WO2009059363A1 - Procédé et appareil pour la récupération de matière biologique en suspension - Google Patents

Procédé et appareil pour la récupération de matière biologique en suspension Download PDF

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Publication number
WO2009059363A1
WO2009059363A1 PCT/AU2008/001643 AU2008001643W WO2009059363A1 WO 2009059363 A1 WO2009059363 A1 WO 2009059363A1 AU 2008001643 W AU2008001643 W AU 2008001643W WO 2009059363 A1 WO2009059363 A1 WO 2009059363A1
Authority
WO
WIPO (PCT)
Prior art keywords
suspension solution
biological material
container
filter
filter means
Prior art date
Application number
PCT/AU2008/001643
Other languages
English (en)
Inventor
Lawrence William Hirst
Original Assignee
Lawrence William Hirst
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from AU2007906048A external-priority patent/AU2007906048A0/en
Application filed by Lawrence William Hirst filed Critical Lawrence William Hirst
Priority to CA2704846A priority Critical patent/CA2704846A1/fr
Priority to NZ585963A priority patent/NZ585963A/en
Publication of WO2009059363A1 publication Critical patent/WO2009059363A1/fr
Priority to US12/774,439 priority patent/US20100275650A1/en
Priority to AU2010202366A priority patent/AU2010202366B2/en

Links

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00—Sampling; Preparing specimens for investigation
    • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • G01N1/40—Concentrating samples
    • G01N1/4077—Concentrating samples by other techniques involving separation of suspended solids
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N1/00—Preservation of bodies of humans or animals, or parts thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/71—Suction drainage systems
    • A61M1/79—Filters for solid matter
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00—General characteristics of the apparatus
    • A61M2205/12—General characteristics of the apparatus with interchangeable cassettes forming partially or totally the fluid circuit
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2210/00—Anatomical parts of the body
    • A61M2210/06—Head
    • A61M2210/0612—Eyes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/508—Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00—Sampling; Preparing specimens for investigation
    • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • G01N1/40—Concentrating samples
    • G01N1/4077—Concentrating samples by other techniques involving separation of suspended solids
    • G01N2001/4088—Concentrating samples by other techniques involving separation of suspended solids filtration
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00—Metal working
    • Y10T29/49—Method of mechanical manufacture
    • Y10T29/49588—Jewelry or locket making

Definitions

  • the present invention relates generally to a method of providing a promotional avenue for medical clinics by way of producing a personalized keepsake for their clients.
  • keepsake items often embellish the item with names, dates or other information, or provide a surrounding such as a jewellery piece to contain or show off the item.
  • provision of a keepsake of this kind may be considered a goodwill or promotional tool for a service offering.
  • a dental practitioner or other provider may actively promote the encapsulation or presentation of a first tooth as a special service, in order to attract business or simply differenciate the services of that outlet by developing goodwill with the client.
  • Cataract surgery is commonly conducted via a procedure call phacoemulsification, whereby the patient's clouded lens is broken up and removed via a tube through a small incision in the eye.
  • the lens material is broken into small fragments by ultrasonic pulses and is ejected via suction into a containment cassette located within the operating machine.
  • the cassettes accumulate the lens material and the fluid media used to irrigate the procedure, and the individual patient cassette is normally removed and discarded following the procedure.
  • the phacoemulsification method has become the standard procedure for routine cataract surgery, and the cassette-type collection of fluid and lens material is common, though the exact configuration of the equipment and performance varies. Importantly, the ability remains, by way of removing a connection or other port, to access the material accumulated within the cassette for most, if not all types of phacoemulsification systems.
  • the present invention is directed to a method and apparatus for recovery of suspended biological material, which may at least partially overcome at least one of the abovementioned disadvantages or provide the consumer with a useful or commercial choice.
  • the present invention in one form, resides broadly in an apparatus for recovery of suspended biological material from a solution, the apparatus including a suspension solution container to temporarily hold the suspension solution, extraction means to apply extractive force to the container to extract the suspension solution temporarily held therein and the filter means sized to separate the suspended biological material from the suspension solution.
  • the invention resides in a phacoemulsification separation apparatus for recovery of suspended biological material from a solution formed during phacoemulsification, the apparatus including a suspension solution container to temporarily hold the solution, extraction means to apply extractive force to the container to extract the solution temporarily held therein and the filter means sized to separate the suspended biological material from the solution.
  • the invention resides in a method for recovery of suspended biological material from a solution the method including the steps of a temporarily collecting the solution in a solution container, applying extractive force to the container to extract the solution temporarily held therein and filtering the solution through filter means sized to separate the suspended biological material from the solution.
  • the invention resides in a method for creation of a keepsake or memento from biological material recovered following removal during a medical procedure, the method including the steps of collecting the biological material in a solution, temporarily collecting the solution in a solution container, applying extractive force to the container to extract the solution temporarily held therein and filtering the solution through filter means sized to separate the suspended biological material as a filtrate from the solution, removing the filtrate from the filter means into a container, filling of the container with a measured amount of stabilizer fluid, and capping the container to seal the container.
  • the invention relates to an apparatus for recovery of a suspended biological material from a solution.
  • a phacoemulsification procedure results in a collection of the biological material in an irrigation fluid.
  • the fluid and biological material normally collected in a container, commonly known in the art as a cassette.
  • the cassette is normally quite small, approximately the size of B5 stationery and is normally manufactured of a transparent plastic.
  • the cassette has at least one opening in order to accept the collected material and irrigation fluid.
  • the cassette will preferably be removed to a controlled environment away from the patient, for the collection of the biological material.
  • the cassette will preferably be considered as a primary collection vessel.
  • the present invention includes extraction means.
  • the extraction means is normally provided as a plurality of components and connected to perform the function.
  • connection means will normally be provided to connect to the opening of the cassette through which the contents of the cassette can be removed. Normally, substantially all of the contents of the cassette are removed and the separation of the biological material from the remainder of the solution will be undertaken coincident with the removal from the cassette. Further, the biological material will normally be retained and the irrigation fluid will normally be wasted.
  • the connection means preferably includes a shaped connector.
  • the shaped connector will normally be provided in the form of a tapered stopper.
  • a particularly preferred form of the tapered stopper is a frustoconical member with a central bore extending through the stopper from a larger circular face to a smaller circular face.
  • the stopper will be manufactured from a resilient material in order to adapt the stopper to mate with openings of different dimension. The resilient material also typically creates an air/water proof seal between the stopper and the cassette opening.
  • the degree to which the stopper is tapered and the resilience of the material used may vary.
  • the stopper will provide a simple and quick connection which is air/fluid tight and typically will not require special training in order to connect the stopper to the cassette.
  • the extraction means also preferably includes a fluid conveyance tube.
  • the fluid conveyance tube is preferably attached to the stopper, normally by insertion of at least a portion of the tube into the bore of the stopper.
  • the fluid conveyance tube is also preferably associated with filter means.
  • the filter means is provided in an in-line configuration such that fluid extracted from the cassette must pass through the filter means.
  • a preferred form of filter means is provided in a two-part housing including an upper and lower housing portion with the upper and lower housing portion designated with reference to the flow direction and the lower housing portion being downstream of the upper housing portion.
  • each portion of the two-part housing is connectable to the other portion to allow separation.
  • a threaded connection is preferred but is not the only type of connection which may be used.
  • Grip means may be provided on one or both of the housing portions, preferably both.
  • Each portion of the filter housing will typically be manufactured from a plastic material, preferably a transparent plastic to enable a user to monitor the filtration process.
  • the filter housing will typically include a filter screen or similar.
  • the filter screen is preferably convex to the flow direction. Normally, the filter screen will be attached peripherally to the lower portion of the filter housing. It is particularly preferred that an upper surface of the filter screen be easily accessible with minimal exposed edges, corners or recesses in which material can be caught during removal which may limit the amount of collected biological material.
  • the openings in the filter screen will typically sized to separate the biological material particles large enough to be visible to the naked eye.
  • the phacoemulsification procedure results in material similar in size to fine sand and with a density which is suitably low to enable gentle agitation of the cassette during the removal process to produce a relatively homogenous mixture of the biological particles and irrigation fluid.
  • the filter screen is a stainless steel screen having openings of approximately 0 .4 mm in diameter.
  • the filter will normally be connected in line with a fluid conveyance tube leading from the stopper to the upper portion and a second fluid conveyance tube leading from the lower portion of the filter for the waste irrigation fluid.
  • a waste outlet Located downstream of the filter is preferably a waste outlet and also a means to apply extractive force to the cassette and its contents.
  • the extractive force is normally applied through the use or application of a vacuum to the cassette although the cassette may alternatively be emptied by gravity draining for example or other similar process.
  • the preferred means for applying the vacuum is a syringe or similar, preferably of approximately 30 mL in capacity. Other means may be used alternatively such as a plumbed vacuum, Venturi or similar.
  • a common volume of the cassette used in the phacoemulsification procedure is between 50-200 mL and the irrigation liquid is normally a balanced salt solution.
  • an in-line check valve or non-return valve is included between the filter and the means for applying extractive force to enable multiple extractions to remove and expel waste irrigation fluid from the cassette.
  • the waste outlet is provided in the form of a waste tube connected downstream of the check valve or nonreturn valve but prior to the means for applying extractive force. Where a waste tube is provided, the free end of the waste tube may be weighted to ensure the directionality of the expelled stream.
  • An example of an appropriate instrument is a spatula, preferably shaped to enable manipulation of the collected material into a secondary collection vessel.
  • the preferred form of secondary collection vessel is typically jewellery or a wearable memento.
  • a particularly preferred form is that of a vial with a cap or the closure.
  • the vial is preferably a wearable vial such as a pendant, hearings, cufflinks or other. Whilst this embodiment relates to the collection of relatively small amounts of biological material, the method and apparatus of the present invention may be expanded to incorporate larger volumes of biological material into more substantial secondary collection vessels such as paper weights or other items.
  • a funnel or similar will normally be provided or used according to the method.
  • the funnel is normally located in all relative to an opening of the secondary collection vessel.
  • the cap or cover of the secondary collection vessel is preferably permanently attached to the vessel once the biological material (and any other material) has been inserted into the secondary collection vessel.
  • the means or method of fixing the cap to the vessel may be any suitable means including using an engineered tolerance closure or a suitable fast acting adhesive or bonding agent.
  • fluid will be added to the secondary collection vessel prior to sealing. Normally the fluid will stabilise the biological material and may also act to disperse the material within the vessel.
  • a preferred form of fluid is an approximately 70% alcohol solution which also has an added benefit of a low vaporisation temperature thereby reducing the amount of residue should any spillage or overflow occur.
  • the fluid may be added by any manner of application to the secondary collection vessel including from a bulk source or from a metered dose applicator such as a syringe, squirt bottle or the like.
  • the secondary collection vessel may be temporarily housed or arranged such that handling or correct orientation of the vessel is not required during the transfer of the material.
  • a handling fixture may be provided which may incorporate a broad base for stability and may be internally configured to align and retain a variety of forms of secondary collection vessel.
  • the secondary collection vessel will be retained in an upright position by the handling fixture by provision of a corresponding shaped opening in the handling fixture.
  • the handling fixture is preferably transparent is such that the secondary collection vessel (and other elements) are visible when located in the handling fixture.
  • a preferred configuration of includes a lower portion to at least temporarily hold the secondary collection vessel.
  • the lower portion also has a receiving opening and a shaped cavity internally configured to align and retain various forms of secondary collection vessel.
  • At least one upper portion is provided and also includes a shaped receiving opening.
  • the shaped opening in the at least one upper portion is internally configured to align and retain a cap for the secondary collection vessel.
  • there will be a pair of interchangeable upper portions a first upper portion used in conjunction with the lower portion in order to insert material and fluid into the secondary collection vessel and a second upper portion used to cap the secondary collection vessel once the first upper portion has been removed from the lower portion.
  • the upper and lower portions may have corresponding shaped means in order to positively align the upper and lower portions during use.
  • the most preferred process following the separation of the biological material includes the steps of: • Loading of the secondary collection vessel in the form of a pendant body to the handling fixture;
  • the elements described above may be supplied to the clinic facility in kit form, such that re-usable and consumable components may be organized and waste minimized. It is anticipated that the extraction and filter components, plus the orientation fixtures suited to the various jewellery formats are re-usable items, requiring only a general flush and clean between applications or periodically, and the jewelry components, such as a variety or pendant bodies and caps may be supplied in bulk form, for selection according to patient requirements. Enclosure elements (jewelry pieces or otherwise) may be designed to accommodate a modular assembly system, allowing customization of the final presented product. Various accessories for the jewelry item may also be provided, such as necklaces, cufflink findings, clasps, pins or strings.
  • the product may be provided with a marking or otherwise applied graphic or labeling element which identifies the clinic or practitioner responsible for the procedure and supply.
  • This marking may be applied at component production level, such as embossing on plastic parts, or by a post-applied print or label affixed following assembly of the product.
  • the processing of the lens material, from reclamation from the phacoemulsification cassette to presentation to the patient should be a very rapid process, requiring minimal training and dexterity of the operator. Given that the patient is almost immediately mobile and able to leave the surgery within 15 minutes to half and hour of surgery, the process should preferably allow the keepsake to leave with the patient and should also not overly consume the time of clinic staff.
  • Alternate methods of lens or other material encapsulation may include incorporation into a rapid-curing resin or other means of capturing and sealing the material.
  • the capture of the material may be designed to maximize the visual impact of the keepsake, by addition of sparkling features or materials that impart flow, motion or other eye-catching or novel features.
  • a high-end application of the concept may include a longer or more involved method of material processing, such as resin impregnation or casting, such that the finished product is not provided immediately and the finished piece may be much more complex, functional or visually spectacular.
  • Provision of this system either as an immediate or follow-up patient service, must be considered within the context of a clinic marketing strategy and must consider the implications of privacy, patient consent and health and safety aspects of the use of human biological material.
  • Figure 1 illustrates a preferred embodiment of an extraction kit according to the present invention.
  • FIG 2 is a perspective illustration of a preferred filter used in the extraction kit illustrated in Figure 1 opened to show the filter screen.
  • Figure 3 is a perspective view of the filter screen as illustrated in Figure 2 showing the biological material collected on the filter screen.
  • Figure 4 illustrates a preferred step in the method of collection of the biological material namely using a spatula to remove the material from the filter screen.
  • Figure 5 is a perspective view of two preferred embodiments of vials and respective caps which may be used in the present invention.
  • Figure 6 is a perspective view of the vials and caps of Figure 5 in a capped condition.
  • Figure 7 is a perspective view from the front of a preferred embodiment of handling fixture used according to the present invention.
  • Figure 8 is a perspective view of the handling fixture illustrated in Figure 7 with a funnel in position.
  • Figure 9 is a perspective view of the handling fixture illustrated in Figures 7 and 8 showing an upper portion of the handling fixture of the preferred embodiment used to close the vial.
  • a method and apparatus for creation of a keepsake or memento from biological material recovered following removal during a medical procedure, particularly phacoemulsification, is provided.
  • the phacoemulsification method has become the standard procedure for routine cataract surgery, and the collection of fluid and lens material removed during the procedure into a collection cassette 10 is common, though the exact configuration of the equipment and performance varies. Importantly, the ability remains, by way of removing a connection or other port, to access the material accumulated within the cassette 10 for most, if not all types of phacoemulsification systems. Once the cassette 10 is accessible, the material within (including the irrigation fluid) may be withdrawn in order to selectively retain the lens material. In the preferred embodiment illustrated in Figure 1, this access includes the use of a tapered, resilient stopper 11 which provides a sealed connection to an extraction tube 12 via the appropriate port or opening in the cassette 10. The taper and resilience of the stopper 11 should accommodate various port sizes and or shapes, depending on the phacoemulsification system.
  • the extracted fluid is entrained via the tube 12 through a filtration component 13 by way of a vacuum or gravity draining.
  • suction to ensure rapid extraction is applied by a large syringe 14.
  • a common volume of material is 50 to 20OmL of balanced salt solution, thus, the preferred embodiment includes vacuum extraction by way of a large syringe (3OmL) and a suitable check valve 15 enabling multiple pump strokes to alternately suck and expel waste irrigation fluid.
  • a waste tube 16 is provided with a weight 17 to ensure the waste stream is directed to an appropriate drain.
  • the preferred filter 13 is provided in two parts with an upper 18 and lower 19 portion (defined by their relative position in the flow path with the lower portion downstream), which are formed or otherwise labeled to indicate the flow direction therein.
  • the portions are easily separable by a user by means of a knurled or grippable edges, in order to access the collected lens material without loss or contamination.
  • the filter screen 20 located in the filter 13 is sufficiently coarse to only collect particles large enough to be easily visible. It is common for lens particles 21 delivered by phacoemulsification to be sized similarly to fine sand, with a density suitably low to enable the cassette 10 to be agitated gently to produce a relatively homogenous mixture of particles 21 and suspension or irrigation fluid.
  • the illustrated preferred embodiment incorporating a stainless steel filter screen 20 has apertures approximately 0.4mm diameter, which captures a suitable amount of material for processing.
  • the lens particles/material 21 accumulates on the filter screen 20 within the filter 13.
  • opening of the filter 13 exposes the filter screen 20 such that the lens particles/material 21 which tends to cling to the screen 20 face can be scraped away for collection as illustrated in Figure 4.
  • the filter screen 20 is exposed such that the entire face is accessible and no edges or corners limit the amount of collected material that may be scraped away.
  • a spatula 22 or other suitable tool may be provided to scrape the filter screen 20.
  • This tool may also be shaped to enable manipulation of the lens material (which retains the consistency of damp brown sugar) into a secondary collection vessel 23.
  • the secondary collection vessel 23 of the illustrated embodiment takes the form of a piece of jewellery or wearable memento.
  • the lens particles/material 21 are loaded into the secondary container
  • FIG. 23 in a manner that is hygienic and safe for the operator.
  • the spatula 22 is configured to be received by a small funnel 24 located partially in the open neck of the secondary collection vessel 23, such that no material is lost in the process.
  • Figures 5 and 6 illustrate preferred embodiments of the secondary collection vessel 23 in the form of jewellery pieces which as illustrated, take the form of a vial 25 with a cap 26, which, when capped, can be worn or carried as a pendant.
  • the jewellery pieces, particularly the vials 25 can be housed or arranged such that handling or correct orientation of the small parts is not required.
  • FIG. 7 A preferred configuration of equipment to achieve this is illustrated in Figure 7 in which the vial 25 is retained in an upright position by a handling fixture.
  • the handling fixture illustrated includes an upper 27 and a lower 28 portion, with the lower portion 28 incorporating a broad base 29 for stability.
  • the lower portion 28 also has a receiving opening 30 and shaped cavity (not shown) for a vial 25, internally configured to align and retain various vial forms.
  • the upper portion 27 also includes a shaped receiving opening 31.
  • the shaped opening 31 in the upper portion 27 is internally configured to align and retain a cap 26 for the vial 25.
  • the handling fixture portions 27, 28 of the illustrated embodiment are transparent, such that the vial and other elements are visible.
  • a fluid to both biologically stabilize and allow the lens particles/material 21 to disperse and drift in the vial 25 is added.
  • a suitable fluid for both these actions is
  • the handling fixture may also allow orientation of the cap 26, such that the filling and correct closure process require no contact between reclaimed lens particles/material 21 and the clinic operator.
  • Fixation of the cap 26 to the vial 25 may be by an engineered tolerance closure, or a suitable fast-acting adhesive or bonding agent.
  • the preferred process therefore includes the steps of:

Abstract

L'invention porte sur un appareil pour la récupération de matière biologique en suspension à partir d'une solution contenant une suspension. L'appareil comprend un conteneur de solution contenant une suspension pour contenir de façon temporaire la solution contenant une suspension, des moyens d'extraction pour appliquer une force d'extraction au conteneur afin d'extraire la solution contenant une suspension temporairement contenue dans celui-ci et les moyens de filtration dimensionnés pour séparer la matière biologique en suspension à partir de la solution contenant une suspension.
PCT/AU2008/001643 2007-11-05 2008-11-05 Procédé et appareil pour la récupération de matière biologique en suspension WO2009059363A1 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
CA2704846A CA2704846A1 (fr) 2007-11-05 2008-11-05 Procede et appareil pour la recuperation de matiere biologique en suspension
NZ585963A NZ585963A (en) 2007-11-05 2008-11-05 A method and apparatus for recovery of suspended biological material
US12/774,439 US20100275650A1 (en) 2007-11-05 2010-05-05 Method and Apparatus for Recovery of Suspended Biological Material
AU2010202366A AU2010202366B2 (en) 2007-11-05 2010-06-04 A Method And Apparatus For Recovery Of Suspended Biological Material

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AU2007906048A AU2007906048A0 (en) 2007-11-05 A Method And Apparatus For Recovery Of Suspended Biological Material
AU2007906048 2007-11-05

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US12/774,439 Continuation-In-Part US20100275650A1 (en) 2007-11-05 2010-05-05 Method and Apparatus for Recovery of Suspended Biological Material
AU2010202366A Division AU2010202366B2 (en) 2007-11-05 2010-06-04 A Method And Apparatus For Recovery Of Suspended Biological Material

Publications (1)

Publication Number Publication Date
WO2009059363A1 true WO2009059363A1 (fr) 2009-05-14

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Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/AU2008/001643 WO2009059363A1 (fr) 2007-11-05 2008-11-05 Procédé et appareil pour la récupération de matière biologique en suspension

Country Status (4)

Country Link
US (1) US20100275650A1 (fr)
CA (1) CA2704846A1 (fr)
NZ (1) NZ585963A (fr)
WO (1) WO2009059363A1 (fr)

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CN113376001A (zh) * 2021-07-12 2021-09-10 国家海洋局北海环境监测中心 一种浮游植物样品杂质去除装置及其使用方法

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DE102011118929A1 (de) * 2011-11-21 2013-05-23 Kautex Textron Gmbh & Co. Kg Nebenflüssigkeitsbehälter für ein Kfz
CN113539007A (zh) * 2021-09-07 2021-10-22 中国人民解放军陆军特色医学中心 一种白内障教学用超声乳化白内障吸除训练器

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US20040038425A1 (en) * 2002-08-26 2004-02-26 Ferguson Gary William Method of depositing material and density gradients of material from sample suspensions and filter devices for same
US20040069714A1 (en) * 2002-10-11 2004-04-15 Ferguson Gary William Filter apparatus and methods to capture a desired amount of material from a sample suspension for monolayer deposition, analysis or other uses

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Publication number Priority date Publication date Assignee Title
US3731806A (en) * 1971-03-01 1973-05-08 Pelam Inc Specimen analysis device
US6599271B1 (en) * 1999-04-13 2003-07-29 Syntec, Inc. Ophthalmic flow converter
US20040038425A1 (en) * 2002-08-26 2004-02-26 Ferguson Gary William Method of depositing material and density gradients of material from sample suspensions and filter devices for same
US20040069714A1 (en) * 2002-10-11 2004-04-15 Ferguson Gary William Filter apparatus and methods to capture a desired amount of material from a sample suspension for monolayer deposition, analysis or other uses

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113376001A (zh) * 2021-07-12 2021-09-10 国家海洋局北海环境监测中心 一种浮游植物样品杂质去除装置及其使用方法

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Publication number Publication date
NZ585963A (en) 2012-05-25
CA2704846A1 (fr) 2009-05-14
US20100275650A1 (en) 2010-11-04

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