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Microelectromechanical devices useful for manipulating cells or embryos, kits thereof, methods of making same, and methods of use thereof

a micro-electromechanical and embryonic technology, applied in the field of micro-electromechanical systems (mems) devices for the manipulation of cells or embryos, can solve the problems of insufficient optimization, poor viability of cultured oocytes and embryos, and the enormity of the demand placed on technical staff by these procedures, so as to facilitate the identification of an individual oocyte, facilitate the identification of a single oocyte, and facilitate the effect of cell manipulation speed and

Inactive Publication Date: 2009-01-29
MATHEWS SHEPHERD MCKAY & BRUNEAU P A
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0023]The rigors of the physical manipulation of these cells during assisted reproduction procedures as well as the sheer enormity of the demand that these procedures place on technical staff represents two of the main reasons for failure. Any improvements in terms of efficiencies to these procedures which result in higher rates of success as well as increased capacity for processing is of great value.
[0024]Methodologies for the tracking of oocytes and embryos during isolation and manipulation for purposes such as animal husbandry, embryo tagging, and tracking of manipulated or treated oocytes over time and through space are rudimentary at present. Current protocols utilize the segregation of oocytes and embryos into individual wells or drops of culture medium entrapped under inert oil layers. The viability of cultured oocytes and embryos is enhanced by the co-culture of several oocytes or embryos within a relatively small volume. A device which would facilitate the identification of an individual oocyte or embryo distinctly from other oocytes or embryos would allow the co-culture of many differently treated or coded oocytes or embryos in one volume of media. Further, the ability to permanently label a particular oocyte or embryo in such a way as to allow coding of the treatment of each oocyte or embryo into the label is desirable.
[0025]It is an object of the invention to provide MEMS devices, kits, and methods of uses thereof, to enable rapid and easy manipulation of cells or groups of cells including but not limited to culture cells, oocytes, embryos, or sperm. More specifically, the present invention allows for an automated method of manipulating cells which does not rely heavily upon the ability of the person performing the manipulation. Further, the present invention allows for the manipulation of many cells simultaneously.
[0031]5. cytoplasmic transfer for the transfer of cytoplasmic material from one cell to another to reduce infertility of oocytes or embryos;

Problems solved by technology

At present the outcome of these procedures, being technically demanding and relatively novel and as such, not optimized, is very poor.
The rigors of the physical manipulation of these cells during the generation of transgenic animals, intracytoplasmic sperm injection, assisted hatching, enucleation, nuclear transfers and cytoplasmic transfer as well as the sheer enormity of the demand that these procedures place on technical staff represents two of the main reasons for failure.

Method used

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  • Microelectromechanical devices useful for manipulating cells or embryos, kits thereof, methods of making same, and methods of use thereof
  • Microelectromechanical devices useful for manipulating cells or embryos, kits thereof, methods of making same, and methods of use thereof
  • Microelectromechanical devices useful for manipulating cells or embryos, kits thereof, methods of making same, and methods of use thereof

Examples

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examples

[0698]The following protocols and experimental methods and materials are employed in the Examples that follow.

Superovulation

[0699]Mice (i.e., RB Swiss, (CBA*C57BL6 / J)fl) are given 5 i.u. / ml Pregnant Mares Serum Gonadotrophin (PMSG) interperitoneally (i.p.). At 46 to 48 hours post injection a second injection is i.p. administered providing 5 i.u. / ml Human Chorionic Gonadotrophin (hCG) in Phosphate Buffered Saline (PBS). If mating is desired, females are placed with males immediately.

Blastocyst Flush

[0700]The uterus is removed from 3.5 day pregnant mice and placed into sterile PBS. Using a sterile fine forceps the mesometrium is trimmed and the ovaries, oviducts, the utero-tubal junction, and the cervical bifurcation are dissected from both of the uterine horns. The uterine horn is flushed using a syringe of DMEM (Dulbecco's Modification of Eagle's Medium (Mod.) 1× (DMEM) with L-Glutamine, 4.5 g / L Glucose and Sodium Pyruvate; Fisher Scientific cat. # MT10013CM) with HEPES with a blunt...

example

The In Vitro Culture Device Operation of In Vitro Culture Device

[0745]After having been placed in an environmental controlling instrument of the present invention, the single layer or multi-layer in vitro culture device is loaded with fluids (i.e., culture media), any bubbles being purged by gentle pressure being applied to the system through the loading / removal compartments or through the input and output enclosed channels. Oocytes or embryos, having been attached to labelable zona anchor MEMS devices that are attractive to the movement tracks of the in vitro culture device, are added to the loading compartment (i.e., by mouth pipette, by robotic means, by other cell handling means). The environmental controlling instrument CPU is provided with the desired culture conditions, time, and amendment parameters. The environmental controlling instrument CPU actuates the travel of the cells on the movement tracks through out the single or multi-layer in vitro culture device, provides cult...

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Abstract

The present invention relates generally to microelectromechanical systems (MEMS) devices for the manipulation of cells or groups of cells, such as oocytes, embryos, and sperm. In particular, the present invention relates to Cell Labeling MEMS devices (2F), Microinjection MEMS devices, IntraCytoplasmic Sperm Injection (“ICSI”) MEMS devices, Zona Coring MEMS devices, Enucleation MEMS devices, Enucleation / Nuclear Transfer MEMS devices, and Cytoplasmic Transfer MEMS devices. The present invention also relates to kits containing the MEMS devices of the present invention.

Description

[0001]The present application is a continuation-in-part application of U.S. Provisional Application No. 60 / 130,802 filed Apr. 23, 1999; U.S. Provisional Application No. 60 / 147,802 filed Aug. 9, 1999, and U.S. Provisional Application No. 60 / 149,269 filed Aug. 17, 1999. The disclosures of the above-identified applications are incorporated herein by reference in their entirety.FIELD OF THE INVENTION[0002]The present invention relates generally to microelectromechanical systems (MEMS) devices for the manipulation of cells or groups of cells, such as oocytes, embryos, and sperm. In particular, the present invention relates to Cell Labeling MEMS devices, Labelable Zona Anchor MEMS devices, Microinjection MEMS devices, IntraCytoplasmic Sperm Injection (“ICSI”) MEMS devices, Zona Coring MEMS devices, Enucleation MEMS devices, Enucleation / Nuclear Transfer MEMS devices, and cytoplasmic transfer MEMS devices. The present invention also relates to kits containing the MEMS devices of the present...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C12N15/00C23F1/00C12M1/00H01L21/02B23P15/00B44C1/22C12MC12M1/22C12M1/34C12M3/00C12N5/00C12N5/08C12N11/08C12N11/14D04B9/00D04B9/20
CPCB01L3/5027C12M35/04C12M21/06
Inventor PALACIOS-BOYCE, MONICA
Owner MATHEWS SHEPHERD MCKAY & BRUNEAU P A
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