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You are here: BAILII >> Databases >> England and Wales Court of Appeal (Civil Division) Decisions >> Tate & Lyle Technology Ltd v Roquette Freres [2010] EWCA Civ 1049 (11 October 2010) URL: http://www.bailii.org/ew/cases/EWCA/Civ/2010/1049.html Cite as: [2010] EWCA Civ 1049, [2011] FSR 3 |
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ON APPEAL FROM THE HIGH COURT OF JUSTICE
CHANCERY DIVISION
PATENTS COURT
MR JUSTICE LEWISON
Strand, London, WC2A 2LL |
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B e f o r e :
LORD JUSTICE RICHARDS
and
LORD JUSTICE SULLIVAN
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Tate & Lyle Technology Ltd |
Claimant Respondent |
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- And - |
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Roquette Frčres |
Defendant Appellant |
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WordWave International Limited
A Merrill Communications Company
165 Fleet Street, London EC4A 2DY
Tel No: 020 7404 1400, Fax No: 020 7404 1424
Official Shorthand Writers to the Court)
Colin Birss Q.C. and Thomas Mitcheson (instructed by Linklaters LLP) for the Respondent
Hearing dates: 26-27 July 2010
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Crown Copyright ©
Lord Justice Lloyd:
Introduction
The background to the patent
"4. Sugars are saccharides. Saccharides come in many different forms. Some are monosaccharides, some disaccharides, others trisaccharides and so on. The prefix denotes the degree of polymerisation (i.e. the number of small molecules bonded together) and is abbreviated to DP in some of the prior art. Thus a trisaccharide can be abbreviated to DP3. Saccharides can also be divided into oligosaccharides and polysaccharides. The former have more than one identical molecule bonded together but not very many. If they have many they are polysaccharides.
5. The process of making maltitol crystals begins with a starch (typically from corn, potatoes or wheat). The starch is first liquefied by the addition of enzymes or acids. Once liquefied, any enzyme is deactivated and saccharification can take place. Saccharification is also carried out by means of enzymes which break down the long polysaccharide chains into shorter ones. Specific enzymes are added to hydrolyse the polysaccharides so as to yield the required type of sugar. On the way to making maltitol, it is necessary to yield maltose, so the additive will be a maltogenic enzyme. Maltose itself consists of two units of glucose linked together and is thus a disaccharide. But the maltogenic enzyme will also produce maltotriose, which consists of three units of glucose linked together and is thus a trisaccharide. There are other by-products of enzymatic maltose production (e.g. panose and maltotetraose). The hydrolysation results in a hydrolysate. This is filtered to remove insoluble material. It is also typically purified by column chromatography or molecular sieving to remove unwanted sugars.
6. The purified hydrolysate is then hydrogenated. This converts the sugars into sugar alcohols in the form of a syrup. Hydrogenation of the maltose in the hydrolysate will result in maltitol within the syrup. Hydrogenation of the maltotriose in the hydrolysate will result in maltotriitol within the syrup. The hydrogenated equivalents of other by-products of maltose production are sorbitol, panitol and maltotetraitol. Since the object of the exercise is the production of maltitol crystals, the presence of maltotriitol and other by-products is regarded as an impurity.
7. The syrup is then crystallised. Even if they are not polymorphic, crystals can grow in different ways, and exhibit different shapes. The different shapes are properly called "habits". However, the patent in suit describes the different shapes as different "forms"; which is an alternative descriptor. These different habits form as a result of the symmetry of the internal crystal structure and the relative growth rates of the crystal faces. Thus if molecules of maltitol accumulate at one face more rapidly than at another, long needle-like crystals are formed. If, on the other hand, the crystals accumulate at the same rate at the competing faces, the resulting crystals are likely to be more cubic in nature. There is no accepted nomenclature for the different habits that crystals take. Different adjectives are used by different people to describe what is essentially the same habit. Thus Roquette have described the same habit as "bipyramidal", "arrondi" (round) and "pavé" (like a cobblestone). Others have described the same habit as "parallelepipedal"."
The patent in suit
"The use of maltotriitol to modify or control the form of maltitol crystals."
"The extent of the protection conferred by a European patent or a European patent application shall be determined by the claims. Nevertheless the description and drawings shall be used to interpret the claims."
"Article 69 should not be interpreted as meaning that the extent of the protection conferred by a European patent is to be understood as that defined by the strict, literal meaning of the wording used in the claims, the description and drawings being employed only for the purpose of resolving an ambiguity found in the claims. Nor should it be taken to mean that the claims serve only as a guideline and that the actual protection conferred may extend to what, from a consideration of the description and drawings by a person skilled in the art, the patent proprietor has contemplated. On the contrary, it is to be interpreted as defining a position between these extremes which combines a fair protection for the patent proprietor with a reasonable degree of legal certainty for third parties."
"Finally purposive construction leads one to eschew the kind of meticulous verbal analysis which lawyers are too often tempted by their training to indulge."
"The present invention concerns the use of maltotriitol to modify or control the form of maltitol crystals."
"20. … The specification begins by introducing maltitol, and explains that it was first presented in syrup form, then in powder form, and that it has been known in crystalline form since 1980. These crystals are anhydrous maltitol which are subject to wide-ranging patent protection on behalf of the HAYASHIBARA company. The specification then describes two forms of processes for crystallisation: the massé technique and crystallisation in water. These are almost the only processes in industrial use. The products obtained by these methods are of very variable crystallinity and not all are particularly well suited to certain applications such as chewing gum or chocolate. It also gives other examples of situations in which crystals produced by these techniques are not satisfactory. The particular defects to which it draws attention are those of not flowing easily, being liable to cake or knot, poor solubility, being bad vehicles for compression and not meeting the criteria for identification and purity set by the different pharmacopoeias [0008].
21. The problem that Roquette set out to solve is described in [0009]. It sought "to perfect maltitol compositions which do not have the flow, caking, dissolving or compression defects presented by known maltitol powders." It continues by asserting [0010] that while working to perfect these compositions it "was able to isolate, in a surprising and unexpected way, two particular forms of maltitol crystals, one bipyramidal and the other prismatic."
22. The key teaching of the patent is set out in [0011]. It says:
"It has indeed demonstrated that, against all expectation, the form of the maltitol crystals was a function of the maltotriitol content of a maltitol syrup intended for crystallisation. The Applicant company has noted that by controlling the maltotriitol content of a maltitol syrup, it was possible to direct the form of the maltitol crystals towards one or other of the forms or towards a mix of the two forms, when this maltitol syrup is subjected to a crystallisation stage."
23. The bipyramidal crystal is described as made up of two regular tetrahedrons of base 50-500µm, to make an octahedron with edge length of 50-500µm. The experts agree that the octahedron is in fact made up of two square pyramids rather than two tetrahedrons. The prismatic crystal is described as consisting of plane faces constituting a tetrahedron and 100-400µm long by 20-100µm wide.
24. The patent goes on to explain the merits and demerits of the two different habits: [0014] to [0016]. A semi-crystallised mass of maltitol with bipyramidal crystals is more viscous than one with prismatic crystals. The bipyramidal crystal provides a more thickened mass before refining which is useful in the production of chocolate, and a greater consistency of flow which is useful in the production of pharmaceutical coatings etc. On the other hand the prismatic crystal is more compressible and so enables low-crystal content caking in the manufacture of chewing gum centres and the like.
25. The patent continues with a description of the two crystal habits. At [0027] to [0030] the patent explains that differences in habit are caused by different quantities of maltotriitol. Less than 1% maltotriitol and the crystals are bipyramidal in habit. More than 4% maltotriitol and the crystals are prismatic in habit. Between 1% and 4% and the crystals are a heterogeneous mixture of the two habits. These data are subsequently tabulated at [0077] (although one figure in the table is in the wrong place). At [0034] the patent repeats its key teaching:
"One of the essential characteristics of the invention is therefore to vary the maltotriitol contents of the maltitol syrups to be crystallised while advantageously retaining a reduced content of maltosyl 1,6 maltitol."
26. However, although this paragraph teaches that the maltotriitol content of the maltitol syrup can be varied, it also proposes a number of other ways in which the maltotriitol level can be controlled. The patent goes on to explain that the maltotriitol content of the syrup may be controlled either upstream or downstream. It proposes three different ways of controlling the maltotriitol content upstream (all of which result in the ultimate reduction of maltotriitol content) and two different ways of controlling the maltotriitol content downstream (one of which reduces and the other of which increases the maltotriitol content). The upstream methods of controlling the maltotriitol content of the syrup include alteration of the hydrolysate before hydrogenation (e.g. by molecular sieving). At this stage, there is no maltotriitol present in the hydrolysate, because that comes into existence only after hydrogenation. What is present in the hydrolysate at that stage is its forerunner: maltotriose. The patent explains that all these possibilities for controlling the maltotriitol content may be used singly or in combination: [0038].
27. The patent continues with a long (and largely irrelevant) description of the process by which the syrup is obtained. However, the patent explains ([0047]) that at the first stage of saccharification:
"it is already possible to control the maltotriose content (which after hydrogenation leads to maltotriitol) … by adjusting the amount of maltogenic a-amylase as a function of the maltotriose content and therefore of the form of the maltitol crystals that it is wished to obtain."
28. The patent thus teaches that one way of controlling the crystal habit is by adjusting the maltotriose content of the hydrolysate with the result that the amount of maltotriitol content of the syrup after hydrogenation is likewise controlled. This is reflected in [0071] and [0072] of the specification, which explain:
"[0071] According to a first version of the process, a series of steps is applied to the maltitol syrup obtained in the preceding hydrogenation stage as follows
- possibly carrying out a chromatographic fractionation, known per se, so as to obtain a maltitol rich fraction and a more or less rich maltotriitol fraction as a function of the form of crystals required
- concentrating the maltitol rich fraction
- crystallising and separating the formed maltitol crystals
- recycling the crystallisation mother liquors upstream of the chromatographic fractionation stage
[0072] According to a second version of the process, a series of steps is applied to the maltitol syrup obtained in the preceding hydrogenation stage as follows
- concentrating the maltitol syrup
- crystallising and separating the formed maltitol crystals."
29. The first version adjusts the maltotriitol content of the syrup after hydrogenation, but the second version does not. The maltotriitol content has already been determined by the adjustment of the maltotriose content of the hydrolysate; and thus after hydrogenation the syrup merely requires concentration and crystallisation. A similar process is described in [0074] where the maltotriose content of the hydrolysate is again adjusted before hydrogenation.
30. The patent gives one example to illustrate the claim [0076]. In the example the syrup to be crystallised is concentrated and placed in a dish. Crystallised maltitol is then added, and the dish is cooled. The crystals are thus formed. There is no adjustment to the maltotriitol content of the syrup. The tabular results of the example simply record that "different bases are used".
31. As one might expect, the patent culminates in the claims. It is necessary to describe some of the claims that were subsequently abandoned or disallowed by the Opposition Division of the EPO. Claims 1 and 4 as granted claimed the two types of crystal: bipyramidal and prismatic respectively. These claims have been abandoned, because neither of these crystal habits was new. Each had been disclosed by the prior art. Granted claims 2 and 5 claimed compositions comprising those crystals respectively and claim 7 was to a composition comprising both kinds. These claims have also been abandoned for similar reasons. The granted patent also contained claims to processes for making the bipyramidal and prismatic crystals (and mixtures) in claims 3, 6 and 8. Those claims mentioned the maltotriitol content as appropriate (lower than 1% for bipyramidal, more than 4% for prismatic and in between for a mixture). These process claims have also been abandoned because the processes for making crystals using the specified maltotriitol content had also been anticipated by prior art.
32. Granted claim 9 was:
"A process for directing the form of the maltitol crystals, characterised in that it consists in controlling the maltotriitol content of the maltitol syrup to be crystallised.""
The issue of construction
"To direct the form of the maltitol crystals, the maltotriitol content of the maltitol syrup is controlled. This control of the maltotriitol content of the maltitol syrup to be crystallised may be carried out upstream and/or downstream of the crystallisation stage."
i) if the composition of the basis, i.e. the maltitol syrup, is such that maltitol exceeds 99%, then the crystals are homogeneous and bipyramidal in form;
ii) with a maltitol content of 93.5% and a maltotriitol content of 3.8%, the crystals are heterogeneous, both bipyramidal and prismatic in form;
iii) with a maltitol content of 90.1%, sorbitol 5.2%, maltotetraitol 3.8% and maltotriitol 0.9%, then the form is homogeneous and bipyramidal;
iv) whereas with 96% maltitol and 4% maltotriitol, the crystals are homogeneous and prismatic.
Discussion
"So the skilled reader is taken to suppose that the patentee knew some patent law – that his claim is for the purpose of defining the monopoly and that it should be for something new. Knowledge of that may well affect how the claim is read – for instance one would not expect the patentee to have used language which covered what he expressly acknowledged was old."
"because the skilled reader knows that the patentee is trying to claim something which he, the patentee, considers to be new, he will be strongly averse to ascribe to the claim a meaning which covers that which the patentee acknowledges is old."
Lord Justice Richards
Lord Justice Sullivan