Saffron treatment method for mammalian maladies

Abstract

A variety of medicinal compounds comprising Crocus sativus for the treatment of a plurality of medical ailments are described. A method of creating a Crocus sativus extract is also described. In addition, a variety of embodiments and methods of utilizing inhalation therapeutic delivery mechanisms including nebulizers and vaporizers for the vaporization of Crocus sativus comprising medicinal compounds and extracts are disclosed.

Claims

1. A primary container suitable for delivering a medicinal formulation for inhalation therapy, the primary container comprising: a secondary enclosure positioned within the primary container, wherein the enclosure comprises an absorbent material; a mixture comprising Crocus sativus extract residing within the secondary enclosure, wherein the adsorbent material encases the mixture within the secondary enclosure; and wherein the primary container is receivable within an electronic cigarette.

2. The primary container of claim 1 wherein a release valve is positioned within an opening of the primary container, wherein the release valve is capable of opening and closing the primary container opening.

3. The primary container of claim 1 wherein the primary container is a canister capable of withstanding a vapor pressure contained within an interior therewithin.

4. The primary container of claim 1 wherein the mixture comprises a solvent selected from the group consisting of water, ethyl alcohol and combinations thereof.

5. The primary container of claim 1 wherein the primary container is receivable within an inhaler device.

6. The primary container of claim 1 wherein a propellant resides within the secondary enclosure.

7. The primary container of claim 4 wherein the mixture comprises a concentration of at least 0.01 mg of Crocus sativus extract to about 1 ml of solvent.

8. The primary container of claim 1 wherein the mixture further comprises an herb, a petroleum jelly, a spice, a vitamin, turmeric, lavender, cinnamon, mint, and combinations thereof.

9. The primary container of claim 1 wherein the secondary enclosure comprises a bag, a pillow, or a pouch.

10. A primary container suitable for delivering a medicinal formulation for inhalation therapy, the primary container comprising: a secondary container positioned within the primary container, wherein the secondary container comprises an adsorbent material; a mixture comprising Crocus sativus extract residing within the secondary container, wherein the adsorbent material encases the mixture within the secondary container; and wherein the primary container is receivable within an electronic cigarette.

11. The primary container of claim 10 wherein the medicinal formulation further comprises an aromatic, an herb, a hydrocarbon, a flavoring, a glycerol, a spice, a petroleum jelly, an oil, a tincture, a vitamin, or a combination thereof.

12. The primary container of claim 10 wherein the medicinal formulation comprises a solvent selected from the group consisting of water, ethyl alcohol, vinegar, and combinations thereof.

13. The primary container of claim 10 wherein the primary container is receivable within an inhaler device or an electronic cigarette.

14. The primary container of claim 10 wherein the secondary container comprises a bag, a pillow, or a pouch.

15. A primary container suitable for delivering a medicinal formulation for inhalation therapy, the primary container comprising: a secondary container positioned within the primary container, wherein the secondary container comprises an adsorbent material selected from the group consisting of cotton, a paper, a woven fabric, a non-woven fabric, and combinations thereof; a mixture comprising Crocus sativus extract residing within the secondary container, wherein the adsorbent material encases the mixture therewithin; and wherein the primary container is receivable within an electronic cigarette.

16. The primary container of claim 15 wherein the medicinal formulation further comprises an aromatic, an herb, a hydrocarbon, a flavoring, a glycerol, a spice, a petroleum jelly, an oil, a tincture, a vitamin, or a combination thereof.

17. The primary container of claim 15 wherein the medicinal formulation comprises a solvent selected from the group consisting of water, ethyl alcohol, vinegar, and combinations thereof.

18. The primary container of claim 15 wherein the primary container is receivable within an inhaler device or an electronic cigarette.

19. The primary container of claim 15 wherein the secondary container comprises a bag, a pillow, or a pouch.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a flow chart of a preferred Crocus sativus extraction process of the present invention.

(2) FIG. 2 illustrates a cross-sectional view of an embodiment of an inhaler device that may be used to deliver the Crocus sativus extract or therapeutic mixture thereof.

(3) FIG. 3A shows a cross-sectional view of an embodiment of a jet nebulizer that may be used to deliver the Crocus sativus extract or therapeutic mixture thereof.

(4) FIG. 3B is a cross-sectional view of an embodiment of an ultrasonic nebulizer that may be used to deliver the Crocus sativus extract or therapeutic mixture thereof.

(5) FIG. 4 illustrates a cross-sectional view of an embodiment of a portable inhaler that may be used to deliver the Crocus sativus extract or therapeutic mixture thereof.

(6) FIG. 5 is a cross-sectional view of an embodiment of an electronic cigarette which may be used to deliver the Crocus sativus extract or therapeutic mixture thereof.

SUMMARY OF THE PRESENT INVENTION

(7) The present invention is directed to the use of saffron (Crocus sativus) in the treatment of various medical maladies affecting the mammalian body. Crocus sativus, commonly known as saffron, is a perennial stemless herb that is widely cultivated in different parts of the world, particularly Greece, India, Iran, and Spain. Saffron has been known to be used in traditional medicine as an anodyne, antidepressant, sedative, respiratory decongestant, anticatarrhal, expectorant, antispasmodic, eupeptic, stomachic, carminative, diaphoretic, gingival sedative, aphrodisiac, and emmenagogue.

(8) In view of its wide range of medical uses, saffron has undergone extensive phytochemical and biochemical studies with a variety of biologically active constituents being isolated (Srivastava, R.). Chemical studies of Crocus sativus stigmas appear to indicate that it possesses medically beneficial carotenoids such as crocetin (also called -crocetin or crocetin-I), its glycosidic forms being digentiobioside (crocin), gentiobioside, glucoside, gentioglucoside and diglucoside, -crocetin (monomethyl ester), -crocetin (dimethylester), trans crocetin isomer, 13-cis-crocetin, -carotene, -carotene, lycopene, zeaxanthin and mangicrocin, a xanthone-carotenoid glycosidic conjugate (Bhargava, V. K.). These carotenoids and other constituents contained within Crocus sativus are currently being investigated for a number of medical ailments, such as the treatment of Alzheimer's disease, respiratory disorders, Parkinson's disease seizures, diabetes, blood pressure disorders and cancer (Bhargava, V. K. and Abdullaev, F. I.). In addition, studies by M. Agha-Hosseini et al, have shown Crocus sativus to be particularly beneficial in the treatment of pre-menstrual symptoms.

(9) The present invention, therefore, provides methods and embodiments for optimization of the medicinal benefits of saffron. Specifically, embodiments of Crocus sativus comprising extracts, compounds and mixtures are provided for use in the treatment of various medical ailments, particularly for the treatment of pre-menstrual symptoms.

(10) In addition, embodiments and methods are provided for use of Crocus sativus comprising extracts, compounds and mixtures for use with various inhalation apparatus and methods such as vaporization and nebulization.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

(11) Before saffron can be used for its medicinal properties, it is first modified to extract, modify and concentrate the carotenoids comprised within the Crocus sativus. FIG. 1 is a flow chart that illustrates a preferred embodiment of the Crocus sativus extraction process of the present invention. In the embodiment, a constituent mixture comprising Crocus sativus is steeped in a heated solvent or liquid to extract and concentrate the Crocus sativus therewithin. The steeped Crocus sativus extract may then be mixed with other solvents and/or chemicals to further modify the medicinal mixture. This modification process preferably utilizes a steeping of the Crocus sativus combined with other optional herbs and extracts in a heated solvent. The steeping process preferably extracts and concentrates the carotenoids comprised within the Crocus sativus.

(12) In a first step of the preferred process, a solvent, such as water is heated to a desired temperature. In step 2, the constituents comprising Crocus sativus are added to the heated solvent and are allowed to steep in the solvent for a period of time to thereby extract and concentrate the medicinal properties of the Crocus sativus. In the following step, the extract constituents are removed from the solvent and the extract is cooled, for example, to room temperature. The Crocus sativus concentrated extract is now ready to be utilized for therapeutic applications, particularly with an inhalation delivery device.

(13) In addition, other constituents may also be added to the saffron and steeped together. Examples of additional non-limiting constituents that may be added to the mixture include herbs and spices such as turmeric, lavender, cinnamon, various mints, flavorings, vitamins, aromatics or other organic materials. In a preferred embodiment, at least one of the constituents may be soluble in water, ethyl alcohol or a mixture thereof.

(14) In a preferred embodiment, Crocus sativus is added to water, such as distilled water. Other liquids or solvents such as, but not limited to, hydrocarbons, oils such as hemp and vegetable oils, alcohols such as ethyl alcohol, vegetable glycerins, tinctures, vinegar, glycerol, ether, infused liquids or combinations thereof, may be used as a steeping solvent. For the purpose of the present invention, the term steep is defined as soaking in a liquid such as water to soften, cleanse, extract or infuse a constituent. The term extract is defined herein as a preparation containing the active ingredient of a substance in concentrated form. The term infusion is defined herein as the extraction of an active substance through the use of steeping. The term tincture is defined herein as an extract from a plant or animal. Tinctures may comprise a variety of solvents including but not limited to ethyl alcohol, vinegar, glycerol, ether and propylene glycol. A tincture comprising Crocus sativus may be placed directly in the mouth, such as on the tongue or alternatively may be positioned within an inhaler, nebulizer, vaporizer or container thereof.

(15) In a preferred embodiment, the solvent, such as water is first heated to about 100 C. (212 F.) at which point the solvent is removed from the heat source. Saffron is then added to the heated solvent, i.e., water, to extract and concentrate the Crocus sativus. The saffron may comprise any commercially available form. Non-limiting examples are as dried threads, as a powder or combination thereof. In addition, the saffron may be contained within a fabric, a paper envelope or package such that the solvent and the Crocus sativus extract is able to permeate therethrough. The form of the package is non-limiting and may comprise a pouch, a pillow, a bag, or similar container. Alternatively, the saffron may be added directly into the solvent without being placed within a separate package or container. The steeped medium may be prepared in advance and may be bottled for future use.

(16) The saffron may be steeped using a non-limiting combination of time intervals and solvent temperatures. For example, saffron may be steeped for a longer period of time in a solvent (i.e., water) having a temperature of 10 C. (50 F.) as compared to steeping in a solvent having a temperature of about 96 C. (205 F.). Table 1 shown below, illustrates an embodiment of the relationship between solvent temperature and steeping time. In a preferred embodiment, steeping time may range from about 30 seconds to about 15 minutes. However, a preferred steeping time ranges from about 1 minute to about 5 minutes.

(17) TABLE-US-00001 TABLE 1 Solvent Temperature Steeping Time ( C.) (minutes) 10 15 35 10 60 5 85 3 100 1

(18) In addition, the amount of saffron added to the solvent also affects the optimal steeping time interval. In general, the more saffron added to the solvent, a longer steeping time is required to extract an effective therapeutic amount of Crocus sativus. A preferred steeping temperature is about 65 C. (150 F.) for a period of time commensurate with the amount of saffron added. Table 2 shown below, illustrates preferred steeping times for different amounts of saffron. These time intervals should be added to the previously given time intervals based on liquid temperature. For example, when steeping about one gram of saffron at 60 C., the total preferred steeping time is about 7 minutes, 5 minutes for 60 C. solvent (Table 1) and an additional 2 minutes for the additional 0.75 g of saffron.

(19) TABLE-US-00002 TABLE 2 Amount of Saffron Additional Steeping Time (g) Interval (minutes) 0.25 0 0.50 1 1.0 2 2.0 4 3.0 6

(20) Color of the steeped solvent may be used as an indicator to determine the concentration level of extraction. The concentration level of extraction is important, as the darker the infused solvent appears, typically the more concentrated the Crocus sativus extract. Thus, concentration of the extract can be controlled by analysis of the color and hue of the appearance of the extract. Color intensity may range from a light yellow to a darker orange color. The longer the time interval the saffron is steeped at a given temperature, generally the deeper and darker the extract color and, subsequently, the more concentrated the infusion or extract. Also affecting color and infusion or extract concentration is the amount of saffron being steeped. In general, the greater the amount of saffron being steeped, the deeper and darker the color and, subsequently, the more concentrated the infusion or extract. Therapeutic saffron steep levels will vary from individual to individual. In a preferred embodiment, the concentration of Crocus sativus in the solvent is at least about 0.01 mg/ml. In a more preferred embodiment, the concentration of the Crocus sativus in the ranges from about 0.01 mg/ml to about 10 mg/ml. The solvent may comprise water, ethyl alcohol, or combinations thereof.

(21) Once the saffron is steeped, the infused solvent may either be placed in a steamer or humidifier, a nebulizer, an aerosol delivery device, such as an inhaler or similar vaporizing or humidifying apparatus. Other therapeutic agents may be added to the infused solvent. Delivery of the vapor or mist may be assisted using oxygen, compressed air, or ultrasonic power.

(22) A non-limiting example for preparing a steeped inhalation medium is as follows. Heat about 235 ml or about 235 g of water, preferably distilled water, to a temperature of about 100 C. Remove the water from the heat and allow the water to cool to a temperature of about 65 C. (150 F.) It is important to allow any solvent being used to steep saffron to cool to at least 65 C. (150 F.) before steeping, otherwise the therapeutic advantage of the steeped agent may be significantly diminished, and might even be rendered ineffective.

(23) After the solvent reaches the desired temperature, about 0.25 g of the Crocus sativus stigma or other saffron form is added to the heated solvent and allowed to steep from about 5 to about 10 minutes, depending upon the desired concentration strength. After the concentration of the Crocus sativus is achieved, the steeping constituents are removed from the infused solvent, for example by a straining process. The extract is then cooled to about 25 C. at which it is then placed within a container or chamber for inhalation therapy.

(24) The mixture comprising the solvent and Crocus sativus is preferably stirred until the desired concentration is achieved, as evidenced by the preferred color change of the steeped mixture. In a preferred embodiment, the mixture of the Crocus sativus and solvent is steeped such that the color of the mixture changes to an orange color having a Pantone identification number of 144C. Typically, the steeping mixture changes from a brown color, having a Pantone identification number ranging from 127C to 129C, to a darker brown, having a Pantone identification number ranging from 135C to 137C or in the Pantone identification number 1375 color family, and then finally to an orange color, having a Pantone identification number of 144C.

(25) The Pantone Color Matching System is a standardized color reproduction system that may be used to accurately reproduce the intensity and hue of a color. The system uses standardized color mixtures to accurately replicate various shades and intensity of colors. The Pantone Matching System may be used as a means by which to assess readiness of the steeped medium for use in inhalation therapy. Pantone Guides provide a number of color swatches for color matching. Pantone is a registered trademark of Pantone LLC, of Carlstadt, N.J.

(26) FIG. 2 illustrates an embodiment of an inhaler 10 that may be used to deliver the Crocus sativus infusion or medicinal extract. In a preferred embodiment, the inhaler 10 comprises a housing 12 having an opening 14 that extends to a mouth piece 16. In a preferred embodiment, a distal end 18 of the opening 14 is designed to receive an inhaler container or vessel 20, such as a sealed inhaler canister and an opening proximal end 22 that comprises the inhaler mouth piece 16. The inhaler mouth piece 16 is designed to channel the released therapeutic aerosol comprising the Crocus sativus mixture to a patient. In addition, the inhaler 10 comprises an actuation mechanism 24. The actuation mechanism 24 activates the release of a therapeutic aerosol 26 from within the inhaler container or canister 20.

(27) In a preferred embodiment, the actuation mechanism 24 comprises a moveable mechanism member 28 that operates a container release valve 30 that enables the contents within the container to expel out. In a preferred embodiment illustrated in FIG. 2, the moveable mechanism member 28 compresses against a distal end 32 of the release valve 30. When compressed, the contents contained within the inhaler container 20 expel out through the valve 30. The movable mechanism member 28 may comprise a moveable portion of a sidewall 34 of the housing 12 or may comprise an actuation button 36 that when depressed, causes the release of the contents contained within the inhaler container 20.

(28) In a preferred embodiment, a medicinal therapeutic mixture 38 comprising the Crocus sativus extract, infusion or combination thereof, is contained within the sealed inhaler container or canister 20. In addition to the Crocus sativus extract, other solvents or medicinal compounds such as ethyl alcohol, glycerin and tinctures may be mixed with the Crocus sativus and contained within an interior 40 of the container 20. In addition, a propellant such as a chlorofluorocarbon or a hydrofluoroalkane may be comprised within the container 20. The propellant is preferably mixed with the medicinal therapeutic mixture 38 comprising the Crocus sativus extract. In addition, the propellant provides an aerosol medium with which the Crocus sativus extract or infusion mixture thereof is expelled from within the container 20. Once expelled from the container 20, the aerosol Crocus sativus 26 travels through the mouth piece 16 of the inhaler 10, where it is thus inhaled by a patient.

(29) FIG. 3A illustrates a generalized embodiment of a jet nebulizer 42 that may be used to create an aerosol 44 of the medicinal therapeutic mixture 38 comprising the Crocus sativus extract. In a preferred embodiment, the jet nebulizer 42 comprises a reservoir 46 within which the therapeutic mixture 38 comprising the Crocus sativus extract or infusion may reside. In addition, the jet nebulizer 42 comprises a housing 48 having first and second openings 50, 52. In a preferred embodiment, the first opening 50 extends to a mouth piece 54 that interfaces with a patient. The second opening 52 comprises a gas intake end 56. In a preferred embodiment, ambient air enters through the gas intake end 56. As shown in the figure, a compressed gas carried by a tube 58 is introduced into the reservoir 46. The compressed gas forces the medicinal therapeutic mixture 38 comprising the Crocus sativus through a baffle 60 at which pressure from the air intake end 56 creates the aerosol mist 44 comprising the Crocus sativus. The aerosol mist 44 is then inhaled by a patient through the mouthpiece 54. In a preferred embodiment, the compressed gas may comprise ambient air, oxygen, an inert gas, or combinations thereof.

(30) FIG. 3B illustrates a generalized embodiment of an ultrasonic nebulizer 62 which may be used to produce a therapeutic aerosol 64 of the therapeutic mixture 38 comprising the Crocus sativus extract or infusion thereof. As previously mentioned, the ultrasonic nebulizer 62 utilizes an oscillating or vibrating transducer 66 that creates the aerosol particles 64. In this case the aerosol particles 64 comprise the infused Crocus sativus mixture. As shown, the ultrasonic nebulizer 62 comprises a housing 68 having a reservoir portion 70. In a preferred embodiment, the Crocus sativus infusion mixture 38 resides within the reservoir portion 70. In addition, the transducer 66, such as a piezoelectric transducer, is submerged within the Crocus sativus infusion mixture. In a preferred embodiment, the transducer 66 is positioned on an interior surface 74 of a bottom sidewall 76 of the reservoir 70. Vibration of the transducer 66 within the therapeutic mixture 38 comprising the Crocus sativus infusion mixture creates a plurality of aerosol particles 64 which escape from the reservoir container 70. As shown, electrical power is supplied to the transducer 66 through an electrically connected power source 72.

(31) In addition, as shown, the nebulizer 62 has a first opening 76 that extends through a sidewall 78 of the housing 68. The first opening 76 extends to a mouth piece 80 that interfaces with a patient. A second opening 82 opposed from the first opening 76, extends through a second portion 84 of the housing sidewall 78. The second opening 82 comprises an air intake designed to receive a gas such as compressed air, oxygen, an inert gas or combinations thereof. Pressure created by the air or gas entering the intake opening 82 forces the aerosol 64, created by the transducer 66, out through the mouthpiece 80 where it is inhaled by a patient.

(32) In another embodiment, a portable inhaler device 86 such as the embodiment shown in FIG. 4 may be used as a vehicle in which a therapeutic mixture 88 comprising the Crocus sativus is inhaled. The inhaler 86 comprises a housing 90 having an elongated length 92 that extends between opposing first and second housing ends 94, 96. In a preferred embodiment, the inhaler housing 90 comprises an enclosure formed in an elongated tubular form. In a preferred embodiment, the inhaler housing 90 extends to an annular opening 98 at the second housing end 96. The opening 98 extends through a housing sidewall 100 and provides access to an interior housing region 102. In addition, the opening 98 acts as the interface to the patient. In a preferred embodiment, the inhaler 86 shown in FIG. 4, is positionable within a nose of a patient, wherein the medical therapeutic mixture 88 therewithin is inhaled. Alternatively, the opening 98 of the inhaler 86 may be positioned within the patient's mouth to facilitate inhalation of the Crocus sativus extract.

(33) In a preferred embodiment, the therapeutic mixture 88 comprising the Crocus sativus extract, infusion mixture or compound thereof resides within the interior region 102 of the inhaler 86. In addition, a mixture comprising ethyl alcohol, a wax, petroleum jelly, polymeric material or combinations thereof may be mixed with the Crocus sativus to thus form a therapeutic compound 104 that is positionable within the interior 102 of the inhaler housing 90. A wick 106 or a fillable packaging 108 may reside within the inhaler housing 90. Preferably at least a portion of the wick 106 may reside within the Crocus sativus comprising mixture 88 or compound 104. The wick 106 may be made of cotton or other absorbent material. The wick 106 may also be soaked in the saffron infusion or extract or may be added by droplets to the wick 106 (from 5 to 30 or more) and then assembled for inhaling.

(34) A cap 110 may be positioned over the opening 98 to prevent evaporation or contamination of the therapeutic mixture 88 or compound 104 residing within the housing 90. The inhaler housing 90 may be made of a polymer, plastic, metal, cardboard, glass, composite or other such structural material.

(35) In another embodiment, the inhaler 86 may house commercially available saffron that may be packaged within the fillable packing or secondary container 108 such as, but not limited to, a cotton pillow, a woven or non-woven fabric, or an absorbent paper pouch, that resides within the nose inhaler housing 90. In a preferred embodiment, the saffron within the secondary container 108 may be activated with water (or other solvent such as ethyl alcohol). Individuals may conduct repeated periodic inhalation until therapeutic relief is achieved.

(36) In a preferred embodiment, the secondary container 108 may comprise a pouch, bag or a pillow that encloses an amount of Crocus sativus. The secondary container 108 may be constructed by enclosing an amount of an extract constituent, such as Crocus sativus within about a 3 cm to 4 cm by a 1 cm to 2 cm area of material on three sides. The secondary container 108 is formed by, for example but not limited to, folding or sealing three of the sides of the material together. In a preferred embodiment, about 0.5 g to about 3 g of Crocus sativus stigma or other saffron form is inserted into this 3 sided sealed package. After the saffron is positioned inside the container 108, the fourth side of the material is sealed along with the other three sides. The secondary container 108, comprising the extract constituent is then placed within the housing 90 of the inhaler 86. About 3 ml to 9 ml of distilled water, preferably having a temperature greater than 10 C. is then poured onto the filled secondary package 108.

(37) In addition to vaporizing the Crocus sativus infusion or extract into an aerosol mist, as previously described, a concentrated form of a medicinal compound 104 may be made by combining the Crocus sativus with a variety of non-limiting oils, waxes, gels, petroleum jelly, ethyl alcohol, or other solvents. In this embodiment, the Crocus sativus may be mixed with a combination of these oils, waxes, and/or alcohols to create a concentrated hardened medicinal compound of Crocus sativus. In an embodiment, the medicinal compound 104 may be positioned within the inhaler 86 illustrated in FIG. 4. In addition to vaporizing the hardened medicinal Crocus sativus compound, it is further contemplated that the medicinal compound 104 may be ingested. Such an ingestible Crocus sativus comprising compound may contain ingestible materials such as, but not limited to ingestible oils, waxes, ethyl alcohol, flavorings, herbs such as cinnamon, turmeric, mint as well as vitamins, water and alcohol soluble additives and/or hardeners. Furthermore, it is contemplated that the Crocus sativus extract or infusion mixture may be ingested itself or applied to the skin. Such a mixture for topical applications may also comprise a cream or oil designed for application to the skin.

(38) In an embodiment, vaporization of the medicinal therapeutic mixture 38 comprising the Crocus sativus infusion, and/or the Crocus sativus comprising medicinal compound 104, may be accomplished through contact with a heat source (not shown) such as a heated surface. A heated or non-heated forced air source (not shown) may also be used in combination with the heat source to facilitate vaporization of the Crocus sativus comprising mixture. The emanation of such a vapor resulting from the heating of the medicinal compound 104 or mixture 38 may be directly inhaled from a vaporization device such as a humidifier (not shown), through a connector device (not shown), such as but not limited to a mask, a tube, a balloon or a nose piece that is connectable to the vaporization device (not shown). The Crocus sativus medicinal compound or infusion is preferably deposited within a chamber of the vaporization device such that it is in contact with the heat source.

(39) Vaporizers typically reach temperatures between about 680 C. (360 F.) and 806 C. (430 F.) which is a temperature capable of vaporizing the Crocus sativus infusion mixture 38 or medicinal compound 104. Digitally controlled vaporizers may be used by individuals preferring to set specific vaporization temperatures. Generally, temperatures less than 842 C. (450 F.) are used as organic matter burns above that temperature, potentially contaminating the vapors with toxic materials.

(40) In another embodiment, a humidifier (not shown) containing the infused saffron 38 or medicinal compound 104 may be placed in a room without the aid of a connector device (not shown). In this embodiment, the vaporized Crocus sativus comprising infusion mixture 38 or medicinal compound 104 is emanated through the air surrounding the humidifier. Inhalation of the saffron infused steam may be achieved by the individual's presence within the room being humidified. Inhalation can occur while sleeping, working, or other activity being conducted within a room to provide treatment of a medical ailment, such as reducing pre-menstrual symptoms.

(41) In another embodiment, the Crocus sativus extract 38 and/or medical compound 104 may be vaporized using an electric cigarette 112 as shown in FIG. 5. The electronic cigarette 112 typically comprises a heating element 114, i.e., an atomizer that heats a liquid or material contained within an electronic cigarette container or cartridge 116 until it reaches its vaporization point. The mixture 38, in this case, the Crocus sativus comprising extract or infusion mixture or compound 104, as previously discussed, is contained within the electronic cigarette container or cartridge 116 that resides within an electronic cigarette housing 118. A micro-controller 120 connected to an electrical power source 122 may be used to activate the atomizer 114 and vaporize the Crocus sativus extract contained therewithin. An operating indicator 130 such as a light emitting diode (LED) or other light source may be controller by the micro-controller 120 to indicate that the heating element 114 is operating.

(42) In a preferred embodiment, heat emanating from the heating element 114 heats the electronic cigarette container 116, converting the therapeutic mixture 38 comprising the Crocus sativus extract or infusion mixture into an aerosol particle vapor 124 that is inhaled by a user. Alternatively, the heating element 114 may also heat the Crocus sativus comprising compound 104 which may be contained therewithin, thus converting it into aerosol particle vapor 124. The aerosol vapor particles 124 are delivered through an opening 126 of the housing 118 which serves as a mouth piece 128 through which a user may inhale, thus forcing the vapor 124 into the lungs of the user. The electronic cigarette delivery concept provides a vapor, or steam comprising Crocus sativus that may be inhaled into the lungs to provide instantaneous therapy and relief of the various medical ailments previously discussed. The above detailed description and examples are intended for purposes of illustrating the invention and are not to be construed as limited.