Microcomplex for use in photoepilation process to obtain it and composition containing it

Abstract

The present invention relates to a microcomplex containing a modified nanoparticle adsorbed on a host microparticle and to a process to obtain it. The microcomplex is particularly useful for photoepilation. The present invention also relates to a composition containing the microcomplex and to the method for enhanced photoepilation based on the microcomplexes.

Claims

1. A microcomplex for use in photoepilation comprising: a nanocomplex which comprise a nanoparticle of a material selected from the group consisting of metals, semiconductors and their mixtures, supporting a Localized Surface Plasmon Resonance, which is coated by forming at least a bond, coordinate or covalent, with at least a polycationic polymer or a heterobifunctional compound which comprises at least a thiol group on one end of the molecule and at least a positively charged functional group on the other end; adsorbed on the surface of a host particle with a diameter comprised between 100 nm and 2000 nm; the microcomplex have a Z potential higher than 10 my.

2. The microcomplex according to claim 1 wherein the diameter of the host particle is comprised between 200 nm and 500 nm.

3. The microcomplex according to claim 2 wherein the host particle is silica.

4. The microcomplex according to claim 3 wherein the silica is a modified silica with amines group.

5. The microcomplex according to claim 1, wherein the microcomplex presents a localized surface plasmon resonance maximum between 700 and 900 nm.

6. The microcomplex according to claim 1, wherein the nanoparticle is a gold nanorod.

7. The microcomplex according to claim 1, wherein the polycationic polymer is a polyamine or polyimine containing polymer.

8. The microcomplex according to claim 7 wherein the polycationic polymer is chitosan or polyethyleneimine.

9. A process for the preparation of the microcomplex according to claim 1, which comprises: a) adding a suspension of nanoparticle coated with at least a polycationic polymer to a host microparticle with a diameter comprises between 100 nm and 2000 nm, under ultrasounds to obtain microcomplexes, and b) separating the microcomplexes obtained in the step a).

10. A process for the preparation of the microcomplex according to claim 1, which comprises: a) mixing amino modified host microspheres with a diameter comprises between 100 nm and 2000 nm with a surfactant coated nanoparticles to produce a suspension, b) sonicating the suspension c) incubating under stirring to obtain a microcomplex, and d) coating the resulting microcomplex with a polycationic polymer.

11. A composition comprising the microcomplex as defined in claim 1.

12. Photoepilation method which comprises the steps of (i) applying to the skin surface the composition for topical application as defined in claim 11, and (ii) applying a radiation from a radiation source to said surface of the skin.

13. Photoepilation method as described in claim 12 on which the radiation source is a LED device emitting in a wavelength ranging from 700 to 1200 nm.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 shows the comparative spectrum of gold nanorods adsorbed (show a peak on 792.5) or not (show a peak on 800.1) onto a silica microparticle surface.

(2) FIG. 2 shows the scanning electron microscopy (SEM) of gold nanorods adsorbed onto a silica microparticle surface.

(3) FIG. 3A shows the Two Photon Luminescence (TPL) image of a hair root incubated with gold-chitosan nanocomplexes. FIG. 3B shows an image of a hair root incubated with silica-gold-chitosan macrocomplexes.

(4) FIG. 4A, 4B. 4C show an illustrative example of the damage observed at 9 joul/cm.sup.2. FIG. 4A Untreated hairs, FIG.4B Silica gold microcomplexe, FIG. 4C gold nanocomplexes.

(5) FIG. 5 shows an estimation of the average damage observed for each treatment. Gold untreated hairs (black), gold chitosan nanocomplexes (grey) and silica-gold-chitosan macrocomplexes (white) at 3 J/cm.sup.2, 5 J/cm.sup.2, 7 J/cm.sup.2 and 9 J/cm.sup.2.

(6) FIG. 6 shows a representation of the relative hair root damage at different energies (abcisas, J/cm.sup.2) for different sizes of the host microparticle (nanocomplex (black square, and different silica microparticle of 235 (grey), 519 (white) and 2000 nm (black) diameter respectively).

(7) FIG. 7 shows a comparison of the hair root damage at 5 J/cm.sup.2 as a function of the host microparticle diameter in nm.

(8) FIG. 8 shows TPL image of a hair root incubated with silica aminated nanorods microcomplexes.

DETAILED DESCRIPTION OF THE INVENTION

(9) As mentioned above, an aspect of the present invention relates to a microcomplex for use in photoepilation comprising a nanocomplex which comprise a nanoparticle of a material selected from the group consisting of metals, semiconductors and their mixtures, supporting a Localized Surface Plasmon Resonance, which is coated by forming at least a bond, coordinate or covalent, with at least a polycationic polymer or a heterobifunctional compound which comprises at least a thiol group on one end of the molecule and at least a positively charged functional group on the other end; adsorbed on the surface of a host particle with a diameter comprised between 100 nm and 2000 nm; the microcomplex have a positive Z potential higher than 10 mV.

(10) The term host particle as used herein refers to particles which are essentially spherical form made of silica, modified silica, cellulose, modified cellulose as for example carboxymethyl cellulose or particles made of polyanionic polymers such as polystyrene sulfonate or polyacrylates. Preferred the host particle is made of silica or activated silica microparticles or surface modified silica microparticles (either with carboxylate, sulfonate, amine groups, epoxy groups or other organic groups). In a particular embodiment the host particle is made of activated silica and in a second particular embodiment the host particle is made of silica modified with amine groups.

(11) In a more preferred embodiment the diameter of the host particle is comprised between 200 nm and 500 nm.

(12) In an embodiment the Z potential is comprised between 10 mV and 150 mV.

(13) In a particular embodiment the metal nanoparticle is a gold nanoparticle.

(14) The nanoparticle presents in the microcomplex of the present invention are designed to present a LSP maximum contained between 650-1200 nm, which is the window where the absorption and thus the photoheating of the biological tissues is minimal. In this way, the contrast of absorption between the microcomplexes and the surrounding tissues is maximized and the possible photothermal damage caused to the surrounding tissues and/or glands is avoided.

(15) A choice of a resonance centered at around 700-900 nm is motivated by the subsequent minimum absorption (photoheating) of biological tissues.

(16) According to a preferred embodiment the microcomplex of the invention presents a localized surface plasmon resonance maximum between 700 and 900 nm.

(17) Furthermore, recent numerical studies enabled to quantify the influence of the geometry of gold NPs on its heating ability. It was demonstrated that the optical field intensity within the metal is the main parameter to be maximized in order to increase the temperature of the NP. This is the reason why, for a given illumination, elongated gold NPs (known as nanorod (NR)) generate more heat than gold nanospheres of the same volume. Considering all above-mentioned parameters, one can design gold NRs to act as efficient punctual heat-sources to be remotely controllable by light. Importantly, the temperature profile associated to a punctual heat source decays in 1/r, where r is the distance from the source.

(18) Therefore according to a preferred embodiment the microcomplex of the invention comprises a gold nanorod.

(19) Hair fibers are strongly keratinized conferring to the hair cuticle high polyanionic, therefore in a preferred embodiment the polycationic polymer is a polyamine or polyimine containing polymer; in a more preferred embodiment the polycationic polymer is quaternary ammonium polymer such as the polyquaternium-n series polymers, polyallyl ammonium polymers and copolymers thereof with polyamines, polyglycosamines and/or polyimines as polyethyleneimine. Among these polymers Chitosan (poly-glucosamine) and polyethyleneimine are polycationic polymers having strong affinity to gold by the formation of multiple weak covalent/coordination bonds leading to strongly charged polycationic (positively charges) nanoparticles. Therefore in a particular embodiment the polycationic polymer is chitosan or polyethyleneimine.

(20) In another embodiment of the invention a heterobifunctional compound is used. The heterobifunctional compound refers to a compound that comprises at least a thiol group on one end of the molecule and at least a positively charged functional group on the other end. Among these compounds Self Assembling Monolayer forming compounds are preferentially used. These compounds from the groups mercapto-(alkyl)-amino/dimethyl amino/quaternary ammonium:
HS(CH.sub.2).sub.nNH.sub.3
HS(CH.sub.2).sub.nN(CH.sub.3).sub.2
HS(CH.sub.2).sub.nN(CH.sub.3).sub.3.sup.+Cl.sup.

(21) In another embodiment of the invention the chain (CH.sub.2).sub.n can be replaced by a polyoxy-ethylene chain with the general formula: (CH.sub.2CH.sub.2O).sub.n, using then the series of heterobifunctional polyethylene glycols to obtain positively charged surfaces in the nanoparticles.

(22) According to another embodiment of the invention said chemical compound specifically binds through receptor-mediated processes, to a molecule target present on the basal cells of the hair. Examples of said compounds in this case are antibodies, which can be obtained and thereafter chemically modified to be grafted to the NP surface according to well known methods.

(23) In another aspect of the invention the composition of the invention is cosmetically or pharmaceutically acceptable. According to a particular embodiment the composition is an aqueous suspension. The composition may however be also in form of a gel, milk, lotion, ointment or cream. The microcomplexes are present in a cosmetically efficient amount. Under cosmetically efficient amount is to be understood the minimum amount to achieve a photoepilation effect in a photoepilation method. The composition may further contain other cosmetically or pharmaceutically acceptable ingredients such as solvent or cosmetic additives or vehicles.

(24) Another aspect refers to a photoepilation method which comprises the steps of (i) applying to the skin surface the composition for topical application as defined above, and (ii) applying a radiation to said surface of the skin. According to a particular embodiment the light source is an IPL with a light delivered through a head piece window defining a set area of illumination (emitting between 600-1000 nm). In this case, according to another particular embodiment a higher absorption contrast is achieved by filtering out the emission that does not overlap with the Plasmon resonance, minimizing melanin absorption and thus tissue heating without contributing to hair damage.

(25) The light source can also be a laser device emitting in a wavelength which match with the maximum absorption of the microcomplexes LSP, and in a range between 700-1100 nm. Another aspect refers to the possibility offered by the microcomplexes defined above to decrease the energy necessary to obtain an efficient hair removal. This aspect open the possibility to enlarge the technic to other less powerful light sources as LEDs (Light Emitting Devices). According to a particular embodiment the light source is a LED emitting in a wavelength that matches the maximum of absorption of the microcomplexes and particularly in the range from 700 nm to 1100 nm.

(26) The possibility offered of using lower energy emitting devices also permits to use larger application surfaces which would result in time reduced treatment sessions.

EXAMPLES

(27) The following examples are provided for illustrative means, and are not meant to be limiting of the present invention.

Example 1

Synthesis of the Microcomplexes of the Invention

(28) Preparation of the Microcomplexes

(29) Chitosan covered gold nanorods presenting a surface plasmon resonance (SPR) absorption maximum around 800 nm were prepared as described in the patent application WO2013079105 and maintained in lactate buffer 5 mM pH 6. The nanoparticle suspension presented an absorption maximum of around 6 UA corresponding to 0.2 mg/mL of gold. 10 mL of the nanorod suspension were added of 2.5 mg of silica (SiO.sub.2) microparticles of 0.235 micrometers under ultrasounds. The resulting suspension was then kept at room temperature and the formed microcomplexes decanted. Excess nanoparticles were removed and the microcomplexes washed twice with 5 mM lactate buffer pH 6.

(30) The FIG. 1 compares the absorption spectra of the microcomplexes and the dispersed gold nanocomplexes, indicating that absorption properties remain almost unchanged.

(31) The FIG. 2 shows a SEM micrography showing that the nanocomplexes accumulate at the microparticles surface.

Example 2

Comparative Example, Nanocomplex Versus Microcomplexes

(32) Nanocomplexes versus microcomplexes: delivery to the hair

(33) Fairs hairs isolated from pork skin and containing the whole root were incubated during 5 minutes in two suspensions of gold-chitosan nanocomplexes and silica-gold-chitosan microcomplexes. The characteristics of the two suspensions were as follows: gold nanorods covered in surface with chitosan presenting and absorption maximum at 800 nm of about 7 UA; gold nanorods covered in surface with chitosan and then adsorbed in the surface of 235 nm silica microparticles and presenting and absorption maximum around 800 nm of about 6 UA.

(34) Hairs were incubated at room temperature during 5 minutes and then washed extensively with water. The FIG. 3A and the FIG. 3B show a TPL image of two hairs after incubation with each of the two suspensions showing strong interaction of both nano and microcomplexes with the hair root.

(35) Nanocomplexes Versus Microcomplexes: Photothermal Efficiency

(36) The incubated hair samples were placed on microscopy slides before being illuminated with IPL. Exposure was performed with a single 30 millisec pulse of 4 different energies (3, 5, 7 and 9 joules/cm.sup.2). Using a high pass filter at 755 nm the light wavelength range was limited to 755-1200 nm in order to reduce the contribution of melanin to heating.

(37) Damage to the hair root was estimated visually by the change in colour and shape induced by IPL exposure (5 hairs per treated slide).

(38) The FIG. 4 A shows that at 9 joul/cm.sup.2 no effect is observed on gold complex untreated hairs while the hair root is destroyed either for nanocomplexes (FIG. 4C) or microcomplexes (FIG. 4B).

(39) The FIG. 5 shows comparative effect of IPL on fair hairs for gold untreated hairs, gold chitosan nanocomplexes and silica-gold-chitosan macrocomplexes. IPL consisted on a 30 msec single shot on isolated hairs placed in a microscopy slide. From FIG. 5, we observed a substantial increase of the heating efficiency of silica-gold microcomplexes over nanocomplexes, especially for low fluences.

(40) Study of Heating Efficacy as a Function of the Host Microparticle Particle Size

(41) Three sizes of microcomplexes were prepared by incubating silica microparticles with chitosan covered nanorods as described in Example 1.

(42) In this experiment three sizes of silica microparticles were used (0.235 m, 0.519 m and 2 m). Isolated pork fair hairs were incubated 5 minutes in each microcomplex suspension and then treated with IPL filtered at 755 nm at different energy levels.

(43) The amount of damaged to hairs root was estimated by evaluation in changes in shape and color of the hairs using a computer assisted image analysis software. Results are presented in FIG. 6. From these results an optimum size of the microcomplex to effectively transfer heat to the hair root is found to be around 200-500 nm.

(44) FIG. 7 shows an optimum host micropaticle size around 250 nm, which is more noticeable at 5 J/cm.sup.2.

Example 3

Preparation of Microcomplexes of Gold Nanorods on Aminated Silica Microparticles

(45) Gold nanorods presenting a maximum SPR are prepared as described in the Example 1. The nanorods suspension is centrifuged and the resulting pellet is re-suspended adjusting the CTAB (Cetyl Trimethyl Ammonium Bromide) concentration to 5 mM.

(46) 8 ml of the nanorods suspension are mixed with 2 ml of ethanol and 200 microliters of a silica-aminated microparticles of 237 nm diameter suspension at 50 mg/ml. The resulting suspension is sonicated at 45 C. during 15 minutes, incubated at 45 C. during 2 hours and then left to stand overnight at 30 C. under gentle stirring.

(47) Excess of nanorods are eliminated by decantation and the resulting microcomplexes are washed extensively with pure water.

(48) The resulting microcomplexes are then suspended in a solution of chitosan at 0.5 mg/ml and left stand overnight under gentle stirring at 30 C. This step is devoted to eliminate any CTAB left on the microcomplexes and to passivate the exposed surface of the nanorods linked with a polyaminated polymer.

(49) The microcomplexes resulting are finally washed extensively with pure water.

Example 4

Adsorption of Silica-amino Nanorods Microcomplexes to Hair Roots

(50) Fair pork hairs were incubated 10 minutes in an aqueous suspension of the silica aminated-nanorod microcomplexes (0.5 mg/ml) described in the Example 3.

(51) After this period hairs were washed with water and placed in microscope slides to observe the adsorption of microcomplexes at the keratinized hair root by Two Photon Luminescence (TPL), which is specific of the nanorods structure.

(52) FIG. 8 shows an image of a hair root on which the microcomplexes are effectively adsorbed.