Chitosan-pluronic complex and nano-carrier comprising same

Abstract

The present invention relates to a transdermal nano-carrier and, more specifically, to a nano-carrier having a chitosan-based nano-sponge structure. According to the present invention, as a nano-carrier having enhanced transdermal delivery on the basis of a complex containing chitosan is provided, it is possible to effectively deliver drugs, cosmetic materials, etc. into the skin.

Claims

1. A nanocarrier for transdermal penetration comprising a chitosan-pluronic complex in which chitosan is substituted at both ends of a pluronic polymer, and further comprising a pluronic polymer, wherein the chitosan-substituted pluronic polymer is represented by the following chemical formula 1,
(PEO)a-(PPO)b-(PEO)a  [Chemical Formula 1] wherein the PEO is polyethylene oxide, the PPO is polypropylene oxide, and the a and b are each independently an integer of 1 to 300, and wherein a weight ratio of the chitosan-pluronic complex and the pluronic polymer further comprised in the nanocarrier is 8:2.

2. The nanocarrier of claim 1, wherein the chitosan-pluronic complex includes chitosan having a molecular weight of 3 to 760 kDa.

3. The nanocarrier of claim 1, wherein the nanocarrier has a size of 500 nm or less.

4. The nanocarrier of claim 1, wherein the nanocarrier has a surface charge value of 0 to 50 mV.

5. The nanocarrier of claim 1, wherein the nanocarrier has a loading efficiency of 90% or more for Nile red.

6. The nanocarrier of claim 1, wherein the nanocarrier is a nanocarrier for transdermal penetration or oral administration.

7. A method of manufacturing the nanocarrier for transdermal penetration according to claim 1, the method comprising the steps of: (a) mixing a pluronic polymer with chitosan to prepare a complex in which chitosan is substituted at an end of the pluronic polymer; (b) mixing the complex with the pluronic polymer in the presence of a solvent to prepare a mixture; (c) dropping the mixture on distilled water; and (d) stirring the mixture-dropped distilled water.

8. The method of claim 7, wherein the step (a) comprises mixing chitosan with a molecular weight of 3 to 760 kDa.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a schematic diagram of a nanocarrier according to an embodiment of the present disclosure.

(2) FIG. 2 is .sup.1H-NMR analysis results of a reaction group-introduced pluronic polymer according to an embodiment of the present disclosure.

(3) FIG. 3 is .sup.1H-NMR analysis results of a chitosan-pluronic complex according to an embodiment of the present disclosure.

(4) FIG. 4 is results of measuring sizes and surface charge values of a nanocarrier according to an embodiment of the present disclosure.

(5) FIG. 5 is results of measuring amounts of chitosan on the surface of a nanocarrier according to an embodiment of the present disclosure.

(6) FIG. 6 is results of measuring stability values of a nanocarrier according to an embodiment of the present disclosure.

(7) FIG. 7 is results of analyzing drug loading efficiencies of a nanocarrier according to an embodiment of the present disclosure.

(8) FIG. 8 is results of analyzing cytotoxicity values of a nanocarrier according to an embodiment of the present disclosure.

(9) FIG. 9 is results of measuring skin penetration rate values of a drug using a nanocarrier according to an embodiment of the present disclosure.

(10) FIG. 10 is results of measuring skin penetration distribution images of a drug using a nanocarrier according to an embodiment of the present disclosure.

DESCRIPTION OF EXEMPLARY EMBODIMENTS

(11) Hereinafter, the present disclosure will be described in more detail through Examples. It will be obvious to a person having ordinary skill in the art that these examples are illustrative purposes only and are not to be construed to limit the scope of the present disclosure.

Example 1. Introducing a Reaction Group at Both End Groups of a Pluronic Polymer

(12) A reaction was performed on 323 mg of p-NPC (p-nitrophenyl chloroformate, 10 molar ratio) having excellent reactivity with amine at ends of 2 g of a polymer of Pluronic (Pluronic F127, (PEO).sub.a-(PPO).sub.b-(PEO).sub.a; the a and b are each independently an integer of 1 to 300) in 30 ml of dichloromethane (DCM). A reaction was performed at 0° C. for 24 hours using 130 μl of pyridine (10 mr) as a catalyst. Thereafter, a purification process was performed three times in cold ether to remove unreacted p-NPC and pyridine.

(13) The above-mentioned manufacturing process is illustrated in the following reaction formula 1:

(14) ##STR00001##

Measurement Example 1. .SUP.1.H-NMR Analysis of p-NPC-Pluronic

(15) After freeze-drying a p-NPC-Pluronic polymer manufactured in the above-mentioned Example 1 in a powdery state, .sup.1H-NMR was analyzed by dissolving the freeze-dried p-NPC-Pluronic polymer into D.sub.2O. The .sup.1H-NMR analysis results are illustrated in FIG. 2. Referring to FIG. 2, it can be confirmed that pyridine has completely been removed (substitution rate>98%, purity of 100%).

Example 2. Preparing Chitosan-Pluronic Complexes

(1) Example 2-1. Preparing a 3 kDa Chitosan-Pluronic Complex

(16) After dissolving 300 mg of the p-NPC-Pluronic polymer in DMSO to substitute chitosan at both ends of a p-NPC-Pluronic polymer manufactured in the above-mentioned Example 1, a reaction process was performed at room temperature for 12 hours by adding 900 mg of 3 kDa chitosan along with triethylamine (TEA) as a catalyst to the p-NPC-Pluronic polymer dissolved in DMSO. Thereafter, in order to improve purity, unreacted chitosan was precipitated in acetone and removed, and unreacted TEA and p-NPC were removed from cold ether. Further, in order to improve purity, the impurity-removed chitosan-pluronic complex was freeze-dried in a powdery state after dialyzing the chitosan-pluronic complex in a deionized water, thereby removing impurities from the dialyzed chitosan-pluronic complex. The above-described preparation process is illustrated in the following reaction formula 2.

(2) Example 2-2. Preparing a 10 kDa Chitosan-Pluronic Complex

(17) The 10 kDa chitosan-pluronic complex was prepared by the same method as in Example 2-1 except that 10 kDa chitosan was used.

(18) ##STR00002##

Measurement Example 2. .SUP.1.H-NMR Analysis of Chitosan-Pluronic Complexes

(19) After performing a .sup.1H-NMR analysis process by dissolving chitosan-pluronic complexes in a powdery state prepared in Examples 2-1 and 2-2 in D.sub.2O, results of the process are shown in FIG. 3. Referring to FIG. 3 (a result of a left graph: using of 3 kDa chitosan (Example 2-1), a result of a right graph: using of 10 kDa chitosan (Example 2-2)), it can be confirmed that chitosan-pluronic complexes having a substitution rate of 98% or more irrespective of molecular weights of the chitosans can be prepared.

Example 3. Manufacturing Nanocarriers

(20) Nanocarriers (3 kDa chitosan-substituted nanocarrier: Chi.sub.3k-NS, 10 kDa chitosan-substituted nanocarrier: Chi.sub.10k-NS)) were manufactured through nanoprecipitation by adjusting a ratio of the chitosan-pluronic complex prepared in Example 2 prepared in the above-mentioned Example 2 to pluronic. More specifically, after dissolving a 3 kDa or 10 kDa chitosan-substituted chitosan-pluronic complex prepared in the above-mentioned Example 2 and pluronic to a concentration of 10 mg/ml of acetone (99%, sigma aldrich) at weight ratio of 5:5, 8:2, and 10:0 to prepare mixed solutions, and slowing injecting 1 ml of the mixed solutions at a rate of 0.1 ml/min into 5 ml of deionized water that had been stirring at a rotation speed of 500 rpm, the mixed solutions were reacted with the deionized water at room temperature for 12 hours or more, and an acetone solvent was naturally evaporated and removed in the reaction process. The above-described manufacturing process is illustrated in the following reaction formula 3:

(21) ##STR00003##

Measurement Example 3. Measuring Sizes and Surface Charges of Nanocarriers

(22) After filtering the nanocarriers manufactured in the above-mentioned Example 3 with a 0.2 μm syringe filter to obtain nanosponges, and analyzing sizes and surface charge values of 2 mg/ml of the nanosponges using DLS (ELS-8000, Otsuka Electronics Co., Japan) equipment, the analysis results are illustrated in FIG. 4.

(23) Referring to FIG. 4, the manufactured nanocarriers show uniform distributions and sizes of 140 nm or less in all groups, and differences in sizes according to mixing ratios and molecular weights of chitosans are not shown to be great.

(24) However, as results of measuring surface charge values, in case of formulations into which large amounts of chitosans are injected according to mixing ratios of the chitosan-pluronic complexes and pluronic, measured surface charge values shown higher positive charges (about +11 mV.fwdarw.about +18 mV), and differences in surface charge values according to the molecular weights of chitosans have not been observed.

Measurement Example 5. Measuring Chitosan Amounts on Surfaces of Nanocarriers

(25) A measurement process was performed using Ninhydin assay to quantitatively analyze chitosan amounts on surfaces of the nanocarriers manufactured in the above-mentioned Example 3. After mixing nanocarrier solutions with Nin-hydrin reagents (2% solutions) at a volume ratio of 1:1 to obtain mixed solutions, the mixed solutions were reacted at a 90° C. condition for 30 minutes to obtain final reaction solutions. After quantitatively measuring amounts of chitosans by measuring 570 nm UV absorbance values of the final reaction solutions (violet), measurement results of the chitosan amounts are illustrated in FIG. 5.

(26) Referring to FIG. 5, more amounts of chitosans exist in case of formulations into which more amounts of chitosans are injected according to mixing ratios.

Measurement Example 6. Stability Evaluation of Nanocarriers

(27) An analysis process was performed using DLS equipment to check if agglomeration phenomena of the nanocarriers were exhibited by time at conditions (PBS (pH 7.4), 37° C.) similar to an in vivo environment to evaluate stability of the nanocarriers manufactured in the above-mentioned Example 3. More specifically, after observing if stabilities of chitosans were maintained under conditions of 37° C. and 100 rpm for 7 days, observation results of the stabilities of chitosans are illustrated in FIG. 6. Referring to FIG. 6, it can be confirmed that the nanocarriers can be stable in the in vivo environment according as it is observed that the agglomeration phenomena are not exhibited, and uniform sizes of the nanocarriers are well maintained for 0 to 7 days.

Measurement Example 7. Evaluating Drug Loading Efficiencies and Characteristics of Drug-Loaded Nanocarriers

(28) The nanocarriers were loaded along with Nile red (ex.530 nm/em.635 nm) which had hydrophobic characteristics as a model drug and could exhibit red fluorescence when manufacturing nanocarriers. As results of analyzing loading efficiencies, about 95% of high loading efficiencies were exhibited.

(29) After loading drugs, results of observing variations in sizes and surface charge values of the nanocarriers are illustrated in FIG. 7. Referring to FIG. 7, although a minute difference exists between sizes and surface charge values of the nanocarriers before and after loading the drugs in all conditions, there is not the difference statistically. Accordingly, it can be confirmed that the drugs are stably collected in hydrophobic polymer portions inside nanosponges.

Measurement Example 8. Evaluating Nanocarrier Cytotoxicity

(30) After applying Mouse Embryonic fibrolast cell line (NIH/3T3, passage #15, 1×10.sup.4 cells/wess) to 96 well cell culture plates, the 96 well cell culture plates having the Mouse Embryonic fibrolast cell line applied thereto were stabilized for about 12 hours (cell culture medium: DEMS including 10% of FBS and 1% of antibiotics)

(31) After manufacturing nanocarriers having Nile red as a model drug loaded thereon in an amount of 1,000 μg/ml, adding the nanocarriers to cells, the nanocarriers added to the cells were cultured for 24 hours. After analyzing effects of the nanocarriers on cell metabolism in each group using WST-8 evaluation method, analysis results are illustrated in FIG. 8.

(32) Referring to FIG. 8, it can be confirmed that the nanocarriers are excellent in bio compatibility without causing cytotoxicity up to the amount of 1,000 μg/ml in all conditions.

Measurement Example 9. Evaluating Skin Penetration Rates of Drugs

(33) After injecting 5 ml of PBS, i.e., a release buffer into a receptor chamber of Franz type diffusion cell to experiment skin penetration of drugs, and covering human cadaver skin with a size of 1.5×1.5 cm.sup.2 between the receptor chamber and a donor chamber, 2 mg/ml of each of samples (nanocarriers having a drug (Nile red) loaded thereon) was injected into a donor portion of Franz cell.

(34) An analysis process was performed by measuring amounts of the drugs penetrating the skin after adjusting temperature and rotation speed of the receptor chamber to 37° C. and 600 rpm and recovering the drug-loaded nanocarriers as much as 500 μl for a sampling time of 0.5, 1, 2, 4, 8, 12, 18, or 24 hours.

(35) Referring to FIG. 9, when nanocarrier formulations rather than control groups (drugs themselves) are used, it can be confirmed that skin penetration rates of the drugs are increased 4 times or more. Particularly, the highest skin penetration rates of the drugs were observed at formulations (3k-8:2) having the nanocarriers mixed with the chitosan at a ratio of 8:2 in nanocarriers substituted with 3 kDa chitosan's (skin penetration rates of the formulations (3k-8:2) were improved as much as about 8 times compared to the control groups).

(36) Further, it can be confirmed that, in case of nanocarrier formulations using 3 kDa chitosan rather than nanocarrier formulations having the nanocarriers substituted with 10 kDa chitosan, it can be confirmed that molecular weight of chitosan may also have an effect on the skin penetration rates of the drugs according as skin penetration rates of drugs are improved.

(37) After completing a skin penetration experiment of the drugs, skins were fixed in a 1-% neutral formalin solution for 12 hours or more to confirm how the drugs were distributed in the skins. After mixing the fixed skins with an OCT compound, allowing OCT compound-mixed skins to be frozen in liquid nitrogen of −20° C. or less, and cutting the frozen skins to a thickness of 20 μm through a cryo-section device (−25° C.), sampling was made by attaching the cut skins to glass. After washing samples with deionized water and observing distribution statuses of a model drug (Nile red) in the skins with a fluorescence microscope, observation results are illustrated in FIG. 10.

(38) Referring to FIG. 10, it is observed that drugs having hydrophobicity and low molecular characteristics are collected in stratum corneum in a control group using a drug (Nile red) alone without using a nanocarrier, while it is observed that the drug is evenly spread to an epidermal layer and a dermal layer by permeating the stratum corneum in a group of using the nanocarrier.

(39) Particularly, it has been confirmed that the formulations (Chi.sub.3k-NS) can be used as a novel platform to deliver various incurable disease treating drugs into the skin according as a high amount of fluorescence is observed from a formulation (Chi.sub.3k-NS) having the nanocarriers mixed with the 3 kDa chitosan at a ratio of 8:2, i.e., an optimal formulation condition.

(40) As described above, the present disclosure has an effect of enabling a drug, a cosmetic material or the like to be efficiently delivered into the skin by providing a nanocarrier with improved skin penetration rate having its roots in a complex including chitosan.

(41) Further, the present disclosure has an effect enabling the drug, the cosmetic material or the like to be stably delivered even in an in vivo environment by minimizing an agglomeration phenomenon of the nanocarrier.

(42) Further, the present disclosure has an effect of providing a nanocarrier for transdermal penetration which has excellent bio compatibility since the nanocarrier does not cause cytotoxicity.

(43) Although the present disclosure has been described along with the accompanying drawings, this is only one of various examples including the gist of the present disclosure and has an object of enabling a person having ordinary skill in the art to easily practice the invention. Accordingly, it is evident that the present disclosure is not limited to the aforementioned examples. Accordingly, the range of protection of the present disclosure should be interpreted based on the following claims, and all of technological spirits within the equivalents of the present disclosure may fall within the range of right of the present disclosure by changes, substitutions and replacements without departing from the gist of the present disclosure. Furthermore, it is evident that the configurations of some drawings have been provided to more clearly describe configurations and have been more exaggerated or reduced than actual configurations.