FIXATIVE SOLUTION AND METHOD OF PREPARATION OF BIOLOGICAL SAMPLE

Abstract

Aspects of the disclosure relate to a fixative containing carboxylic acid, preferably acetic acid, for parasitological samples. In some aspects the disclosure relates to an aqueous fixative solution for parasitological samples comprising: a) a C2 to C6 carboxylic acid (preferably acetic acid) at a concentration of 0.5M or greater; and b) a C2 to C6 carboxylate salt or halide salt at a concentration of 0.02M or greater, preferably 0.04M or greater. An optional composition comprises 1.3M acetic acid, 12 mM sodium benzoate, 0.9% calcium chloride, 0.9% calcium bromide, 100 pg/ml menthol and 350 pg/ml thymol. The fixative is free of formaldehyde or other hazardous compounds, and exhibits good killing and staining properties when used with parasitological samples such as ova and helminths.

Description

FIELD OF THE INVENTION

The present invention relates to a fixative solution for the histological fixation of biological samples and to a method of preparation of biological samples for examination, for example, by microscopy.

BACKGROUND

The invention is concerned particularly but not exclusively with a fixative solution suitable for fixation of living organisms, especially parasitological samples, such as helminth ova or Giardia lamblia for example.

A fixative solution for such applications is required to kill the organism (which may be pathogenic) and to preserve their cellular structure so that they can subsequently be examined microscopically, typically after staining with a stain such as Trypan blue, Lugol's iodine or Trichrome stain, for example. The microscopic appearance of the sample after staining is affected by the fixative solution, but it is difficult or impossible to predict the effect of a given formulation of fixative on the staining properties.

Formaldehyde has been widely used in fixative solutions (for example, in aqueous solution as formalin) but is toxic, carcinogenic and generally hazardous to the environment.

Other fixatives have been used but in many cases are also hazardous.

More recently, non-hazardous fixatives have been developed, for example, as disclosed in GB 2528426A (Reardon) and WO92/19951A (Streck Lab) but there remains a need for fixative solutions which will reliably kill parasitical organisms such as helminths which, having a tough outer layer, are highly resistant to the penetration of fixative. Cell death is difficult to achieve in a short time if highly toxic chemicals such as formaldehyde are ruled out.

An object of the present invention is therefore to provide a relatively non-hazardous fixative that is suitable for histological fixing of parasitological samples in particular.

A further object of the invention is to provide a fixative and method of preparation of biological samples that results in good staining properties.

SUMMARY

Accordingly, the invention provides an aqueous fixative solution for biological samples comprising:

• a) a C2 to C6 carboxylic acid at a concentration of 0.5M or greater
• b) a C2 to C6 carboxylate salt or halide salt at a concentration of 0.02M or greater, preferably 0.04M or greater.

Optionally, said C2 to C6 carboxylic acid is acetic acid.

Optionally, the concentration of C2 to C6 carboxylic acid is 0.9M or greater, more preferably 1.3M or greater. Optionally, the concentration of the of C2 to C6 carboxylic acid is no greater than 3.5M.

It has been found that such concentrations of carboxylic acid (particularly acetic acid) result in a rapid killing of biological organisms such as helminth ova, for example, without requiring a toxic additive such as formaldehyde.

In an optional, yet preferred embodiment, the concentration of acetic acid is below 10% w/v. A concentration below this limit is classified as non-corrosive.

The carboxylate salt or halide salt of component b) may for example be the salt of an alkali or alkaline earth metal or of ammonium other cation that confers reasonable solubility.

Optionally, component b) is a calcium or magnesium halide salt.

More preferably, component b) comprises calcium chloride at a concentration of at least 0.06M, preferably at least 0.08M, preferably at least 0.1M, and/or calcium bromide at a concentration of at least 0.06M, preferably at least 0.08M, preferably at least 0.1 M.

It has been found that such halide salts help preserve the cellular structure, possibly an osmoregulatory effect involving the halide salts counteracting the turgor effect of the carboxylic acid.

Optionally, the fixative further comprises: c) a bacteriostatic or fungistatic concentration of benzoic acid or sorbic acid or a salt thereof.

Optionally, component c) is a benzoate salt at a concentration of at least 5 mM, more preferably at least 10 mM.

Component c) as defined above may help to preserve the sample against decomposition.

Optionally, the fixative further comprises: d) a biocidal essential oil component in a concentration of at least 50 μg/ml.

The biocidal essential oil may for example be bacteriostatic or bactericidal or fungistatic or fungicidal.

Optionally, said biocidal essential oil component d) is one or more of: menthol, thymol, pulegol, dihydrocarveol, piperitol, menthone, menthene, o-cymene, p-cymene, citronellal, carvacrol, eugenol, 4-carvo-menthol (termpinen-4-ol), allicin or camphor. Optionally, the essential oil component is present in its naturally-occurring stereoisomeric or enantiomeric form.

Desirably said biocidal essential oil component d) comprises menthol and thymol.

It has been found that such essential oils facilitate cell death and thus shorten the time needed for fixing.

In preferred, yet optional embodiments:

• i) said carboxylic acid component a) is acetic acid at a concentration of 0.8M to 1.75M,
• ii) said halide salt component b) is calcium chloride at a concentration of 70 to 100 mM plus calcium bromide at a concentration of 30 mM to 50 mM and
• iii) said benzoic acid salt component c) is at a concentration of 5 mM to 15 mM benzoate.

In particularly preferred, yet still optional embodiments:

• i) said carboxylic acid component a) is acetic acid at a concentration of 1.2M to 1.75M,
• ii) said halide salt component b) is calcium chloride at a concentration of 70 to 100 mM plus calcium bromide at a concentration of 30 mM to 50 mM and
• iii) said benzoic acid salt component c) is at a concentration of 5 mM to 15 mM benzoate.

The above embodiments advantageously may result in particularly good staining properties.

In a further preferred embodiment:

• i) said carboxylic acid component a) is acetic acid at a concentration of 0.8M to 1.75M,
• ii) said halide salt component b) is calcium chloride and/or calcium bromide at a total concentration of from 1.0 to 4.5M and
• iii) said benzoic acid salt component c) is at a concentration of 5 mM to 125 mM benzoate.

In certain preferred embodiments component b) is a halide salt at a concentration of 0.3M to 6M, preferably 1M to 5M, most preferably 1M to 4M.

Such embodiments have been found suitable for use as flotation solutions, having a density sufficiently great to float cysts or ova or other organisms of interest, thereby facilitating their separation and identification.

In such embodiments the fixative optionally includes a non-polar solute which increases the density of the fixative solution to above 1.1 g/ml, preferably above 1.2 g/ml. most preferably from 1.2 g/ml to 1.4 g/ml.

Preferably the non-polar solute is a soluble carbohydrate, preferably a sugar, preferably sucrose or glucose or fructose or maltose, or any combination thereof.

An additional aspect of the invention for which protection is sought provides a method of preparing a biological sample for examination comprising fixing the sample with an aqueous fixative solution as defined above.

Optionally, the biological sample is a living organism. Optionally, the biological sample is a parasitological sample.

In a preferred embodiment the biological sample is stained after fixing, for example, with an azo dye, or with iodine, or with a trichrome stain. Other stains can also be used.

Other preferred features are defined in the claims.

Within the scope of this application it is expressly intended that the various aspects, embodiments, examples and alternatives set out in the preceding paragraphs, in the claims and/or in the following description, and in particular the individual features thereof, may be taken independently or in any combination. That is, all embodiments and/or features of any embodiment or example can be combined in any suitable way and/or combination, unless such features are incompatible. The applicant reserves the right to change any originally filed claim or file any new claim accordingly, including the right to amend any originally filed claim to depend from and/or incorporate any feature of any other claim although not originally claimed in that manner.

DETAILED DESCRIPTION

A study was conducted to validate the effectiveness of a number of formulations of fixative in accordance with the invention in order to determine both their effectiveness to denature a cell (i.e. make inert from an infectious perspective) and to preserve cellular morphology for a prolonged period of time.

To achieve this, three types of stain were used, namely:

• • 1. Lugol's Iodine staining to determine morphology
  • 2. Trypan Blue staining to determine viability
  • 3. Trichrome stain commonly used laboratory procedure.

Initially all substances were tested using a live sample of Giardia lamblia, which is a flagellated protozoan parasite commonly found around the world. Its abundance in numbers and delicate internal structures made this a suitable candidate for testing. Samples of Trichuris suis (whipworm) were also tested with the most viable formulation (Example 8) to see mainly whether the fixative was able to denature a typical helminth ova in an acceptable amount of time.

Example 1

200 ml of fixative was prepared with the following formulation:

• • 185 ml distilled water
  • 15 ml of Glacial Acetic Acid (7.5% solution—1.3M)
  • 0.06 g Sodium Benzoate—2 mM
  • 2.22 g Calcium Chloride—100 mM

Example 2

200 ml of fixative was prepared with the following formulation:

• • 181 ml distilled water
  • 19 ml of Glacial Acetic Acid (9.5% solution—1.65M)
  • 0.36 g Sodium Benzoate—12 mM
  • 3.00 g Calcium Chloride—100 mM
  • 4.72 g Calcium Bromide

Example 3

200 ml of fixative was prepared with the following formulation:

• • 181 ml distilled water
  • 19 ml of Glacial Acetic Acid (9.5% solution—1.65M)
  • 0.36 g Sodium Benzoate—12 mM
  • 1.8 g Calcium Chloride—0.9%
  • 1.8 g Calcium Bromide 0.9%

Example 4

200 ml of fixative was prepared with the following formulation:

• • 190 ml distilled water
  • 10 ml of Glacial Acetic Acid (5% solution—0.87M)
  • 0.36 g Sodium Benzoate—12 mM
  • 1.8 g Calcium Chloride—0.9%
  • 1.8 g Calcium Bromide 0.9%

Example 5

200 ml of fixative was prepared with the following formulation:

• • 181 ml distilled water
  • 19 ml of Glacial Acetic Acid (9.5% solution—1.65M)
  • 0.36 g Sodium Benzoate—12 mM
  • 1.8 g Calcium Chloride—0.9%
  • 1.8 g Calcium Bromide 0.9%
  • 0.04 g Menthol crystals—200 μg/ml (around half of maximum solubility)
  • 0.125 g Thymol—625 μg/ml (around 70% of maximum solubility)

Example 6

200 ml of fixative was prepared with the following formulation:

• • 181 ml distilled water
  • 19 ml of Glacial Acetic Acid (9.5% solution—1.65M)
  • 0.36 g Sodium Benzoate—12 mM
  • 1.8 g Calcium Chloride—0.9%
  • 1.8 g Calcium Bromide 0.9%
  • 0.02 g Menthol crystals—100 μg/ml (around a quarter of max solubility)
  • 0.07 Thymol—350 μg/ml (around 39% of maximum solubility)

Example 7

200 ml of fixative was prepared with the following formulation:

• • 190 ml distilled water
  • 10 ml of Glacial Acetic Acid (5% solution—0.87M)
  • 0.36 g Sodium Benzoate—12 mM
  • 1.8 g Calcium Chloride—0.9%
  • 1.8 g Calcium Bromide 0.9%
  • 0.02 g Menthol crystals—100 μg/ml (around a quarter of max solubility)
  • 0.07 Thymol—350 μg/ml (around 39% of maximum solubility)

Example 8

200 ml of fixative was prepared with the following formulation:

• • 185 ml distilled water
  • 15 ml of Glacial Acetic Acid (7.5% solution—1.3M)
  • 0.36 g Sodium Benzoate—12 mM
  • 1.8 g Calcium Chloride—0.9%
  • 1.8 g Calcium Bromide 0.9%
  • 0.02 g Menthol crystals—100 μg/ml (around a quarter of max solubility)
  • 0.07 Thymol—350 μg/ml (around 39% of maximum solubility)

Example 9

200 ml of fixative was prepared with the following formulation:

• • 185 ml distilled water
  • 15 ml of Glacial Acetic Acid (7.5% solution—1.3M)
  • 0.36 g Sodium Benzoate—12 mM
  • 1.8 g Calcium Chloride—0.9%
  • 1.8 g Calcium Bromide 0.9%
  • 0.04 g Menthol crystals—200 μg/ml (around a quarter of max solubility)

Example 10

200 ml of fixative was prepared with the following formulation:

• • 185 ml distilled water
  • 15 ml of Glacial Acetic Acid (7.5% solution—1.3M)
  • 0.36 g Sodium Benzoate—12 mM
  • 1.8 g Calcium Chloride—0.9%
  • 1.8 g Calcium Bromide 0.9%
  • 0.07 Thymol—350 μg/ml (around 39% of maximum solubility)

Example 11

200 ml of fixative was prepared with the following formulation:

• • 185 ml distilled water
  • 15 ml of Glacial Acetic Acid (7.5% solution—1.3M)
  • 0.36 g Sodium Benzoate—12 mM
  • 1.8 g Calcium Chloride—0.9%
  • 1.8 g Calcium Bromide 0.9%
  • 0.2 ml Triton X-100—0.001%
  • (The use of Trition® surfactant negates the use of ELISA).

Example 12

Live Giardia samples were received and checked for morphology and to ensure correct cellular structure etc.

200 μl of Live Giardia were inculcated into each of the test solutions (3.3 ml) contained within a Mini Parasep SF® faecal parasite concentrator device.

This was carried out in duplicate, with:

• • a. One sample containing just the fixative (Sample 1); and
  • b. One sample containing the fixative mixed with a consistent sample of raw stool (Sample 2)

This was immediately followed by centrifugation at 400 g for 2 minutes. A 15 μl sample was then taken from the base of each sedimentation tube to be mounted on a microscope slide with 15 μl of Trypan blue stain added. As viability of the cysts was the main reason for this step, each sample was centrifuged immediately after the addition of the Live Giardia, and mounted directly after centrifugation.

Samples were left for a period of 24 hours and then 15 μl was taken to check morphology with Lugol's iodine and Trypan Blue of Sample 1.

Samples were left for a period of 48 hours and then 15 μl was once again taken to check morphology with Lugol's iodine of Sample 1.

Samples were left for a period of 5 days and then 15 μl was once again taken to check morphology with Lugol's iodine of both samples.

Trichrome stains were conducted for all samples which still showed good morphology, with samples being taken from Sample 1.

Further morphology testing was carried out for all samples which passed this point after a period of 2 months.

The results for the formulations of the above Examples are shown in the Table 1.0 below, together with comparative results for 10% formalin, the commercially available fixatives SAF (formaldehyde-based, containing methanol and also 2% acetic acid), Alcorfix (containing methanol, ethanol, isopropanol, zinc sulphate and 4.8% acetic acid), PVA (containing methanol, ethanol and zinc sulphate) and Safefix (containing 1-(cis-3-chloroallyl)-3,5,7-triaza-1-azoniaadamantane chloride), and also distilled water, as a control.

TABLE 1.0
	Cell	Cell	Cell	Cell	Cell	Cell	Cell
	viability	viability	structure	structure	structure	structure	structure
	after 2	after 24	after 24	after 48	after 1	after 1	after 2
	mins	hours	hours	hours	week	week	months
	(Trypan	(Trypan	(Lugol's	(Lugol's	(Lugol's	(Trichrome	(Lugol's
Fixative	blue)	blue)	Iodine)	Iodine)	Iodine)	stain)	Iodine)
10% Formalin	Clear		Good	Excellent	Good	Good	Good
	(cross-		structure	structure	structure	definition	structure
	linking -
	test
	invalid)
SAF	Clear		Excellent	Excellent	Excellent	Reasonable	Acceptable
	(cross-		structure	structure	structure	definition	structure
	linking -
	test
	invalid)
Alcorfix	Minimal	Dark blue	Excellent	Excellent	Excellent	Good	Excellent
	blue in	ingress	structure	structure	structure	definition	structure
	cell wall	(Cell
	(start of	death)
	cell
	death)
PVA	Clear	Dark blue	Excellent	Good	Excellent	Good	Excellent
	(Cell	ingress	structure	structure	structure	definition	structure
	viable)	(Cell
		death)
SafeFix	Clear	Clear (Cell	Acceptable	Excellent	Good		Poor
	(Cell	appears	structure	structure	structure		structure
	viable)	viable)
Distilled	Clear	Clear (Cell	Excellent	Acceptable	Poor	Poor	Poor/Complete
water	(Cell	viable)	structure	structure	structure	definition	cellular
	viable)						degeneration
Example 1	Dark	Dark blue	Excellent	Excellent	Excellent	Good	Good
	blue in	in cell wall	structure	structure	structure	definition	structure
	cell wall	and light
	(Cell	blue
	death)	cytoplasm
		(Cell
		death)
Example 2	Dark	Dark blue	Excellent	Excellent	Excellent	Reasonable	Excellent
	blue in	in cell wall	structure	structure	structure	definition	structure
	cell wall	and light
	(Cell	blue
	death)	cytoplasm
		(Cell
		death)
Example 3	Dark	Dark blue	Excellent	Excellent	Excellent	Reasonable	Good
	blue in	in cell wall	structure	structure	structure	definition	structure
	cell wall	and light
	(Cell	blue
	death)	cytoplasm
		(Cell
		death)
Example 4	Dark	Dark blue	Excellent	Excellent	Excellent	Poor	Excellent
	blue in	in cell wall	structure	structure	structure	definition	structure
	cell wall	and light
	(Cell	blue
	death)	cytoplasm
		(Cell
		death)
Example 5	Dark	Dark blue	Excellent	Excellent	Excellent	Reasonable	Excellent
	blue in	in cell wall	structure	structure	structure	definition	structure
	cell wall	and dark
	(Cell	blue
	death)	cytoplasm
		(Cell
		death)
Example 6	Dark	Dark blue	Excellent	Excellent	Excellent	Reasonable	Excellent
	blue in	in cell wall	structure	structure	structure	definition	structure
	cell wall	and light
	(Cell	blue
	death)	cytoplasm
		(Cell
		death)
Example 7	Dark	Dark blue	Excellent	Excellent	Excellent	Good	Good
	blue in	in cell wall	structure	structure	structure	definition	structure
	cell wall	and light
	(Cell	blue
	death)	cytoplasm
		(Cell
		death)
Example 8	Dark	Dark blue	Excellent	Excellent	Excellent	Excellent	Excellent
	blue in	in cell wall	structure	structure	structure	definition	structure
	cell wall	and light
	(Cell	blue
	death)	cytoplasm
		(Cell
		death)
Example 9	Dark	Dark blue	Excellent	Excellent	Excellent	Good	Good
	blue in	in cell wall	structure	structure	structure	definition	structure
	cell wall	and light
	(Cell	blue
	death)	cytoplasm
		(Cell
		death)
Example 10	Dark	Dark blue	Excellent	Excellent	Excellent	Good	Good
	blue in	in cell wall	structure	structure	structure	definition	structure
	cell wall	and light
	(Cell	blue
	death)	cytoplasm
		(Cell
		death)
Example 11	Dark	Dark blue	Excellent	Acceptable	Excellent	Poor
	blue in	in cell wall	structure	structure	structure	definition
	cell wall	and dark
	(Cell	blue
	death)	cytoplasm
		similar to
		Alcorfix
		(Cell
		death)

The fixatives of Examples 5 to 11 gave particularly good results, with the Example 8 formulation currently being considered the best.

Preferred aqueous fixative solutions of the present invention can be used with e.g. faecal parasite concentrator devices.

Such devices are commercially available e.g. as the Parasep® or ParaPRO® devices or the devices shown in WO2017/187165A, in the name of the present applicants, for example.

Such devices typically utilise a mixing chamber and a receiving chamber separated by a filter.

In use, a fixative solution and a faecal sample are introduced into the mixing chamber and agitated in contact to liquefy the sample. The liquified sample is then filtered and the filtrate, (containing e.g. ova and cysts which pass through the filter) is collected in the receiving chamber.

The fixative solution ensures that the filtrate is not biologically hazardous. The filtrate can then be examined under the microscope to identify e.g. the ova and cysts.

For example, a mini Parasep® device can be used, which will typically hold 3.3 ml of fixative solution within the mixing tube. A 0.5-1.0 g sample of stool is added to the mixing tube before the tube is sealed with a vertical filter attached to a sedimentation tube. The sample is then vortexed, inverted and typically centrifuged for 2 minutes at 400 g (dependent on filter version). The filter and mixing tube can then be removed and a sample taken from the pellet found at the base of the sedimentation tube. This is then mounted on a microscope slide, where a stain may be added before the sample is examined for the presence of parasitic organisms.

In some cases, it is desirable for the fixative solution to float the ova and cysts so that they can be more readily identified and separated from the solution. Such solutions are known as flotation solutions.

Such flotation solutions can for example be used in a mini Parasep® device as follows:

A 0.5-1.0 g sample of stool is added to the mixing tube before the tube is sealed with a vertical filter attached to a sedimentation tube. The sample is then vortexed, inverted and squeezed by hand to pressurise the vessel, forcing the filtration of the sample. The solution is left to rest for 3 minutes, before an inoculation loop is used to remove a layer from the top of the liquid (which will be holding the majority of the parasitic ova and cysts if present). This is then mounted on a microscope slide, where a stain may be added before the sample is examined for the presence of parasitic organisms.

The following Examples relate to formulations of flotation solutions. The volumes of fixative are approximate whereas the masses and (in the case of glacial acetic acid) volume of the components are exact. The specific gravity values (density compared to pure water) are also exact.

A series of high specific gravity fixative solutions were prepared as follows:

Example 13

Approximately 500 ml of fixative was prepared with the following formulation:

• • 231.25 ml de-ionised water
  • 250 g cane sugar
  • 18.75 ml of Glacial Acetic Acid (3.75 v/v % solution—0.66M)
  • 0.45 g Sodium Benzoate—0.09% (6.25 mM)
  • 2.25 g Calcium Chloride—0.45% (0.041 M)
  • 2.25 g Calcium Bromide hydrate—0.41% (0.021M)
  • 0.025 g Menthol—0.005%
  • 0.0875 g Thymol—0.0175%

The specific gravity of the resulting fixative was 1.265.

This formulation was one of the most effective of the high density formulations in Examples 13 to 28. In a variant of this formulation (Example 28), a higher proportion of cane sugar was employed in order to raise the specific gravity of the fixative solution to about 1.29.

Example 14

Approximately 500 ml of fixative was prepared with the following formulation:

• • 231.25 ml de-ionised water
  • 250 g cane sugar
  • 18.75 ml of Glacial Acetic Acid (3.75 v/v % solution—0.66M)
  • 1.8 g Sodium Benzoate—0.36% (25 mM)
  • 40 g Calcium Chloride—8.0% (0.72M)
  • 2.25 g Calcium Bromide hydrate—0.41% (0.021M)
  • 0.025 g Menthol—0.005%
  • 0.0875 g Thymol—0.0175%
  • The specific gravity of the resulting fixative was 1.245.

Example 15

Approximately 500 ml of fixative was prepared with the following formulation:

• • 231.25 ml de-ionised water
  • 230 g cane sugar
  • 18.75 ml of Glacial Acetic Acid (3.75 v/v % solution—0.66M)
  • 0.5 g Sodium Benzoate—0.10% (6.9 mM)
  • 60 g Calcium Chloride—12.0% (1.08M)
  • 2.25 g Calcium Bromide hydrate—0.41% (0.021M)
  • 0.025 g Menthol—0.005%
  • 0.0875 g Thymol—0.0175%
  • The specific gravity of the resulting fixative was 1.272

Example 16

Approximately 500 ml of fixative was prepared with the following formulation:

• • 231.25 ml de-ionised water
  • 200 g cane sugar
  • 18.75 ml of Glacial Acetic Acid (3.75 v/v % solution—0.66M)
  • 0.5 g Sodium Benzoate—0.10% (6.9 mM)
  • 60 g Calcium Chloride—12.0% (1.08M)
  • 2.25 g Calcium Bromide hydrate—0.41% (0.021M)
  • 0.025 g Menthol—0.005%
  • 0.0875 g Thymol—0.0175%
  • The specific gravity of the resulting fixative was 1.297.

Example 17

Approximately 500 ml of fixative was prepared with the following formulation:

• • 231.25 ml de-ionised water
  • 180 g cane sugar
  • 18.75 ml of Glacial Acetic Acid (3.75 v/v % solution—0.66M)
  • 0.25 g Sodium Benzoate—0.050% (3.5 mM)
  • 80 g Calcium Chloride—16.0% (1.44M)
  • 2.25 g Calcium Bromide hydrate—0.41% (0.021M)
  • 0.025 g Menthol—0.005%
  • 0.0875 g Thymol—0.0175%
  • The specific gravity of the resulting fixative was 1.324.

Example 18

Approximately 850 ml of fixative was prepared with the following formulation:

• • 462.5 ml de-ionised water
  • 200 g cane sugar
  • 37.5 ml of Glacial Acetic Acid (4.4 v/v % solution—0.66M)
  • 0.50 g Sodium Benzoate—0.059% (3.5 mM)
  • 390 g Calcium Chloride dihydrate—34.7% (3.12M)
  • 4.5 g Calcium Bromide hydrate—0.48% (0.024M)
  • 0.050 g Menthol—0.0059%
  • 0.175 g Thymol—0.021%
  • The specific gravity of the resulting fixative was 1.310.

Example 19

Approximately 400 ml of fixative was prepared with the following formulation:

• • 231.25 ml de-ionised water
  • 50 g cane sugar
  • 18.75 ml of Glacial Acetic Acid (4.7 v/v % solution—0.82M)
  • 0.25 g Sodium Benzoate—0.063% (4.33 mM)
  • 250 g Calcium Chloride dihydrate—47.1% (4.25M)
  • 2.25 g Calcium Bromide hydrate—0.52% (0.026M)
  • 0.025 g Menthol—0.0063%
  • 0.0875 g Thymol—0.022%
  • The specific gravity of the resulting fixative was 1.360.

Example 20

Approximately 450 ml of fixative was prepared with the following formulation:

• • 231.25 ml de-ionised water
  • 25 g cane sugar
  • 21 ml of Glacial Acetic Acid (4.7 v/v % solution—0.82M)
  • 0.25 g Sodium Benzoate—0.055% (3.89 mM)
  • 250 g Calcium Chloride dihydrate—42.0% (3.78M)
  • 2.25 g Calcium Bromide hydrate—0.46% (0.023M)
  • 0.025 g Menthol—0.0056%
  • 0.0875 g Thymol—0.019%
  • The specific gravity of the resulting fixative was 1.330.

Example 21

Approximately 850 ml of fixative was prepared with the following formulation:

• • 462.5 ml de-ionised water
  • 360 g cane sugar
  • 37.5 ml of Glacial Acetic Acid (4.4 v/v % solution—0.77M)
  • 0.50 g Sodium Benzoate—0.059% (4.08 mM)
  • 200 g Calcium Chloride dihydrate—17.8% (1.60M)
  • 4.5 g Calcium Bromide hydrate—0.49% (0.024M)
  • 0.050 g Menthol—0.0059%
  • 0.175 g Thymol—0.021%
  • The specific gravity of the resulting fixative was 1.308.

Example 22

Approximately 950 ml of fixative was prepared with the following formulation:

• • 550 ml de-ionised water
  • 360 g cane sugar
  • 37.5 ml of Glacial Acetic Acid (3.9 v/v % solution—0.69M)
  • 200 g Calcium Chloride dihydrate—15.9% (1.43M)
  • 4.5 g Calcium Bromide hydrate—0.44% (0.022M)
  • 0.050 g Menthol—0.0053%
  • 0.175 g Thymol—0.018%
  • The specific gravity of the resulting fixative was 1.280.

Example 23

Approximately 820 ml of fixative was prepared with the following formulation:

• • 500 ml de-ionised water
  • 280 g cane sugar
  • 37.5 ml of Glacial Acetic Acid (4.5 v/v % solution—0.80M)
  • 200 g Calcium Chloride dihydrate—18.4% (1.66M)
  • 4.5 g Calcium Bromide hydrate—0.51% (0.025M)
  • 0.050 g Menthol—0.0061%
  • 0.175 g Thymol—0.021%
  • The specific gravity of the resulting fixative was 1.270.

Example 24

Approximately 800 ml of fixative was prepared with the following formulation:

• • 500 ml de-ionised water
  • 200 g cane sugar
  • 37.5 ml of Glacial Acetic Acid (4.9 v/v % solution—0.82M)
  • 240 g Calcium Chloride—30.9% (2.70M)
  • 4.5 g Calcium Bromide hydrate—0.52% (0.027M)
  • 0.050 g Menthol—0.0063%
  • 0.175 g Thymol—0.022%
  • The specific gravity of the resulting fixative was 1.330.

Example 25

Approximately 420 ml of fixative was prepared with the following formulation:

• • 231.25 ml de-ionised water
  • 100 g cane sugar
  • 18.75 ml of Glacial Acetic Acid (4.5 v/v % solution—0.78M)
  • 0.45 g Sodium Benzoate—0.11% (7.44 mM)
  • 15 g Calcium Chloride—3.57% (0.32M)
  • 2.25 g Calcium Bromide hydrate—0.49% (0.025M)
  • 0.025 g Menthol—0.0059%
  • 0.0875 g Thymol—0.021%
  • 30 g Citric acid—7.1% (0.037M)
  • The specific gravity of the resulting fixative was 1.288.

Example 26

Approximately 400 ml of fixative was prepared with the following formulation:

• • 250 ml de-ionised water
  • 100 g cane sugar
  • 20.0 ml of Glacial Acetic Acid (5.0 v/v % solution—0.87M)
  • 0.45 g Sodium Benzoate—0.11% (7.44 mM)
  • 90 g Calcium Chloride—22.5% (2.03M)
  • 2.25 g Calcium Bromide hydrate—0.52% (0.026M)
  • 0.025 g Menthol—0.0063%
  • 0.0875 g Thymol—0.022%
  • 60 g Citric acid—15.0% (0.78M)
  • The specific gravity of the resulting fixative was 1.296.

Example 27

Approximately 420 ml of fixative was prepared with the following formulation:

• • 250 ml de-ionised water
  • 50 g cane sugar
  • 20.0 ml of Glacial Acetic Acid (4.8 v/v % solution—0.83M)
  • 0.45 g Sodium Benzoate—0.11% (7.44 mM)
  • 200 g Calcium Chloride dihydrate 36.0% (3.24M)
  • 2.25 g Calcium Bromide hydrate 0.49% (0.025M)
  • 0.025 g Menthol—0.0059%
  • 0.0875 g Thymol—0.021%
  • 60 g Citric acid—14.3% (0.74M)
  • The specific gravity of the resulting fixative was 1.337.

Example 28

Approximately 5100 ml of fixative was prepared with the following formulation:

• • 2300 ml de-ionised water
  • 3750 g cane sugar
  • 375 ml of Glacial Acetic Acid (7.4 v/v % solution—1.3M)
  • 4.5 g Sodium Benzoate—0.88% (6.1 mM)
  • 60 g Calcium Chloride—1.2% (0.11M)
  • 30 g Calcium Bromide hydrate 0.59% (0.027M)
  • 0.25 g Menthol—0.049%
  • 0.875 g Thymol—0.017%
  • The specific gravity of the resulting fixative was approximately 1.29.
  • This SG formulation is the most preferred of Examples 14 to 28.

Magnesium halides may be substituted for the calcium halides in the Examples.

It is considered that similar results would be obtained if the concentrations of the acetic acid in the Examples were varied by about ±0.3M or more and that acceptable results would be obtained over broader ranges as defined in the claims. It is considered that similar results would be obtained if the concentrations of the remaining components in the Examples were varied by at least ±10%, possibly ±20% or more of their stated values and that acceptable results would be obtained over a wider range of concentrations.

In general, the upper limit of halide salt concentration is set only by the solubility of each particular salt in the fixative solution.

Claims

1. An aqueous fixative solution for biological samples comprising: a) a C2 to C6 carboxylic acid at a concentration of 0.5M or greater;b) an alkaline earth halide salt at a concentration of 0.02M or greater; andc) a biocidal essential oil component in a concentration of at least 50 μg/ml.

2. An aqueous fixative solution according to claim 1, wherein said C2 to C6 carboxylic acid is acetic acid.

3. An aqueous fixative solution according to claim 1, wherein the concentration of alkaline earth halide salt is 0.04M or greater.

4. An aqueous fixative solution according to claim 1, wherein the concentration of C2 to C6 carboxylic acid is 1.3M or greater.

5. An aqueous fixative solution according to claim 2, wherein the concentration of acetic acid is below 10% w/v.

6. An aqueous fixative solution according to claim 1, wherein component b) is a calcium or magnesium halide salt.

7. An aqueous fixative solution according to claim 6, wherein component b) comprises calcium chloride at a concentration of at least 0.06M, and/or calcium bromide at a concentration of at least 0.06M.

8. An aqueous fixative solution according to claim 1 wherein component b) is a halide salt at a concentration of 0.3M to 6M.

9. An aqueous fixative solution according to claim 1 further comprising a non-polar solute which increases the density of the fixative solution to above 1.1 g/ml.

10. An aqueous fixative solution according to claim 9 wherein the non-polar solute is a soluble carbohydrate, selected from the group consisting of: sugar, sucrose, glucose, fructose, maltose and any combination thereof.

11. An aqueous fixative solution according to claim 1, further comprising: d) a bacteriostatic or fungistatic concentration of benzoic acid or sorbic acid or a salt thereof.

12. (canceled)

13. An aqueous fixative solution according to claim 12 wherein said biocidal essential oil component c) is selected from the group consisting of: menthol, thymol, pulegol, dihydrocarveol, piperitol, menthone, menthene, o-cymene, p-cymene, citronellal, carvacrol, eugenol, 4-carvo-menthol (termpinen-4-ol), allicin and camphor.

14. An aqueous fixative solution according to claim 12 wherein said biocidal essential oil component c) comprises menthol and thymol.

15. An aqueous fixative solution according to claim 11 wherein: i) said carboxylic acid component a) is acetic acid at a concentration of 0.8M to 1.75M;ii) said alkaline earth halide salt component b) is calcium chloride at a concentration of 70 mM to 100 mM plus calcium bromide at a concentration of 30 mM to 50 mM; andiii) said component (d) is a benzoic acid salt at a concentration of 5 mM to 15 mM benzoate.

16. An aqueous fixative solution according to claim 11 wherein: i) said carboxylic acid component a) is acetic acid at a concentration of 1.2M to 1.75M;ii) said alkaline earth halide salt component b) is calcium chloride at a concentration of 70 mM to 100 mM plus calcium bromide at a concentration of 30 mM to 50 mM; andiii) said component (d) is a benzoic acid salt at a concentration of 5 mM to 15 mM benzoate.

17. An aqueous fixative solution according to claim 11 wherein: i) said carboxylic acid component a) is acetic acid at a concentration of 0.8M to 1.75M;ii) said alkaline earth halide salt component b) is calcium chloride and/or calcium bromide at a total concentration of from 1.0M to 4.5M; andiii) said component (d) is a benzoic acid salt at a concentration of 5 mM to 125 mM benzoate.

18. A method of preparing a biological sample for examination comprising fixing the sample with an aqueous fixative solution as claimed in claim 1.

19. A method according to claim 18 wherein the biological sample is a living organism.

20. A method according to claim 18 wherein the biological sample is a parasitological sample.

21. A method according to claim 20 wherein the density of the aqueous fixative solution is sufficient to float eggs or larvae or cysts or oocysts in the parasitological sample and is preferably in the range 1.2 g/ml to 1.4 g/ml, more preferably 1.25 g/ml to 1.35 g/ml.

22. A method according to claim 18 wherein the biological sample is stained after fixing.

23. A method according to claim 22 wherein the biological sample is stained with an azo dye, or with iodine, or with a trichrome stain.