出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2012/12/04 17:19:10」(JST)
| Alcian blue stain | |
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Other names
Alcian blue 8GX, Ingrain blue 1, C.I. 74240, "chloromethylated copper phthalocyanine-thiourea reaction products" |
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| Identifiers | |
| CAS number | 33864-99-2 Y |
| PubChem | 3084579 |
| ChemSpider | 2341620 Y |
| Jmol-3D images | Image 1 Image 2 |
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SMILES
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InChI
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| Properties | |
| Molecular formula | C56H68Cl4CuN16S4 |
| Molar mass | 1298.86 g mol−1 |
| Y (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
Alcian blues (IPA ′al·shən ′blü[1]), are a family of polyvalent basic dyes, of which, the Alcian blue 8G (also called Ingrain blue 1, and C.I. 74240, formerly called Alcian blue 8GX from the name of a batch of an ICI product) has been historically the most common and the most reliable member.[2] It is used to stain acidic polysaccharides such as glycosaminoglycans in cartilages and other body structures, some types of mucopolysaccharides, sialylated glycocalyx of cells etc. For many of these targets it is one of the most widely used cationic dyes for both light and electron microscopy. Use of alcian blue has historically been a popular staining method in histology especially for light microscopy in paraffin embedded sections and in semithin resin sections. The tissue parts that specifically stain by this dye become blue to bluish-green after staining and are called "Alcianophilic" (akin to "eosinophilic" or "sudanophilic"). Alcian blue staining can be combined with H&E staining, PAS staining and van Gieson staining methods. Alcian blue can be used to quantitate acidic glycans both in microspectrophotometric quantitation in solution or for staining glycoproteins in polyacrylamide gels or on western blots. Biochemists had used it to assay acid polysaccharides in urine since 1960s for diagnosis of diseases like mucopolysaccharidosis but from 1970's, partly due to lack of availability of Alcian and partly due to length and tediousness of the procedure, alternative methods had to be developed e.g. Dimethyl methylene blue (DMB) method.[3]
Prof. J E Scott, the first person outside the dye Industry to crack the chemical secret of this dye comments:
In addition to its wide use as a stain Alcian blue has also been used in other diverse applications e.g. gelling agent for lubricating fluids, modifiers for electrodes, charged coating agents etc.
Contents
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The Monstral blue found to coat the inside of copper vessels used to process phthalic acid derivatives had lead to the discovery of Phthalocyanine in 1907. Attracted by the brilliance, stability and insolubility of this chromophore, attempts were made to reversibly modify it so that it would be carried into fabric in a solution and then easily precipitated (ingrained) into an unleachable but finely well dispersed deposit (hence the name "ingrain dyeing"). From this attempt, Alcian Blue (Ingrain blue 1) was first synthesized by the ICI dyestuffs department under N. H. Haddock and Wood in the early 1940s and patented in 1947 (Patent numbers: GB 586340 and GB 587636),[5] originally as a textile dye. In 1950 it was used by Steedman as a selective dye for mucins.[6] While the popularity of Alcian blue expanded exponentially, the difficulty involved in its production due to environmentally hazardous intermediate steps made its availability difficult and ICI stopped producing it by 1973. Many of the alternate sources sold similar looking color products with unreliable staining.
Prof J.E. Scott worked to decipher the chemistry of Alcian blue which was known only to the Industry but kept as a tight trade secret. After spending 3 man-years of effort (which would have been unnecessary had the industry released the results)in 1972 he published the structure of Alcian blue and was able to get ICI to confirm it in 1973, incidentally in the same time that ICI also had just stopped producing it.[7]
After the interim crisis since 1970s when ICI had to stop, there have now been environmentally safe alternative industrial manufacturing of this dye that is supposed to work as well as 8GX but is called 8G since it is made differently.[8] In attempt to answer what was the importance of discovering an alternative method of manufacturing this compound, a company (Anatech Ltd, USA) which remanufactured Alcian Blue says:
According to Elsevier's dictionary of chemoetymology the Alcian in Alcian Blue might have been coined by contraction (and slight alteration) of phthalocyanine.".[9] Oxford online dictionary mentions that it was a trademark and also specifies[10]
This hypothesis is consistent with the name of Alcian green which is a tetraphenyl-phthalocyanine with copper.[11]
However Prof. J.E. Scott who had cracked the Chemistry of Alcian Blue himself and later received confirmation from the manufacturer (ICI) wrote that Alcian was a trademark that ICI preferred to be spelt starting with a capital "A", and he presumes it came from the old English word "halcyon", which has a "romantic and poetic associations with the kingfisher bird and calm seas".[12] Prof. Scott also states that Alcian green was merely a mixture of Alcian Blue and Alcian yellow and not a single compound, which is also supported by thin layer chromatography data from various sources e.g. works by another dye expert Prof. R.W. Horobin - one of the two chief editors of the 10th edition of the 75 year old "Conn's Biological Stains Manual" published on behalf of the Biological Stain Commission.[13]
Alcian Yellow is an azo dye which neither has a phthalocyanine ring nor any of the colors of the Kingfisher, but in common with Alcian blue, has hydrolyzable charged thiouronium side-chains and similar stability of the final stained product. On the other hand there are other phthalocyanine dyes like Luxol fast blue and Durazol blue which have not acquired "Alcian" as a part of their names.[14]
The solid Alcian Blue is obtained as greenish-black (or sometimes dark bluish violet[15]) crystals with metallic sheen. The aqueous solution is bright greenish-blue. Though the compound alcian blue itself is unstable (see stability below) the staining it produces is stable and light fast (i.e. does not bleach).
Unlike tricyclic thiazines (e.g. toluidine blue, methylene blue and azure A etc.) which are metachromatic due to switching from monomeric to stacked aggregates, Alcian blue is apparently orthochromatic. In common with Astra blue and other similar dyes, this property that it does not change color either by change in concentration or by combination with substrates, makes it very suitable for microspectrophotometry. The apparent lack of metachromasia is not because it is truly orthochromatic but because "it is already fully metachromatic" in aqueous solution.[16]
In aqueous solution large numbers of AB molecules stack together as micelles of very large size, too large to be even dialysed. Thus even at a fairly high dilution, it has an absorption maximum at ~600-615 nm which is actually not the absorption maximum of a dye monomer but that of the multimer. Since the absorbed light is of yellow orange spectrum, the transmitted/reflected light is perceived by our eye as the complementary color of slightly greenish blue or cyan. In aqueous solution Alcian blues continue to be metachromatic at molar concentrations one hundredth those at which toluidine blue is mainly orthochromatic. Only a very small shoulder of the absorption curve at 670-680 nm represent the monomeric dye which is usually the minority and becomes even lesser minority (<108M) in presence of salts. However when the solvent is DMSO- a non-protic solvent of moderately high dielectric constant, Alcian blue does not aggregate and a big monomeric absorption peak can be well visualized. A similar spectral shift to the longer monomeric peak is also observed when nonpolar solvents like ethanol (or ethanol water mixture) is used as a vehicle or when nonionic detergents like Triton X-100 are used, that make exogenous micelles.
Alcians blue carries Phthalocyanine one of the most highly colored chromophores yet known with a molar extinction of 120,000 i.e. AB is detectable at half the molar concentration of popular dyes like toluidine blue, tryarylmethanes (e.g. pararosaniline and the analogous Schiff bases used in PAS stain, Crystal violet in Gram stain) etc.
It is water soluble. When each of the pair of substituents on the pendant group nitrogens are toluyl, the solubility in water at 20° is about 9.5% w/w ; and similarly a few other solubilities are: 6.0% in absolute ethanol, 6.0% in Cellosolve and 3.25% ethylene glycol, whereas it is practically insoluble in xylene.[17] In relative/partitioning terms, Alcian Blue 8G has a (octanol) Partition coefficient "LogP" of -9.7, suggesting it is rather water soluble (lipid soluble if LogP>0, and good lipid stains generally have a LogP>+7).[18] Methanol is an acceptable substitute for ethanol as a potential vehicle for Alcian blue, but isopropanol is not, because, within a few hours all of suspended Alcian blue precipitates if isopropanol is tried as a vehicle.[19]
The sample compound with Merck index number 218 has a melting point of 148°C.
It is a tetravalent basic (cationic) dye with a copper (Cu2+, coordination 4 of 6, orbital configuration d9 with Jahn–Teller distortion) phthalocyanine nucleus (CuPc) with three or four pendent isothiouronium side chains imparting its bulkiness and positive charges. In order to qualify as an alcian blye family member there has to be at least 2 side chains and the mixtures often have 3 chains in average to qualify as 8G. Four tetramethylisothiouronium groups per molecule are shown in the picture. ICI had claimed an average of about three side chains per molecule, but analyses by Prof Scotts lab suggested between three and four. Most of them are at the 2(3) positions, as in the formula and sometimes a cartoon representation uses the methylene bridge criss crossing across the bond between these two positions to indicate that it could bind either of these two positions. A large number of isomers, differing in the positions of the cationic groups, are possible. Alcian blue 7GX carries fewer isothiouronium groups than 8GX. Similarly 5GX and 2GX may have even fewer side groups but it was not rigorously proven.
The phthalocyanine aromatic nucleus has a large Conjugated system which has a CBN (Conjugated bond number) of 48.[20] However it is the charges on the isothiouronium side groups that still keeps it water soluble. These side groups can carry bulkier alkyl or aryl substituents rather than the 8x2 methyl groups as in the image given. These groups split off from the macrocyclic ring during the washing at the end of staining or by rather mind conditions (e.g. pH above 5.6) or during spontaneous degradation.
The metals in the Phthallocyanine nucleus and substituted groups directly attached to the aromatic nucleus determine colors of the members of the metal phthallocyanine family e.g. Alcian Blue and the copper phthalocyanine itself are blue, but brominated or chlorinated copper phthalocyanine and sulfonated copper phthalocyanine are green.
Alcian Blue has a relatively high solubility in salt solutions and stains slower than other dyes. By changing pH or ambient salt concentrations characteristic staining patterns can be obtained.
At pH 1.0 it stains only sulfated polysaccharides and at pH 2.5 also stains carboxyl group containing sugars such as sialic acids and uronic acids intensify the stain of hyaluronic acids which would also stain albeit relatively weakly by their half sulfate esters at pH 1.0.[21]
A staining method where at a fixed pH of about 5.5, different critical salt concentration (Classically MgCl2, but NaCl, KCl, LiBr are potential alternatives) can be used where the smaller (faster diffusing) salt cation competes with alcian blue to bind to the anionic sites. Target material specific critical electrolyte concentration (CEC) is supposed to selectively identify sulphated, carboxylated and phosphated structures for example as the targets.
Alcian blue 8G as an exception to most other dyes can deteriorate even in the solid state, changing to an insoluble pigment, unless it is the pyridine variant of alcian blue (Alcian Blue-tetrakis(methylpyridinium) chloride, CAS 123439-83-8, CB6503730, PubChem 24860335).[22] The solution is unstable at pH 5.6 and above, unless MgCl2 is used as a stabilizer. According to Prof. John A. Kiernan - one of the two chief editors of the 10th edition of the 75 year old "Conn's Biological Stains Manual" published on behalf of the Biological Stain Commission:[23]
Nucleic acids are generally basophilic because they have a very high density of negative charge due to the sugar phosphate backbone. However in contrast to other basic i.e. cationic dyes, Alcian blue usually (given the right pH and salt concentrations, and normal temperature and duration in minutes, not hours) preferably stains acidic glycosaminoglycans but not the chromatin and nissel substance, the mechanism of which had been a mystery for a long time and various theories were proposed. Though the presumed basis of the staining is its positive charge attracted to negative structures (e.g. acidic sugars), bulkiness (width 2.5-3 nm, compared to toluidine blue ~0.7 x1.1 nm[24]) makes its diffusion very slow in less permeable parts of the tissue and thus prevent it from staining highly negative yet compact structures such as chromatin and nissel substance.[25] However prolonged staining (few days at 25°C) or DNA denaturing conditions may allow Alcian blue to also stain the nucleus. The isolation of the positive charge from the aromatic electron cloud by the intervening methylene bridges makes the localized positive charged regions "hard" ions in contrast to soft ions where the charge is delocalized over the whole aromatic pi cloud.[26] When these hard cations encounter the hard anions e.g. in form of sulfate they form salts without regard for the precise chemical nature of the anion. The resulting salts are highly stable but can be slowly exchanged with high concentration of salts. Washing with water or alkali treatment after staining causes base catalyzed hydrolysis and removal of the pendant positively charged side chains and the resulting compound is Phthalocyanine Blue which forms a blue water insoluble dye precipitate.[27] The precipitates are so robust that they withstand harsh conditions like PAS or other counterstaining and also dehydration and embedding treatments (in contrast toluidine blue is partially extracted away during dehydration). This unleachability is the chemical basis of the ingrain dyeing for which AB (Ingrain blue 1) was originally designed by the dye industry.
The historic Alcian Blue varied so much batch to batch that only the 8GX (e.g. not even the 8GS) batch produced by ICI was later decided to be the biologically useful ones. Commercially available batches usually contained about 49% of the actual dye and rest used to be Sulfate, boric acid, dextrin and other impurities and by variou sextraction methods up to 80% pure extracts can be made. Actually the dye does not necessary contain all 4 substituents but might contain 2 or 3 of them and have various geometric isomers. But anyhow the manufacture of 8GX by ICI had stopped by Mid-1970s because of environmental hazards and very small lots were available that were received from alternate sources. Only recently Alcian Blue has been re manufactured in bulk using safer procedures but the newer product does not have the suffix X (or S) since the manufacture process (and the exact product composition) is somewhat different.[28]
Alcian blue is an eye and respiratory tract irritant. Solid Alcian blue is a combustible powder and should never be handled close to heat or a naked flame. Heating Alcian blue produces toxic fumes of nitrogen compounds. It can react violently if mixed with oxidising materials. The solution of Alcian blue is a skin sensitiser and corrosive (partly due to the acidic pH needed to maintain it unhydrolyzed in solution) and harmful by skin absorption. Most vendor MSDS (Material safety datasheet) mention that effect of ingestion not known or target organ not known. However some do mention that potential target organs are teeth and kidneys.[29]
This stain was originally discovered by ICI in 1940s as a member of the competitive dye industry for the purpose of industrial dying. It was used for some time for staining textiles, leather products and inks. ICI sold thousands of tons of alcian blue and filed multiple patents regarding its manufacturing process to keep its chemistry a tight secret. However ICI had had trouble with the dye's solubility under textile dyeing conditions, and various process changes in manufacturing were made during the 1950s and 1960s.
Trypanocidal drug suramin is polysulfated and gives a positive alcian blue reaction even at pH 1.[30] Thus, in tissues from a patient on Suramin Alcian blue cannot be used or interpreted reliably.
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In addition to its use as a dye or stain Alcian blue also finds other material science uses.
Alcian blue has been used as an adhesive to help stick glycol methacrylate sections to glass slides (which have negatively charged silicate groups).[31]
Alcian blue carrying a large aromatic surface that can participate in Van der Waal's interaction as well as multiple licalized charges. Thus it can be coated onto surfaces and significantly modify surface property and charge. Some cells in culture grow better on surfaces coated with positive charge like poly-L-lysine or polyornithine or Alcian blue. Alcian blue coated surfaces hold onto the negatively charge glycocalyx so tight that it can even be used to cover a layer of cells and then float it up to peel off the roof ("unroofing") to study the cytoplasmic side of the plasma membrane.[32]
Alcian Blue has been used as a gelling agent for lubricating fluids [33] likely due to the stacking properties of this macrocylic aromatic compound.
Another application is "Alcian Blue Modified Carbon Paste Electrode" (ABMCPE) which acts as a highly sensitive redox sensor compared to Bare Carbon Paste Electrode (BCPE) and exhibits strong "promoting" effect and stability.[34]
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