Polymer, thermosensitive carrier and use thereof

Abstract

Disclosed herein are a novel polymer, a thermosensitive carrier prepared using the same and use thereof. The novel polymer is essentially composed of a PEO-PPO-PEO block copolymer and silane.

Claims

1. A thermosensitive carrier, comprising: a gold nanorod; and an outer coating entrapping the gold nanorod, wherein the outer coating is comprised of an organic/inorganic amphilic thermosensitive polymer, having a structure as shown in Formula (1): ##STR00002## wherein the x is 98 y is 68, and z is 98.

2. The thermosensitive carrier according to claim 1, further comprising a pharmaceutical composition entrapped by the outer coating.

3. The thermosensitive carrier according to claim 2, wherein the pharmaceutical composition is an anti-cancer agent.

4. A method for treating cancer in a subject, comprising: administering to the subject a therapeutically effective amount of the thermosensitive carrier according to claim 2.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) To make the above and other objectives, features, advantages, and embodiments of the present invention more apparent, the present invention is described with reference to accompanying drawings, in which:

(2) FIG. 1 is a flow chart of a method for synthesizing the present polymer according to an embodiment of the present invention;

(3) FIG. 2 is an NMR spectrum of the present polymer according to an embodiment of the present invention;

(4) FIG. 3 is an IR spectrum of the present polymer according to an embodiment of the present invention;

(5) FIG. 4 is a flow chart of a method for preparing a thermosensitive carrier according to another embodiment of the present invention;

(6) FIG. 5A is a transmission electron microscope (TEM) photo of the present gold nanorods;

(7) FIG. 5B is a TEM photo of the present thermosensitive carrier;

(8) FIG. 6 shows results of dynamic light scattering of the thermosensitive carrier according to an embodiment of the present invention;

(9) FIG. 7 shows a drug release profile of the present controlled release thermosensitive carrier according to an embodiment of the present invention with or without irradiation with laser at 808 nm;

(10) FIG. 8A shows results of temperature increment measured after the present controlled release thermosensitive carrier is injected into mice with tumors via the tail vein and the tumor site is irradiated for 30 s with laser at 808 nm according to an embodiment of the present invention; and

(11) FIG. 8B shows a growth profile of a tumor in 14 days after irradiation with laser at 808 nm is administered to the tumor site as shown in FIG. 8A.

DETAILED DESCRIPTION OF DISCLOSED EMBODIMENTS

(12) To make the description of the present disclosure more thorough and complete, the implementations and specific embodiments of the present invention are exemplarily described hereinafter. However, the implementations and specific embodiments of the present invention are not limited thereto.

(13) Unless otherwise stated, the scientific and technical terms used in the specification have the same meaning as commonly understood by those of ordinary skill in the art. Moreover, the referent used in the specification may be singular or plural, unless otherwise indicated.

(14) The term subject or patient refers to an animal that can receive the thermosensitive carrier of the present invention. In a preferred embodiment, the animal is a mammal and particularly human.

(15) The term cancer may be a non-solid or solid tumor. For example, the cancer includes, but is not limited to, leukemia, lymphoma, diaphysial osteosarcoma, multiple myeloma, testis carcinoma, thyroid cancer, prostate cancer, throat cancer, cervical cancer, nasopharyngeal cancer, breast cancer, colorectal cancer, pancreatic cancer, head and neck cancer, esophageal cancer, rectal cancer, lung cancer, liver cancer, brain cancer, melanoma or skin cancer.

(16) As used in the specification, the term about generally means that the actual value is within 10%, 5%, 1%, or 0.5% of a particular value or range. About indicates herein that the actual value falls within an acceptable standard error of the average, depending on the considerations of persons of ordinary skill in the art. Besides the case in the experimental examples, or unless stated specifically otherwise, it should be understood that the range, amounts, values, and percentages used herein are all modified by about. Accordingly, unless stated otherwise, the values or parameters disclosed in the specification and appended claims are all rough values and may be changed as desired.

(17) To solve the problem existing in the prior art, the present invention provides a new polymer and a thermosensitive carrier. In contrast to the prior art, the anti-cancer drugs and especially lipid soluble anti-cancer drugs can really be entrapped by the thermosensitive carrier prepared by using the new polymer material in the present invention. The thermosensitive carrier of the present invention can prevent the natural release of drugs entrapped in the carrier without the aid of additional materials, such that the drug release can be accurately controlled, thereby reducing the occurrence of side effects. Moreover, the thermosensitive carrier of the present invention can combine the chemotherapy and the thermal therapy together to produce a synergistic therapeutic effect, thus greatly increasing the tumor treatment efficiency. Meanwhile, the thermosensitive carrier of the present invention also has a good biocompatibility and a low toxicity.

(18) Numerous examples are given below to illustrate various implementations of the present invention, whereby the technical contents disclosed in the present invention can be practiced by those of ordinary skill in the art based on the disclosure in the specification. Accordingly, the examples given below are not intended to limit the protection scope of the present invention. Furthermore, all the literatures cited in the specification are incorporated herein by reference in their entirety.

(19) In the present disclosure, a controlled release thermosensitive carrier is formed by entrapping gold nanorods and a lipid soluble anti-cancer drug in a special organic/inorganic amphilic thermosensitive polymer, whereby light to heat conversion is effected by absorbing the laser by the gold nanorods, and the polymer deforms under compression with the heat energy, to press and release the anti-cancer drug. In this way, both the thermal therapy and the chemotherapy are achieved.

EXAMPLE 1

Synthesis of Polymer of the Present Invention

(20) The main scheme for chemical synthesis in this example was shown in FIG. 1. The synthesis steps were as follows. The PEO-PPO-PEO block polymer used in this example was the F127 polymer (MW=12600). 10 g of F127 was dissolved in 100 ml of N-methyl-2-pyrrolidone (NMP), and then 0.2 g of succinic anhydride (SA) and 0.2 g of 4-(dimethyl-amino)pyridine (DMAP) were added and heated to about 60 C. The reaction was continued for 24 hrs under a nitrogen atmosphere, to obtain a product F127-carboxylate. Then, 0.2 ml of thionyl chloride, 0.2 ml of triethyl amine (TEA) and 0.3 ml of 3-aminopropyl triethoxysilane (APTES) were added and reacted for 24 hrs. After reaction, the product was extracted with ether (3). In this manner, a OH functional group on the F127 polymer was chemically converted into a SiOH functional group, and a silylated organic/inorganic amphilic thermosensitive polymer, that is, the polymer of the present invention (the structure as shown in Formula (1); referred to as Silane-127 hereinafter) was formed. After characterization by NMR and IR sepectrometry, the results are shown in FIGS. 2 and 3 respectively.

(21) FIG. 2 is a proton-NMR spectrum of silane-F127. It can be found from FIG. 2 that there are obvious shifts and additional peaks in the proton-NMR spectrum of the F127 polymer modified with silane. It can be inferred that the peak at 1.22 ppm is attributed to the contribution of the hydrogen atoms on SiOCH2-CH3, and the peak at 4.7 ppm is attributed to the contribution of the hydrogen atoms on CH2-CH2-O in the F127 polymer. Furthermore, the change of function groups on silane-F127 compared with F127 is determined by IR sepectrometry in this example. The determination results are shown in FIG. 3. It can be found from FIG. 3 that the peak at 1100 cm.sup.1 is attributed to SiOH and the peaks at 1650 cm.sup.1 and 1550 cm.sup.1 are attributed CONH. Based on the results from proton-NMR, carbon-NMR, and IR sepectrometry, the structure of the polymer silane-F127 according to the present invention can be determined.

EXAMPLE 2

Synthesis of Thermosensitive Carrier According to the Present Invention

(22) 2.1 Synthesis of Oil Soluble Gold Nanorods

(23) 0.3645 g of cetyltrimethyl-ammonium bromide (CTAB) was dissolved in 5 ml of deionized water, and stirred for 30 min. Then, 5 ml of 510.sup.4 M gold (III) chloride hydrate (HAuCl4) was added, and 0.6 ml of 110.sup.2 M sodium borohydride (NaBH4) was slowly added, upon which the color of the solution changed from clear yellow to clear brown, that is, the nano gold seeds were gradually formed. Finally, the formulated gold nanorod growth solution (1.385 g of cetyltrimethylammonium bromide (CTAB) dissolved in 38 ml of deionized water, 2 ml of 110.sup.2 M hydrogen tetrachloroaurate (III) trihydrate (HAuCl4), 0.4 ml of 0.1 M silver nitrate (AgNO3), and 0.22 ml of 1 M L-ascorbic acid) was added to the nano gold seed solution. After 24 h reaction, gold nanorods were produced. Then, cetyltrimethylammonium bromide (CTAB) on the surface of gold nanorods was removed and 300 L of 1-octadecanethiol was added and reacted, to produce the oil soluble gold nanorods.

(24) 2.2 Synthesis of Controlled Release Thermosensitive Carriers (SFGRs)

(25) The main scheme for synthesizing the thermosensitive carrier in this example was shown in FIG. 4. A 2 wt % solution of the polymer silane-F127 was formulated in deionized water. Then, the 2 wt % solution of the polymer silane-F127 was evenly shaken for 3 min in an ultrasonic homogenizer together with the oil soluble gold nanorods and a lipid soluble anti-cancer drug (paclitaxel) dissolved in chloroform, upon which the solution was cloudy. Subsequently, the solution was transferred to a hot plate, heated to about 60 C., and magnetically stirred. After the oily solution was removed, the remaining solution was clear. The aqueous ammonia was added to subject the silyloxy group to hydrolysis and condensation. In this manner, the controlled release thermosensitive carrier of the present invention was obtained. The carrier was finally analyzed by transmission electron microscopy and dynamic light scattering.

(26) FIGS. 5A and 5B are TEM photos of the gold nanorods and thermosensitive carrier according to the present invention respectively. It can be clearly seen from the photo in FIG. 5B that the thermosensitive carrier does entrap the gold nanorods, and a layer of silicon oxide is formed on the surface. The results of dynamic light scattering show that the thermosensitive carrier of the present invention has a particle size of about 120 nm, as shown in FIG. 6.

EXAMPLE 3

Drug Release Profile of the Thermosensitive Carrier According to the Present Invention

(27) The thermosensitive carrier prepared in Example 2 was used in this example for determining the drug release profile. The results show that the thermosensitive carrier entrapping the anti-cancer drug has an excellent entrapment effect, and the drug cannot be naturally released.

(28) The paclitaxel concentration released was measured by HPLC and calculated. Before irradiation with laser at 808 nm is administered, the drug molecules are well entrapped (no more than 5% of the drug is naturally released), and the carrier is useful as a system for long-term entrapment of the drug. However, after 30 s-irradiation with laser at 808 nm is administered, an absorption peak of the drug molecules can be immediately detected by HPLC. It is found from calculation that up to 70% of the drug is released, suggesting that after irradiation with laser, the light energy is absorbed and converted into heat energy by the thermosensitive carrier of the present invention, such that the thermosensitive polymer is contracted and compressed, to release the drug. The drug is released rapidly, to achieve a controlled release effect, as shown in FIG. 7.

EXAMPLE 4

Efficacy of the Thermosensitive Carrier According to the Present Invention in Animal Model of Tumor

(29) The thermosensitive carrier prepared in Example 2 was intravenously injected into mice xenografted with A549 human lung cancer cells, and circulated for 12 hrs in the mice. Continuous 30 s-irradiation with laser at 808 nm was administered at the tumor site. The results are shown in FIG. 8A.

(30) Thermal effect is produced at the tumor site immediately in the mice administered with the thermosensitive carrier of the present invention. It is found from consecutive 14 days observation after the 30 s-irradiation with laser at 808 nm is administered at day 1 that the tumors of the mice almost disappear completely, and the calculation result of the tumor volume is shown in FIG. 8B.

(31) The results of this experimental example confirm that the thermosensitive carrier of the present invention can accurately control the drug release, deliver the drug precisely to the tumor site, and effectively reduce the tumor size in the animal model, thus having a significant therapeutic effect.

(32) It can be known from the results obtained in all the examples above that the thermosensitive carrier of the present invention has an efficient thermal therapeutic effect in-vitro and in-vivo. Meanwhile, the thermosensitive carrier of the present invention may be loaded with, and effectively control the release of an anti-cancer drug.

(33) The specific examples disclosed above are not intended to limit the protection scope of the present invention. Modifications may be made by those of ordinary skill in the art without departing from the principle and spirit of the present invention. Therefore, the scope of the present invention is defined by the claims.