the chemical compounds present. To the best of their knowledge, this is the first time that a color-based array has been used to visually detect a wide range of vaporized chemicals.

 

finger print
Color tells a story. Arrays consist of series of tiny dots containing different metalloporphyrins that produce unique color change patterns upon exposure to chemical vapors. Researchers are building a library of color "fingerprints" for various chemicals.

 

Photo credit: K. S. Suslick, N. A. Rakow

In the 17 August 2000 issue of Nature, Suslick and Rakow describe making an array of 10 metalloporphyrin dye complexes by combining 5,10,15,20-tetraphenylporphyrin with 10 metals including iron, copper, manganese, and cobalt. Then the metalloporphyrin dyes were spotted onto reverse phase silica thin-layer-chromatography plates. The metalloporphyrin array was then exposed to chemical vapors specifically chosen to represent a wide range of functional chemical groups commonly found in environmental pollutants. The functional chemical groups included amines, alcohols, arenes, ethers, phosphines, thioethers, thiols, and ketones. Within 30 seconds to 5 minutes after exposure, unique color fingerprints were obtained at exposure concentrations ranging from 2 parts per million to 100 parts per billion. In contrast, the human nose is generally sensitive to most compounds at a concentration of a few parts per million. "The sensitivity of our artificial nose is 10 to 100 times better than that [of the human nose] for many compounds," says Suslick.

Each functional chemical group is easily distinguished from the others, and family resemblances occur among chemically similar species, such as pyridine and n-hexylamine. Smell-seeing also detects more than volatile organic compounds. Permanent gases such as carbon monoxide, phosphine, hydrogen sulfide, and airborne ammonia are detected by the metalloporphyrins as well. In addition to identifying single chemical compounds, the metalloporphyrin array is proving a good way to identify mixtures of vapors. Color change patterns for mixtures containing 2-4 components are distinctly different from those for single compounds. For complex mixtures, it is often sufficient to recognize a fingerprint pattern rather than the makeup of individual components. For example, perfume manufacturers may detect counterfeit products by measuring the unique fingerprints of legitimate products. "We can generate unique color fingerprints and compare them without knowing the hundreds of components in the perfume," says Suslick.

The ability to attach chemical substituents--for instance, phenyl groups-- to porphyrins, then combine them with metals, means that an infinite number of metalloporphyrin dyes are theoretically available to cover a broad range of environmental chemicals. However, in practice Suslick believes that an array containing 25-36 different metalloporphyrins is probably sufficient to cover any foreseeable future use.

Advantages of Seeing Smells

Metalloporphyrin arrays eliminate the subjectivity associated with smell and odors. "One person may think an odor is terrible, and another may think it's not so bad," says Suslick. Smell-seeing is an excellent way to quantitatively compare aromas and measure the actual amounts of smell compounds. For instance, people living downwind of a hog farm could measure the quantity of each smell compound and monitor an acceptable level of air quality. Or smell-seeing could sniff out insecticides near farmland, bacteria causing infections in hospitals, spoilage in the food industry, or dangerous chemicals such as benzene in the workplace. The Illinois team is working on establishing sensitivities for all chemicals monitored by the Occupational Safety and Health Administration through metalloporphyrin arrays and smell-seeing.

The smell-seeing approach differs from several other commercial and experimental designs for artificial noses, which largely rely on polymers that swell when they come in contact with a vaporized chemical. When polymers swell, they trigger a measurable response such as a change in electrical conductivity, or cause a dye to fluoresce in a probe molecule. However, all systems that use polymer swelling suffer from the caveat that ambient water vapor and humidity change the sensitivity of the system, says Rakow. Because they're polar, polymers preferentially absorb water vapor more than they do the many organic chemicals they're intended to detect. Consequently, small changes in ambient humidity distort the reliability of polymer-based systems. "Unfortunately, relative humidity is one thing in the environment that changes most dramatically," says Suslick.

 

diagram

 

Drawing a picture of scent. The smell-seeing rig (above) uses nitrogen gas to create saturated chemical vapors to which metalloporphyrin arrays are exposed. Scanning and comparing "before" and "after" images yields a unique color change pattern for each chemical, which can be compared to the color fingerprint library for identification. A new "smell camera" (right) is an affordable way to quickly detect chemicals in the field.
Photo credit: K. S. Suslick, N. A. Rakow

In contrast, metalloporphyrin dyes used in the smell-seeing approach are mounted on reverse phase silica gel plates, which provide a hydrophobic surface that greatly reduces interference from water vapor. For instance, as reported in the Nature paper, a color fingerprint obtained from exposing an array to n-hexylamine vapor was identical to one from an array spiked heavily with water vapor.

The ability to easily detect chemicals in the presence of large amounts of water vapor also makes the smell-seeing method more sensitive for trace levels of odors and more specific for many different odors than polymer-based systems. The metalloporphyrins form reversible chemical bonds when they come in contact with chemical vapors. This is a much stronger interaction than the simple adsorption that occurs between polymers and vapors. "In principle and in practice, [this system has] greater sensitivity and specificity because of the discrete nature of the bonding that adsorption onto polymers does not permit," says Suslick.

A sensor based on the smell-seeing technique may be available by September 2001. A company called ChemSensing, Inc., is being set up in Champaign to develop and market a smell-seeing device. The first commercial product will be called a "smell camera" and will incorporate an inexpensive digital camera to measure colorimetric changes to detect chemicals like those described in the Nature paper. "The beauty of using dyes," says Rakow, "is that you only need a simple imaging device, so a digital camera could be interfaced with a PalmPilot." The goal is to make the product affordable--about $1,000 per unit. Still to be determined is the best way to manufacture the array of metalloporphyrin dyes. "We want to rapidly and uniformly put down the pattern of spots so when the color changes, it pops out at you and you can see it," says Suslick. One method being tested is ink-jet printing technology, used by companies that make DNA arrays.

Carol Potera

 

Suggested Reading

Rakow NA, Suslick KS. A colorimetric sensor array for odour visualization. Nature 406(6797):710-713 (2000).

Bhyrappa P, Vaijayanthimala G, Suslick KS. Shape-selective ligation to dendrimer-metalloporphyrins. J Am Chem Soc 121:262-263 (1999).

Suslick KS, Rakow NA, Kosal ME, Chou JH. The materials chemistry of porphyrins and metalloporphyrins. J Porphyrins Phthalocyanines 4(4):407-413 (2000).

 

진보블로그 공감 버튼트위터로 리트윗하기페이스북에 공유하기딜리셔스에 북마크

How people can smell - smell process

 

http://www.senseofsmell.org/feature/smell101/lesson1/01.php

 

Whether for finding food, avoiding predators or choosing a mate, the sense of smell is critical for the existence of almost all creatures. We humans, able to distinguish over 10,000 different odor molecules, utilize our sense of smell for a multitude of activities from enjoying the aroma of freshly brewed coffee to deciding whom not to sit next to on the bus. In the last 15 years scientists have made great advances to our understanding of how our nose detects odor molecules and our brain processes the resulting information that gives rise to the sensation of smell.

diagram courtesy of Leffingwell.com

Every time we inhale, currents of air swirl up through the nostrils, over the bony turbinates, to a “sheet” about the size of a small postage stamp that contains millions of olfactory receptor neurons. This is the olfactory epithelium.

diagram courtesy of Leffingwell.com

Each of the millions of olfactory neurons has minuscule filaments (cilia) extending from its knob.  This knob is located at the tip of the olfactory neuron and the cilia project from the knob directly into the atmosphere.  This is the only part of the brain that projects into the atmosphere.   The cilia contain olfactory receptors, specialized proteins that bind low molecular weight molecules (odorants).  One of the big breakthroughs of the past 15 years was the discovery by L. Buck and R. Axel of a large multi-gene family that encode for these olfactory receptors.  Each receptor has a pocket (binding site) that is just the right shape to bind either a specific molecule or a group of structurally similar molecules. The interaction of the right molecule with the right receptor causes the receptor to change its shape (structural conformation). This conformational change gives rise to an electrical signal that goes first to the olfactory bulb and then to the areas of the brain that convert the electrical signal to a smell.  

In 1996, Peter Mombaerts found that olfactory neurons containing the same olfactory receptor, while randomly scattered within one of four spatial zones of the olfactory epithelium, project to only two specific areas (glomeruli) in the olfactory bulb.  These findings suggest that the bulb transfers information that is broadly distributed in the olfactory epithelium into a highly organized information map that is in essence a map of the information provided by the different olfactory receptors. Systematic studies have shown that different odorants are represented by distinct spatial activity patterns in the glomerular layer of the olfactory bulb.  These results in turn suggest a combinatorial mechanism for olfactory coding wherein the responses of olfactory receptors to odorants produce spatial patterns of olfactory bulb activity that are characteristic for a given odorant or blend of odorants, e.g. a perfume.  Thus, it appears that these spatial patterns of activity create the information that leads to recognition of odor quality and intensity and discrimination between odors.  This information is processed at higher levels of the olfactory system and in the brain giving rise to the perception of smell.

진보블로그 공감 버튼트위터로 리트윗하기페이스북에 공유하기딜리셔스에 북마크