Massachusetts Institute of Technology

Max-planck-gesellschaft Zur F&#xf6;rderung Der Wissenschaften E. V.

Affinity Biosensors, LLC

Thomas P Burg

Scott R Manalis

Philip Dextras

Sungmin Son

Yao-Chung Weng

Andrea Kristine Bryan

William H Grover

Michel Godin

Margherita Bassu

Andreas Heinrich Dietzel

Subra Suresh

Kenneth Babcock

Jungchul Lee

Ken Babcock

Foelke Purr

Yara Mejia

Raffaele Faoro

Amneet Gulati

Sangwon Byun

Ethoxy-nonafluorobutane (CFOCH) is used as an immersion medium for immersing an immersion objective of a cryo-light microscope. The cryo-light microscope comprising an immersion objective, a front lens mount holding a front lens of the immersion objective, a sample holder and a cold stage carrying the sample holder further has a heating device coupling a heat flow into the front lens mount.

Cryo-light microscope and immersion medium for cryo-light microscopy

For comparing first optical properties of a first fluid with second optical properties of a second fluid a first transparent grating having a grating constant is made of the first liquid, and a second transparent grating also having the grating constant is made of the second liquid. The second transparent grating is arranged at a lateral offset of less than 45% of the grating constant with regard to the first transparent grating such that grating bars of the first and second transparent gratings are arranged side by side. Coherent light is directed onto the first and second transparent gratings such that light which passed through the grating bars of the first and second transparent gratings forms a diffraction pattern comprising intensity maxima. Two light intensities of two intensity maxima of a same order higher than zero are measured and compared to each other.

Method and apparatus for comparing optical properties of two liquids

The method and apparatus of the present invention detects changes in cell biomechanics caused by any of a variety of diseases and conditions. In one embodiment, the method and apparatus of the invention detect infection of red blood cells. In one embodiment, the invention is a method and apparatus comprising a microfluidic channel with a constriction, for trapping infected red blood cells while allowing healthy red blood cells to deform and pass through the channel. In another embodiment, the invention comprises a suspended microchannel resonator for detecting and counting red blood cells at the constriction of the microfluidic channel.

Method and apparatus for high throughput diagnosis of diseased cells with microchannel devices

Methods and apparatus for improving measurements of particle or cell characteristics, such as mass, in Suspended Microchannel Resonators (SMR's). Apparatus include in particular designs for trapping particles in SMR's for extended measurement periods. Methods include techniques to provide differential measurements by varying the fluid density for repeated measurements on the same particle or cell.

Method and apparatus for trapping single particles in microfluidic channels

Mass cytometry method. In one aspect, the method includes providing a sample having at least one cell type and mixing the sample with material such as nanoparticles functionalized with affinity molecules for the at least one cell type. The sample is transported through a suspended microchannel resonator to record a mass histogram and a cell count for the at least one cell type is determined from the histogram.

Flow cytometry methods and immunodiagnostics with mass sensitive readout

Method for determining buoyant mass and deformability of a cell. The method includes introducing the cell into a suspended microchannel resonator that includes a constriction near a distal location in the resonator. A first frequency shift in the resonator is monitored as a cell moves to the distal location in the resonator, the first frequency shift being related to the buoyant mass of the cell. Transit time of the cell through the constriction is measured by monitoring a second frequency shift as a result of a change in cell location as it passes through the constriction, whereby deformability is determined from the measured buoyant mass and transit time.

Apparatus and method for measuring buoyant mass and deformability of single cells

Methods and apparatus for improving measurements of particle or cell characteristics, such as mass, in Suspended Microchannel Resonators (SMR's). Apparatus include in particular designs for trapping particles in SMR's for extended measurement periods and for changing the fluid properties within the SMR during the extended periods. Methods include techniques to provide for cell growth over time and over time in response to changing fluid properties to aid in determining parameters such as drug resistance and drug susceptibility.

Method and apparatus for extended time and varying environment measurements of single particles in microfluidic channels

Measurements of the mass and surface charge of microparticles are employed in the characterization of many types of colloidal dispersions. The suspended microchannel resonator (SMR) is capable of measuring individual particle masses with femtogram resolution. The high sensitivity of the SMR resonance frequency to changes in particle position in the SMR channel is employed to determine the electrophoretic mobility of discrete particles in an applied electric field. When an oscillating electric field is applied to the suspended microchannel, the transient resonance frequency shift corresponding to a particle transit can be analyzed to extract both the buoyant mass and electrophoretic mobility of each particle. These parameters, together with the mean particle density, can be used to compute the size, absolute mass, and surface charge of discrete particles.

Method and apparatus for integrated measurement of the mass and surface charge of discrete microparticles using a suspended microchannel resonator

Methods and apparatus for improving measurements of particle or cell characteristics, such as mass, in Susppended Microchannel Resonators (SMR's). Apparatus include in particular designs for trapping particles in SMR's for extended measurement periods. Methods include techniques to provide differential measurements by varying the fluid density for repeated measurements on the same particle or cell.

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Goettingen, Germany

Thomas P Burg