阅读说明：本技术 一种生物可降解两性离子聚碳酸酯及其应用 (Biodegradable zwitterionic polycarbonate and application thereof ) 是由 陈维 陈莹 黄德春 钟伊南 于 2020-03-05 设计创作，主要内容包括：本发明公开了一种生物可降解两性离子聚碳酸酯及其应用,主要是利用含有羟基官能团的化合物或聚合物为引发剂开环聚合环碳酸酯单体,得到功能性聚合物,丙烯酰胺类两性离子化合物与二巯基类化合物反应合成巯基化两性离子化合物,最后功能性聚合物和巯基化两性离子化合物进行Michael加成反应,即得所述生物可降解两性离子聚碳酸酯,本发明聚合物简单易合成,其聚合分子量可控,能自组装纳米药物,可用于肿瘤,炎症等多种疾病治疗,也可用于抗菌支架涂层。与以往研究相比,此类生物可降解聚合物制备简单,抗蛋白吸附能力强,减少免疫反应,其有望在生物医学领域有着广泛的应用前景。(The invention discloses a biodegradable zwitterionic polycarbonate and application thereof, and the biodegradable zwitterionic polycarbonate is mainly prepared by ring-opening polymerization of a cyclic carbonate monomer by using a compound or a polymer containing a hydroxyl functional group as an initiator to obtain a functional polymer, reacting an acrylamide zwitterionic compound with a dimercapto compound to synthesize a mercapto zwitterionic compound, and finally carrying out Michael addition reaction on the functional polymer and the mercapto zwitterionic compound. Compared with the previous research, the biodegradable polymer has the advantages of simple preparation, strong protein adsorption resistance and immune reaction reduction, and is expected to have wide application prospect in the field of biomedicine.)

1. A biodegradable zwitterionic polycarbonate is characterized in that a compound or polymer containing a hydroxyl functional group is mainly used as an initiator to carry out ring opening polymerization on a cyclic carbonate monomer to obtain a functional polymer, an acrylamide zwitterionic compound and a dimercapto compound react to synthesize a mercapto zwitterionic compound, and finally the functional polymer and the mercapto zwitterionic compound are subjected to Michael addition reaction to obtain the biodegradable zwitterionic polycarbonate.

2. The biodegradable zwitterionic polycarbonate of claim 1, wherein the cyclic carbonate monomer is selected from compounds represented by the following structures:

wherein R is₂Is selected from H or CH₃。

3. The biodegradable zwitterionic polycarbonate of claim 1, wherein the compound or polymer containing hydroxyl functional groups is selected from isopropanol, polyethylene glycol or benzyl alcohol.

4. The biodegradable zwitterionic polycarbonate of claim 1, wherein the acrylamide-based zwitterionic compound is selected from compounds represented by the following structures:

5. the biodegradable zwitterionic polycarbonate of claim 1, wherein the dimercapto-based compound is selected from compounds represented by the following structures:

6. the biodegradable zwitterionic polycarbonate of claim 1, wherein the acrylamide zwitterionic compound and the dimercapto compound are reacted in an organic solvent by adding organic amine to synthesize a thiolated zwitterionic compound.

7. Nanoparticles made of the biodegradable zwitterionic polycarbonate of any one of claims 1-6.

8. Use of the biodegradable zwitterionic polycarbonate of any one of claims 1-6 in the preparation of an anti-tumor medicament.

Technical Field

The invention relates to a biodegradable zwitterionic polycarbonate with nonspecific protein adsorption resistance, and a preparation method and application thereof, and belongs to the technical field of high polymer materials.

Background

The adsorption of proteins on the surface of materials is a very common phenomenon and brings many adverse effects to people. For example, nonspecific adsorption of proteins can cause biomedical materials to cause cells to adsorb, spread, proliferate, and even die on their surfaces; decreasing the sensitivity of the biosensor, etc. The protein is strongly adsorbed on the hydrophobic surface, and the hydrophobic surface destroys the protein structure to denature and inactivate the protein. Therefore, hydrophilic substances are constructed on the surface of the material, so that the adsorption of nonspecific proteins can be resisted. In the past decades, people have been devoted to research on polyethylene glycol (PEG) and Phosphorylcholine (PC) substances as materials for resisting nonspecific protein adsorption, but PEG has relatively poor stability and is easily oxidized in a biological environment. Meanwhile, studies have shown that the PEG modified protein drug carrier can induce the phenomenon of accelerating blood clearance, which is related to the immune reaction induced by PEG. Therefore, these drawbacks prevent the PEG-based derivatives from being used for a long period of time to varying degrees.

As described above, the nonspecific protein-resistant adsorbent can improve the effect to some extent. Zwitterionic polymers are a class of polymers that contain zwitterionic groups or a mixture of anionic and cationic end groups in the polymer chain. The polymer is characterized in that: the polymer molecular chain contains both anionic groups and cationic groups, and the total number of positive and negative charges is equal. For this reason, zwitterionic polymers can be broadly classified into two categories: one type is an amphoteric polyelectrolyte with positively and negatively charged groups 1:1 distributed over two or more different monomers, e.g. with mixed charges-N⁺(CH₃)₃and-SO₃ ^-/COO^-The compound of (1), etc.; another type is amphoteric poly with positively and negatively charged groups on the same monomerThe compounds, i.e., salt-based polymers, such as those commonly referred to as betaine-based polymers, include phosphate betaine, sulfonate betaine, and carboxylate betaine polymers.

Due to the unique chain structure, the zwitterionic polymer has excellent chemical properties, good thermal stability and hydration performance, and has attracted wide attention worldwide in recent years. Up to now, many new and functionalized zwitterionic polymers have been synthesized and applied to various fields of the petroleum industry, biomedical materials, drug synthesis, sewage treatment, and the like. Regarding the application of zwitterionic materials in the biomedical field, two major areas are mainly focused on: in the microscopic field, the method is mainly used for drug slow release and gene vectors; in the macroscopic field, it is mainly used for modifying biological materials. In recent years, two methods, namely 'grafted-from' and 'grafted-on', are utilized to polymerize and graft the zwitterionic liquid on the surface of the biological material to form the zwitterionic polymer brush, and experiments show that the zwitterionic polymer brush has good protein adsorption resistance, and compared with the traditional material, the zwitterionic polymer brush has good biocompatibility, antibacterial property and anticoagulant property. In this respect, Yang et al (Biomaterials,2009.30(29): p.5617-5621.) modify the gold nanoparticles with PCBAA, although the particles modified with PEG have equivalent anti-protein adsorption capacity in 10% serum, in undiluted serum, the anti-nonspecific protein adsorption capacity is higher than that of the traditional PEG modified particles, and the stability of the gold nanoparticles is obviously increased by the high-efficiency nonfoulding performance. Jiang et al (biomaterials.2011; 32:4604-8.) have utilized CB to prepare degradable multifunctional nanogels that exhibit very low macrophage phagocytosis and significant uptake by human venous endothelial cells, which implies low interaction with their immune system and high selectivity for targeting cells. The amphoteric ion polymer is also grafted to the surfaces of metal, glass and the like through atom transfer radical polymerization, self-assembly method and other polymerization, has good protein adsorption resistance, antibacterial adhesion resistance and anticoagulation capacity, and is environment-friendly.

Biodegradable polymers generally have good biocompatibility and biomechanical properties, are eventually degraded in vivo by enzymatic or non-enzymatic pathways to the exclusion of the body, and the degradation products are also biocompatible. Such polymers have been widely used in various fields, particularly in biomedical fields, such as biodegradable sutures, biological stent materials, drug delivery vehicles, and the like. In order to meet more demands, synthetic biodegradable polymers have also been rapidly developed. The task group of the Shizu teacher discloses a cyclic carbonate monomer containing acrylate functional groups and preparation and application thereof (CN 101633654). The cyclic carbonate monomer is easy to prepare, and can conveniently carry out different modification on acrylate functional groups through Michael addition reaction, so that the side chain of a polymer contains functional groups such as hydroxyl, carboxyl, amino and the like. Research has shown that the combination of Michael addition reactions is an efficient and feasible method for synthesizing biologically active materials. Therefore, the cyclic carbonate has more obvious bioactivity and controllable degradation performance and mechanical performance than natural degradable polymers.

In summary, polyethylene glycol shielding is by far the most successful strategy to overcome these drawbacks in clinical tumor therapy, and a number of pegylated proteins have been marketed. However, clinically, therapeutic-induced anti-PEG antibodies have attracted serious attention for the future of pegylated therapeutic drugs.

Disclosure of Invention

The purpose of the invention is as follows: in view of the above application problems, the main object of the present invention is to provide a biodegradable zwitterionic polycarbonate and its preparation and application.

The technical scheme is as follows: in order to achieve the purpose of the invention, the invention adopts the following technical scheme:

a biodegradable zwitterionic polycarbonate is prepared by mainly utilizing a compound or a polymer containing a hydroxyl functional group as an initiator to carry out ring opening polymerization on a cyclic carbonate monomer to obtain a functional polymer, reacting an acrylamide zwitterionic compound with a dimercapto compound to synthesize a mercapto zwitterionic compound, and finally carrying out Michael addition reaction on the functional polymer and the mercapto zwitterionic compound.

Preferably, the method comprises the following steps:

the cyclic carbonate monomer is selected from compounds represented by the following structures:

wherein R is₂Is selected from H or CH₃。

The compound or polymer containing hydroxyl functional groups is selected from isopropanol, polyethylene glycol or benzyl alcohol.

The acrylamide zwitterionic compound is selected from compounds shown in the following structures:

the dimercapto compound is selected from compounds shown in the following structures:

adding organic amine into an organic solvent for reaction between the acrylamide zwitterionic compound and the dimercapto compound to synthesize the sulfhydrylation zwitterionic compound.

The structural formula of the biodegradable zwitterionic polycarbonate is shown as the general formula (I):

wherein:

R₁is an initiator unit, wherein when the initiator is selected from polyethylene glycol, the molecular weight of the initiator is 1000-20000;

R₂is selected from H or CH₃；

R₃Being two of a mercapto zwitterionic compound unitA zwitterionic group;

x＝5～100，y＝1-50。

as a further preferred scheme, the biodegradable zwitterionic polycarbonate can be prepared by the following method:

isopropanol is used as an initiator, dichloromethane is used as a solvent, bis (bistrimethylsilyl) amine zinc is used as a catalyst, an acrylate carbonate monomer is selected for ring-opening polymerization to prepare a hydrophobic polymer, an acrylamide zwitterionic compound and a dimercapto compound are reacted to synthesize a mercapto zwitterionic compound, N-dimethylformamide and methanol are used as a mixed solvent, the zwitterionic compound is successfully modified on a side chain of the acrylate carbonate through Michael addition reaction, and finally the zwitterionic polycarbonate is prepared.

The invention also provides nanoparticles prepared from the biodegradable zwitterionic polycarbonate.

The zwitterionic polycarbonate and the nanoparticles are used as drug carriers, so that long circulation of drugs can be promoted, and immunogenicity is reduced.

The invention finally provides the application of the biodegradable zwitterionic polycarbonate in the preparation of antitumor drugs.

The nano-particles, taking nano-micelles as an example, are prepared by a solvent dialysis displacement method, and the preferable specific steps are as follows: firstly, dissolving the zwitterionic polymer in a mixed solvent of N, N-dimethylformamide and methanol, then filling the mixture into a dialysis bag, and dialyzing the mixture in deionized water or a PB7.4 buffer solution medium, wherein the dialysis medium is periodically replaced.

The zwitterionic nano-micelle has high stability in pH 7.4, and the size of the nano-particles is stable when 10 wt% of BSA is added. The zwitter-ion nano-particle is demonstrated to form a layer of physical and energy barrier through water molecules which are very tightly combined on the surface, so that the capacity of resisting nonspecific adsorption of proteins is obtained.

The zwitter-ion nano micelle obtained by the technical scheme can wrap hydrophobic drugs through hydrophobic effect, and the hydrophobic drugs are selected from paclitaxel and the like.

Preferably, the coating method comprises the steps of dissolving the zwitterionic polymer in a mixed solvent of N, N-dimethylformamide and methanol, adding a hydrophobic drug, filling into a dialysis bag, dialyzing in deionized water or a PB7.4 buffer solution medium, periodically replacing the dialysis medium, and finally dialyzing to remove the mixed solvent and the unencapsulated drug to finally obtain the hydrophobic drug-coated polymer micelle;

the zwitterion nano micelle medicine carrying system can promote the long circulation of the medicine in vivo and has the effect of reducing the immunogenicity.

The invention designs and synthesizes the zwitterion polymers with different molecular weights, and the zwitterion nano-micelle with a certain concentration has stronger stability by detecting the action condition between the polymers with different molecular weights and Bovine Serum Albumin (BSA), thereby promoting the in vivo long circulation of the medicament and reducing the immunogenicity.

The technical effects are as follows: compared with the prior art, the invention provides a preparation method and application of biodegradable zwitterionic polycarbonate, the polymer is simple and easy to synthesize, the polymerization molecular weight is controllable, nano-drugs can be self-assembled, and the biodegradable zwitterionic polycarbonate can be used for treating various diseases such as tumors and inflammations and also can be used for antibacterial stent coatings. Compared with the previous research, the biodegradable polymer has the advantages of simple preparation, strong protein adsorption resistance and immune reaction reduction, and is expected to have wide application prospect in the field of biomedicine.

Drawings

FIG. 1 hydrogen NMR spectra of Polymer 1(PAC) (8k) from example 1;

FIG. 2 shows the hydrogen nuclear magnetic spectrum of intermediate 1(CB) in example 1;

FIG. 3 shows the hydrogen nuclear magnetic spectrum of thiolated zwitterion (TCB) in example 1;

FIG. 4 shows the hydrogen NMR spectrum of the zwitterionic polymer PAC (TCB) (8k) in example 1;

FIG. 5 shows the particle size of the zwitterionic polymer micelle obtained in example 2;

FIG. 6 shows the particle size change of the zwitterionic polymer micelle obtained in example 2 under the condition of 10% wt. bovine serum albumin;

FIG. 7 shows the results of hemolysis test on the zwitterionic polymer micelle obtained in example 2;

FIG. 8 shows the results of the toxicity test of the zwitterionic polymer micelle obtained in example 2 on Hela cells (24h, 48 h).

Detailed Description

The invention is further described with reference to the accompanying drawings and specific examples.