Vadivelu et al., 2018 - Google Patents
Cryoprotectant-free freezing of cells using liquid marbles filled with hydrogelVadivelu et al., 2018
View PDF- Document ID
- 312580776160155444
- Author
- Vadivelu R
- Kashaninejad N
- Sreejith K
- Bhattacharjee R
- Cock I
- Nguyen N
- Publication year
- Publication venue
- ACS applied materials & interfaces
External Links
Snippet
Cryopreservation without cryoprotectant remains a significant challenge for the re- establishment of cell culture after freeze–thaw. Thus, finding an alternative and a simple cryopreservation method is necessary. Liquid marble (LM)-based digital microfluidics is a …
- 239000007788 liquid 0 title abstract description 74
Classifications
-
- 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, AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N1/00—Preservation of bodies of humans or animals, or parts thereof
- A01N1/02—Preservation of living parts
- A01N1/0205—Chemical aspects
- A01N1/021—Preservation or perfusion media, liquids, solids or gases used in the preservation of cells, tissue, organs or bodily fluids
- A01N1/0221—Freeze-process protecting agents, i.e. substances protecting cells from effects of the physical process, e.g. cryoprotectants, osmolarity regulators like oncotic agents
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICRO-ORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING OR MAINTAINING MICRO-ORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
- C12N5/06—Animal cells or tissues; Human cells or tissues ; Not used, see subgroups
- C12N5/0602—Vertebrate cells
- C12N5/0603—Embryonic cells ; Embryoid bodies
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Vadivelu et al. | Cryoprotectant-free freezing of cells using liquid marbles filled with hydrogel | |
Whaley et al. | Cryopreservation: an overview of principles and cell-specific considerations | |
Meneghel et al. | Cryopreservation as a key element in the successful delivery of cell-based therapies—a review | |
Akiyama et al. | Cryoprotectant-free cryopreservation of mammalian cells by superflash freezing | |
Asghar et al. | Preserving human cells for regenerative, reproductive, and transfusion medicine | |
Ozimic et al. | Sperm cryopreservation today: approaches, efficiency, and pitfalls | |
Tomás et al. | Extracellular antifreeze protein significantly enhances the cryopreservation of cell monolayers | |
Zhang et al. | Emerging technologies in medical applications of minimum volume vitrification | |
Huang et al. | Alginate hydrogel microencapsulation inhibits devitrification and enables large‐volume low‐CPA cell vitrification | |
Huang et al. | Advanced technologies for the preservation of mammalian biospecimens | |
He et al. | Vitrification by ultra-fast cooling at a low concentration of cryoprotectants in a quartz micro-capillary: a study using murine embryonic stem cells | |
Bailey et al. | Synthetically scalable poly (ampholyte) which dramatically enhances cellular cryopreservation | |
Yu et al. | Interfacial interactions of sucrose during cryopreservation detected by Raman spectroscopy | |
Matsumura et al. | Cryopreservation of a two-dimensional monolayer using a slow vitrification method with polyampholyte to inhibit ice crystal formation | |
de Vries et al. | Bulk droplet vitrification: an approach to improve large-scale hepatocyte cryopreservation outcome | |
Chen et al. | Small‐volume vitrification for human spermatozoa in the absence of cryoprotectants by using Cryotop | |
Murray et al. | Low DMSO cryopreservation of stem cells enabled by macromolecular cryoprotectants | |
Ohnishi et al. | Effect of the silk protein sericin on cryopreserved rat islets | |
Lu et al. | Scalable production and cryostorage of organoids using core–shell decoupled hydrogel capsules | |
Bissoyi et al. | Cryopreservation of liver-cell spheroids with macromolecular cryoprotectants | |
Sart et al. | Cryopreservation of pluripotent stem cell aggregates in defined protein‐free formulation | |
Diaz-Dussan et al. | Trehalose-based polyethers for cryopreservation and three-dimensional cell scaffolds | |
Bai et al. | Cryopreservation in the era of cell therapy: revisiting fundamental concepts to enable future technologies | |
Jeong et al. | Vitrification for cryopreservation of 2D and 3D stem cells culture using high concentration of cryoprotective agents | |
Tessier et al. | Effect of ice nucleation and cryoprotectants during high subzero-preservation in endothelialized microchannels |