Patent Application
20230364242
The present invention relates to a complex containing a water-soluble β-blocker and lecithin, a method for producing the complex, an external pharmaceutical composition containing the complex, and the like.
Infantile hemangiomas are defined by clinical practice guidelines for hemangiomas and vascular malformations as lesions of this nature with tumorous proliferation of abnormal vascular endothelial cells. It is known that infantile hemangioma is the most frequent tumor occurring in infants, the incidence of all infants is 0.8%, and the incidence of female infants is approximately three times higher than that of male infants. In 40% of patients, no hemangiomas are present at birth, and cell proliferation begins and rapidly increases within the first few weeks of life. Thereafter, the hemangiomas increase and rise up to 6 to 20 months after birth, and then slowly regress from 1 year and 6 months to 5 years of age. Generation sites are head and neck 60%, trunk 25%, and limbs 15%. There are many cases where spontaneous regression occurs over time, but after increase, there is a problem in terms of appearance such as cutaneous atrophic scar, wrinkle scar, vasodilation, skin depigmentation, pigmentation, and deformation due to residual subcutaneous tumor.
Hitherto, a method of waiting for spontaneous regression by follow-up, surgical treatment, laser treatment, steroid local injection or treatment by internal administration has been mainly performed, but in recent years, a remarkable tumor reduction effect by internal administration of a β-blocker (for example, propranolol) has been reported, and in Japan, Hemangiol (registered trademark) syrup has been approved for adaptation to infantile hemangioma.
However, the internal administration of the β-blocker has a decrease in blood pressure, hypoglycemia, bradycardia and the like as side effects due to systemic administration, and a safety problem remains as a problem (Non Patent Literature 1).
Therefore, a treatment by locally administering a β-blocker such as propranolol or timolol as an external pharmaceutical composition has been attempted, and a report has been made that the effect has been recognized (Non Patent Literatures 2 and 3).
For example, propranolol has been reported for photolysis (Photochem, Photobiol. Sci., 2002, 1, 136-140, Environ. Sci. Technol., 2007, 41, 803-810), and it is known that decomposition particularly proceeds in an aqueous solution. As described above, some β-blockers have a risk of photolysis. Therefore, caution is required in the preparation of an external pharmaceutical composition containing a β-blocker, which has a higher risk of exposure to natural light or the like as compared with oral preparations.
In addition, as external pharmaceutical compositions containing a β-blocker, an aqueous gel agent, a cream, an ointment, and the like have been reported (WO 2009/050567 A, WO 2010/122442 A), but these do not satisfy both transdermal absorbability and skin retention. In particular, when an external pharmaceutical composition containing a β-blocker is applied to hemangiomas such as infantile hemangiomas, it is necessary to consider balance between transdermal absorbability and skin retention.
Therefore, an object of the present invention is to provide a composition containing a β-blocker, which has a low risk of photolysis of the β-blocker and is excellent in the balance between transdermal absorbability and skin retention.
The present inventors have conceived an idea that if a β-blocker (propranolol) is used as a complex with something and can be always allowed to present in oil, there is almost no contact with dissolved oxygen or water even when exposed to natural light, and thus there is a possibility that the risk of photolysis is suppressed.
Then, as a result of intensive studies based on this idea, it has been found that lecithin, which is a biocompatible material, can easily form a complex with a β-blocker (propranolol), and these complexes can be stably dispersed in oil to form a complex dispersion.
External preparations such as cream preparations prepared using these complex dispersions suppress photolysis and are excellent in the balance between transdermal absorbability and skin retention, and thus have completed the present invention.
Therefore, the present invention provides the following.
It is considered that a preparation prepared using a dispersion in oil of a complex composed of a β-blocker (propranolol) and lecithin can be expected as an external therapeutic agent for infantile hemangioma because the risk of photolysis of the β-blocker is low and the balance between transdermal absorbability and skin retention is excellent.
On the other hand, the particles in the complex dispersion provided as one embodiment of the present invention are monodisperse, and can be produced with good reproducibility. These utilize the high affinity between a water-soluble β-blocker and lecithin, and can be easily produced using existing production facilities.
<Complex or Complex Dispersion>
The present invention provides a complex containing a water-soluble β-blocker and lecithin (hereinafter, also referred to as “β-blocker/lecithin complex”) or a dispersion containing the complex in an oily base material.
The “complex” of the present invention means a so-called reverse micelle in which a water-soluble β-blocker and lecithin interact with each other by a non-covalent bond, and these molecules are self-assembled into particles, a particulate S/O type complex in which the water-soluble β-blocker is partially or entirely coated with lecithin, or a mixture of the reverse micelle and the S/O type complex. The average particle size when the complex containing the water-soluble β-blocker and lecithin of the present invention is dispersed in an oily base material is, for example, approximately 1 to approximately 50 nm, preferably approximately 2 to approximately 30 nm, and more preferably approximately 3 to approximately 20 nm.
In the present invention, the numerical range indicated using “to” indicates a range including the numerical values described before and after “to” as the minimum value and the maximum value, respectively.
The “water-soluble β-blocker” used in the present invention is not particularly limited as long as it is a β-blocker soluble in water. The “soluble in water” means that the amount of water required to dissolve 1 g or 1 mL of the water-soluble active ingredient is less than 100 mL to the extent that it dissolves within 30 minutes, for example, when vigorously shaken at 20±5° C. every 5 minutes for 30 seconds. Examples of such a water-soluble β-blocker include “sparingly soluble”, “soluble”, “easily soluble”, or “extremely soluble” defined in the Japanese Pharmacopoeia.
Examples of the water-soluble β-blocker include, but are not limited to, propranolol, timolol, alprenolol, bupranolol, bufetrol, oxprenolol, atenolol, bisoprolol, betaxolol, bevantolol, metoprolol, acebutolol, celiprolol, nipradilol, tilisolol, nadolol, indenolol, carteolol, pindolol, bunitrolol, landiolol, esmolol, arotinolol, carvedilol, labetalol, amosulalol, and salts thereof, and these may be used alone or in combination of two or more thereof.
In one embodiment of the present invention, the water-soluble β-blocker contains at least one selected from propranolol, timolol, acebutolol, atenolol, carteolol, nadolol, metoprolol, and salts thereof.
In one embodiment of the present invention, the water-soluble β-blocker is propranolol or a salt thereof.
In one embodiment of the present invention, the water-soluble β-blocker is propranolol hydrochloride.
The content of the water-soluble β-blocker is not particularly limited as long as the object of the present invention can be achieved, but is, for example, approximately 10 to approximately 50 wt %, and preferably approximately 20 to approximately 40 wt %, based on the total amount of the complex of the present invention.
The “lecithin” used in the present invention is not particularly limited as long as it is lecithin, and may be naturally derived (for example, soy lecithin, egg yolk lecithin, or the like) or synthetically derived. Examples of the lecithin include those containing phosphatidylcholine, phosphatidylethanolamine, phosphatidylinositol, phosphatidylserine, sphingomyelin, and the like.
In one embodiment of the present invention, the lecithin contains phosphatidylcholine.
In one embodiment of the present invention, lecithin contains at least one of phosphatidylcholine represented by formula I:
In one embodiment of the present invention, lecithin contains approximately 80 wt % or more, preferably approximately 90 wt % or more, and more preferably 94 wt % or more of phosphatidylcholine (preferably phosphatidylcholine represented by formula I).
In one embodiment of the present invention, the lecithin is soy lecithin. The soy lecithin may be, for example, those appropriately available from reagent supply companies such as LIPOID AG and NOF Corporation.
The content of lecithin is not particularly limited as long as the object of the present invention can be achieved, but is, for example, approximately 40 to approximately 90 wt %, and preferably approximately 50 to approximately 80 wt %, based on the total amount of the complex of the present invention.
Alternatively, the weight ratio of the water-soluble β-blocker to lecithin contained in the complex of the present invention is not particularly limited as long as the object of the present invention can be achieved, but is, for example, approximately 1:1 to approximately 1:10, and preferably approximately 1:1 to approximately 1:3.
The “dispersion” or “complex dispersion” of the present invention means a dispersion containing a β-blocker/lecithin complex in an oily base material.
The “oily base material” used in the present invention is, for example, a substance known as a base material for pharmaceuticals, quasi-pharmaceutical products, cosmetics, nutritional supplements, or agricultural chemicals, and is not particularly limited as long as it dissolves lecithin.
Examples of the oily base material include, but are not limited to, fatty acid esters having 8 to 20 carbon atoms such as cetyl 2-ethylhexanoate, isopropyl myristate (IPM), and isopropyl palmitate (IPP), terpenes such as squalane and squalene, vegetable fats and oils such as soybean oil, jojoba oil, almond oil, and olive oil, animal fats and oils such as horse oil, synthetic oils such as silicone oil, and mineral oils such as liquid paraffin and white petrolatum, and these may be used alone or in combination of two or more thereof.
In one embodiment of the present invention, the oily base material is fatty acid esters having 10 to 16 carbon atoms, vegetable fats and oils, or mineral oils, and is preferably isopropyl myristate (IPM), soybean oil, or liquid paraffin.
<Method for Producing Complex or Complex Dispersion>
The β-blocker/lecithin complex of the present invention or a dispersion in oil containing the complex can be produced by several methods. This is considered to be due to the high stability of the intermediate formed due to the high affinity between the water-soluble β-blocker and lecithin. The production method is roughly divided into an in-liquid drying method in which a dispersion containing a complex is produced at once in a system and a method in which the dispersion is once dehydrated via a gel-like substance.
In-Liquid Drying Method
This method is a method in which lecithin is heated and dissolved in an oily base material, a water-soluble β-blocker aqueous solution is added thereto and stirred, and then the mixture is dehydrated under reduced pressure to produce a transparent dispersion containing a complex at once.
The feature of this method is that a dispersion having a controlled particle size can be produced only by adding a water-soluble β-blocker aqueous solution to lecithin dissolved in an oily base material as described above, stirring the mixture, and then dehydrating the mixture without using a special shearing device. In addition, when the ratio of lecithin and the water-soluble β-blocker is appropriately set at the time of forming a complex, it is possible to produce a dispersion with high reproducibility by a single operation regardless of its scale.
The amount of the oily base material is not particularly limited, and is appropriately set according to the content in the final product. For example, an oily base material is used in an amount of approximately 3 to approximately 30 times, and preferably approximately 5 to approximately 10 times the weight of lecithin used. By using the oily base material in an amount of 3 times, and preferably 5 times or more, formation of coarse particles is suppressed, and a transparent dispersion is obtained.
The β-blocker aqueous solution means an aqueous solution in which a water-soluble β-blocker is dissolved. The β-blocker aqueous solution may further contain a pH adjusting agent or the like as long as the object of the present invention can be achieved. The β-blocker aqueous solution can be prepared by a known method. The concentration of the water-soluble β-blocker in theβ-blocker aqueous solution is not particularly limited, and can be appropriately adjusted according to the solubility of the β-blocker to be used, the desired concentration and content, and the like.
When the β-blocker aqueous solution is added to the oily base material in which lecithin is dissolved, the oily base material may be once returned to around room temperature, or the β-blocker aqueous solution can be added under heating conditions as long as it is within a range in which rapid evaporation of moisture can be suppressed.
The dehydration step is performed by heating and decompressing the oily base material at a temperature equal to or lower than the boiling point of the oily base material. The heating temperature is not particularly limited, and varies depending on the oily base material to be used, but the heating is performed at, for example, 50° C. to 80° C., and preferably 60° C. to 75° C. Examples of the embodiment include a method of using a decompression device such as an aspirator or a vacuum pump while heating and stirring, a method of using an evaporator, and the like.
Production Method of Dehydrating via Gel-Like Substance
On the other hand, a complex or a dispersion containing the complex can be produced via a gel-like substance. The gel-like substance used in the present invention is composed of only a β-blocker aqueous solution and lecithin, and is in a gel to semi-solid state in which the β-blocker aqueous solution is contained in lecithin.
Further, the methods via a gel-like substance are classified into two types depending on its drying mode. The first is a method in which a gel-like substance or an aqueous dispersion thereof is dried to form a complex of a β-blocker and lecithin, and the second is a method in which an oily base material is added to a gel-like substance and dried in a liquid to form a complex dispersion.
The gel-like substance can be obtained by kneading a water-soluble β-blocker, water, and lecithin (preferably, a β-blocker aqueous solution and lecithin). The kneading step can be performed by a known method, and can be performed until a uniform gel-like substance is formed. Instruments and devices used for kneading are not particularly limited as long as they can be usually used by those skilled in the art. Examples of the instrument/machine used for kneading include a spatula, a mortar, a stirrer, a mechanical stirrer, a mixer, a rotation-revolution mixer, a multi-bead shocker, and the like. The kneading can be performed, for example, at room temperature until a gel-like substance uniform in appearance is obtained after mixing the water-soluble β-blocker, water, and lecithin (preferably, after mixing the β-blocker aqueous solution and lecithin). In addition, operability of kneading may be improved by sufficiently immersing lecithin in a β-blocker aqueous solution before kneading.
The weight ratio of water to lecithin is not particularly limited, but is, for example, approximately 5:1 to approximately 1:1, preferably approximately 3:1 to approximately 2:1, and more preferably approximately 2:1.
Next, a complex or a complex dispersion can be produced by subjecting the gel-like substance thus obtained to a drying step.
(i) Method of Directly Freeze-Drying Gel-Like Substance
Freezing of the gel-like substance may be, for example, a method usually performed by those skilled in the art. For example, a dry bath prepared by adding dry ice to liquid nitrogen or a solvent such as acetone or methanol can be used. The frozen gel-like substance is freeze-dried for approximately 12 hours to approximately 24 hours to produce a complex, and an oily base material is added to the obtained complex, and the mixture is sufficiently stirred until transparently dispersed, whereby a complex dispersion can be produced.
(ii) Method of Drying Aqueous Dispersion of Gel-Like Substance
The method for obtaining the aqueous dispersion of the gel-like substance may be, for example, a method usually performed by those skilled in the art, and examples thereof include a method in which water is added to the gel-like substance and the mixture is stirred using a stirrer, a mechanical stirrer, or the like until it becomes uniform. The weight ratio of the gel-like substance to water is not particularly limited, but is, for example, approximately 1:1 to approximately 1:20, preferably approximately 1:5 to approximately 1:10, and more preferably approximately 1:9.
The obtained aqueous dispersion is freeze-dried in the same manner as in (i), or dried using a spray dryer (or a spray freeze-dryer), whereby a complex can be produced. In addition, an oily base material is added to the obtained complex, and the mixture is sufficiently stirred until transparently dispersed, whereby a complex dispersion can be produced. When the aqueous dispersion is used, not only operability of the gel-like substance is improved and movement between the steps is facilitated, but also the range of drying methods that can be used may be expanded.
(iii) Method of Adding Oily Base Material to Gel-Like Substance and Drying in Liquid
It is also possible to produce a complex dispersion by adding an oily base material to a gel-like substance and dehydrating the mixture under reduced pressure under heating conditions. The oily base material, the dehydration method, and the like to be used are the same as those in the “in-liquid drying method” described above.
The obtained dispersion containing the β-blocker/lecithin complex is transparent and can have high dispersion stability. Furthermore, when the complex is dispersed in fatty acid esters, addition of a certain amount of soybean oil may particularly improve light stability and dispersion stability. The dispersion thus obtained can be appropriately applied to various existing preparation formulations.
Application of Complex Containing β-Blocker and Lecithin
The complex of the β-blocker and lecithin of the present invention or a dispersion containing the same can be used for diseases, disorders and symptoms that can be treated or prevented by the β-blocker, and the like. Examples of the diseases, disorders, and symptoms that can be treated or prevented by the β-blocker include, but are not limited to, hypertension including essential hypertension, angina, arrhythmia, migraine, hemangioma including infantile hemangioma, and the like.
In one embodiment of the present invention, there is provided the β-blocker/lecithin complex of the present invention or the dispersion containing the same for using in the treatment or prevention of hypertension including essential hypertension, angina, arrhythmia, migraine, or hemangioma including infantile hemangioma.
In one embodiment of the present invention, there is provided the β-blocker/lecithin complex of the present invention or the dispersion containing the same for using in the treatment or prevention of infantile hemangioma.
In one embodiment of the present invention, there is provided a use of the β-blocker/lecithin complex of the present invention or the dispersion containing the same for preparing a medicament for treating or preventing hypertension including essential hypertension, angina, arrhythmia, migraine, or hemangioma including infantile hemangioma.
In one embodiment of the present invention, there is provided a use of the β-blocker/lecithin complex of the present invention or the dispersion containing the same for preparing a medicament for treating or preventing infantile hemangioma is provided.
In one embodiment of the present invention, there is provided a method for treating or preventing hypertension including essential hypertension, angina, arrhythmia, migraine, or hemangioma including infantile hemangioma, comprising administering an effective amount of the β-blocker/lecithin complex of the present invention or the dispersion containing the same.
In one embodiment of the present invention, there is provided a method for treating or preventing infantile hemangioma, comprising administering an effective amount of the β-blocker/lecithin complex of the present invention or the dispersion comprising the same.
External Pharmaceutical Composition
In one embodiment of the present invention, an external pharmaceutical composition containing the β-blocker/lecithin complex of the present invention or the dispersion containing the same is provided.
In addition to the β-blocker/lecithin complex of the present invention or the dispersion containing the same, the external pharmaceutical composition of the present invention may contain additives that are acceptable in the field of pharmaceuticals and cosmetics, such as excipients, lubricants, binders, disintegrants, emulsifiers, stabilizers, flavoring agents, diluents, gelling agents, and water, as necessary.
The content of the β-blocker in the external pharmaceutical composition of the present invention is not particularly limited, and can be appropriately adjusted according to the purpose.
The external pharmaceutical composition of the present invention may be formulated into a cream (a W/O type cream, an O/W type cream, or the like), a gel agent (for example, an oil gel agent or the like), an emulsion, a suspending agent, a patch (a tape agent, a cataplasm agent, or the like), or the like together with the above additives as necessary with reference to a known method or the like.
For example, in the case of a W/O type cream, a mineral oil such as white petrolatum and an emulsion stabilization aid such as stearyl alcohol are heated and dissolved to form an oil phase. Next, a lipophilic nonionic surfactant and a heated aqueous phase are added dropwise to the oil phase and sufficiently emulsified. When the emulsification is completed, a dispersion containing the β-blocker/lecithin complex of the present invention may be added, stirred until it becomes uniform in a heated state, and allowed to cool to obtain a W/O type cream.
Examples of the lipophilic nonionic surfactant include sorbitan monooleate, sorbitan sesquioleate, polyoxyethylene-hydrogenated castor oil, polyoxyethylene (2) oleyl ether, and the like.
In the case of an O/W type cream, for example, an O/W type cream may be obtained by heating purified water containing a surfactant having a high HLB value and various additives (for example, preservatives such as ethyl parahydroxybenzoate and propyl parahydroxybenzoate, solubilizing agents such as propylene glycol, and the like), dropping the oil phase similarly heated, stirring the mixture in a heated state until it becomes uniform, and allowing the mixture to cool.
In the case of an oil gel agent, for example, dextrin palmitate, which is an oil thickening/gelling agent, may be added to a mineral oil such as liquid paraffin, and heated and dissolved, then a dispersion containing the β-blocker/lecithin complex of the present invention may be gradually added and stirred, stirring may be stopped when the dispersion becomes uniform, and then the dispersion may be allowed to cool to room temperature to obtain an oil gel agent.
In one embodiment of the present invention, the external pharmaceutical composition of the present invention which is a W/O type cream is provided.
By using a W/O type cream, it is possible to impart light stability while maintaining high transdermal absorbability and retention. In addition, in these dosage forms, drying of the agent after application is suppressed, so that there is no precipitation of a gelling agent that causes a problem when an aqueous gel agent is applied. Therefore, itchy sensation of the affected part associated with the precipitation of the gelling agent is reduced, and the risk of scratching the affected part is reduced.
In one embodiment of the present invention, there is provided the external pharmaceutical composition of the present invention for treating or preventing hypertension including essential hypertension, angina, arrhythmia, migraine, or hemangioma including infantile hemangioma.
In one embodiment of the present invention, the external pharmaceutical composition of the present invention for treating or preventing infantile hemangioma is provided.
The present invention will be described in more detail with reference to the following examples, but the present invention is not limited thereto.
The following reagents were used.
As an emulsifier used in the emulsification step, CLEARMIX manufactured by M Technique Co., Ltd. was used.
Preparation of Dispersion Containing Propranolol Hydrochloride-Soy Lecithin Complex
Purified water (2.0 g) was added to propranolol hydrochloride (0.5 g), and completely dissolved in a hot water bath at 50° C. to prepare an aqueous solution of propranolol hydrochloride. Separately, soy lecithin (1.0 g) and isopropyl myristate (5.0 g) were added to an eggplant flask, and completely dissolved in a hot water bath at 75° C., then the aqueous solution of propranolol hydrochloride prepared was added dropwise, and the mixture was stirred for approximately 10 minutes.
The obtained suspension was dried under reduced pressure at 75° C. for 1 hour and then allowed to cool to obtain a desired dispersion.
Purified water (2.0 g) was added to propranolol hydrochloride (0.4 g), and completely dissolved in a hot water bath at 50° C. to prepare an aqueous solution of propranolol hydrochloride. The aqueous solution of propranolol hydrochloride prepared was added to soy lecithin (1.0 g), and the mixture was sealed and immersed at room temperature for approximately 3 hours. The mixture was kneaded with a spatula until it became uniform to obtain a gel-like substance. The obtained gel-like substance was frozen with dry ice-acetone and dried in a freeze-dryer for approximately 19 hours. Isopropyl myristate (10 g) was added to the obtained dried product, and the mixture was stirred until it was uniformly dispersed to obtain a desired dispersion.
Purified water (30.6 g) was added to a gel-like substance prepared in the same manner as in Example 2, and the mixture was stirred until it was uniformly dispersed to obtain an aqueous dispersion of a gel-like substance. Subsequently, the obtained aqueous dispersion (17.0 g) was frozen in dry ice-acetone and dried in a freeze-dryer for approximately 19 hours. Isopropyl myristate (5.0 g) was added to the dried product thus obtained, and the mixture was stirred until it was uniformly dispersed to obtain a desired dispersion.
Isopropyl myristate (10 g) was added to a gel-like substance prepared in the same manner as Example 2, and the mixture was dried under reduced pressure in a warm bath at 75° C. for 30 minutes and then allowed to cool to obtain a desired dispersion.
All of the complex dispersions prepared in Examples 1 to 4 were transparent, and their particle sizes were also equivalent (see Test Example 1).
Preparation of External Pharmaceutical Composition Containing Propranolol Hydrochloride-Soy Lecithin Complex Dispersion
Japanese Pharmacopoeia white petrolatum, Japanese Pharmacopoeia stearyl alcohol, and polyoxyethylene (2) oleyl ether were each weighed in a container, and stirred in a hot water bath at 75° C. until they became uniform. The mixture was attached to an emulsifier, and purified water was added dropwise thereto while stirring at 75° C. and 4,500 rpm. After approximately 10 minutes, when the whole mixture became uniform, a complex dispersion prepared in the same manner as in Example 1 and Japanese Pharmacopoeia soybean oil were added thereto, and the mixture was further heated and stirred for 10 minutes. The container was pulled up from the hot water bath, and the mixture was stirred until the temperature reached room temperature while being allowed to cool, thereby obtaining a desired W/O type cream.
Table 1 and Table 2 show the amounts (weight ratios) of the reagents used for preparation of the creams of Examples 5 to 7 and Examples 8 to 10, respectively.
Purified water [20.1 g (40.2 wt %)], sodium lauryl sulfate [0.9 g (1.8 wt %)], and Japanese Pharmacopoeia propylene glycol [2.5 g (5.0 wt %)] were each weighed in necessary amounts in a container, and stirred in a hot water bath at 75° C. until the mixture became uniform to form an aqueous phase. On the other hand, Japanese Pharmacopoeia white petrolatum [10 g (20 wt %)], Japanese Pharmacopoeia stearyl alcohol [5.0 g (10 wt %)], and a complex dispersion [11.5 g (23.0 wt %)] prepared in the same manner as in Example 2 were added to another container, and stirred in a hot water bath at 75° C. until the mixture became uniform to form an oil phase. The oil phase was added dropwise while the aqueous phase was heated and stirred in a hot water bath at 75° C., and stirred until it became uniform. The mixture was taken out from the hot water bath and allowed to cool overnight to obtain a desired O/W type cream.
Purified liquid paraffin [27.5 g (55.0 wt %)] was weighed in a container, and dextrin palmitate [2.5 g (5.0 wt %)] was added little by little. The mixture was sufficiently stirred at room temperature, and then completely dissolved in a warm bath at 75° C. A complex dispersion [20.0 g (40.0 wt %)] prepared in the same manner as in Example 2 was added to the resulting mixed liquid, and the mixture was stirred at 75° C. until it became uniform. The stirring was stopped at 75° C., and the mixture was placed in a container and cooled to room temperature over approximately 12 hours to obtain a desired oil gel agent.
Propranolol hydrochloride (0.2 g) was weighed into a container, and phosphate buffered saline (20 mL) was added thereto, then the mixture was heated to 70° C. while stirring. Hydroxypropylmethyl cellulose [0.9 g, (4.5% (w/v))] was added thereto and suspended, then cooled and stirred until transparent to obtain a gel agent of Comparative Example 1.
Japanese Pharmacopoeia white petrolatum [40 g, (40 wt %)], Japanese Pharmacopoeia stearyl alcohol 20 g, (20 wt %)], and polyoxyethylene (2) oleyl ether [5.0 g, (5 wt %)] were each weighed in a container, and stirred in a hot water bath at 75° C. until they became uniform to form an oil phase. On the other hand, propranolol hydrochloride [1.0 g (1.0 wt %)] and purified water [34.0 g (34 wt %)] were weighed in required amounts in different containers, and completely dissolved in a hot water bath at 75° C. to form an aqueous phase. The oil phase was attached to an emulsifier, and the aqueous phase was added dropwise while stirring at 75° C. and 4,500 rpm, and the mixture was emulsified for approximately 10 minutes. The container was pulled up from the hot water bath, and the mixture was stirred until the temperature reached room temperature while being allowed to cool, thereby obtaining a desired W/O type cream.
Japanese Pharmacopoeia white petrolatum, Japanese Pharmacopoeia stearyl alcohol, and polyoxyethylene (2) oleyl ether were each weighed in a container, and stirred in a hot water bath at 75° C. until they became uniform. The mixture was attached to an emulsifier, and an aqueous solution of propranolol hydrochloride was added dropwise thereto while stirring the mixture at 75° C. and 4,500 rpm. After approximately 10 minutes, when the whole mixture became uniform, isopropyl myristate in which soy lecithin was heated and dissolved in advance and Japanese Pharmacopoeia soybean oil were added thereto, and the mixture was further heated and stirred for 10 minutes. The container was pulled up from the hot water bath, and the mixture was stirred until the temperature reached room temperature while being allowed to cool, thereby obtaining a desired W/O type cream.
Table 3 shows the amount (weight ratio) of each reagent used for preparing the creams of Comparative Examples 3 to 4.
In-liquid drying was performed in the same manner as in Example 1 using sucrose laurate or sucrose erucate, which is a surfactant having a low HLB value, instead of using soy lecithin, but a suspension was formed, and a transparent dispersion could not be obtained.
The particle size of the complex dispersion obtained in Examples 1 to 4 was measured using Zetasizer Nano ZS (manufactured by Malvern Panalytical) measured using a dynamic light scattering method (DLS). For the measurement, a glass cell was used, and physical property values [viscosity: 6.6 mPa·s (20° C.), refractive index: 1.434] of EXCEPARL IPM were used. Also, the average particle size indicates the average value (nm) of the particle size distribution by scattering intensity. The results are shown in
The average particle size in the complex dispersion prepared in Example 1 was 4.701 nm (PDI: 0.126) (
The average particle size of the dispersion when the amount of propranolol hydrochloride was changed was as follows.
The average particle size in the complex dispersion prepared in Example 2 was 4.443 nm (PDI: 0.105) (
The average particle size of the aqueous dispersion of the gel-like substance obtained in Example 3 was 494.4 nm (PDI: 0.363) (
The average particle size of the complex dispersion obtained in Example 4 was 4.478 nm (PDI: 0.106) (
Skin of a hairless mouse [trade name: “Laboskin”, manufactured by Hoshino Laboratory Animals, Inc.] was attached to a vertical Franz cell (10 mm in line) manufactured by Asahi Glassplant Inc. As a receiver liquid of the cell, a phosphate buffer (manufactured by FUJIFILM Wako Pure Chemical Corporation) was used.
The formulations obtained in Examples 5 to 10 and Comparative Examples 1, 3 and 4 were applied (50 mg) to the skin of a hairless mouse, and a test was performed at 37° C. for 24 hours. The propranolol concentration in the receiver liquid was measured by HPLC at 3 hours and 6 hours after the start of the test, 3 hours before the end of the test, and at the end of the test. The results are shown in
The measurement conditions of HPLC are as follows.
As is apparent from
As is apparent from
An appropriate amount of each of the formulations obtained in Examples 5, 6, 7, and 9 and Comparative Examples 1, 2, and 4 was put in a glass bottle, and color tone change due to accumulation of exposure to light was evaluated with a light stability test apparatus [model: LTL-200A-14WCD (manufactured by Nagano Science Co., Ltd.)]. For the formulations of Example 6 and Comparative Examples 1 and 2, the purity was measured by HPLC after exposure to light.
The test conditions are shown below.
Light source: D65 lamp, temperature: 25° C., relative humidity: 60% RH
Illuminance: 4.00 klx, integrated illuminance: 1200 klx·h
The measurement by HPLC was performed under the same conditions as in Test Example 2 except that the measurement wavelength was 254 nm. Appearance photographs of the formulations before and after exposure to light are shown in
As is apparent from
A main decomposition product of Comparative Example 2 is a peak appearing at approximately 3.3 minutes on the HPLC chart of
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-165384 | Sep 2020 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2021/036088 | 9/30/2021 | WO |
