STABILIZED ANTI-CANCER COLD ATMOSPHERIC PLASMA (CAP)-STIMULATED MEDIA AND METHODS FOR PREPARING AND USING THE SAME

Abstract

This disclosure relates to stabilized anti-cancer cold atmospheric plasma (CAP)-stimulated media, to methods for preparing such media, and to methods of treatment using such media.

Description

This application claims the benefit of U.S. Provisional Application No. 62/247,223, filed Oct. 28, 2015, which is incorporated by reference in its entirety.

FIELD OF THE INVENTION

The present invention relates to stabilized anti-cancer cold atmospheric plasma (CAP)-stimulated media, to methods for preparing such media, and to methods of treatment using such media.

BACKGROUND OF THE INVENTION

Over the past decade, cold atmospheric plasma (CAP) has shown a selective anti-cancer capacity both in vitro (see, e.g., Refs. 1-8) and in vivo (see, e.g., Refs. 9-13). Various types of CAP devices have been used to directly irradiate cancer cells cultured in the multi-well plates (see, e.g., Refs. 4 and 14), petri-dishes (see, e.g., Refs. 1 and 15), or tumor tissues (see, e.g., Refs. 9 and 12). Recently, plasma-stimulated medium (PSM) has exhibited a significant anti-cancer capacity, as strong as the direct CAP treatment on glioblastoma cells (References 16-18), lung carcinoma cells (see, e.g., Ref. 9), and bladder cancer cells (see, e.g., Ref. 20). Additionally, it has been reported that microsecond-pulsed plasma-activated media is able to selectively inhibit the growth of lung cancer (H460) cells rather than normal lung cancer (L132) cells (see, e.g., Ref. 21). The selective apoptosis in the PSM treated glioblastoma cells (see, e.g., Ref. 22), further confirms that PSM is a selective anti-cancer tool. The injection of PSM into mice also significantly inhibits the growth of tumors (see, e.g., Ref. 23). PSM may therefore have wide applications in cancer treatment including specific situations where CAP cannot reach deep seated tumors or when the CAP device is not portable.

The CAP-originated reactive species are thought to be the main factor in cancer cell death and growth inhibition (see, e.g., Ref. 24). When CAP interacts with the medium, both reactive oxygen species (ROS) such as hydroxyl free radicals (OH) (see, e.g., Ref. 25) and hydrogen peroxide (H₂O₂) (see, e.g., Refs. 19 and 26) and reactive nitrogen species (RNS) such as nitric oxide (NO) (see, e.g., Ref. 27) and nitrite (NO₂⁻) (see, e.g., Refs. 17 and 28) are dissolved in the aqueous solution. Among them, H₂O₂ has been found to mainly contribute to the death of cancer cells after the direct CAP irradiation on cancer cells (References 29-31) or the indirect CAP irradiation on the culture medium (see, e.g., Refs. 18 and 19).

For pharmaceutical reasons, PSM should be stable when stored. To date, the largest disadvantage of PSM for future clinical application is its degradation during storage. PSM gradually loses its anti-cancer capacity during storage between room temperature (see, e.g., Refs. 17 and 19) and a few degrees above the freezing point of water (see, e.g., Ref. 19).

To date, the sole strategy to inhibit the degradation of PSM during storage is to freeze it at low temperature (−80° C.), However, according to the description of most manufacturers of cell culture media, the ideal storage temperature range for medium is between 2° C. to 8° C., rather than under freezing conditions. Thus, considering the clinical application prospective, PSM should at least be stable at such a temperature range. No method has been reported to date regarding improving the stability of PSM between the recommended storage temperature range of between 2° C. and 8° C.

There is therefore a need for CAP-stimulated medium that exhibit enhanced stability, such that they may be stored at temperatures between, for example, about 2° C. and about 8° C., while retaining its anti-cancer activity.

SUMMARY OF THE INVENTION

The present invention relates to stabilized anti-cancer cold atmospheric plasma-stimulated media (CAPSM), to methods for preparing such stabilized media and to methods treatment using such media. This disclosure not only addresses ways to increase the anti-cancer capacity of CAPSM, but also significantly improve the stability of such media without compromising the CAPSM therapeutic potential in, for example, cancer treatment.

The inventors have found that the degradation of PSM is mainly due to reaction between the plasma-originated reactive species generated during CAP treatment and one or more components in Dulbecco's Modified Eagle Medium (DMEM). Based on this finding, both the reactive species (such as H₂O₂ ) in PSM and the anti-cancer capacity of PSM can be significantly stabilized during storage (e.g., at 8° C. and −25° C.) for at least 3 days (such as, e.g., 3-7 days). In addition, the inventors have surprisingly found that addition of, for example, a tyrosine derivative, such as 3-nitro-L -tyrosine, to the medium (e.g. Dulbecco's Modified Eagle Medium, DMEM) can mitigate the degradation of reactive species (such as H₂O₂) in the media, allowing for the enhanced retention of activity (such as anti-cancer activity), for example, at 8° C. during storage.

Accordingly, in one aspect, the present invention relates to a stabilized cold atmospheric plasma-stimulated media (CAPSM), such as an anti-cancer CAPSM

In one embodiment, the CAP-stimulated media comprises phosphate buffered saline (PBS), Dulbecco's Modified Eagle Medium (DMEM), or a combination thereof.

In one embodiment, the CAP-stimulated media comprises phosphate buffered saline (PBS). In another embodiment, the CAP-stimulated media comprises Dulbecco's Modified Eagle Medium (DMEM).

In one embodiment, any of the CAP-stimulated media described herein is stable for a period of up to 7 days, such as up to 6 days, up to 5 days, up to 4 days or up to 3 days, for example, between about 1 and about 7 days, about 1 and about 6 days, about 1 and about 5 days, about 1 and about 4 days or about 1 and about 3 days, or for about 1 day, about 2 days or about 3 days.

In one embodiment, any of the CAP-stimulated media described herein is stable at a temperature of between about −25° C. and about 25° C., such as between about −25° C. and about 22° C., between about 0° C. and about 22° C., between about 0° C. and about 8° C. or between about 2° C. and about 8° C.

In one embodiment, any of the CAP-stimulated media described herein is stable at a temperature of between about −25° C. and about 25° C., such as between about −25° C. and about 22° C., between about 0° C. and about 22° C., between about 0° C. and about 8° C. or between about 2° C. and about 8° C., for a period of up to 7 days, such as up to 6 days, up to 5 days, up to 4 days or up to 3 days, for example, between about 1 and about 7 days, about 1 and about 6 days, about 1 and about 5 days, about 1 and about 4 days or about 1 and about 3 days, or for about 1 day, about 2 days or about 3 days.

In one embodiment, any of the CAP-stimulated media described herein is free of cysteine, or methionine, or a combination thereof.

In one embodiment, any of the CAP-stimulated media described herein is free of phenylalanine.

In one embodiment, any of the CAP-stimulated media described herein is free of cysteine, or methionine, or phenylalanine, or any combination thereof.

In one embodiment, any of the CAP-stimulated media described herein is free of phenol red.

In one embodiment, any of the CAP-stimulated media described herein is free of cysteine, or methionine, or phenylalanine, or phenol red, or any combination thereof.

In one embodiment, any of the plasma stimulated media described herein comprises glutamine.

In one embodiment, any of the CAP-stimulated media described herein further comprise 3-nitro-L-tyrosine.

In additional embodiments, the 3-nitro-L-tyrosine is present in the CAP-stimulated media at a concentration of up to about 9 mM, such as between about 1 and about 5 mM, for example, at a concentration of about 1 mM, about 2 mM, about 3 MM, or about 4 mM.

In another aspect, the present invention relates to a method of (i) stabilizing and/or (ii) enhancing the activity (e.g., anti-cancer activity) of CAP-stimulated stimulated media.

In one embodiment, the method comprises stabilizing the CAP-stimulated media. In one embodiment, the method comprises enhancing the activity of the CAP-stimulated media.

In one embodiment, the method comprises reducing the amount of cysteine, or methionine, or a combination thereof, in the media.

In another embodiment, the method comprises reducing the amount of phenylalanine in the media.

In another embodiment, the method comprises reducing the amount of cysteine, or methionine, or phenylalanine, or any combination thereof, in the media.

In another embodiment, the method comprises reducing the amount of phenol red in the media.

In another embodiment, the method comprises reducing the amount of cysteine, or methionine, or phenylalanine, or phenol red, or any combination thereof, in the media.

In another embodiment, the method comprises adding 3-nitro-L-tyrosine to the media. For example, the 3-nitro-L-tyrosine may be added to the CAP-stimulated media at a concentration of up to about 9 mM, such as between about 1 and about 5 mM, for example, at a concentration of about 1 mM, about 2 mM, about 3 MM, or about 4 mM.

In another embodiment, the method comprises (i) reducing the amount of cysteine, or methionine, or phenylalanine, or phenol red, or any combination thereof, in the media and (ii) adding 3-nitro-L-tyrosine to the media.

In another embodiment, the method comprises

reducing the amount of cysteine, methionine, or a combination thereof, in the media;

(ii) reducing the amount of phenylalanine in the media;

(iii) reducing the amount of phenol red in the media;

(iv) adding 3-nitro-L-tyrosine to the media; or

(v) any combination of (i)-(iv).

In another aspect, the present invention relates to a method of treating a target tissue.

In one embodiment, the method comprises administering (e.g., administering to a patient in need of such treatment) a CAP-stimulated media according to any of the embodiments described herein.

In one embodiment, the method comprises treating cancerous and/or precancerous tissue (e.g., cancerous and/or precancerous cells).

In one embodiment, the target tissue comprises lung, bladder, brain or skin tissue (e.g., lung bladder, brain or skin cells), or any combination thereof.

In a further aspect, the present invention related to a method of enhancing the activity (e.g., anti-cancer activity) of CAP-stimulated media, the method comprising (i) increasing the diameter of the well (e.g., in a multi-plate well), and/or (ii) decreasing the gap between the plasma tube and the surface of the media during the CAP-stimulated treatment.

In one embodiment, the method comprises increasing the diameter of the well (e.g., in a multi-plate well) during the treatment. The diameter of the well may be increased by decreasing the number of wells per plate.

In additional embodiments, for example, as the well diameter increases from 11.00 mm (48 wells per plate) to 15.6 mm diameter (24 well per plate), from 15.6 mm to 22.1 mm diameter (12 wells per plate), or from 22.1 mm to 34.8 mm diameter (6 wells per plate), the diameter of the well increases by about 42%, about 42% and about 57%, respectively.

In additional embodiments, for example, as the number of wells per plate decreases from 48 (11.00 mm diameter) to 24 (15.6 mm diameter), from 24 to 12 (22.1 mm diameter), or from 12 to 6 (34.8 mm diameter), the diameter of the well increases by about 42%, about 42% and about 57%, respectively.

In another embodiment, the method comprises decreasing the gap between the plasma tube and the surface of the media during the treatment.

In one embodiment, the gap between the plasma tube and the surface of the media during the treatment is about 4 cm, about 3.5 cm, about 3 cm, about 2.5 cm or about 2 cm. The gap may be decreased from any larger diameter to any lower diameter, as recited herein.

For example, the gap may be decreased from about 4 cm to about 3.5 cm, from about 3.5 cm to about 3 cm, from about 3 cm to about 2.5 cm or from about 2.5 cm to about 2 cm. As a further example, the gap may be decreased from about 4 cm to about 3.5 cm, from about 4 cm to about 3 cm, from about 4 cm to about 2.5 cm or from about 4 cm to about 2 cm.

In additional embodiments, the gap is decreased by about 25%, about 20%, about 17%, or about 14%.

BRIEF DESCRPTION OF THE DRAWINGS

FIG. 1 depicts (a) an examplary CAP device, and (b) the general research strategy using PSM to affect cancer cells seeded in a multi-well plate.

FIG. 2 depicts, as described in Example 1, (a) the change of H₂O₂ concentration in CAP -stimulated DMEM (left column) and PBS (right column) during storage at 8° C. and 22° C. for 26 hours; (b) the change of H₂O₂ concentration in CAP-stimulated PBS during storage at 8° C. for 7 days; (c) the change of H₂O₂ concentration in CAP-stimulated PBS during the storage at 8° C. and −25° C. for 3 days; (d) the change of anti-cancer capacity of the CAP-stimulated PBS during storage at 8° C. and −25° C. for 3 days; (e) the effect of the cold plasma-stimulated PBS on the cell viability of U87MG (left column), PA-TU-8988T (middle column), and MDA-MB-231 (right column) cells cultured in CAP-stimulated PBS; and (f) the change of H₂O₂ concentration in 37.3 μM H₂O₂ containing PBS during the storage at 8° C. for 3 days. The volume of solution for each well was 1 mL for all experiments. The treatment time for (a-d) was 1 minute and 2 minutes, respectively. Results are presented as the mean±standard deviation (s.d.) of three independently repeated experiments performed in triplicate (a-c and f) or in sextuplicate (d and e). For the cell viability, the data have been normalized to corresponding control group. Student's t-test was performed and the significance is indicated as ***p<0.005.

FIG. 3 depicts, as described in Example 2, (a) the change of H₂O₂ concentration in CAP -stimulated PBS containing specific components in DMEM during the storage at 22° C. for 26 hours (immediately: left column; stored at 22° C. for 26 hours: right column) (b) the change of H₂O₂ concentration in CAP-stimulated cysteine/methionine-free DMEM, cysteine-free DMEM, methionine-free DMEM, and standard DMEM during storage at 8° C. for 3 days (immediately: left column; stored at 8° C. for 3 days: right column); and (c) the change of anti-cancer capacity of the CAP-stimulated cysteine/methionine-free DMEM, cysteine-free DMEM, methionine-free DMEM, and standard DMEM during storage at 8° C. for 3 days (immediately: left column; stored at 8° C. for 3 days: right column). For all experiments, the volume of solution and the treatment time in each well was 1 mL and 1 minute. Results are presented as the mean±s.d. of three independently repeated experiments performed in triplicate (a and b) or in sextuplicate (c). For the cell viability, the data have been normalized to corresponding control group. Student's t-test was performed and the significance is indicated as *p<0.05, **p<0.01, ***p<0.005.

FIG. 4 depicts the effect of phenol red on the H₂O₂ concentration in DMEM during CAP treatment. During the CAP treatment, 1 mL of DMEM in 12-well plate was treated by CAP for 1 min. Results are presented as the mean±s.d. of three repeated experiments in triplicate.

FIG. 5 depicts, as described in Example 3, (a) the change of H₂O₂ concentration in 34.5 μM H₂O₂ containing DMEM during storage at −25° C. for 3 days; (b) the change of H₂O₂ concentration in 37.3 μM H₂O₂ containing PBS during storage at −25° C. for 3 days; (c) the change of H₂O₂ concentration in CAP-stimulated PBS containing specific component(s) in DMEM during storage at −25° C. (immediately: left column; stored a−25° C.: right column); (d) the change of H₂O₂ concentration in CAP-stimulated cysteine/methionine-free DMEM, cysteine-free DMEM, methionine-free DMEM, and standard DMEM during storage at −25° C. for 3 days (immediately: left column; stored at −25° C. for 3 days: right column); and (e) the anti-cancer capacity of CAP -stimulated cysteine/methionine-free DMEM, cysteine-free DMEM, methionine free DMEM, and standard DMEM during storage at −25° C. for 3 days (1 minute: left column; 2 minutes: right column). For all experiments, the volume of solution in each well was 1 mL. The treatment time was 1 minute (c and d). Results are presented as the mean±s.d. of three independently repeated experiments performed in triplicate (a-d) or in sextuplicate (e). For the cell viability, the data have been normalized to corresponding control group. Student's t-test was performed and the significance is indicated as ***p<0.005.

FIG. 6 depicts, as described in Example 4, (a) chemical formulas for phenylalanine, tyrosine, and 3-nitro-L-tyrosine; (b) the change of H₂O₂ concentration in CAP-stimulated standard DMEM, phenylalanine-containing DMEM, tyrosine-containing DMEM, and 3-nitro-L-tyrosine containing DMEM during storage at 8° C. for 26 hours (immediately: left column; stored at 8° C. for 26 hours: right column); (c) the change of H₂O₂ concentration in CAP-stimulated standard DMEM (left column) and 3-nitro-L-tyrosine containing DMEM (right column) during storage at 8° C. for 3 days; (d) the change of anti-cancer capacity of CAP-stimulated standard DMEM (left column) and 3-nitro-L-tyrosine-containing DMEM (right column) during storage at 8° C. for 3 days; (e) the change of H₂O₂ concentration in CAP-stimulated single amino acid containing PBS and double amino acid containing PBS during storage at 22° C. for 26 hours (immediately: left column; stored at 22° C. for 26 hours: right column), the corresponding concentrations of cysteine, methionine, phenylalanine, and 3-nitro-L-tyrosine in PBS were 0.2 mM, 0.2 mM, 0.4 mM and 2 mM, respectively; f) the change of H₂O₂ concentration in CAP-stimulated 3-nitro-L-tyrosine containing DMEM at different concentrations during storage at 8° C. for 3 days (immediately: left column; stored at 8° C. for 3 days: right column); and (g) the change of H₂O₂ concentration in CAP-stimulated standard DMEM (left column) and 3-nitro-L-tyrosine containing DMEM (right column) during storage at −25° C. for 3 days. For all experiments, the volume of solution in each well was 1 mL. The treatment time was 1 minute for (b, e, and f) and 2 minutes for (c, d, and g). Results are presented as the mean±s.d. of three independently repeated experiments performed in triplicate (b, c, and e-g) or in sextuplicate (d). For the cell viability, the data have been normalized to corresponding control group. Student's t-test was performed and the significance is indicated as *p<0.05, **p<0.01, ***p<0.005.

FIG. 7 depicts the effect of well diameter of the multi-plate well on the H₂O₂ concentration and anti-cancer capacity of the CAP stimulated media. The diameter of the well in a 48-well plate, 24-well plate, 12-well plate, and 6-well plate is 11.0 mm, 15.6 mm, 22.1 mm, and 34.8 mm, respectively. FIG. 7(a) shows the relative H₂O₂ concentration in the CAP-stimulated media. FIG. 7(b) shows the anti-cancer capacity of the CAP-stimulated media on U87MG cells with a confluence of 2×10⁴ cells/mL. FIG. 7(c) shows the anti-cancer capacity of the CAP-stimulated media on MDA-MB-231 cells with a confluence of 2×10⁴ cells/mL. Cells were cultured in 1 mL of the CAP -stimulated media from different multi-well plates. The treatment time was 1 min. Results are presented as the mean±s.d. of three repeated experiments performed in triplicate (a) or in sextuplicate (b and c).

FIG. 8 the effect of the gap between the plasma tube and the media surface during the CAP treatment on the H₂O₂ concentration and anti-cancer capacity of the CAP-stimulated media. FIG. 8(a) shows the relative H₂O₂ concentration in 1 mL of the CAP-stimulated media. FIG. 8(b) shows the anti-cancer capacity of the CAP-stimulated media on U87MG cells with a confluence of 2×10⁴ cells/mL. FIG. 8(c) shows the anti-cancer capacity of the CAP-stimulated media on MDA-MB -231 cells with a confluence of 2×10⁴ cells/mL. Cells were cultured in 1 mL of CAP-stimulated media. The treatment time was 1 min. Results are presented as the mean±s.d. of three repeated experiments performed in triplicate (a) or in sextuplicate (b and c).

FIG. 9 depicts a pre-operative axial post-gadolinium magnetic resonace (MR) image displaying a left temporal glioblastoma (FIG. 9A), and a post-operative axial post-gadolinium MR image displaying a residual line of enhancing tumor (FIG. 9B, light arrow). The surgical resection cavity (dark arrow) is filled with CAPSM (light coloration).

DETAILED DESCRIPTION OF THE INVENTION

Definitions

Unless defined otherwise, all technical and scientific terms used herein generally have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.

The term “comprising” is open ended and, in connection with a composition, refers to the elements recited. The term “comprising” as used in connection with the compositions described herein can alternatively cover compositions “consisting essentially of” or “consisting of” the recited components.

The terms “stable” and “stabilized” as used herein mean, in certain embodiments, that less than about 25%, such as less than about 20%, less than about 15%, less than about 10%, less than about 9%, less than about 8%, less than about 7%, less than about 6%, less than about 5%, less than about 4%, less than about 3%, less than about 2%, less than about 1%, less than about 0.5%, or less than about 0.1% of the concentration of the active species (such as H₂O₂) in the media decomposes, for example, during a specified period of time at a specified temperature (e.g., when stored between about 2° C. and about 8° C. for at a period of least 3 days (such as, e.g., 3-7 days).

EXAMPLES

The present invention will now be further described by way of the following non-limiting examples. In applying the disclosure of these examples, it should be kept clearly in mind that the examples are merely illustrative of the present invention and should not be construed as limiting the scope of the invention in any way as many variations and equivalents that are encompassed by the present invention will become apparent to those skilled in the art upon reading the present disclosure.

The CAP Device

The CAP device (FIG. 1a) is a helium CAP jet generator which has been used in a series of studies (see, e.g., Refs. 17, 18 and 32-34). The CAP jet is generated between the central electrode and the grounded ring electrode. The carrying gas is helium with a flow of 4.7 L/min, controlled by a flow meter. The output voltage is 3.16 kV. Any suitable CAP device can be utilized, such as shown in, e.g., International Publication No. WO 12/167089, which is hereby incorporated by reference in its entirety.

The general research strategy described herein is illustrated in FIG. 1b. 1 mL of PSM was made by the vertical irradiation on the medium in a well on a 12-well plate. Then, the PSM was transferred to a 1.5 mL centrifuge tube by pipette. The centrifuge tubes were stored in refrigerators with different internal temperatures (8° C. and −25° C.) for 3 days. Additionally, some centrifuge tubes were stored at 22° C., for the investigation of PSM degradation at room temperature. Ultimately, the PSM was either transferred to culture the seeded cancer cells in a 96-well plate or transferred into a black wall 96-well plate to measure for H₂O₂ concentration. Because PBS is not suitable for cell culture, the protocols used to transfer the CAP-stimulated PBS are slightly different from those used to transfer the CAP-stimulated DMEM.

Methods

Medium and Cell Cultures

Standard Dulbecco's modified Eagle's medium (11965-118), modified cysteine/methionine/glutamine-free DMEM (21013-024), modified arginine/lysine/glutamine-free DMEM (A14431-01) and PBS (14040-133) were purchased from Thermo Fisher Scientific (Waltham, Mass.). All DMEM and PBS were mixed with 1% (v/v) antibiotic (penicillin and streptomycin) (Thermo Fisher Scientific) before any experiments were performed. Human glioblastoma (U87MG) cells, pancreatic cancer (PA-TU-8988T) cells and human breast cancer (MDA-MB-231) cells were obtained from George Washington University. All cancer cell lines were seeded with a confluence of 3×104 cells/mL and a volume of 100 μL in each well on a 96-well plate and were cultured for 6 hours in a complete media composed of Dulbecco's modified Eagle's medium supplemented with 10% (v/v) fetal bovine serum (Thermo Fisher Scientific). and 1% (v/v) antibiotic (penicillin and streptomycin) solution under standard cell culture conditions (a humidified, 37° C., 5% CO₂ environment). In each experiment, 6 wells in a single column on the 96-well plate were seeded with cancer cells.

Preparation of CAP-Stimulated PBS and DMEM

The protocols to prepare PSM are the same among different experiments. 1 mL of PBS or DMEM (or modified DMEM, such as cysteine/methionine-free DMEM) in a well on a Corning™ Falcon™ 12-well plate was treated by CAP for 1 or 2 minutes. The gap between the end of dielectric plasma tube and the bottom of 12-well plate was 3 cm.

Preparation of H₂O₂ Containing PBS and DMEM

H₂O₂ containing PBS and H₂O₂ containing DMEM were prepared by adding 30 wt % H₂O₂ solution to PBS and DMEM, respectively. The H₂O₂ concentration in the H₂O₂ containing PBS and H₂O₂ containing DMEM were the same as the H₂O₂ concentration in the CAP-treated (for 1 minute) 1 mL of PBS or DMEM in the 12-well plate, respectively.

Preparation of Specific Component Containing PBS and DMEM

The amino acid(s) containing PBS, calcium containing PBS, magnesium containing PBS, glucose containing PBS, phenol red containing PBS, and amino acid(s) containing DMEM were prepared by adding and dissolving specific amino acid(s), calcium chloride solution, magnesium chloride solution, D-glucose, phenol red solution or an amino acid derivative (such as 3-nitro-L -tyrosine) in PBS and DMEM, respectively. With the exception of PBS and DMEM, the added components were purchased from Sigma Aldrich.

Affecting the Growth of Cancer Cells Seeded in a 96-Well Plate by CAP-Stimulated DMEM or PBS

First, the initial culture medium which had been cultured cells for 6 hours was removed before this step. Then, for the CAP-stimulated DMEM, 100 μL of treated DMEM was transferred from a well on the 12-well plate (or other tubes stored in a refrigerator) to a well on the 96-well plate, in which 3×103 cancer cells were seeded and had been cultured for 6 hours. In each experiment, 6 wells in a single column on the 96-well plate were seeded with cancer cells. In the control group, the DMEM used to culture cancer cells was the untreated DMEM. For the CAP -stimulated PBS, 100 μL of untreated DMEM was first transferred into the well seeded with 3×103 cancer cells on the 96-well plate. Then, 100 μL of treated PBS was transferred into the well which contained 100 μL of untreated DMEM and 3×103 cancer cells. Thus, after this step, the total volume of the mixed medium in each well seeded with cancer cells was 200 μL. For the control group, the PBS transferred into the well was not treated. Ultimately, for the above two cases, the cancer cells on the 96-well plate were cultured under a standard cell culture condition (a humidified, 37° C., 5% CO₂ environment) for 3 days.

Measuring and Processing Cell Viability

The cancer cells in the 96-well plates were cultured in the 96-well plate under standard cell culture conditions (a humidified, 37° C., 5% CO₂ environment) for 3 days. Then, according to the standard protocols provided by manufacturer, the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diophenyltetrazolium bromide, Thermo Fisher Scientific) assay was performed as follows. 0.7 mg/mL MTT-DMEM solution was prepared by dissolving MTT powder in standard DMEM. The the DMEM which had been used to culture the treated cells for 72 hours was then removed from wells on 96-well plate. Cells were then cultured in the MTT-DMEM solution under standard culture conditions for 3 hours. In each well, the volume of MTT-DMEM was replaced by 100 μL of 0.4% (v/v) hydrochloric acid containing isopropanol solution. The 96-well plate filled with hydrochloric acid containing isopropanol solution was then read by a Hybrid Technology H1 microplate reader (BioTek Instruments, Winooski, Vt.) at a 570 nm of absorbance. To facilitate the formation of violet solution, the 96-well plate was shook for 1 min before the treatment. In each independent experiment, 6 wells in a single column on the 96-well plate were seeded with cancer cells for the cell viability test. The average value of measured cell viability from 6 wells was regarded as the cell viability measured from one independent experiment. To facilitate understanding of the data, all data about cell viability shown in the Figures has been normalized to the control group by dividing the measured cell viability of the experimental group by the measured cell viability of the control group. The final data shown in all Figures are the mean±s.d. of the normalized cell viability from three independently repeated experiments.

Measuring H₂O₂ Concentration.

50 μL of CAP-stimulated medium or PBS to be analyzed for H₂O₂ concentration was transferred to a well on a black-wall Corning™ Falcon™ 96-well clear bottom plate in triplicate. Subsequently, according to standard protocols provided by Sigma Aldrich (St. Louis, Mo.), the H₂O₂ concentration in the cold plasma-stimulated medium was measured as follows. First, 50 μL of red peroxidase substrate stock solution, 200 μL of peroxidase stock solution, and 4.75 ml of assay buffer were mixed to prepare H₂O₂ probe solution. 50 μL of probe solution was then added in the black 96-well plate and mixed with 50 μL of the CAP-stimulated medium or PBS. After 30 min of storage at the room temperature, with protecting from light, a Hybrid Technology H1 microplate reader (BioTek Instruments, Winooski, Vt.) was used to measure the fluorescence with an excitation wavelength at 540 nm and an emission wavelength at 590 nm. The final measured fluorescent strength of the experimental group was obtained by deducting the measured fluorescence of the control group from the measured fluorescence of the experimental group. The standard H₂O₂ solution was used to prepare the standard H₂O₂ concentration-fluorescence curve. Based on this standard curve, we obtained the H₂O₂ concentration in CAP-stimulated medium or PBS. The triplicate experiments were independently repeated for three times

Example 1

The Mechanism of PBS Degradation

To understand the mechanism of PSM degradation, H₂O₂ generation in CAP-stimulated DMEM and PBS after 26 hours of storage (at 8° C. or 22° C.) was compared. As can be seen from FIG. 2, the H₂O₂ in the CAP-stimulated PBS was stable during storage. In contrast, most of the H₂O₂ in the plasma-stimulated DMEM had been lost after 26 hours storage at either 8° C. or 22° C. (FIG. 2a). The higher storage temperature for PSM, the more degradation occurs in PSM (FIG. 2a). The CAP-stimulated PBS has higher a H₂O₂ concentration than the CAP-stimulated DMEM (FIG. 2a).

The H₂O₂ concentration in the CAP-stimulated PBS was not only stable over 7 days of storage at 8° C. (FIG. 2b) but also stable over 3 days at −25° C. (FIG. 2c). The stable anti-cancer capacity of the CAP-stimulated PBS over 3 days at 8° C. and −25° C. was further confirmed by using the corresponding treated PBS to affect the growth of breast cancer (MDA-MB-231) cells (FIG. 2d). In addition, FIG. 2e shows that that the CAP-stimulated PBS can also effectively inhibit the growth of glioblastoma (U87MG) cells and pancreatic cancer (PA-TU-8988T) cells with a dose -dependent manner, making it a stable anti-cancer PSM over a wide temperature range. As shown in FIG. 2f, the H₂O₂ containing PBS experienced a slight degradation over storage at 820 C. for 3 days, which is similar to the slight degradation observed in the CAP-stimulated PBS (FIG. 2c). The H₂O₂ in PBS experiences a natural degradation during the storage at 8° C. Thus, the gradual H₂O₂ consumption in the cold CAP-stimulated DMEM is likely due to the combined effect of the natural degradation of H₂O₂ in aqueous solution and the reaction between H₂O₂ and one or more components in the DMEM. The latter mainly controls the degradation at 8° C.

Example 2

The Effect of Components in DMEM on the Degradation of PBS

The effect of several specific components in DMEM on the PSM degradation was also investigated. A comparison between DMEM and PBS reveals that 15 amino acids, glucose, calcium ion, magnesium ion, and phenol red are the main composition differences between DMEM and PBS.

Accordingly, 15 specific amino acids solutions, 1 glucose solution, 2 saline solutions (CaCl₂, MgCl₂), and 1 phenol red solution were respectively made by adding or dissolving the specific component in PBS according to their concentrations in the standard DMEM. After the CAP treatment and subsequent 26 hours of storage at 22° C., the H₂O₂ concentrations in these solutions were measured and compared with the corresponding H₂O₂ concentration in the solution immediately following the CAP treatment (FIG. 3a). The H₂O₂ in the CAP-stimulated PBS is relatively stable over the storage. In contrast, most of the studied components cause different levels of H₂O₂ degradation in the CAP-stimulated PBS-based solution, except tryptophan, tyrosine, and lysine. Cysteine and methionine cause the most significant degradation of the H₂O₂ during the storage at room temperature. Phenylalanine also causes noticeable degradation of the H₂O₂ . Based on these data, a modified DMEM that is free of cysteine, methionine, and/or phenylalanine (or any combination thereof) will be a stable PSM. CAP-stimulated cysteine/methionine/glutamine free DMEM was compared with CAP-stimulated arginine/lysine/glutamine free DMEM and CAP -stimulated standard DMEM. It was found that only the former was stable during storage at 22° C. for 26 hours. The absence of arginine and lysine did not inhibit the H₂O₂ degradation in PSM. These results are consistent with the trends revealed in FIG. 3a.

To prepare DMEM free of both cysteine and methionine, 4 mM glutamine was added to cysteine/methionine/glutamine free DMEM. Based on this cysteine/methionine free DMEM, modified DMEM without cysteine (but containing methionine) and modified DMEM without methionine (but containing cysteine) were also prepared as described herein. The effect of cysteine and methionine on the stability of PSM was then investigated. After three days of storage at 8° C., only the CAP-stimulated cysteine/methionine free DMEM showed strong capacity for inhibiting the H₂O₂ degradation (FIG. 3b). As can also be seen from FIG. 3b, the presence of either cysteine or methionine (or a combination thereof), results in noticeable H₂O₂ degradation in PSM during storage. The anti-cancer capacity of these PSM on breast cancer (MDA-MB-231) cells was also investigated. In contrast to the experiments performed in the immediately treated media, 3 days of storage at 8° C. causes noticeable degradation of the anti-cancer capacity of PSM, even for the modified DMEM that is free of cysteine and methionine (FIG. 3c). However, compared with other three cases, the cysteine/methionine free DMEM exhibits the strongest capacity to retain the effective species in PSM. Without wishing to be bound by theory, there may be two reasons that the cysteine/methionine free DMEM does not completely inhibit the H₂O₂ degradation. The first may be that additional components other than cysteine and methionine in DMEM may also contribute to the instability of PSM during the storage (FIG. 3a). Modified DMEM without all these reactive components may be as stable as PBS after the CAP irradiation. The second possibility is that some reactive species other than H₂O₂ may also contribute to the anti-cancer capacity of PSM.

FIG. 4 shows the effect of phenol red on the anti-cancer activity of DMEM. As can be seen from FIG. 4, the presence phenol red in the medium significantly consumes H₂O₂ generated during the CAP treatment. The concentration in the CAP stimulated DMEM without phenol red is nearly 100% greater than that observed in the cap stimulated DMEM containing phenol red. Phenol red acts as a pH value indicator in DMEM, and is not necessary for the growth of cells. Accordingly, for the application of CAPSM, a medium (e.g., DMEM) that is free of phenol red will be more suitable for the application of CAP in cancer treatment.

Example 3

The Effect of Components under Freezing Conditions

Despite that the typically accepted optimized storage temperature for the culture medium should be between 2 and 8° C., cryopreservation of PSM may still be necessary under certain circumstances. For example, for most refrigerators utilized in pharmacies, the temperature in the freezing chamber is around −20° C. PSM has, however, been found to even further degrade when stored at temperature around −20° C., than when stored at 22° C. (see, e.g., Ref. 17) or at 4° C. (see, e.g., Ref. 19). A general observation is that freezing aggravates the degradation of PSM. As shown in FIG. 2, both the H₂O₂ concentration (FIG. 2c) and the anti-cancer capacity (FIG. 2d) of the CAP-stimulated PBS are stably retained during the storage at −25° C. Thus, the degradation of the CAP-stimulated DMEM should also be due to the reaction between components in DMEM and the plasma-originated reactive species, such as H₂O₂. To verify this, the stability of H₂O₂ containing DMEM and H₂O₂ containing PBS under freezing conditions for 3 days was investigated. As seen in FIG. 5, and in contrast to the immediately prepared H₂O₂ containing DMEM and immediately prepared H₂O₂ containing PBS, H₂O₂ is completely consumed (FIG. 5a) and is well retained (FIG. 5b) in the frozen DMEM and the frozen PBS at −25° C., respectively. Accordingly, the plasma-originated (or other source originated) H₂O₂ naturally tends to strongly react with specific components in DMEM under freezing conditions. In addition, similar to the trend shown in FIG. 2f, H₂O₂ also shows a natural tendency to be slightly consumed in PBS during the freezing storage. Thus, the degradation of H₂O₂ in PSM under freezing conditions is likely also due to the reaction between H₂O₂ and the components in media and a natural degradation in aqueous solution. The former is likely the main factor.

A further investigation was conducted into which component(s) in DMEM contribute to the degradation of PSM during the freezing storage. This was performed by comparing the degradation of H₂O₂ in 15 amino acids solutions, 1 glucose solution, 2 saline solutions (CaCl₂, MgCl₂), 1 phenol red solution, and PBS. As shown in FIG. 5c, cysteine and methionine remain the two most reactive components in DMEM consuming the plasma-originated H₂O₂ during the freezing storage. However, in contrast to the trend shown in FIG. 3a, all studied components tend to aggravate the degradation of H₂O₂ in the cold plasma-stimulated PBS at −25° C., including tyrosine, tryptophan, and lysine, which actually inhibit the degradation of H₂O₂ in the CAP-stimulated PBS at 8° C. (FIG. 3a). Under freezing conditions, the H₂O₂ degradation in the methionine solution is stronger than that in the cysteine solution.

The anti-degradation effect of the cysteine/methionine-free DMEM under freezing conditions using the above mentioned methods was also investigated. The appearance of either of cysteine and methionine in DMEM will result in the complete consumption of H₂O₂ after 3 days of storage at −25° C. (FIG. 5d). Cysteine-free DMEM is slightly more resistant to degradation of the H₂O₂ than methionine-free DMEM, which is consistent with the trend revealed in FIG. 5c that methionine is more reactive with H₂O₂ than cysteine during the freezing storage. For the cysteine/methionine-free DMEM, more than half of the H₂O₂ has been consumed during the 3 days of storage at −25° C., which is also consistent with trend shown in FIG. 5c that many other components in DMEM also contribute to the instability of PSM. Ultimately, the anti-cancer capacity of these modified DMEM on MDA-MB-231 cells was compared. When the CAP treatment time is just 1 minute (FIG. 5e), the difference between the four experimental groups is not pronounced. Such phenomenon may be due to the low concentration of residual H₂O₂ or reactive species in frozen CAP-stimulated cysteine/methionine-free DMEM, which are too weak to cause a noticeable anti-cancer effect (FIG. 5d). When the CAP treatment time extends to 2 minutes (FIG -cancer capacity of PSM. In contrast, the CAP-stimulated cysteine/methionine free DMEM still causes a 60% anti-cancer growth effect.

Example 4: Addition of 3-Nitro-L-Tyrosine

Based on the results shown in FIG. 3a, it can be seen that tyrosine increases the H₂O₂ concentration in CAP-stimulated PBS during storage at 8° C. Among 15 amino acids in DMEM, only tyrosine and phenylalanine have an aromatic ring structures (FIG. 6a). However, phenylalanine causes noticeable H₂O₂ degradation in the CAP-stimulated PBS during the storage at 8° C. (FIG. 3a). The structural difference between tyrosine and phenylalanine is a hydroxyl substituent on the aromatic ring (FIG. 6a), suggesting that modification of the aromatic ring of an amino acid such as tyrosine may enhances the capacity of the amino acid to inhibit the degradation of H₂O₂ during storage, e.g., at 8° C.

2 mM 3-nitro-L-tyrosine containing DMEM, 2 mM phenylalanine containing DMEM, and 2 mM tyrosine containing DMEM were prepared by dissolving 3-nitro-L-tyrosine, phenylalanine, and tyrosine powders, respectively, in standard DMEM. Subsequently, the stability of H₂O₂ in the CAP -stimulated DMEM, tyrosine-containing DMEM, phenylalanine-containing DMEM, and 3-nitro-L -tyrosine-containing DMEM stored at 8° C. were compared. 3-nitro-L-tyrosine significantly inhibits the degradation of H₂O₂ in PSM (FIG. 6b). In contrast, tyrosine and phenylalanine do not improve the stability of PSM (FIG. 5b). Furthermore, it was observed that some H₂O₂ degradation occurs in the CAP-stimulated 3-nitro-L-tyrosine-containing DMEM and the CAP-stimulated standard DMEM after the storage at 8° C. for 3 days (FIG. 6c). However, despite 60% of plasma-originated H₂O₂ being lost during storage, the CAP-stimulated 3-nitro-L-tyrosine-containing DMEM is more effective than the CAP-stimulated standard DMEM, in which 74% of plasma-originated H₂O₂ is lost during the 3 days of storage. Moreover, after storage, the CAP-stimulated 3-nitro-L-tyrosine -containing DMEM still shows a noticeable anti-breast cancer cell capacity as strong as the immediately treated 3-nitro-L-tyrosine-containing DMEM (FIG. 6d). In contrast, the anti-cancer capacity of the CAP-stimulated standard DMEM significantly decays during the storage (FIG. 6d).

To determine the anti-degradation mechanism of 3-nitro-L-tyrosine in the CAP-stimulated DMEM, it was first investigated whether 3-nitro-L-tyrosine was able to inhibit the H₂O₂ degradation in 0.2 mM cysteine containing PBS, 0.2 mM methionine containing PBS, and 0.4 mM phenylalanine containing PBS. As shown in FIG. 6e, 2 mM 3-nitro-L-tyrosine is able to completely inhibit the H₂O₂ degradation in all three CAP-stimulated amino acid containing PBS solutions at 22° C. Accordingly, the CAP-stimulated DMEM may be stabilized by 3-nitro-L-tyrosine through inhibiting the reaction between some components in DMEM (such as, for example, cysteine, methionine and phenylalanine) with the plasma-originated H₂O₂. The concentration effect of 3-nitro-L-tyrosine on its anti-degradation effect in the CAP-stimulated DMEM was also studied. For the CAP-stimulated 3-nitro-L-tyrosine containing DMEM, the residual H₂O₂ after 3 days of storage increases as the concentration of 3-nitro-L-tyrosine increases from 1 mM to 4 mM (FIG. 6f). After 3 days of storage at 8° C., 4 mM 3-nitro-L-tyrosine-containing DMEM loses 30% of the H₂O₂ originated from the CAP treatment. In contrast, the standard DMEM loses 81% of the plasma-originated H₂O₂ (FIG. 6f). FIG. 6g shows the effect after storage at −25° C. for 3 days.

Example 5

Effect of Well Diameter

FIG. 7 shows how the H₂O₂ concentration and the anti-cancer capacity of the CAP -stimulated media (10% FBS+90% DMEM) can be controlled by the diameter of well on the multi -well plate used in the CAP treatment. FIG. 7a shows the relative H₂O₂ concentration in 1 mL of CAPSM. FIGS. 7b and 7c show the relative viability of glioblastoma (U87) cells (2×10⁴ cells/ml) (FIG. 7b) and breast cancer (MDA-MB-231) cells (2×10⁴ cells/ml) (FIG. 7c) cultured in 1 mL of CAPSM from different multi-wells plates. The treatment times for (b) and (c) were 1 minute. Cells were then cultured for 3 days before the cell viability measurement. The results are presented as the mean±s.d. of three repeated experiments performed in sextuplicate.

As can be seen from FIG. 7, increasing the diameter of the well on a multi-well plate increases the anti-cancer activity of the CAPSM. The diameter of well in a 48-well plate, 24-well plate, 12-well plate, and 6-well plate is 11.0 mm, 15.6 mm, 22.1 mm, and 34.8 mm, respectively. The anti-cancer capacity (the ratio of the decreased cell viability and the initial cell viability, which is also equal to the difference between 1 and the relative cell viability) of the CAP-stimulated media on U87MG cells increase from about 29% to about 75% as the diameter of well increases from 11.0 mm to 34.8 mm. Similarly, the anti-cancer capacity of the CAP-stimulated media on MDA-MB-231 cells increases from about 67% to about 75% as the diameter of well increases from 11.0 mm to 34.8 mm.

Example 6

Effect of the Gap distance Between the Plasma Tube and the Medium Surface

FIG. 8 shows how the H₂O₂ 2 concentration and the anti-cancer capacity of the CAP -stimulated media (10% FBS+90% DMEM) can be controlled by adjusting the gap between the plasma tube and the surface of media during the CAP treatment. FIG. 8a shows the relative H₂O₂ concentration in 1 mL of CAPSM. FIGS. 8b and 8c show the relative viability of U87 cells (FIG. 8b) and MDA-MB-231 cells (FIG. 8c) cultured in 1 mL of CAPSM. For all figures, the CAP treatment time was 1 minute. 6-well plates were used during the CAP treatment. The seeding cell confluence was 2×10⁴ cells/ml. Cells were then cultured for 3 days before the cell viability measurement. Results are presented as the mean±s.d. of three repeated experiments performed in sextuplicate.

As can be seen from FIG. 8, decreasing the gap between the plasma tube and the surface of the medium during CAP treatment increases the anti-cancer activity of the CAPSM. The anti-cancer capacity (the ratio of the decreased cell viability and the initial cell viability, which is also equal to the difference between 1 and relative cell viability) of the CAP-stimulated media on U87MG cells increases from about 51% to about 61% as the gap decreases from 4 cm to 2 cm. Similarly, the anti -cancer capacity of the CAP-stimulated media on MDA-MB-231 cells increases from about 62% to about 70% as the gap decreases from 4cm to 2cm.

Example 8

Magnetic Resonance Imaging

FIG. 9 shows a pre-operative axial post-gadolinium magnetic resonace (MR) image displaying a left temporal glioblastoma (FIG. 9A), and a post-operative axial post-gadolinium MR image displaying a residual line of enhancing tumor (FIG. 9B, light arrow) following direct injection of a CAPSM according to the present disclosure into the brain tumor. The surgical resection cavity (dark arrow) is filled with CAPSM (light coloration).

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The present invention is not to be limited in scope by the specific embodiments described herein. Indeed, various modifications of the invention in addition to those described herein will become apparent to those skilled in the art from the foregoing description and the accompanying figures. Such modifications are intended to fall within the scope of the appended claims.

Patents, patent applications, publications, product descriptions, and protocols are cited throughout this application, the disclosures of which are incorporated herein by reference in their entireties for all purposes.

Claims

1. A stabilized cold atmospheric plasma-stimulated anti-cancer medium,

2. The medium of claim 1, wherein the medium comprises phosphate buffered saline (PBS), Dulbecco's Modified Eagle Medium (DMEM), or a combination thereof.

3. The medium according to claim 1, wherein the medium comprises phosphate buffered saline (PBS).

4. The medium according to claim 1, wherein the medium comprises Dulbecco's Modified Eagle Medium (DMEM).

5. The medium according to claim 1, wherein the medium is stable for a period of up to 7 days, up to 6 days, up to 5 days, up to 4 days or up to 3 days.

6. The medium according to claim 1, wherein the medium is stable for between about 1 and about 7 days, about 1 and about 6 days, about 1 and about 5 days, about 1 and about 4 days or about 1 and about 3 days.

7. The medium according to claim 1, wherein the medium is stable at a temperature of between about −25° C. and about 25° C., between about −25° C. and about 22° C., between about 0° C. and about 22° C., between about 0° C. and about 8° C. or between about 2° C. and about 8° C.

8. The medium according to claim 1, wherein the medium is free of cysteine, methionine, or a combination thereof.

9. The medium according to claim 1, wherein the medium is free of phenylalanine.

10. The medium according to claim 1, wherein the medium is free of phenol red.

11. The medium according to claim 1. wherein the medium comprises 3-nitro-L-tyrosine.

12. The medium according to claim herein the 3-nitro-L-tyrosine is present in the plasma-stimulated media at a concentration of up to 9 mM.

13. The medium according to claim 11, wherein the 3-nitro-L-tyrosine is present in the plasma-stimulated media at a concentration of between about 1 and about 5 mM.

14. The medium according to claim 11, wherein the 3-nitro-L-tyrosine is present in the plasma-stimulated media at a concentration of about 1 mM, about 2 mM. about 3 MM. or about 4 mM.

15. A method of stabilizing and/or enhancing the anti-cancer activity of cold atmospheric plasma-stimulated media, the method comprising:

(i) reducing the amount of cysteine, methionine, or a combination thereof, in the media;

(ii) reducing the amount of phenylalanine in the media;

(iii) reducing the amount of phenol red in the media;

(iv) adding 3-nitro-tyrosine to the media; or

(v) any combination of (i)-(iv).

16. A method of treating a target tissue comprising administering to a patient in need of such treatment a medium according to claim 1.

17. The method according to claim 16, wherein the tissue is cancerous tissue.

18. The method according to claim 16, wherein the tissue comprises lung tissue, bladder tissue, brain tissue, skin tissue, or any combination thereof.

19. A method of enhancing the anti-cancer activity of cold atmospheric plasma—

stimulated media, the method comprising;

(i) increasing the diameter of the well in a multi-plate well,

(ii) decreasing the gap between the plasma tube and the surface of the media during the cold atmospheric plasma treatment; or

(iii) any combination of (i) and (ii).

20. The method according to claim 19, wherein the diameter of the well is increased by about 42% or about 57%.

21. The method according to claim 19, wherein the gap is decreased by about 25%, about 20%, about 17%, or about 14%.