Patent Application
20240008527
The present invention concerns a process for the manufacture of marked cellulose acetate fibres, an apparatus for marking cellulose acetate fibres, a process for the detection of at least one information item on marked cellulose acetate fibres or on products comprising marked cellulose acetate fibres, a process for the manufacture of a tow bale comprising marked cellulose acetate fibres, a tow bale, a tow, a filter and a cigarette comprising marked cellulose acetate fibres.
Counterfeit products are causing damage to trade and governments, as illicit trading and counterfeiting harms originators by flushing the markets with illicit products and circumventing tax and customs regulations, thus harming governments aiming to enforce tax and customs laws. Attempts have been made to distinguish counterfeit products from original products by marking of products, making it possible to determine if a product is counterfeit or original. For example, US2016/0168781 discloses a method of marking fibres, wherein fibres are being marked with a nucleic acid marker with the aim to determine whether the fibrous material is authentic or counterfeit.
One of the products which are particularly prone to black market and counterfeiting are cigarettes, which are subject to tax and customs regulations in a large variety of countries. It is thus desirable to make cigarettes distinguishable with respect to original or counterfeit nature of the cigarette. WO2016/179220 discloses, for example, marked cigarette filters, wherein the marking is achieved by etching, barcode or printing. Such markings can be subject to damage, caused by physical damage or biological disintegration or degradation of the filter, thus disabling the detecting mechanism. It is further possible that even these markings can be subject to imitation and counterfeiting.
There is thus still a need to provide marked cellulose acetate fibres, which are often comprised in cigarettes and upstream products thereof, which are marked in a manner which is more resistant to physical damage and biological disintegration of the cigarettes and upstream products thereof. It is further desirable to provide a marking for these products which makes it possible to trace the origin of such products. By providing information items, such as producer, date, place, batch, fibre characteristics and product line, a product comprising the marked cellulose acetate fibres can be traced by identifying the markings on the product to its origin. It is possible for involved parties, such as police and customs, to match the obtained information with production information from the product providers, which are able by identifying through warehouse and distribution information from where the product originates, where it was originally intended to be shipped and traded. This not only allows distinction between counterfeit and original products, but provides valuable information for the prosecution of criminal activities and responsible individuals and organizations.
The invention thus concerns a process for the manufacture of marked cellulose acetate fibres comprising a step wherein a plurality of cellulose acetate fibres are provided; a step wherein a marker comprising at least one polynucleotide is deposited onto at least a portion of the cellulose acetate fibres, thereby marking the cellulose acetate fibres. The invention further concerns an apparatus for marking cellulose acetate fibres with at least one polynucleotide; a process for the detection of at least one information item by identifying the nucleotide sequence comprised in the at least one polynucleotide with which cellulose acetate fibres are marked; a process for the manufacture of a tow bale comprising cellulose acetate fibres marked with at least one polynucleotide; cellulose acetate fibres marked with at least one polynucleotide marker, tow, tow bale, filter and cigarette comprising such cellulose acetate fibres.
In the present invention, designations in singular are intended to include the plural; for example, “a fibre” is intended to denote also “more than one fibre” or “a plurality of fibres”.
All aspects and embodiments of the present invention are combinable.
In the context of the present invention, the term “comprising” is intended to include the meaning of “consisting of”.
The invention concerns a process for the manufacture of marked cellulose acetate fibres comprising:
The term “polynucleotide” intends to denote polymers comprising a plurality of nucleotides or nucleotide analogues. According to the present invention, “polynucleotide” denotes, for example, fragments of DNA or RNA, in particular artificial fragments of DNA or RNA. The length of the polynucleotide often is equal to or greater than 6 nucleotides, preferably equal to or greater than 12 nucleotides, and even more preferably equal to or greater than 15 nucleotides. The length of the polynucleotide often is equal to or less than 200 nucleotides, preferably equal to or less than 100 nucleotides, and even more preferably equal to or less than 50 nucleotides. Polynucleotides with a nucleotide length of from 6 to 200 nucleotides are also denoted as oligonucleotide. In one aspect of the present invention, the length of the polynucleotide can also exceed 200, such as 300, 400 or even more than 500 nucleotides. Lengths of up to 2000 nucleotides can be suitable. Preferably, the at least one polynucleotide comprises from 6 to 200 nucleotides. The nucleotides present in the polynucleotide are the naturally occurring nucleotides, such as adenine, cytosine, guanine, thymine and uracil, any of their derivatives, such as 5-fluorocytosine, 5-fluorouracil, 5-methylcytosine, 5-hydroxymethylcytosine, dideoxynucleotides, cordycepin and other artificial nucleotides and derivatives of nucleotides.
The polynucleotide according to the present invention can be a polynucleotide with a natural nucleotide sequence, such as plant or animal polynucleotide, for example obtained by digestion of plant or animal RNA or DNA, or, which is preferred, a non-natural polynucleotide with a predefined non-natural nucleotide sequence. The preferred non-natural polynucleotides can be obtained through methods skilled in the art, for example by applying the phosphoramidite method.
The at least one polynucleotide marker deposited on the cellulose acetate fibres preferably not only makes it possible to distinguish counterfeit from original products comprising such fibres. In a preferred aspect, the at least one polynucleotide encodes information comprising at least one information item selected from the group consisting of producer, date, place, batch, fibre characteristics and product line. Such information items generally can comprise any information suitable to detect the origin of the marked cellulose acetate fibres or products comprising these fibres. The information is encoded by the specific nucleotide sequence present in the at least one polynucleotide. Suitably, the sequence is confidential and specific for certain producers, dates, places, batches, fibre characteristics and product lines. Due to the high variability of the sequence and simultaneous high specificity of the sequence as defined by its originator, it is difficult if not possible to imitate these markers. A further advantage is that it is virtually impossible to remove the markers from the products, as it is known that by assaying techniques such as PCR even small amounts of marker suffice to allow detection. The marker generally is resistant against usual physical and biological stress to which the products comprising the marked cellulose acetate fibres can be exposed, and, due to its specificity, can be well distinguished from any artefacts, such as DNA from a different source.
The step of providing a plurality of cellulose acetate fibres can comprise the mere provision of cellulose acetate fibres which have been obtained from a commercial source. The manufacturing process can also comprise the following steps: (a) spinning cellulose acetate fibres from a dope comprising a solvent and cellulose acetate; (b) forming tow from the cellulose acetate fibres; (c) crimping the tow; (d) drying the tow; wherein the at least one polynucleotide is deposited onto at least a portion of the cellulose acetate fibres between or during either of steps (a) to (d). The general concept of steps (a) to (d) are known from e.g. P. Rustemeyer, Macromol. Symp. 2004, 208, 267-291. The deposition of the at least one polynucleotide can be effected on sections of the tow, or over the full length of the tow. The at least one polynucleotide preferably is applied as at least one aqueous or at least one alcoholic solution. In one aspect, the at least one polynucleotide is activated, for example alkaline activated, at deposition. Suitably, the deposition of the at least one polynucleotide is performed by metering a defined amount of at least one polynucleotide onto at least a portion of the cellulose acetate fibres or tow comprising cellulose acetate fibres.
Alternatively, the cellulose acetate fibres can be dipped into at least one solution of the polynucleotide. In one aspect, the at least one polynucleotide is applied consecutively as two or more solutions. The at least one oligonucleotide can also be formulated into at least one solid formulation, such as a tablet. The solid formulation can comprise at least one auxiliary ingredient as known from, for example, the pharmaceutical or food industry, such as a binder or a coating. The solid formulation is then contacted with the at least one solvent, such as the aqueous or alcoholic solvent, prior to application to the cellulose acetate fibres.
According to the present invention, the deposition of the at least one polynucleotide on the cellulose acetate fibres or the tow comprising the cellulose acetate fibres can be effected between or during either of steps (a) to (d). In one aspect, the at least one polynucleotide can be present in the dope spun in step (a), or in the spinning auxiliary, for example spinning oil, employed in step (a). In a preferred aspect, the at least one polynucleotide is deposited onto at least a portion of the cellulose acetate fibres between steps (c) and (d). This has the advantage that any contamination of surroundings, fibres or tow can be minimized, and the at least one polynucleotide can be easily replaced for the next production batch with another polynucleotide. The risk of creating artefacts is minimized by this procedure. It has been shown that the deposition of the at least one polynucleotide before the drying step has no disadvantage with respect to stability or reliability of the marker.
The invention concerns further an apparatus for marking cellulose acetate fibres, the apparatus comprising:
Preferably, the apparatus has a metering device, making it possible to dose the exact amount per unit cellulose acetate fibre or tow or per time. Suitable transport systems adapted to transport the cellulose acetate fibres are known from the general concept of manufacturing cellulose acetate fibres and tows comprising such fibres, such as processes comprising spinning, crimping and drying steps.
Another object of the present invention is a process for the detection of at least one information item selected from the group consisting of producer, date, place, batch, fibre characteristics and product line comprised in the nucleotide sequence of the at least one polynucleotide on cellulose acetate fibres marked with at least one polynucleotide or on products comprising cellulose acetate fibres marked with at least one polynucleotide, comprising:
Products comprising cellulose acetate fibres marked with at least one polynucleotide can be, for example, cellulose acetate tow, filters comprising the cellulose acetate tow, tow bales comprising cellulose acetate tow and cigarettes comprising the filters comprising cellulose acetate fibres. The process for the detection of at least one information item can further comprise the step of extracting the at least one polynucleotide from the sample of cellulose acetate fibres marked with at least one polynucleotide or the products comprising cellulose acetate fibres marked with at least one polynucleotide, by suitable extraction methods such as treatment with an aqueous buffer. A process for the detection of at least one information item selected from the group consisting of producer, date, place, batch, fibre characteristics and product line comprised in the nucleotide sequence of the at least one polynucleotide on cellulose acetate fibres marked with at least one polynucleotide or on products comprising cellulose acetate fibres marked with at least one polynucleotide, can further comprise: providing a plurality of cellulose acetate fibres; depositing at least one polynucleotide marker onto at least a portion of the cellulose acetate fibres; thereby producing marked cellulose acetate fibres; and further may optionally comprise manufacturing a product comprising cellulose acetate fibres marked with at least one polynucleotide, for example manufacturing of filters from filter tow comprising cellulose acetate fibres marked with at least one polynucleotide. The assaying of the sample of cellulose acetate fibres marked with at least one polynucleotide or the products comprising cellulose acetate fibres marked with at least one polynucleotide to identify the nucleotide sequence comprised in the at least one polynucleotide preferably comprises a PCR technique.
The invention also concerns a process for the manufacture of a tow bale comprising cellulose acetate fibres marked with at least one polynucleotide marker, which comprises the steps of (a) spinning cellulose acetate fibres from a dope comprising a solvent and cellulose acetate; (b) forming tow from the cellulose acetate fibres; (c) crimping the tow; (d) drying the tow; wherein the at least one polynucleotide is deposited onto at least a portion of the cellulose acetate fibres between or during either of steps (a) to (d), and which further comprises the steps of (e) baling the tow and (f) packaging the tow bale. It is preferred that the deposition of the at least one polynucleotide marker is performed between steps (c) and (d). The steps for (e) baling the tow and (f) packaging the tow bale are known, for example, from WO2016/174162.
Another object of the present invention concerns cellulose acetate fibres marked with at least one polynucleotide marker. Such fibres are obtainable, for example, by the processes according to the present invention for concerning the manufacture of marked cellulose acetate fibres.
Yet another object of the present invention concerns tow or tow bale comprising cellulose acetate fibres marked with at least one polynucleotide marker according to the present invention.
The invention also concerns a filter comprising cellulose acetate fibres marked with at least one polynucleotide marker according to the present invention. The filter is a filter for gas, aerosol or liquid, preferably a filter for a gas or aerosol, and most preferably a cigarette filter filtering cigarette smoke. The manufacture of cigarette filters from tow comprising cellulose acetate fibres is generally known, for example from P. Rustemeyer, “Filter Rods and Cellulose Acetate—Life-Cycle from the Tree to the Consumer”, 1998, 325023650, BATCo US DOJ v Philipp Morris, which can be obtained through http://legacy.library.ucsf.edu/tid/iun71a99/pdf.
Another object of the present invention is a cigarette comprising cellulose acetate fibres marked with at least one polynucleotide marker, preferably comprising the filter according to the present invention.
Should the disclosure of any patents, patent applications, and publications which are incorporated herein by reference conflict with the description of the present application to the extent that it may render a term unclear, the present description shall take precedence.
The following examples are intended to further explain the invention without limiting it.
A 12-mer oligonucleotide, encoding producer, product line and date was diluted in aqueous solution to a concentration of 2 μg/m3.
This oligomer solution was applied to the cellulose acetate fibres corresponding to about 0.3 ng oligonucleotide/kg cellulose acetate fibres, and the cellulose acetate fibres were dried.
A plurality of samples of the dried cellulose acetate fibres with a weight of 100 mg each were tested by routine DNA detection methods to provide forensic authentication. The oligonucleotide was detected after PCR amplification in every analysed sample, and the encoded information matched with the originating production batch. >50% of the oligonucleotide amount applied was detected.
| Number | Date | Country | Kind |
|---|---|---|---|
| 17173747.1 | May 2017 | EP | regional |
This application is a continuation of U.S. patent application Ser. No. 16/616,230, filed on Nov. 22, 2019, which is a national phase filing under 35 USC 371 of International Application No. PCT/EP2018/061020, filed on Apr. 30, 2018, which claims priority of European Patent Application No. 17173747.1, filed on May 31, 2017, the entire contents of which are hereby incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 16616230 | Nov 2019 | US |
| Child | 18473007 | US |
