Patent Application
20090081281
1. Field of the Invention
The present invention generally relates to lipid based drug delivery system. In particular, it relates to highly flexible, penetrating liposomal formulations loaded with photosensitizers that can transport the photosensitizer across the skin barrier into a deeper layer for treating dermatological problems and other cancerous or precancerous skin conditions.
2. Invention Disclosure Statement
Skin has been used for decades as a site for topical administration of drug for treating dermatological problems, for cosmetic application and for treating cancerous and precancerous conditions in skin. The main aim of a topical drug delivery system is to maximize the delivery of therapeutic agent in the formulation through stratum corneum, into deeper layers of the skin. Other aims are to promote uniform absorption, to offer controlled delivery of the therapeutic agents and to reduce side effects.
The skin is a complex membrane composed of different layers. Its upper layer, stratum corneum, is the main physical barrier for percutaneous penetration of drug applied topically. There are several different pharmaceutical products which are targeted through the skin into the body and these include transdermal drug delivery systems (patches), liposomes, creams, ointments, lotions, gels as well as subcutaneous implants. In contrast to the traditional oral drug administration, the use of transdermal drug delivery by-passes first pass metabolism of the liver, the acidic environment of the gastrointestinal tract, and problems of absorption in the stomach etc.
In topical administration, penetration rate is influenced by many factors like molecular weight of the drug, drug carrier, interaction of carrier with the skin and many others. The permeability of the drug molecule is directly related to its lipophilicity and inversely proportional to molecular size. Attempts have been made to overcome this limitation. Different drug delivery systems are described in the prior art to overcome the skin barrier.
Liposomes have been much investigated as a system for dermal application. But most studies have shown that these liposome vesicles are not very efficient in penetrating the physical skin barrier as these conventional liposome vesicles are rigid. Specialized liposomal which are flexible to pass through the skin are being explored Transfersomes in one such flexible liposomes example described by Gregor Ceve in U.S. Pat. No. 6,165,500 for systemic administration of insulin. Transfersomes are lipid vesicles that incorporate molecular edge activators, which can deform and squeeze through microspores in stratum corneum. Similarly niosomes and ethosomes are other carrier used for dermal application of drug. Ethosomes are liposomes high in ethanol content which fluidizes the ethosomal lipids and stratum corneum bilayer thus allowing the penetration; while niosomes uses nonionic surfactant.
Many of the above described drug carrier systems are not efficient enough to transport the photosensitizer across the skin barrier, as most of them face a lot of stability related problems e.g. deformation of the liposome vesicle to pass through the skin pore can cause damage to carrier system leading to leakage of the active compound carried in the liposome. Other problems are liposome vesicles can aggregate on passing the skin barrier reducing their efficiency and ability to bring the photo drug to the desired treatment site.
The success of this drug delivery system depends on the ability of the drug to penetrate through the skin in sufficient quantities to achieve its desired therapeutic effect. It has been shown that fluidization of intercellular domains and thus altering the stratum corneum is a possible mechanism for enhanced transport of drug encapsulated vesicles.
Different methods are used in the prior art to modify the barrier properties of the stratum corneum and to enhance drug penetration through skin which include use of chemical penetration enhancers; iontophoresis, which is administrating ionic therapeutic agents through skin using a low level of electric current; and, phonophoresis which uses ultrasound energy to increase penetration through skin.
Photodynamic therapy (PDT) is one of the most promising new techniques being explored for use in a variety of medical applications and is known as a well-recognized treatment for the destruction of tumors. The use of PDT for the treatment of various types of disease is limited due to the inherent features of photosensitizers. These include their high cost, extended retention in the host organism, skin photo toxicity, low solubility in physiological solutions (which reduces its usefulness for intravascular administration as it can provoke thromboembolic accidents), and low targeting effectiveness. These disadvantages generally lead to the administration of very high doses of a photosensitizer, which dramatically increase the possibility of accumulation of the photosensitizer in non-damaged tissues and the accompanying risks of affecting non-damaged sites.
Since the application of photodynamic therapy is used in treating many dermatological problems and also in cancerous and precancerous skin conditions it is necessary to develop an effective drug delivery system which can be applied topically. So as to optimize and target the abnormal cells in the skin and beneath, by topical application thus reducing the side effects like skin photosensitivity in the other normal skin cells.
Drug delivery systems designed in the present invention are better than the prior art systems. These delivery systems can effectively penetrate the skin barrier and optimize the drug concentration in deeper layer of the skin.
Present invention aims at overcoming the impermeability of intact human skin to penetration in a reversible and non-damaging manner as well as to design therapeutically effective intradermal drug delivery systems for transporting hydrophobic photosensitizers for administering photodynamic therapy.
It is an objective of the present invention to formulate a suitable highly flexible, penetrating liposomal carrier system for topical application.
It is another objective of the present invention to use this delivery system for faster and efficient transport of hydrophobic photosensitizer across stratum corneum.
It is a further objective of the present invention to use the new formulation for optimizing and targeting photosensitizer through topical administration to deeper layers within the skin.
It is yet another objective of this invention to increase the drug penetration across the skin barrier as well as decreasing the side effects on the skin.
Briefly stated, the present invention provides a highly flexible penetrating liposomal carrier system, formulated with enhanced skin penetration properties. This specialized formulation of a highly flexible penetrating liposomal delivery system comprises one or more phospholipids, lysophosphatides and hydrophobic photosensitizers. This new formulation can squeeze the liposomal particles through intercellular regions of stratum corneum as an intact structures, and in this way, deliver encapsulated photosensitizer to the epidermis, dermis, hypodermis and surroundings. The penetrating liposomal formulations provide therapeutically effective amounts of a hydrophobic photosensitizer through topical application with better skin penetration thus improving drug targeting and the efficacy of photodynamic therapy (PDT).
A penetrating liposomal formulation is a specialized topical drug delivery system that can reach cells in the deeper skin layer but avoids systemic absorption of the drug thus minimizing side effects. Highly specialized penetrating liposomal formulation of present invention comprises of one or more phospholipids, one or more lysophosphatides and a hydrophobic photosensitizer. These new formulations are highly specialized flexible liposomes which can easily penetrate through stratum corneum and reach the deeper cells of the skin layer even when they are topically applied. This allows the drug to be delivered without significant side effects which are commonly reported with systemic administration.
Topical applications of dermatological drugs can now be used to achieve a localized therapeutic effect on or beneath the application site. The principal goals of topical drug delivery are to maximize the delivery of the drug or active ingredient from the formulation through the stratum corneum, upper epidermis, and into deeper subcutaneous tissue, to minimize the further absorption through the skin into the systemic circulation, and further to promote a more uniform absorption, to reduce dose frequency and to improve the cosmetic or aesthetic appeal of the dosage form.
As with other routes of administration, transport across the skin is also associated with several disadvantages, the main being, not all drugs are suitable candidates for topical administration. A number of physicochemical parameters have been identified to influence drug uptake by skin such as size of the vesicles, molecular weight that influences the diffusion process, and variations in penetration rates in different skin types. In other words the skin permeability of the molecule is directly proportional to its lipophilicity and inversely proportional to molecular size. Sometime it is seen that damaged stratum corneum shows increased permeability compared to intact skin layer. Hyperproliferation of stratum corneum was found to increase permeability due to reduced barrier properties.
The new penetrating liposomal formulation of this invention overcomes most of the drawbacks seen in the convention delivery systems. These new formulations show enhanced shelf life, non-aggregated and stable with better load carrying capacity. The penetrating liposome vesicle is formulated at nano scale to help easy transport through the skin barrier, since particle size is an important criterion for transdermal penetration. These newly formulated penetrating liposome particles can squeeze themselves through intercellular regions of stratum corneum as intact structures, and by this way, deliver encapsulated photosensitizer to the dermis.
The present invention is further illustrated by the following examples, but is not limited thereby.
A specialized penetrating liposome formulation of mTHPC also called Temoporfin was prepared according to the following general procedure:
Ethanolic solution of lipids (3:1) is vigorously mixed with a vortexer in a sealed glass vessel for 5 minute. Then m-THPC and penetration enhancer were added and the mixture was again mixed. This was followed by ultrasonication for 5 minute. A suitable amount of phosphate buffer saline pH 7.4 was added drop wise to hydrate the mixture and is mixed again with a vortexer for 5 minute followed by is ultrasonication. The resultant mixture is then extruded (filtrated) through different polycarbonate filtrate with pore sizes form 400 nm up to 50 nm. The entire process is performed at room temperature.
Using the foregoing procedure, a highly penetrating liposomal formulation for m-THPC was prepared as follows:
The Phospholipon 80 is a commercially available lipid mixture comprising of about 73.0-76.0% by weight (3-sn-phosphatidyl) choline, maximum 6% by weight (3-sn-lysophosphatidyl) choline, maximum 7% by weight cephalin and maximum 7% by weight phosphatidic acid. (Phospholipon 80 used in the preparation of penetrating liposomes in the present invention; is supplied by Phospholipid GmbH; Nattermannallee 1; D-50829 Köln, Germany).
Different lipid mixtures can be used other than Phospholipon 80 which includes commercially available Phospholipon 50 (comprising of about min. 50% by weight 3-Sn-phosphatidyl choline and max. 6% by weight 3-Sn-Lysophosphatidyl choline), Phospholipon 90 (comprising of minimum about 90% by weight 3-Sn-Phosphatidyl choline, max. 6% by weight 3-Sn-lysophosphatidyl choline and max. 3% by weight tocopherol) and Phospholipon 100 as well as mixtures from other phospholipids.
Penetration enhancer is used to increase skin permeability by reversibly damaging the physiochemical nature of the stratum corneum to reduce its diffusional resistance. A good skin penetration enhancer should be non-irritating, pharmacological inert, non-toxic, and should be easy to be used with other ingredients of the formulation. In the above formulations, terpenes such as Cineol (2,2,4-trimethyl-3-oxabicyclo[2.2.2]octane), Citral (3,7-dimethyl-2,6-octadienal) and Limonen (1-methyl-4-pro-1-en-2-yl-cyclohexene) are used as penetration enhancers to improve the absorption of highly penetrating liposomal formulated mTHPC through the stratum corneum barrier of the skin. Many terpenes have been classified as GRAS (Generally Regarded As Safe) by FDA. Penetration enhancer can help the new penetrating liposomal formulation to easily pass through main skin barrier by increasing the fluidity of stratum corneum, thereby reducing its resistance. Phospholipids used in the new liposomal formulation of the present invention show better deformability to the vesicles resulting in better skin permeation.
a. Standard Highly Flexible Penetrating Liposome Without mTHPC (Stored at 4° C.) for 0 day, 3, 6, and 12 months.
b. Stability Data for Highly Flexible Penetrating Liposome with Different Concentration of mTHPC Prepared by Ultra Turrax Method.
c. Stability for Penetrating Liposome with 0.75 mg THPC/ml Content.
Example 1 (storage temperature 4° C.)
Example 2 (storage temperature 4° C.)
The above data shows a penetrating liposomal mTHPC formulation which is stable.
Stability Data for Penetrating Liposomal Formulation with Different Lipids
The above stability data shows that the much preferred lipid for formulation is Ph 80 in isopropanol compared to Ph 50 in propylene glycol in regard to long-term shelf life. For applications where much shorter shelf lives are appropriate the Ph 50 system can also be used. The effective diameter of the liposome produced from Ph 80 in Isopropanol over a period of time shows better stability compared to the Ph50 in propylene glycol. Thus Ph 80 is a preferred embodiment over the Ph 50 in preparing liposomes for most applications.
Diluted solutions of this penetrating liposomes with mTHPC where measured at two different wavelengths to estimate the percentage of drug (mTHPC) lost during the filtration through 0.2 μm and 0.02 μm filters. Penetrating liposomes were able to cross the 0.02 μm membrane system without substantial loss of drug, whereas conventional liposomes are not. This shows the high flexibility of the liposome as they are able to cross membranes with a pore size of less than 20% of their own diameter. The difference of the mTHPC content at two different wavelengths (649 and 703 nm) was calculated to show that there no net loss of mTHPC content was observed between before and after filtration. This demonstrates a high efficiency of encapsulation of the drug.
Localization of mTHPC Within the Specialized Penetrating Liposomal Formulation
Gel filtration of highly specialized liposomal formulation performed on Sephadex G50 columns. As shown in
In vivo studies were performed in female NMR1 mice of 6 to 8 week old, inoculated with HT29 human colorectal carcinoma cell. Of the three treatment groups, 1st group served as a control while 2nd and 3rd group received the new penetrating liposomal formulated mTHPC on left thigh and tumor respectively. In the treatment groups the mTHPC content is checked at different time periods to study the effectiveness of the new penetrating liposomal formulation in transferring drug through the skin barrier to the targeted region in deeper layers of the skin. Four mice for each treatment group were sacrificed to record the mTHPC content in blood, skin, treated skin, tumor, muscle, liver and spleen at 0, 0.5, 3 and 6 hours after topical application of the new penetrating liposomal formulated mTHPC.
Second group of mice were treated with penetrating liposomal formulation loaded with mTHPC, which, was applied topical on the tumor and the mTHPC wet weight concentration in blood, liver, muscle, skin, skin treated, spleen and tumor at different time interval is plotted in
In all the above studies the mTHPC concentration in other tissues especially liver and spleen was lowered considerably thus reducing the toxicity to these critical tissues in the body.
Having described preferred embodiments of the invention with reference to the accompanying drawings, it is to be understood that the invention is not limited to the precise embodiments, and that various changes and modifications may be effected therein by those skilled in the art without departing from the scope or spirit of the invention as defined in the appended claims.
This application claims the benefit of U.S. Provisional Application Ser. No. 60/799,373 filed May 10, 2006, and U.S. Full Application filled on May 4, 2007, both of which are incorporated by reference herein.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US2007/011045 | 5/8/2007 | WO | 00 | 10/31/2008 |
| Number | Date | Country | |
|---|---|---|---|
| 60799373 | May 2006 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 11800147 | May 2007 | US |
| Child | 12226893 | US |
