Disclosed are methods for separating carbon nanotubes on the basis of a specified parameter, such as length. The methods include labelling of the carbon nanotubes with a biological moiety, followed by SDS-PAGE and staining, to separate the carbon nanotubes on the basis of length and/or characterize their length. In some embodiments, egg-white lysozyme, conjugated covalently onto single-walled carbon nanotubes surfaces using carbodiimide method, followed by SDS-PAGE and visualization of the single-walled nanotubes using silver staining, provides high resolution characterization of length of the single-walled carbon nanotubes. This high precision, inexpensive, rapid and simple separation method obviates the need for centrifugation, additional chemical analyses, and expensive spectroscopic techniques such as Raman spectroscopy to visualize carbon nanotube bands. The disclosed methods find utility in quality-control in the manufacture of carbon nanotubes of specific lengths.

The present disclosure relates to a carbon nanotube wire includes a carbon nanotube aggregate constituted of a plurality of carbon nanotubes. In the plurality of carbon nanotubes, a mean length of the plurality of carbon nanotubes is not larger than 150 μm, a CV value of the mean length is not smaller than 0.40, a mean diameter of the plurality of carbon nanotubes is smaller than 4 nm, a CV value of the mean diameter is not smaller than 0.18, and a proportion of carbon nanotubes with lengths not smaller than 3 μm is not less than 60%.

A nanocarbon separation device includes a separation tank that is configured to accommodate a dispersion liquid including nanocarbons, a first electrode provided at an upper part in the separation tank, a second electrode provided at a lower part in the separation tank, an evaluation unit that is configured to evaluate a physical state or a chemical state of the dispersion liquid, and a determination unit that is configured to determine a separation state between metallic nanocarbons and semiconducting nanocarbons included in the dispersion liquid from the physical state or the chemical state.

A nanocarbon separation device includes a separation tank that is configured to accommodate a dispersion liquid including nanocarbons, a first electrode provided at an upper part in the separation tank, a second electrode provided at a lower part in the separation tank, an evaluation unit that is configured to evaluate a physical state or a chemical state of the dispersion liquid, and a determination unit that is configured to determine a separation state between metallic nanocarbons and semiconducting nanocarbons included in the dispersion liquid from the physical state or the chemical state.

Provided herein is a nanopore structure, which in one aspect is a “carbon nanotube porin”, that comprises a short nanotube with an associated lipid coating. Also disclosed are compositions and methods enabling the preparation of such nanotube/lipid complexes. Further disclosed is a method for therapeutics delivery that involves a drug delivery agent comprising a liposome with a NT loaded with a therapeutic agent, introducing the therapeutic agent into a cell or a tissue or an organism; and subsequent release of the therapeutic agents into a cell.

Provided herein is a nanopore structure, which in one aspect is a “carbon nanotube porin”, that comprises a short nanotube with an associated lipid coating. Also disclosed are compositions and methods enabling the preparation of such nanotube/lipid complexes. Further disclosed is a method for therapeutics delivery that involves a drug delivery agent comprising a liposome with a NT loaded with a therapeutic agent, introducing the therapeutic agent into a cell or a tissue or an organism; and subsequent release of the therapeutic agents into a cell.

Provided herein is a nanopore structure, which in one aspect is a “carbon nanotube porin”, that comprises a short nanotube with an associated lipid coating. Also disclosed are compositions and methods enabling the preparation of such nanotube/lipid complexes. Further disclosed is a method for therapeutics delivery that involves a drug delivery agent comprising a liposome with a NT loaded with a therapeutic agent, introducing the therapeutic agent into a cell or a tissue or an organism; and subsequent release of the therapeutic agents into a cell.

Provided herein is a nanopore structure, which in one aspect is a “carbon nanotube porin”, that comprises a short nanotube with an associated lipid coating. Also disclosed are compositions and methods enabling the preparation of such nanotube/lipid complexes. Further disclosed is a method for therapeutics delivery that involves a drug delivery agent comprising a liposome with a NT loaded with a therapeutic agent, introducing the therapeutic agent into a cell or a tissue or an organism; and subsequent release of the therapeutic agents into a cell.

A nanocarbon separation device includes a separation tank that is configured to accommodate a dispersion liquid including nanocarbons, a first electrode that is provided at an upper part in the separation tank, a second electrode that is provided at a lower part in the separation tank, an evaluation unit that is configured to evaluate a physical state or a chemical state of the dispersion liquid, and a fractionation unit that is configured to fractionate the dispersion liquid based on the physical state or the chemical state.

A nanocarbon separation device includes a separation tank that is configured to accommodate a dispersion liquid including nanocarbons, a first electrode that is provided at an upper part in the separation tank, a second electrode that is provided at a lower part in the separation tank, an evaluation unit that is configured to evaluate a physical state or a chemical state of the dispersion liquid, and a fractionation unit that is configured to fractionate the dispersion liquid based on the physical state or the chemical state.