US 11,421,194 B2Granted

Pumpless platform for high-throughput dynamic multicellular culture and chemosensitivity evaluation

AssigneesThe Trustees of the Stevens Institute of Technology, Hackensack Meridian Health Center for Discovery and Innovation

InventorsWoo Lee, Zhehuan Chen, Jenny Zilberberg

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Abstract

The described invention provides an ex vivo dynamic multiple myeloma cancer niche contained in a pumpless perfusion culture device. The dynamic multiple myeloma cancer niche includes (a) a three-dimensional tissue construct containing a dynamic ex vivo bone marrow niche, which contains a mineralized bone-like tissue containing viable osteoblasts self-organized into cohesive multiple cell layers and an extracellular matrix secreted by the viable adherent osteoblasts; and a microenvironment dynamically perfused by nutrients and dissolved gas molecules; and (b) human myeloma cells seeded from a biospecimen composition comprising mononuclear cells and the multiple myeloma cells. The human myeloma cells are in contact with osteoblasts of the bone marrow niche, and the viability of the human myeloma cells is maintained by the multiple myeloma cancer niche.

Claims25

Dependent claims

An in vitro multiwell plate-based pumpless perfusion culture device comprising, from top to bottom:

(i) a bottomless multi-well plate comprising a plurality of bottomless wells, wherein four adjacent sequential wells comprise a culture chamber;
(ii) a first micropatterned pressure-sensitive adhesive (PSA) layer attached to a bottom surface of the culture chamber;
(iii) a polymer layer comprising four holes vertically aligned with the four adjacent sequential wells of the culture chamber, the polymer layer being attached to a bottom surface of the first micropatterned PSA layer;
(iv) a second micropatterned PSA layer attached to a bottom surface of the polymer layer;
(v) a third micropatterned PSA layer that connects the four adjacent sequential wells, wherein the third micropatterned PSA layer is attached to a bottom surface of the second micropatterned PSA layer;
(vi) a transparent, optical grade glass layer attached to the bottom surface of the third micropatterned PSA layer that forms a bottom surface for the plurality of wells and that seals the multi-well plate-based pumpless perfusion culture device;
(vii) a rocking platform for holding the multi-well plate, characterized by rocking speed and an adjustable rocking/tilt angle;
wherein the four adjacent sequential wells that comprise the culture chamber comprise an inlet well, a cell seeding port well, a cell chamber well, and an outlet well;
wherein the first micropatterned PSA layer is effective to maintain stable liquid droplets and to prevent medium evaporation by covering the inlet well, cell seeding port well, and outlet well of the first polymer layer;
wherein the inlet and outlet wells are configured as reservoirs for culture medium and to generate hydrostatic pressure differential between the wells;
wherein the cell seeding port well is adapted to receive a biological sample of cells;
wherein an intermediate layer is disposed between the second micropatterned PSA layer and the third micropatterned PSA layer, the intermediate layer including a first polymer membrane effective to cover the inlet well and to control the flow rate of medium in the culture chamber, and a second polymer membrane different from the first polymer membrane, disposed adjacent to the first polymer membrane and effective to cover the cell chamber well and to hold the medium within the culture chamber during cell seeding and culture;
and
wherein the second micropatterned PSA layer is effective to adhere and seal the first and second polymer membranes in the culture chamber.

11 more elements

An ex vivo multiple myeloma cancer niche contained in a device, in which flow of minute amounts of liquids or dissolved gas molecules, is controlled by microfluidics (a microfluidic device) comprising:

(a) an ex vivo bone marrow microenvironment perfused by nutrients and dissolved gas molecules (a bone marrow niche) comprising viable osteoblasts seeded on a surface of the microfluidic device and cultured to form 3D nodular structures that comprise a 3D bone-like tissue,
the 3D bone-like tissue being characterized by an extracellular matrix secreted by the viable osteoblasts;
and
(b) a multiple myeloma tumor biospecimen comprising viable human multiple myeloma cells;
the microfluidic device comprising, from top to bottom:
(i) a bottomless multi-well plate comprising a plurality of bottomless wells, wherein four adjacent sequential wells comprise a culture chamber;
(ii) a first micropatterned pressure-sensitive adhesive (PSA) layer attached to a bottom surface of the culture chamber;
(iii) a polymer layer comprising four holes vertically aligned with the four adjacent sequential wells of the culture chamber, the polymer layer being attached to a bottom surface of the first micropatterned PSA layer;
(iv) a second micropatterned PSA layer attached to a bottom surface of the polymer layer;
(v) a third micropatterned PSA layer that connects the four adjacent sequential wells, wherein the third micropatterned PSA layer is attached to a bottom surface of the second micropatterned PSA layer;
(vi) a transparent, optical grade glass layer attached to the bottom surface of the third micropatterned PSA layer that forms a bottom surface for the plurality of wells and that seals the multi-well plate-based pumpless perfusion culture device;
(vii) a rocking platform for holding the multi-well plate, characterized by rocking speed and an adjustable rocking/tilt angle;
wherein the four adjacent sequential wells that comprise the culture chamber comprise an inlet well, a cell seeding port well, a cell chamber well, and an outlet well;
wherein the first micropatterned PSA layer is effective to maintain stable liquid droplets and to prevent medium evaporation by covering the inlet well, cell seeding port well, and outlet well of the first polymer layer;
wherein the inlet and outlet wells are configured as reservoirs for culture medium and to generate hydrostatic pressure differential between the wells;
wherein the cell seeding port well is adapted to receive a biological sample of cells;
wherein an intermediate layer is disposed between the second micropatterned PSA layer and the third micropatterned PSA layer, the intermediate layer including a first polymer membrane effective to cover the inlet well and to control the flow rate of medium in the culture chamber, and a second polymer membrane different from the first polymer membrane, disposed adjacent to the first polymer membrane and effective to cover the cell chamber well and to hold the medium within the culture chamber during cell seeding and culture;
and
wherein the second micropatterned PSA layer is effective to adhere and seal the first and second polymer membranes in the culture chamber;
wherein the microfluidic device is effective to control flow of minute amounts of the liquids, nutrients and dissolved gas molecules in the multiple myeloma cancer niche;
wherein the ex vivo multiple myeloma cancer niche is responsive to changing conditions of perfusion of the ex vivo multiple myeloma cancer niche by the minute amounts of liquids, nutrients and dissolved gas molecules in the microfluidic device;
and
wherein formation of an ex vivo multiple myeloma microenvironment in the microfluidic device is effective to recapitulate spatial and temporal characteristics of a multiple myeloma cancer niche in vivo and to maintain viability of the multiple myeloma cells in the multiple myeloma cancer niche in the microfluidic device ex vivo.

20 more elements

A method for preparing an ex vivo multiple myeloma cancer niche contained in a device in which flow of minute amounts of liquids or dissolved gas molecules is controlled by microfluidics (a microfluidic device), the microfluidic device comprising, from top to bottom:

(i) a bottomless multi-well plate comprising a plurality of bottomless wells, wherein four adjacent sequential wells comprise a culture chamber;
(ii) a first micropatterned pressure-sensitive adhesive (PSA) layer attached to a bottom surface of the culture chamber;
(iii) a polymer layer comprising four holes vertically aligned with the four adjacent sequential wells of the culture chamber, the polymer layer being attached to a bottom surface of the first micropatterned PSA layer;
(iv) a second micropatterned PSA layer attached to a bottom surface of the polymer layer;
(v) a third micropatterned PSA layer that connects the four adjacent sequential wells, wherein the third micropatterned PSA layer is attached to a bottom surface of the second micropatterned PSA layer;
(vi) a transparent, optical grade glass layer attached to the bottom surface of the third micropatterned PSA layer that forms a bottom surface for the plurality of wells and that seals the multi-well plate-based pumpless perfusion culture device;
(vii) a rocking platform for holding the multi-well plate, characterized by rocking speed and an adjustable rocking/tilt angle;
wherein the four adjacent sequential wells that comprise the culture chamber comprise an inlet well, a cell seeding port well, a cell chamber well, and an outlet well;
wherein the first micropatterned PSA layer is effective to maintain stable liquid droplets and to prevent medium evaporation by covering the inlet well, cell seeding port well, and outlet well of the first polymer layer;
wherein the inlet and outlet wells are configured as reservoirs for culture medium and to generate hydrostatic pressure differential between the wells;
wherein the cell seeding port well is adapted to receive a biological sample of cells;
wherein an intermediate layer is disposed between the second micropatterned PSA layer and the third micropatterned PSA layer, the intermediate layer including a first polymer membrane effective to cover the inlet well and to control the flow rate of medium in the culture chamber, and a second polymer membrane different from the first polymer membrane, disposed adjacent to the first polymer membrane and effective to cover the cell chamber well and to hold the medium within the culture chamber during cell seeding and culture;
and
wherein the second micropatterned PSA layer is effective to adhere and seal the first and second polymer membranes in the culture chamber;
the method comprising:
(a) constructing an ex vivo bone marrow microenvironment perfused by nutrients and dissolved gas molecules (a bone marrow niche) in the microfluidic device by:
(i) seeding a surface of the microfluidic device with viable osteoblasts;
and
(ii) culturing the cells to form 3D nodular structures that comprise a 3D bone-like tissue;
the 3D bone-like tissue being characterized by an extracellular matrix secreted by the viable adherent osteoblasts;
(b) preparing a multiple myeloma tumor biospecimen composition comprising viable human multiple myeloma cells from a subject and plasma autologous to the subject;
and
(c) seeding the ex vivo bone marrow microenvironment perfused by nutrients and dissolved gas molecules with the multiple myeloma tumor biospecimen, and forming an ex vivo microenvironment in the microfluidics device effective to recapitulate spatial and temporal characteristics of a multiple myeloma cancer niche in vivo and to maintain viability of the multiple myeloma cells in the multiple myeloma cancer niche in the microfluidics device ex vivo;
wherein the microfluidic device is effective to control flow of minute amounts of the liquids, nutrients and dissolved gas molecules in the multiple myeloma cancer niche;
wherein the ex vivo multiple myeloma cancer niche in the microfluidic device is responsive to changing conditions of perfusion of the ex vivo multiple myeloma cancer niche by the minute amounts of liquids, nutrients and dissolved gas molecules in the microfluidics device.

22 more elements

A method for assessing chemotherapeutic efficacy of a test chemotherapeutic agent on viable human multiple myeloma cells seeded in an ex vivo microenvironment effective to recapitulate spatial and temporal characteristics of a multiple myeloma cancer niche and to maintain viability of the myeloma cells (a multiple myeloma cancer niche) obtained from a subject comprising:

(a) preparing an in vitro microfluidic device comprising, from top to bottom:
(i) a bottomless multi-well plate comprising a plurality of bottomless wells, wherein four adjacent sequential wells comprise a culture chamber;
(ii) a first micropatterned pressure-sensitive adhesive (PSA) layer attached to a bottom surface of the culture chamber;
(iii) a polymer layer comprising four holes vertically aligned with the four adjacent sequential wells of the culture chamber, the polymer layer being attached to a bottom surface of the first micropatterned PSA layer;
(iv) a second micropatterned PSA layer attached to a bottom surface of the polymer layer;
(v) a third micropatterned PSA layer that connects the four adjacent sequential wells, wherein the third micropatterned PSA layer is attached to a bottom surface of the second micropatterned PSA layer;
(vi) a transparent, optical grade glass layer attached to the bottom surface of the third micropatterned PSA layer that forms a bottom surface for the plurality of wells and that seals the multi-well plate-based pumpless perfusion culture device;
(vii) a rocking platform for holding the multi-well plate, characterized by a rocking speed and an adjustable rocking/tilt angle;
wherein the four adjacent sequential wells that comprise the culture chamber comprise an inlet well, a cell seeding port well, a cell chamber well, and an outlet well;
wherein the first micropatterned PSA layer is effective to maintain stable liquid droplets and to prevent medium evaporation by covering the inlet well, cell seeding port well, and outlet well of the first polymer layer;
wherein the inlet and outlet wells are configured as reservoirs for culture medium and to generate hydrostatic pressure differential between the wells;
wherein the cell seeding port well is adapted to receive a biological sample of cells;
wherein an intermediate layer is disposed between the second micropatterned PSA layer and the third micropatterned PSA layer, the intermediate layer including a first polymer membrane effective to cover the inlet well and to control the flow rate of medium in the culture chamber, and a second polymer membrane different from the first polymer membrane, disposed adjacent to the first polymer membrane and effective to cover the cell chamber well and to hold the medium within the culture chamber during cell seeding and culture;
and
wherein the second micropatterned PSA layer is effective to adhere and seal the first and second polymer membranes in the culture chamber;
(b) constructing an ex vivo bone marrow microenvironment perfused by nutrients and dissolved gas molecules (a bone marrow niche) by
(1) seeding a surface of the culture chamber of the in vitro microfluidic device of (a) with a population of cells comprising osteoblasts;
(2) culturing the cells with a culture medium through the channel region for a time effective for the cells to form a confluent layer on the bottom surface of the channel, to then form multiple cell layers and to then form 3D nodular structures that comprise a 3D bone-like tissue;
the 3D bone like tissue being characterized by a mineralized bone-like tissue comprising (a) viable osteoblasts self-organized into cohesive multiple cell layers and (b) an extracellular matrix secreted by the viable adherent osteoblasts;
(c) preparing a multiple myeloma tumor biospecimen composition by:
(1) acquiring a multiple myeloma tumor biospecimen from the subject, wherein the biospecimen comprises viable multiple myeloma cells;
and
(2) adding plasma autologous to the subject to the viable multiple myeloma cells;
(3) bringing the biospecimen composition of (c)(2) comprising viable multiple myeloma cells in contact with the osteoblasts of the ex vivo bone marrow microenvironment perfused by nutrients and dissolved gas molecules to seed the ex vivo bone marrow microenvironment with the viable multiple myeloma cells, the ex vivo bone marrow microenvironment perfused by nutrients and dissolved gas molecules and the seeded multiple myeloma cells in contact with the osteoblasts of the ex vivo bone marrow microenvironment forming an ex vivo microenvironment effective to recapitulate spatial and temporal characteristics of a multiple myeloma cancer niche and to maintain viability of the human multiple myeloma cells (a multiple myeloma cancer niche);
and
(d) testing chemotherapeutic efficacy of a chemotherapeutic agent on the viable human multiple myeloma cells maintained in the ex vivo multiple myeloma cancer niche of (c)(3) in the test chamber of (a) by
(1) contacting the ex vivo multiple myeloma cancer niche comprising viable human myeloma cells with a test chemotherapeutic agent;
and
(2) comparing at least one of viability and level of apoptosis of the multiple myeloma cells in the multiple myeloma cancer niche in the presence of the test chemotherapeutic agent to an untreated control;
and
(e) initiating therapy to treat the multiple myeloma in the patient with the test chemotherapeutic agent if the test chemotherapeutic agent is effective to significantly (P<0.05) reduce viability of the multiple myeloma cells or to increase apoptosis of the multiple myeloma cells, compared to the untreated control.

28 more elements

Dependencies are inferred from the claim text.

Facts

Application: 16/703,218Filed 4 Dec 2019 · us provisional application
Priority: 6 Dec 2018
Published: US 2020/0181551 A111 Jun 2020
Granted: 23 Aug 2022
Term ends: Not estimatedThe source records don’t support an estimate.

Classification32 codes

C12M 21/08
Bioreactors or fermenters specially adapted for specific uses: for producing artificial tissue or for ex-vivo cultivation of tissue
G01N 33/5088
Supracellular entities, e.g. tissue, organisms: of vertebrates
B01L 3/502707
By integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g.…
B01L 3/502746
By integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g.…