WO2021212031A1 - Ingestible sampling device - Google Patents
Ingestible sampling device Download PDFInfo
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- WO2021212031A1 WO2021212031A1 PCT/US2021/027770 US2021027770W WO2021212031A1 WO 2021212031 A1 WO2021212031 A1 WO 2021212031A1 US 2021027770 W US2021027770 W US 2021027770W WO 2021212031 A1 WO2021212031 A1 WO 2021212031A1
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- WO
- WIPO (PCT)
- Prior art keywords
- ingestible
- sampling device
- sponge
- cell sampling
- cap
- Prior art date
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- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
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- A61B10/02—Instruments for taking cell samples or for biopsy
- A61B2010/0216—Sampling brushes
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- C—CHEMISTRY; METALLURGY
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- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
Definitions
- the invention relates to cell sampling devices.
- the present invention relates to ingestible cell sampling devices for sampling cells in a subject, and methods of use for detecting abnormalities in a subject using the same.
- an ingestible cell sampling device may be used to collect cells from the surface of the gastrointestinal tract of a patient.
- various issues exist with the cell sampling devices currently used including difficulty or unpleasantness in swallowing and retrieving the device, detachment of the sponge from the string during use, and/or laceration to the esophagus of the patient upon withdrawal of the device. Accordingly, what is needed are improved ingestible cell sampling devices for use in a subject.
- the device comprises an abrasive sponge housed within a dissolvable capsule, a molded cap, and a string attached to the molded cap.
- the abrasive sponge comprises reticulated foam.
- the abrasive sponge is compressible. The sponge may be retained in a compressed state by the dissolvable capsule.
- the abrasive sponge when in an uncompressed state, has a shape configured to maximize an exterior dimension while minimizing the total amount of sponge to be contained in a capsule.
- the abrasive sponge is formed to have concavities or indentations, and/or to have a void space, as may be provided by removing at least one portion of the abrasive sponge prior to compressing the sponge into the dissolvable capsule, e.g., from inside the sponge, and/or from the top, bottom, and/or side of the abrasive sponge.
- the dissolvable capsule comprises one or more openings, such that a portion of the abrasive sponge is exposed to the external environment at the one or more openings.
- the dissolvable capsule comprises a first closed end and a second closed end.
- the dissolvable capsule comprises a first closed end and a second open end.
- the molded cap comprises an internal surface in contact with an external surface of one end of the capsule and an exterior surface in contact with the external environment. In some embodiments, the molded cap comprises an internal surface in contact with the abrasive sponge and an exterior surface in contact with the external environment. In some embodiments, the molded cap comprises an interior surface in contact with the abrasive sponge and an exterior surface. The exterior surface of the molded cap may be in contact with an internal surface of one end of the capsule. In some embodiments, the interior surface of the molded cap is attached to the abrasive sponge by an adhesive, which is preferably dissolvable.
- the string is attached to the molded cap by a knot. In some embodiments, the string is attached to the molded cap by an adhesive. In some embodiments, the string is attached to the molded cap by a knot and adhesive.
- the string may comprise a suture. In some embodiments, the string passes through a portion of the abrasive sponge.
- a method of obtaining a cell sample from a subject comprises providing the ingestible cell sampling device described herein to the subject, and removing all or a portion of the ingestible cell sampling device from the subject.
- the ingestible cell sampling device may be removed from the subject within 10 minutes of providing the ingestible cell sampling device to the subject.
- the technology provides an ingestible cell sampling device and systems comprising such a device, e.g., for conducting a cell sampling method using a device as described herein.
- An ingestible cell sampling device comprising: i) an abrasive sponge housed within a dissolvable capsule, the dissolvable capsule comprising an exterior surface exposed to an external environment; ii) a molded cap; and iii) a string having a first end attached to the molded cap.
- the abrasive sponge comprises at least one void space.
- the dissolvable capsule comprises one or more openings, wherein a portion of the abrasive sponge is exposed to the external environment at the one or more openings.
- the dissolvable capsule comprises a first end and a second end, wherein: a) the first end is closed and the second end is closed; or b) the first end is closed and the second end is open.
- the molded cap comprises a cap interior surface and a cap exterior surface, wherein the cap interior surface is in contact with the exterior surface of the capsule at the first closed end, and the cap exterior surface is in contact with the external environment.
- the molded cap comprises a cap interior surface and a cap exterior surface, wherein the cap interior surface is in contact with the abrasive sponge.
- molded cap comprises a cap interior surface in contact with the abrasive sponge and a cap exterior surface in contact with the external environment.
- a system or kit for obtaining a cell sample from a subject comprising an ingestible cell sampling device of any of the preceding embodiments; and further comprising one or more of: i) a container to receive an abrasive sponge comprising collected cells; ii) a cell preservative reagent, preferably a buffer reagent; iii) a microscope slide; iv) an assay plate; v) a local anesthetic treatment, preferably a local anaesthetic spray; vi) a component of a drinkable solution; preferably a pre-mixed drinkable solution; and vii) a lubricant, preferably a lubricant gel or liquid.
- a method of obtaining a cell sample from a subject comprising: i) orally administering an abrasive sponge housed within a dissolvable capsule of a ingestible cell sampling device of any one of embodiments 1-21 to the subject, and ii) withdrawing from the subject the abrasive sponge, wherein the abrasive sponge collects a cell sample from the subject during the withdrawing.
- the at least one biomarker comprises DNA comprising at least a portion of a gene selected from the group consisting of NDRG4, ZNF682, VAV3, BMP3, ZNF568, FER1L4, ANKRD13B, CD ID, CDKN2A , CHST2, CNNM1, DI03, DOCK2, DTX1, ELMOl, FERMT3, FLIl, GRIN2D, HUNK, JAM3, LRRC4, OPLAH, PDGFD, PKIA, PPP2R5C, QKI, SEP9, SFMBT2,
- assaying the at least one biomarker comprises determining the DNA to determine the methylation state of the gene.
- biomarkers from the group consisting of NDRG4, ZNF682, VAV3, BMP3, ZNF568, FER1L4, ANKRD13B, CD ID, CDKN2A , CHST2, CNNM1, DI03, DOCK2, DTX1, ELMOl, FERMT3, FLIl, GRIN2D, HUNK, JAM3, LRRC4, OPLAH, PDGFD, PKIA, PPP2R5C, QKI, SEP9, SFMBT2,
- assaying the at least one biomarker comprises assaying the methylation state of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, or 33 genes from the group consisting of NDRG4, ZNF682, VAV3, BMP3, ZNF568, FER1L4, ANKRD13B, CD ID, CDKN2A , CHST2, CNNM1, DI03, DOCK2, DTX1, ELMOl, FERMT3, FLIl, GRIN2D, HUNK, JAM3, LRRC4, OPLAH, PDGFD, PKIA, PPP2R5C, QKI, SEP9, SFMBT2,
- assaying the at least one biomarker comprises assaying the methylation state of at least one gene selected from the group consisting of: ANKRD13B, CHST2, CNNM1, DOCK2, DTX1, FER1L4, FERMT3,
- assaying the at least one biomarker comprises assaying the methylation state of at least one gene selected from the group consisting of: BMP 3, NDRG4, VAV3, SFMBT2, DI03, HUNK, ELMOl, CD ID, CDKN2A, and OPLAH.
- assaying the at least one biomarker comprises assaying the methylation state of at least one gene selected from the group consisting of NDRG4, ZNF682, VAV3, BMP 3, ZNF568, and FLR11.4.
- the term “or” is an inclusive “or” operator and is equivalent to the term “and/or” unless the context clearly dictates otherwise.
- the term “based on” is not exclusive and allows for being based on additional factors not described, unless the context clearly dictates otherwise.
- the meaning of “a”, “an”, and “the” include plural references.
- the meaning of “in” includes “in” and “on.”
- composition “consisting essentially of’ recited elements may contain an unrecited contaminant at a level such that, though present, the contaminant does not alter the function of the recited composition as compared to a pure composition, i.e., a composition “consisting of’ the recited components.
- abrasive refers to a material capable of removing cells from a surface, and preferably collecting the cells removed from the surface.
- abrasive may indicate a material capable of removing cells from the esophagus of a subject.
- an abrasive material is capable of removing cells from a surface (e.g., the esophagus) without causing damage to the esophagus.
- esophageal disorder refers to types of disorder associated with the esophagus and/or esophageal tissue. Examples of esophageal disorders include, but are not limited to, Barrett's esophagus (BE), Barrett's esophageal dysplasia (BED), Barrett's esophageal low-grade dysplasia (BE-LGD), Barrett's esophageal high-grade dysplasia (BE- HGD), and esophageal adenocarcinoma (EAC).
- BE Barrett's esophagus
- BED Barrett's esophageal dysplasia
- BE-LGD Barrett's esophageal low-grade dysplasia
- BE- HGD Barrett's esophageal high-grade dysplasia
- EAC esophageal adenocarcinoma
- the “ingestible cell sampling device” of the technology comprises an ingestible portion, e.g., an “ingestible assembly” comprising an abrasive sponge housed within a dissolvable capsule and attached to a string; and a non-ingestible portion, e.g., a portion of the string that is not ingested during use, which is preferably attached to a handle.
- an ingestible portion e.g., an “ingestible assembly” comprising an abrasive sponge housed within a dissolvable capsule and attached to a string
- a non-ingestible portion e.g., a portion of the string that is not ingested during use, which is preferably attached to a handle.
- handle as used herein in reference to a non-swallowable component of an ingestible sampling device suitable for a user or a third party to hold, e.g., oral administration of the ingestible assembly of the ingestible cell sampling device.
- molded means any suitable means of fabricating a component, e.g., a cap or capsule, including but not limited to injection molding, compression molding, transfer molding, sintering, various means of 3-D additive printing, stereolithography, and machining.
- capsule refers to any component or material serving to surround or encase a sponge, preferably in a manner that renders the sponge swallowable.
- the capsule is dissolvable.
- a capsule encompasses any material or device that encloses a sponge, preferably a sponge in a compressed state, and that provides an surface suitable for swallowing, e.g., a surface of sufficient smoothness and/or slickness to facilitate swallowing of the sponge.
- a capsule may be formed separately, e.g., as a molded empty container in which a sponge is later partially or completely enclosed, or a capsule may be formed as part of process of encasing the sponge, e.g., as a coating, wrapping, or other binding treatment applied during or after compression of the sponge, and having the effect of holding the enclosed sponge in the compressed state.
- cap as used herein in reference to an ingestible sampling device refers to a rigid or semi-rigid component attached or attachable at or near an end of a string of the ingestible sampling device, preferably comprising one or more holes or openings for attachment of the string, e.g., with a loop or knot.
- a cap component of the ingestible assembly is shaped to be suitable for swallowing, e.g., having a cupped shape that follow an external contour of a a capsule, or being shaped to fit within a capsule.
- buttons as used herein in reference to an ingestible sampling device refers to a rigid or semi-rigid component attached or attachable at or near an end of a string of the ingestible sampling device, preferably comprising one or more holes or openings for attachment of the string, e.g., with a loop or knot.
- the term “button” is an example of a molded cap having a disk-like shape. In some embodiments, a button is sized to fit within the dissolvable capsule of the ingestible sampling device.
- saying refers to qualitatively assessing or quantitatively measuring an aspect of a sample, e.g., assessing or measuring the presence, amount, state, or functionality of a target entity, e.g., a biomarker.
- string refers broadly to any cord, thread, filament, cable, strand, fiber, ribbon, webbing, suture, lacing, or other flexible tethering material, including materials that are a single filament, and that comprise multiple filaments, e.g., comprising one or more strands that are, for example, twisted, braided, woven, fused, or otherwise combined to form a string, and may comprise strands or filaments of the same or different natural, synthetic, or hybrid material, e.g., silk, cotton, polyester, nylon, polypropylene, cellulose, and the like.
- a string or individual filaments of a string may be solid, e.g., a single cord or filament of a flexible material such as nylon or polypropylene, or a string may comprise one or more hollow strands, e.g., a tubing of nylon, polypropylene, or other flexible material.
- a string may comprise one or more informative markings, e.g., calibration markings indicating, for example, a distance between a marking and an end of the string.
- a series of calibration markings may be provided along the string, and may be at evenly spaced intervals, or at intervals of different lengths.
- reticulated refers to a porous, low density material, e.g., a foam. Reticulated material comprises open pores or cells, with few intact closed cells.
- compressible refers to a material that is capable of being reversibly forced or pressed into a smaller space or narrower compass in at least one dimension, and that is capable of expanding to an uncompressed dimension when the compressing force is removed.
- biomarker and “marker” are used interchangeably, and refer to a biological material (e.g., a nucleic acid, or a region of a nucleic acid, or a protein) that may be used to distinguish non-normal cells (e.g., cancer cells) from normal cells, e.g., based on presence, absence, or status (e.g., methylation state or mutation) of the marker substance.
- biological materials include, without limitation, nucleic acids, polypeptides, carbohydrates, fatty acids, cellular components (e.g., cell membranes and mitochondria), and whole cells.
- markers are particular nucleic acid regions (e.g., genes, intragenic regions, specific loci, etc.). Regions of nucleic acid or protein that are biomarkers may be referred to, e.g., as “marker genes,” “marker regions,” “marker sequences,” “marker loci,” etc.
- the terms “patient” or “subject” refer to organisms to be subject to various tests provided by the technology.
- the term “subject” includes animals, preferably mammals, including humans.
- the subject is a primate.
- the subject is a human.
- sample is used in its broadest sense. In one sense it can refer to an animal cell or tissue. In another sense, it refers to a specimen or culture obtained from any source, as well as biological and environmental samples. Biological samples encompass fluids, solids, tissues, and gases. Environmental samples include environmental material such as surface matter, soil, water, and industrial samples. These examples are not to be construed as limiting the sample types applicable to the present invention.
- cell sample refers to a sample that comprises a cell (e.g., an intact cell from a subject) or cellular material (e.g., material from cells from the subject that are not intact cells).
- a “methylation state”, “methylation profile”, and “methylation status” of a nucleic acid molecule refers to the presence of absence of one or more methylated nucleobases in the nucleic acid molecule.
- a nucleic acid molecule containing a methylated cytosine is considered methylated (e.g., the methylation state of the nucleic acid molecule is methylated).
- a nucleic acid molecule that does not contain any methylated nucleotides is generally considered unmethylated.
- the methylation state of a particular nucleic acid sequence can indicate the methylation state of every base in the sequence or can indicate the methylation state of a subset of the bases (e.g., of one or more cytosines) within the sequence, or can indicate information regarding regional methylation density within the sequence with or without providing precise information of the locations within the sequence the methylation occurs.
- the methylation state describes the state of methylation of a nucleic acid (e.g., a genomic sequence).
- the methylation state refers to the characteristics of a nucleic acid segment at a particular genomic locus relevant to methylation.
- Such characteristics include, but are not limited to, whether any of the cytosine (C) residues within this DNA sequence are methylated, the location of methylated C residue(s), the frequency or percentage of methylated C throughout any particular region of a nucleic acid, and allelic differences in methylation due to, e.g., difference in the origin of the alleles.
- nucleic acid detection assay refers to any method of determining the nucleotide composition of a nucleic acid of interest. Nucleic acid detection assays include but are not limited to, DNA sequencing methods, probe hybridization methods, structure specific cleavage assays (e.g., the INVADER assay, (Hologic, Inc.) and are described, e.g, in U.S. Patent Nos. 5,846,717, 5,985,557, 5,994,069, 6,001,567, 6,090,543, and 6,872,816; Lyamichev et al., Nat.
- target nucleic acid is amplified (e.g., by polymerase chain reaction, e.g., as described by K.B. Mullis in U.S. Patent Nos. 4,683,195, 4,683,202, and 4,965,188) and amplified nucleic acid is detected simultaneously using an invasive cleavage assay.
- Assays configured for performing a detection assay e.g., invasive cleavage assay
- an amplification assay are described in U.S. Pat. No. 9,096,893, incorporated herein by reference in its entirety for all purposes.
- QuARTS method Additional amplification plus invasive cleavage detection configurations, termed the QuARTS method, are described in, e.g., in U.S. Pat. Nos. 8,361,720; 8,715,937; 8,916,344; and 9,212,392, each of which is incorporated herein by reference for all purposes. Additional modified QuARTS methods, termed LQAS AND TELQAS, are described in, e.g., U.S. Patent Publication No. US20200248233A1, U.S. Patent No. 10,648,025, International Application Publication No. WQ202104172 1 , and International Application publication No. W02020206256A1.
- invasive cleavage structure refers to a cleavage structure comprising i) a target nucleic acid, ii) an upstream nucleic acid (e.g. , an invasive or “INVADER” oligonucleotide), and iii) a downstream nucleic acid (e.g., a probe), where the upstream and downstream nucleic acids anneal to contiguous regions of the target nucleic acid, and where an overlap forms between the a 3' portion of the upstream nucleic acid and duplex formed between the downstream nucleic acid and the target nucleic acid.
- an upstream nucleic acid e.g. , an invasive or “INVADER” oligonucleotide
- a downstream nucleic acid e.g., a probe
- an overlap occurs where one or more bases from the upstream and downstream nucleic acids occupy the same position with respect to a target nucleic acid base, whether or not the overlapping base(s) of the upstream nucleic acid are complementary with the target nucleic acid, and whether or not those bases are natural bases or non-natural bases.
- the 3' portion of the upstream nucleic acid that overlaps with the downstream duplex is a non base chemical moiety such as an aromatic ring structure, e.g., as disclosed, for example, in U.S. Pat. No. 6,090,543, incorporated herein by reference in its entirety.
- one or more of the nucleic acids may be attached to each other, e.g., through a covalent linkage such as nucleic acid stem-loop, or through a non-nucleic acid chemical linkage (e.g., a multi-carbon chain).
- a covalent linkage such as nucleic acid stem-loop
- a non-nucleic acid chemical linkage e.g., a multi-carbon chain.
- the term “flap endonuclease assay” includes “INVADER” invasive cleavage assays, QuARTS assays, LQAS and TELQAS assays, as described above.
- a “flap oligonucleotide” refers to an oligonucleotide cleavable in a detection assay, such as an invasive cleavage assay, by a flap endonuclease.
- a flap oligonucleotide forms an invasive cleavage structure with other nucleic acids, e.g., a target or template nucleic acid and an invasive oligonucleotide.
- Flap assay reagents may optionally contain a target or template nucleic acid to which an invasive oligonucleotide and flap oligonucleotide bind.
- flap assay reagents comprise a Mg ++ flap assay buffer, as discussed herein.
- the term “flap endonuclease” refers to a structure-specific nucleolytic enzyme that cleaves a nucleic acid flap structure, e.g., an invasive cleavage structure.
- Flap endonuclease include, e.g., 5' -exonuclease domains of the DNA polymerase I proteins of Eubacteria and the FEN-1 proteins of Eukarya and Archaea. (Kaiser, el al, supra). Flap endonucleases may cleave additional structures, e.g., pseudo-Y, 5' overhang, and gap structures.
- overlap endonuclease substrate refers to a nucleic acid flap structure, e.g., an invasive cleavage structure, that is recognized and cleaved by a flap endonuclease, such as a FEN-1 endonuclease.
- FEN-1 refers to a non polymerase flap endonuclease from a eukaryote or archaeal organism, as encoded by a FEN-1 gene. See, e.g., Kaiser, et al., supra, WO 02/070755, and US Patent No. US 7,122,364, which are incorporated by reference herein in their entireties for all purposes.
- FEN-1 activity refers to any enzymatic activity of a FEN-1 enzyme.
- FEN-1 endonucleases also comprise modified FEN-1 proteins, e.g., chimerical proteins comprising portions of FEN-1 enzymes from different organisms, and enzymes comprising one or more mutations (e.g., substitutions, deletions, insertions, etc.), as described in WO 02/070755, and US Patent No. US 7,122,364.
- modified FEN-1 proteins e.g., chimerical proteins comprising portions of FEN-1 enzymes from different organisms, and enzymes comprising one or more mutations (e.g., substitutions, deletions, insertions, etc.), as described in WO 02/070755, and US Patent No. US 7,122,364.
- flap endonuclease assay refers to a detection assay in which formation and cleavage of a flap endonuclease substrate is used to evaluate a sample for the presence of or an amount of a target analyte, e.g. , a target nucleic acid.
- flap assay reagents or “invasive cleavage assay reagents” refers to a collection of all reagents required for performing a flap assay or invasive cleavage assay.
- flap assays generally include oligonucleotides for forming an invasive cleavage structure, a flap endonuclease and, optionally, a FRET cassette or 5' hairpin FRET reporter.
- Flap assay reagents may optionally contain a target to which the invasive oligonucleotide and flap oligonucleotide bind.
- FRET cassette refers to a hairpin oligonucleotide that contains a fluorophore moiety and a nearby quencher moiety that quenches the fluorophore.
- Hybridization of a cleaved flap e.g., from cleavage of a target-specific probe in a PCR-flap assay assay
- a FRET cassette produces a secondary substrate for the flap endonuclease, e.g., a FEN-1 enzyme. Once this substrate is formed, the 5' fluorophore-containing base can be cleaved from the cassette by the flap endonuclease, thereby generating a fluorescence signal.
- a FRET cassette comprises an unpaired 3' portion to which a cleavage product, e.g., a portion of a cleaved flap oligonucleotide, can hybridize to from an invasive cleavage structure cleavable by a FEN-1 endonuclease.
- a cleavage product e.g., a portion of a cleaved flap oligonucleotide
- PCR-flap assay is used interchangeably with the term “PCR-invasive cleavage assay” and refers to an assay configuration combining PCR target amplification and detection of the amplified DNA by formation of a first overlap cleavage structure comprising amplified target DNA, and a second overlap cleavage structure comprising a cleaved 5' flap from the first overlap cleavage structure and a labeled reporter oligonucleotide, e.g., a “FRET cassette” or 5' hairpin FRET reporter oligonucleotide.
- a labeled reporter oligonucleotide e.g., a “FRET cassette” or 5' hairpin FRET reporter oligonucleotide.
- the assay reagents comprise a mixture containing DNA polymerase, FEN-1 endonuclease, a primary probe comprising a portion complementary to a target nucleic acid, and a FRET cassette or 5' hairpin FRET reporter, and the target nucleic acid is amplified by PCR and the amplified nucleic acid is detected simultaneously (i.e.. detection occurs during the course of target amplification).
- PCR-flap assays include the QuARTS assays described in U.S. Pat. Nos. 8,361,720; 8,715,937; and 8,916,344, and the amplification assays of US Pat. No. 9,096,893 (for example, as diagrammed in Figure 1 of that patent), each of which is incorporated herein by reference in its entirety.
- PCR-flap assay reagents refers to one or more reagents for detecting a target nucleic acid in a PCR-flap assay, the reagents comprising nucleic acid molecules capable of participating in amplification of a target nucleic acid and in formation of a flap endonuclease substrate in the presence of the target nucleic acid, preferably in a mixture containing DNA polymerase, FEN-1 endonuclease and a FRET cassette or 5' hairpin FRET reporter.
- FRET refers to fluorescence resonance energy transfer, a process in which moieties (e.g., fluorophores) transfer energy e.g., among themselves, or, from a fluorophore to a non-fluorophore (e.g. , a quencher molecule).
- FRET involves an excited donor fluorophore transferring energy to a lower-energy acceptor fluorophore via a short-range (e.g., about 10 nm or less) dipole-dipole interaction.
- FRET involves a loss of fluorescence energy from a donor and an increase in fluorescence in an acceptor fluorophore.
- FRET energy can be exchanged from an excited donor fluorophore to a non-fluorescing molecule (e.g., a quenching molecule).
- a non-fluorescing molecule e.g., a quenching molecule.
- FRET is known to those of skill in the art and has been described (See, e.g., Stryer et ak, 1978, Ann. Rev. Biochem., 47:819; Selvin, 1995, Methods Enzymok, 246:300; Orpana, 2004 Biomol Eng 21, 45-50; Olivier, 2005 Mutant Res 573, 103-110, each of which is incorporated herein by reference in its entirety).
- kit refers to any delivery system for delivering materials.
- kits include systems that allow for the storage, transport, delivery, or use of devices and/or for processing samples obtained with devices (e.g., drinkable solutions, lubricants, or anesthetics for use of a swallowable device, sample stabilizing reagents; sample processing reagents such as particles, buffers, denaturants, oligonucleotides, filters, assay reaction components, etc. in the appropriate containers) and/or supporting materials (e.g., sample processing or sample storage vessels, written instructions for performing a procedure, etc.) from one location to another.
- devices e.g., drinkable solutions, lubricants, or anesthetics for use of a swallowable device, sample stabilizing reagents; sample processing reagents such as particles, buffers, denaturants, oligonucleotides, filters, assay reaction components, etc. in the appropriate containers
- supporting materials e.g., sample processing or sample storage vessels, written instructions for performing a procedure, etc.
- kits include one or more enclosure
- fragmented kit refers to a delivery system comprising two or more separate containers that each contains a subportion of the total kit components.
- the containers may be delivered to the intended recipient together or separately.
- a first container may contain materials for sample collection and a buffer.
- a first container may contain materials for sample collection and a cell stabilization buffer.
- a second container may contain reagents for detection of the one or more biomarkers.
- a second container may contain capture oligonucleotides and denaturant.
- fragmente Analyte specific reagents
- any delivery system comprising two or more separate containers that each contains a subportion of the total kit components are included in the term “fragmented kit.”
- a fragmented kit may contain analyte specific reagents, reagents for DNA extraction, and/or bisulfite conversion reagents.
- a fragmented kit comprising analyte specific reagents may be used in conjunction with a commercially available kit for DNA extraction.
- the kit may comprise reagents for sample collection and a cell stabilization buffer, and may be used in conjunction with a suitable kit for DNA extraction to isolate DNA From the sample prior to detecting one or more biomarkers, such as biomarkers described herein.
- kits refers to a delivery system containing all of the components for sample collection, processing, and assaying in a single container (e.g., in a single box housing each of the desired components).
- kit includes both fragmented and combined kits.
- system refers to a collection of articles for use for a particular purpose, e.g., a collection of devices, reagents, and instruments for collecting a sample (e.g., in preparation for analyzing the sample), or for collecting, processing and/or analyzing a sample for a particular purpose.
- the articles of a system comprise instructions for use, as information supplied on e.g., an article, on paper, on recordable media (e.g., DVD, flash drive, etc.).
- instructions direct a user to an online location, e.g., a website for viewing, hearing, and/or downloading instructions.
- instructions or other information are provided as an application (“app”) for a mobile device.
- FIGS. 1 A-1D show various embodiments of the dissolvable capsule described herein.
- FIG. 1A shows a capsule having a first closed end and a second closed end.
- FIG. IB shows a capsule having a first closed end and a second open end.
- FIG. 1C shows a capsule having a first closed end and a second closed end and multiple openings.
- FIG. ID shows a capsule having a first closed end and a second open end and multiple openings.
- FIG. 2 shows an embodiment of the ingestible cell sampling device described herein.
- the device comprises an abrasive sponge housed in a compressed state within a dissolvable capsule having a first closed end and a second closed end, a spherical molded cap having an interior surface in contact with the exterior surface of the second closed end, and a suture attached to the molded cap.
- FIG. 3 shows an embodiment of the ingestible cell sampling device described herein.
- the device comprises an abrasive sponge housed in a compressed state within a dissolvable capsule having a first closed end and a second closed end, a spherical molded cap having an interior surface in contact with the exterior surface of the second closed end, and a suture attached to the molded cap.
- the device further includes multiple openings along the cylindrical edge of the dissolvable capsule, such that the abrasive sponge is exposed to the external environment at these openings.
- FIG. 4 shows an embodiment of the ingestible cell sampling device described herein.
- the device comprises an abrasive sponge housed in a compressed state within a dissolvable capsule having a first closed end and a second open end, a spherical molded cap having an interior surface in contact with the abrasive sponge, and a suture attached to the molded cap.
- the molded cap covers the second open end of the dissolvable capsule.
- FIG. 5 shows an embodiment of the ingestible cell sampling device described herein.
- the device comprises an abrasive sponge housed in a compressed state within a dissolvable capsule having a first closed end and a second open end, a spherical molded cap having an interior surface in contact with the abrasive sponge, and a suture attached to the molded cap.
- the molded cap covers the second open end of the dissolvable capsule.
- the device further comprises multiple openings along the cylindrical edge of the dissolvable capsule.
- FIGS. 6A-6D show various embodiments of the abrasive sponge described herein.
- FIG. 6A shows a cylindrical shaped abrasive sponge comprising a portion of material from the center removed. Approximately 25% of the material from the center of the sponge is removed.
- FIG. 6B shows a similar sponge wherein a larger portion of material from the center is removed. Approximately 50% of the material from the center of the sponge is removed.
- FIG. 6C shows a cylindrical sponge wherein multiple portions from the edge of the sponge are removed to create a pinwheel shape from the top view.
- FIG. 6D shows a cylindrical sponge wherein multiple portions from the edge of the sponge are removed to create a cross shape from the top view.
- FIGS. 7A-7B show various views of an abrasive sponge wherein a portion (about 25%) of material from the center of the sponge is removed.
- the suture material passes through the abrasive sponge and attaches to the molded cap.
- the uncompressed diameter of the abrasive sponge is about 30 mm (FIG. 7 A).
- a portion of material is removed from the center of the abrasive sponge, and the abrasive sponge is attached to the interior surface of the molded cap by an adhesive (FIG. 7B).
- FIGS. 8A-8B show various views of an abrasive sponge wherein a portion (about 50%) of material from the center of the sponge is removed.
- the suture material passes through the abrasive sponge and attaches to the molded cap.
- the uncompressed diameter of the abrasive sponge is about 30 mm (FIG. 8 A).
- a portion of material is removed from the center of the abrasive sponge, and the abrasive sponge is attached to the interior surface of the molded cap by an adhesive (FIG. 8B).
- FIGS. 9A-9B show various views of an abrasive sponge wherein multiple portions of material from the edge of the sponge are removed.
- the uncompressed diameter of the abrasive sponge is about 30 mm (FIG. 9A).
- Multiple portions of material from the edge of the sponge are removed, to generate a sponge having a pinwheel shape from the top view (FIG. 9B).
- FIGS. 10A-10B show various views of an abrasive sponge wherein multiple portions of material from the edge of the sponge are removed.
- the uncompressed diameter of the abrasive sponge is about 30 mm (FIG. 10A).
- Multiple portions of material from the edge of the sponge are removed, to generate a sponge having a cross shape from the top view (FIG. 10B).
- FIGS. 11 A-l ID show various embodiments of methods for attaching the string to the molded cap.
- FIG. 11 A shows an embodiment where the suture is attached to the molded cap by means of a knot.
- the molded cap sits on the outside of a closed end of the capsule.
- FIG. 1 IB shows an embodiment where the molded cap covers an open end of the capsule.
- the string is attached to the molded cap by means of a knot
- the molded cap comprises an elongated cylindrical edge, the circumference of which fits within the circumference of the open end of the capsule.
- FIG. 11C shows an embodiment where the molded cap is a button. The button fits within the capsule and the string is attached to the button by means of a knot.
- FIG. 1 ID shows an embodiment where the molded cap is a button. The button fits within the capsule and the string is attached to the button by means of a knot.
- FIG. 12 shows multiple views of the embodiment for attachment shown in FIG. 11A.
- the molded cap comprises two holes through which the string is threaded (left).
- the knot to secure the string to the cap is tied on the inside of the molded cap (center).
- the molded cap fits over a closed end of the dissolvable capsule, such that the interior surface of the molded cap is in contact with the exterior surface of the closed end of the capsule (right).
- FIG. 13 shows multiple views of the embodiment for attachment shown in FIG. 1 IB.
- the molded cap comprises two holes through which the string is threaded (left).
- the knot to secure the string to the cap is tied on the inside of the molded cap (center).
- the molded cap comprises an elongated cylindrical edge, the circumference of which fits within the circumference of the open end of the capsule (center, right).
- the exterior surface of the molded cap is in contact with the external environment.
- FIG. 14 shows multiple views of the embodiment for attachment shown in FIG. 11C.
- the molded cap is a button.
- the button comprises two holes through which the string is threaded (left).
- the knot to secure the string to the button is tied on the inside of the molded cap (center).
- the string may be secured to the molded cap by use of an adhesive.
- the button fits within the capsule (right).
- FIG. 15 shows multiple views of the embodiment for attachment shown in FIG. 1 ID.
- the molded cap is a button.
- the button comprises a bar feature molded into the cap (left).
- the string wraps around the bar feature, and the knot to secure the string to the button is tied on the inside of the molded cap (center).
- the string may be secured to the button (e.g., to the bar feature) by an adhesive.
- the button fits within the capsule (right).
- FIG. 16 shows multiple views of an exemplary embodiment of the ingestible cell sampling device as described herein.
- the device comprises dissolvable capsule having a first closed end and a second closed end.
- the device comprises a spherical molded cap having an exterior surface in contact with the interior surface of the second closed end, and a suture attached to the molded cap.
- An abrasive sponge may be housed in a compressed state within the dissolvable capsule, such that the interior surface of the spherical molded cap is in contact with the abrasive sponge.
- Exemplary side, top, and angled views of the molded cap are shown on the right.
- the molded cap comprises two holes to allow attachment of the suture, and is slightly recessed on top to account for suture thickness.
- FIG. 17 shows multiple views of an exemplary embodiment of the ingestible cell sampling device as described herein.
- the device comprises dissolvable capsule having a first closed end and a second closed end.
- the device comprises a spherical molded cap having an exterior surface in contact with the interior surface of the second closed end, and a suture attached to the molded cap.
- An abrasive sponge may be housed in a compressed state within the dissolvable capsule, such that the interior surface of the spherical molded cap is in contact with the abrasive sponge.
- Exemplary side, top, and angled views of the molded cap are shown on the right.
- the molded cap comprises two holes to allow attachment of the suture, and is slightly recessed on top to account for suture thickness.
- the holes are slightly larger than the holes shown in the embodiment of FIG. 16.
- the larger holes for this device compared to those shown in FIG. 16 may permit different (e.g. larger) knots to be used to attach the suture to the
- FIG. 18 shows multiple views of an exemplary embodiment of the ingestible cell sampling device as described herein.
- the device comprises dissolvable capsule having a first closed end and a second open end.
- An abrasive sponge may be housed in a compressed state within the dissolvable capsule.
- the device comprises a spherical molded cap having an interior surface in contact with the abrasive sponge, and a suture attached to the molded cap.
- the exterior surface of the spherical molded cap is exposed to the external environment.
- the molded cap covers the second open end of the dissolvable capsule. Exemplary side, top, and angled views of the molded cap are shown on the right.
- the molded cap comprises two holes to allow attachment of the suture, and is slightly recessed on top to account for suture thickness.
- FIG. 19 shows multiple views of an exemplary embodiment of the ingestible cell sampling device as described herein.
- the device comprises dissolvable capsule having a first closed end and a second open end.
- An abrasive sponge may be housed in a compressed state within the dissolvable capsule.
- the device comprises a spherical molded cap having an interior surface in contact with the abrasive sponge, and a suture attached to the molded cap.
- the exterior surface of the molded cap is exposed to the external environment.
- the molded cap covers the second open end of the dissolvable capsule. Exemplary side, top, and angled views of the molded cap are shown on the right.
- the molded cap comprises two holes to allow attachment of the suture, and is slightly recessed on top to account for suture thickness.
- FIG. 20 shows multiple views for an exemplary embodiment of a handle as described herein.
- the handle has a hook shape.
- the handle “pinches” the dissolvable capsule within a set of grippers at one end of the handle.
- the other end of the handle is a hook.
- the suture may be wound around any suitable portion of the handle.
- the ingestible device may be removed and the suture may be unwound.
- the device may be ingested by the subject, while the subject or a third party holds on to the hook end of the handle.
- FIG. 21 shows an exemplary embodiment of a handle as described herein.
- the handle comprises a cavity in which the dissolvable capsule may be placed.
- the suture may be wound around a separate portion of the handle, as shown. When wound, the suture may be held in place by a suitable amount of tension.
- the handle may comprise tabs, which may be squeezed to remove tension from the suture and allow for facile removal of the suture from the handle, without the need to unwind the entire length of the suture.
- FIG. 22 shows another exemplary embodiment of a handle as described herein.
- the handle may be circular in shape.
- the handle comprises a cavity in which the dissolvable capsule may be placed.
- the suture may be wound around the external edge of the circular handle, such as along a slightly recessed channel extending along the outer edge of the handle.
- the suture may be tied in such as a position, which may be facilitated by a single hole placed in the circular handle.
- the suture may be untied and unwound from the circular handle to allow for the subject to ingest the device.
- FIG. 23 shows another exemplary embodiment of a handle as described herein.
- the handle is a T-shape.
- the handle comprises a cavity in which the dissolvable capsule may be placed.
- the suture may be held in place by winding the suture around the handle.
- FIG. 24 shows an exemplary embodiment of a handle as described herein.
- the handle comprises a flat surface on one end, and a hook shape on the opposing end.
- the flat surface comprises a cavity in which the dissolvable capsule may be placed.
- the flat surface additionally comprises a plurality of openings to provide a variety of suitable attachment sites for the suture.
- FIGS. 25A-25F show exemplary assay designs for detecting biomarkers of esophageal disorders in a sample.
- the technology relates to cell sampling devices.
- the present invention relates to ingestible cell sampling devices and their use in methods for detecting various abnormalities in a subject.
- the ingestible cell sampling devices described herein are advantageous in that the devices provide improved safety for use in a subject.
- the ingestible cell sample devices described herein comprise a handle to facilitate ease of use by the subject.
- the handle provides a suitable surface for the user or a third party to hold onto during ingestion of the dissolvable capsule component of the device, thereby preventing loss within the subject and facilitating facile removal of the device following a suitable duration of time.
- the ingestible cell sampling devices described herein are designed to prevent detachment of the string from the molded cap, thus preventing loss of the device within a subject.
- the ingestible cell sampling devices described herein are designed to minimize the risk of the sponge detaching from the string during retrieval of the device, thus also preventing loss of the device within the subject.
- the devices described herein use materials that prevent laceration to the esophagus upon withdrawal of the device. The devices are easily swallowed by the subject, with a rapid dissolution of the capsule and expansion of the sponge, thus minimizing the total time required to collect an esophageal sample from the subject.
- the sponge comprises multiple features that enable for maximal surface area to capture sufficient tissue from a subject. Accordingly, described herein are ingestible cell sampling devices with maximal sampling capabilities having enhanced safety and tolerability for use in a subject.
- ingestible cell sampling devices comprise an abrasive sponge housed within a dissolvable capsule, a molded cap, and a string attached to the molded cap.
- the abrasive sponge may comprise any suitable material.
- the material is capable of being compressed and retained in a compressed state by the dissolvable capsule.
- the abrasive sponge may comprise a reticulated material.
- the reticulated material comprises 10-35 pores per inch of material.
- the reticulated material may comprise about 10, about 15, about 20, about 25, about 30, or about 35 pores per inch of material.
- the material may be any suitable porous, low-density material capable of collecting esophageal cells from a subject.
- the abrasive sponge may comprise reticulated polyurethane.
- the abrasive sponge comprises a reticulated polyester material.
- the abrasive sponge comprises a reticulated polyether material.
- the porosity of the abrasive sponge may be at least 80%.
- the porosity may be at least 80%, at least 81%, at least 82%, at least 83%, at least 84%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99%.
- the abrasive sponge may be of any suitable size and shape.
- the size and shape of the sponge may depend on the size of the capsule.
- the abrasive sponge is of a suitable size and shape to allow for compression into a capsule suitable for oral administration (e.g. ingestion), and subsequent facile removal from the esophagus and throat of a subject after dissolution of the capsule and restoration of the sponge to its uncompressed size.
- the sponge may be cylindrical in shape.
- the sponge may be cylindrical in shape with a diameter (e.g. the diameter of the circular portion forming the shaft of the cylinder) of about 20-400 mm in an uncompressed shape.
- the diameter may be about 20 mm, about 25 mm, about 30 mm, about 35 mm, or about 40 mm in an uncompressed state.
- the sponge may be cylindrical in shape with a diameter of 20 mm, 21 mm, 22 mm, 23 mm, 24 mm, 25 mm, 26 mm, 27 mm, 28 mm, 29 mm, or 30 mm in an uncompressed state.
- the sponge may be spherical in shape.
- the sponge may be spherical in shape with a diameter of about 20-40 mm in an uncompressed state.
- the sponge may be spherical in shape with a diameter of about 20 mm, about 25 mm, about 30 mm, about 35 mm, or about 40 mm in an uncompressed state.
- the sponge may be spherical in shape with a diameter of 20 mm, 21 mm, 22 mm, 23 mm, 24 mm, 25 mm, 26 mm, 27 mm, 28 mm, 29 mm, or 30 mm in an uncompressed state.
- the abrasive sponge may be compressed to a suitable size and housed within the dissolvable capsule in a compressed state.
- the compressed sponge may have a diameter of about 1 mm to about 15 mm.
- the compressed sponge may have a diameter of 1 mm, 2 mm, 3 mm, 4 mm, 5 mm, 6 mm, 7 mm, 8 mm, 9 mm, 10 mm, 11 mm,
- the dissolution of the dissolvable capsule releases the abrasive sponge from compression and allows the abrasive sponge to expand.
- the abrasive sponge expands to its uncompressed size following dissolution of the dissolvable capsule.
- the abrasive sponge expands to substantially the same size as its original, uncompressed size prior to packaging within the capsule. As a nonlimiting example, the abrasive sponge may expand to within 10% of the original, uncompressed size following dissolution of the dissolvable capsule.
- the sponge may expand to within 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, or 10% of the original, uncompressed size following dissolution of the dissolvable capsule.
- the original, uncompressed size may be 30 mm and the sponge may expand to 27-30 mm following dissolution of the capsule.
- the uncompressed sponge is uniform in shape.
- the uncompressed sponge may be uniformly spherical in shape.
- the uncompressed sponge may be uniformly cylindrical in shape.
- the uncompressed sponge may be spherical in shape with a protrusion that extends a portion of the abrasive sponge material into the dissolvable capsule. This protrusion is exemplified in FIG. 8B.
- the abrasive sponge is formed to have concavities or indentations, or other external or internal spaces devoid of sponge material (“void spaces”), as may be provided by removing at least one portion of the abrasive sponge.
- void spaces devoid of sponge material
- a “removed” portion of a sponge refers a void space in the shaped abrasive sponge, e.g., a portion that would be removed from a simple solid form, e.g., a sphere or cylinder, to produce the final shape comprising one or more void spaces.
- an abrasive sponge may be manufactured in a final form that comprises such a void space, such that no sponge material need be physically “removed” during manufacture.
- at least one portion of material may be removed from the center of the abrasive sponge.
- the sponge may be cylindrical in shape and a portion of the material may be removed from the center of the sponge.
- the sponge may be spherical in shape and a portion of the material may be removed from the center of the abrasive sponge.
- FIG. 6A and 6B such embodiments are exemplified in FIG. 6A and 6B.
- at least one portion of material may be removed from at least one outer edge of the abrasive sponge.
- the sponge may be cylindrical in shape and at least one portion of the material may be removed from the edge of the abrasive sponge.
- the sponge may be spherical in shape and at least one portion of the material may be removed from the edge of the abrasive sponge.
- FIG. 6C and 6D Various embodiments are exemplified in FIG. 6C and 6D.
- multiple portions of material may be removed from the edge of the sponge to generate a pinwheel shape (as shown in FIG. 6C) or a cross-shape (as shown in FIG. 6D), when the sponge is viewed from the top.
- Any suitable sized portion may be removed from the sponge. For example, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, or more of the material may be removed from the sponge. In some embodiments, removal of a portion of the material facilitates compression of the sponge into a suitable sized capsule for ingestion by a subject. In some embodiments, removal of a portion of the material from the sponge facilitates rapid expansion of the sponge following dissolution of the dissolvable capsule. In some embodiments, removal of a portion of the material from the sponge increases the surface area of the sponge available for collecting esophageal cells in the subject.
- the abrasive sponge is housed within a dissolvable capsule. Accordingly, the abrasive sponge may be compressed into a cylindrical shape to fit into the dissolvable capsule.
- the dissolvable capsule may comprise any suitable material.
- the dissolvable capsule may comprise gelatin, starch, or a cellulosic material as known in the art.
- the dissolvable may be a vegan or vegetarian capsule (e.g., exclusive of all animal products, or free of products from certain types of animals; e.g. gelatin-free capsule).
- the dissolvable capsule may be made of a suitable material.
- the dissolvable capsule comprises a suitable material that dissolves within 10 minutes of entering the stomach cavity of a subject.
- the dissolvable capsule may dissolve approximately within 10 minutes, within 9 minutes, within 8 minutes, within 7 minutes, within 6 minutes, within 5 minutes, within 4 minutes, within 3 minutes, within 2 minutes, or within 1 minute of exposure to the stomach cavity of a subject.
- the dissolvable capsule dissolves within 5 minutes of exposure to the stomach cavity of the subject.
- the dissolvable capsule comprises a first closed end and a second closed end.
- a dissolvable capsule comprising a first closed end and a second open end is shown in FIG. 1A.
- the dissolvable capsule comprises a first closed end and a second open end.
- a dissolvable capsule comprising a first closed end and a second open end is shown in FIG. IB.
- the dissolvable capsule comprises one or more openings, such that a portion of the abrasive sponge is exposed to the external environment at the one or more openings. The presence of one or more openings may facilitate a faster dissolution time of the capsule upon ingestion by a subject.
- the dissolvable capsule comprises one opening.
- the dissolvable capsule comprises two or more openings. Representative images of capsules containing one or more openings are shown in FIG. 1C (capsule having a first closed end and a second open end) and FIG. ID (capsule having a first closed end and a second open end).
- the one or more openings may be any suitable size and shape that allow for exposure of the abrasive sponge to the external environment without substantially diminishing the ability of the capsule to retain the sponge in a compressed state.
- the one or more openings may be in any suitable location on the dissolvable capsule.
- the dissolvable capsule may comprise one or more openings on a closed end of the capsule.
- the dissolvable capsule may comprise one or more openings on a cylindrical edge of the capsule.
- the ingestible cell sampling device further comprises a molded cap.
- the molded cap is hemispherical in shape.
- the molded cap is cylindrical in shape (e.g., a button).
- the molded cap is connected to the capsule.
- the molded cap may be connected to the capsule by an adhesive.
- the molded cap is connected to the abrasive sponge.
- the molded cap may be connected to the abrasive sponge by an adhesive.
- the molded cap fits within the capsule.
- the cell sampling device may comprise a capsule comprising a first closed end and a second closed end, and a hemispherical molded cap may cover one of the closed ends of the capsule.
- the molded cap may comprise an internal surface in contact with an external surface of one end of the capsule and an exterior surface in contact with the external environment (as exemplified in FIG. 2 and FIG. 3).
- the molded cap comprises an interior surface in contact with the abrasive sponge and an exterior surface.
- the exterior surface may be in contact with the external environment.
- the capsule may comprise a first closed end and a second open end, and the molded cap may cover the second open end of the capsule.
- the molded cap may comprise an elongated cylindrical edge, the circumference of which fits within the circumference of the capsule (as exemplified in FIG. 4).
- the molded cap comprises an interior surface in contact with the abrasive sponge and an exterior surface in contact with an internal surface of one end of the capsule.
- the capsule may comprise a first closed end and a second closed end, and a hemispherical molded cap may comprise an interior surface in contact with the abrasive sponge and an exterior surface in contact with the internal surface of one closed end of the capsule (e.g., the molded cap is fitted within the capsule).
- the capsule may comprise a first closed end and a second closed end, and a cylindrically shaped molded cap (e.g., a button) may be fitted inside the capsule.
- the button may be fitted inside the capsule such that the rim of the molded cap is in contact with the capsule, the bottom surface of the molded cap is in contact with the abrasive sponge, and the top surface of the molded cap is not in direct contact with the interior surface of the capsule (as exemplified in FIG. 14 and FIG. 15).
- the cell sampling device comprises a capsule comprising a first closed end and a second closed end, and a hemispherical molded cap may fit within the capsule.
- the cell sampling may comprise a hemispherical molded cap having an exterior surface in contact with the interior surface of the second closed end, and a suture attached to the molded cap.
- An abrasive sponge may be housed in a compressed state within the dissolvable capsule, such that the interior surface of the spherical molded cap is in contact with the abrasive sponge.
- Such an embodiment is shown, for example, in FIG. 16 and FIG. 17.
- the interior surface of the molded cap may be attached to the abrasive sponge.
- the interior surface of the molded cap may be attached to the abrasive sponge by an adhesive.
- the molded cap may be attached to the capsule (e.g. by an adhesive).
- the ingestible cell sampling device further comprises a string attached to the molded cap.
- the string may be attached to the molded cap by any suitable means, including but not limited to crimping, over-molding, adhesive, melting, wrapping, or taping.
- the string is attached to the molded cap by an adhesive.
- the string is attached to the molded cap by a knot. Any suitable type of knot may be used.
- the knot may be a hitch knot.
- the term “hitch knot” refers to a type of knot used to tie a string to an object or to another string.
- hitch knots include an alternate ring hitching, anchor bend variant, bale sling hitch, barrel hitch, becket hitch, blackwall hitch, blake's hitch, boom hitch, bottom loaded release hitch, buntline hitch, cat's paw, chain hitch, clinging clara, clove hitch, continuous ring hitching, cow hitch variant, cow hitch with toggle, cow hitch, double half hitches, Farrimond friction hitch, garda hitch, ground-line hitch, half hitch, halter hitch, highpoint hitch, highwayman's hitch, hitching tie, icicle hitch, killick hitch, knute hitch, lighterman's hitch, magnus hitch, marline hitching, marlinespike hitch, masthead knot, midshipman's hitch, acquirer hitch, acquirer hitch, acquirer friction hitch, ossel hitch, palomar knot, pile hitch, prusik knot, reverse half hitch
- the knot may be a binding knot.
- binding knot refers to a type of knot used to keep an object or multiple objects together, using a string that passes at least once around them. Suitable binding knots include, for example, a boa knot, a bottle sling, a bowline knot, a constrictor knot, a corned beef knot, a granny knot, a ground line hitch, a Miller’s knot, a Packer’s knot, a reef knot, a strangle knot, a surgeon’s knot, a thief knot, a jamming knot, a sheet bend, or a common whipping knot.
- the type of knot may be selected to allow for ease of manufacturing while also providing a stable means of connecting the string to the molded cap.
- the molded cap may comprise any suitable feature to enable attachment of the string to the cap.
- the molded cap may comprise two holes through which the string can be threaded and tied into a suitable knot.
- the string can be threaded through the first hole, pass through the external environment, and re-enter the interior of the capsule by passing through the second hole, before a knot can be tied on the interior of the capsule.
- the molded cap may comprise a bar on which the string can be secured (as shown in FIG. 1 ID).
- the string may comprise any suitable material.
- the string may be a suture material (e.g. surgical suture material).
- the suture material may be made from a variety of materials, including biological materials or synthetic materials.
- the suture material may comprise synthetic materials such as nylon, polyester, PVDF, polypropylene, or combinations thereof.
- the string should be of a suitable thickness to allow for facile ingestion by the subject without causing lacerations to the throat.
- the string has a thickness of 0.3 mm to 0.7 mm.
- the string may have a thickness of 0.3 mm, 0.35 mm, 0.4 mm, 0.45 mm, 0.5 mm, 0.55 mm, 0.6 mm, 0.65 mm, or 0.7 mm.
- the string should be of a suitable length to allow for retrieval of the device after dissolution of the dissolvable capsule in the subject. Accordingly, the string should be long enough to allow for the abrasive sponge contained within the dissolvable capsule to reach the stomach cavity of the subject, while retaining enough string for the subject or a physician to be able to grip the string to initiate retrieval of the device.
- the string may be at least 60 cm long. In some embodiments, the string may be 60cm to 80cm long.
- the string may be 60 cm, 61 cm, 62 cm, 63 cm, 64 cm, 65 cm, 66 cm, 67 cm, 68c cm, 69 cm, 70 cm, 71 cm, 72 cm, 73 cm, 74 cm, 75 cm, 76 cm, 77 cm, 78 cm, 79 cm, or 80 cm long.
- the string may comprise markings on the string to judge the amount of string that has been swallowed. Such markings would assist in determining that the dissolvable capsule has traveled to the desired area (e.g. the stomach cavity of the subject).
- the markings may be spaced any suitable distance apart. For example, the markings may be spaced 1-80 cm apart. For example, the markings may be placed about 1 cm, about 5 cm, about 10 cm, about 15 cm, about 20 cm, about 25 cm, about 30 cm, about 35 cm, or about 40 cm apart.
- the string should have a suitable tensile strength to minimize the risk of the string breaking during ingestion and/or retrieval of the device.
- the string should have a suitable tensile strength to allow for the string to be pulled to retrieve the device from the subject after dissolution of the dissolvable capsule.
- the ingestible device may comprise a handle or a grip to facilitate retrieval of the device and/or prevent swallowing of the entire string.
- the ingestible device may comprise a handle attached to the end of the string that is not attached to the moldable cap or button.
- the ingestible device may comprise a handle or a grip on the end of the string that does not contain the capsule.
- the handle or grip may be of any suitable size and shape to facilitate retrieval and prevent swallowing of the string.
- the handle or grip may be an open shape (e.g. bar shape, T-shape, X-shape, hook shape, etc.) or a closed shape (e.g. circular or semi-circular shape, rectangular shape, triangular shape, etc.), and may be formed from the same material as the string (e.g., may be a loop or knot in the string) or may comprise different material (e.g., plastic, metal, etc.).
- Suitable handles are demonstrated herein, in particular in FIGS. 21, 22, 23, and 24.
- the handle also serves as means to store the ingestible device prior to use in a subject.
- the handle may comprise a cavity in which the dissolvable capsule may be contained.
- the handle may also comprise a means to wind the string (e.g., suture) around the handle during storage.
- the handle pinches dissolvable capsule ingestible device within a set of grippers at one end of the handle.
- the handle may comprise a mechanism to loosen or unlock the grippers, thereby releasing the dissolvable capsule prior to use in a subject.
- the other end of the handle e.g. the end opposite to the grippers
- is a hook Such an embodiment is shown in FIG. 20.
- the handle comprises a flat surface containing a cavity in which the dissolvable capsule may be placed and a segment around which the suture may be wrapped.
- the handle may further comprise a means to release tension on the suture, thereby facilitating removal of the length of suture without the need for unwinding.
- FIG. 21 Such an embodiment is shown, for example, in FIG. 21.
- the handle comprises tabs, which may be squeezed to remove tension from the suture and allow for facile removal of the suture from the handle.
- the handle is circular in shape.
- the handle comprises a flat surface containing a cavity in which the dissolvable capsule may be placed.
- the suture may be wound around the external edge of the circular handle, such as along a slightly recessed channel extending along the outer edge of the handle.
- the suture may be tied in such as a position, which may be facilitated by a single hole placed in the circular handle.
- the suture may be untied and unwound from the circular handle to allow for the subject to ingest the device. Such an embodiment is shown in FIG. 22.
- the handle is a T-shape.
- the top cross section of the T may comprise a cavity in which the dissolvable capsule may be placed, whereas the perpendicular cross section may be used to wind the suture around the handle.
- the handle comprises a modified hook shape with multiple attachment sites to which the suture may be secured.
- FIG. 24 shows an exemplary embodiment of a handle as described herein.
- the handle comprises a flat surface on one end, and a hook shape on the opposing end.
- the flat surface comprises a cavity in which the dissolvable capsule may be placed.
- the flat surface additionally comprises a plurality of openings to provide a variety of suitable attachment sites for the suture.
- the string passes through a portion of the abrasive sponge. Accordingly, passing the string through the sponge will help secure the sponge to the molded cap, such that the sponge is not lost within the subject after dissolution of the dissolvable capsule.
- the string passes through at least one surface of the dissolvable capsule.
- the string may pass through the first closed end of the dissolvable capsule, through the abrasive sponge, and then attach to the molded cap.
- the string may pass through the first closed end of the dissolvable capsule, through the abrasive sponge, through the second closed end of the dissolvable capsule, and then attach to the molded cap.
- the end of the string not attached to the molded cap may be attached to a handle, as described above.
- the methods comprise providing an ingestible cell sampling device described herein to the subject.
- Suitable methods for providing an ingestible cell sampling device to a subject are described in U.S. Patent No. 4,735,214, U S. Patent No 10,327,742, and U.S. Patent No. 10,292,687, each of which are incorporated herein by reference in their entireties.
- the subject may swallow the ingestible cell sampling device described herein and a suitable amount of time may pass prior to retrieving the device from the subject.
- the subject may swallow the ingestible cell sampling device and 10 minutes or less may be allowed to pass prior to retrieval. For example, 10 minutes, 9 minutes, 8 minutes, 7 minutes,
- a stabilization buffer may comprise any suitable agent or combination of agents that prevent unwanted damage to the cells (e.g. cell lysis) or damage/degradation of the nucleic acids (e.g. DNA or RNA) contained within the cell sample.
- esophageal cells are harvested from the abrasive sponge and analyzed to determine whether an esophageal disorder is present in the subject. Analysis may be performed by any suitable method, including protein-based tests, tissue/cell examinations (e.g., microscopy or other visual inspections), and/or nucleic acid detection assays. For example, analysis may be performed by protein-based techniques to analyze one or more biomarkers of interest. Protein-based techniques include, for example, immunohistochemistry, ELISA, western blot, flow cytometry, fluorescent in-situ hybridization (FISH), fluorescence analysis of cell sorting (FACS), mass spectrometry, etc.
- protein-based techniques include, for example, immunohistochemistry, ELISA, western blot, flow cytometry, fluorescent in-situ hybridization (FISH), fluorescence analysis of cell sorting (FACS), mass spectrometry, etc.
- protein-based techniques may be performed using one or more antibodies against at least one biomarker protein of interest.
- the biomarker protein(s) may be detected using an antibody capable of reacting with the protein(s), and subsequent visualization of the antibody.
- the antibody may be a polyclonal antibody or a monoclonal antibody.
- the use of secondary, tertiary or further antibodies may advantageously employed in order to amplify the signal and facilitate detection.
- esophageal cells are harvested from the abrasive sponge and examined to determine whether an esophageal disorder is present in the subject.
- cells may be harvested from the sponge, plated on an appropriate medium, and examined by microscopy or other visual examination to determine whether characteristics indicative of an esophageal disorder are present in the cells.
- cells may be harvested from the sponge, plated, and inspected using a microscope to determine whether one or more cancer cells are present.
- diagnosis of an esophageal disorder may be made by visualization of a specific cell type, such as a columnar cell, which may be indicative of gastroesphageal reflux disease or complications thereof, including Barrett’s Esophagus or esophageal adenocarcinoma.
- a specific cell type such as a columnar cell, which may be indicative of gastroesphageal reflux disease or complications thereof, including Barrett’s Esophagus or esophageal adenocarcinoma.
- esophageal cells are harvested from the abrasive sponge and one or more nucleic acid detection assays are performed to determine whether an esophageal disorder is present in the subject.
- esophageal cells may be harvested from the abrasive sponge following use in a subject, and the cells may be analyzed by one or more nucleic acid detection assays to detect levels of one or more biomarkers of an esophageal disorder. Suitable methods (e.g. nucleic acid detection assays) and biomarkers for detecting esophageal disorders are described in U.S. Pat. Appl. Ser. No.
- 10,435,755 (including, e.g., BMP3, NDRG4, VAV3, SFMBT2, DI03, HUNK, ELMOl, CD ID, CDKN2A; and OPLAH), both of which are incorporated herein by reference in their entireties.
- Exemplary assay designs for suitable biomarkers ZNF682, NDRG4, and VAV3 are discussed in more detail, below.
- esophageal cells may be harvested from the abrasive sponge and the levels of one or more biomarkers selected from ZNF682, NDRG4, and VAV3 may be determined. In some embodiments, levels of ZNF682, NDRG4, and VA V 3 may be determined. In some embodiments, detecting an esophageal disorder may comprise measuring DNA methylation levels of the one or more biomarkers.
- the biomarker may be ZNF682.
- Exemplary primers and probes for ZNF682 are shown in FIG. 16A.
- the ZNF682 forward primer may comprise 5 ’AGTTTATTTTGGGAAGAGTCGCG3 ’ (SEQ ID NO: 3)
- the reverse primer may comprise 5’CCATTATCCCCGCAATCGAA3’ (SEQ ID NO: 4)
- the probe may comprise 5’CGCGCCGAGGGCGCGTTTTTGCGTT/3C6/3’(SEQ ID NO: 5).
- the biomarker may be VAV3.
- Exemplary primers and probes for VA V 3 are shown in FIG. 16B.
- the VAV3 forward primer may comprise 5’TCGGAGTCGAGTTTAGCGC3’ (SEQ ID NO: 8) and the reverse primer may comprise 5 ’ CGAAATCGAAAAAAC AAAAACCGC3 ’ (SEQ ID NO: 9).
- VAV3 may be detected by one probe or two probes.
- VAV3 may be detected by the probe (arm 1) 5 CGCCGAGGCGGCGTTCGCGA/3C6/3’ (SEQ ID NO: 10) and/or the probe (arm 5) 5 CCACGGACGCGGCGTTCGCGA/3C6/3’ (SEQ ID NO: 11).
- the biomarker may be NDRG4.
- Exemplary primers and probes for NDRG4 are shown in FIG. 16C.
- the NDRG4 forward primer may comprise 5 ’ CGGTTTTCGTTCGTTTTTTCG3 ’ (SEQ ID NO: 14)
- the reverse primer may comprise 5’CCGCCTTCTACGCGACTA3’ (SEQ ID NO: 15)
- the probe may comprise 5 ’ CCACGGACGGTTCGTTTATCG/3C6/3 ’ (SEQ ID NO: 16).
- the biomarker may be bone morphogenic protein 3 ⁇ BMP 3).
- the biomarker may be ZNF568. In some embodiments, the biomarker may be BMP 3 and ZNF568.
- one or a group of biomarkers for analyzing a sample collected from an esophagus may be selected from the group consisting of NDRG4, ZNF682, VAV3, BMP3, ZNF568, FER1L4, ANKRD13B, CD ID, CDKN2A , CHST2, CNNM1, DI03, DOCK2, DTX1, ELMOl, FERMT3, FLIl, GRIN2D, HUNK, JAM3, LRRC4, OPLAH, PDGFD, PKIA, PPP2R5C, QKI, SEP9, SFMBT2, SLC12A8, TBX15, TSPYL5, ZNF304, and ZNF671.
- Biomarkers selected from this group may comprise 1 biomarker, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, or 33 biomarkers, alone or in any combination or subcombination, without limitation.
- the biomarker or group of biomarkers is selected from the group consisting of ANKRDJ3B CHST2, CNNM1, DOCK2, DTX1, FER1L4, FERMT3, FLIl, GRIN2D, JAM3, LRRC4, OPLAH, PDGFD,
- the biomarker or group of biomarkers is selected from the group consisting of BMP 3, NDRG4, VAV3, SFMBT2, DIO 3, HUNK, ELMOl, CD1D, CDKN2A, and OPLAH. In some embodiments, the biomarker or group of biomarkers is selected from the group consisting of NDRG4, ZNF682, VAV3, BMP 3,
- the group of biomarkers comprises the group consisting of NDRG4, ZNF682, VAV3, BMP 3, ZNF568, and FLR11.4.
- the one or more biomarkers are normalized against a reference marker. Suitable methods and reference markers are described in U.S. Patent No. 10,465,248 and U.S. Patent Application No. US 16/318,580, the entire contents of each of which are incorporated herein by reference.
- the reference marker is selected from b-actin, ZDHHC1, and B3GALT6.
- the reference marker may be ZDHHCl.
- Exemplary primers and probes for ZDHHCl are shown in FIG. 16D.
- the ZDHHCl forward primer comprises 5 ’ GTCGGGGTCGATAGTTTACG3 ’ (SEQ ID NO: 19)
- the reverse primer comprises 5’ACTCGAACTCACGAAAACG3’ (SEQ ID NO: 20)
- the probe comprises 5 CCACGGACGGACGAACGCACG/3C6/3’ (SEQ ID NO: 21).
- the reference marker may be B3GALT6.
- Exemplary primers and probes for B3GALT6 are shown in FIG. 16E.
- the B3GALT6 forward primer comprises 5 ’ GGTTTATTTTGGTTTTTTGAGTTTTCGG3 ’ (SEQ ID NO: 24)
- the reverse primer comprises 5’TCCAACCTACTATATTTACGCGAA3’ (SEQ ID NO:25)
- the probe comprises 5 ’CCACGGACGGCGGATTTAGGG/3C6/3 ’ (SEQ ID NO: 26).
- the reference marker may be b-actin.
- Exemplary primers and probes for b-actin are shown in FIG. 16F.
- the b-actin forward primer comprises 5 ’ GTGTTTGTTTTTTTGATTAGGTGTTTAAGA3 ’ (SEQ ID NO: 32)
- the reverse primer comprises 5’CTTTACACCAACCTCATAACCTTATC3’ (SEQ ID NO:33)
- the probe comprises 5 ’ GACGCGGAGATAGTGTTGTGG/3C6/3 ’ (SEQ ID NO:34).
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AU2021257479A AU2021257479A1 (en) | 2020-04-17 | 2021-04-16 | Ingestible sampling device |
EP21788930.2A EP4135592A4 (en) | 2020-04-17 | 2021-04-16 | Ingestible sampling device |
US17/996,032 US20230190243A1 (en) | 2020-04-17 | 2021-04-16 | Ingestible sampling device |
CN202180032612.7A CN115605138A (en) | 2020-04-17 | 2021-04-16 | Ingestible sampling device |
JP2022562444A JP2023522629A (en) | 2020-04-17 | 2021-04-16 | ingestible sampling device |
CA3174354A CA3174354A1 (en) | 2020-04-17 | 2021-04-16 | Ingestible sampling device |
KR1020227038078A KR20230026300A (en) | 2020-04-17 | 2021-04-16 | Ingestible Sampling Device |
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EP (1) | EP4135592A4 (en) |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2023224945A1 (en) * | 2022-05-16 | 2023-11-23 | Pavmed, Inc. | Device for collecting a biological sample |
US11987847B2 (en) | 2014-03-31 | 2024-05-21 | Mayo Foundation For Medical Education And Research | Detecting colorectal neoplasm |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4735214A (en) * | 1986-09-05 | 1988-04-05 | Berman Irwin R | Gastrointestinal diagnostic capsule and method of use |
WO2011058316A1 (en) * | 2009-11-13 | 2011-05-19 | Medical Research Council | Cell sampling device |
US20130296738A1 (en) * | 2012-05-04 | 2013-11-07 | Given Imaging Ltd. | Device and method for in vivo cytology acquisition |
US20160081671A1 (en) * | 2014-09-18 | 2016-03-24 | Covidien Lp | Use of expansion-force elements in a compressible cell collection device |
KR20160128136A (en) * | 2015-04-28 | 2016-11-07 | 서울대학교산학협력단 | Peroral apparatus for clinical specimen collection in gastrointestinal tract and method for the same |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3683890A (en) * | 1970-10-02 | 1972-08-15 | Charles B Beal | Carrier system for delivery of an end of an elongated member to the upper gastrointestinal tract |
US7449001B2 (en) * | 2001-05-17 | 2008-11-11 | Fargklamman Ab | Sampling device and method for obtaining samples of internal body substances and method for producing a sampling device |
ITPS20010019A1 (en) * | 2001-06-26 | 2002-12-26 | Muretto Pietro Aurelio Gaetano | ENDOGASTRIC CAPSULE |
GB0521521D0 (en) * | 2005-10-21 | 2005-11-30 | Medical Res Council | Diagnostic methods and kits |
US10292687B2 (en) * | 2014-08-15 | 2019-05-21 | Covidien Lp | Designs and methods to facilitate swallowing of a tethered cell collection device |
CN107532124B (en) * | 2015-03-27 | 2022-08-09 | 精密科学公司 | Detection of esophageal disorders |
WO2018144562A1 (en) * | 2017-01-31 | 2018-08-09 | University Of Kansas | Imaging and collection device and related systems and methods |
-
2021
- 2021-04-16 US US17/996,032 patent/US20230190243A1/en active Pending
- 2021-04-16 JP JP2022562444A patent/JP2023522629A/en active Pending
- 2021-04-16 CN CN202180032612.7A patent/CN115605138A/en active Pending
- 2021-04-16 US US17/233,199 patent/US20220071605A1/en active Pending
- 2021-04-16 EP EP21788930.2A patent/EP4135592A4/en active Pending
- 2021-04-16 CA CA3174354A patent/CA3174354A1/en active Pending
- 2021-04-16 KR KR1020227038078A patent/KR20230026300A/en active Search and Examination
- 2021-04-16 AU AU2021257479A patent/AU2021257479A1/en active Pending
- 2021-04-16 WO PCT/US2021/027770 patent/WO2021212031A1/en unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4735214A (en) * | 1986-09-05 | 1988-04-05 | Berman Irwin R | Gastrointestinal diagnostic capsule and method of use |
WO2011058316A1 (en) * | 2009-11-13 | 2011-05-19 | Medical Research Council | Cell sampling device |
US20130296738A1 (en) * | 2012-05-04 | 2013-11-07 | Given Imaging Ltd. | Device and method for in vivo cytology acquisition |
US20160081671A1 (en) * | 2014-09-18 | 2016-03-24 | Covidien Lp | Use of expansion-force elements in a compressible cell collection device |
KR20160128136A (en) * | 2015-04-28 | 2016-11-07 | 서울대학교산학협력단 | Peroral apparatus for clinical specimen collection in gastrointestinal tract and method for the same |
Non-Patent Citations (2)
Title |
---|
IQBAL UMAIRA , SIDDIQUE OSAMAB,, OVALLE ANAISB , ANWAR HAFSAD , MOSS, STEVEN F: "Safety and efficacy of a minimally invasive cell sampling device (‘Cytosponge’) in the diagnosis of esophageal pathology: a systematic review", EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, vol. 30, no. 11, 1 November 2018 (2018-11-01), pages 1261 - 1269, XP009539648, DOI: 10.1097/MEG.0000000000001210 * |
See also references of EP4135592A4 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11987847B2 (en) | 2014-03-31 | 2024-05-21 | Mayo Foundation For Medical Education And Research | Detecting colorectal neoplasm |
WO2023224945A1 (en) * | 2022-05-16 | 2023-11-23 | Pavmed, Inc. | Device for collecting a biological sample |
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US20230190243A1 (en) | 2023-06-22 |
EP4135592A4 (en) | 2024-04-17 |
EP4135592A1 (en) | 2023-02-22 |
KR20230026300A (en) | 2023-02-24 |
CA3174354A1 (en) | 2021-10-21 |
CN115605138A (en) | 2023-01-13 |
JP2023522629A (en) | 2023-05-31 |
AU2021257479A1 (en) | 2022-11-10 |
US20220071605A1 (en) | 2022-03-10 |
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