Patent Application
20240408160
The present invention relates to methods for preparing parsnip extracts with enhanced physiological activities, compositions comprising the parsnip extracts prepared by the methods, and methods for promoting respiratory health by using the compositions.
Mammals, including humans, suffer from various respiratory symptoms and diseases due to genetic or environmental factors, and there is an urgent need for innovative solutions to effectively prevent, improve, or treat these respiratory symptoms or diseases.
As reported in, e.g., J Clin Invest, 111:291-297, 2003; N Engl J. Med. 2001; 44(5): 350-62; Toshio Hirano, Cytokine molecular biology, World Science, 2002; Am J Respir Crit Care Med, 2013, 187:347-365; Am J Respir Crit Care Med, 2009, 180:396-406; Biol Pharm Bull, 2012, 35:1752-1760; Am J Respir Crit Care Med, 1997 155, 1441-1447; Am J Physiol Lung CellMol Physiol, 2010, 298: L262-L269; Am J Respir Cell Mol Biol, 2013, 48:531-539;Eur Respir J, 1998, 12:1200-1208; LOS One. 2014 May 15; 9(5): e97784; Respir Res. 2015May 22; 16:59.; J Immunol Res. 2017; 2017:6710278; Respirology. 2016 April; 21(3): 467-75;and Am J Respir Crit Care Med 154(1): 76-81, 1996, which are incorporated herein by reference, research on bronchial asthma and chronic obstructive pulmonary disease is actively underway. However, there are few functional foods or drugs to effectively prevent, improve, or treat bronchial asthma and chronic obstructive disease.
The present invention provides a method for pre-treating raw parsnips into aged parsnips and extracting these aged parsnips to produce parsnip extracts having physiological activities higher than those of raw parsnips. Also, it provides a composition comprising the parsnip extracts having enhanced physiological activities. In addition, it provides a method for promoting respiratory health and/or preventing, improving, or treating respiratory symptoms or diseases by using the composition.
In one aspect, the present invention provides a composition for promoting respiratory health. More specifically, in one aspect, the present invention provides a composition for promoting respiratory health, the composition comprising processed parsnip extracts having a total polyphenol content greater than that of unprocessed raw (natural) parsnips. The promotion of respiratory health may include preventing, improving, or treating diseases, disorders, conditions, or symptoms associated with respiratory diseases. Respiratory diseases may include bronchial asthma or chronic obstructive pulmonary disease. The processed parsnip extracts of the present invention may preferably have a total polyphenol content of at least 1.5 times, preferably at least 2 times, and mor preferably at least 3 times more than the raw parsnips.
In accordance with an embodiment of the present invention, raw parsnips are heat-dried at a predetermined range of temperature (or a predetermined temperature) for a predetermined period of time (or a predetermined time) to the point where the color of the raw parsnips changes to brown or black, and then the extraction process is applied to obtain the extract. As an example, the predetermined range of temperature can be adjusted to a temperature between about 50° C. and about 70° C., and the predetermined period can be adjusted to a period between about 10 and about 30 days. As another example, the predetermined range of temperature can be adjusted to a temperature between about 55° C. and about 65° C., and the predetermined c period can be adjusted to a period between about 10 and about 20 days. As another example, the predetermined range of temperature can be adjusted to a temperature between about 70° C. and about 90° C., and the predetermined period can be adjusted to a period between about 3 and about 10 days. As another example, the predetermined range of temperature can be adjusted to a temperature between about 85° C. and about 90° C., and the predetermined period can be adjusted to a period between 3 and 10 days. According to some other embodiments, the predetermined range of temperature and the predetermined period of time can be adjusted to such an extent that the color of the raw parsnips changes to brown or black and/or that the total polyphenol content of the processed parsnips becomes greater than the total polyphenol content of the raw parsnips.
In another aspect, the present invention provides a method for preparing the extract. More specifically, in another aspect, the present invention provides a method of preparing processed aged parsnip extracts having a total polyphenol content greater than (e.g., at least 2 times greater than) that of unprocessed raw (natural) parsnips. The preparation method includes the steps of heat drying raw parsnips for a predetermined period of time at a predetermined range of temperature, adding alcohol, water, or a mixture thereof to the thus heat-dried parsnips, filtering the supernatant after extraction, and removing unnecessary components. In accordance with an embodiment of the present invention, the heat drying step may be conducted to such an extent that the color of the raw parsnips changes to brown or black and that the total polyphenol content of the processed parsnips becomes greater than the total polyphenol content of the raw parsnips.
The above and other aspects of the invention and representative embodiments of the invention are described in more detail below.
12A is the standard line used to measure the DPPH radical scavenging activity of the parsnip extract according to the another embodiment of the present invention, and .12B is a graph showing the DPPH radical scavenging activity of the parsnip extract sample according to the another embodiment of the present invention. Group A refers to a test group to which the parsnip extract prepared in Example 1 of the present invention, Group P refers to a test group to which the parsnip extract prepared in Example 6 of the present invention, and CONT refers to a control group to which extracts obtained from raw parsnips without performing the pretreatment (aging) process.
For the purpose of promoting an understanding of the principles of the present disclosure, reference will now be made to the embodiments illustrated in the drawings, and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of this disclosure is thereby intended.
In the present disclosure the term “about” can allow for a degree of variability in a value or range, for example, within 10%, within 5%, or within 1% of a stated value or of a stated limit of a range.
In the present disclosure the term “substantially” can allow for a degree of variability in a value or range, for example, within 90%, within 95%, or within 99% of a stated value or of a stated limit of a range.
In this document, the terms “a,” “an,” or “the” are used to include one or more than one unless the context clearly dictates otherwise.
The term “or” is used to refer to a nonexclusive “or” unless otherwise indicated.
In addition, it is to be understood that the phraseology or terminology employed herein, and not otherwise defined, is for the purpose of description only and not of limitation. Any use of section headings is intended to aid reading of the document and is not to be interpreted as limiting. Further, information that is relevant to a section heading may occur within or outside of that section. Furthermore, all publications, patents, and patent documents referred to in this document are incorporated by reference herein in their entirety, as though individually incorporated by reference. In the event of inconsistent usages between this document and those documents so incorporated by reference, the usage in the incorporated references should be considered supplementary to that of this document; for irreconcilable inconsistencies, the usage in this document controls.
In one aspect, the present invention provides parsnip extracts having physiological activities greater than raw parsnips. In accordance with an embodiment of the prevent invention, raw parsnips are pretreated to make aged or processed parsnips, and the aged or processed parsnips are subjected to an extraction process, thereby preparing the parsnip extracts of the invention. The parsnip extracts of the invention have physiological activities greater than raw parsnips.
A process of pretreating raw parsnips was reported in Plant Foods for Human Nutrition (2020) 75:292-297), but the process takes too much time (4 weeks) to complete and requires high temperature (80° C.) heat treatment and a high level of humidity (95%), which limits its application in industrial sites. There is an urgent need for a new method of pre-treating raw parsnips with a shorter period of time and milder process conditions.
According to embodiments of the present invention, it is possible to obtain parsnip extracts with significantly improved physiological activities compared to raw parsnips by pre-treating raw parsnips with mild process conditions and/or for a relatively short time.
In accordance with embodiments of the invention, raw parsnips are pretreated to make aged parsnips. The raw parsnips can be cut into pieces before pretreatment. The shape (e.g., round, spherical, cuboid, cube, etc.) and size (e.g., large, medium, small, etc.) can be adjusted accordingly as needed. During the pretreatment process, temperature, time, and/or pressure can be set appropriately.
For example, the temperature can suitably be heated to about 40˜90° C., 45˜85° C., 50˜80° C., 55˜75° C., or 60˜70° C. However, the above-listed ranges are only examples, and the temperature can be adjusted accordingly as needed. The heating can be suitably conducted for a predetermined period of time. For example, it can be heated for about 1˜30days, 5˜25 days, 10˜20 days, or 13˜17 days. However, the above-listed ranges are only illustrative, and the heating period can be adjusted accordingly as needed. The pressure condition can suitably be adjusted appropriately during the heating. For example, it can be done under atmospheric pressure conditions or at high pressure. However, the above pressure conditions are only examples, and the pressure conditions can be adjusted accordingly as needed. For example, the heating and drying process can be conducted either wet or dry. If necessary, wet drying and dry drying can be used together.
After the pretreatment, water, alcohol, or a mixture thereof is added for extraction. The type of alcohol can be appropriately selected according to needs. Preferably, ethanol may be chosen. The concentration of alcohol can be adjusted as needed. Preferably, about 10˜45% alcohol can be used. Preferably, about 15˜40% alcohol can be used. Even more preferably, 20˜30% alcohol can be used. However, these alcohol concentration ranges are only illustrative and can be adjusted as needed. Preferably, water, alcohol, or a water/alcohol mixture can be used in greater amount than the raw parsnips (e.g., 2, 3, 4, 5, 6, . . . times raw parsnips).
Thereafter, the aged parsnips are extracted in a stirring shaker. The temperature and time for the extraction can be selected according to needs. For example, they can be extracted at room temperature for 24 hours. Supernatants are filtered after the extraction, and additional extraction can be conducted, if needed. All supernatants obtained in the extraction process are collected, and the collected supernatants are concentrated under reduced pressure to remove residual organic solvents and treated with nitrogen to remove residual moisture.
In another aspect, the present invention provides a composition comprising the parsnip extracts having physiological activities greater than raw parsnips for use in preventing, improving (alleviating), or treating respiratory diseases, disorders, conditions, or symptoms.
As used herein, the term “composition” is intended to contain the extract obtained by the above-described methods or contain any other product resulting directly or indirectly from the extract. The term “composition” is intended to contain a combination of at least one of the extract and at least one of the product resulting from the extract, a combination of two or more of the extracts, or a combination of two or more of the products resulting from the extracts.
As used herein, the term “composition” refers to a mixture of a pharmaceutically or therapeutically active component (ingredient) with one or more other components, which may be chemically or biologically active or inactive. Such components may include, but not limited to, carriers, stabilizers, diluents, dispersing agents, suspending agents, thickening agents, excipients, and adjuvants.
Any suitable pharmaceutically acceptable carriers, stabilizers, diluents, dispersing agents, suspending agents, thickening agents, excipients, and adjuvants known to those of ordinary skill in the art for use in pharmaceutical compositions may be selected and employed in the compositions described herein. As used herein, the term “acceptable” with respect to a formulation, composition, or ingredient, as used herein, means having no persistent detrimental effect on the general health of the subject being treated. As used herein, the term “carrier” refers to chemical or biological material that can facilitate the incorporation of a therapeutically active ingredient(s) into cells or tissues. Examples of the pharmaceutically acceptable carrier include lactose, dextrose, sucrose, sorbitol, mannitol, starch, acacia gum, calcium phosphate, alginate, gelatin, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, water, syrup, methyl cellulose, methylhydroxybenzoate, propylhydroxybenzoate, talc, magnesium stearate, mineral oil, and the like, but it is not limited thereto.
Suitable excipients may include, for example, water, pharmaceutically acceptable organic solvents such as paraffins (e.g., petroleum fractions), vegetable oils (e.g. groundnut or sesame oil), mono-or polyfunctional alcohols (e.g., ethanol or glycerol), carriers such as natural mineral powders (e.g., kaoline, clays, talc, chalk), synthetic mineral powders (e.g., highly dispersed silicic acid and silicates), sugars (e.g., cane sugar, lactose and glucose), emulsifiers (e.g., lignin, spent sulphite liquors, methylcellulose, starch and polyvinylpyrrolidone), and lubricants (e.g., magnesium stearate, talc, stearic acid and sodium lauryl sulphate).
The compositions described herein may be in the form of a solid, liquid, or gas (aerosol). For example, they may be in the form of tablets (coated tablets) made of, for example, collidone or shellac, gum Arabic, talc, titanium dioxide or sugar, capsules (gelatin), solutions (aqueous or aqueous-ethanolic solution), syrups containing the active substances, emulsions or inhalable powders (of various saccharides such as lactose or glucose, salts and mixture of these excipients with one another), and aerosols (propellant-containing or-free inhale solutions). Also, the compositions described herein may be formulated for sustained or slow release.
In still another aspect, the present invention provides a method of using a composition comprising the parsnip extracts having enhanced physiological activities to promote respiratory health and/or to prevent, improve, or treat respiratory symptoms, conditions, or diseases.
As used herein, the term “treat,” “treating” or “treatment” refers to methods of alleviating, abating, ameliorating, inhibiting, relieving, stopping, or preventing a disease, disorder, condition, or symptom. The term also refers to methods of alleviating, abating, ameliorating, inhibiting, relieving, stopping, or preventing the underlying causes of the disease, disorder, condition, or symptom.
As used herein, the term “subject” or “patient” encompasses mammals and non-mammals. Examples of mammals include, but are not limited to, humans, chimpanzees, apes monkeys, cattle, horses, sheep, goats, swine; rabbits, dogs, cats, rats, mice, guinea pigs, and the like. Examples of non-mammals include, but are not limited to, birds, fishes and the like.
As used herein, the term “administration” or “administering” of the subject composition refers to providing a composition of the invention and/or a prodrug thereof to a subject in need of treatment.
As used herein, the term “effective amount” or “therapeutically effective amount” refer to a sufficient amount of an active ingredient(s) described herein being administered which will, for example, relieve to some extent one or more of the symptoms of the disease or condition being treated. The result can be reduction and/or alleviation of the signs, symptoms, or causes of a disease, or any other desired alteration of a biological system. For example, an “effective amount” for therapeutic uses is the amount of the composition as disclosed herein required to provide a clinically significant decrease in disease symptoms. An appropriate “effective” amount in any individual case may be determined using techniques, such as a dose-escalation study.
In addition, such compositions may be administered singly or in combination with one or more additional functional or therapeutic agents. The methods of administration of such compositions may include, but are not limited to, intravenous administration, inhalation, oral administration, rectal administration, parenteral, intravitreal administration, subcutaneous administration, intramuscular administration, intranasal administration, dermal administration, topical administration, ophthalmic administration, buccal administration, tracheal administration, bronchial administration, sublingual administration or optic administration. The method of administration of the composition is determined according to the degree of symptoms. In addition, the dosage of the active ingredient in the composition may vary depending on the route of administration, the severity of the disease, the age, the sex, and weight of the patient, and may be administered once to several times a day.
Compositions provided herein may be administered by way of known formulations, including tablets, capsules or elixirs for oral administration, suppositories for rectal administration, sterile solutions or suspensions for parenteral or intramuscular administration, lotions, gels, ointments or creams for topical administration, and the like. In some embodiments, such compositions are formulated as tablets, pills, capsules, a liquid, an inhalant, a nasal spray solution, a suppository, a solution, a gel, an emulsion, an ointment, eye drops, or ear drops.
The therapeutically effective amount may vary depending on, among others, the disease indicated, the severity of the disease, the age and relative health of the subject, the potency of the compound administered, the mode of administration and the treatment desired. The required dosage will also vary depending on the mode of administration, the particular condition to be treated and the effect desired.
The above and other embodiments and uses will be apparent to one skilled in the art in light of the present disclosures. The following examples are provided merely as illustrative of various embodiments and shall not be construed to limit the invention in any way.
Hereinafter, the present invention will be described in more detail through examples. These examples are only intended to illustrate the present invention in more detail, and it will be apparent to those skilled in the art that the scope of the present invention is not limited by these examples according to the gist of the present invention.
Raw parsnips were peeled, washed, and cut to pieces so that each piece was about 200g. The parsnip pieces were placed in a drying chamber maintained at 55° C.˜65° C. and heat-dried for at least 10 days. 30% alcohol (or a mixture of alcohol and water) was added to the heat-dried parsnip pieces. The extraction was performed at room temperature (20° C. ˜25° C.) for 24 hours in a stirred incubator (125 rpm). The supernatant was filtered by a filter paper (Whatman No 4). The parsnips remaining on the filter paper were extracted one more time under the same conditions, and the supernatant was collected one more time. The thus-obtained final processed parsnip extract was subjected to reduced pressure extraction to remove residual organic solvents and then subjected to nitrogen treatment to remove residual moisture. The preparation process is illustrated in
1. Determination of Total Polyphenol Content
2.5 mg/mL, 5.0 mg/mL, and 10.0 mg/mL of the final processed parsnip extracts prepared in Example 1 were prepared. 100 μL of 2.5 mg/mL of the final processed parsnip extract and 200 μL of 2% Na2CO3 were reacted for 3 minutes, 100 μL of 5.0 mg/mL of the final processed parsnip extract and 200 μL of 2% Na2CO3 were reacted for 3 minutes, and 100 μL of 10.0 mg/mL of the final processed parsnip extract and 200 μL of 2% Na2CO3were reacted for 3 minutes. To the resulting mixtures, 10 μL of 50% Folin-ciocalteu reagent was added and reacted for 3 minutes, and then absorbance was measured at 720 nm. As for a blank, the organic solvent (i.e., 15% DMSO), which was used to dissolve parsnip extract, was mixed and reacted with 2% Na2CO3 for 3 minutes. For the control, 50% Folin-ciocalteu reagent was added to the blank (i.e., the mixture of 15% DMSO and 2% Na2CO3) and reacted for 3 minutes. The content of total polyphenols was shown against a calibration curve using gallic acid.
As shown in
2. DPPH Radical Scavenging Activity
To evaluate the antioxidant properties of the processed parsnips, the DPPH radical scavenging test was performed in addition to the analysis of the total polyphenol content. 2.5 mg/mL, 5.0 mg/mL, and 10.0 mg/mL of the final processed parsnip extracts prepared in Example 1 were prepared. 20 μL of 2.5 mg/mL of the final processed parsnip extract and 80 μL of 0.3 mM DPPH (2,2-diphenyl-1-picrylhydrazyl) reagent were reacted for 1 hour under dark condition, 20 μL of 5.0 mg/mL of the final processed parsnip extract and 80 μL of 0.3 mM DPPH (2,2-diphenyl-1-picrylhydrazyl) reagent were reacted for 1 hour under dark condition, and 20 μL of 10.0 mg/mL of the final processed parsnip extract and 80 μL of 0.3mM DPPH (2,2-diphenyl-1-picrylhydrazyl) reagent were reacted for 1 hour under dark condition. Then, absorbance was measured at 720 nm. As for a blank optical density, 20 μL of the organic solvent (i.e., 10% DMSO), which was used to dissolve parsnip extract, was mixed with 80 μL of 100% ethanol for 1 hour, and as for the control optical density, 20 μL of the organic solvent (i.e., 10% DMSO) was mixed with 0.3 mM DPPH (80 μL) and then reacted for 1 hour. Antioxidant activity was calculated by the following formula.
As shown in
1. Cytotoxicity Assay
Based on the results of Example 2, it was observed that after a certain period of time (e.g., 20 days), the physiological activity of the processed parsnip did not increase linearly even if additional dry heating processing was conducted. Experiments were conducted to establish the maximum concentration of processed parsnips (20-day aged parsnips) that do not cause cytotoxicity. To verify that the processed parsnips have inhibitory effect on respiratory inflammation, BEAS-2B human bronchial epithelial cells were cultured at 37° C. and 5% CO2 saturation. The cultured cells are dispensed at a 96-well place with conditions of 5×104 cells/cm2 for cytotoxicity experiments and stabilized for 12 hours, and the processed parsnips (here, 20-day processed parsnips) were treated at various concentrations. More specifically, the concentrations were 0 mg/mL (in this case, phosphate buffered saline was treated instead of the processed parsnip), 0.625 mg/mL, 1.25 mg/mL, 2.5 mg/mL, 5 mg/mL, and 10 mg/mL. After 24 hours, cell viability was determined by MTT assay, and the highest concentration (here, 2.5 mg/mL) that did not affect the cell viability was determined (
Acrolein is one of the indicators of air pollution and is a highly reactive aldehyde family. It is known to not only cause oxidative stress in cells but also bind to various macromolecules (e.g., DNA or proteins) and induce inflammatory responses and apoptosis. Based on the results of the above-mentioned study, it was evaluated at the cellular level whether parsnip extract processed for 20 days under non-toxic treatment conditions had a significant preventive effect on acrolein-induced inflammation. More specifically, the processed parsnip extract of the present invention was treated to human bronchial epithelial cells (BEAS-2B cells), and then 160 μM of acrolein was treated. Gene expression in the signaling system associated with inflammation was analyzed. As shown in
Similarly, it was also verified at the cellular level whether the processed parsnip extract of the present invention has a significant effect of treating acrolein-induced inflammation under non-toxic treatment conditions. More specifically, 160 μM of acrolein was treated to BEAS-2B human bronchial epithelial cells, and then the processed parsnip extracts were treated. Gene expression of signaling systems involved in inflammation was analyzed. Although not shown here, we could obtain results similar to
1. Inflammatory Markers
Based on the results of the above cell experiments, C57BL6 mice were used to verify the effect of the processed parsnip on markers of respiratory inflammation. More specifically, C57BL6 male mice were orally administered with 10 mg/kg bw of the processed parsnip extract in accordance with the present invention for 2 weeks. From day 9, acrolein was nasally administered for 5 days (nasal installation; 10 μg/kg bw). On day 14, the animals were sacrificed, and inflammatory markers were analyzed (
2. Cytokine Protein Content
The protein content of various pro-inflammatory cytokines contained in the blood samples obtained from the test animal was analyzed. The inflammatory cytokines in the blood shown in
3. Inflammatory Gene Expression in Lung Tissue
In addition to the systemic inflammatory response identified in
4. H&E Staining Assay for Lung Tissue
Histological analysis of the lung tissue was performed by H&E staining. As shown in
5. PAS Staining Assay for Lung Tissue
The lung tissue was PAS stained to determine the degree of mucus accumulation in the lung tissue. As shown in
As in the cell model study, in the animal model study, it was verified whether the processed parsnip extract of the present invention at a concentration not causing toxicity has a significant effect to treat acrolein-induced inflammation. More specifically, acrolein was first treated to C57BL6 male mice, the processed parsnip extract was then treated, and inflammatory markers were analyzed. Although not shown here, we could obtain results similar to those shown in
As in Example 1, raw parsnips were peeled, washed, and cut to pieces so that each piece was about 200 g. The parsnip pieces were placed in a drying chamber maintained at 85˜90° C. and heat-dried for 6 days. 30% alcohol (or a mixture of alcohol and water) was added to the heat-dried parsnip pieces. The extraction was performed at room temperature (20˜25° C.) for 24 hours in a stirred incubator (125 rpm). The supernatant was filtered by a filter paper (Whatman No 4). The parsnips remaining on the filter paper were extracted one more time under the same conditions, and the supernatant was collected one more time. The thus-obtained final processed parsnip extract was subjected to reduced pressure extraction to remove residual organic solvents and then subjected to nitrogen treatment to remove residual moisture. The preparation process is illustrated in
1. DPPH Radical Scavenging Activity
To evaluate the antioxidant properties of the processed parsnips, the DPPH radical scavenging test was performed. 2.5 mg/mL, 5.0 mg/mL, and 10.0 mg/mL of the final processed parsnip extracts prepared in Example 1 were prepared. 20 μL of 2.5 mg/ml of the final processed parsnip extract and 180 μL of 0.2 mM DPPH (2,2-diphenyl-1-picrylhydrazyl) reagent were reacted for 1 hour under dark condition, 20 μL of 5.0 mg/mL of the final processed parsnip extract and 180 μL of 0.2 mM (2,2-diphenyl-1-picrylhydrazyl) reagent were reacted for 1 hour under dark condition, and 20 μL of 10.0 mg/mL of the final processed parsnip extract and 180 μL of 0.2 mM (2,2-diphenyl-1-picrylhydrazyl) reagent were reacted for 30 minutes under dark condition. Then, absorbance was measured at 517 nm.
For the control, vitamin C (0˜100 ug/mL) was reacted with DPPH reagent under the same conditions. Using the measured absorbance value, a standard line (
2. ABTS Radical Scavenging Activity
The antioxidant activity of the processed parsnip extracts was assayed by using 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid (ABTS) and 2,2-Azobis(2-methylpropionamidine)dihydrochloride (AAPH). ABTS was dissolved in 100 mL of PBS at a concentration of 2.5 mM, heated at 70° C. for 1 hour, and cooled at room temperature for 20˜30 minutes. AAPH was dissolved in 100 mL of PBS at a concentration of 1 mM, heated at 70° C. for 1 hour, and cooled at room temperature for 20˜30 minutes. As a standard solution, vitamin C was prepared by continuous dilution from 100 μg/mL to 0 μg/mL. The sample solution was continuously diluted so that the absorbance at 734 nm could be between 0.65 and 0.9. 10 μL of the standard solution and 10 μL of the sample solution respectively were placed in a 96-well plate, 190 μL of ABTS solution was added, and the mixture was reacted at room temperature for 10 minutes. Based on the absorbance data read at 734 nm, the radical scavenging activity of the sample was calculated by reading against the vitamin C concentration by using the standard equation (
1. Cytotoxicity Assay
To verify whether the antioxidant activity of processed parsnip extracts according to the present invention acts as a protective effect on lung cells, the efficacy test was conducted by using human primary bronchial/tracheal epithelial cells. The cells were cultured in 37° C., 5% CO2 environment with 10% FBS and 1% penicillin-streptomycin in DMEM/F-12medium. The cells were inoculated in a 96-well plate at a density of 5×104 cells/well and were grown for 24 hours. The parsnip extracts at various concentrations (0, 25, 50, 100, 200,and 400 μg/mL) were prepared, 100 μL of the respective parsnip extractions were added to the well, and the cells were incubated for 24 hours. MTT solution was prepared in PBS at a concentration of 5 mg/mL, 10 μL of the MTT solution was added to each well to make the final concentration of 0.5 mg/mL, and the cells were incubated for 4 hours. The medium was removed, and 100 μL of DMSO was added to dissolve the formazan crystals. Absorbance was measured at 570 nm, and background absorbance at 630 nm was calibrated. Cell viability was calculated as a percentage compared to the control group. All experiments were repeated three times. Data were expressed as mean±standard deviation. Statistical analysis was performed using GraphPad Prism using one-way analysis of variance (ANOVA) and Tukey's post-hoc test. A p-value of less than 0.05 was considered statistically significant. As shown in
2. Effect of Processed Parsnip Extract to Protect Lung Cell from Inflammation Induced by Acrolein
Experiments were conducted with the maximum concentration of processed parsnips that do not cause cytotoxicity. 20 ug/mL of LPS was administered to a group for 24 hours to induce inflammation. The processed parsnip extract sample B and LPS were treated to the other group. After 24 hours, cell viability was determined by MTT assay (
Similarly, it was also verified at the cellular level whether the processed parsnip extract of the present invention has a significant effect of treating LPS-induced inflammation under non-toxic treatment conditions. More specifically, LPS was treated to human primary bronchial/tracheal epithelial cells, and then the processed parsnip extracts were treated. Gene expression of signaling systems involved in inflammation was analyzed. Although not shown here, we could obtain results similar to
The present application claims priority to U.S. Application No. 63/507,468 filed on Jun. 11, 2023 and U.S. Application No. 63/515,341 filed on Jul. 25, 2023, which applications are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| 63507468 | Jun 2023 | US | |
| 63515341 | Jul 2023 | US |
